Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 2483 |
| ensemblid | ENSG00000109536.13 |
| hgncid | 3954 |
| symbol | FRG1 |
| name | FSHD region gene 1 |
| refseq_nuc | NM_004477.3 |
| refseq_prot | NP_004468.1 |
| ensembl_nuc | ENST00000226798.9 |
| ensembl_prot | ENSP00000226798.4 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 189940872 |
| end | 189963192 |
| strand | + |
| ver | v1.2 |
| region | chr4:189940872-189963192 |
| region5000 | chr4:189935872-189968192 |
| regionname0 | FRG1_chr4_189940872_189963192 |
| regionname5000 | FRG1_chr4_189935872_189968192 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 258 | 346 | 93 | 56 | 140 | 14 | 42 | 112 | FRG1_chr4_189935872_189968192 | FRG1 | MAEYS others(253): Show |
chr4 | 189935872 | 189968192 |
| a0002 | 0/0 | 258 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | MAEYS others(253): Show |
chr4 | 189935872 | 189968192 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 774 | 155 | 21 | 34 | 65 | 8 | 26 | FRG1_chr4_189935872_189968192 | FRG1 | ATGGC others(769): Show |
chr4 | 189935872 | 189968192 | ||
| a0001c0002 | 0/0 | 774 | 114 | 29 | 16 | 50 | 6 | 13 | FRG1_chr4_189935872_189968192 | FRG1 | ATGGC others(769): Show |
chr4 | 189935872 | 189968192 | ||
| a0001c0003 | 0/0 | 774 | 77 | 43 | 6 | 25 | 0 | 3 | FRG1_chr4_189935872_189968192 | FRG1 | ATGGC others(769): Show |
chr4 | 189935872 | 189968192 | ||
| a0002c0004 | 0/0 | 774 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | ATGGC others(769): Show |
chr4 | 189935872 | 189968192 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 978 | 154 | 21 | 34 | 65 | 8 | 25 | FRG1_chr4_189935872_189968192 | FRG1 | GGGTT others(973): Show |
chr4 | 189935872 | 189968192 |
| a0001c0001t0012 | 0/0 | 978 | 1 | 0 | 0 | 0 | 0 | 1 | FRG1_chr4_189935872_189968192 | FRG1 | GGGTT others(973): Show |
chr4 | 189935872 | 189968192 |
| a0001c0002t0002 | 0/0 | 978 | 68 | 20 | 14 | 18 | 5 | 11 | FRG1_chr4_189935872_189968192 | FRG1 | GGGTT others(973): Show |
chr4 | 189935872 | 189968192 |
| a0001c0002t0004 | 0/0 | 978 | 36 | 2 | 2 | 30 | 1 | 1 | FRG1_chr4_189935872_189968192 | FRG1 | GGGTT others(973): Show |
chr4 | 189935872 | 189968192 |
| a0001c0002t0006 | 0/0 | 978 | 5 | 5 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | GGGTT others(973): Show |
chr4 | 189935872 | 189968192 |
| a0001c0002t0008 | 0/0 | 978 | 2 | 0 | 0 | 2 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | GGGTT others(973): Show |
chr4 | 189935872 | 189968192 |
| a0001c0002t0010 | 0/0 | 978 | 1 | 0 | 0 | 0 | 0 | 1 | FRG1_chr4_189935872_189968192 | FRG1 | GGGTT others(973): Show |
chr4 | 189935872 | 189968192 |
| a0001c0002t0011 | 0/0 | 978 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | GGGTT others(973): Show |
chr4 | 189935872 | 189968192 |
| a0001c0002t0013 | 0/0 | 978 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | GGGTT others(973): Show |
chr4 | 189935872 | 189968192 |
| a0001c0003t0002 | 0/0 | 978 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | GGGTT others(973): Show |
chr4 | 189935872 | 189968192 |
| a0001c0003t0003 | 0/0 | 978 | 39 | 13 | 1 | 25 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | GGGTT others(973): Show |
chr4 | 189935872 | 189968192 |
| a0001c0003t0005 | 0/0 | 978 | 30 | 23 | 4 | 0 | 0 | 3 | FRG1_chr4_189935872_189968192 | FRG1 | GGGTT others(973): Show |
chr4 | 189935872 | 189968192 |
| a0001c0003t0007 | 0/0 | 978 | 5 | 4 | 1 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | GGGTT others(973): Show |
chr4 | 189935872 | 189968192 |
| a0001c0003t0009 | 0/0 | 978 | 2 | 2 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | GGGTT others(973): Show |
chr4 | 189935872 | 189968192 |
| a0002c0004t0005 | 0/0 | 978 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | GGGTT others(973): Show |
chr4 | 189935872 | 189968192 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 65 | 1 | 12 | 40 | 3 | 9 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0001t0001g0004 | 0/0 | 8 | 6 | 2 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0001t0001g0006 | 0/0 | 6 | 1 | 2 | 2 | 1 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0001t0001g0007 | 0/0 | 6 | 0 | 0 | 3 | 0 | 3 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0001t0001g0009 | 0/0 | 5 | 1 | 2 | 0 | 1 | 1 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0001t0001g0012 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0001t0001g0013 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0001t0001g0081 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0001t0012g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0002t0002g0002 | 0/0 | 32 | 5 | 10 | 5 | 4 | 8 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0002t0002g0005 | 0/0 | 8 | 0 | 0 | 7 | 0 | 1 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0002t0002g0015 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0002t0002g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0002t0002g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0002t0002g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0002t0002g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0002t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0002t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0002t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0002t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0002t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0002t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0002t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0002t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0002t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0002t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0002t0004g0002 | 0/0 | 18 | 2 | 1 | 13 | 1 | 1 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0002t0004g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0002t0004g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0002t0004g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0002t0004g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0002t0004g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0002t0004g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0002t0004g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0002t0004g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0002t0004g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0002t0004g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0002t0004g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0002t0004g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0002t0006g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0002t0006g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0002t0006g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0002t0006g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0002t0008g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0002t0010g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0002t0011g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0002t0013g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0003t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0003t0003g0003 | 0/0 | 30 | 8 | 0 | 22 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0003t0003g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0003t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0003t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0003t0003g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0003t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0003t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0003t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0003t0003g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0003t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0003t0005g0008 | 0/0 | 6 | 3 | 3 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0003t0005g0010 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0003t0005g0011 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0003t0005g0019 | 0/0 | 3 | 1 | 0 | 0 | 0 | 2 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0003t0005g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0003t0005g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0003t0005g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0003t0005g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0003t0005g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0003t0005g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0003t0005g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0003t0005g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0003t0007g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0003t0007g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0003t0007g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0001c0003t0009g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| a0002c0004t0005g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | GBR | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0030 | EUR | GBR | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0073 | EUR | GBR | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | GBR | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0012 | EUR | FIN | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG00280 | hp2 | a0001 | c0002 | t0002 | g0002 | EUR | FIN | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG00408 | hp2 | a0001 | c0002 | t0004 | g0002 | EAS | CHS | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG00438 | hp1 | a0001 | c0002 | t0004 | g0110 | EAS | CHS | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG00544 | hp1 | a0001 | c0002 | t0002 | g0102 | EAS | CHS | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | CHS | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG00558 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | CHS | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG00558 | hp2 | a0001 | c0002 | t0004 | g0117 | EAS | CHS | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG00597 | hp1 | a0001 | c0002 | t0004 | g0002 | EAS | CHS | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG00621 | hp2 | a0001 | c0002 | t0004 | g0002 | EAS | CHS | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG00639 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PUR | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG00642 | hp2 | a0001 | c0002 | t0004 | g0037 | AMR | PUR | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG00733 | hp2 | a0001 | c0002 | t0002 | g0115 | AMR | PUR | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG00735 | hp2 | a0001 | c0003 | t0007 | g0063 | AMR | PUR | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG00741 | hp1 | a0001 | c0003 | t0005 | g0008 | AMR | PUR | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG01069 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PUR | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG01070 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PUR | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG01071 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | PUR | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG01071 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PUR | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG01081 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | PUR | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG01081 | hp2 | a0001 | c0003 | t0005 | g0010 | AMR | PUR | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG01099 | hp1 | a0001 | c0003 | t0005 | g0008 | AMR | PUR | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG01109 | hp1 | a0001 | c0003 | t0005 | g0008 | AMR | PUR | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG01168 | hp1 | a0001 | c0002 | t0002 | g0015 | AMR | PUR | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG01168 | hp2 | a0001 | c0002 | t0002 | g0111 | AMR | PUR | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG01175 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PUR | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG01243 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PUR | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | CLM | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG01358 | hp1 | a0001 | c0002 | t0002 | g0104 | AMR | CLM | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG01358 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | CLM | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | CLM | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG01361 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | CLM | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG01496 | hp1 | a0001 | c0002 | t0004 | g0002 | AMR | CLM | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG01515 | hp1 | a0001 | c0002 | t0002 | g0002 | EUR | IBS | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG01516 | hp1 | a0001 | c0002 | t0002 | g0002 | EUR | IBS | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG01517 | hp2 | a0001 | c0002 | t0002 | g0002 | EUR | IBS | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG01884 | hp1 | a0001 | c0003 | t0005 | g0084 | AFR | ACB | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG01884 | hp2 | a0001 | c0002 | t0002 | g0105 | AFR | ACB | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG01891 | hp1 | a0001 | c0003 | t0005 | g0011 | AFR | ACB | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG01891 | hp2 | a0001 | c0003 | t0003 | g0003 | AFR | ACB | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PEL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG01934 | hp2 | a0001 | c0003 | t0003 | g0061 | AMR | PEL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PEL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG02015 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | KHV | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG02055 | hp1 | a0001 | c0003 | t0005 | g0008 | AFR | ACB | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG02055 | hp2 | a0001 | c0002 | t0002 | g0116 | AFR | ACB | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG02056 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | KHV | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG02083 | hp2 | a0001 | c0002 | t0004 | g0107 | EAS | KHV | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG02129 | hp1 | a0001 | c0002 | t0004 | g0002 | EAS | KHV | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG02132 | hp2 | a0001 | c0002 | t0004 | g0002 | EAS | KHV | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | ACB | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG02155 | hp2 | a0001 | c0002 | t0002 | g0039 | EAS | CDX | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG02257 | hp1 | a0001 | c0003 | t0005 | g0008 | AFR | ACB | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG02257 | hp2 | a0001 | c0002 | t0002 | g0015 | AFR | ACB | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG02258 | hp1 | a0001 | c0002 | t0006 | g0022 | AFR | ACB | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG02258 | hp2 | a0001 | c0003 | t0002 | g0096 | AFR | ACB | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG02280 | hp1 | a0001 | c0003 | t0003 | g0003 | AFR | ACB | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | ACB | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG02451 | hp2 | a0001 | c0002 | t0002 | g0015 | AFR | ACB | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG02523 | hp1 | a0001 | c0003 | t0003 | g0003 | EAS | KHV | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG02572 | hp1 | a0001 | c0003 | t0003 | g0003 | AFR | GWD | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG02572 | hp2 | a0001 | c0003 | t0005 | g0091 | AFR | GWD | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG02615 | hp1 | a0001 | c0002 | t0002 | g0097 | AFR | GWD | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG02615 | hp2 | a0001 | c0003 | t0003 | g0049 | AFR | GWD | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG02622 | hp1 | a0001 | c0003 | t0003 | g0058 | AFR | GWD | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG02622 | hp2 | a0001 | c0002 | t0002 | g0002 | AFR | GWD | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG02647 | hp1 | a0001 | c0002 | t0002 | g0113 | AFR | GWD | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG02647 | hp2 | a0001 | c0003 | t0009 | g0023 | AFR | GWD | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG02683 | hp1 | a0001 | c0002 | t0002 | g0002 | SAS | PJL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG02698 | hp1 | a0001 | c0002 | t0002 | g0100 | SAS | PJL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG02723 | hp1 | a0001 | c0003 | t0007 | g0016 | AFR | GWD | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG02723 | hp2 | a0001 | c0003 | t0005 | g0010 | AFR | GWD | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG02735 | hp2 | a0001 | c0002 | t0002 | g0037 | SAS | PJL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG02809 | hp1 | a0001 | c0002 | t0002 | g0114 | AFR | GWD | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG02809 | hp2 | a0001 | c0003 | t0005 | g0034 | AFR | GWD | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG02818 | hp1 | a0001 | c0003 | t0007 | g0016 | AFR | GWD | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG02818 | hp2 | a0001 | c0002 | t0004 | g0002 | AFR | GWD | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG02886 | hp1 | a0001 | c0003 | t0005 | g0011 | AFR | GWD | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG02895 | hp1 | a0001 | c0002 | t0002 | g0020 | AFR | GWD | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG02895 | hp2 | a0001 | c0002 | t0002 | g0015 | AFR | GWD | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG02897 | hp2 | a0001 | c0002 | t0002 | g0020 | AFR | GWD | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG02922 | hp1 | a0001 | c0003 | t0005 | g0011 | AFR | ESN | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG02922 | hp2 | a0001 | c0003 | t0007 | g0016 | AFR | ESN | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG02965 | hp1 | a0001 | c0002 | t0002 | g0099 | AFR | ESN | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG02965 | hp2 | a0001 | c0002 | t0002 | g0038 | AFR | ESN | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | ESN | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG02970 | hp2 | a0001 | c0002 | t0002 | g0112 | AFR | ESN | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG02976 | hp1 | a0001 | c0002 | t0011 | g0041 | AFR | ESN | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG02976 | hp2 | a0001 | c0003 | t0005 | g0036 | AFR | ESN | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG03017 | hp2 | a0001 | c0002 | t0002 | g0002 | SAS | PJL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG03098 | hp1 | a0001 | c0002 | t0006 | g0044 | AFR | MSL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG03098 | hp2 | a0001 | c0003 | t0005 | g0008 | AFR | MSL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG03130 | hp1 | a0001 | c0003 | t0005 | g0010 | AFR | ESN | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG03139 | hp1 | a0002 | c0004 | t0005 | g0092 | AFR | ESN | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG03139 | hp2 | a0001 | c0003 | t0003 | g0003 | AFR | ESN | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG03195 | hp1 | a0001 | c0003 | t0003 | g0003 | AFR | ESN | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG03195 | hp2 | a0001 | c0002 | t0006 | g0042 | AFR | ESN | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG03209 | hp1 | a0001 | c0002 | t0006 | g0022 | AFR | MSL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG03209 | hp2 | a0001 | c0002 | t0002 | g0002 | AFR | MSL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG03225 | hp1 | a0001 | c0002 | t0013 | g0045 | AFR | MSL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG03239 | hp2 | a0001 | c0002 | t0002 | g0002 | SAS | PJL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG03453 | hp1 | a0001 | c0003 | t0005 | g0034 | AFR | MSL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG03453 | hp2 | a0001 | c0003 | t0005 | g0035 | AFR | MSL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG03486 | hp1 | a0001 | c0003 | t0005 | g0085 | AFR | MSL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG03486 | hp2 | a0001 | c0003 | t0003 | g0003 | AFR | MSL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG03491 | hp2 | a0001 | c0002 | t0002 | g0002 | SAS | PJL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG03492 | hp1 | a0001 | c0002 | t0002 | g0002 | SAS | PJL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG03516 | hp1 | a0001 | c0003 | t0005 | g0035 | AFR | ESN | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | ESN | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG03540 | hp2 | a0001 | c0002 | t0004 | g0002 | AFR | GWD | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG03579 | hp2 | a0001 | c0003 | t0005 | g0052 | AFR | MSL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG03654 | hp2 | a0001 | c0002 | t0010 | g0094 | SAS | PJL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG03688 | hp2 | a0001 | c0003 | t0005 | g0019 | SAS | STU | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG03710 | hp1 | a0001 | c0002 | t0002 | g0005 | SAS | PJL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG03831 | hp1 | a0001 | c0001 | t0012 | g0001 | SAS | BEB | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG03831 | hp2 | a0001 | c0002 | t0002 | g0002 | SAS | BEB | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG03834 | hp1 | a0001 | c0003 | t0005 | g0019 | SAS | BEB | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | BEB | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | BEB | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG03942 | hp2 | a0001 | c0003 | t0005 | g0090 | SAS | BEB | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG04115 | hp1 | a0001 | c0002 | t0002 | g0002 | SAS | STU | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | BEB | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | STU | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | STU | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG04204 | hp2 | a0001 | c0002 | t0004 | g0002 | SAS | STU | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | STU | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA18522 | hp1 | a0001 | c0003 | t0005 | g0010 | AFR | YRI | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA18522 | hp2 | a0001 | c0003 | t0003 | g0003 | AFR | YRI | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | CHB | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | CHB | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA18906 | hp1 | a0001 | c0003 | t0003 | g0050 | AFR | YRI | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA18906 | hp2 | a0001 | c0002 | t0002 | g0002 | AFR | YRI | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA18941 | hp2 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA18942 | hp1 | a0001 | c0002 | t0004 | g0118 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA18945 | hp1 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA18947 | hp2 | a0001 | c0002 | t0004 | g0014 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA18948 | hp1 | a0001 | c0002 | t0002 | g0106 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA18948 | hp2 | a0001 | c0002 | t0004 | g0046 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA18952 | hp2 | a0001 | c0002 | t0004 | g0002 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA18954 | hp1 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA18956 | hp1 | a0001 | c0002 | t0004 | g0021 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA18957 | hp1 | a0001 | c0002 | t0008 | g0002 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA18959 | hp2 | a0001 | c0002 | t0004 | g0002 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA18960 | hp2 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA18962 | hp1 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA18964 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA18965 | hp2 | a0001 | c0002 | t0004 | g0014 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA18966 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA18967 | hp1 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA18968 | hp1 | a0001 | c0002 | t0004 | g0108 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA18969 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA18970 | hp2 | a0001 | c0002 | t0004 | g0021 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA18972 | hp2 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA18973 | hp2 | a0001 | c0002 | t0002 | g0109 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA18974 | hp1 | a0001 | c0002 | t0004 | g0021 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA18975 | hp2 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA18979 | hp1 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA18980 | hp1 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA18981 | hp1 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA18981 | hp2 | a0001 | c0002 | t0004 | g0014 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA18982 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA18985 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA18988 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA18992 | hp2 | a0001 | c0002 | t0002 | g0039 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA18994 | hp1 | a0001 | c0003 | t0003 | g0060 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA18995 | hp2 | a0001 | c0002 | t0004 | g0002 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA18999 | hp1 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA19000 | hp1 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA19000 | hp2 | a0001 | c0002 | t0004 | g0002 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA19002 | hp2 | a0001 | c0002 | t0004 | g0095 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA19003 | hp2 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA19004 | hp2 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA19006 | hp1 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA19009 | hp1 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA19012 | hp1 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | LWK | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA19030 | hp2 | a0001 | c0003 | t0005 | g0010 | AFR | LWK | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA19043 | hp1 | a0001 | c0002 | t0002 | g0002 | AFR | LWK | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA19043 | hp2 | a0001 | c0002 | t0006 | g0043 | AFR | LWK | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA19054 | hp1 | a0001 | c0002 | t0004 | g0040 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA19054 | hp2 | a0001 | c0003 | t0003 | g0062 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA19056 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA19065 | hp1 | a0001 | c0002 | t0004 | g0014 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA19065 | hp2 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA19068 | hp1 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA19068 | hp2 | a0001 | c0002 | t0008 | g0002 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA19075 | hp1 | a0001 | c0002 | t0004 | g0103 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA19075 | hp2 | a0001 | c0002 | t0004 | g0002 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA19079 | hp2 | a0001 | c0002 | t0004 | g0002 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA19081 | hp2 | a0001 | c0003 | t0003 | g0003 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA19082 | hp1 | a0001 | c0002 | t0004 | g0002 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA19083 | hp2 | a0001 | c0002 | t0004 | g0002 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA19084 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA19085 | hp2 | a0001 | c0002 | t0002 | g0098 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA19090 | hp1 | a0001 | c0002 | t0004 | g0040 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA19090 | hp2 | a0001 | c0003 | t0003 | g0059 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA19240 | hp1 | a0001 | c0003 | t0007 | g0089 | AFR | YRI | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA19240 | hp2 | a0001 | c0002 | t0002 | g0038 | AFR | YRI | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA20129 | hp1 | a0001 | c0003 | t0009 | g0023 | AFR | ASW | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA20129 | hp2 | a0001 | c0003 | t0003 | g0048 | AFR | ASW | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA20805 | hp1 | a0001 | c0002 | t0004 | g0002 | EUR | TSI | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA20805 | hp2 | a0001 | c0002 | t0002 | g0101 | EUR | TSI | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA20905 | hp1 | a0001 | c0002 | t0002 | g0002 | SAS | GIH | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0069 | SAS | GIH | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | ACB | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG02486 | hp2 | a0001 | c0003 | t0003 | g0055 | AFR | ACB | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG02559 | hp1 | a0001 | c0002 | t0002 | g0002 | AFR | ACB | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG02559 | hp2 | a0001 | c0003 | t0005 | g0036 | AFR | ACB | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG03471 | hp1 | a0001 | c0003 | t0003 | g0003 | AFR | MSL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG03471 | hp2 | a0001 | c0003 | t0005 | g0011 | AFR | MSL | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | USA | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| HG06807 | hp2 | a0001 | c0003 | t0005 | g0011 | AFR | USA | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA18955 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | USA | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA21309 | hp1 | a0001 | c0003 | t0005 | g0019 | AFR | LWK | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| NA21309 | hp2 | a0001 | c0002 | t0002 | g0020 | AFR | LWK | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0081 | REF | REF | FRG1_chr4_189935872_189968192 | FRG1 | chr4 | 189935872 | 189968192 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:189961868 | G | A | 1 | a0002 | 1 | HG03139.hp1 | missense_variant | MODERATE | c.676G>A | p.Glu226Lys | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 8/9 | 814/978 | 676/777 | 226/258 | chr4 | 189961868 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:189941027 | C | T | 3 | a0001c0002 a0001c0003 a0002c0004 |
192 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(189): Show |
synonymous_variant | LOW | c.18C>T | p.Tyr6Tyr | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/9 | 156/978 | 18/777 | 6/258 | chr4 | 189941027 | |||
| chr4:189955040 | C | T | 1 | a0001c0002 | 114 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(111): Show |
synonymous_variant | LOW | c.321C>T | p.Ile107Ile | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 5/9 | 459/978 | 321/777 | 107/258 | chr4 | 189955040 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:189940880 | C | G | 5 | a0001c0003t0003 a0001c0003t0005 a0001c0003t0007 others(2): Show |
77 | HG00735.hp2 HG00741.hp1 HG01081.hp2 others(74): Show |
5_prime_UTR_variant | MODIFIER | c.-130C>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/9 | 130 | chr4 | 189940880 | ||||||
| chr4:189940887 | G | A | 2 | a0001c0003t0005 a0002c0004t0005 |
31 | HG00741.hp1 HG01081.hp2 HG01099.hp1 others(28): Show |
5_prime_UTR_variant | MODIFIER | c.-123G>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/9 | 123 | chr4 | 189940887 | ||||||
| chr4:189940892 | C | T | 1 | a0001c0002t0013 | 1 | HG03225.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-118C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/9 | chr4 | 189940892 | |||||||
| chr4:189940923 | C | T | 1 | a0001c0002t0008 | 2 | NA18957.hp1 NA19068.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-87C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/9 | chr4 | 189940923 | |||||||
| chr4:189940928 | T | C | 13 | a0001c0002t0002 a0001c0002t0004 a0001c0002t0006 others(10): Show |
192 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(189): Show |
5_prime_UTR_variant | MODIFIER | c.-82T>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/9 | 82 | chr4 | 189940928 | ||||||
| chr4:189940929 | C | G | 5 | a0001c0003t0003 a0001c0003t0005 a0001c0003t0007 others(2): Show |
77 | HG00735.hp2 HG00741.hp1 HG01081.hp2 others(74): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-81C>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/9 | chr4 | 189940929 | |||||||
| chr4:189940948 | C | T | 6 | a0001c0002t0004 a0001c0002t0011 a0001c0003t0003 others(3): Show |
109 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(106): Show |
5_prime_UTR_variant | MODIFIER | c.-62C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/9 | 62 | chr4 | 189940948 | ||||||
| chr4:189940949 | C | G | 1 | a0001c0002t0010 | 1 | HG03654.hp2 | 5_prime_UTR_variant | MODIFIER | c.-61C>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/9 | 61 | chr4 | 189940949 | ||||||
| chr4:189940949 | C | T | 1 | a0001c0002t0013 | 1 | HG03225.hp1 | 5_prime_UTR_variant | MODIFIER | c.-61C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/9 | 61 | chr4 | 189940949 | ||||||
| chr4:189940971 | A | G | 5 | a0001c0003t0003 a0001c0003t0005 a0001c0003t0007 others(2): Show |
77 | HG00735.hp2 HG00741.hp1 HG01081.hp2 others(74): Show |
5_prime_UTR_variant | MODIFIER | c.-39A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/9 | 39 | chr4 | 189940971 | ||||||
| chr4:189940983 | C | T | 1 | a0001c0003t0009 | 2 | HG02647.hp2 NA20129.hp1 |
5_prime_UTR_variant | MODIFIER | c.-27C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/9 | 27 | chr4 | 189940983 | ||||||
| chr4:189940987 | C | T | 5 | a0001c0003t0003 a0001c0003t0005 a0001c0003t0007 others(2): Show |
77 | HG00735.hp2 HG00741.hp1 HG01081.hp2 others(74): Show |
5_prime_UTR_variant | MODIFIER | c.-23C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/9 | 23 | chr4 | 189940987 | ||||||
| chr4:189940996 | A | C | 1 | a0001c0002t0006 | 5 | HG02258.hp1 HG03098.hp1 HG03195.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-14A>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/9 | 14 | chr4 | 189940996 | ||||||
| chr4:189940999 | T | C | 5 | a0001c0003t0003 a0001c0003t0005 a0001c0003t0007 others(2): Show |
77 | HG00735.hp2 HG00741.hp1 HG01081.hp2 others(74): Show |
5_prime_UTR_variant | MODIFIER | c.-11T>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/9 | 11 | chr4 | 189940999 | ||||||
| chr4:189941000 | T | G | 5 | a0001c0002t0002 a0001c0002t0004 a0001c0002t0008 others(2): Show |
108 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(105): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-10T>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/9 | chr4 | 189941000 | |||||||
| chr4:189941009 | C | T | 1 | a0001c0001t0012 | 1 | HG03831.hp1 | 5_prime_UTR_variant | MODIFIER | c.-1C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/9 | 1 | chr4 | 189941009 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:189941132 | C | T | 37 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0015 others(34): Show |
106 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.62+61C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/8 | chr4 | 189941132 | |||||||
| chr4:189941222 | C | T | 1 | a0001c0002t0010g0094 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.62+151C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/8 | chr4 | 189941222 | |||||||
| chr4:189941271 | A | G | 1 | a0001c0002t0004g0021 | 3 | NA18956.hp1 NA18970.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.62+200A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/8 | chr4 | 189941271 | |||||||
| chr4:189941291 | G | A | 1 | a0001c0002t0004g0095 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.62+220G>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/8 | chr4 | 189941291 | |||||||
| chr4:189941356 | G | A | 43 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0015 others(40): Show |
113 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.62+285G>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/8 | chr4 | 189941356 | |||||||
| chr4:189941402 | C | T | 1 | a0001c0003t0009g0023 | 2 | HG02647.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.62+331C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/8 | chr4 | 189941402 | |||||||
| chr4:189941434 | C | T | 5 | a0001c0002t0002g0015 a0001c0002t0002g0113 a0001c0002t0002g0114 others(2): Show |
8 | HG00733.hp2 HG01168.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.62+363C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/8 | chr4 | 189941434 | |||||||
| chr4:189941554 | C | G | 1 | a0001c0001t0001g0093 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.62+483C>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/8 | chr4 | 189941554 | |||||||
| chr4:189941637 | T | C | 2 | a0001c0002t0002g0037 a0001c0002t0004g0037 |
2 | HG00642.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.62+566T>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/8 | chr4 | 189941637 | |||||||
| chr4:189941643 | C | T | 1 | a0001c0002t0002g0112 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.62+572C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/8 | chr4 | 189941643 | |||||||
| chr4:189941726 | A | G | 3 | a0001c0003t0005g0008 a0001c0003t0005g0091 a0002c0004t0005g0092 |
8 | HG00741.hp1 HG01099.hp1 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.62+655A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/8 | chr4 | 189941726 | |||||||
| chr4:189941813 | G | C | 1 | a0001c0001t0001g0047 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.62+742G>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/8 | chr4 | 189941813 | |||||||
| chr4:189941872 | T | C | 1 | a0001c0001t0001g0012 | 4 | HG00280.hp1 HG00639.hp1 HG01069.hp1 others(1): Show |
intron_variant | MODIFIER | c.62+801T>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/8 | chr4 | 189941872 | |||||||
| chr4:189941972 | C | G | 39 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0015 others(36): Show |
108 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.62+901C>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/8 | chr4 | 189941972 | |||||||
| chr4:189942067 | T | A | 3 | a0001c0003t0003g0048 a0001c0003t0003g0049 a0001c0003t0003g0050 |
3 | HG02615.hp2 NA18906.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.62+996T>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/8 | chr4 | 189942067 | |||||||
| chr4:189942442 | T | G | 1 | a0001c0002t0002g0112 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.63-760T>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/8 | chr4 | 189942442 | |||||||
| chr4:189942443 | C | T | 1 | a0001c0002t0002g0112 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.63-759C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/8 | chr4 | 189942443 | |||||||
| chr4:189942505 | A | G | 1 | a0001c0003t0005g0036 | 2 | HG02559.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.63-697A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/8 | chr4 | 189942505 | |||||||
| chr4:189942563 | T | C | 1 | a0001c0001t0001g0051 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.63-639T>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/8 | chr4 | 189942563 | |||||||
| chr4:189942567 | A | G | 1 | a0001c0003t0005g0090 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.63-635A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/8 | chr4 | 189942567 | |||||||
| chr4:189942587 | T | A | 45 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0015 others(42): Show |
115 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.63-615T>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/8 | chr4 | 189942587 | |||||||
| chr4:189942688 | G | A | 1 | a0001c0003t0005g0052 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.63-514G>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/8 | chr4 | 189942688 | |||||||
| chr4:189942860 | C | A | 39 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0015 others(36): Show |
108 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.63-342C>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/8 | chr4 | 189942860 | |||||||
| chr4:189942930 | C | G | 1 | a0001c0002t0002g0112 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.63-272C>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/8 | chr4 | 189942930 | |||||||
| chr4:189942978 | A | G | 1 | a0001c0003t0009g0023 | 2 | HG02647.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.63-224A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/8 | chr4 | 189942978 | |||||||
| chr4:189942997 | C | T | 4 | a0001c0002t0006g0022 a0001c0002t0006g0042 a0001c0002t0006g0043 others(1): Show |
5 | HG02258.hp1 HG03098.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.63-205C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 1/8 | chr4 | 189942997 | |||||||
| chr4:189943355 | T | G | 2 | a0001c0001t0001g0024 a0001c0001t0001g0053 |
3 | NA18950.hp1 NA18967.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.133+83T>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189943355 | |||||||
| chr4:189943388 | A | G | 1 | a0001c0003t0007g0089 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.133+116A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189943388 | |||||||
| chr4:189943487 | G | A | 2 | a0001c0001t0001g0025 a0001c0001t0001g0054 |
3 | NA18972.hp1 NA18980.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.133+215G>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189943487 | |||||||
| chr4:189943499 | A | G | 1 | a0001c0002t0002g0039 | 2 | HG02155.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.133+227A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189943499 | |||||||
| chr4:189943777 | G | A | 1 | a0001c0003t0002g0096 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.133+505G>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189943777 | |||||||
| chr4:189943798 | A | T | 44 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0015 others(41): Show |
114 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.133+526A>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189943798 | |||||||
| chr4:189943882 | A | G | 1 | a0001c0001t0001g0088 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.133+610A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189943882 | |||||||
| chr4:189943998 | G | C | 1 | a0001c0002t0010g0094 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.133+726G>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189943998 | |||||||
| chr4:189944133 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.133+861C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189944133 | |||||||
| chr4:189944240 | G | A | 44 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0015 others(41): Show |
114 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.133+968G>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189944240 | |||||||
| chr4:189944241 | A | G | 1 | a0001c0002t0010g0094 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.133+969A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189944241 | |||||||
| chr4:189944246 | G | A | 1 | a0001c0002t0010g0094 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.133+974G>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189944246 | |||||||
| chr4:189944613 | CT | C | 44 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0015 others(41): Show |
114 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.133+1352delT | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 189944613 | ||||||
| chr4:189944721 | G | A | 1 | a0001c0001t0001g0026 | 2 | NA18950.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.133+1449G>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189944721 | |||||||
| chr4:189944773 | G | C | 38 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0015 others(35): Show |
107 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.133+1501G>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189944773 | |||||||
| chr4:189944895 | T | A | 1 | a0001c0001t0001g0087 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.133+1623T>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189944895 | |||||||
| chr4:189944941 | A | C | 44 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0015 others(41): Show |
114 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.133+1669A>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189944941 | |||||||
| chr4:189945043 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.133+1771C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189945043 | |||||||
| chr4:189945243 | T | A | 3 | a0001c0003t0003g0048 a0001c0003t0003g0049 a0001c0003t0003g0050 |
3 | HG02615.hp2 NA18906.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.133+1971T>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189945243 | |||||||
| chr4:189945257 | T | C | 1 | a0001c0003t0005g0036 | 2 | HG02559.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.133+1985T>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189945257 | |||||||
| chr4:189945376 | C | T | 1 | a0001c0002t0002g0111 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.133+2104C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189945376 | |||||||
| chr4:189945386 | A | G | 13 | a0001c0003t0005g0008 a0001c0003t0005g0010 a0001c0003t0005g0011 others(10): Show |
31 | HG00741.hp1 HG01081.hp2 HG01099.hp1 others(28): Show |
intron_variant | MODIFIER | c.133+2114A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189945386 | |||||||
| chr4:189945400 | C | T | 44 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0015 others(41): Show |
114 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.133+2128C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189945400 | |||||||
| chr4:189945463 | T | C | 1 | a0001c0003t0003g0055 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.133+2191T>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189945463 | |||||||
| chr4:189945526 | C | T | 1 | a0001c0001t0001g0083 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.133+2254C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189945526 | |||||||
| chr4:189945608 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.133+2336C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189945608 | |||||||
| chr4:189945609 | G | C | 1 | a0001c0001t0001g0056 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.133+2337G>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189945609 | |||||||
| chr4:189945698 | A | G | 1 | a0001c0001t0001g0009 | 5 | HG00140.hp2 HG01070.hp1 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.133+2426A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189945698 | |||||||
| chr4:189945773 | A | C | 4 | a0001c0002t0006g0022 a0001c0002t0006g0042 a0001c0002t0006g0043 others(1): Show |
5 | HG02258.hp1 HG03098.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.133+2501A>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189945773 | |||||||
| chr4:189945852 | T | C | 2 | a0001c0003t0005g0010 a0001c0003t0005g0084 |
6 | HG01081.hp2 HG01884.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.133+2580T>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189945852 | |||||||
| chr4:189946175 | C | T | 44 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0015 others(41): Show |
114 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.133+2903C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189946175 | |||||||
| chr4:189946280 | CATAAA | C | 44 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0015 others(41): Show |
114 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.133+3012_133+3016d others(7): Show |
FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 189946280 | ||||||
| chr4:189946286 | A | G | 1 | a0001c0001t0001g0080 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.133+3014A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189946286 | |||||||
| chr4:189946311 | C | CAA | 9 | a0001c0002t0002g0106 a0001c0002t0004g0046 a0001c0002t0004g0107 others(6): Show |
10 | HG02083.hp2 HG02258.hp1 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.133+3053_133+3054d others(4): Show |
FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 189946311 | ||||||
| chr4:189946311 | C | CAAA | 31 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0015 others(28): Show |
100 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.133+3052_133+3054d others(5): Show |
FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 189946311 | ||||||
| chr4:189946336 | T | C | 1 | a0001c0002t0006g0042 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.133+3064T>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189946336 | |||||||
| chr4:189946395 | G | T | 1 | a0001c0001t0001g0051 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.133+3123G>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189946395 | |||||||
| chr4:189946672 | G | A | 1 | a0001c0001t0001g0027 | 2 | NA19060.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.133+3400G>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189946672 | |||||||
| chr4:189946709 | T | C | 4 | a0001c0002t0006g0022 a0001c0002t0006g0042 a0001c0002t0006g0043 others(1): Show |
5 | HG02258.hp1 HG03098.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.133+3437T>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189946709 | |||||||
| chr4:189946714 | A | G | 1 | a0001c0002t0010g0094 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.133+3442A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189946714 | |||||||
| chr4:189946783 | T | C | 1 | a0001c0001t0001g0057 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.133+3511T>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189946783 | |||||||
| chr4:189946845 | G | T | 43 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0015 others(40): Show |
110 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.133+3573G>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189946845 | |||||||
| chr4:189947099 | T | G | 67 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0015 others(64): Show |
185 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(182): Show |
intron_variant | MODIFIER | c.133+3827T>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189947099 | |||||||
| chr4:189947143 | G | A | 1 | a0001c0001t0001g0051 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.133+3871G>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189947143 | |||||||
| chr4:189947146 | C | A | 1 | a0001c0003t0003g0048 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.133+3874C>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189947146 | |||||||
| chr4:189947241 | A | G | 1 | a0001c0001t0001g0012 | 4 | HG00280.hp1 HG00639.hp1 HG01069.hp1 others(1): Show |
intron_variant | MODIFIER | c.133+3969A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189947241 | |||||||
| chr4:189947246 | T | G | 72 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0015 others(69): Show |
192 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(189): Show |
intron_variant | MODIFIER | c.133+3974T>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189947246 | |||||||
| chr4:189947252 | T | C | 13 | a0001c0003t0005g0008 a0001c0003t0005g0010 a0001c0003t0005g0011 others(10): Show |
31 | HG00741.hp1 HG01081.hp2 HG01099.hp1 others(28): Show |
intron_variant | MODIFIER | c.133+3980T>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189947252 | |||||||
| chr4:189947286 | T | C | 1 | a0001c0003t0009g0023 | 2 | HG02647.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.133+4014T>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189947286 | |||||||
| chr4:189947321 | C | T | 71 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0015 others(68): Show |
191 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(188): Show |
intron_variant | MODIFIER | c.133+4049C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189947321 | |||||||
| chr4:189947322 | G | C | 71 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0015 others(68): Show |
191 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(188): Show |
intron_variant | MODIFIER | c.133+4050G>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189947322 | |||||||
| chr4:189947324 | C | CATAAG | 71 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0015 others(68): Show |
191 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(188): Show |
intron_variant | MODIFIER | c.133+4054_133+4055i others(7): Show |
FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 189947324 | ||||||
| chr4:189947442 | C | A | 7 | a0001c0003t0003g0003 a0001c0003t0003g0055 a0001c0003t0003g0058 others(4): Show |
36 | HG01891.hp2 HG01934.hp2 HG02280.hp1 others(33): Show |
intron_variant | MODIFIER | c.133+4170C>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189947442 | |||||||
| chr4:189947478 | G | A | 3 | a0001c0003t0005g0008 a0001c0003t0005g0091 a0002c0004t0005g0092 |
8 | HG00741.hp1 HG01099.hp1 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.133+4206G>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189947478 | |||||||
| chr4:189947703 | C | G | 9 | a0001c0003t0003g0003 a0001c0003t0003g0048 a0001c0003t0003g0050 others(6): Show |
38 | HG01891.hp2 HG01934.hp2 HG02280.hp1 others(35): Show |
intron_variant | MODIFIER | c.133+4431C>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189947703 | |||||||
| chr4:189947718 | A | G | 14 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0012 others(11): Show |
32 | HG00280.hp1 HG00639.hp1 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.134-4444A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189947718 | |||||||
| chr4:189947764 | T | C | 4 | a0001c0002t0006g0022 a0001c0002t0006g0042 a0001c0002t0006g0043 others(1): Show |
5 | HG02258.hp1 HG03098.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.134-4398T>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189947764 | |||||||
| chr4:189947915 | C | G | 68 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0015 others(65): Show |
186 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(183): Show |
intron_variant | MODIFIER | c.134-4247C>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189947915 | |||||||
| chr4:189948092 | G | A | 1 | a0001c0002t0002g0097 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.134-4070G>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189948092 | |||||||
| chr4:189948118 | G | T | 44 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0015 others(41): Show |
114 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.134-4044G>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189948118 | |||||||
| chr4:189948206 | T | G | 10 | a0001c0003t0003g0003 a0001c0003t0003g0048 a0001c0003t0003g0049 others(7): Show |
39 | HG01891.hp2 HG01934.hp2 HG02280.hp1 others(36): Show |
intron_variant | MODIFIER | c.134-3956T>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189948206 | |||||||
| chr4:189948222 | G | T | 44 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0015 others(41): Show |
114 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.134-3940G>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189948222 | |||||||
| chr4:189948244 | G | A | 38 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0015 others(35): Show |
107 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.134-3918G>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189948244 | |||||||
| chr4:189948256 | G | C | 38 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0015 others(35): Show |
107 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.134-3906G>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189948256 | |||||||
| chr4:189948511 | C | G | 7 | a0001c0003t0003g0003 a0001c0003t0003g0055 a0001c0003t0003g0058 others(4): Show |
36 | HG01891.hp2 HG01934.hp2 HG02280.hp1 others(33): Show |
intron_variant | MODIFIER | c.134-3651C>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189948511 | |||||||
| chr4:189948520 | A | G | 1 | a0002c0004t0005g0092 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.134-3642A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189948520 | |||||||
| chr4:189948549 | T | A | 44 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0015 others(41): Show |
114 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.134-3613T>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189948549 | |||||||
| chr4:189948828 | C | T | 1 | a0001c0001t0001g0075 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.134-3334C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189948828 | |||||||
| chr4:189948841 | C | A | 37 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0015 others(34): Show |
106 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.134-3321C>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189948841 | |||||||
| chr4:189948968 | A | C | 7 | a0001c0003t0003g0003 a0001c0003t0003g0055 a0001c0003t0003g0058 others(4): Show |
36 | HG01891.hp2 HG01934.hp2 HG02280.hp1 others(33): Show |
intron_variant | MODIFIER | c.134-3194A>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189948968 | |||||||
| chr4:189948969 | G | A | 1 | a0001c0003t0003g0058 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.134-3193G>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189948969 | |||||||
| chr4:189949318 | T | G | 1 | a0001c0002t0004g0117 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.134-2844T>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189949318 | |||||||
| chr4:189949356 | A | G | 1 | a0001c0001t0001g0074 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.134-2806A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189949356 | |||||||
| chr4:189949417 | A | G | 5 | a0001c0003t0005g0010 a0001c0003t0005g0035 a0001c0003t0005g0036 others(2): Show |
11 | HG01081.hp2 HG01884.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.134-2745A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189949417 | |||||||
| chr4:189949765 | T | C | 44 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0015 others(41): Show |
114 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.134-2397T>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189949765 | |||||||
| chr4:189949769 | A | G | 1 | a0001c0003t0005g0052 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.134-2393A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189949769 | |||||||
| chr4:189949817 | T | C | 44 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0015 others(41): Show |
114 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.134-2345T>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189949817 | |||||||
| chr4:189949920 | G | A | 1 | a0001c0002t0002g0113 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.134-2242G>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189949920 | |||||||
| chr4:189949924 | A | G | 1 | a0001c0002t0002g0105 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.134-2238A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189949924 | |||||||
| chr4:189949988 | C | T | 1 | a0001c0002t0002g0104 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.134-2174C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189949988 | |||||||
| chr4:189950042 | T | TTTTG | 4 | a0001c0002t0006g0022 a0001c0002t0006g0042 a0001c0002t0006g0043 others(1): Show |
5 | HG02258.hp1 HG03098.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.134-2104_134-2101d others(6): Show |
FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 189950042 | ||||||
| chr4:189950421 | T | C | 1 | a0001c0002t0011g0041 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.134-1741T>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189950421 | |||||||
| chr4:189950660 | A | C | 1 | a0001c0003t0005g0085 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.134-1502A>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189950660 | |||||||
| chr4:189950707 | A | G | 1 | a0001c0002t0006g0044 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.134-1455A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189950707 | |||||||
| chr4:189950841 | G | A | 68 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0015 others(65): Show |
186 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(183): Show |
intron_variant | MODIFIER | c.134-1321G>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189950841 | |||||||
| chr4:189950852 | T | C | 1 | a0001c0003t0009g0023 | 2 | HG02647.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.134-1310T>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189950852 | |||||||
| chr4:189950938 | A | G | 1 | a0001c0002t0010g0094 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.134-1224A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189950938 | |||||||
| chr4:189950947 | T | C | 1 | a0001c0002t0006g0022 | 2 | HG02258.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.134-1215T>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189950947 | |||||||
| chr4:189951092 | G | T | 72 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0015 others(69): Show |
192 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(189): Show |
intron_variant | MODIFIER | c.134-1070G>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189951092 | |||||||
| chr4:189951304 | G | T | 1 | a0001c0001t0001g0073 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.134-858G>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189951304 | |||||||
| chr4:189951388 | A | G | 1 | a0001c0002t0002g0038 | 2 | HG02965.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.134-774A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189951388 | |||||||
| chr4:189951444 | C | T | 1 | a0001c0002t0010g0094 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.134-718C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189951444 | |||||||
| chr4:189951489 | CA | C | 32 | a0001c0001t0001g0054 a0001c0002t0006g0022 a0001c0002t0006g0042 others(29): Show |
83 | HG00735.hp2 HG00741.hp1 HG01081.hp2 others(80): Show |
intron_variant | MODIFIER | c.134-656delA | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 189951489 | ||||||
| chr4:189951489 | CAA | C | 40 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0015 others(37): Show |
109 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.134-657_134-656del others(2): Show |
FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 189951489 | ||||||
| chr4:189951539 | C | T | 44 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0015 others(41): Show |
114 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.134-623C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189951539 | |||||||
| chr4:189951552 | C | T | 2 | a0001c0003t0005g0019 a0001c0003t0005g0090 |
4 | HG03688.hp2 HG03834.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.134-610C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189951552 | |||||||
| chr4:189951623 | T | C | 44 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0015 others(41): Show |
114 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.134-539T>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189951623 | |||||||
| chr4:189951633 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.134-529G>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189951633 | |||||||
| chr4:189951650 | C | T | 44 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0015 others(41): Show |
114 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.134-512C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189951650 | |||||||
| chr4:189951727 | A | G | 1 | a0001c0001t0001g0033 | 2 | HG02897.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.134-435A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189951727 | |||||||
| chr4:189951739 | C | T | 4 | a0001c0002t0006g0022 a0001c0002t0006g0042 a0001c0002t0006g0043 others(1): Show |
5 | HG02258.hp1 HG03098.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.134-423C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189951739 | |||||||
| chr4:189951881 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.134-281C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189951881 | |||||||
| chr4:189951888 | A | T | 44 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0015 others(41): Show |
114 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.134-274A>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189951888 | |||||||
| chr4:189951939 | T | C | 13 | a0001c0003t0005g0008 a0001c0003t0005g0010 a0001c0003t0005g0011 others(10): Show |
31 | HG00741.hp1 HG01081.hp2 HG01099.hp1 others(28): Show |
intron_variant | MODIFIER | c.134-223T>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189951939 | |||||||
| chr4:189951962 | T | G | 44 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0015 others(41): Show |
114 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.134-200T>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189951962 | |||||||
| chr4:189952005 | T | G | 68 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0015 others(65): Show |
186 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(183): Show |
intron_variant | MODIFIER | c.134-157T>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189952005 | |||||||
| chr4:189952007 | A | C | 68 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0015 others(65): Show |
186 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(183): Show |
intron_variant | MODIFIER | c.134-155A>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189952007 | |||||||
| chr4:189952029 | A | G | 119 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(116): Show |
339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.134-133A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | chr4 | 189952029 | |||||||
| chr4:189952099 | CA | C | 44 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0015 others(41): Show |
114 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.134-55delA | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 189952099 | ||||||
| chr4:189952367 | C | G | 1 | a0001c0003t0009g0023 | 2 | HG02647.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.259+80C>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 3/8 | chr4 | 189952367 | |||||||
| chr4:189952634 | G | A | 1 | a0001c0001t0001g0026 | 2 | NA18950.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.259+347G>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 3/8 | chr4 | 189952634 | |||||||
| chr4:189952797 | G | A | 44 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0015 others(41): Show |
114 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.260-271G>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 3/8 | chr4 | 189952797 | |||||||
| chr4:189952860 | C | T | 2 | a0001c0001t0001g0078 a0001c0001t0001g0087 |
2 | HG02145.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.260-208C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 3/8 | chr4 | 189952860 | |||||||
| chr4:189953039 | T | C | 1 | a0001c0003t0009g0023 | 2 | HG02647.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.260-29T>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 3/8 | chr4 | 189953039 | |||||||
| chr4:189953165 | T | G | 2 | a0001c0003t0005g0010 a0001c0003t0005g0084 |
6 | HG01081.hp2 HG01884.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.317+40T>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 4/8 | chr4 | 189953165 | |||||||
| chr4:189953218 | G | A | 1 | a0001c0001t0001g0028 | 2 | HG00544.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.317+93G>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 4/8 | chr4 | 189953218 | |||||||
| chr4:189953314 | G | GA | 80 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0012 others(77): Show |
212 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(209): Show |
intron_variant | MODIFIER | c.317+197dupA | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr4 | 189953314 | ||||||
| chr4:189953314 | G | GAA | 5 | a0001c0003t0005g0010 a0001c0003t0005g0035 a0001c0003t0005g0036 others(2): Show |
11 | HG01081.hp2 HG01884.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.317+196_317+197dup others(2): Show |
FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr4 | 189953314 | ||||||
| chr4:189953349 | T | A | 1 | a0001c0001t0001g0064 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.317+224T>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 4/8 | chr4 | 189953349 | |||||||
| chr4:189953357 | C | T | 1 | a0001c0001t0001g0032 | 2 | NA18747.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.317+232C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 4/8 | chr4 | 189953357 | |||||||
| chr4:189953359 | G | A | 1 | a0001c0003t0009g0023 | 2 | HG02647.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.317+234G>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 4/8 | chr4 | 189953359 | |||||||
| chr4:189953380 | G | A | 67 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0015 others(64): Show |
184 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(181): Show |
intron_variant | MODIFIER | c.317+255G>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 4/8 | chr4 | 189953380 | |||||||
| chr4:189953600 | C | T | 44 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0015 others(41): Show |
114 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.317+475C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 4/8 | chr4 | 189953600 | |||||||
| chr4:189953622 | T | C | 4 | a0001c0003t0005g0008 a0001c0003t0005g0011 a0001c0003t0005g0091 others(1): Show |
13 | HG00741.hp1 HG01099.hp1 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.317+497T>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 4/8 | chr4 | 189953622 | |||||||
| chr4:189953680 | T | C | 23 | a0001c0003t0003g0003 a0001c0003t0003g0048 a0001c0003t0003g0049 others(20): Show |
70 | HG00741.hp1 HG01081.hp2 HG01099.hp1 others(67): Show |
intron_variant | MODIFIER | c.317+555T>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 4/8 | chr4 | 189953680 | |||||||
| chr4:189953739 | G | T | 1 | a0001c0003t0009g0023 | 2 | HG02647.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.317+614G>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 4/8 | chr4 | 189953739 | |||||||
| chr4:189953746 | T | TA | 4 | a0001c0002t0006g0022 a0001c0002t0006g0042 a0001c0002t0006g0043 others(1): Show |
5 | HG02258.hp1 HG03098.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.317+625dupA | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr4 | 189953746 | ||||||
| chr4:189953797 | T | G | 1 | a0001c0003t0005g0052 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.317+672T>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 4/8 | chr4 | 189953797 | |||||||
| chr4:189953883 | A | G | 3 | a0001c0001t0001g0018 a0001c0001t0001g0072 a0001c0001t0001g0082 |
5 | HG00735.hp1 HG01258.hp1 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.317+758A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 4/8 | chr4 | 189953883 | |||||||
| chr4:189953901 | G | A | 3 | a0001c0002t0004g0014 a0001c0002t0004g0095 a0001c0002t0004g0108 |
6 | NA18947.hp2 NA18965.hp2 NA18968.hp1 others(3): Show |
intron_variant | MODIFIER | c.317+776G>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 4/8 | chr4 | 189953901 | |||||||
| chr4:189954036 | A | G | 1 | a0001c0002t0013g0045 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.317+911A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 4/8 | chr4 | 189954036 | |||||||
| chr4:189954047 | A | G | 1 | a0001c0001t0001g0071 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.317+922A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 4/8 | chr4 | 189954047 | |||||||
| chr4:189954099 | A | T | 1 | a0001c0002t0011g0041 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.318-938A>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 4/8 | chr4 | 189954099 | |||||||
| chr4:189954207 | TA | T | 3 | a0001c0003t0005g0008 a0001c0003t0005g0091 a0002c0004t0005g0092 |
8 | HG00741.hp1 HG01099.hp1 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.318-821delA | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr4 | 189954207 | ||||||
| chr4:189954382 | A | G | 1 | a0001c0003t0007g0063 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.318-655A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 4/8 | chr4 | 189954382 | |||||||
| chr4:189954398 | TAAG | T | 4 | a0001c0003t0005g0019 a0001c0003t0005g0034 a0001c0003t0005g0085 others(1): Show |
7 | HG02809.hp2 HG03453.hp1 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.318-637_318-635del others(3): Show |
FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr4 | 189954398 | ||||||
| chr4:189954399 | AAG | A | 44 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0015 others(41): Show |
114 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.318-634_318-633del others(2): Show |
FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr4 | 189954399 | ||||||
| chr4:189954522 | A | C | 1 | a0001c0003t0005g0035 | 2 | HG03453.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.318-515A>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 4/8 | chr4 | 189954522 | |||||||
| chr4:189954525 | G | A | 1 | a0001c0002t0010g0094 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.318-512G>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 4/8 | chr4 | 189954525 | |||||||
| chr4:189954593 | TTC | T | 10 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0020 others(7): Show |
12 | HG00558.hp1 HG02258.hp1 HG02897.hp2 others(9): Show |
intron_variant | MODIFIER | c.318-442_318-441del others(2): Show |
FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr4 | 189954593 | ||||||
| chr4:189954594 | TC | T | 35 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0015 others(32): Show |
99 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.318-442delC | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 4/8 | chr4 | 189954594 | |||||||
| chr4:189954595 | C | T | 1 | a0001c0002t0002g0116 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.318-442C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 4/8 | chr4 | 189954595 | |||||||
| chr4:189954621 | G | T | 1 | a0001c0003t0002g0096 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.318-416G>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 4/8 | chr4 | 189954621 | |||||||
| chr4:189954654 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.318-383G>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 4/8 | chr4 | 189954654 | |||||||
| chr4:189954788 | G | T | 1 | a0001c0002t0004g0103 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.318-249G>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 4/8 | chr4 | 189954788 | |||||||
| chr4:189955455 | A | ATCT | 68 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0015 others(65): Show |
186 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(183): Show |
intron_variant | MODIFIER | c.432+306_432+308dup others(3): Show |
FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr4 | 189955455 | ||||||
| chr4:189955682 | G | GT | 4 | a0001c0003t0005g0019 a0001c0003t0005g0034 a0001c0003t0005g0085 others(1): Show |
7 | HG02809.hp2 HG03453.hp1 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.432+532dupT | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr4 | 189955682 | ||||||
| chr4:189955831 | A | T | 1 | a0001c0002t0002g0102 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.432+680A>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 5/8 | chr4 | 189955831 | |||||||
| chr4:189955917 | A | G | 2 | a0001c0002t0010g0094 a0001c0002t0011g0041 |
2 | HG02976.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.432+766A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 5/8 | chr4 | 189955917 | |||||||
| chr4:189956037 | A | G | 2 | a0001c0003t0003g0049 a0001c0003t0003g0050 |
2 | HG02615.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.432+886A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 5/8 | chr4 | 189956037 | |||||||
| chr4:189956138 | A | G | 1 | a0001c0001t0001g0070 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.432+987A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 5/8 | chr4 | 189956138 | |||||||
| chr4:189956201 | A | T | 54 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0015 others(51): Show |
153 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.432+1050A>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 5/8 | chr4 | 189956201 | |||||||
| chr4:189956408 | T | G | 1 | a0001c0002t0002g0114 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.433-990T>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 5/8 | chr4 | 189956408 | |||||||
| chr4:189956413 | G | C | 1 | a0001c0002t0006g0022 | 2 | HG02258.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.433-985G>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 5/8 | chr4 | 189956413 | |||||||
| chr4:189956554 | C | T | 1 | a0001c0002t0006g0043 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.433-844C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 5/8 | chr4 | 189956554 | |||||||
| chr4:189956555 | A | G | 69 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0015 others(66): Show |
187 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(184): Show |
intron_variant | MODIFIER | c.433-843A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 5/8 | chr4 | 189956555 | |||||||
| chr4:189956672 | G | T | 1 | a0001c0002t0002g0101 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.433-726G>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 5/8 | chr4 | 189956672 | |||||||
| chr4:189956709 | T | G | 51 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0015 others(48): Show |
133 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.433-689T>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 5/8 | chr4 | 189956709 | |||||||
| chr4:189956724 | G | A | 1 | a0001c0001t0001g0066 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.433-674G>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 5/8 | chr4 | 189956724 | |||||||
| chr4:189956834 | G | C | 4 | a0001c0002t0006g0022 a0001c0002t0006g0042 a0001c0002t0006g0043 others(1): Show |
5 | HG02258.hp1 HG03098.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.433-564G>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 5/8 | chr4 | 189956834 | |||||||
| chr4:189957037 | G | A | 10 | a0001c0003t0003g0003 a0001c0003t0003g0048 a0001c0003t0003g0049 others(7): Show |
39 | HG01891.hp2 HG01934.hp2 HG02280.hp1 others(36): Show |
intron_variant | MODIFIER | c.433-361G>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 5/8 | chr4 | 189957037 | |||||||
| chr4:189957167 | CCTA | C | 3 | a0001c0001t0001g0007 a0001c0001t0001g0032 a0001c0001t0001g0079 |
9 | HG02083.hp1 HG02698.hp2 HG03710.hp2 others(6): Show |
intron_variant | MODIFIER | c.433-227_433-225del others(3): Show |
FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr4 | 189957167 | ||||||
| chr4:189957225 | T | A | 1 | a0001c0003t0003g0059 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.433-173T>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 5/8 | chr4 | 189957225 | |||||||
| chr4:189957230 | G | T | 4 | a0001c0002t0006g0022 a0001c0002t0006g0042 a0001c0002t0006g0043 others(1): Show |
5 | HG02258.hp1 HG03098.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.433-168G>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 5/8 | chr4 | 189957230 | |||||||
| chr4:189957258 | G | C | 1 | a0001c0002t0004g0118 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.433-140G>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 5/8 | chr4 | 189957258 | |||||||
| chr4:189957317 | A | G | 51 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0015 others(48): Show |
133 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.433-81A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 5/8 | chr4 | 189957317 | |||||||
| chr4:189957357 | A | G | 3 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0070 |
12 | HG00099.hp1 HG00140.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.433-41A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 5/8 | chr4 | 189957357 | |||||||
| chr4:189957362 | T | C | 1 | a0001c0003t0007g0089 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.433-36T>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 5/8 | chr4 | 189957362 | |||||||
| chr4:189957383 | A | AT | 69 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0015 others(66): Show |
187 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(184): Show |
intron_variant | MODIFIER | c.433-12dupT | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr4 | 189957383 | ||||||
| chr4:189957552 | C | CTGTA | 11 | a0001c0003t0003g0003 a0001c0003t0003g0048 a0001c0003t0003g0049 others(8): Show |
41 | HG01891.hp2 HG01934.hp2 HG02280.hp1 others(38): Show |
intron_variant | MODIFIER | c.537+52_537+55dupGT others(2): Show |
FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 189957552 | ||||||
| chr4:189957587 | G | C | 38 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0015 others(35): Show |
107 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.537+85G>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 6/8 | chr4 | 189957587 | |||||||
| chr4:189957653 | A | G | 52 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0015 others(49): Show |
134 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.537+151A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 6/8 | chr4 | 189957653 | |||||||
| chr4:189957672 | T | G | 52 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0015 others(49): Show |
134 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.537+170T>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 6/8 | chr4 | 189957672 | |||||||
| chr4:189957752 | C | T | 5 | a0001c0003t0005g0010 a0001c0003t0005g0035 a0001c0003t0005g0036 others(2): Show |
11 | HG01081.hp2 HG01884.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.537+250C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 6/8 | chr4 | 189957752 | |||||||
| chr4:189958105 | G | GTTTTCTC | 38 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0015 others(35): Show |
107 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.537+608_537+614dup others(7): Show |
FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 189958105 | ||||||
| chr4:189958138 | C | A | 4 | a0001c0003t0005g0008 a0001c0003t0005g0011 a0001c0003t0005g0091 others(1): Show |
13 | HG00741.hp1 HG01099.hp1 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.537+636C>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 6/8 | chr4 | 189958138 | |||||||
| chr4:189958170 | C | T | 63 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0015 others(60): Show |
175 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.537+668C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 6/8 | chr4 | 189958170 | |||||||
| chr4:189958233 | T | C | 1 | a0001c0003t0003g0060 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.537+731T>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 6/8 | chr4 | 189958233 | |||||||
| chr4:189958292 | C | T | 5 | a0001c0003t0005g0010 a0001c0003t0005g0035 a0001c0003t0005g0036 others(2): Show |
11 | HG01081.hp2 HG01884.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.537+790C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 6/8 | chr4 | 189958292 | |||||||
| chr4:189958345 | T | C | 63 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0015 others(60): Show |
175 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.537+843T>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 6/8 | chr4 | 189958345 | |||||||
| chr4:189958596 | G | A | 1 | a0001c0002t0013g0045 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.537+1094G>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 6/8 | chr4 | 189958596 | |||||||
| chr4:189958633 | G | A | 2 | a0001c0003t0003g0049 a0001c0003t0003g0050 |
2 | HG02615.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.537+1131G>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 6/8 | chr4 | 189958633 | |||||||
| chr4:189958666 | T | C | 4 | a0001c0002t0002g0005 a0001c0002t0002g0098 a0001c0002t0002g0106 others(1): Show |
11 | HG00558.hp1 HG03710.hp1 NA18948.hp1 others(8): Show |
intron_variant | MODIFIER | c.537+1164T>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 6/8 | chr4 | 189958666 | |||||||
| chr4:189958672 | A | C | 1 | a0001c0001t0001g0018 | 3 | HG00735.hp1 HG01258.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.537+1170A>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 6/8 | chr4 | 189958672 | |||||||
| chr4:189958696 | A | T | 1 | a0001c0001t0001g0053 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.537+1194A>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 6/8 | chr4 | 189958696 | |||||||
| chr4:189958774 | A | C | 52 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0015 others(49): Show |
134 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.537+1272A>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 6/8 | chr4 | 189958774 | |||||||
| chr4:189958781 | A | AT | 44 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0015 others(41): Show |
114 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.537+1285dupT | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 189958781 | ||||||
| chr4:189958827 | A | G | 1 | a0001c0001t0001g0017 | 3 | HG01257.hp2 HG01258.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.537+1325A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 6/8 | chr4 | 189958827 | |||||||
| chr4:189959022 | G | C | 1 | a0001c0001t0001g0029 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.537+1520G>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 6/8 | chr4 | 189959022 | |||||||
| chr4:189959121 | A | G | 1 | a0001c0002t0002g0020 | 3 | HG02895.hp1 HG02897.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.537+1619A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 6/8 | chr4 | 189959121 | |||||||
| chr4:189959136 | A | G | 63 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0015 others(60): Show |
175 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.538-1612A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 6/8 | chr4 | 189959136 | |||||||
| chr4:189959194 | T | G | 1 | a0001c0001t0001g0067 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.538-1554T>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 6/8 | chr4 | 189959194 | |||||||
| chr4:189959254 | A | G | 52 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0015 others(49): Show |
134 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.538-1494A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 6/8 | chr4 | 189959254 | |||||||
| chr4:189959475 | G | A | 1 | a0001c0003t0009g0023 | 2 | HG02647.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.538-1273G>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 6/8 | chr4 | 189959475 | |||||||
| chr4:189959508 | C | T | 4 | a0001c0003t0005g0008 a0001c0003t0005g0011 a0001c0003t0005g0091 others(1): Show |
13 | HG00741.hp1 HG01099.hp1 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.538-1240C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 6/8 | chr4 | 189959508 | |||||||
| chr4:189959649 | A | G | 1 | a0001c0002t0011g0041 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.538-1099A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 6/8 | chr4 | 189959649 | |||||||
| chr4:189959698 | G | A | 52 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0015 others(49): Show |
134 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.538-1050G>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 6/8 | chr4 | 189959698 | |||||||
| chr4:189959894 | TACCAGAA others(60): Show |
T | 1 | a0001c0003t0005g0091 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.538-810_538-744del others(67): Show |
FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 189959894 | ||||||
| chr4:189959940 | C | T | 1 | a0001c0002t0008g0002 | 2 | NA18957.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.538-808C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 6/8 | chr4 | 189959940 | |||||||
| chr4:189960114 | G | T | 2 | a0001c0001t0001g0031 a0001c0001t0001g0077 |
3 | HG02109.hp2 HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.538-634G>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 6/8 | chr4 | 189960114 | |||||||
| chr4:189960283 | T | C | 51 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0015 others(48): Show |
133 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.538-465T>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 6/8 | chr4 | 189960283 | |||||||
| chr4:189960381 | C | T | 52 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0015 others(49): Show |
134 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.538-367C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 6/8 | chr4 | 189960381 | |||||||
| chr4:189960536 | A | G | 37 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0015 others(34): Show |
106 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.538-212A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 6/8 | chr4 | 189960536 | |||||||
| chr4:189960552 | A | T | 11 | a0001c0003t0003g0003 a0001c0003t0003g0048 a0001c0003t0003g0049 others(8): Show |
41 | HG01891.hp2 HG01934.hp2 HG02280.hp1 others(38): Show |
intron_variant | MODIFIER | c.538-196A>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 6/8 | chr4 | 189960552 | |||||||
| chr4:189960658 | AATC | A | 10 | a0001c0003t0003g0003 a0001c0003t0003g0048 a0001c0003t0003g0049 others(7): Show |
39 | HG01891.hp2 HG01934.hp2 HG02280.hp1 others(36): Show |
intron_variant | MODIFIER | c.538-86_538-84delAT others(1): Show |
FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 189960658 | ||||||
| chr4:189960678 | T | C | 1 | a0001c0001t0001g0030 | 2 | HG00099.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.538-70T>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 6/8 | chr4 | 189960678 | |||||||
| chr4:189960699 | G | C | 1 | a0001c0002t0002g0097 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.538-49G>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 6/8 | chr4 | 189960699 | |||||||
| chr4:189961059 | G | A | 1 | a0001c0002t0002g0099 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.629+220G>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 7/8 | chr4 | 189961059 | |||||||
| chr4:189961083 | G | A | 4 | a0001c0002t0006g0022 a0001c0002t0006g0042 a0001c0002t0006g0043 others(1): Show |
5 | HG02258.hp1 HG03098.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.629+244G>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 7/8 | chr4 | 189961083 | |||||||
| chr4:189961217 | A | C | 1 | a0001c0003t0005g0052 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.629+378A>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 7/8 | chr4 | 189961217 | |||||||
| chr4:189961338 | C | T | 1 | a0001c0001t0001g0069 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.630-484C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 7/8 | chr4 | 189961338 | |||||||
| chr4:189961418 | T | C | 1 | a0001c0002t0011g0041 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.630-404T>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 7/8 | chr4 | 189961418 | |||||||
| chr4:189961445 | T | A | 1 | a0001c0003t0003g0061 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.630-377T>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 7/8 | chr4 | 189961445 | |||||||
| chr4:189961493 | C | T | 1 | a0001c0001t0001g0071 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.630-329C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 7/8 | chr4 | 189961493 | |||||||
| chr4:189961531 | C | G | 1 | a0001c0002t0011g0041 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.630-291C>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 7/8 | chr4 | 189961531 | |||||||
| chr4:189961537 | A | G | 1 | a0001c0002t0002g0115 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.630-285A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 7/8 | chr4 | 189961537 | |||||||
| chr4:189961676 | G | A | 1 | a0001c0001t0001g0051 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.630-146G>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 7/8 | chr4 | 189961676 | |||||||
| chr4:189961807 | A | G | 1 | a0001c0001t0001g0068 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.630-15A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 7/8 | chr4 | 189961807 | |||||||
| chr4:189962132 | C | T | 2 | a0001c0003t0003g0062 a0001c0003t0005g0036 |
3 | HG02559.hp2 HG02976.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.740+200C>T | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 8/8 | chr4 | 189962132 | |||||||
| chr4:189962150 | T | A | 1 | a0001c0002t0006g0043 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.740+218T>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 8/8 | chr4 | 189962150 | |||||||
| chr4:189962522 | G | A | 1 | a0001c0002t0002g0100 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.741-571G>A | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 8/8 | chr4 | 189962522 | |||||||
| chr4:189962559 | C | CT | 11 | a0001c0003t0003g0003 a0001c0003t0003g0048 a0001c0003t0003g0049 others(8): Show |
41 | HG01891.hp2 HG01934.hp2 HG02280.hp1 others(38): Show |
intron_variant | MODIFIER | c.741-526dupT | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | 189962559 | ||||||
| chr4:189962567 | T | TA | 4 | a0001c0002t0006g0022 a0001c0002t0006g0042 a0001c0002t0006g0043 others(1): Show |
5 | HG02258.hp1 HG03098.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.741-525dupA | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | 189962567 | ||||||
| chr4:189962704 | CAAG | C | 2 | a0001c0003t0007g0016 a0001c0003t0007g0063 |
4 | HG00735.hp2 HG02723.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.741-384_741-382del others(3): Show |
FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | 189962704 | ||||||
| chr4:189962903 | A | G | 1 | a0001c0002t0013g0045 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.741-190A>G | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 8/8 | chr4 | 189962903 | |||||||
| chr4:189962930 | T | C | 52 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0015 others(49): Show |
134 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.741-163T>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 8/8 | chr4 | 189962930 | |||||||
| chr4:189963062 | A | C | 1 | a0001c0001t0001g0077 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.741-31A>C | FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 8/8 | chr4 | 189963062 | |||||||
| chr4:189963070 | T | TTTC | 63 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0015 others(60): Show |
175 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.741-21_741-20insCT others(1): Show |
FRG1 | ENSG00000109536.13 | transcript | ENST00000226798.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | 189963070 |