Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 150946 |
| ensemblid | ENSG00000157833.13 |
| hgncid | 27172 |
| symbol | GAREM2 |
| name | GRB2 associated regulator of MAPK1 subtype 2 |
| refseq_nuc | NM_001168241.2 |
| refseq_prot | NP_001161713.1 |
| ensembl_nuc | ENST00000401533.7 |
| ensembl_prot | ENSP00000384593.1 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 26173088 |
| end | 26189663 |
| strand | + |
| ver | v1.2 |
| region | chr2:26173088-26189663 |
| region5000 | chr2:26168088-26194663 |
| regionname0 | GAREM2_chr2_26173088_26189663 |
| regionname5000 | GAREM2_chr2_26168088_26194663 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 874 | 283 | 79 | 70 | 94 | 11 | 28 | 71 | GAREM2_chr2_26168088_26194663 | GAREM2 | MEKLA others(869): Show |
chr2 | 26168088 | 26194663 |
| a0002 | 0/1 | 874 | 12 | 2 | 5 | 1 | 1 | 2 | 1 | GAREM2_chr2_26168088_26194663 | GAREM2 | MEKLA others(869): Show |
chr2 | 26168088 | 26194663 |
| a0003 | 0/0 | 874 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | MEKLA others(869): Show |
chr2 | 26168088 | 26194663 |
| a0004 | 0/0 | 874 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | MEKLA others(869): Show |
chr2 | 26168088 | 26194663 |
| a0005 | 0/0 | 874 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | MEKLA others(869): Show |
chr2 | 26168088 | 26194663 |
| a0006 | 0/0 | 874 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | MEKLA others(869): Show |
chr2 | 26168088 | 26194663 |
| a0007 | 0/0 | 874 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | MEKLA others(869): Show |
chr2 | 26168088 | 26194663 |
| a0008 | 0/0 | 874 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | MEKLA others(869): Show |
chr2 | 26168088 | 26194663 |
| a0009 | 0/0 | 874 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | MEKLA others(869): Show |
chr2 | 26168088 | 26194663 |
| a0010 | 0/0 | 874 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | MEKLA others(869): Show |
chr2 | 26168088 | 26194663 |
| a0011 | 0/0 | 874 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GAREM2_chr2_26168088_26194663 | GAREM2 | MEKLA others(869): Show |
chr2 | 26168088 | 26194663 |
| a0012 | 0/0 | 874 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GAREM2_chr2_26168088_26194663 | GAREM2 | MEKLA others(869): Show |
chr2 | 26168088 | 26194663 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2622 | 196 | 58 | 46 | 70 | 2 | 20 | GAREM2_chr2_26168088_26194663 | GAREM2 | ATGGA others(2617): Show |
chr2 | 26168088 | 26194663 | ||
| a0001c0002 | 0/0 | 2622 | 57 | 3 | 16 | 22 | 8 | 8 | GAREM2_chr2_26168088_26194663 | GAREM2 | ATGGA others(2617): Show |
chr2 | 26168088 | 26194663 | ||
| a0001c0004 | 0/0 | 2622 | 9 | 9 | 0 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | ATGGA others(2617): Show |
chr2 | 26168088 | 26194663 | ||
| a0001c0005 | 0/0 | 2622 | 7 | 4 | 3 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | ATGGA others(2617): Show |
chr2 | 26168088 | 26194663 | ||
| a0001c0006 | 1/0 | 2622 | 6 | 1 | 2 | 2 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | ATGGA others(2617): Show |
chr2 | 26168088 | 26194663 | ||
| a0001c0007 | 0/0 | 2622 | 3 | 1 | 2 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | ATGGA others(2617): Show |
chr2 | 26168088 | 26194663 | ||
| a0001c0008 | 0/0 | 2622 | 2 | 2 | 0 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | ATGGA others(2617): Show |
chr2 | 26168088 | 26194663 | ||
| a0001c0012 | 0/0 | 2622 | 1 | 0 | 0 | 0 | 1 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | ATGGA others(2617): Show |
chr2 | 26168088 | 26194663 | ||
| a0001c0015 | 0/0 | 2622 | 1 | 0 | 1 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | ATGGA others(2617): Show |
chr2 | 26168088 | 26194663 | ||
| a0001c0018 | 0/0 | 2622 | 1 | 1 | 0 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | ATGGA others(2617): Show |
chr2 | 26168088 | 26194663 | ||
| a0002c0003 | 0/1 | 2622 | 12 | 2 | 5 | 1 | 1 | 2 | GAREM2_chr2_26168088_26194663 | GAREM2 | ATGGA others(2617): Show |
chr2 | 26168088 | 26194663 | ||
| a0003c0009 | 0/0 | 2622 | 2 | 0 | 2 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | ATGGA others(2617): Show |
chr2 | 26168088 | 26194663 | ||
| a0004c0016 | 0/0 | 2622 | 1 | 0 | 1 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | ATGGA others(2617): Show |
chr2 | 26168088 | 26194663 | ||
| a0005c0017 | 0/0 | 2622 | 1 | 0 | 1 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | ATGGA others(2617): Show |
chr2 | 26168088 | 26194663 | ||
| a0006c0020 | 0/0 | 2622 | 1 | 0 | 1 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | ATGGA others(2617): Show |
chr2 | 26168088 | 26194663 | ||
| a0007c0019 | 0/0 | 2622 | 1 | 0 | 0 | 1 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | ATGGA others(2617): Show |
chr2 | 26168088 | 26194663 | ||
| a0008c0013 | 0/0 | 2622 | 1 | 1 | 0 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | ATGGA others(2617): Show |
chr2 | 26168088 | 26194663 | ||
| a0009c0021 | 0/0 | 2622 | 1 | 1 | 0 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | ATGGA others(2617): Show |
chr2 | 26168088 | 26194663 | ||
| a0010c0010 | 0/0 | 2622 | 1 | 1 | 0 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | ATGGA others(2617): Show |
chr2 | 26168088 | 26194663 | ||
| a0011c0014 | 0/0 | 2622 | 1 | 0 | 0 | 1 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | ATGGA others(2617): Show |
chr2 | 26168088 | 26194663 | ||
| a0012c0011 | 0/0 | 2622 | 1 | 0 | 0 | 1 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | ATGGA others(2617): Show |
chr2 | 26168088 | 26194663 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4164 | 183 | 51 | 42 | 69 | 2 | 19 | GAREM2_chr2_26168088_26194663 | GAREM2 | GCCCG others(4159): Show |
chr2 | 26168088 | 26194663 |
| a0001c0001t0002 | 0/0 | 4164 | 2 | 0 | 2 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | GCCCG others(4159): Show |
chr2 | 26168088 | 26194663 |
| a0001c0001t0006 | 0/0 | 4164 | 2 | 2 | 0 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | GCCCG others(4159): Show |
chr2 | 26168088 | 26194663 |
| a0001c0001t0007 | 0/0 | 4160 | 3 | 1 | 2 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | GCCCG others(4155): Show |
chr2 | 26168088 | 26194663 |
| a0001c0001t0009 | 0/0 | 4164 | 1 | 1 | 0 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | GCCCG others(4159): Show |
chr2 | 26168088 | 26194663 |
| a0001c0001t0010 | 0/0 | 4187 | 1 | 1 | 0 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | GCCCG others(4182): Show |
chr2 | 26168088 | 26194663 |
| a0001c0001t0011 | 0/0 | 4164 | 1 | 1 | 0 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | GCCCG others(4159): Show |
chr2 | 26168088 | 26194663 |
| a0001c0001t0012 | 0/0 | 4164 | 1 | 0 | 0 | 0 | 0 | 1 | GAREM2_chr2_26168088_26194663 | GAREM2 | GCCCG others(4159): Show |
chr2 | 26168088 | 26194663 |
| a0001c0001t0013 | 0/0 | 4164 | 1 | 0 | 0 | 1 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | GCCCG others(4159): Show |
chr2 | 26168088 | 26194663 |
| a0001c0001t0014 | 0/0 | 4164 | 1 | 1 | 0 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | GCCCG others(4159): Show |
chr2 | 26168088 | 26194663 |
| a0001c0002t0001 | 0/0 | 4164 | 11 | 0 | 7 | 0 | 4 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | GCCCG others(4159): Show |
chr2 | 26168088 | 26194663 |
| a0001c0002t0002 | 0/0 | 4164 | 40 | 0 | 6 | 22 | 4 | 8 | GAREM2_chr2_26168088_26194663 | GAREM2 | GCCCG others(4159): Show |
chr2 | 26168088 | 26194663 |
| a0001c0002t0005 | 0/0 | 4164 | 6 | 3 | 3 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | GCCCG others(4159): Show |
chr2 | 26168088 | 26194663 |
| a0001c0004t0004 | 0/0 | 4164 | 9 | 9 | 0 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | GCCCG others(4159): Show |
chr2 | 26168088 | 26194663 |
| a0001c0005t0003 | 0/0 | 4164 | 3 | 0 | 3 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | GCCCG others(4159): Show |
chr2 | 26168088 | 26194663 |
| a0001c0005t0006 | 0/0 | 4164 | 2 | 2 | 0 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | GCCCG others(4159): Show |
chr2 | 26168088 | 26194663 |
| a0001c0005t0008 | 0/0 | 4164 | 2 | 2 | 0 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | GCCCG others(4159): Show |
chr2 | 26168088 | 26194663 |
| a0001c0006t0003 | 1/0 | 4164 | 6 | 1 | 2 | 2 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | GCCCG others(4159): Show |
chr2 | 26168088 | 26194663 |
| a0001c0007t0001 | 0/0 | 4164 | 3 | 1 | 2 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | GCCCG others(4159): Show |
chr2 | 26168088 | 26194663 |
| a0001c0008t0005 | 0/0 | 4164 | 2 | 2 | 0 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | GCCCG others(4159): Show |
chr2 | 26168088 | 26194663 |
| a0001c0012t0001 | 0/0 | 4164 | 1 | 0 | 0 | 0 | 1 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | GCCCG others(4159): Show |
chr2 | 26168088 | 26194663 |
| a0001c0015t0015 | 0/0 | 4164 | 1 | 0 | 1 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | GCCCG others(4159): Show |
chr2 | 26168088 | 26194663 |
| a0001c0018t0001 | 0/0 | 4164 | 1 | 1 | 0 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | GCCCG others(4159): Show |
chr2 | 26168088 | 26194663 |
| a0002c0003t0001 | 0/1 | 4164 | 12 | 2 | 5 | 1 | 1 | 2 | GAREM2_chr2_26168088_26194663 | GAREM2 | GCCCG others(4159): Show |
chr2 | 26168088 | 26194663 |
| a0003c0009t0001 | 0/0 | 4164 | 2 | 0 | 2 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | GCCCG others(4159): Show |
chr2 | 26168088 | 26194663 |
| a0004c0016t0001 | 0/0 | 4164 | 1 | 0 | 1 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | GCCCG others(4159): Show |
chr2 | 26168088 | 26194663 |
| a0005c0017t0001 | 0/0 | 4164 | 1 | 0 | 1 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | GCCCG others(4159): Show |
chr2 | 26168088 | 26194663 |
| a0006c0020t0001 | 0/0 | 4164 | 1 | 0 | 1 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | GCCCG others(4159): Show |
chr2 | 26168088 | 26194663 |
| a0007c0019t0001 | 0/0 | 4164 | 1 | 0 | 0 | 1 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | GCCCG others(4159): Show |
chr2 | 26168088 | 26194663 |
| a0008c0013t0001 | 0/0 | 4164 | 1 | 1 | 0 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | GCCCG others(4159): Show |
chr2 | 26168088 | 26194663 |
| a0009c0021t0003 | 0/0 | 4164 | 1 | 1 | 0 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | GCCCG others(4159): Show |
chr2 | 26168088 | 26194663 |
| a0010c0010t0004 | 0/0 | 4164 | 1 | 1 | 0 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | GCCCG others(4159): Show |
chr2 | 26168088 | 26194663 |
| a0011c0014t0001 | 0/0 | 4164 | 1 | 0 | 0 | 1 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | GCCCG others(4159): Show |
chr2 | 26168088 | 26194663 |
| a0012c0011t0001 | 0/0 | 4164 | 1 | 0 | 0 | 1 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | GCCCG others(4159): Show |
chr2 | 26168088 | 26194663 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 51 | 18 | 14 | 12 | 1 | 6 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0001t0001g0003 | 0/0 | 21 | 0 | 3 | 18 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0001t0001g0004 | 0/0 | 10 | 1 | 0 | 7 | 0 | 2 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0001t0001g0005 | 0/0 | 8 | 0 | 8 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0001t0001g0007 | 0/0 | 8 | 8 | 0 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0001t0001g0009 | 0/0 | 5 | 0 | 3 | 0 | 1 | 1 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0001t0001g0010 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0001t0001g0013 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0001t0001g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0001t0001g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0001t0002g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0001t0006g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0001t0007g0001 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0001t0009g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0001t0010g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0001t0011g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0001t0012g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0001t0013g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0001t0014g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0002t0001g0011 | 0/0 | 5 | 0 | 4 | 0 | 1 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0002t0001g0016 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0002t0001g0033 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0002t0002g0002 | 0/0 | 26 | 0 | 5 | 18 | 2 | 1 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0002t0002g0020 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0002t0002g0021 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0002t0002g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0002t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0002t0005g0008 | 0/0 | 6 | 3 | 3 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0004t0004g0006 | 0/0 | 8 | 8 | 0 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0004t0004g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0005t0003g0017 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0005t0006g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0005t0008g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0006t0003g0012 | 1/0 | 5 | 0 | 2 | 2 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0006t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0007t0001g0001 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0007t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0008t0005g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0012t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0015t0015g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0001c0018t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0002c0003t0001g0001 | 0/1 | 9 | 2 | 3 | 1 | 1 | 1 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0002c0003t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0002c0003t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0002c0003t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0003c0009t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0004c0016t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0005c0017t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0006c0020t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0007c0019t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0008c0013t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0009c0021t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0010c0010t0004g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0011c0014t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| a0012c0011t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0016 | EUR | GBR | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG00099 | hp2 | a0002 | c0003 | t0001 | g0001 | EUR | GBR | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG00140 | hp1 | a0001 | c0002 | t0002 | g0002 | EUR | GBR | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG00140 | hp2 | a0001 | c0012 | t0001 | g0001 | EUR | GBR | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | CHS | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG00642 | hp2 | a0004 | c0016 | t0001 | g0009 | AMR | PUR | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG00733 | hp1 | a0001 | c0002 | t0005 | g0008 | AMR | PUR | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG00735 | hp1 | a0002 | c0003 | t0001 | g0061 | AMR | PUR | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG00735 | hp2 | a0001 | c0002 | t0001 | g0016 | AMR | PUR | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0063 | AMR | PUR | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG00741 | hp1 | a0005 | c0017 | t0001 | g0001 | AMR | PUR | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0011 | AMR | PUR | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG01069 | hp1 | a0001 | c0005 | t0003 | g0017 | AMR | PUR | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG01069 | hp2 | a0001 | c0006 | t0003 | g0012 | AMR | PUR | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG01070 | hp1 | a0002 | c0003 | t0001 | g0001 | AMR | PUR | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG01070 | hp2 | a0001 | c0002 | t0001 | g0016 | AMR | PUR | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0016 | AMR | PUR | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG01071 | hp2 | a0001 | c0005 | t0003 | g0017 | AMR | PUR | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG01074 | hp1 | a0001 | c0002 | t0001 | g0011 | AMR | PUR | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG01074 | hp2 | a0001 | c0002 | t0005 | g0008 | AMR | PUR | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG01081 | hp2 | a0002 | c0003 | t0001 | g0001 | AMR | PUR | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0011 | AMR | PUR | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG01099 | hp2 | a0006 | c0020 | t0001 | g0011 | AMR | PUR | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG01106 | hp2 | a0001 | c0005 | t0003 | g0017 | AMR | PUR | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG01109 | hp1 | a0002 | c0003 | t0001 | g0060 | AMR | PUR | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG01167 | hp1 | a0001 | c0002 | t0005 | g0008 | AMR | PUR | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG01167 | hp2 | a0001 | c0001 | t0007 | g0001 | AMR | PUR | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG01168 | hp1 | a0001 | c0007 | t0001 | g0036 | AMR | PUR | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG01168 | hp2 | a0003 | c0009 | t0001 | g0029 | AMR | PUR | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG01169 | hp1 | a0003 | c0009 | t0001 | g0029 | AMR | PUR | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG01169 | hp2 | a0001 | c0001 | t0007 | g0001 | AMR | PUR | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG01175 | hp1 | a0001 | c0002 | t0002 | g0085 | AMR | PUR | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG01175 | hp2 | a0001 | c0007 | t0001 | g0001 | AMR | PUR | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG01192 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | PUR | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | CLM | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG01261 | hp1 | a0001 | c0002 | t0001 | g0011 | AMR | CLM | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | CLM | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG01496 | hp2 | a0001 | c0015 | t0015 | g0001 | AMR | CLM | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG01516 | hp1 | a0001 | c0002 | t0001 | g0033 | EUR | IBS | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG01516 | hp2 | a0001 | c0002 | t0001 | g0011 | EUR | IBS | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG01517 | hp1 | a0001 | c0002 | t0001 | g0033 | EUR | IBS | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | IBS | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG01884 | hp1 | a0001 | c0004 | t0004 | g0048 | AFR | ACB | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG01928 | hp1 | a0002 | c0003 | t0001 | g0001 | AMR | PEL | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG01981 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PEL | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PEL | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG02004 | hp1 | a0001 | c0006 | t0003 | g0012 | AMR | PEL | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG02004 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PEL | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG02015 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | KHV | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | KHV | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG02040 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | KHV | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG02055 | hp2 | a0001 | c0008 | t0005 | g0025 | AFR | ACB | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | KHV | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG02080 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | KHV | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG02129 | hp1 | a0007 | c0019 | t0001 | g0003 | EAS | KHV | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG02129 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | KHV | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | KHV | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG02135 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | KHV | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG02155 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | CDX | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CDX | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG02258 | hp1 | a0002 | c0003 | t0001 | g0001 | AFR | ACB | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG02280 | hp2 | a0001 | c0007 | t0001 | g0001 | AFR | ACB | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PEL | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG02300 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | PEL | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG02622 | hp2 | a0001 | c0004 | t0004 | g0006 | AFR | GWD | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG02630 | hp2 | a0001 | c0004 | t0004 | g0006 | AFR | GWD | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG02647 | hp1 | a0008 | c0013 | t0001 | g0027 | AFR | GWD | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG02717 | hp1 | a0001 | c0005 | t0006 | g0035 | AFR | GWD | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG02717 | hp2 | a0001 | c0004 | t0004 | g0006 | AFR | GWD | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG02723 | hp1 | a0001 | c0001 | t0009 | g0004 | AFR | GWD | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG02895 | hp2 | a0001 | c0001 | t0010 | g0001 | AFR | GWD | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG02897 | hp2 | a0001 | c0005 | t0006 | g0035 | AFR | GWD | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ESN | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | ESN | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG02976 | hp2 | a0001 | c0004 | t0004 | g0006 | AFR | ESN | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG03017 | hp1 | a0001 | c0002 | t0002 | g0002 | SAS | PJL | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG03041 | hp1 | a0002 | c0003 | t0001 | g0001 | AFR | GWD | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | MSL | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG03098 | hp2 | a0001 | c0001 | t0011 | g0018 | AFR | MSL | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG03130 | hp1 | a0001 | c0008 | t0005 | g0025 | AFR | ESN | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ESN | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | ESN | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | MSL | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG03225 | hp2 | a0001 | c0005 | t0008 | g0024 | AFR | MSL | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG03239 | hp2 | a0002 | c0003 | t0001 | g0028 | SAS | PJL | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG03453 | hp1 | a0009 | c0021 | t0003 | g0038 | AFR | MSL | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG03486 | hp1 | a0001 | c0005 | t0008 | g0024 | AFR | MSL | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG03491 | hp1 | a0001 | c0002 | t0002 | g0021 | SAS | PJL | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG03491 | hp2 | a0001 | c0002 | t0002 | g0088 | SAS | PJL | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG03492 | hp1 | a0001 | c0002 | t0002 | g0021 | SAS | PJL | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ESN | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG03516 | hp2 | a0001 | c0002 | t0005 | g0008 | AFR | ESN | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG03540 | hp2 | a0001 | c0004 | t0004 | g0006 | AFR | GWD | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG03654 | hp1 | a0001 | c0002 | t0002 | g0021 | SAS | PJL | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG03669 | hp1 | a0001 | c0002 | t0002 | g0020 | SAS | PJL | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG03704 | hp2 | a0001 | c0001 | t0012 | g0003 | SAS | PJL | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG03710 | hp2 | a0001 | c0002 | t0002 | g0034 | SAS | PJL | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | BEB | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | BEB | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | BEB | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG04184 | hp1 | a0001 | c0002 | t0002 | g0034 | SAS | BEB | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG04184 | hp2 | a0002 | c0003 | t0001 | g0001 | SAS | BEB | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | STU | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | STU | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | STU | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA18522 | hp2 | a0001 | c0001 | t0006 | g0023 | AFR | YRI | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | CHB | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA18940 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA18947 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA18950 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA18950 | hp2 | a0002 | c0003 | t0001 | g0001 | EAS | JPT | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA18960 | hp1 | a0001 | c0002 | t0002 | g0052 | EAS | JPT | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA18965 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA18967 | hp1 | a0001 | c0006 | t0003 | g0012 | EAS | JPT | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA18967 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA18969 | hp2 | a0011 | c0014 | t0001 | g0003 | EAS | JPT | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA18974 | hp1 | a0001 | c0002 | t0002 | g0087 | EAS | JPT | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA18979 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA18993 | hp1 | a0001 | c0002 | t0002 | g0086 | EAS | JPT | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA18994 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA19003 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA19011 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA19011 | hp2 | a0012 | c0011 | t0001 | g0003 | EAS | JPT | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA19030 | hp1 | a0001 | c0004 | t0004 | g0006 | AFR | LWK | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA19030 | hp2 | a0001 | c0004 | t0004 | g0006 | AFR | LWK | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | LWK | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA19043 | hp2 | a0001 | c0018 | t0001 | g0041 | AFR | LWK | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA19057 | hp2 | a0001 | c0002 | t0002 | g0084 | EAS | JPT | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA19058 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA19067 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA19070 | hp2 | a0001 | c0006 | t0003 | g0012 | EAS | JPT | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA19077 | hp1 | a0001 | c0001 | t0013 | g0010 | EAS | JPT | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA19090 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA20129 | hp2 | a0001 | c0001 | t0006 | g0023 | AFR | ASW | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA20752 | hp1 | a0001 | c0002 | t0002 | g0002 | EUR | TSI | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA20752 | hp2 | a0001 | c0002 | t0002 | g0020 | EUR | TSI | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA20805 | hp1 | a0001 | c0002 | t0002 | g0020 | EUR | TSI | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG01123 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | CLM | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG02109 | hp2 | a0001 | c0002 | t0005 | g0008 | AFR | ACB | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG03471 | hp1 | a0010 | c0010 | t0004 | g0047 | AFR | MSL | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG03471 | hp2 | a0001 | c0002 | t0005 | g0008 | AFR | MSL | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | USA | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| HG06807 | hp2 | a0001 | c0001 | t0007 | g0001 | AFR | USA | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA20300 | hp1 | a0001 | c0004 | t0004 | g0006 | AFR | USA | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | USA | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA21309 | hp1 | a0001 | c0001 | t0014 | g0057 | AFR | LWK | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| NA21309 | hp2 | a0001 | c0006 | t0003 | g0083 | AFR | LWK | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| homoSapiens | chm13v2 | a0002 | c0003 | t0001 | g0001 | REF | REF | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| homoSapiens | grch38p0 | a0001 | c0006 | t0003 | g0012 | REF | REF | GAREM2_chr2_26168088_26194663 | GAREM2 | chr2 | 26168088 | 26194663 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:26173254 | C | A | 1 | a0010 | 1 | HG03471.hp1 | missense_variant | MODERATE | c.34C>A | p.Arg12Ser | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 1/6 | 167/4164 | 34/2625 | 12/874 | chr2 | 26173254 | |||
| chr2:26173303 | G | A | 1 | a0012 | 1 | NA19011.hp2 | missense_variant | MODERATE | c.83G>A | p.Arg28His | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 1/6 | 216/4164 | 83/2625 | 28/874 | chr2 | 26173303 | |||
| chr2:26184345 | A | G | 1 | a0007 | 1 | HG02129.hp1 | missense_variant | MODERATE | c.497A>G | p.Lys166Arg | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 4/6 | 630/4164 | 497/2625 | 166/874 | chr2 | 26184345 | |||
| chr2:26185068 | A | G | 3 | a0002 a0003 a0005 |
14 | HG00099.hp2 HG00735.hp1 HG00741.hp1 others(11): Show |
missense_variant | MODERATE | c.1220A>G | p.Gln407Arg | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 4/6 | 1353/4164 | 1220/2625 | 407/874 | chr2 | 26185068 | |||
| chr2:26186252 | G | A | 1 | a0003 | 2 | HG01168.hp2 HG01169.hp1 |
missense_variant | MODERATE | c.1492G>A | p.Gly498Ser | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 5/6 | 1625/4164 | 1492/2625 | 498/874 | chr2 | 26186252 | |||
| chr2:26186269 | C | A | 1 | a0008 | 1 | HG02647.hp1 | missense_variant | MODERATE | c.1509C>A | p.Ser503Arg | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 5/6 | 1642/4164 | 1509/2625 | 503/874 | chr2 | 26186269 | |||
| chr2:26186270 | C | T | 1 | a0004 | 1 | HG00642.hp2 | missense_variant | MODERATE | c.1510C>T | p.Pro504Ser | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 5/6 | 1643/4164 | 1510/2625 | 504/874 | chr2 | 26186270 | |||
| chr2:26187508 | C | T | 1 | a0009 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.1876C>T | p.Pro626Ser | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 6/6 | 2009/4164 | 1876/2625 | 626/874 | chr2 | 26187508 | |||
| chr2:26187671 | C | A | 1 | a0005 | 1 | HG00741.hp1 | missense_variant | MODERATE | c.2039C>A | p.Pro680His | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 6/6 | 2172/4164 | 2039/2625 | 680/874 | chr2 | 26187671 | |||
| chr2:26187911 | C | T | 1 | a0011 | 1 | NA18969.hp2 | missense_variant | MODERATE | c.2279C>T | p.Ala760Val | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 6/6 | 2412/4164 | 2279/2625 | 760/874 | chr2 | 26187911 | |||
| chr2:26187961 | C | T | 1 | a0006 | 1 | HG01099.hp2 | missense_variant | MODERATE | c.2329C>T | p.Arg777Cys | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 6/6 | 2462/4164 | 2329/2625 | 777/874 | chr2 | 26187961 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:26176345 | G | A | 17 | a0001c0001 a0001c0004 a0001c0005 others(14): Show |
240 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(237): Show |
splice_region_variant&synonymous_variant | LOW | c.114G>A | p.Gly38Gly | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 2/6 | 247/4164 | 114/2625 | 38/874 | chr2 | 26176345 | |||
| chr2:26184406 | G | T | 1 | a0001c0018 | 1 | NA19043.hp2 | synonymous_variant | LOW | c.558G>T | p.Gly186Gly | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 4/6 | 691/4164 | 558/2625 | 186/874 | chr2 | 26184406 | |||
| chr2:26184442 | G | A | 1 | a0001c0008 | 2 | HG02055.hp2 HG03130.hp1 |
synonymous_variant | LOW | c.594G>A | p.Ala198Ala | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 4/6 | 727/4164 | 594/2625 | 198/874 | chr2 | 26184442 | |||
| chr2:26185195 | T | C | 16 | a0001c0001 a0001c0002 a0001c0007 others(13): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
synonymous_variant | LOW | c.1347T>C | p.Asp449Asp | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 4/6 | 1480/4164 | 1347/2625 | 449/874 | chr2 | 26185195 | |||
| chr2:26185228 | T | G | 1 | a0001c0012 | 1 | HG00140.hp2 | synonymous_variant | LOW | c.1380T>G | p.Arg460Arg | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 4/6 | 1513/4164 | 1380/2625 | 460/874 | chr2 | 26185228 | |||
| chr2:26186350 | C | T | 1 | a0001c0015 | 1 | HG01496.hp2 | synonymous_variant | LOW | c.1590C>T | p.Leu530Leu | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 5/6 | 1723/4164 | 1590/2625 | 530/874 | chr2 | 26186350 | |||
| chr2:26187345 | C | T | 1 | a0001c0007 | 3 | HG01168.hp1 HG01175.hp2 HG02280.hp2 |
synonymous_variant | LOW | c.1713C>T | p.Pro571Pro | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 6/6 | 1846/4164 | 1713/2625 | 571/874 | chr2 | 26187345 | |||
| chr2:26187699 | T | C | 2 | a0001c0004 a0010c0010 |
10 | HG01884.hp1 HG02622.hp2 HG02630.hp2 others(7): Show |
synonymous_variant | LOW | c.2067T>C | p.Ser689Ser | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 6/6 | 2200/4164 | 2067/2625 | 689/874 | chr2 | 26187699 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:26173111 | A | T | 1 | a0001c0015t0015 | 1 | HG01496.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-110A>T | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 1/6 | chr2 | 26173111 | |||||||
| chr2:26173118 | G | T | 1 | a0001c0001t0014 | 1 | NA21309.hp1 | 5_prime_UTR_variant | MODIFIER | c.-103G>T | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 1/6 | 103 | chr2 | 26173118 | ||||||
| chr2:26188364 | G | A | 2 | a0001c0001t0009 a0001c0005t0008 |
3 | HG02723.hp1 HG03225.hp2 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*107G>A | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 6/6 | 107 | chr2 | 26188364 | ||||||
| chr2:26188616 | C | T | 1 | a0001c0001t0013 | 1 | NA19077.hp1 | 3_prime_UTR_variant | MODIFIER | c.*359C>T | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 6/6 | 359 | chr2 | 26188616 | ||||||
| chr2:26188651 | A | T | 2 | a0001c0004t0004 a0010c0010t0004 |
10 | HG01884.hp1 HG02622.hp2 HG02630.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*394A>T | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 6/6 | 394 | chr2 | 26188651 | ||||||
| chr2:26188672 | C | T | 1 | a0001c0001t0012 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*415C>T | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 6/6 | 415 | chr2 | 26188672 | ||||||
| chr2:26188805 | G | A | 2 | a0001c0001t0002 a0001c0002t0002 |
42 | HG00140.hp1 HG00738.hp2 HG01123.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*548G>A | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 6/6 | 548 | chr2 | 26188805 | ||||||
| chr2:26188971 | A | T | 2 | a0001c0002t0005 a0001c0008t0005 |
8 | HG00733.hp1 HG01074.hp2 HG01167.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*714A>T | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 6/6 | 714 | chr2 | 26188971 | ||||||
| chr2:26188984 | C | T | 1 | a0001c0001t0011 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*727C>T | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 6/6 | 727 | chr2 | 26188984 | ||||||
| chr2:26189016 | TCATC | T | 1 | a0001c0001t0007 | 3 | HG01167.hp2 HG01169.hp2 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*765_*768delATCC | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 6/6 | 765 | INFO_REALIGN_3_PRIME | chr2 | 26189016 | |||||
| chr2:26189025 | C | T | 23 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0010 others(20): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(228): Show |
3_prime_UTR_variant | MODIFIER | c.*768C>T | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 6/6 | 768 | chr2 | 26189025 | ||||||
| chr2:26189245 | G | A | 2 | a0001c0004t0004 a0010c0010t0004 |
10 | HG01884.hp1 HG02622.hp2 HG02630.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*988G>A | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 6/6 | 988 | chr2 | 26189245 | ||||||
| chr2:26189381 | C | T | 2 | a0001c0001t0006 a0001c0005t0006 |
4 | HG02717.hp1 HG02897.hp2 NA18522.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1124C>T | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 6/6 | 1124 | chr2 | 26189381 | ||||||
| chr2:26189588 | T | TCTTGCAG others(16): Show |
1 | a0001c0001t0010 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1332_*1354dupCTTG others(19): Show |
GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 6/6 | 1355 | INFO_REALIGN_3_PRIME | chr2 | 26189588 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:26173512 | C | T | 8 | a0001c0001t0001g0005 a0001c0001t0001g0092 a0001c0001t0001g0093 others(5): Show |
15 | HG01081.hp1 HG01192.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.112+180C>T | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 1/5 | chr2 | 26173512 | |||||||
| chr2:26173526 | C | G | 1 | a0001c0002t0002g0021 | 3 | HG03491.hp1 HG03492.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.112+194C>G | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 1/5 | chr2 | 26173526 | |||||||
| chr2:26173601 | G | A | 1 | a0001c0007t0001g0036 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.112+269G>A | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 1/5 | chr2 | 26173601 | |||||||
| chr2:26173751 | T | G | 1 | a0001c0001t0001g0037 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.112+419T>G | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 1/5 | chr2 | 26173751 | |||||||
| chr2:26173865 | G | A | 1 | a0001c0001t0001g0022 | 2 | HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.112+533G>A | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 1/5 | chr2 | 26173865 | |||||||
| chr2:26174071 | G | A | 15 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(12): Show |
34 | HG00408.hp1 HG00639.hp1 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.112+739G>A | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 1/5 | chr2 | 26174071 | |||||||
| chr2:26174185 | C | A | 1 | a0001c0002t0005g0008 | 6 | HG00733.hp1 HG01074.hp2 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.112+853C>A | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 1/5 | chr2 | 26174185 | |||||||
| chr2:26174320 | C | T | 2 | a0001c0001t0001g0090 a0001c0001t0001g0091 |
2 | HG02055.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.112+988C>T | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 1/5 | chr2 | 26174320 | |||||||
| chr2:26174339 | G | A | 1 | a0001c0005t0008g0024 | 2 | HG03225.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.112+1007G>A | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 1/5 | chr2 | 26174339 | |||||||
| chr2:26174380 | CT | C | 1 | a0001c0005t0003g0017 | 3 | HG01069.hp1 HG01071.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.112+1049delT | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 1/5 | chr2 | 26174380 | |||||||
| chr2:26174387 | G | T | 1 | a0001c0001t0001g0028 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.112+1055G>T | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 1/5 | chr2 | 26174387 | |||||||
| chr2:26174550 | G | T | 1 | a0001c0005t0006g0035 | 2 | HG02717.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.112+1218G>T | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 1/5 | chr2 | 26174550 | |||||||
| chr2:26174754 | T | C | 8 | a0001c0002t0005g0008 a0001c0004t0004g0006 a0001c0004t0004g0048 others(5): Show |
24 | HG00733.hp1 HG01069.hp1 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.112+1422T>C | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 1/5 | chr2 | 26174754 | |||||||
| chr2:26174792 | C | T | 4 | a0001c0004t0004g0006 a0001c0004t0004g0048 a0001c0005t0003g0017 others(1): Show |
13 | HG01069.hp1 HG01071.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.112+1460C>T | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 1/5 | chr2 | 26174792 | |||||||
| chr2:26174823 | G | T | 1 | a0001c0001t0001g0089 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.112+1491G>T | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 1/5 | chr2 | 26174823 | |||||||
| chr2:26174864 | T | C | 16 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(13): Show |
35 | HG00408.hp1 HG00639.hp1 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.113-1480T>C | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 1/5 | chr2 | 26174864 | |||||||
| chr2:26174876 | A | T | 1 | a0001c0001t0001g0097 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.113-1468A>T | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 1/5 | chr2 | 26174876 | |||||||
| chr2:26174975 | G | T | 1 | a0001c0001t0001g0015 | 4 | HG02257.hp2 HG02486.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-1369G>T | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 1/5 | chr2 | 26174975 | |||||||
| chr2:26175039 | G | C | 1 | a0001c0001t0001g0051 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.113-1305G>C | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 1/5 | chr2 | 26175039 | |||||||
| chr2:26175040 | C | G | 1 | a0001c0001t0001g0051 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.113-1304C>G | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 1/5 | chr2 | 26175040 | |||||||
| chr2:26175075 | C | CCA | 15 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(12): Show |
30 | HG00408.hp1 HG00639.hp1 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.113-1252_113-1251d others(4): Show |
GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 26175075 | ||||||
| chr2:26175075 | C | CCACA | 8 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0042 others(5): Show |
18 | HG01884.hp1 HG02257.hp2 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.113-1254_113-1251d others(6): Show |
GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 26175075 | ||||||
| chr2:26175094 | T | C | 1 | a0001c0002t0002g0052 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.113-1250T>C | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 1/5 | chr2 | 26175094 | |||||||
| chr2:26175111 | C | T | 1 | a0001c0002t0002g0020 | 3 | HG03669.hp1 NA20752.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.113-1233C>T | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 1/5 | chr2 | 26175111 | |||||||
| chr2:26175247 | C | T | 11 | a0001c0002t0001g0033 a0001c0002t0002g0002 a0001c0002t0002g0020 others(8): Show |
42 | HG00140.hp1 HG01123.hp2 HG01175.hp1 others(39): Show |
intron_variant | MODIFIER | c.113-1097C>T | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 1/5 | chr2 | 26175247 | |||||||
| chr2:26175455 | G | A | 100 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(97): Show |
247 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(244): Show |
intron_variant | MODIFIER | c.113-889G>A | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 1/5 | chr2 | 26175455 | |||||||
| chr2:26175466 | A | C | 75 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(72): Show |
187 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(184): Show |
intron_variant | MODIFIER | c.113-878A>C | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 1/5 | chr2 | 26175466 | |||||||
| chr2:26175528 | TG | T | 41 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(38): Show |
86 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.113-811delG | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 26175528 | ||||||
| chr2:26175638 | G | A | 1 | a0001c0006t0003g0083 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.113-706G>A | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 1/5 | chr2 | 26175638 | |||||||
| chr2:26175697 | A | G | 5 | a0001c0004t0004g0006 a0001c0004t0004g0048 a0001c0005t0003g0017 others(2): Show |
15 | HG01069.hp1 HG01071.hp2 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.113-647A>G | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 1/5 | chr2 | 26175697 | |||||||
| chr2:26175711 | G | A | 1 | a0001c0005t0008g0024 | 2 | HG03225.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.113-633G>A | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 1/5 | chr2 | 26175711 | |||||||
| chr2:26175899 | A | C | 100 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(97): Show |
247 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(244): Show |
intron_variant | MODIFIER | c.113-445A>C | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 1/5 | chr2 | 26175899 | |||||||
| chr2:26175930 | C | G | 1 | a0001c0001t0001g0051 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.113-414C>G | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 1/5 | chr2 | 26175930 | |||||||
| chr2:26175931 | G | C | 1 | a0001c0001t0001g0051 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.113-413G>C | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 1/5 | chr2 | 26175931 | |||||||
| chr2:26175970 | C | T | 1 | a0001c0002t0005g0008 | 6 | HG00733.hp1 HG01074.hp2 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.113-374C>T | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 1/5 | chr2 | 26175970 | |||||||
| chr2:26175973 | G | A | 2 | a0001c0001t0001g0009 a0004c0016t0001g0009 |
6 | HG00639.hp2 HG00642.hp2 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.113-371G>A | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 1/5 | chr2 | 26175973 | |||||||
| chr2:26176024 | G | A | 1 | a0001c0001t0001g0092 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.113-320G>A | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 1/5 | chr2 | 26176024 | |||||||
| chr2:26176074 | C | T | 34 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0022 others(31): Show |
101 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(98): Show |
intron_variant | MODIFIER | c.113-270C>T | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 1/5 | chr2 | 26176074 | |||||||
| chr2:26176112 | C | T | 2 | a0001c0002t0005g0008 a0009c0021t0003g0038 |
7 | HG00733.hp1 HG01074.hp2 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.113-232C>T | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 1/5 | chr2 | 26176112 | |||||||
| chr2:26176203 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.113-141C>T | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 1/5 | chr2 | 26176203 | |||||||
| chr2:26176237 | T | A | 1 | a0001c0001t0001g0026 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.113-107T>A | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 1/5 | chr2 | 26176237 | |||||||
| chr2:26176265 | C | T | 1 | a0001c0005t0008g0024 | 2 | HG03225.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.113-79C>T | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 1/5 | chr2 | 26176265 | |||||||
| chr2:26176309 | T | TTCCCCTC others(1): Show |
16 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(13): Show |
35 | HG00408.hp1 HG00642.hp1 HG01433.hp2 others(32): Show |
intron_variant | MODIFIER | c.113-31_113-24dupCC others(6): Show |
GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 26176309 | ||||||
| chr2:26176319 | C | T | 1 | a0001c0004t0004g0048 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.113-25C>T | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 1/5 | chr2 | 26176319 | |||||||
| chr2:26176572 | C | T | 1 | a0001c0002t0002g0088 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.253+88C>T | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 2/5 | chr2 | 26176572 | |||||||
| chr2:26176601 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.253+117G>A | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 2/5 | chr2 | 26176601 | |||||||
| chr2:26176612 | C | G | 34 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0022 others(31): Show |
101 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(98): Show |
intron_variant | MODIFIER | c.253+128C>G | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 2/5 | chr2 | 26176612 | |||||||
| chr2:26176640 | C | G | 1 | a0010c0010t0004g0047 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.253+156C>G | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 2/5 | chr2 | 26176640 | |||||||
| chr2:26176685 | T | C | 1 | a0010c0010t0004g0047 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.253+201T>C | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 2/5 | chr2 | 26176685 | |||||||
| chr2:26176876 | C | T | 37 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(34): Show |
74 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.253+392C>T | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 2/5 | chr2 | 26176876 | |||||||
| chr2:26177069 | A | C | 1 | a0009c0021t0003g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.253+585A>C | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 2/5 | chr2 | 26177069 | |||||||
| chr2:26177318 | G | A | 1 | a0009c0021t0003g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.253+834G>A | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 2/5 | chr2 | 26177318 | |||||||
| chr2:26177473 | A | G | 4 | a0001c0004t0004g0006 a0001c0004t0004g0048 a0001c0005t0003g0017 others(1): Show |
13 | HG01069.hp1 HG01071.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.253+989A>G | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 2/5 | chr2 | 26177473 | |||||||
| chr2:26177599 | C | T | 41 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(38): Show |
86 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.253+1115C>T | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 2/5 | chr2 | 26177599 | |||||||
| chr2:26177718 | C | T | 1 | a0001c0002t0002g0087 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.253+1234C>T | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 2/5 | chr2 | 26177718 | |||||||
| chr2:26177909 | C | G | 100 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(97): Show |
247 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(244): Show |
intron_variant | MODIFIER | c.253+1425C>G | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 2/5 | chr2 | 26177909 | |||||||
| chr2:26178068 | C | T | 4 | a0001c0002t0005g0008 a0001c0005t0008g0024 a0001c0008t0005g0025 others(1): Show |
11 | HG00733.hp1 HG01074.hp2 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.253+1584C>T | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 2/5 | chr2 | 26178068 | |||||||
| chr2:26178205 | G | A | 1 | a0001c0005t0006g0035 | 2 | HG02717.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.253+1721G>A | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 2/5 | chr2 | 26178205 | |||||||
| chr2:26178290 | T | G | 2 | a0001c0005t0008g0024 a0001c0008t0005g0025 |
4 | HG02055.hp2 HG03130.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.253+1806T>G | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 2/5 | chr2 | 26178290 | |||||||
| chr2:26178410 | AC | A | 80 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(77): Show |
214 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(211): Show |
intron_variant | MODIFIER | c.253+1937delC | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 26178410 | ||||||
| chr2:26178494 | G | C | 3 | a0001c0004t0004g0006 a0001c0004t0004g0048 a0010c0010t0004g0047 |
10 | HG01884.hp1 HG02622.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.253+2010G>C | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 2/5 | chr2 | 26178494 | |||||||
| chr2:26178611 | G | T | 96 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(93): Show |
236 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(233): Show |
intron_variant | MODIFIER | c.253+2127G>T | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 2/5 | chr2 | 26178611 | |||||||
| chr2:26178661 | C | T | 100 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(97): Show |
247 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(244): Show |
intron_variant | MODIFIER | c.253+2177C>T | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 2/5 | chr2 | 26178661 | |||||||
| chr2:26178721 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.253+2237C>T | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 2/5 | chr2 | 26178721 | |||||||
| chr2:26178830 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.253+2346G>A | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 2/5 | chr2 | 26178830 | |||||||
| chr2:26178868 | G | GC | 17 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(14): Show |
36 | HG00408.hp1 HG00639.hp1 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.253+2387dupC | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 26178868 | ||||||
| chr2:26178883 | G | GGGAGGCG others(11): Show |
3 | a0001c0001t0001g0010 a0001c0001t0001g0079 a0001c0001t0013g0010 |
7 | NA18940.hp1 NA18960.hp2 NA18964.hp2 others(4): Show |
intron_variant | MODIFIER | c.253+2404_253+2405i others(20): Show |
GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 26178883 | ||||||
| chr2:26178883 | G | GGGAGGCG others(17): Show |
8 | a0001c0001t0001g0007 a0001c0001t0001g0018 a0001c0001t0001g0030 others(5): Show |
18 | HG02071.hp2 HG02572.hp2 HG02615.hp1 others(15): Show |
intron_variant | MODIFIER | c.253+2404_253+2405i others(26): Show |
GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 26178883 | ||||||
| chr2:26178883 | G | GGGAGGCG others(23): Show |
22 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0019 others(19): Show |
53 | HG00408.hp2 HG00558.hp2 HG01081.hp1 others(50): Show |
intron_variant | MODIFIER | c.253+2404_253+2405i others(32): Show |
GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 26178883 | ||||||
| chr2:26178883 | G | GGGAGGCG others(29): Show |
2 | a0001c0001t0001g0075 a0001c0001t0001g0080 |
2 | HG02015.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.253+2404_253+2405i others(38): Show |
GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 26178883 | ||||||
| chr2:26178883 | G | GGGAGGCG others(35): Show |
3 | a0001c0001t0001g0076 a0001c0001t0001g0081 a0001c0001t0001g0095 |
3 | HG00558.hp1 HG02293.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.253+2404_253+2405i others(44): Show |
GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 26178883 | ||||||
| chr2:26178883 | G | GGGAGGCG others(41): Show |
2 | a0001c0001t0001g0077 a0001c0001t0001g0078 |
2 | NA18944.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.253+2404_253+2405i others(50): Show |
GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 26178883 | ||||||
| chr2:26178889 | A | AGGAGGCG others(10): Show |
1 | a0001c0001t0001g0046 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.253+2415_253+2416i others(19): Show |
GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 26178889 | ||||||
| chr2:26178889 | A | AGGAGGCG others(11): Show |
3 | a0001c0001t0001g0009 a0001c0001t0001g0055 a0004c0016t0001g0009 |
7 | HG00639.hp2 HG00642.hp2 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.253+2416_253+2417i others(20): Show |
GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 26178889 | ||||||
| chr2:26178889 | A | AGGAGGCG others(17): Show |
1 | a0001c0001t0001g0056 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.253+2416_253+2417i others(26): Show |
GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 26178889 | ||||||
| chr2:26178889 | A | AGGAGGCG others(23): Show |
29 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0026 others(26): Show |
92 | HG00099.hp2 HG00140.hp2 HG00733.hp2 others(89): Show |
intron_variant | MODIFIER | c.253+2416_253+2417i others(32): Show |
GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 26178889 | ||||||
| chr2:26178889 | A | AGGAGGCG others(5): Show |
4 | a0001c0001t0001g0064 a0001c0004t0004g0006 a0001c0004t0004g0048 others(1): Show |
11 | HG01884.hp1 HG02622.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.253+2412_253+2423d others(14): Show |
GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 26178889 | ||||||
| chr2:26178889 | A | AGGAGGCG others(17): Show |
3 | a0001c0001t0001g0013 a0001c0001t0001g0039 a0001c0001t0001g0040 |
6 | HG00642.hp1 HG01433.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.253+2423_253+2424i others(26): Show |
GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 26178889 | ||||||
| chr2:26178889 | A | AGGAGGCG others(23): Show |
11 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0015 others(8): Show |
29 | HG00408.hp1 HG01069.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.253+2423_253+2424i others(32): Show |
GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 26178889 | ||||||
| chr2:26178889 | A | AGGAGGCG others(29): Show |
2 | a0001c0001t0001g0043 a0001c0001t0001g0044 |
2 | HG02486.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.253+2423_253+2424i others(38): Show |
GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 26178889 | ||||||
| chr2:26178889 | A | AGGAGGCG others(35): Show |
1 | a0001c0001t0001g0045 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.253+2423_253+2424i others(44): Show |
GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 26178889 | ||||||
| chr2:26178889 | A | C | 41 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(38): Show |
86 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.253+2405A>C | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 2/5 | chr2 | 26178889 | |||||||
| chr2:26178902 | GGAGGCA | G | 4 | a0001c0002t0005g0008 a0001c0005t0008g0024 a0001c0008t0005g0025 others(1): Show |
11 | HG00733.hp1 HG01074.hp2 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.253+2424_253+2429d others(8): Show |
GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 26178902 | ||||||
| chr2:26178908 | A | G | 3 | a0001c0001t0001g0013 a0001c0001t0001g0039 a0001c0001t0001g0040 |
6 | HG00642.hp1 HG01433.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.253+2424A>G | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 2/5 | chr2 | 26178908 | |||||||
| chr2:26179052 | A | C | 4 | a0001c0004t0004g0006 a0001c0004t0004g0048 a0001c0005t0003g0017 others(1): Show |
13 | HG01069.hp1 HG01071.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.253+2568A>C | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 2/5 | chr2 | 26179052 | |||||||
| chr2:26179143 | C | G | 1 | a0001c0005t0008g0024 | 2 | HG03225.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.253+2659C>G | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 2/5 | chr2 | 26179143 | |||||||
| chr2:26179187 | C | A | 1 | a0001c0001t0001g0071 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.253+2703C>A | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 2/5 | chr2 | 26179187 | |||||||
| chr2:26179190 | G | T | 4 | a0001c0002t0005g0008 a0001c0005t0008g0024 a0001c0008t0005g0025 others(1): Show |
11 | HG00733.hp1 HG01074.hp2 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.253+2706G>T | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 2/5 | chr2 | 26179190 | |||||||
| chr2:26179215 | C | T | 1 | a0001c0002t0002g0085 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.253+2731C>T | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 2/5 | chr2 | 26179215 | |||||||
| chr2:26179260 | G | C | 1 | a0001c0005t0003g0017 | 3 | HG01069.hp1 HG01071.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.253+2776G>C | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 2/5 | chr2 | 26179260 | |||||||
| chr2:26179426 | T | A | 1 | a0001c0001t0001g0046 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.253+2942T>A | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 2/5 | chr2 | 26179426 | |||||||
| chr2:26179625 | G | A | 2 | a0001c0002t0002g0084 a0001c0002t0002g0086 |
2 | NA18993.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.253+3141G>A | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 2/5 | chr2 | 26179625 | |||||||
| chr2:26179725 | G | C | 96 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(93): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.253+3241G>C | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 2/5 | chr2 | 26179725 | |||||||
| chr2:26179977 | A | G | 103 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(100): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(255): Show |
intron_variant | MODIFIER | c.254-2990A>G | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 2/5 | chr2 | 26179977 | |||||||
| chr2:26179994 | C | T | 3 | a0001c0002t0005g0008 a0001c0005t0008g0024 a0001c0008t0005g0025 |
10 | HG00733.hp1 HG01074.hp2 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.254-2973C>T | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 2/5 | chr2 | 26179994 | |||||||
| chr2:26180114 | G | T | 2 | a0001c0002t0001g0011 a0006c0020t0001g0011 |
6 | HG00741.hp2 HG01074.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.254-2853G>T | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 2/5 | chr2 | 26180114 | |||||||
| chr2:26180133 | G | T | 3 | a0001c0001t0001g0027 a0001c0001t0001g0055 a0008c0013t0001g0027 |
3 | HG02109.hp1 HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.254-2834G>T | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 2/5 | chr2 | 26180133 | |||||||
| chr2:26180388 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.254-2579C>T | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 2/5 | chr2 | 26180388 | |||||||
| chr2:26180727 | C | G | 1 | a0001c0008t0005g0025 | 2 | HG02055.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.254-2240C>G | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 2/5 | chr2 | 26180727 | |||||||
| chr2:26180881 | G | A | 1 | a0001c0001t0001g0031 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.254-2086G>A | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 2/5 | chr2 | 26180881 | |||||||
| chr2:26180897 | G | A | 103 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(100): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(255): Show |
intron_variant | MODIFIER | c.254-2070G>A | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 2/5 | chr2 | 26180897 | |||||||
| chr2:26181305 | G | T | 2 | a0001c0001t0001g0074 a0001c0001t0001g0075 |
2 | HG02132.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.254-1662G>T | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 2/5 | chr2 | 26181305 | |||||||
| chr2:26181310 | T | C | 1 | a0001c0001t0001g0066 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.254-1657T>C | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 2/5 | chr2 | 26181310 | |||||||
| chr2:26181340 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.254-1627C>T | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 2/5 | chr2 | 26181340 | |||||||
| chr2:26181341 | A | G | 1 | a0001c0001t0001g0073 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.254-1626A>G | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 2/5 | chr2 | 26181341 | |||||||
| chr2:26181352 | C | T | 103 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(100): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(255): Show |
intron_variant | MODIFIER | c.254-1615C>T | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 2/5 | chr2 | 26181352 | |||||||
| chr2:26181570 | T | C | 3 | a0001c0002t0005g0008 a0001c0008t0005g0025 a0009c0021t0003g0038 |
9 | HG00733.hp1 HG01074.hp2 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.254-1397T>C | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 2/5 | chr2 | 26181570 | |||||||
| chr2:26181641 | T | G | 37 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(34): Show |
74 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.254-1326T>G | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 2/5 | chr2 | 26181641 | |||||||
| chr2:26181792 | C | T | 2 | a0001c0002t0005g0008 a0001c0008t0005g0025 |
8 | HG00733.hp1 HG01074.hp2 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.254-1175C>T | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 2/5 | chr2 | 26181792 | |||||||
| chr2:26181906 | A | G | 103 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(100): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(255): Show |
intron_variant | MODIFIER | c.254-1061A>G | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 2/5 | chr2 | 26181906 | |||||||
| chr2:26181965 | A | G | 1 | a0001c0001t0001g0019 | 3 | NA18981.hp2 NA19070.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.254-1002A>G | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 2/5 | chr2 | 26181965 | |||||||
| chr2:26182147 | C | G | 103 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(100): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(255): Show |
intron_variant | MODIFIER | c.254-820C>G | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 2/5 | chr2 | 26182147 | |||||||
| chr2:26182245 | T | C | 1 | a0001c0001t0001g0090 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.254-722T>C | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 2/5 | chr2 | 26182245 | |||||||
| chr2:26182444 | C | A | 1 | a0001c0001t0014g0057 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.254-523C>A | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 2/5 | chr2 | 26182444 | |||||||
| chr2:26182537 | C | G | 2 | a0001c0002t0005g0008 a0001c0008t0005g0025 |
8 | HG00733.hp1 HG01074.hp2 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.254-430C>G | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 2/5 | chr2 | 26182537 | |||||||
| chr2:26182549 | A | G | 1 | a0002c0003t0001g0061 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.254-418A>G | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 2/5 | chr2 | 26182549 | |||||||
| chr2:26182565 | G | A | 1 | a0001c0002t0002g0034 | 2 | HG03710.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.254-402G>A | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 2/5 | chr2 | 26182565 | |||||||
| chr2:26182814 | C | A | 1 | a0001c0001t0001g0093 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.254-153C>A | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 2/5 | chr2 | 26182814 | |||||||
| chr2:26182881 | G | C | 1 | a0009c0021t0003g0038 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.254-86G>C | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 2/5 | chr2 | 26182881 | |||||||
| chr2:26183116 | A | G | 103 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(100): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(255): Show |
intron_variant | MODIFIER | c.384+19A>G | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 3/5 | chr2 | 26183116 | |||||||
| chr2:26183238 | T | C | 1 | a0001c0001t0001g0072 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.384+141T>C | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 3/5 | chr2 | 26183238 | |||||||
| chr2:26183466 | GTAATCCC others(4): Show |
G | 5 | a0001c0004t0004g0006 a0001c0004t0004g0048 a0001c0005t0003g0017 others(2): Show |
15 | HG01069.hp1 HG01071.hp2 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.384+370_384+380del others(11): Show |
GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 3/5 | chr2 | 26183466 | |||||||
| chr2:26183478 | C | T | 1 | a0002c0003t0001g0060 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.384+381C>T | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 3/5 | chr2 | 26183478 | |||||||
| chr2:26183700 | A | C | 8 | a0001c0002t0005g0008 a0001c0004t0004g0006 a0001c0004t0004g0048 others(5): Show |
24 | HG00733.hp1 HG01069.hp1 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.385-533A>C | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 3/5 | chr2 | 26183700 | |||||||
| chr2:26183720 | TCAAA | T | 95 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(92): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.385-492_385-489del others(4): Show |
GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 26183720 | ||||||
| chr2:26183897 | C | T | 14 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(11): Show |
32 | HG00408.hp1 HG00639.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.385-336C>T | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 3/5 | chr2 | 26183897 | |||||||
| chr2:26184111 | C | T | 1 | a0003c0009t0001g0029 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.385-122C>T | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 3/5 | chr2 | 26184111 | |||||||
| chr2:26184156 | T | C | 1 | a0001c0001t0001g0039 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.385-77T>C | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 3/5 | chr2 | 26184156 | |||||||
| chr2:26184192 | G | C | 2 | a0001c0001t0001g0090 a0001c0001t0001g0091 |
2 | HG02055.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.385-41G>C | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 3/5 | chr2 | 26184192 | |||||||
| chr2:26185282 | T | C | 2 | a0001c0001t0001g0039 a0001c0001t0001g0040 |
2 | HG03831.hp1 HG04199.hp2 |
splice_region_variant&intron_variant | LOW | c.1428+6T>C | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 4/5 | chr2 | 26185282 | |||||||
| chr2:26185287 | G | T | 1 | a0001c0001t0001g0058 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1428+11G>T | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 4/5 | chr2 | 26185287 | |||||||
| chr2:26185344 | C | T | 1 | a0001c0001t0001g0039 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1428+68C>T | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 4/5 | chr2 | 26185344 | |||||||
| chr2:26185461 | G | T | 3 | a0001c0001t0001g0015 a0001c0001t0001g0042 a0001c0001t0001g0059 |
6 | HG02257.hp2 HG02486.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1428+185G>T | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 4/5 | chr2 | 26185461 | |||||||
| chr2:26185798 | G | A | 1 | a0001c0006t0003g0083 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1429-391G>A | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 4/5 | chr2 | 26185798 | |||||||
| chr2:26185927 | T | C | 1 | a0001c0001t0001g0062 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1429-262T>C | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 4/5 | chr2 | 26185927 | |||||||
| chr2:26186105 | C | G | 1 | a0001c0001t0001g0067 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1429-84C>G | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 4/5 | chr2 | 26186105 | |||||||
| chr2:26186113 | C | T | 2 | a0001c0001t0001g0076 a0001c0001t0001g0081 |
2 | HG00558.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.1429-76C>T | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 4/5 | chr2 | 26186113 | |||||||
| chr2:26186582 | T | C | 1 | a0001c0002t0002g0088 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1598+224T>C | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 5/5 | chr2 | 26186582 | |||||||
| chr2:26186803 | C | G | 2 | a0001c0001t0001g0009 a0004c0016t0001g0009 |
6 | HG00639.hp2 HG00642.hp2 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.1599-428C>G | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 5/5 | chr2 | 26186803 | |||||||
| chr2:26186924 | A | G | 2 | a0001c0001t0001g0018 a0001c0001t0011g0018 |
3 | HG02809.hp2 HG03098.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1599-307A>G | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 5/5 | chr2 | 26186924 | |||||||
| chr2:26186943 | C | G | 1 | a0001c0001t0001g0078 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1599-288C>G | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 5/5 | chr2 | 26186943 | |||||||
| chr2:26187017 | G | A | 1 | a0001c0001t0014g0057 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1599-214G>A | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 5/5 | chr2 | 26187017 | |||||||
| chr2:26187081 | G | A | 100 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(97): Show |
248 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(245): Show |
intron_variant | MODIFIER | c.1599-150G>A | GAREM2 | ENSG00000157833.13 | transcript | ENST00000401533.7 | protein_coding | 5/5 | chr2 | 26187081 |