Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 2208 |
| ensemblid | ENSG00000104921.15 |
| hgncid | 3612 |
| symbol | FCER2 |
| name | Fc epsilon receptor II |
| refseq_nuc | NM_001220500.2 |
| refseq_prot | NP_001207429.1 |
| ensembl_nuc | ENST00000597921.6 |
| ensembl_prot | ENSP00000471974.1 |
| mane_status | MANE Select |
| chr | chr19 |
| start | 7688776 |
| end | 7702131 |
| strand | - |
| ver | v1.2 |
| region | chr19:7688776-7702131 |
| region5000 | chr19:7683776-7707131 |
| regionname0 | FCER2_chr19_7688776_7702131 |
| regionname5000 | FCER2_chr19_7683776_7707131 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 321 | 360 | 66 | 72 | 180 | 13 | 27 | 138 | FCER2_chr19_7683776_7707131 | FCER2 | MEEGQ others(316): Show |
chr19 | 7683776 | 7707131 |
| a0002 | 0/0 | 321 | 79 | 28 | 9 | 16 | 4 | 22 | 9 | FCER2_chr19_7683776_7707131 | FCER2 | MEEGQ others(316): Show |
chr19 | 7683776 | 7707131 |
| a0003 | 0/0 | 321 | 7 | 0 | 3 | 3 | 1 | 0 | 2 | FCER2_chr19_7683776_7707131 | FCER2 | MEEGQ others(316): Show |
chr19 | 7683776 | 7707131 |
| a0004 | 0/0 | 321 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | MEEGQ others(316): Show |
chr19 | 7683776 | 7707131 |
| a0005 | 0/0 | 321 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | MEEGQ others(316): Show |
chr19 | 7683776 | 7707131 |
| a0006 | 0/0 | 321 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | MEEGQ others(316): Show |
chr19 | 7683776 | 7707131 |
| a0007 | 0/0 | 321 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | MEEGQ others(316): Show |
chr19 | 7683776 | 7707131 |
| a0008 | 0/0 | 321 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | MEEGQ others(316): Show |
chr19 | 7683776 | 7707131 |
| a0009 | 0/0 | 321 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | MEEGQ others(316): Show |
chr19 | 7683776 | 7707131 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 963 | 227 | 34 | 47 | 115 | 11 | 18 | FCER2_chr19_7683776_7707131 | FCER2 | ATGGA others(958): Show |
chr19 | 7683776 | 7707131 | ||
| a0001c0003 | 0/0 | 963 | 60 | 21 | 6 | 26 | 2 | 5 | FCER2_chr19_7683776_7707131 | FCER2 | ATGGA others(958): Show |
chr19 | 7683776 | 7707131 | ||
| a0001c0004 | 0/0 | 963 | 40 | 6 | 17 | 16 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | ATGGA others(958): Show |
chr19 | 7683776 | 7707131 | ||
| a0001c0005 | 0/0 | 963 | 31 | 4 | 2 | 22 | 0 | 3 | FCER2_chr19_7683776_7707131 | FCER2 | ATGGA others(958): Show |
chr19 | 7683776 | 7707131 | ||
| a0001c0012 | 0/0 | 963 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | ATGGA others(958): Show |
chr19 | 7683776 | 7707131 | ||
| a0001c0017 | 0/0 | 963 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | ATGGA others(958): Show |
chr19 | 7683776 | 7707131 | ||
| a0002c0002 | 0/0 | 963 | 63 | 22 | 8 | 12 | 4 | 17 | FCER2_chr19_7683776_7707131 | FCER2 | ATGGA others(958): Show |
chr19 | 7683776 | 7707131 | ||
| a0002c0006 | 0/0 | 963 | 11 | 2 | 1 | 4 | 0 | 4 | FCER2_chr19_7683776_7707131 | FCER2 | ATGGA others(958): Show |
chr19 | 7683776 | 7707131 | ||
| a0002c0009 | 0/0 | 963 | 4 | 3 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | ATGGA others(958): Show |
chr19 | 7683776 | 7707131 | ||
| a0002c0014 | 0/0 | 963 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | ATGGA others(958): Show |
chr19 | 7683776 | 7707131 | ||
| a0003c0008 | 0/0 | 963 | 4 | 0 | 3 | 0 | 1 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | ATGGA others(958): Show |
chr19 | 7683776 | 7707131 | ||
| a0003c0010 | 0/0 | 963 | 3 | 0 | 0 | 3 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | ATGGA others(958): Show |
chr19 | 7683776 | 7707131 | ||
| a0004c0007 | 0/0 | 963 | 5 | 5 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | ATGGA others(958): Show |
chr19 | 7683776 | 7707131 | ||
| a0005c0016 | 0/0 | 963 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | ATGGA others(958): Show |
chr19 | 7683776 | 7707131 | ||
| a0006c0011 | 0/0 | 963 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | ATGGA others(958): Show |
chr19 | 7683776 | 7707131 | ||
| a0007c0013 | 0/0 | 963 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | ATGGA others(958): Show |
chr19 | 7683776 | 7707131 | ||
| a0008c0015 | 0/0 | 963 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | ATGGA others(958): Show |
chr19 | 7683776 | 7707131 | ||
| a0009c0018 | 0/0 | 963 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | ATGGA others(958): Show |
chr19 | 7683776 | 7707131 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1585 | 225 | 34 | 46 | 114 | 11 | 18 | FCER2_chr19_7683776_7707131 | FCER2 | AGAAG others(1580): Show |
chr19 | 7683776 | 7707131 |
| a0001c0001t0004 | 0/0 | 1617 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | AGAAG others(1612): Show |
chr19 | 7683776 | 7707131 |
| a0001c0001t0006 | 0/0 | 1585 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | AGAAG others(1580): Show |
chr19 | 7683776 | 7707131 |
| a0001c0003t0001 | 0/0 | 1585 | 43 | 16 | 0 | 24 | 0 | 3 | FCER2_chr19_7683776_7707131 | FCER2 | AGAAG others(1580): Show |
chr19 | 7683776 | 7707131 |
| a0001c0003t0002 | 0/0 | 1521 | 16 | 4 | 6 | 2 | 2 | 2 | FCER2_chr19_7683776_7707131 | FCER2 | AGAAG others(1516): Show |
chr19 | 7683776 | 7707131 |
| a0001c0003t0007 | 0/0 | 1585 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | AGAAG others(1580): Show |
chr19 | 7683776 | 7707131 |
| a0001c0004t0001 | 0/0 | 1585 | 40 | 6 | 17 | 16 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | AGAAG others(1580): Show |
chr19 | 7683776 | 7707131 |
| a0001c0005t0001 | 0/0 | 1585 | 21 | 4 | 0 | 14 | 0 | 3 | FCER2_chr19_7683776_7707131 | FCER2 | AGAAG others(1580): Show |
chr19 | 7683776 | 7707131 |
| a0001c0005t0002 | 0/0 | 1521 | 10 | 0 | 2 | 8 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | AGAAG others(1516): Show |
chr19 | 7683776 | 7707131 |
| a0001c0012t0001 | 0/0 | 1585 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | AGAAG others(1580): Show |
chr19 | 7683776 | 7707131 |
| a0001c0017t0001 | 0/0 | 1585 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | AGAAG others(1580): Show |
chr19 | 7683776 | 7707131 |
| a0002c0002t0001 | 0/0 | 1585 | 59 | 22 | 8 | 8 | 4 | 17 | FCER2_chr19_7683776_7707131 | FCER2 | AGAAG others(1580): Show |
chr19 | 7683776 | 7707131 |
| a0002c0002t0003 | 0/0 | 1585 | 4 | 0 | 0 | 4 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | AGAAG others(1580): Show |
chr19 | 7683776 | 7707131 |
| a0002c0006t0001 | 0/0 | 1585 | 11 | 2 | 1 | 4 | 0 | 4 | FCER2_chr19_7683776_7707131 | FCER2 | AGAAG others(1580): Show |
chr19 | 7683776 | 7707131 |
| a0002c0009t0001 | 0/0 | 1585 | 4 | 3 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | AGAAG others(1580): Show |
chr19 | 7683776 | 7707131 |
| a0002c0014t0001 | 0/0 | 1585 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | AGAAG others(1580): Show |
chr19 | 7683776 | 7707131 |
| a0003c0008t0001 | 0/0 | 1585 | 3 | 0 | 2 | 0 | 1 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | AGAAG others(1580): Show |
chr19 | 7683776 | 7707131 |
| a0003c0008t0005 | 0/0 | 1553 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | AGAAG others(1548): Show |
chr19 | 7683776 | 7707131 |
| a0003c0010t0001 | 0/0 | 1585 | 3 | 0 | 0 | 3 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | AGAAG others(1580): Show |
chr19 | 7683776 | 7707131 |
| a0004c0007t0001 | 0/0 | 1585 | 5 | 5 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | AGAAG others(1580): Show |
chr19 | 7683776 | 7707131 |
| a0005c0016t0001 | 0/0 | 1585 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | AGAAG others(1580): Show |
chr19 | 7683776 | 7707131 |
| a0006c0011t0001 | 0/0 | 1585 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | AGAAG others(1580): Show |
chr19 | 7683776 | 7707131 |
| a0007c0013t0001 | 0/0 | 1585 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | AGAAG others(1580): Show |
chr19 | 7683776 | 7707131 |
| a0008c0015t0001 | 0/0 | 1585 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | AGAAG others(1580): Show |
chr19 | 7683776 | 7707131 |
| a0009c0018t0001 | 0/0 | 1585 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | AGAAG others(1580): Show |
chr19 | 7683776 | 7707131 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 16 | 1 | 7 | 4 | 2 | 2 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0002 | 0/0 | 13 | 1 | 4 | 6 | 0 | 2 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0003 | 0/0 | 10 | 0 | 3 | 7 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0005 | 0/0 | 9 | 0 | 0 | 8 | 1 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0007 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0008 | 0/0 | 7 | 0 | 3 | 4 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0010 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0012 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0014 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0020 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0026 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0028 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0033 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0047 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0051 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0055 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0056 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0057 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0059 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0061 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0100 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0118 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0004g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0001t0006g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0003t0001g0009 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0003t0001g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0003t0001g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0003t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0003t0001g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0003t0001g0054 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0003t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0003t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0003t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0003t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0003t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0003t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0003t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0003t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0003t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0003t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0003t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0003t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0003t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0003t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0003t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0003t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0003t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0003t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0003t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0003t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0003t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0003t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0003t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0003t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0003t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0003t0002g0011 | 0/0 | 6 | 0 | 5 | 0 | 1 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0003t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0003t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0003t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0003t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0003t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0003t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0003t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0003t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0003t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0003t0002g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0003t0007g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0004t0001g0006 | 0/0 | 8 | 0 | 8 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0004t0001g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0004t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0004t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0004t0001g0045 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0004t0001g0058 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0004t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0004t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0004t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0004t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0004t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0004t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0004t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0004t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0004t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0004t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0004t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0004t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0004t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0004t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0004t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0004t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0004t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0004t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0004t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0004t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0004t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0005t0001g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0005t0001g0029 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0005t0001g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0005t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0005t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0005t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0005t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0005t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0005t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0005t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0005t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0005t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0005t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0005t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0005t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0005t0002g0013 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0005t0002g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0005t0002g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0005t0002g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0012t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0001c0017t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0002c0002t0001g0004 | 0/0 | 9 | 0 | 3 | 0 | 1 | 5 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0002c0002t0001g0018 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0002c0002t0001g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0002c0002t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0002c0002t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0002c0002t0001g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0002c0002t0001g0053 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0002c0002t0001g0060 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0002c0002t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0002c0002t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0002c0002t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0002c0002t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0002c0002t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0002c0002t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0002c0002t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0002c0002t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0002c0002t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0002c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0002c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0002c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0002c0002t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0002c0002t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0002c0002t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0002c0002t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0002c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0002c0002t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0002c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0002c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0002c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0002c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0002c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0002c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0002c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0002c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0002c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0002c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0002c0002t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0002c0002t0003g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0002c0002t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0002c0006t0001g0016 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0002c0006t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0002c0006t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0002c0006t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0002c0006t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0002c0006t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0002c0006t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0002c0006t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0002c0006t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0002c0009t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0002c0009t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0002c0009t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0002c0014t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0003c0008t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0003c0008t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0003c0008t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0003c0008t0005g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0003c0010t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0003c0010t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0003c0010t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0004c0007t0001g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0004c0007t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0004c0007t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0005c0016t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0006c0011t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0007c0013t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0008c0015t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| a0009c0018t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0026 | EUR | GBR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0034 | EUR | GBR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0089 | EUR | GBR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG00140 | hp2 | a0002 | c0002 | t0001 | g0260 | EUR | GBR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0094 | EUR | FIN | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG00280 | hp2 | a0001 | c0003 | t0002 | g0011 | EUR | FIN | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | FIN | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG00323 | hp2 | a0002 | c0002 | t0001 | g0004 | EUR | FIN | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG00423 | hp1 | a0002 | c0002 | t0003 | g0129 | EAS | CHS | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | CHS | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG00438 | hp1 | a0001 | c0003 | t0001 | g0009 | EAS | CHS | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG00438 | hp2 | a0002 | c0002 | t0001 | g0064 | EAS | CHS | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | CHS | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | CHS | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG00597 | hp1 | a0001 | c0003 | t0001 | g0009 | EAS | CHS | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | CHS | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG00609 | hp1 | a0001 | c0005 | t0002 | g0013 | EAS | CHS | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG00609 | hp2 | a0002 | c0002 | t0001 | g0246 | EAS | CHS | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | CHS | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG00621 | hp2 | a0002 | c0006 | t0001 | g0016 | EAS | CHS | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG00642 | hp1 | a0001 | c0005 | t0002 | g0269 | AMR | PUR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | CHS | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG00673 | hp2 | a0002 | c0006 | t0001 | g0125 | EAS | CHS | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG00733 | hp1 | a0003 | c0008 | t0005 | g0175 | AMR | PUR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG00735 | hp2 | a0001 | c0004 | t0001 | g0006 | AMR | PUR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG00741 | hp2 | a0001 | c0003 | t0002 | g0011 | AMR | PUR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG01069 | hp1 | a0001 | c0003 | t0002 | g0011 | AMR | PUR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG01069 | hp2 | a0001 | c0004 | t0001 | g0006 | AMR | PUR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG01070 | hp2 | a0002 | c0002 | t0001 | g0004 | AMR | PUR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | PUR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG01071 | hp2 | a0001 | c0003 | t0002 | g0011 | AMR | PUR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG01074 | hp2 | a0002 | c0002 | t0001 | g0130 | AMR | PUR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG01099 | hp1 | a0001 | c0004 | t0001 | g0006 | AMR | PUR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG01106 | hp2 | a0005 | c0016 | t0001 | g0181 | AMR | PUR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG01109 | hp2 | a0002 | c0002 | t0001 | g0223 | AMR | PUR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG01167 | hp1 | a0001 | c0004 | t0001 | g0045 | AMR | PUR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG01167 | hp2 | a0002 | c0002 | t0001 | g0018 | AMR | PUR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG01169 | hp1 | a0001 | c0004 | t0001 | g0045 | AMR | PUR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0275 | AMR | PUR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG01192 | hp1 | a0001 | c0003 | t0002 | g0011 | AMR | PUR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG01192 | hp2 | a0002 | c0002 | t0001 | g0131 | AMR | PUR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG01243 | hp2 | a0001 | c0005 | t0002 | g0270 | AMR | PUR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG01255 | hp1 | a0001 | c0003 | t0002 | g0011 | AMR | CLM | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG01255 | hp2 | a0003 | c0008 | t0001 | g0277 | AMR | CLM | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | CLM | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG01261 | hp1 | a0002 | c0006 | t0001 | g0067 | AMR | CLM | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0284 | AMR | CLM | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG01346 | hp2 | a0001 | c0003 | t0002 | g0110 | AMR | CLM | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG01358 | hp1 | a0001 | c0004 | t0001 | g0031 | AMR | CLM | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG01361 | hp2 | a0001 | c0004 | t0001 | g0006 | AMR | CLM | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | CLM | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | CLM | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG01496 | hp2 | a0001 | c0004 | t0001 | g0261 | AMR | CLM | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0057 | EUR | IBS | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0051 | EUR | IBS | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG01516 | hp1 | a0002 | c0002 | t0001 | g0259 | EUR | IBS | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0057 | EUR | IBS | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | ACB | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG01884 | hp2 | a0002 | c0002 | t0001 | g0019 | AFR | ACB | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG01891 | hp1 | a0002 | c0014 | t0001 | g0085 | AFR | ACB | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG01891 | hp2 | a0001 | c0004 | t0001 | g0162 | AFR | ACB | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG01928 | hp1 | a0006 | c0011 | t0001 | g0188 | AMR | PEL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG01928 | hp2 | a0001 | c0004 | t0001 | g0169 | AMR | PEL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG01943 | hp1 | a0001 | c0004 | t0001 | g0031 | AMR | PEL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0285 | AMR | PEL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG01952 | hp1 | a0001 | c0004 | t0001 | g0006 | AMR | PEL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG01952 | hp2 | a0002 | c0002 | t0001 | g0108 | AMR | PEL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG01975 | hp1 | a0001 | c0004 | t0001 | g0266 | AMR | PEL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PEL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG01978 | hp1 | a0001 | c0001 | t0006 | g0177 | AMR | PEL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG01993 | hp2 | a0001 | c0004 | t0001 | g0006 | AMR | PEL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PEL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02004 | hp2 | a0003 | c0008 | t0001 | g0114 | AMR | PEL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | KHV | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | KHV | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02027 | hp2 | a0001 | c0003 | t0002 | g0210 | EAS | KHV | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02040 | hp2 | a0001 | c0003 | t0001 | g0282 | EAS | KHV | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02055 | hp1 | a0002 | c0002 | t0001 | g0123 | AFR | ACB | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | KHV | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | KHV | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02074 | hp1 | a0001 | c0003 | t0001 | g0054 | EAS | KHV | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02074 | hp2 | a0001 | c0004 | t0001 | g0183 | EAS | KHV | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02080 | hp1 | a0001 | c0004 | t0001 | g0267 | EAS | KHV | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02083 | hp1 | a0001 | c0003 | t0001 | g0279 | EAS | KHV | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02083 | hp2 | a0001 | c0003 | t0001 | g0054 | EAS | KHV | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | KHV | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | KHV | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02132 | hp1 | a0003 | c0010 | t0001 | g0271 | EAS | KHV | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02132 | hp2 | a0001 | c0003 | t0001 | g0106 | EAS | KHV | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | KHV | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02145 | hp1 | a0002 | c0002 | t0001 | g0088 | AFR | ACB | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02145 | hp2 | a0002 | c0009 | t0001 | g0041 | AFR | ACB | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02155 | hp1 | a0001 | c0004 | t0001 | g0025 | EAS | CDX | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CDX | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CDX | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02257 | hp1 | a0002 | c0009 | t0001 | g0041 | AFR | ACB | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | ACB | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02258 | hp1 | a0001 | c0003 | t0001 | g0074 | AFR | ACB | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02273 | hp1 | a0001 | c0004 | t0001 | g0058 | AMR | PEL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02273 | hp2 | a0001 | c0004 | t0001 | g0006 | AMR | PEL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02280 | hp1 | a0002 | c0002 | t0001 | g0084 | AFR | ACB | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02280 | hp2 | a0001 | c0005 | t0001 | g0042 | AFR | ACB | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PEL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02300 | hp1 | a0001 | c0004 | t0001 | g0189 | AMR | PEL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PEL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | ACB | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02451 | hp2 | a0002 | c0002 | t0001 | g0035 | AFR | ACB | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | KHV | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02572 | hp1 | a0001 | c0003 | t0001 | g0017 | AFR | GWD | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02572 | hp2 | a0002 | c0002 | t0001 | g0019 | AFR | GWD | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02602 | hp1 | a0002 | c0002 | t0001 | g0168 | SAS | PJL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02602 | hp2 | a0001 | c0003 | t0001 | g0092 | SAS | PJL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02615 | hp1 | a0004 | c0007 | t0001 | g0086 | AFR | GWD | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0292 | AFR | GWD | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02622 | hp1 | a0002 | c0002 | t0001 | g0040 | AFR | GWD | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0283 | AFR | GWD | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02630 | hp1 | a0002 | c0002 | t0001 | g0049 | AFR | GWD | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02630 | hp2 | a0001 | c0004 | t0001 | g0159 | AFR | GWD | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02647 | hp2 | a0001 | c0003 | t0007 | g0291 | AFR | GWD | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02683 | hp1 | a0001 | c0003 | t0002 | g0276 | SAS | PJL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02683 | hp2 | a0001 | c0003 | t0001 | g0116 | SAS | PJL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0079 | SAS | PJL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | GWD | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02723 | hp1 | a0002 | c0006 | t0001 | g0290 | AFR | GWD | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02723 | hp2 | a0004 | c0007 | t0001 | g0024 | AFR | GWD | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02735 | hp1 | a0002 | c0002 | t0001 | g0004 | SAS | PJL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02738 | hp2 | a0002 | c0002 | t0001 | g0004 | SAS | PJL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02809 | hp1 | a0001 | c0003 | t0001 | g0017 | AFR | GWD | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02809 | hp2 | a0002 | c0002 | t0001 | g0214 | AFR | GWD | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02818 | hp2 | a0001 | c0003 | t0002 | g0216 | AFR | GWD | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02886 | hp1 | a0001 | c0003 | t0002 | g0152 | AFR | GWD | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02886 | hp2 | a0001 | c0017 | t0001 | g0288 | AFR | GWD | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02895 | hp2 | a0002 | c0002 | t0001 | g0053 | AFR | GWD | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02896 | hp1 | a0001 | c0005 | t0001 | g0215 | AFR | GWD | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02896 | hp2 | a0004 | c0007 | t0001 | g0024 | AFR | GWD | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02897 | hp1 | a0004 | c0007 | t0001 | g0024 | AFR | GWD | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02897 | hp2 | a0002 | c0002 | t0001 | g0053 | AFR | GWD | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02922 | hp1 | a0001 | c0004 | t0001 | g0156 | AFR | ESN | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02922 | hp2 | a0001 | c0003 | t0001 | g0017 | AFR | ESN | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02965 | hp1 | a0001 | c0005 | t0001 | g0042 | AFR | ESN | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02965 | hp2 | a0001 | c0003 | t0001 | g0146 | AFR | ESN | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02970 | hp1 | a0002 | c0002 | t0001 | g0158 | AFR | ESN | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02970 | hp2 | a0002 | c0002 | t0001 | g0120 | AFR | ESN | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | ESN | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02976 | hp2 | a0002 | c0002 | t0001 | g0040 | AFR | ESN | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG03017 | hp1 | a0002 | c0006 | t0001 | g0016 | SAS | PJL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG03017 | hp2 | a0002 | c0006 | t0001 | g0083 | SAS | PJL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG03041 | hp1 | a0001 | c0003 | t0001 | g0145 | AFR | GWD | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG03098 | hp1 | a0001 | c0003 | t0001 | g0036 | AFR | MSL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG03098 | hp2 | a0004 | c0007 | t0001 | g0066 | AFR | MSL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG03130 | hp1 | a0001 | c0003 | t0001 | g0023 | AFR | ESN | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG03130 | hp2 | a0001 | c0004 | t0001 | g0157 | AFR | ESN | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG03139 | hp1 | a0002 | c0002 | t0001 | g0019 | AFR | ESN | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG03139 | hp2 | a0002 | c0002 | t0001 | g0075 | AFR | ESN | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG03195 | hp1 | a0001 | c0004 | t0001 | g0219 | AFR | ESN | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG03195 | hp2 | a0001 | c0003 | t0001 | g0023 | AFR | ESN | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG03209 | hp1 | a0001 | c0004 | t0001 | g0286 | AFR | MSL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | MSL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG03225 | hp1 | a0002 | c0006 | t0001 | g0163 | AFR | MSL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG03225 | hp2 | a0002 | c0002 | t0001 | g0161 | AFR | MSL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG03239 | hp1 | a0002 | c0002 | t0001 | g0004 | SAS | PJL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG03453 | hp1 | a0001 | c0003 | t0001 | g0050 | AFR | MSL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG03453 | hp2 | a0007 | c0013 | t0001 | g0080 | AFR | MSL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG03486 | hp1 | a0002 | c0002 | t0001 | g0202 | AFR | MSL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG03486 | hp2 | a0001 | c0003 | t0001 | g0023 | AFR | MSL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG03490 | hp1 | a0002 | c0002 | t0001 | g0018 | SAS | PJL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG03491 | hp1 | a0002 | c0002 | t0001 | g0060 | SAS | PJL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG03491 | hp2 | a0002 | c0002 | t0001 | g0134 | SAS | PJL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG03492 | hp2 | a0002 | c0002 | t0001 | g0060 | SAS | PJL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | ESN | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG03516 | hp2 | a0002 | c0002 | t0001 | g0078 | AFR | ESN | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG03579 | hp1 | a0001 | c0003 | t0001 | g0050 | AFR | MSL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG03579 | hp2 | a0002 | c0002 | t0001 | g0049 | AFR | MSL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG03654 | hp1 | a0002 | c0006 | t0001 | g0101 | SAS | PJL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG03654 | hp2 | a0001 | c0003 | t0001 | g0009 | SAS | PJL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0253 | SAS | PJL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG03688 | hp1 | a0002 | c0002 | t0001 | g0090 | SAS | STU | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG03688 | hp2 | a0002 | c0002 | t0001 | g0132 | SAS | STU | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG03704 | hp1 | a0001 | c0005 | t0001 | g0082 | SAS | PJL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG03710 | hp1 | a0002 | c0006 | t0001 | g0115 | SAS | PJL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG03831 | hp1 | a0002 | c0002 | t0001 | g0004 | SAS | BEB | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0235 | SAS | BEB | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG03834 | hp1 | a0001 | c0005 | t0001 | g0029 | SAS | BEB | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG03834 | hp2 | a0002 | c0002 | t0001 | g0252 | SAS | BEB | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0243 | SAS | BEB | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG03927 | hp2 | a0002 | c0002 | t0001 | g0018 | SAS | BEB | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG03942 | hp1 | a0001 | c0003 | t0002 | g0105 | SAS | BEB | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0241 | SAS | BEB | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG04115 | hp1 | a0002 | c0002 | t0001 | g0224 | SAS | STU | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0069 | SAS | STU | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0239 | SAS | BEB | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG04199 | hp1 | a0002 | c0002 | t0001 | g0244 | SAS | STU | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG04199 | hp2 | a0002 | c0009 | t0001 | g0201 | SAS | STU | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG04204 | hp1 | a0002 | c0002 | t0001 | g0004 | SAS | STU | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG04228 | hp1 | a0001 | c0004 | t0001 | g0148 | SAS | STU | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | YRI | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | YRI | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | CHB | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18612 | hp2 | a0002 | c0006 | t0001 | g0126 | EAS | CHB | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18747 | hp1 | a0002 | c0002 | t0001 | g0222 | EAS | CHB | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | YRI | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | YRI | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18940 | hp2 | a0002 | c0002 | t0003 | g0022 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18942 | hp1 | a0001 | c0004 | t0001 | g0187 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18942 | hp2 | a0001 | c0005 | t0001 | g0242 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18943 | hp1 | a0001 | c0003 | t0002 | g0213 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18944 | hp1 | a0001 | c0004 | t0001 | g0058 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18945 | hp2 | a0001 | c0005 | t0001 | g0029 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18946 | hp1 | a0001 | c0003 | t0001 | g0063 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18946 | hp2 | a0001 | c0005 | t0002 | g0013 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18950 | hp1 | a0001 | c0004 | t0001 | g0278 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18950 | hp2 | a0001 | c0003 | t0001 | g0230 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18952 | hp2 | a0001 | c0012 | t0001 | g0196 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18953 | hp2 | a0001 | c0005 | t0002 | g0037 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18954 | hp2 | a0002 | c0002 | t0001 | g0256 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18957 | hp1 | a0001 | c0005 | t0001 | g0194 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18960 | hp1 | a0001 | c0003 | t0001 | g0232 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18961 | hp2 | a0001 | c0003 | t0001 | g0198 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18962 | hp1 | a0001 | c0003 | t0001 | g0093 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18967 | hp1 | a0001 | c0003 | t0001 | g0009 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18969 | hp2 | a0001 | c0003 | t0001 | g0091 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18970 | hp2 | a0001 | c0001 | t0004 | g0274 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18971 | hp2 | a0001 | c0005 | t0001 | g0046 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18972 | hp1 | a0001 | c0005 | t0002 | g0013 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18973 | hp2 | a0001 | c0004 | t0001 | g0124 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18975 | hp1 | a0001 | c0003 | t0001 | g0095 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18975 | hp2 | a0008 | c0015 | t0001 | g0096 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18977 | hp1 | a0001 | c0005 | t0001 | g0046 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18977 | hp2 | a0002 | c0002 | t0003 | g0022 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18979 | hp2 | a0001 | c0003 | t0001 | g0009 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18980 | hp2 | a0001 | c0003 | t0001 | g0099 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18982 | hp1 | a0001 | c0003 | t0001 | g0009 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18985 | hp2 | a0002 | c0002 | t0001 | g0238 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18986 | hp1 | a0001 | c0004 | t0001 | g0044 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18988 | hp1 | a0001 | c0004 | t0001 | g0151 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18988 | hp2 | a0001 | c0005 | t0001 | g0027 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18989 | hp1 | a0001 | c0003 | t0001 | g0068 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18991 | hp1 | a0001 | c0005 | t0001 | g0027 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18993 | hp2 | a0001 | c0005 | t0001 | g0029 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18994 | hp1 | a0002 | c0002 | t0001 | g0257 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18994 | hp2 | a0001 | c0005 | t0001 | g0218 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18998 | hp2 | a0001 | c0004 | t0001 | g0044 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA19000 | hp2 | a0001 | c0004 | t0001 | g0025 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA19001 | hp1 | a0001 | c0004 | t0001 | g0184 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA19003 | hp1 | a0001 | c0005 | t0001 | g0195 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA19004 | hp1 | a0002 | c0002 | t0001 | g0098 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA19005 | hp1 | a0001 | c0003 | t0001 | g0247 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA19007 | hp2 | a0001 | c0005 | t0002 | g0013 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA19030 | hp1 | a0001 | c0003 | t0001 | g0036 | AFR | LWK | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA19030 | hp2 | a0001 | c0003 | t0001 | g0137 | AFR | LWK | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA19043 | hp1 | a0001 | c0003 | t0001 | g0147 | AFR | LWK | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | LWK | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA19055 | hp2 | a0001 | c0005 | t0001 | g0191 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA19056 | hp2 | a0001 | c0005 | t0001 | g0027 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA19059 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA19059 | hp2 | a0001 | c0004 | t0001 | g0025 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA19062 | hp1 | a0001 | c0003 | t0001 | g0273 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA19062 | hp2 | a0001 | c0003 | t0001 | g0121 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA19064 | hp1 | a0003 | c0010 | t0001 | g0205 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA19064 | hp2 | a0001 | c0005 | t0001 | g0192 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA19066 | hp1 | a0001 | c0004 | t0001 | g0268 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA19066 | hp2 | a0001 | c0005 | t0002 | g0013 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA19067 | hp2 | a0002 | c0006 | t0001 | g0016 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA19079 | hp1 | a0001 | c0003 | t0001 | g0212 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA19080 | hp1 | a0001 | c0004 | t0001 | g0185 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA19080 | hp2 | a0003 | c0010 | t0001 | g0209 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA19081 | hp1 | a0002 | c0002 | t0001 | g0255 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA19082 | hp1 | a0001 | c0004 | t0001 | g0265 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA19082 | hp2 | a0001 | c0005 | t0002 | g0013 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA19084 | hp1 | a0001 | c0005 | t0002 | g0037 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA19084 | hp2 | a0002 | c0002 | t0003 | g0022 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA19087 | hp1 | a0001 | c0003 | t0001 | g0127 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA19091 | hp1 | a0001 | c0005 | t0001 | g0139 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA19240 | hp1 | a0001 | c0003 | t0002 | g0199 | AFR | YRI | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA19240 | hp2 | a0002 | c0002 | t0001 | g0293 | AFR | YRI | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA20129 | hp1 | a0002 | c0009 | t0001 | g0077 | AFR | ASW | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | ASW | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA20752 | hp1 | a0002 | c0002 | t0001 | g0133 | EUR | TSI | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA20752 | hp2 | a0001 | c0003 | t0002 | g0128 | EUR | TSI | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA20805 | hp1 | a0003 | c0008 | t0001 | g0174 | EUR | TSI | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0026 | EUR | TSI | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA20905 | hp1 | a0009 | c0018 | t0001 | g0155 | SAS | GIH | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA20905 | hp2 | a0001 | c0005 | t0001 | g0150 | SAS | GIH | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG01123 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | CLM | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG01123 | hp2 | a0001 | c0004 | t0001 | g0006 | AMR | CLM | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02109 | hp1 | a0001 | c0005 | t0001 | g0248 | AFR | ACB | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02109 | hp2 | a0002 | c0002 | t0001 | g0035 | AFR | ACB | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02486 | hp1 | a0001 | c0003 | t0001 | g0289 | AFR | ACB | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | ACB | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | ACB | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG02559 | hp2 | a0001 | c0003 | t0002 | g0142 | AFR | ACB | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | MSL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | MSL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | USA | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | USA | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | USA | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | USA | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | LWK | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | LWK | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0118 | REF | REF | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0100 | REF | REF | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:7689213 | A | G | 1 | a0007 | 1 | HG03453.hp2 | missense_variant | MODERATE | c.946T>C | p.Ser316Pro | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 11/11 | 1148/1585 | 946/966 | 316/321 | chr19 | 7689213 | |||
| chr19:7689215 | G | A | 1 | a0004 | 5 | HG02615.hp1 HG02723.hp2 HG02896.hp2 others(2): Show |
missense_variant | MODERATE | c.944C>T | p.Pro315Leu | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 11/11 | 1146/1585 | 944/966 | 315/321 | chr19 | 7689215 | |||
| chr19:7689308 | C | T | 1 | a0005 | 1 | HG01106.hp2 | missense_variant | MODERATE | c.851G>A | p.Arg284Gln | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 11/11 | 1053/1585 | 851/966 | 284/321 | chr19 | 7689308 | |||
| chr19:7689422 | G | T | 1 | a0009 | 1 | NA20905.hp1 | missense_variant | MODERATE | c.737C>A | p.Ala246Asp | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 11/11 | 939/1585 | 737/966 | 246/321 | chr19 | 7689422 | |||
| chr19:7690464 | C | T | 1 | a0008 | 1 | NA18975.hp2 | missense_variant | MODERATE | c.563G>A | p.Arg188Gln | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 9/11 | 765/1585 | 563/966 | 188/321 | chr19 | 7690464 | |||
| chr19:7696869 | C | T | 1 | a0006 | 1 | HG01928.hp1 | missense_variant | MODERATE | c.425G>A | p.Arg142Gln | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/11 | 627/1585 | 425/966 | 142/321 | chr19 | 7696869 | |||
| chr19:7697554 | C | T | 1 | a0003 | 7 | HG00733.hp1 HG01255.hp2 HG02004.hp2 others(4): Show |
missense_variant | MODERATE | c.226G>A | p.Gly76Ser | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 5/11 | 428/1585 | 226/966 | 76/321 | chr19 | 7697554 | |||
| chr19:7698362 | G | A | 2 | a0002 a0009 |
80 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(77): Show |
missense_variant | MODERATE | c.184C>T | p.Arg62Trp | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 4/11 | 386/1585 | 184/966 | 62/321 | chr19 | 7698362 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:7689235 | A | G | 1 | a0001c0012 | 1 | NA18952.hp2 | synonymous_variant | LOW | c.924T>C | p.Pro308Pro | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 11/11 | 1126/1585 | 924/966 | 308/321 | chr19 | 7689235 | |||
| chr19:7689325 | G | A | 1 | a0001c0017 | 1 | HG02886.hp2 | synonymous_variant | LOW | c.834C>T | p.Gly278Gly | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 11/11 | 1036/1585 | 834/966 | 278/321 | chr19 | 7689325 | |||
| chr19:7689340 | G | A | 1 | a0002c0014 | 1 | HG01891.hp1 | synonymous_variant | LOW | c.819C>T | p.Cys273Cys | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 11/11 | 1021/1585 | 819/966 | 273/321 | chr19 | 7689340 | |||
| chr19:7690170 | G | A | 10 | a0001c0003 a0001c0005 a0001c0012 others(7): Show |
178 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(175): Show |
synonymous_variant | LOW | c.717C>T | p.His239His | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 10/11 | 919/1585 | 717/966 | 239/321 | chr19 | 7690170 | |||
| chr19:7698817 | A | G | 7 | a0001c0004 a0001c0005 a0001c0012 others(4): Show |
86 | HG00609.hp1 HG00621.hp2 HG00642.hp1 others(83): Show |
synonymous_variant | LOW | c.60T>C | p.Arg20Arg | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 3/11 | 262/1585 | 60/966 | 20/321 | chr19 | 7698817 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:7688835 | G | A | 1 | a0002c0002t0003 | 4 | HG00423.hp1 NA18940.hp2 NA18977.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*358C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 11/11 | 358 | chr19 | 7688835 | ||||||
| chr19:7688879 | G | GCATCTGG others(25): Show |
1 | a0001c0001t0004 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*282_*313dupAGAGTA others(26): Show |
FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 11/11 | 313 | chr19 | 7688879 | ||||||
| chr19:7688879 | GCATCTGG others(25): Show |
G | 1 | a0003c0008t0005 | 1 | HG00733.hp1 | 3_prime_UTR_variant | MODIFIER | c.*282_*313delAGAGTA others(26): Show |
FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 11/11 | 282 | chr19 | 7688879 | ||||||
| chr19:7688879 | GCATCTGG others(57): Show |
G | 2 | a0001c0003t0002 a0001c0005t0002 |
26 | HG00280.hp2 HG00609.hp1 HG00642.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*250_*313delAGAGTA others(58): Show |
FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 11/11 | 250 | chr19 | 7688879 | ||||||
| chr19:7688920 | G | A | 1 | a0001c0001t0001 | 1 | HG02155.hp2 | 3_prime_UTR_variant | MODIFIER | c.*273C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 11/11 | 273 | chr19 | 7688920 | ||||||
| chr19:7688929 | G | C | 3 | a0001c0003t0001 a0002c0002t0001 a0002c0014t0001 |
9 | HG01884.hp2 HG01891.hp1 HG02280.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*264C>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 11/11 | 264 | chr19 | 7688929 | ||||||
| chr19:7689169 | C | A | 1 | a0001c0001t0006 | 1 | HG01978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*24G>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 11/11 | 24 | chr19 | 7689169 | ||||||
| chr19:7689184 | T | C | 1 | a0001c0003t0007 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 11/11 | 9 | chr19 | 7689184 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:7689448 | G | A | 1 | a0007c0013t0001g0080 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.729-18C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 10/10 | chr19 | 7689448 | |||||||
| chr19:7689474 | G | T | 1 | a0002c0006t0001g0290 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.729-44C>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 10/10 | chr19 | 7689474 | |||||||
| chr19:7689558 | G | C | 1 | a0002c0002t0001g0079 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.729-128C>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 10/10 | chr19 | 7689558 | |||||||
| chr19:7689659 | C | T | 88 | a0001c0001t0001g0102 a0001c0003t0001g0023 a0001c0003t0001g0036 others(85): Show |
125 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.729-229G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 10/10 | chr19 | 7689659 | |||||||
| chr19:7689682 | C | G | 1 | a0001c0001t0001g0015 | 4 | NA18983.hp1 NA19001.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.729-252G>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 10/10 | chr19 | 7689682 | |||||||
| chr19:7689705 | C | A | 5 | a0001c0001t0001g0190 a0001c0001t0001g0200 a0001c0001t0001g0262 others(2): Show |
5 | NA18960.hp2 NA18973.hp2 NA19003.hp2 others(2): Show |
intron_variant | MODIFIER | c.729-275G>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 10/10 | chr19 | 7689705 | |||||||
| chr19:7689705 | C | T | 135 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0061 others(132): Show |
190 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.729-275G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 10/10 | chr19 | 7689705 | |||||||
| chr19:7689743 | T | C | 134 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0061 others(131): Show |
189 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.729-313A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 10/10 | chr19 | 7689743 | |||||||
| chr19:7689790 | C | T | 122 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0061 others(119): Show |
171 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.729-360G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 10/10 | chr19 | 7689790 | |||||||
| chr19:7689810 | G | C | 135 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0061 others(132): Show |
190 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.728+349C>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 10/10 | chr19 | 7689810 | |||||||
| chr19:7689816 | G | T | 135 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0061 others(132): Show |
190 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.728+343C>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 10/10 | chr19 | 7689816 | |||||||
| chr19:7689819 | A | G | 135 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0061 others(132): Show |
190 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.728+340T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 10/10 | chr19 | 7689819 | |||||||
| chr19:7689880 | C | T | 135 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0061 others(132): Show |
190 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.728+279G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 10/10 | chr19 | 7689880 | |||||||
| chr19:7689897 | C | T | 4 | a0002c0014t0001g0085 a0004c0007t0001g0024 a0004c0007t0001g0066 others(1): Show |
6 | HG01891.hp1 HG02615.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.728+262G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 10/10 | chr19 | 7689897 | |||||||
| chr19:7689912 | G | A | 135 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0061 others(132): Show |
190 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.728+247C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 10/10 | chr19 | 7689912 | |||||||
| chr19:7689966 | C | A | 1 | a0001c0001t0001g0136 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.728+193G>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 10/10 | chr19 | 7689966 | |||||||
| chr19:7690026 | G | A | 138 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0038 others(135): Show |
193 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.728+133C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 10/10 | chr19 | 7690026 | |||||||
| chr19:7690031 | T | C | 138 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0038 others(135): Show |
193 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.728+128A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 10/10 | chr19 | 7690031 | |||||||
| chr19:7690053 | C | T | 4 | a0001c0001t0001g0038 a0001c0001t0001g0153 a0001c0001t0001g0197 others(1): Show |
5 | HG01891.hp2 HG02818.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.728+106G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 10/10 | chr19 | 7690053 | |||||||
| chr19:7690056 | A | C | 132 | a0001c0001t0001g0038 a0001c0001t0001g0153 a0001c0001t0001g0197 others(129): Show |
185 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.728+103T>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 10/10 | chr19 | 7690056 | |||||||
| chr19:7690078 | T | C | 132 | a0001c0001t0001g0038 a0001c0001t0001g0153 a0001c0001t0001g0197 others(129): Show |
185 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.728+81A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 10/10 | chr19 | 7690078 | |||||||
| chr19:7690082 | A | G | 132 | a0001c0001t0001g0038 a0001c0001t0001g0153 a0001c0001t0001g0197 others(129): Show |
185 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.728+77T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 10/10 | chr19 | 7690082 | |||||||
| chr19:7690085 | C | T | 132 | a0001c0001t0001g0038 a0001c0001t0001g0153 a0001c0001t0001g0197 others(129): Show |
185 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.728+74G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 10/10 | chr19 | 7690085 | |||||||
| chr19:7690132 | C | G | 1 | a0002c0002t0001g0168 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.728+27G>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 10/10 | chr19 | 7690132 | |||||||
| chr19:7690145 | G | A | 6 | a0001c0001t0001g0038 a0001c0001t0001g0153 a0001c0001t0001g0197 others(3): Show |
7 | HG01891.hp2 HG02615.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.728+14C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 10/10 | chr19 | 7690145 | |||||||
| chr19:7690273 | A | G | 126 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(123): Show |
178 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(175): Show |
splice_region_variant&intron_variant | LOW | c.622-8T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 9/10 | chr19 | 7690273 | |||||||
| chr19:7690327 | C | T | 126 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(123): Show |
178 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.622-62G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 9/10 | chr19 | 7690327 | |||||||
| chr19:7690348 | G | A | 1 | a0001c0001t0001g0178 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.621+58C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 9/10 | chr19 | 7690348 | |||||||
| chr19:7690355 | T | TC | 66 | a0001c0003t0001g0023 a0001c0003t0001g0036 a0001c0003t0001g0050 others(63): Show |
91 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.621+50dupG | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 9/10 | chr19 | 7690355 | |||||||
| chr19:7690372 | T | C | 2 | a0001c0001t0001g0166 a0001c0004t0001g0219 |
2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.621+34A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 9/10 | chr19 | 7690372 | |||||||
| chr19:7690399 | A | G | 125 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(122): Show |
177 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(174): Show |
splice_region_variant&intron_variant | LOW | c.621+7T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 9/10 | chr19 | 7690399 | |||||||
| chr19:7690583 | T | C | 123 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(120): Show |
175 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.470-26A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7690583 | |||||||
| chr19:7690586 | G | T | 123 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(120): Show |
175 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.470-29C>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7690586 | |||||||
| chr19:7690592 | T | C | 123 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(120): Show |
175 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.470-35A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7690592 | |||||||
| chr19:7690593 | G | A | 123 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(120): Show |
175 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.470-36C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7690593 | |||||||
| chr19:7690596 | A | G | 123 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(120): Show |
175 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.470-39T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7690596 | |||||||
| chr19:7690599 | G | A | 123 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(120): Show |
175 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.470-42C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7690599 | |||||||
| chr19:7690600 | C | T | 56 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0054 others(53): Show |
83 | HG00280.hp2 HG00438.hp1 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.470-43G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7690600 | |||||||
| chr19:7690632 | A | G | 123 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(120): Show |
175 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.470-75T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7690632 | |||||||
| chr19:7690685 | G | A | 123 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(120): Show |
175 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.470-128C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7690685 | |||||||
| chr19:7690695 | C | T | 1 | a0002c0002t0001g0130 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.470-138G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7690695 | |||||||
| chr19:7690696 | A | G | 121 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(118): Show |
173 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.470-139T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7690696 | |||||||
| chr19:7690807 | C | T | 6 | a0001c0001t0001g0038 a0001c0001t0001g0153 a0001c0001t0001g0197 others(3): Show |
7 | HG01891.hp2 HG02615.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.470-250G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7690807 | |||||||
| chr19:7690830 | A | G | 123 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(120): Show |
175 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.470-273T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7690830 | |||||||
| chr19:7690859 | A | G | 123 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(120): Show |
175 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.470-302T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7690859 | |||||||
| chr19:7690909 | G | C | 45 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0054 others(42): Show |
60 | HG00438.hp1 HG00597.hp1 HG00733.hp1 others(57): Show |
intron_variant | MODIFIER | c.470-352C>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7690909 | |||||||
| chr19:7691026 | C | T | 15 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0043 others(12): Show |
26 | HG02015.hp1 HG02015.hp2 HG02071.hp1 others(23): Show |
intron_variant | MODIFIER | c.470-469G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691026 | |||||||
| chr19:7691043 | A | G | 1 | a0001c0003t0002g0152 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.470-486T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691043 | |||||||
| chr19:7691051 | T | TATCACCA others(177): Show |
1 | a0001c0001t0001g0166 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.470-495_470-494ins others(184): Show |
FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691051 | |||||||
| chr19:7691051 | T | TATCATCA others(85): Show |
1 | a0003c0008t0005g0175 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.470-495_470-494ins others(92): Show |
FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691051 | |||||||
| chr19:7691056 | C | T | 122 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(119): Show |
174 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.470-499G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691056 | |||||||
| chr19:7691078 | G | A | 1 | a0003c0008t0005g0175 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.470-521C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691078 | |||||||
| chr19:7691078 | G | GGCCCCTC others(85): Show |
39 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0054 others(36): Show |
54 | HG00438.hp1 HG00597.hp1 HG01255.hp2 others(51): Show |
intron_variant | MODIFIER | c.470-522_470-521ins others(92): Show |
FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691078 | |||||||
| chr19:7691078 | G | GGCCCCTC others(85): Show |
67 | a0001c0003t0001g0023 a0001c0003t0001g0036 a0001c0003t0001g0050 others(64): Show |
92 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.470-522_470-521ins others(92): Show |
FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691078 | |||||||
| chr19:7691078 | G | GGCCCCTC others(85): Show |
1 | a0004c0007t0001g0086 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.470-522_470-521ins others(92): Show |
FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691078 | |||||||
| chr19:7691092 | C | T | 36 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0032 others(33): Show |
51 | HG01109.hp1 HG01891.hp2 HG01934.hp2 others(48): Show |
intron_variant | MODIFIER | c.470-535G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691092 | |||||||
| chr19:7691121 | C | CTGA | 15 | a0001c0003t0002g0011 a0001c0003t0002g0105 a0001c0003t0002g0110 others(12): Show |
27 | HG00280.hp2 HG00609.hp1 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.470-565_470-564ins others(3): Show |
FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691121 | |||||||
| chr19:7691123 | A | G | 108 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(105): Show |
148 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(145): Show |
intron_variant | MODIFIER | c.470-566T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691123 | |||||||
| chr19:7691124 | A | ATAGCTCA others(82): Show |
15 | a0001c0003t0002g0011 a0001c0003t0002g0105 a0001c0003t0002g0110 others(12): Show |
27 | HG00280.hp2 HG00609.hp1 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.470-568_470-567ins others(89): Show |
FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691124 | |||||||
| chr19:7691124 | A | G | 108 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(105): Show |
148 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(145): Show |
intron_variant | MODIFIER | c.470-567T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691124 | |||||||
| chr19:7691154 | A | T | 1 | a0001c0001t0001g0057 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.470-597T>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691154 | |||||||
| chr19:7691182 | G | A | 123 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(120): Show |
175 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.470-625C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691182 | |||||||
| chr19:7691202 | T | C | 123 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(120): Show |
175 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.470-645A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691202 | |||||||
| chr19:7691237 | T | C | 123 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(120): Show |
175 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.470-680A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691237 | |||||||
| chr19:7691305 | C | T | 123 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(120): Show |
175 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.470-748G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691305 | |||||||
| chr19:7691385 | A | T | 122 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(119): Show |
174 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.470-828T>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691385 | |||||||
| chr19:7691425 | C | T | 122 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(119): Show |
174 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.470-868G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691425 | |||||||
| chr19:7691440 | C | T | 60 | a0001c0003t0001g0023 a0001c0003t0001g0036 a0001c0003t0001g0074 others(57): Show |
84 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.470-883G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691440 | |||||||
| chr19:7691442 | A | C | 122 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(119): Show |
174 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.470-885T>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691442 | |||||||
| chr19:7691445 | G | T | 122 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(119): Show |
174 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.470-888C>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691445 | |||||||
| chr19:7691449 | A | ATAGT | 122 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(119): Show |
174 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.470-893_470-892ins others(4): Show |
FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691449 | |||||||
| chr19:7691465 | A | T | 122 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(119): Show |
174 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.470-908T>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691465 | |||||||
| chr19:7691498 | T | C | 1 | a0001c0001t0001g0056 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.470-941A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691498 | |||||||
| chr19:7691545 | C | T | 1 | a0001c0005t0002g0269 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.470-988G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691545 | |||||||
| chr19:7691577 | A | G | 122 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(119): Show |
174 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.470-1020T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691577 | |||||||
| chr19:7691591 | C | G | 122 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(119): Show |
174 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.470-1034G>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691591 | |||||||
| chr19:7691596 | C | T | 38 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0054 others(35): Show |
51 | HG00438.hp1 HG00597.hp1 HG00733.hp1 others(48): Show |
intron_variant | MODIFIER | c.470-1039G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691596 | |||||||
| chr19:7691709 | G | A | 116 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(113): Show |
168 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.470-1152C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691709 | |||||||
| chr19:7691748 | A | C | 120 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(117): Show |
172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1191T>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691748 | |||||||
| chr19:7691771 | T | C | 119 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(116): Show |
171 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.470-1214A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691771 | |||||||
| chr19:7691820 | T | C | 120 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(117): Show |
172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1263A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691820 | |||||||
| chr19:7691900 | A | G | 1 | a0002c0006t0001g0125 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.470-1343T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691900 | |||||||
| chr19:7691962 | T | C | 120 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(117): Show |
172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1405A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691962 | |||||||
| chr19:7691963 | G | A | 120 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(117): Show |
172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1406C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691963 | |||||||
| chr19:7691964 | T | C | 120 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(117): Show |
172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1407A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691964 | |||||||
| chr19:7691969 | C | A | 120 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(117): Show |
172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1412G>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691969 | |||||||
| chr19:7691970 | ATT | A | 120 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(117): Show |
172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1415_470-1414d others(4): Show |
FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691970 | |||||||
| chr19:7691972 | T | TCACACTC others(137): Show |
1 | a0001c0001t0001g0186 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.470-1416_470-1415i others(146): Show |
FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691972 | |||||||
| chr19:7691972 | T | TCACATTC others(137): Show |
168 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(165): Show |
276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.470-1416_470-1415i others(146): Show |
FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691972 | |||||||
| chr19:7691972 | T | TCACATTC others(281): Show |
1 | a0001c0001t0001g0113 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.470-1416_470-1415i others(290): Show |
FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691972 | |||||||
| chr19:7691972 | T | TCACATTC others(137): Show |
1 | a0001c0001t0001g0015 | 4 | NA18983.hp1 NA19001.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.470-1416_470-1415i others(146): Show |
FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691972 | |||||||
| chr19:7692000 | C | T | 120 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(117): Show |
172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1443G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692000 | |||||||
| chr19:7692012 | C | T | 120 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(117): Show |
172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1455G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692012 | |||||||
| chr19:7692013 | A | G | 120 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(117): Show |
172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1456T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692013 | |||||||
| chr19:7692014 | G | T | 120 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(117): Show |
172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1457C>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692014 | |||||||
| chr19:7692018 | G | A | 120 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(117): Show |
172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1461C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692018 | |||||||
| chr19:7692021 | T | C | 120 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(117): Show |
172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1464A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692021 | |||||||
| chr19:7692024 | A | ATTCACG | 120 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(117): Show |
172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1473_470-1468d others(8): Show |
FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692024 | |||||||
| chr19:7692035 | A | T | 120 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(117): Show |
172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1478T>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692035 | |||||||
| chr19:7692048 | T | C | 120 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(117): Show |
172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1491A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692048 | |||||||
| chr19:7692065 | C | T | 120 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(117): Show |
172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1508G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692065 | |||||||
| chr19:7692067 | A | G | 120 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(117): Show |
172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1510T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692067 | |||||||
| chr19:7692068 | G | A | 137 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0043 others(134): Show |
200 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.470-1511C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692068 | |||||||
| chr19:7692083 | A | T | 120 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(117): Show |
172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1526T>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692083 | |||||||
| chr19:7692089 | C | A | 171 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(168): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.470-1532G>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692089 | |||||||
| chr19:7692096 | T | C | 120 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(117): Show |
172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1539A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692096 | |||||||
| chr19:7692107 | T | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.470-1550A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692107 | |||||||
| chr19:7692108 | T | C | 120 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(117): Show |
172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1551A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692108 | |||||||
| chr19:7692109 | G | A | 120 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(117): Show |
172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1552C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692109 | |||||||
| chr19:7692110 | T | C | 120 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(117): Show |
172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1553A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692110 | |||||||
| chr19:7692113 | T | C | 121 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(118): Show |
173 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.470-1556A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692113 | |||||||
| chr19:7692115 | A | G | 120 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(117): Show |
172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1558T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692115 | |||||||
| chr19:7692125 | C | T | 120 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(117): Show |
172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1568G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692125 | |||||||
| chr19:7692157 | A | G | 120 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(117): Show |
172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1600T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692157 | |||||||
| chr19:7692161 | C | T | 120 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(117): Show |
172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1604G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692161 | |||||||
| chr19:7692164 | A | G | 120 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(117): Show |
172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1607T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692164 | |||||||
| chr19:7692174 | G | A | 135 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0038 others(132): Show |
191 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.470-1617C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692174 | |||||||
| chr19:7692190 | A | T | 1 | a0001c0004t0001g0189 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.470-1633T>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692190 | |||||||
| chr19:7692203 | T | G | 120 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(117): Show |
172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1646A>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692203 | |||||||
| chr19:7692204 | C | T | 120 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(117): Show |
172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1647G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692204 | |||||||
| chr19:7692205 | A | G | 120 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(117): Show |
172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1648T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692205 | |||||||
| chr19:7692210 | G | A | 120 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(117): Show |
172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1653C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692210 | |||||||
| chr19:7692212 | G | A | 120 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(117): Show |
172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1655C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692212 | |||||||
| chr19:7692227 | A | G | 120 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(117): Show |
172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1670T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692227 | |||||||
| chr19:7692233 | A | C | 120 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(117): Show |
172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1676T>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692233 | |||||||
| chr19:7692249 | C | A | 120 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(117): Show |
172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1692G>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692249 | |||||||
| chr19:7692251 | C | T | 120 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(117): Show |
172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1694G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692251 | |||||||
| chr19:7692252 | T | C | 120 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(117): Show |
172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1695A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692252 | |||||||
| chr19:7692253 | G | A | 120 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(117): Show |
172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1696C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692253 | |||||||
| chr19:7692254 | T | C | 120 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(117): Show |
172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1697A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692254 | |||||||
| chr19:7692269 | C | T | 121 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(118): Show |
173 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.470-1712G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692269 | |||||||
| chr19:7692275 | T | G | 120 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(117): Show |
172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1718A>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692275 | |||||||
| chr19:7692288 | C | T | 120 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(117): Show |
172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1731G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692288 | |||||||
| chr19:7692300 | C | T | 120 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(117): Show |
172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1743G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692300 | |||||||
| chr19:7692301 | A | G | 120 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(117): Show |
172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1744T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692301 | |||||||
| chr19:7692306 | G | A | 120 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(117): Show |
172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1749C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692306 | |||||||
| chr19:7692312 | A | C | 120 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(117): Show |
172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1755T>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692312 | |||||||
| chr19:7692318 | G | A | 120 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(117): Show |
172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1761C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692318 | |||||||
| chr19:7692322 | A | G | 4 | a0001c0003t0001g0147 a0004c0007t0001g0024 a0004c0007t0001g0066 others(1): Show |
6 | HG02615.hp1 HG02723.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.470-1765T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692322 | |||||||
| chr19:7692323 | A | T | 120 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(117): Show |
172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1766T>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692323 | |||||||
| chr19:7692329 | C | T | 120 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(117): Show |
172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1772G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692329 | |||||||
| chr19:7692349 | A | G | 120 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(117): Show |
172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1792T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692349 | |||||||
| chr19:7692356 | G | A | 120 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(117): Show |
172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1799C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692356 | |||||||
| chr19:7692369 | CAACAACA others(41): Show |
C | 120 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(117): Show |
172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1860_470-1813d others(50): Show |
FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692369 | |||||||
| chr19:7692440 | C | A | 6 | a0001c0001t0001g0038 a0001c0001t0001g0153 a0001c0001t0001g0197 others(3): Show |
7 | HG01891.hp2 HG02615.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.470-1883G>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692440 | |||||||
| chr19:7692445 | G | A | 120 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(117): Show |
172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1888C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692445 | |||||||
| chr19:7692450 | G | GAACACAT others(6): Show |
1 | a0001c0005t0001g0195 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.470-1906_470-1894d others(15): Show |
FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692450 | |||||||
| chr19:7692462 | G | A | 4 | a0001c0003t0001g0147 a0004c0007t0001g0024 a0004c0007t0001g0066 others(1): Show |
6 | HG02615.hp1 HG02723.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.470-1905C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692462 | |||||||
| chr19:7692485 | A | G | 120 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(117): Show |
172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1928T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692485 | |||||||
| chr19:7692492 | C | T | 3 | a0004c0007t0001g0024 a0004c0007t0001g0066 a0004c0007t0001g0086 |
5 | HG02615.hp1 HG02723.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.470-1935G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692492 | |||||||
| chr19:7692493 | A | G | 120 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(117): Show |
172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1936T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692493 | |||||||
| chr19:7692497 | C | T | 2 | a0001c0001t0001g0166 a0001c0004t0001g0219 |
2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.470-1940G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692497 | |||||||
| chr19:7692500 | G | A | 83 | a0001c0003t0001g0017 a0001c0003t0001g0023 a0001c0003t0001g0036 others(80): Show |
124 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.470-1943C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692500 | |||||||
| chr19:7692501 | C | T | 120 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(117): Show |
172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1944G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692501 | |||||||
| chr19:7692541 | A | G | 120 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(117): Show |
172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1984T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692541 | |||||||
| chr19:7692545 | T | C | 120 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(117): Show |
172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1988A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692545 | |||||||
| chr19:7692570 | G | A | 120 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(117): Show |
172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-2013C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692570 | |||||||
| chr19:7692586 | G | A | 1 | a0002c0002t0001g0079 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.470-2029C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692586 | |||||||
| chr19:7692599 | CCTTACAG others(137): Show |
C | 3 | a0001c0005t0001g0215 a0002c0002t0001g0035 a0002c0002t0001g0078 |
4 | HG02109.hp2 HG02451.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.470-2186_470-2043d others(2): Show |
FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692599 | |||||||
| chr19:7692629 | C | T | 117 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(114): Show |
168 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.470-2072G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692629 | |||||||
| chr19:7692630 | ACCATCG | A | 117 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(114): Show |
168 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.470-2079_470-2074d others(8): Show |
FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692630 | |||||||
| chr19:7692639 | A | G | 6 | a0001c0001t0001g0038 a0001c0001t0001g0153 a0001c0001t0001g0197 others(3): Show |
7 | HG01891.hp2 HG02615.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.470-2082T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692639 | |||||||
| chr19:7692643 | G | A | 117 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(114): Show |
168 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.470-2086C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692643 | |||||||
| chr19:7692649 | C | T | 18 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0043 others(15): Show |
29 | HG02015.hp1 HG02015.hp2 HG02071.hp1 others(26): Show |
intron_variant | MODIFIER | c.470-2092G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692649 | |||||||
| chr19:7692650 | G | A | 1 | a0002c0002t0001g0120 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.470-2093C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692650 | |||||||
| chr19:7692678 | A | G | 119 | a0001c0001t0001g0166 a0001c0003t0001g0009 a0001c0003t0001g0017 others(116): Show |
170 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.470-2121T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692678 | |||||||
| chr19:7692727 | G | A | 117 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(114): Show |
168 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.470-2170C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692727 | |||||||
| chr19:7692729 | T | C | 117 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(114): Show |
168 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.470-2172A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692729 | |||||||
| chr19:7692742 | T | C | 117 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(114): Show |
168 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.470-2185A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692742 | |||||||
| chr19:7692781 | A | G | 120 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(117): Show |
172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-2224T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692781 | |||||||
| chr19:7692842 | C | T | 120 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(117): Show |
172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-2285G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692842 | |||||||
| chr19:7692867 | C | A | 120 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(117): Show |
172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-2310G>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692867 | |||||||
| chr19:7692883 | A | G | 120 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(117): Show |
172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-2326T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692883 | |||||||
| chr19:7692999 | A | G | 1 | a0001c0004t0001g0184 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.470-2442T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692999 | |||||||
| chr19:7693022 | C | T | 18 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0043 others(15): Show |
29 | HG02015.hp1 HG02015.hp2 HG02071.hp1 others(26): Show |
intron_variant | MODIFIER | c.470-2465G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7693022 | |||||||
| chr19:7693028 | C | A | 9 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0061 others(6): Show |
12 | HG01934.hp2 HG02055.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.470-2471G>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7693028 | |||||||
| chr19:7693041 | A | G | 1 | a0001c0004t0001g0278 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.470-2484T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7693041 | |||||||
| chr19:7693113 | C | T | 1 | a0001c0004t0001g0189 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.470-2556G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7693113 | |||||||
| chr19:7693114 | G | A | 120 | a0001c0003t0001g0009 a0001c0003t0001g0017 a0001c0003t0001g0023 others(117): Show |
172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-2557C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7693114 | |||||||
| chr19:7693133 | C | T | 1 | a0007c0013t0001g0080 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.470-2576G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7693133 | |||||||
| chr19:7693151 | T | G | 3 | a0001c0005t0001g0215 a0002c0002t0001g0035 a0002c0002t0001g0078 |
4 | HG02109.hp2 HG02451.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.470-2594A>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7693151 | |||||||
| chr19:7693155 | G | A | 2 | a0001c0003t0001g0050 a0002c0002t0001g0075 |
3 | HG03139.hp2 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.470-2598C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7693155 | |||||||
| chr19:7693209 | G | C | 1 | a0002c0002t0003g0129 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.470-2652C>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7693209 | |||||||
| chr19:7693231 | G | C | 120 | a0001c0001t0001g0039 a0001c0001t0001g0234 a0001c0003t0001g0009 others(117): Show |
173 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.470-2674C>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7693231 | |||||||
| chr19:7693268 | T | A | 153 | a0001c0001t0001g0008 a0001c0001t0001g0028 a0001c0001t0001g0055 others(150): Show |
223 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.470-2711A>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7693268 | |||||||
| chr19:7693272 | G | C | 153 | a0001c0001t0001g0008 a0001c0001t0001g0028 a0001c0001t0001g0055 others(150): Show |
223 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.470-2715C>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7693272 | |||||||
| chr19:7693308 | C | T | 81 | a0001c0003t0001g0023 a0001c0003t0001g0036 a0001c0003t0001g0050 others(78): Show |
120 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.470-2751G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7693308 | |||||||
| chr19:7693374 | G | C | 153 | a0001c0001t0001g0008 a0001c0001t0001g0028 a0001c0001t0001g0055 others(150): Show |
223 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.470-2817C>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7693374 | |||||||
| chr19:7693377 | G | A | 153 | a0001c0001t0001g0008 a0001c0001t0001g0028 a0001c0001t0001g0055 others(150): Show |
223 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.470-2820C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7693377 | |||||||
| chr19:7693417 | A | G | 153 | a0001c0001t0001g0008 a0001c0001t0001g0028 a0001c0001t0001g0055 others(150): Show |
223 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.470-2860T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7693417 | |||||||
| chr19:7693430 | C | G | 154 | a0001c0001t0001g0008 a0001c0001t0001g0028 a0001c0001t0001g0055 others(151): Show |
224 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(221): Show |
intron_variant | MODIFIER | c.470-2873G>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7693430 | |||||||
| chr19:7693443 | A | T | 4 | a0001c0003t0001g0147 a0004c0007t0001g0024 a0004c0007t0001g0066 others(1): Show |
6 | HG02615.hp1 HG02723.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.470-2886T>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7693443 | |||||||
| chr19:7693453 | T | C | 69 | a0001c0001t0001g0008 a0001c0001t0001g0028 a0001c0001t0001g0055 others(66): Show |
98 | HG00280.hp1 HG00438.hp1 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.470-2896A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7693453 | |||||||
| chr19:7693503 | T | C | 1 | a0001c0001t0001g0071 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.470-2946A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7693503 | |||||||
| chr19:7693551 | A | T | 1 | a0002c0002t0001g0120 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.470-2994T>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7693551 | |||||||
| chr19:7693584 | T | A | 172 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0012 others(169): Show |
253 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(250): Show |
intron_variant | MODIFIER | c.470-3027A>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7693584 | |||||||
| chr19:7693591 | G | A | 172 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0012 others(169): Show |
253 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(250): Show |
intron_variant | MODIFIER | c.470-3034C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7693591 | |||||||
| chr19:7693624 | C | CT | 1 | a0001c0003t0001g0017 | 3 | HG02572.hp1 HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.470-3068dupA | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7693624 | |||||||
| chr19:7693642 | T | TTTTTG | 2 | a0002c0002t0001g0035 a0002c0002t0001g0078 |
3 | HG02109.hp2 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.470-3090_470-3086d others(7): Show |
FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7693642 | |||||||
| chr19:7693732 | T | C | 82 | a0001c0001t0001g0292 a0001c0003t0001g0023 a0001c0003t0001g0036 others(79): Show |
121 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.469+3093A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7693732 | |||||||
| chr19:7693733 | G | A | 1 | a0002c0002t0001g0132 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.469+3092C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7693733 | |||||||
| chr19:7693839 | G | A | 44 | a0001c0001t0001g0292 a0001c0003t0001g0023 a0001c0003t0001g0036 others(41): Show |
63 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.469+2986C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7693839 | |||||||
| chr19:7693907 | C | A | 173 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0012 others(170): Show |
253 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(250): Show |
intron_variant | MODIFIER | c.469+2918G>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7693907 | |||||||
| chr19:7693953 | A | AT | 30 | a0001c0001t0001g0021 a0001c0001t0001g0032 a0001c0001t0001g0033 others(27): Show |
37 | HG00544.hp1 HG00621.hp1 HG01257.hp1 others(34): Show |
intron_variant | MODIFIER | c.469+2871dupA | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7693953 | |||||||
| chr19:7693953 | AT | A | 25 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0043 others(22): Show |
38 | HG00741.hp1 HG01169.hp2 HG02015.hp1 others(35): Show |
intron_variant | MODIFIER | c.469+2871delA | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7693953 | |||||||
| chr19:7693953 | ATTTTTTT others(5): Show |
A | 82 | a0001c0001t0001g0292 a0001c0003t0001g0023 a0001c0003t0001g0036 others(79): Show |
121 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.469+2860_469+2871d others(14): Show |
FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7693953 | |||||||
| chr19:7693988 | C | T | 2 | a0002c0002t0001g0131 a0002c0002t0001g0259 |
2 | HG01192.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.469+2837G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7693988 | |||||||
| chr19:7693994 | C | G | 82 | a0001c0001t0001g0292 a0001c0003t0001g0023 a0001c0003t0001g0036 others(79): Show |
121 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.469+2831G>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7693994 | |||||||
| chr19:7694011 | C | T | 82 | a0001c0001t0001g0292 a0001c0003t0001g0023 a0001c0003t0001g0036 others(79): Show |
121 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.469+2814G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7694011 | |||||||
| chr19:7694044 | G | A | 82 | a0001c0001t0001g0292 a0001c0003t0001g0023 a0001c0003t0001g0036 others(79): Show |
121 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.469+2781C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7694044 | |||||||
| chr19:7694064 | T | C | 1 | a0001c0001t0001g0072 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.469+2761A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7694064 | |||||||
| chr19:7694144 | A | G | 72 | a0001c0001t0001g0008 a0001c0001t0001g0028 a0001c0001t0001g0055 others(69): Show |
103 | HG00280.hp1 HG00438.hp1 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.469+2681T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7694144 | |||||||
| chr19:7694147 | G | A | 72 | a0001c0001t0001g0008 a0001c0001t0001g0028 a0001c0001t0001g0055 others(69): Show |
103 | HG00280.hp1 HG00438.hp1 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.469+2678C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7694147 | |||||||
| chr19:7694150 | C | G | 72 | a0001c0001t0001g0008 a0001c0001t0001g0028 a0001c0001t0001g0055 others(69): Show |
103 | HG00280.hp1 HG00438.hp1 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.469+2675G>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7694150 | |||||||
| chr19:7694168 | G | T | 72 | a0001c0001t0001g0008 a0001c0001t0001g0028 a0001c0001t0001g0055 others(69): Show |
103 | HG00280.hp1 HG00438.hp1 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.469+2657C>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7694168 | |||||||
| chr19:7694169 | T | G | 72 | a0001c0001t0001g0008 a0001c0001t0001g0028 a0001c0001t0001g0055 others(69): Show |
103 | HG00280.hp1 HG00438.hp1 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.469+2656A>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7694169 | |||||||
| chr19:7694189 | G | C | 1 | a0002c0002t0001g0168 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.469+2636C>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7694189 | |||||||
| chr19:7694215 | G | C | 19 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0043 others(16): Show |
32 | HG02015.hp1 HG02015.hp2 HG02071.hp1 others(29): Show |
intron_variant | MODIFIER | c.469+2610C>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7694215 | |||||||
| chr19:7694267 | A | G | 4 | a0003c0008t0001g0114 a0003c0008t0001g0174 a0003c0008t0001g0277 others(1): Show |
4 | HG00733.hp1 HG01255.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.469+2558T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7694267 | |||||||
| chr19:7694286 | C | T | 1 | a0001c0004t0001g0185 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.469+2539G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7694286 | |||||||
| chr19:7694304 | G | A | 2 | a0001c0003t0002g0199 a0001c0003t0002g0216 |
2 | HG02818.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.469+2521C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7694304 | |||||||
| chr19:7694319 | T | C | 1 | a0001c0003t0001g0017 | 3 | HG02572.hp1 HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.469+2506A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7694319 | |||||||
| chr19:7694324 | C | T | 5 | a0001c0001t0001g0109 a0001c0001t0001g0164 a0001c0001t0001g0166 others(2): Show |
5 | HG01109.hp1 HG02976.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.469+2501G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7694324 | |||||||
| chr19:7694367 | A | C | 78 | a0001c0001t0001g0292 a0001c0003t0001g0023 a0001c0003t0001g0036 others(75): Show |
115 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.469+2458T>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7694367 | |||||||
| chr19:7694382 | A | G | 3 | a0003c0010t0001g0205 a0003c0010t0001g0209 a0003c0010t0001g0271 |
3 | HG02132.hp1 NA19064.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.469+2443T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7694382 | |||||||
| chr19:7694394 | C | T | 78 | a0001c0001t0001g0292 a0001c0003t0001g0023 a0001c0003t0001g0036 others(75): Show |
115 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.469+2431G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7694394 | |||||||
| chr19:7694583 | G | T | 1 | a0002c0002t0001g0130 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.469+2242C>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7694583 | |||||||
| chr19:7694683 | T | C | 168 | a0001c0001t0001g0008 a0001c0001t0001g0028 a0001c0001t0001g0032 others(165): Show |
240 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.469+2142A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7694683 | |||||||
| chr19:7694734 | G | C | 1 | a0001c0001t0001g0020 | 3 | HG01106.hp1 HG01358.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.469+2091C>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7694734 | |||||||
| chr19:7694790 | C | T | 194 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0012 others(191): Show |
279 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(276): Show |
intron_variant | MODIFIER | c.469+2035G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7694790 | |||||||
| chr19:7694827 | C | T | 3 | a0001c0001t0001g0026 a0001c0001t0001g0228 a0001c0001t0001g0229 |
5 | HG00099.hp1 HG01175.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.469+1998G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7694827 | |||||||
| chr19:7694828 | C | T | 1 | a0001c0004t0001g0124 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.469+1997G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7694828 | |||||||
| chr19:7694829 | G | C | 194 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0012 others(191): Show |
279 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(276): Show |
intron_variant | MODIFIER | c.469+1996C>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7694829 | |||||||
| chr19:7694837 | AT | A | 85 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0038 others(82): Show |
115 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.469+1987delA | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7694837 | |||||||
| chr19:7695134 | T | A | 66 | a0001c0001t0001g0292 a0001c0003t0001g0023 a0001c0003t0001g0036 others(63): Show |
92 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.469+1691A>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7695134 | |||||||
| chr19:7695284 | C | T | 2 | a0001c0001t0001g0179 a0001c0001t0001g0233 |
2 | NA18956.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.469+1541G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7695284 | |||||||
| chr19:7695440 | A | C | 4 | a0001c0003t0001g0017 a0003c0010t0001g0205 a0003c0010t0001g0209 others(1): Show |
6 | HG02132.hp1 HG02572.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.469+1385T>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7695440 | |||||||
| chr19:7695541 | C | T | 1 | a0001c0003t0001g0017 | 3 | HG02572.hp1 HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.469+1284G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7695541 | |||||||
| chr19:7695560 | G | A | 62 | a0001c0001t0001g0292 a0001c0003t0001g0036 a0001c0003t0001g0050 others(59): Show |
86 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.469+1265C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7695560 | |||||||
| chr19:7695596 | C | T | 62 | a0001c0001t0001g0292 a0001c0003t0001g0036 a0001c0003t0001g0050 others(59): Show |
86 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.469+1229G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7695596 | |||||||
| chr19:7695619 | T | TA | 62 | a0001c0001t0001g0292 a0001c0003t0001g0036 a0001c0003t0001g0050 others(59): Show |
86 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.469+1205dupT | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7695619 | |||||||
| chr19:7695723 | C | T | 62 | a0001c0001t0001g0292 a0001c0003t0001g0036 a0001c0003t0001g0050 others(59): Show |
86 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.469+1102G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7695723 | |||||||
| chr19:7695738 | G | A | 7 | a0001c0003t0002g0011 a0001c0003t0002g0105 a0001c0003t0002g0128 others(4): Show |
12 | HG00280.hp2 HG00642.hp1 HG00741.hp2 others(9): Show |
intron_variant | MODIFIER | c.469+1087C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7695738 | |||||||
| chr19:7695783 | G | A | 62 | a0001c0001t0001g0292 a0001c0003t0001g0036 a0001c0003t0001g0050 others(59): Show |
86 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.469+1042C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7695783 | |||||||
| chr19:7695793 | C | T | 3 | a0004c0007t0001g0024 a0004c0007t0001g0066 a0004c0007t0001g0086 |
5 | HG02615.hp1 HG02723.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.469+1032G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7695793 | |||||||
| chr19:7695912 | ATC | A | 3 | a0001c0003t0001g0074 a0002c0002t0001g0246 a0002c0002t0003g0129 |
3 | HG00423.hp1 HG00609.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.469+911_469+912del others(2): Show |
FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7695912 | |||||||
| chr19:7695918 | CTCT | C | 56 | a0001c0001t0001g0292 a0001c0003t0001g0036 a0001c0003t0001g0050 others(53): Show |
80 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.469+904_469+906del others(3): Show |
FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7695918 | |||||||
| chr19:7695920 | C | CT | 24 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(21): Show |
35 | HG00544.hp2 HG00609.hp1 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.469+904dupA | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7695920 | |||||||
| chr19:7695920 | CT | C | 91 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0012 others(88): Show |
125 | HG00280.hp1 HG00438.hp1 HG00639.hp1 others(122): Show |
intron_variant | MODIFIER | c.469+904delA | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7695920 | |||||||
| chr19:7695922 | T | C | 17 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0038 others(14): Show |
21 | HG01891.hp2 HG01934.hp2 HG01975.hp2 others(18): Show |
intron_variant | MODIFIER | c.469+903A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7695922 | |||||||
| chr19:7695949 | C | T | 62 | a0001c0001t0001g0292 a0001c0003t0001g0036 a0001c0003t0001g0050 others(59): Show |
86 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.469+876G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7695949 | |||||||
| chr19:7695957 | C | T | 62 | a0001c0001t0001g0292 a0001c0003t0001g0036 a0001c0003t0001g0050 others(59): Show |
86 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.469+868G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7695957 | |||||||
| chr19:7695975 | T | G | 1 | a0001c0001t0001g0057 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.469+850A>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7695975 | |||||||
| chr19:7696003 | G | A | 62 | a0001c0001t0001g0292 a0001c0003t0001g0036 a0001c0003t0001g0050 others(59): Show |
86 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.469+822C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7696003 | |||||||
| chr19:7696093 | C | G | 1 | a0001c0003t0001g0147 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.469+732G>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7696093 | |||||||
| chr19:7696095 | G | A | 1 | a0001c0001t0001g0264 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.469+730C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7696095 | |||||||
| chr19:7696107 | A | T | 1 | a0001c0004t0001g0267 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.469+718T>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7696107 | |||||||
| chr19:7696140 | G | A | 110 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0012 others(107): Show |
155 | HG00280.hp1 HG00438.hp1 HG00597.hp1 others(152): Show |
intron_variant | MODIFIER | c.469+685C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7696140 | |||||||
| chr19:7696161 | G | A | 1 | a0002c0002t0001g0120 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.469+664C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7696161 | |||||||
| chr19:7696192 | C | T | 8 | a0001c0003t0002g0011 a0001c0003t0002g0105 a0001c0003t0002g0128 others(5): Show |
13 | HG00280.hp2 HG00642.hp1 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.469+633G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7696192 | |||||||
| chr19:7696193 | G | A | 1 | a0007c0013t0001g0080 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.469+632C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7696193 | |||||||
| chr19:7696247 | G | T | 1 | a0001c0003t0001g0017 | 3 | HG02572.hp1 HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.469+578C>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7696247 | |||||||
| chr19:7696333 | T | C | 62 | a0001c0001t0001g0292 a0001c0003t0001g0036 a0001c0003t0001g0050 others(59): Show |
86 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.469+492A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7696333 | |||||||
| chr19:7696336 | C | A | 62 | a0001c0001t0001g0292 a0001c0003t0001g0036 a0001c0003t0001g0050 others(59): Show |
86 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.469+489G>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7696336 | |||||||
| chr19:7696381 | G | A | 2 | a0001c0001t0001g0087 a0001c0001t0001g0204 |
2 | HG03041.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.469+444C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7696381 | |||||||
| chr19:7696393 | G | A | 5 | a0001c0003t0001g0036 a0002c0002t0001g0049 a0002c0002t0001g0123 others(2): Show |
7 | HG02055.hp1 HG02630.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.469+432C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7696393 | |||||||
| chr19:7696527 | C | T | 1 | a0002c0002t0001g0120 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.469+298G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7696527 | |||||||
| chr19:7696528 | G | A | 69 | a0001c0001t0001g0292 a0001c0003t0001g0036 a0001c0003t0001g0050 others(66): Show |
98 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.469+297C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7696528 | |||||||
| chr19:7696560 | A | G | 3 | a0001c0001t0001g0109 a0001c0001t0001g0164 a0001c0004t0001g0286 |
3 | HG01109.hp1 HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.469+265T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7696560 | |||||||
| chr19:7696570 | G | A | 58 | a0001c0001t0001g0008 a0001c0001t0001g0028 a0001c0001t0001g0055 others(55): Show |
86 | HG00280.hp1 HG00438.hp1 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.469+255C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7696570 | |||||||
| chr19:7696586 | G | A | 69 | a0001c0001t0001g0292 a0001c0003t0001g0036 a0001c0003t0001g0050 others(66): Show |
98 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.469+239C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7696586 | |||||||
| chr19:7696608 | CTT | C | 69 | a0001c0001t0001g0292 a0001c0003t0001g0036 a0001c0003t0001g0050 others(66): Show |
98 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.469+215_469+216del others(2): Show |
FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7696608 | |||||||
| chr19:7696623 | G | A | 1 | a0002c0002t0001g0202 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.469+202C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7696623 | |||||||
| chr19:7696631 | G | A | 8 | a0001c0001t0001g0109 a0001c0001t0001g0164 a0001c0001t0001g0166 others(5): Show |
8 | HG01109.hp1 HG02818.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.469+194C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7696631 | |||||||
| chr19:7696781 | A | G | 70 | a0001c0001t0001g0292 a0001c0003t0001g0036 a0001c0003t0001g0050 others(67): Show |
99 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.469+44T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7696781 | |||||||
| chr19:7696795 | G | A | 1 | a0001c0001t0001g0193 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.469+30C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7696795 | |||||||
| chr19:7696799 | T | C | 1 | a0001c0001t0001g0073 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.469+26A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7696799 | |||||||
| chr19:7696916 | T | C | 1 | a0001c0001t0001g0179 | 1 | NA18962.hp2 | splice_acceptor_variant&intron_variant | HIGH | c.380-2A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 7/10 | chr19 | 7696916 | |||||||
| chr19:7696926 | A | G | 188 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0012 others(185): Show |
266 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.380-12T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 7/10 | chr19 | 7696926 | |||||||
| chr19:7696962 | C | T | 1 | a0001c0001t0001g0071 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.380-48G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 7/10 | chr19 | 7696962 | |||||||
| chr19:7696984 | C | A | 1 | a0001c0001t0001g0097 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.379+29G>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 7/10 | chr19 | 7696984 | |||||||
| chr19:7697404 | C | T | 1 | a0001c0004t0001g0261 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.254-106G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 5/10 | chr19 | 7697404 | |||||||
| chr19:7697494 | TCCCCTGC others(2): Show |
T | 81 | a0001c0001t0001g0292 a0001c0003t0001g0017 a0001c0003t0001g0036 others(78): Show |
114 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.253+24_253+32delTT others(7): Show |
FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 5/10 | chr19 | 7697494 | |||||||
| chr19:7697767 | CTA | C | 93 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0032 others(90): Show |
135 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.191-180_191-179del others(2): Show |
FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 4/10 | chr19 | 7697767 | |||||||
| chr19:7697842 | A | C | 1 | a0001c0003t0001g0017 | 3 | HG02572.hp1 HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.191-253T>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 4/10 | chr19 | 7697842 | |||||||
| chr19:7697916 | A | C | 1 | a0001c0001t0001g0227 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.191-327T>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 4/10 | chr19 | 7697916 | |||||||
| chr19:7697939 | C | T | 2 | a0002c0002t0001g0018 a0002c0002t0001g0090 |
4 | HG01167.hp2 HG03490.hp1 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.191-350G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 4/10 | chr19 | 7697939 | |||||||
| chr19:7698025 | G | A | 97 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0032 others(94): Show |
139 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.190+331C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 4/10 | chr19 | 7698025 | |||||||
| chr19:7698066 | G | A | 1 | a0002c0002t0001g0133 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.190+290C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 4/10 | chr19 | 7698066 | |||||||
| chr19:7698092 | C | T | 89 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0032 others(86): Show |
131 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.190+264G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 4/10 | chr19 | 7698092 | |||||||
| chr19:7698159 | C | A | 96 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0043 others(93): Show |
137 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.190+197G>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 4/10 | chr19 | 7698159 | |||||||
| chr19:7698217 | C | T | 1 | a0001c0003t0002g0110 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.190+139G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 4/10 | chr19 | 7698217 | |||||||
| chr19:7698247 | T | C | 1 | a0002c0002t0001g0134 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.190+109A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 4/10 | chr19 | 7698247 | |||||||
| chr19:7698295 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.190+61C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 4/10 | chr19 | 7698295 | |||||||
| chr19:7698329 | A | C | 1 | a0001c0005t0001g0191 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.190+27T>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 4/10 | chr19 | 7698329 | |||||||
| chr19:7698330 | C | A | 1 | a0001c0005t0001g0191 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.190+26G>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 4/10 | chr19 | 7698330 | |||||||
| chr19:7698332 | C | T | 1 | a0001c0001t0001g0109 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.190+24G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 4/10 | chr19 | 7698332 | |||||||
| chr19:7698913 | C | T | 1 | a0001c0003t0001g0091 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.23-59G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 2/10 | chr19 | 7698913 | |||||||
| chr19:7698929 | C | T | 1 | a0001c0001t0001g0071 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.23-75G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 2/10 | chr19 | 7698929 | |||||||
| chr19:7698992 | C | T | 107 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(104): Show |
183 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.23-138G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 2/10 | chr19 | 7698992 | |||||||
| chr19:7699031 | G | A | 140 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(137): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.23-177C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 2/10 | chr19 | 7699031 | |||||||
| chr19:7699044 | A | T | 263 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(260): Show |
410 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(407): Show |
intron_variant | MODIFIER | c.23-190T>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 2/10 | chr19 | 7699044 | |||||||
| chr19:7699091 | A | C | 190 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(187): Show |
286 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(283): Show |
intron_variant | MODIFIER | c.23-237T>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 2/10 | chr19 | 7699091 | |||||||
| chr19:7699097 | C | A | 35 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0012 others(32): Show |
56 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.23-243G>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 2/10 | chr19 | 7699097 | |||||||
| chr19:7699271 | A | G | 149 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(146): Show |
224 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(221): Show |
intron_variant | MODIFIER | c.23-417T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 2/10 | chr19 | 7699271 | |||||||
| chr19:7699477 | G | GT | 6 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0003t0001g0068 others(3): Show |
6 | HG01261.hp1 HG02809.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.22+261dupA | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 2/10 | chr19 | 7699477 | |||||||
| chr19:7699477 | GT | G | 5 | a0001c0001t0001g0020 a0001c0001t0001g0102 a0001c0001t0001g0103 others(2): Show |
9 | HG01106.hp1 HG01358.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.22+261delA | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 2/10 | chr19 | 7699477 | |||||||
| chr19:7699477 | GTTT | G | 7 | a0001c0001t0001g0061 a0001c0001t0001g0122 a0001c0003t0001g0121 others(4): Show |
8 | HG02451.hp1 HG02486.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.22+259_22+261delAA others(1): Show |
FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 2/10 | chr19 | 7699477 | |||||||
| chr19:7699477 | GTTTT | G | 71 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0021 others(68): Show |
114 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.22+258_22+261delAA others(2): Show |
FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 2/10 | chr19 | 7699477 | |||||||
| chr19:7699477 | GTTTTT | G | 146 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(143): Show |
237 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(234): Show |
intron_variant | MODIFIER | c.22+257_22+261delAA others(3): Show |
FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 2/10 | chr19 | 7699477 | |||||||
| chr19:7699487 | T | C | 1 | a0001c0003t0001g0106 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.22+252A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 2/10 | chr19 | 7699487 | |||||||
| chr19:7699488 | T | C | 1 | a0001c0001t0001g0107 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.22+251A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 2/10 | chr19 | 7699488 | |||||||
| chr19:7699512 | G | A | 1 | a0001c0003t0007g0291 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.22+227C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 2/10 | chr19 | 7699512 | |||||||
| chr19:7699550 | G | T | 220 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(217): Show |
355 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(352): Show |
intron_variant | MODIFIER | c.22+189C>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 2/10 | chr19 | 7699550 | |||||||
| chr19:7699587 | C | A | 16 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0172 others(13): Show |
21 | HG00280.hp2 HG00733.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.22+152G>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 2/10 | chr19 | 7699587 | |||||||
| chr19:7699588 | G | A | 8 | a0001c0001t0001g0043 a0001c0001t0001g0164 a0001c0001t0001g0165 others(5): Show |
9 | HG01109.hp1 HG02886.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.22+151C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 2/10 | chr19 | 7699588 | |||||||
| chr19:7699659 | G | GC | 210 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(207): Show |
339 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(336): Show |
intron_variant | MODIFIER | c.22+79dupG | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 2/10 | chr19 | 7699659 | |||||||
| chr19:7699855 | G | A | 146 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(143): Show |
262 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(259): Show |
intron_variant | MODIFIER | c.-85-10C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7699855 | |||||||
| chr19:7699878 | C | G | 6 | a0001c0001t0001g0043 a0001c0001t0001g0164 a0001c0001t0001g0165 others(3): Show |
7 | HG01109.hp1 HG02895.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.-85-33G>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7699878 | |||||||
| chr19:7699886 | T | C | 152 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(149): Show |
269 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(266): Show |
intron_variant | MODIFIER | c.-85-41A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7699886 | |||||||
| chr19:7699899 | C | T | 1 | a0001c0004t0001g0286 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-85-54G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7699899 | |||||||
| chr19:7699900 | A | G | 6 | a0001c0001t0001g0043 a0001c0001t0001g0164 a0001c0001t0001g0165 others(3): Show |
7 | HG01109.hp1 HG02895.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.-85-55T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7699900 | |||||||
| chr19:7699924 | G | A | 13 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0173 others(10): Show |
18 | HG00280.hp2 HG00733.hp1 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.-85-79C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7699924 | |||||||
| chr19:7699926 | C | G | 6 | a0001c0001t0001g0043 a0001c0001t0001g0164 a0001c0001t0001g0165 others(3): Show |
7 | HG01109.hp1 HG02895.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.-85-81G>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7699926 | |||||||
| chr19:7699933 | G | C | 6 | a0001c0001t0001g0043 a0001c0001t0001g0164 a0001c0001t0001g0165 others(3): Show |
7 | HG01109.hp1 HG02895.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.-85-88C>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7699933 | |||||||
| chr19:7699940 | T | C | 6 | a0001c0001t0001g0043 a0001c0001t0001g0164 a0001c0001t0001g0165 others(3): Show |
7 | HG01109.hp1 HG02895.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.-85-95A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7699940 | |||||||
| chr19:7699979 | G | A | 16 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0172 others(13): Show |
21 | HG00280.hp2 HG00733.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.-85-134C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7699979 | |||||||
| chr19:7699988 | A | G | 6 | a0001c0001t0001g0043 a0001c0001t0001g0164 a0001c0001t0001g0165 others(3): Show |
7 | HG01109.hp1 HG02895.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.-85-143T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7699988 | |||||||
| chr19:7699991 | G | C | 5 | a0001c0001t0001g0043 a0001c0001t0001g0164 a0001c0001t0001g0165 others(2): Show |
6 | HG01109.hp1 HG02895.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.-85-146C>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7699991 | |||||||
| chr19:7700119 | C | T | 1 | a0001c0003t0001g0230 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-85-274G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7700119 | |||||||
| chr19:7700263 | T | C | 1 | a0001c0001t0001g0153 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-85-418A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7700263 | |||||||
| chr19:7700289 | A | G | 3 | a0001c0001t0001g0061 a0001c0003t0001g0289 a0001c0017t0001g0288 |
4 | HG02451.hp1 HG02486.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-85-444T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7700289 | |||||||
| chr19:7700328 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-85-483C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7700328 | |||||||
| chr19:7700380 | G | A | 215 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(212): Show |
350 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(347): Show |
intron_variant | MODIFIER | c.-85-535C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7700380 | |||||||
| chr19:7700463 | TCTC | T | 5 | a0001c0001t0001g0026 a0001c0001t0001g0051 a0001c0001t0001g0227 others(2): Show |
8 | HG00099.hp1 HG00639.hp2 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.-85-621_-85-619del others(3): Show |
FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7700463 | |||||||
| chr19:7700506 | CTTTA | C | 215 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(212): Show |
350 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(347): Show |
intron_variant | MODIFIER | c.-85-665_-85-662del others(4): Show |
FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7700506 | |||||||
| chr19:7700565 | A | G | 1 | a0001c0001t0001g0062 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-85-720T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7700565 | |||||||
| chr19:7700633 | G | A | 44 | a0001c0001t0001g0014 a0001c0001t0001g0047 a0001c0001t0001g0048 others(41): Show |
56 | HG00423.hp2 HG00558.hp1 HG01167.hp1 others(53): Show |
intron_variant | MODIFIER | c.-85-788C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7700633 | |||||||
| chr19:7700640 | G | A | 1 | a0009c0018t0001g0155 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-85-795C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7700640 | |||||||
| chr19:7700658 | G | T | 136 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(133): Show |
249 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(246): Show |
intron_variant | MODIFIER | c.-85-813C>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7700658 | |||||||
| chr19:7700704 | G | A | 16 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0172 others(13): Show |
21 | HG00280.hp2 HG00733.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.-85-859C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7700704 | |||||||
| chr19:7700760 | G | A | 1 | a0001c0001t0001g0284 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-85-915C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7700760 | |||||||
| chr19:7700807 | A | G | 11 | a0001c0001t0001g0186 a0001c0001t0001g0190 a0001c0004t0001g0025 others(8): Show |
15 | HG00423.hp2 HG01167.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.-85-962T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7700807 | |||||||
| chr19:7700812 | C | T | 1 | a0002c0006t0001g0290 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-85-967G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7700812 | |||||||
| chr19:7700820 | T | A | 1 | a0001c0001t0001g0285 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-85-975A>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7700820 | |||||||
| chr19:7700842 | G | A | 62 | a0001c0001t0001g0014 a0001c0001t0001g0047 a0001c0001t0001g0048 others(59): Show |
80 | HG00280.hp2 HG00423.hp2 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.-85-997C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7700842 | |||||||
| chr19:7700957 | C | T | 2 | a0001c0001t0001g0225 a0001c0001t0001g0226 |
2 | NA18947.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.-86+1058G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7700957 | |||||||
| chr19:7700964 | C | A | 46 | a0001c0001t0001g0014 a0001c0001t0001g0047 a0001c0001t0001g0048 others(43): Show |
59 | HG00423.hp2 HG00558.hp1 HG01167.hp1 others(56): Show |
intron_variant | MODIFIER | c.-86+1051G>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7700964 | |||||||
| chr19:7701179 | G | A | 1 | a0001c0005t0001g0218 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-86+836C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7701179 | |||||||
| chr19:7701200 | G | A | 1 | a0001c0001t0001g0015 | 4 | NA18983.hp1 NA19001.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.-86+815C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7701200 | |||||||
| chr19:7701388 | T | C | 215 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(212): Show |
350 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(347): Show |
intron_variant | MODIFIER | c.-86+627A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7701388 | |||||||
| chr19:7701401 | G | A | 1 | a0001c0004t0001g0286 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-86+614C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7701401 | |||||||
| chr19:7701667 | T | C | 1 | a0001c0004t0001g0286 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-86+348A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7701667 | |||||||
| chr19:7701673 | G | A | 1 | a0001c0004t0001g0219 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-86+342C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7701673 | |||||||
| chr19:7701703 | A | C | 2 | a0001c0003t0001g0063 a0002c0002t0001g0064 |
2 | HG00438.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.-86+312T>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7701703 | |||||||
| chr19:7701718 | C | A | 4 | a0001c0001t0001g0012 a0001c0001t0001g0220 a0001c0001t0001g0221 others(1): Show |
9 | HG00597.hp2 HG02071.hp1 HG02129.hp1 others(6): Show |
intron_variant | MODIFIER | c.-86+297G>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7701718 | |||||||
| chr19:7701763 | G | A | 1 | a0001c0003t0001g0050 | 2 | HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-86+252C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7701763 | |||||||
| chr19:7701873 | G | T | 1 | a0001c0001t0001g0062 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-86+142C>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7701873 | |||||||
| chr19:7701961 | G | A | 1 | a0002c0002t0001g0222 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-86+54C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7701961 | |||||||
| chr19:7701980 | T | G | 84 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(81): Show |
143 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.-86+35A>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7701980 | |||||||
| chr19:7701985 | T | C | 3 | a0001c0001t0001g0061 a0001c0003t0001g0289 a0001c0017t0001g0288 |
4 | HG02451.hp1 HG02486.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-86+30A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7701985 | |||||||
| chr19:7702003 | C | A | 4 | a0001c0001t0001g0292 a0001c0003t0007g0291 a0002c0002t0001g0293 others(1): Show |
4 | HG02615.hp2 HG02647.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.-86+12G>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7702003 |