Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 79368 |
| ensemblid | ENSG00000132704.16 |
| hgncid | 14875 |
| symbol | FCRL2 |
| name | Fc receptor like 2 |
| refseq_nuc | NM_030764.4 |
| refseq_prot | NP_110391.2 |
| ensembl_nuc | ENST00000361516.8 |
| ensembl_prot | ENSP00000355157.3 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 157745733 |
| end | 157777132 |
| strand | - |
| ver | v1.2 |
| region | chr1:157745733-157777132 |
| region5000 | chr1:157740733-157782132 |
| regionname0 | FCRL2_chr1_157745733_157777132 |
| regionname5000 | FCRL2_chr1_157740733_157782132 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 508 | 374 | 87 | 71 | 168 | 14 | 32 | 126 | FCRL2_chr1_157740733_157782132 | FCRL2 | MLLWS others(503): Show |
chr1 | 157740733 | 157782132 |
| a0002 | 0/0 | 508 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | MLLWS others(503): Show |
chr1 | 157740733 | 157782132 |
| a0003 | 0/0 | 317 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | MLLWS others(312): Show |
chr1 | 157740733 | 157782132 |
| a0004 | 0/0 | 508 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | MLLWS others(503): Show |
chr1 | 157740733 | 157782132 |
| a0005 | 0/0 | 508 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | MLLWS others(503): Show |
chr1 | 157740733 | 157782132 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1524 | 360 | 75 | 69 | 168 | 14 | 32 | FCRL2_chr1_157740733_157782132 | FCRL2 | ATGCT others(1519): Show |
chr1 | 157740733 | 157782132 | ||
| a0001c0002 | 0/0 | 1524 | 11 | 11 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | ATGCT others(1519): Show |
chr1 | 157740733 | 157782132 | ||
| a0001c0004 | 0/0 | 1524 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | ATGCT others(1519): Show |
chr1 | 157740733 | 157782132 | ||
| a0001c0007 | 0/0 | 1524 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | ATGCT others(1519): Show |
chr1 | 157740733 | 157782132 | ||
| a0001c0008 | 0/0 | 1524 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | ATGCT others(1519): Show |
chr1 | 157740733 | 157782132 | ||
| a0002c0003 | 0/0 | 1524 | 3 | 3 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | ATGCT others(1519): Show |
chr1 | 157740733 | 157782132 | ||
| a0003c0005 | 0/0 | 1524 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | ATGCT others(1519): Show |
chr1 | 157740733 | 157782132 | ||
| a0004c0009 | 0/0 | 1524 | 1 | 0 | 0 | 0 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | ATGCT others(1519): Show |
chr1 | 157740733 | 157782132 | ||
| a0005c0006 | 0/0 | 1524 | 1 | 0 | 0 | 0 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | ATGCT others(1519): Show |
chr1 | 157740733 | 157782132 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2589 | 290 | 47 | 56 | 153 | 12 | 21 | FCRL2_chr1_157740733_157782132 | FCRL2 | AGAGT others(2584): Show |
chr1 | 157740733 | 157782132 |
| a0001c0001t0002 | 0/0 | 2589 | 17 | 0 | 3 | 5 | 0 | 9 | FCRL2_chr1_157740733_157782132 | FCRL2 | AGAGT others(2584): Show |
chr1 | 157740733 | 157782132 |
| a0001c0001t0003 | 0/0 | 2589 | 18 | 0 | 6 | 9 | 2 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | AGAGT others(2584): Show |
chr1 | 157740733 | 157782132 |
| a0001c0001t0004 | 0/0 | 2589 | 16 | 16 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | AGAGT others(2584): Show |
chr1 | 157740733 | 157782132 |
| a0001c0001t0006 | 0/0 | 2589 | 8 | 7 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | AGAGT others(2584): Show |
chr1 | 157740733 | 157782132 |
| a0001c0001t0007 | 0/1 | 2589 | 5 | 0 | 3 | 0 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | AGAGT others(2584): Show |
chr1 | 157740733 | 157782132 |
| a0001c0001t0008 | 0/0 | 2589 | 3 | 3 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | AGAGT others(2584): Show |
chr1 | 157740733 | 157782132 |
| a0001c0001t0009 | 0/0 | 2589 | 2 | 2 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | AGAGT others(2584): Show |
chr1 | 157740733 | 157782132 |
| a0001c0001t0010 | 0/0 | 2589 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | AGAGT others(2584): Show |
chr1 | 157740733 | 157782132 |
| a0001c0002t0001 | 0/0 | 2589 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | AGAGT others(2584): Show |
chr1 | 157740733 | 157782132 |
| a0001c0002t0005 | 0/0 | 2589 | 10 | 10 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | AGAGT others(2584): Show |
chr1 | 157740733 | 157782132 |
| a0001c0004t0005 | 0/0 | 2589 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | AGAGT others(2584): Show |
chr1 | 157740733 | 157782132 |
| a0001c0007t0001 | 0/0 | 2589 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | AGAGT others(2584): Show |
chr1 | 157740733 | 157782132 |
| a0001c0008t0002 | 0/0 | 2589 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | AGAGT others(2584): Show |
chr1 | 157740733 | 157782132 |
| a0002c0003t0001 | 0/0 | 2589 | 3 | 3 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | AGAGT others(2584): Show |
chr1 | 157740733 | 157782132 |
| a0003c0005t0001 | 0/0 | 2589 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | AGAGT others(2584): Show |
chr1 | 157740733 | 157782132 |
| a0004c0009t0001 | 0/0 | 2589 | 1 | 0 | 0 | 0 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | AGAGT others(2584): Show |
chr1 | 157740733 | 157782132 |
| a0005c0006t0001 | 0/0 | 2589 | 1 | 0 | 0 | 0 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | AGAGT others(2584): Show |
chr1 | 157740733 | 157782132 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 28 | 0 | 5 | 20 | 0 | 3 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0002 | 0/0 | 10 | 0 | 3 | 4 | 2 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0003 | 0/0 | 9 | 1 | 4 | 0 | 2 | 2 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0004 | 0/0 | 8 | 0 | 2 | 6 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0005 | 0/0 | 7 | 0 | 1 | 6 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0006 | 0/0 | 7 | 0 | 4 | 1 | 0 | 2 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0008 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0009 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0010 | 0/0 | 5 | 2 | 0 | 2 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0013 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0029 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0031 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0033 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0003g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0003g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0004g0014 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0004g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0004g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0004g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0004g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0004g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0004g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0004g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0004g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0004g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0004g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0004g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0006g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0006g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0006g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0006g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0006g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0006g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0006g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0007g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0007g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0007g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0007g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0007g0136 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0008g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0008g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0008g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0009g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0009g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0001t0010g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0002t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0002t0005g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0002t0005g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0002t0005g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0002t0005g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0002t0005g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0002t0005g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0002t0005g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0002t0005g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0002t0005g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0004t0005g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0007t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0001c0008t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0002c0003t0001g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0002c0003t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0003c0005t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0004c0009t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| a0005c0006t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0061 | EUR | GBR | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0029 | EUR | GBR | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0054 | EUR | GBR | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0072 | EUR | GBR | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0135 | EUR | FIN | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0073 | EAS | CHS | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG00423 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | CHS | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | CHS | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | CHS | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | CHS | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | CHS | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | CHS | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG00621 | hp1 | a0001 | c0001 | t0010 | g0168 | EAS | CHS | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | CHS | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0202 | AMR | PUR | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | CHS | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0111 | AMR | PUR | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0055 | AMR | PUR | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG01070 | hp2 | a0001 | c0001 | t0003 | g0019 | AMR | PUR | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0019 | AMR | PUR | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG01106 | hp1 | a0001 | c0001 | t0007 | g0126 | AMR | PUR | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0243 | AMR | PUR | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG01109 | hp1 | a0001 | c0001 | t0006 | g0105 | AMR | PUR | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0205 | AMR | PUR | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0058 | AMR | PUR | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | CLM | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | CLM | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | CLM | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG01346 | hp2 | a0001 | c0001 | t0007 | g0120 | AMR | CLM | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | CLM | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | CLM | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | CLM | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | IBS | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG01516 | hp1 | a0001 | c0001 | t0003 | g0064 | EUR | IBS | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG01884 | hp2 | a0001 | c0001 | t0004 | g0219 | AFR | ACB | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG01891 | hp1 | a0001 | c0001 | t0008 | g0245 | AFR | ACB | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG01891 | hp2 | a0001 | c0001 | t0006 | g0106 | AFR | ACB | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG01934 | hp2 | a0001 | c0001 | t0003 | g0057 | AMR | PEL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PEL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG01981 | hp1 | a0003 | c0005 | t0001 | g0186 | AMR | PEL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PEL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PEL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG02004 | hp2 | a0001 | c0007 | t0001 | g0228 | AMR | PEL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | KHV | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | KHV | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG02055 | hp1 | a0001 | c0001 | t0004 | g0218 | AFR | ACB | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | ACB | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | KHV | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | KHV | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0062 | EAS | KHV | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | KHV | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG02145 | hp2 | a0001 | c0001 | t0008 | g0246 | AFR | ACB | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG02148 | hp2 | a0001 | c0008 | t0002 | g0229 | AMR | PEL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | CDX | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | CDX | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | CDX | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG02257 | hp1 | a0002 | c0003 | t0001 | g0043 | AFR | ACB | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG02257 | hp2 | a0001 | c0002 | t0005 | g0255 | AFR | ACB | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG02258 | hp1 | a0001 | c0001 | t0008 | g0227 | AFR | ACB | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | ACB | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG02280 | hp1 | a0001 | c0001 | t0004 | g0221 | AFR | ACB | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG02300 | hp1 | a0001 | c0001 | t0007 | g0119 | AMR | PEL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | ACB | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG02572 | hp1 | a0001 | c0001 | t0006 | g0108 | AFR | GWD | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0192 | SAS | PJL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG02615 | hp1 | a0001 | c0001 | t0004 | g0041 | AFR | GWD | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG02622 | hp1 | a0001 | c0002 | t0005 | g0248 | AFR | GWD | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | GWD | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG02630 | hp2 | a0002 | c0003 | t0001 | g0043 | AFR | GWD | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0235 | SAS | PJL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG02683 | hp2 | a0004 | c0009 | t0001 | g0189 | SAS | PJL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG02717 | hp1 | a0001 | c0001 | t0004 | g0014 | AFR | GWD | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | GWD | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | GWD | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0199 | SAS | PJL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0198 | SAS | PJL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | GWD | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG02809 | hp2 | a0001 | c0001 | t0004 | g0014 | AFR | GWD | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG02818 | hp1 | a0001 | c0002 | t0005 | g0253 | AFR | GWD | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | GWD | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG02886 | hp1 | a0001 | c0002 | t0005 | g0044 | AFR | GWD | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG02886 | hp2 | a0001 | c0001 | t0006 | g0103 | AFR | GWD | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | GWD | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG02895 | hp2 | a0001 | c0002 | t0005 | g0249 | AFR | GWD | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ESN | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG02922 | hp2 | a0001 | c0002 | t0005 | g0254 | AFR | ESN | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG02965 | hp1 | a0001 | c0002 | t0005 | g0251 | AFR | ESN | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG02965 | hp2 | a0002 | c0003 | t0001 | g0242 | AFR | ESN | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ESN | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG02970 | hp2 | a0001 | c0001 | t0006 | g0107 | AFR | ESN | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | ESN | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG02976 | hp2 | a0001 | c0001 | t0004 | g0222 | AFR | ESN | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0204 | SAS | PJL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG03041 | hp1 | a0001 | c0002 | t0005 | g0044 | AFR | GWD | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG03041 | hp2 | a0001 | c0001 | t0006 | g0104 | AFR | GWD | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | ESN | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | ESN | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG03139 | hp1 | a0001 | c0002 | t0005 | g0247 | AFR | ESN | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | ESN | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | ESN | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG03209 | hp2 | a0001 | c0001 | t0004 | g0146 | AFR | MSL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG03225 | hp1 | a0001 | c0001 | t0006 | g0022 | AFR | MSL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | MSL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0193 | SAS | PJL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG03453 | hp1 | a0001 | c0001 | t0004 | g0014 | AFR | MSL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG03453 | hp2 | a0001 | c0001 | t0009 | g0142 | AFR | MSL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG03486 | hp1 | a0001 | c0004 | t0005 | g0256 | AFR | MSL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG03486 | hp2 | a0001 | c0001 | t0009 | g0141 | AFR | MSL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG03490 | hp1 | a0001 | c0001 | t0007 | g0122 | SAS | PJL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0194 | SAS | PJL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG03516 | hp1 | a0001 | c0001 | t0004 | g0223 | AFR | ESN | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | ESN | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | MSL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG03579 | hp2 | a0001 | c0001 | t0004 | g0224 | AFR | MSL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG03654 | hp1 | a0005 | c0006 | t0001 | g0187 | SAS | PJL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0203 | SAS | PJL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | STU | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0195 | SAS | STU | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | BEB | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | BEB | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0056 | SAS | STU | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | STU | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | BEB | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0234 | SAS | BEB | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0164 | SAS | STU | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | STU | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | STU | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | YRI | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA18522 | hp2 | a0001 | c0001 | t0004 | g0014 | AFR | YRI | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | CHB | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | CHB | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | YRI | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA18906 | hp2 | a0001 | c0002 | t0005 | g0250 | AFR | YRI | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA18951 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0075 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA18983 | hp1 | a0001 | c0001 | t0003 | g0115 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA19003 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0100 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA19030 | hp1 | a0001 | c0001 | t0004 | g0217 | AFR | LWK | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA19030 | hp2 | a0001 | c0002 | t0001 | g0252 | AFR | LWK | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | LWK | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | LWK | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA19059 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | YRI | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA19240 | hp2 | a0001 | c0001 | t0004 | g0220 | AFR | YRI | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA20129 | hp1 | a0001 | c0001 | t0006 | g0022 | AFR | ASW | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ASW | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0076 | EUR | TSI | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | TSI | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0067 | EUR | TSI | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | CLM | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | CLM | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | ACB | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG02109 | hp2 | a0001 | c0001 | t0004 | g0041 | AFR | ACB | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG02486 | hp1 | a0001 | c0001 | t0004 | g0225 | AFR | ACB | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | ACB | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | MSL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | USA | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | USA | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | LWK | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | LWK | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0007 | g0136 | REF | REF | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0033 | REF | REF | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:157767441 | C | A | 1 | a0003 | 1 | HG01981.hp1 | stop_gained | HIGH | c.952G>T | p.Glu318* | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 6/12 | 1011/2589 | 952/1527 | 318/508 | chr1 | 157767441 | |||
| chr1:157767480 | T | A | 1 | a0005 | 1 | HG03654.hp1 | missense_variant | MODERATE | c.913A>T | p.Arg305Trp | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 6/12 | 972/2589 | 913/1527 | 305/508 | chr1 | 157767480 | |||
| chr1:157768692 | A | T | 1 | a0002 | 3 | HG02257.hp1 HG02630.hp2 HG02965.hp2 |
missense_variant | MODERATE | c.605T>A | p.Ile202Asn | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 5/12 | 664/2589 | 605/1527 | 202/508 | chr1 | 157768692 | |||
| chr1:157769983 | G | A | 1 | a0004 | 1 | HG02683.hp2 | missense_variant | MODERATE | c.478C>T | p.Pro160Ser | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 4/12 | 537/2589 | 478/1527 | 160/508 | chr1 | 157769983 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:157766883 | C | T | 2 | a0001c0002 a0001c0004 |
12 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(9): Show |
synonymous_variant | LOW | c.1251G>A | p.Leu417Leu | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/12 | 1310/2589 | 1251/1527 | 417/508 | chr1 | 157766883 | |||
| chr1:157767451 | C | T | 1 | a0001c0004 | 1 | HG03486.hp1 | synonymous_variant | LOW | c.942G>A | p.Gly314Gly | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 6/12 | 1001/2589 | 942/1527 | 314/508 | chr1 | 157767451 | |||
| chr1:157768484 | G | A | 1 | a0001c0007 | 1 | HG02004.hp2 | synonymous_variant | LOW | c.813C>T | p.Gly271Gly | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 5/12 | 872/2589 | 813/1527 | 271/508 | chr1 | 157768484 | |||
| chr1:157768694 | G | A | 1 | a0001c0008 | 1 | HG02148.hp2 | synonymous_variant | LOW | c.603C>T | p.Pro201Pro | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 5/12 | 662/2589 | 603/1527 | 201/508 | chr1 | 157768694 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:157745937 | T | C | 1 | a0001c0001t0006 | 8 | HG01109.hp1 HG01891.hp2 HG02572.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*799A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 12/12 | 799 | chr1 | 157745937 | ||||||
| chr1:157745993 | C | T | 1 | a0001c0001t0004 | 16 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*743G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 12/12 | 743 | chr1 | 157745993 | ||||||
| chr1:157746016 | A | C | 1 | a0001c0001t0007 | 4 | HG01106.hp1 HG01346.hp2 HG02300.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*720T>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 12/12 | 720 | chr1 | 157746016 | ||||||
| chr1:157746044 | C | T | 3 | a0001c0001t0006 a0001c0002t0005 a0001c0004t0005 |
19 | HG01109.hp1 HG01891.hp2 HG02257.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*692G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 12/12 | 692 | chr1 | 157746044 | ||||||
| chr1:157746053 | C | T | 4 | a0001c0001t0006 a0001c0001t0008 a0001c0002t0005 others(1): Show |
22 | HG01109.hp1 HG01891.hp1 HG01891.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*683G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 12/12 | 683 | chr1 | 157746053 | ||||||
| chr1:157746108 | C | G | 1 | a0001c0001t0003 | 18 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*628G>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 12/12 | 628 | chr1 | 157746108 | ||||||
| chr1:157746428 | A | C | 2 | a0001c0001t0002 a0001c0008t0002 |
18 | HG00609.hp2 HG00642.hp2 HG00673.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*308T>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 12/12 | 308 | chr1 | 157746428 | ||||||
| chr1:157746505 | A | G | 1 | a0001c0001t0010 | 1 | HG00621.hp1 | 3_prime_UTR_variant | MODIFIER | c.*231T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 12/12 | 231 | chr1 | 157746505 | ||||||
| chr1:157746610 | G | T | 3 | a0001c0001t0006 a0001c0002t0005 a0001c0004t0005 |
19 | HG01109.hp1 HG01891.hp2 HG02257.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*126C>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 12/12 | 126 | chr1 | 157746610 | ||||||
| chr1:157746625 | C | T | 1 | a0001c0001t0009 | 2 | HG03453.hp2 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*111G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 12/12 | 111 | chr1 | 157746625 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:157746789 | C | T | 17 | a0001c0001t0006g0022 a0001c0001t0006g0103 a0001c0001t0006g0104 others(14): Show |
19 | HG01109.hp1 HG01891.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.1489-15G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 11/11 | chr1 | 157746789 | |||||||
| chr1:157746802 | T | C | 17 | a0001c0001t0006g0022 a0001c0001t0006g0103 a0001c0001t0006g0104 others(14): Show |
19 | HG01109.hp1 HG01891.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.1489-28A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 11/11 | chr1 | 157746802 | |||||||
| chr1:157746830 | A | G | 17 | a0001c0001t0006g0022 a0001c0001t0006g0103 a0001c0001t0006g0104 others(14): Show |
19 | HG01109.hp1 HG01891.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.1488+41T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 11/11 | chr1 | 157746830 | |||||||
| chr1:157746934 | C | G | 17 | a0001c0001t0006g0022 a0001c0001t0006g0103 a0001c0001t0006g0104 others(14): Show |
19 | HG01109.hp1 HG01891.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.1460-35G>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 10/11 | chr1 | 157746934 | |||||||
| chr1:157747007 | C | T | 1 | a0001c0001t0008g0227 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1460-108G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 10/11 | chr1 | 157747007 | |||||||
| chr1:157747046 | T | G | 20 | a0001c0001t0001g0207 a0001c0001t0001g0244 a0001c0001t0002g0192 others(17): Show |
20 | HG00609.hp2 HG00642.hp2 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.1460-147A>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 10/11 | chr1 | 157747046 | |||||||
| chr1:157747073 | A | G | 12 | a0001c0001t0004g0014 a0001c0001t0004g0041 a0001c0001t0004g0146 others(9): Show |
16 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.1460-174T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 10/11 | chr1 | 157747073 | |||||||
| chr1:157747113 | C | T | 17 | a0001c0001t0006g0022 a0001c0001t0006g0103 a0001c0001t0006g0104 others(14): Show |
19 | HG01109.hp1 HG01891.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.1460-214G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 10/11 | chr1 | 157747113 | |||||||
| chr1:157747184 | G | A | 17 | a0001c0001t0006g0022 a0001c0001t0006g0103 a0001c0001t0006g0104 others(14): Show |
19 | HG01109.hp1 HG01891.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.1460-285C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 10/11 | chr1 | 157747184 | |||||||
| chr1:157747238 | A | G | 34 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0013 others(31): Show |
58 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.1460-339T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 10/11 | chr1 | 157747238 | |||||||
| chr1:157747277 | G | C | 17 | a0001c0001t0006g0022 a0001c0001t0006g0103 a0001c0001t0006g0104 others(14): Show |
19 | HG01109.hp1 HG01891.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.1460-378C>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 10/11 | chr1 | 157747277 | |||||||
| chr1:157747280 | T | C | 1 | a0001c0001t0001g0169 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1460-381A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 10/11 | chr1 | 157747280 | |||||||
| chr1:157747305 | ACT | A | 5 | a0001c0001t0001g0017 a0001c0001t0001g0045 a0001c0001t0001g0046 others(2): Show |
6 | HG02145.hp1 HG02280.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.1460-408_1460-407d others(4): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 10/11 | chr1 | 157747305 | |||||||
| chr1:157747386 | G | C | 1 | a0001c0001t0001g0067 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1460-487C>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 10/11 | chr1 | 157747386 | |||||||
| chr1:157747784 | G | A | 17 | a0001c0001t0006g0022 a0001c0001t0006g0103 a0001c0001t0006g0104 others(14): Show |
19 | HG01109.hp1 HG01891.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.1459+769C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 10/11 | chr1 | 157747784 | |||||||
| chr1:157747877 | T | C | 17 | a0001c0001t0006g0022 a0001c0001t0006g0103 a0001c0001t0006g0104 others(14): Show |
19 | HG01109.hp1 HG01891.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.1459+676A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 10/11 | chr1 | 157747877 | |||||||
| chr1:157747995 | T | C | 17 | a0001c0001t0006g0022 a0001c0001t0006g0103 a0001c0001t0006g0104 others(14): Show |
19 | HG01109.hp1 HG01891.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.1459+558A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 10/11 | chr1 | 157747995 | |||||||
| chr1:157748020 | A | G | 17 | a0001c0001t0006g0022 a0001c0001t0006g0103 a0001c0001t0006g0104 others(14): Show |
19 | HG01109.hp1 HG01891.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.1459+533T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 10/11 | chr1 | 157748020 | |||||||
| chr1:157748020 | AT | A | 6 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0074 others(3): Show |
8 | HG00140.hp1 HG03239.hp2 HG03688.hp2 others(5): Show |
intron_variant | MODIFIER | c.1459+532delA | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 10/11 | chr1 | 157748020 | |||||||
| chr1:157748041 | C | T | 17 | a0001c0001t0006g0022 a0001c0001t0006g0103 a0001c0001t0006g0104 others(14): Show |
19 | HG01109.hp1 HG01891.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.1459+512G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 10/11 | chr1 | 157748041 | |||||||
| chr1:157748104 | A | G | 17 | a0001c0001t0006g0022 a0001c0001t0006g0103 a0001c0001t0006g0104 others(14): Show |
19 | HG01109.hp1 HG01891.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.1459+449T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 10/11 | chr1 | 157748104 | |||||||
| chr1:157748189 | C | T | 2 | a0001c0001t0004g0222 a0001c0001t0004g0223 |
2 | HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1459+364G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 10/11 | chr1 | 157748189 | |||||||
| chr1:157748358 | G | T | 1 | a0001c0001t0001g0233 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1459+195C>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 10/11 | chr1 | 157748358 | |||||||
| chr1:157748412 | G | C | 2 | a0001c0001t0006g0022 a0001c0001t0006g0104 |
3 | HG03041.hp2 HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1459+141C>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 10/11 | chr1 | 157748412 | |||||||
| chr1:157748441 | C | CAAAT | 86 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(83): Show |
122 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.1459+108_1459+111d others(6): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 10/11 | chr1 | 157748441 | |||||||
| chr1:157748441 | C | CAAATAAA others(1): Show |
4 | a0001c0001t0001g0125 a0001c0001t0001g0153 a0001c0001t0002g0206 others(1): Show |
4 | HG01952.hp1 HG02451.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1459+104_1459+111d others(10): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 10/11 | chr1 | 157748441 | |||||||
| chr1:157748441 | CAAAT | C | 32 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0025 others(29): Show |
41 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(38): Show |
intron_variant | MODIFIER | c.1459+108_1459+111d others(6): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 10/11 | chr1 | 157748441 | |||||||
| chr1:157748441 | CAAATAAA others(1): Show |
C | 7 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0143 others(4): Show |
7 | HG00741.hp2 HG02074.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1459+104_1459+111d others(10): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 10/11 | chr1 | 157748441 | |||||||
| chr1:157748441 | CAAATAAA others(5): Show |
C | 2 | a0001c0001t0001g0049 a0001c0001t0001g0050 |
2 | HG02486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1459+100_1459+111d others(14): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 10/11 | chr1 | 157748441 | |||||||
| chr1:157748441 | CAAATAAA others(9): Show |
C | 17 | a0001c0001t0006g0022 a0001c0001t0006g0103 a0001c0001t0006g0104 others(14): Show |
19 | HG01109.hp1 HG01891.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.1459+96_1459+111de others(17): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 10/11 | chr1 | 157748441 | |||||||
| chr1:157748491 | C | A | 1 | a0001c0001t0001g0233 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1459+62G>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 10/11 | chr1 | 157748491 | |||||||
| chr1:157748493 | A | T | 248 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(245): Show |
362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.1459+60T>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 10/11 | chr1 | 157748493 | |||||||
| chr1:157748535 | T | G | 86 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(83): Show |
112 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.1459+18A>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 10/11 | chr1 | 157748535 | |||||||
| chr1:157748640 | T | G | 86 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(83): Show |
112 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.1394-22A>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 9/11 | chr1 | 157748640 | |||||||
| chr1:157748855 | T | C | 86 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(83): Show |
112 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.1393+20A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 9/11 | chr1 | 157748855 | |||||||
| chr1:157748990 | A | G | 86 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(83): Show |
112 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.1308-30T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 8/11 | chr1 | 157748990 | |||||||
| chr1:157749045 | G | A | 86 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(83): Show |
112 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.1308-85C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 8/11 | chr1 | 157749045 | |||||||
| chr1:157749056 | A | C | 7 | a0001c0002t0005g0044 a0001c0002t0005g0248 a0001c0002t0005g0249 others(4): Show |
8 | HG02622.hp1 HG02818.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1308-96T>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 8/11 | chr1 | 157749056 | |||||||
| chr1:157749103 | A | G | 1 | a0001c0001t0001g0178 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1308-143T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 8/11 | chr1 | 157749103 | |||||||
| chr1:157749138 | T | C | 1 | a0001c0001t0001g0160 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1308-178A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 8/11 | chr1 | 157749138 | |||||||
| chr1:157749189 | C | CT | 85 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(82): Show |
111 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.1308-230dupA | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 8/11 | chr1 | 157749189 | |||||||
| chr1:157749199 | C | T | 1 | a0001c0001t0001g0074 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1308-239G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 8/11 | chr1 | 157749199 | |||||||
| chr1:157749283 | C | T | 76 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(73): Show |
101 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(98): Show |
intron_variant | MODIFIER | c.1308-323G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 8/11 | chr1 | 157749283 | |||||||
| chr1:157749330 | G | T | 2 | a0002c0003t0001g0043 a0002c0003t0001g0242 |
3 | HG02257.hp1 HG02630.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1307+320C>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 8/11 | chr1 | 157749330 | |||||||
| chr1:157749429 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1307+221C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 8/11 | chr1 | 157749429 | |||||||
| chr1:157749634 | T | C | 10 | a0001c0002t0005g0044 a0001c0002t0005g0247 a0001c0002t0005g0248 others(7): Show |
11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1307+16A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 8/11 | chr1 | 157749634 | |||||||
| chr1:157749690 | T | C | 1 | a0001c0001t0001g0156 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1280-13A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157749690 | |||||||
| chr1:157749738 | G | C | 1 | a0001c0001t0001g0190 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1280-61C>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157749738 | |||||||
| chr1:157749753 | C | T | 1 | a0001c0001t0001g0021 | 2 | NA18973.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.1280-76G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157749753 | |||||||
| chr1:157749909 | G | A | 1 | a0001c0001t0002g0197 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1280-232C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157749909 | |||||||
| chr1:157749943 | T | A | 1 | a0001c0001t0006g0107 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1280-266A>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157749943 | |||||||
| chr1:157749951 | A | T | 10 | a0001c0002t0005g0044 a0001c0002t0005g0247 a0001c0002t0005g0248 others(7): Show |
11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-274T>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157749951 | |||||||
| chr1:157750120 | G | A | 1 | a0001c0007t0001g0228 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1280-443C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157750120 | |||||||
| chr1:157750123 | A | G | 10 | a0001c0002t0005g0044 a0001c0002t0005g0247 a0001c0002t0005g0248 others(7): Show |
11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-446T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157750123 | |||||||
| chr1:157750150 | A | G | 1 | a0001c0001t0001g0052 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1280-473T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157750150 | |||||||
| chr1:157750162 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1280-485G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157750162 | |||||||
| chr1:157750163 | G | A | 10 | a0001c0002t0005g0044 a0001c0002t0005g0247 a0001c0002t0005g0248 others(7): Show |
11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-486C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157750163 | |||||||
| chr1:157750219 | G | A | 69 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(66): Show |
93 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.1280-542C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157750219 | |||||||
| chr1:157750233 | T | C | 1 | a0001c0001t0001g0128 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1280-556A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157750233 | |||||||
| chr1:157750346 | C | A | 10 | a0001c0002t0005g0044 a0001c0002t0005g0247 a0001c0002t0005g0248 others(7): Show |
11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-669G>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157750346 | |||||||
| chr1:157750410 | T | C | 10 | a0001c0002t0005g0044 a0001c0002t0005g0247 a0001c0002t0005g0248 others(7): Show |
11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-733A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157750410 | |||||||
| chr1:157750431 | T | C | 10 | a0001c0002t0005g0044 a0001c0002t0005g0247 a0001c0002t0005g0248 others(7): Show |
11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-754A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157750431 | |||||||
| chr1:157750804 | C | A | 2 | a0001c0001t0008g0245 a0001c0001t0008g0246 |
2 | HG01891.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.1280-1127G>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157750804 | |||||||
| chr1:157750886 | G | C | 13 | a0001c0001t0008g0227 a0001c0001t0008g0245 a0001c0001t0008g0246 others(10): Show |
14 | HG01891.hp1 HG02145.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1280-1209C>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157750886 | |||||||
| chr1:157750911 | A | C | 1 | a0001c0001t0001g0166 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1280-1234T>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157750911 | |||||||
| chr1:157750935 | C | T | 1 | a0001c0001t0008g0227 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1280-1258G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157750935 | |||||||
| chr1:157750940 | T | C | 1 | a0001c0001t0008g0227 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1280-1263A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157750940 | |||||||
| chr1:157751060 | C | T | 1 | a0001c0001t0001g0036 | 2 | NA18957.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.1280-1383G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157751060 | |||||||
| chr1:157751064 | T | C | 4 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(1): Show |
4 | HG01516.hp1 HG02451.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1280-1387A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157751064 | |||||||
| chr1:157751078 | A | G | 1 | a0002c0003t0001g0242 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1280-1401T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157751078 | |||||||
| chr1:157751098 | T | A | 1 | a0001c0001t0003g0073 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1280-1421A>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157751098 | |||||||
| chr1:157751111 | A | G | 10 | a0001c0002t0005g0044 a0001c0002t0005g0247 a0001c0002t0005g0248 others(7): Show |
11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-1434T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157751111 | |||||||
| chr1:157751201 | A | G | 1 | a0001c0001t0001g0063 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1280-1524T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157751201 | |||||||
| chr1:157751208 | T | A | 1 | a0001c0001t0001g0063 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1280-1531A>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157751208 | |||||||
| chr1:157751209 | C | A | 1 | a0001c0001t0001g0063 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1280-1532G>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157751209 | |||||||
| chr1:157751212 | A | G | 1 | a0001c0001t0001g0063 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1280-1535T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157751212 | |||||||
| chr1:157751218 | T | A | 1 | a0001c0001t0001g0063 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1280-1541A>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157751218 | |||||||
| chr1:157751221 | C | T | 1 | a0001c0001t0001g0063 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1280-1544G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157751221 | |||||||
| chr1:157751222 | C | T | 1 | a0001c0001t0001g0063 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1280-1545G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157751222 | |||||||
| chr1:157751224 | T | G | 1 | a0001c0001t0001g0063 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1280-1547A>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157751224 | |||||||
| chr1:157751234 | A | G | 1 | a0001c0001t0001g0212 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1280-1557T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157751234 | |||||||
| chr1:157751332 | G | A | 3 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 |
3 | HG02451.hp2 HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1280-1655C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157751332 | |||||||
| chr1:157751464 | G | A | 10 | a0001c0002t0005g0044 a0001c0002t0005g0247 a0001c0002t0005g0248 others(7): Show |
11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-1787C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157751464 | |||||||
| chr1:157751549 | A | T | 10 | a0001c0002t0005g0044 a0001c0002t0005g0247 a0001c0002t0005g0248 others(7): Show |
11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-1872T>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157751549 | |||||||
| chr1:157751550 | C | T | 20 | a0001c0001t0001g0207 a0001c0001t0001g0244 a0001c0001t0002g0192 others(17): Show |
20 | HG00609.hp2 HG00642.hp2 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.1280-1873G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157751550 | |||||||
| chr1:157751672 | T | C | 1 | a0001c0001t0001g0085 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1280-1995A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157751672 | |||||||
| chr1:157751894 | C | T | 1 | a0001c0001t0003g0075 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1280-2217G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157751894 | |||||||
| chr1:157751894 | CG | C | 3 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 |
3 | HG02451.hp2 HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1280-2218delC | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157751894 | |||||||
| chr1:157751903 | C | CGAGCAAA others(19): Show |
3 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 |
3 | HG02451.hp2 HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1280-2227_1280-222 others(30): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157751903 | |||||||
| chr1:157751904 | T | A | 3 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 |
3 | HG02451.hp2 HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1280-2227A>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157751904 | |||||||
| chr1:157751908 | G | C | 10 | a0001c0002t0005g0044 a0001c0002t0005g0247 a0001c0002t0005g0248 others(7): Show |
11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-2231C>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157751908 | |||||||
| chr1:157751922 | A | G | 10 | a0001c0002t0005g0044 a0001c0002t0005g0247 a0001c0002t0005g0248 others(7): Show |
11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-2245T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157751922 | |||||||
| chr1:157751945 | G | A | 10 | a0001c0002t0005g0044 a0001c0002t0005g0247 a0001c0002t0005g0248 others(7): Show |
11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-2268C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157751945 | |||||||
| chr1:157751949 | T | C | 1 | a0001c0001t0001g0134 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1280-2272A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157751949 | |||||||
| chr1:157752008 | T | C | 2 | a0001c0001t0001g0207 a0001c0001t0001g0244 |
2 | HG03195.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1280-2331A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157752008 | |||||||
| chr1:157752010 | C | T | 3 | a0001c0001t0008g0227 a0001c0001t0008g0245 a0001c0001t0008g0246 |
3 | HG01891.hp1 HG02145.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1280-2333G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157752010 | |||||||
| chr1:157752013 | T | A | 1 | a0001c0001t0001g0131 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1280-2336A>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157752013 | |||||||
| chr1:157752266 | G | A | 10 | a0001c0002t0005g0044 a0001c0002t0005g0247 a0001c0002t0005g0248 others(7): Show |
11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-2589C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157752266 | |||||||
| chr1:157752267 | T | C | 10 | a0001c0002t0005g0044 a0001c0002t0005g0247 a0001c0002t0005g0248 others(7): Show |
11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-2590A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157752267 | |||||||
| chr1:157752318 | A | G | 2 | a0001c0001t0001g0207 a0001c0001t0001g0244 |
2 | HG03195.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1280-2641T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157752318 | |||||||
| chr1:157752548 | G | A | 3 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 |
3 | HG02451.hp2 HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1280-2871C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157752548 | |||||||
| chr1:157752763 | T | C | 1 | a0001c0001t0001g0063 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1280-3086A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157752763 | |||||||
| chr1:157752860 | G | A | 10 | a0001c0002t0005g0044 a0001c0002t0005g0247 a0001c0002t0005g0248 others(7): Show |
11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-3183C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157752860 | |||||||
| chr1:157752920 | G | A | 10 | a0001c0002t0005g0044 a0001c0002t0005g0247 a0001c0002t0005g0248 others(7): Show |
11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-3243C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157752920 | |||||||
| chr1:157753105 | A | T | 7 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(4): Show |
7 | HG00140.hp2 HG00733.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.1280-3428T>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157753105 | |||||||
| chr1:157753365 | C | A | 3 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 |
3 | HG02451.hp2 HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1280-3688G>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157753365 | |||||||
| chr1:157753398 | C | A | 10 | a0001c0002t0005g0044 a0001c0002t0005g0247 a0001c0002t0005g0248 others(7): Show |
11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-3721G>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157753398 | |||||||
| chr1:157753664 | T | C | 1 | a0001c0001t0001g0170 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1280-3987A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157753664 | |||||||
| chr1:157753725 | A | G | 10 | a0001c0002t0005g0044 a0001c0002t0005g0247 a0001c0002t0005g0248 others(7): Show |
11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-4048T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157753725 | |||||||
| chr1:157754045 | C | G | 69 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(66): Show |
93 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.1280-4368G>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157754045 | |||||||
| chr1:157754047 | G | A | 69 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(66): Show |
93 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.1280-4370C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157754047 | |||||||
| chr1:157754049 | A | AATATTTC others(5): Show |
69 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(66): Show |
93 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.1280-4373_1280-437 others(16): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157754049 | |||||||
| chr1:157754050 | C | T | 69 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(66): Show |
93 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.1280-4373G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157754050 | |||||||
| chr1:157754150 | C | T | 1 | a0001c0001t0001g0235 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1280-4473G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157754150 | |||||||
| chr1:157754402 | G | T | 10 | a0001c0002t0005g0044 a0001c0002t0005g0247 a0001c0002t0005g0248 others(7): Show |
11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-4725C>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157754402 | |||||||
| chr1:157754449 | A | C | 10 | a0001c0002t0005g0044 a0001c0002t0005g0247 a0001c0002t0005g0248 others(7): Show |
11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-4772T>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157754449 | |||||||
| chr1:157754471 | G | C | 2 | a0001c0001t0001g0171 a0001c0001t0001g0184 |
2 | HG01192.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1280-4794C>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157754471 | |||||||
| chr1:157754499 | C | A | 1 | a0001c0001t0001g0159 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1280-4822G>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157754499 | |||||||
| chr1:157754773 | C | T | 10 | a0001c0002t0005g0044 a0001c0002t0005g0247 a0001c0002t0005g0248 others(7): Show |
11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-5096G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157754773 | |||||||
| chr1:157754774 | C | T | 10 | a0001c0002t0005g0044 a0001c0002t0005g0247 a0001c0002t0005g0248 others(7): Show |
11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-5097G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157754774 | |||||||
| chr1:157754777 | G | A | 10 | a0001c0002t0005g0044 a0001c0002t0005g0247 a0001c0002t0005g0248 others(7): Show |
11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-5100C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157754777 | |||||||
| chr1:157754832 | G | A | 4 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(1): Show |
4 | HG02451.hp2 HG02647.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1280-5155C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157754832 | |||||||
| chr1:157754870 | G | A | 1 | a0001c0002t0005g0254 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1280-5193C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157754870 | |||||||
| chr1:157754914 | C | T | 10 | a0001c0002t0005g0044 a0001c0002t0005g0247 a0001c0002t0005g0248 others(7): Show |
11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-5237G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157754914 | |||||||
| chr1:157754953 | G | A | 2 | a0001c0001t0001g0069 a0001c0001t0001g0071 |
2 | HG01175.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.1280-5276C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157754953 | |||||||
| chr1:157754965 | C | CA | 19 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0021 others(16): Show |
30 | HG00597.hp2 HG00621.hp2 HG01256.hp2 others(27): Show |
intron_variant | MODIFIER | c.1280-5289dupT | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157754965 | |||||||
| chr1:157754967 | A | G | 1 | a0001c0001t0001g0030 | 2 | HG03139.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1280-5290T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157754967 | |||||||
| chr1:157755006 | C | A | 3 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0007t0001g0228 |
3 | HG02004.hp2 HG02055.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1280-5329G>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157755006 | |||||||
| chr1:157755073 | A | G | 1 | a0001c0001t0001g0150 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1280-5396T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157755073 | |||||||
| chr1:157755123 | A | G | 1 | a0001c0001t0001g0152 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1280-5446T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157755123 | |||||||
| chr1:157755195 | C | T | 10 | a0001c0002t0005g0044 a0001c0002t0005g0247 a0001c0002t0005g0248 others(7): Show |
11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-5518G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157755195 | |||||||
| chr1:157755257 | C | T | 11 | a0001c0001t0007g0119 a0001c0002t0005g0044 a0001c0002t0005g0247 others(8): Show |
12 | HG02257.hp2 HG02300.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1280-5580G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157755257 | |||||||
| chr1:157755325 | G | A | 10 | a0001c0002t0005g0044 a0001c0002t0005g0247 a0001c0002t0005g0248 others(7): Show |
11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-5648C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157755325 | |||||||
| chr1:157755331 | C | A | 10 | a0001c0002t0005g0044 a0001c0002t0005g0247 a0001c0002t0005g0248 others(7): Show |
11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-5654G>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157755331 | |||||||
| chr1:157755420 | G | A | 2 | a0001c0001t0001g0034 a0001c0001t0001g0164 |
3 | HG03017.hp1 HG03831.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1280-5743C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157755420 | |||||||
| chr1:157755474 | T | G | 182 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(179): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.1280-5797A>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157755474 | |||||||
| chr1:157755586 | C | G | 5 | a0001c0001t0001g0017 a0001c0001t0001g0045 a0001c0001t0001g0046 others(2): Show |
6 | HG02145.hp1 HG02280.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.1280-5909G>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157755586 | |||||||
| chr1:157755655 | C | T | 2 | a0001c0001t0001g0035 a0001c0001t0001g0165 |
3 | NA18978.hp1 NA18999.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.1280-5978G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157755655 | |||||||
| chr1:157755800 | T | C | 12 | a0001c0001t0004g0014 a0001c0001t0004g0041 a0001c0001t0004g0146 others(9): Show |
16 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.1280-6123A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157755800 | |||||||
| chr1:157755944 | T | C | 10 | a0001c0002t0005g0044 a0001c0002t0005g0247 a0001c0002t0005g0248 others(7): Show |
11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-6267A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157755944 | |||||||
| chr1:157756044 | G | A | 1 | a0001c0001t0006g0103 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1280-6367C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157756044 | |||||||
| chr1:157756071 | T | A | 5 | a0001c0001t0001g0017 a0001c0001t0001g0045 a0001c0001t0001g0046 others(2): Show |
6 | HG02145.hp1 HG02280.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.1280-6394A>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157756071 | |||||||
| chr1:157756100 | G | T | 10 | a0001c0002t0005g0044 a0001c0002t0005g0247 a0001c0002t0005g0248 others(7): Show |
11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-6423C>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157756100 | |||||||
| chr1:157756212 | A | G | 1 | a0001c0001t0001g0165 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1280-6535T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157756212 | |||||||
| chr1:157756230 | G | A | 1 | a0001c0001t0001g0212 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1280-6553C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157756230 | |||||||
| chr1:157756333 | T | C | 18 | a0001c0001t0002g0192 a0001c0001t0002g0193 a0001c0001t0002g0194 others(15): Show |
18 | HG00609.hp2 HG00642.hp2 HG00673.hp1 others(15): Show |
intron_variant | MODIFIER | c.1280-6656A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157756333 | |||||||
| chr1:157756389 | T | G | 1 | a0001c0001t0001g0173 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1280-6712A>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157756389 | |||||||
| chr1:157756453 | T | C | 10 | a0001c0002t0005g0044 a0001c0002t0005g0247 a0001c0002t0005g0248 others(7): Show |
11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-6776A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157756453 | |||||||
| chr1:157756462 | C | T | 1 | a0001c0001t0001g0239 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1280-6785G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157756462 | |||||||
| chr1:157756468 | A | G | 3 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 |
3 | HG02630.hp1 HG02895.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1280-6791T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157756468 | |||||||
| chr1:157756543 | G | A | 34 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0013 others(31): Show |
58 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.1280-6866C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157756543 | |||||||
| chr1:157756587 | G | A | 10 | a0001c0002t0005g0044 a0001c0002t0005g0247 a0001c0002t0005g0248 others(7): Show |
11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-6910C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157756587 | |||||||
| chr1:157756617 | C | T | 40 | a0001c0001t0001g0017 a0001c0001t0001g0030 a0001c0001t0001g0045 others(37): Show |
42 | HG00609.hp2 HG00642.hp2 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.1280-6940G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157756617 | |||||||
| chr1:157756631 | T | A | 10 | a0001c0002t0005g0044 a0001c0002t0005g0247 a0001c0002t0005g0248 others(7): Show |
11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-6954A>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157756631 | |||||||
| chr1:157756649 | G | T | 1 | a0001c0002t0005g0250 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1280-6972C>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157756649 | |||||||
| chr1:157756662 | C | G | 10 | a0001c0002t0005g0044 a0001c0002t0005g0247 a0001c0002t0005g0248 others(7): Show |
11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-6985G>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157756662 | |||||||
| chr1:157756670 | C | T | 53 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0013 others(50): Show |
82 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.1280-6993G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157756670 | |||||||
| chr1:157756679 | G | GA | 162 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(159): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.1280-7003dupT | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157756679 | |||||||
| chr1:157756679 | GAA | G | 10 | a0001c0002t0005g0044 a0001c0002t0005g0247 a0001c0002t0005g0248 others(7): Show |
11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-7004_1280-700 others(6): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157756679 | |||||||
| chr1:157756696 | G | A | 1 | a0001c0001t0001g0233 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1280-7019C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157756696 | |||||||
| chr1:157756696 | G | C | 10 | a0001c0002t0005g0044 a0001c0002t0005g0247 a0001c0002t0005g0248 others(7): Show |
11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-7019C>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157756696 | |||||||
| chr1:157756886 | C | T | 10 | a0001c0002t0005g0044 a0001c0002t0005g0247 a0001c0002t0005g0248 others(7): Show |
11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-7209G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157756886 | |||||||
| chr1:157757031 | G | C | 3 | a0001c0001t0008g0227 a0001c0001t0008g0245 a0001c0001t0008g0246 |
3 | HG01891.hp1 HG02145.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1280-7354C>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157757031 | |||||||
| chr1:157757100 | T | A | 10 | a0001c0002t0005g0044 a0001c0002t0005g0247 a0001c0002t0005g0248 others(7): Show |
11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-7423A>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157757100 | |||||||
| chr1:157757123 | T | G | 10 | a0001c0002t0005g0044 a0001c0002t0005g0247 a0001c0002t0005g0248 others(7): Show |
11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-7446A>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157757123 | |||||||
| chr1:157757448 | G | A | 1 | a0004c0009t0001g0189 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1280-7771C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157757448 | |||||||
| chr1:157757468 | C | T | 1 | a0001c0001t0008g0227 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1280-7791G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157757468 | |||||||
| chr1:157757508 | C | T | 1 | a0001c0001t0001g0067 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1280-7831G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157757508 | |||||||
| chr1:157757551 | C | T | 10 | a0001c0002t0005g0044 a0001c0002t0005g0247 a0001c0002t0005g0248 others(7): Show |
11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-7874G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157757551 | |||||||
| chr1:157757552 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1280-7875C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157757552 | |||||||
| chr1:157757684 | T | C | 10 | a0001c0002t0005g0044 a0001c0002t0005g0247 a0001c0002t0005g0248 others(7): Show |
11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-8007A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157757684 | |||||||
| chr1:157757701 | A | T | 10 | a0001c0002t0005g0044 a0001c0002t0005g0247 a0001c0002t0005g0248 others(7): Show |
11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-8024T>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157757701 | |||||||
| chr1:157757731 | T | G | 10 | a0001c0002t0005g0044 a0001c0002t0005g0247 a0001c0002t0005g0248 others(7): Show |
11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-8054A>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157757731 | |||||||
| chr1:157757786 | C | A | 10 | a0001c0002t0005g0044 a0001c0002t0005g0247 a0001c0002t0005g0248 others(7): Show |
11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-8109G>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157757786 | |||||||
| chr1:157757831 | G | A | 1 | a0001c0001t0001g0037 | 2 | NA18945.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.1280-8154C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157757831 | |||||||
| chr1:157757835 | G | A | 1 | a0001c0001t0006g0105 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1280-8158C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157757835 | |||||||
| chr1:157757839 | G | C | 10 | a0001c0002t0005g0044 a0001c0002t0005g0247 a0001c0002t0005g0248 others(7): Show |
11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-8162C>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157757839 | |||||||
| chr1:157757841 | A | T | 10 | a0001c0002t0005g0044 a0001c0002t0005g0247 a0001c0002t0005g0248 others(7): Show |
11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-8164T>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157757841 | |||||||
| chr1:157757842 | G | T | 10 | a0001c0002t0005g0044 a0001c0002t0005g0247 a0001c0002t0005g0248 others(7): Show |
11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-8165C>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157757842 | |||||||
| chr1:157757858 | A | G | 1 | a0001c0001t0008g0227 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1280-8181T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157757858 | |||||||
| chr1:157757894 | A | G | 10 | a0001c0002t0005g0044 a0001c0002t0005g0247 a0001c0002t0005g0248 others(7): Show |
11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-8217T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157757894 | |||||||
| chr1:157757897 | G | T | 10 | a0001c0002t0005g0044 a0001c0002t0005g0247 a0001c0002t0005g0248 others(7): Show |
11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-8220C>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157757897 | |||||||
| chr1:157757927 | G | A | 1 | a0001c0001t0001g0176 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1280-8250C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157757927 | |||||||
| chr1:157757956 | C | G | 1 | a0001c0001t0009g0141 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1280-8279G>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157757956 | |||||||
| chr1:157758064 | C | T | 10 | a0001c0002t0005g0044 a0001c0002t0005g0247 a0001c0002t0005g0248 others(7): Show |
11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-8387G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157758064 | |||||||
| chr1:157758094 | T | A | 10 | a0001c0002t0005g0044 a0001c0002t0005g0247 a0001c0002t0005g0248 others(7): Show |
11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-8417A>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157758094 | |||||||
| chr1:157758161 | A | G | 10 | a0001c0002t0005g0044 a0001c0002t0005g0247 a0001c0002t0005g0248 others(7): Show |
11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-8484T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157758161 | |||||||
| chr1:157758293 | G | C | 10 | a0001c0002t0005g0044 a0001c0002t0005g0247 a0001c0002t0005g0248 others(7): Show |
11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1279+8562C>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157758293 | |||||||
| chr1:157758310 | G | A | 10 | a0001c0002t0005g0044 a0001c0002t0005g0247 a0001c0002t0005g0248 others(7): Show |
11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1279+8545C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157758310 | |||||||
| chr1:157758358 | T | C | 3 | a0001c0002t0005g0247 a0001c0002t0005g0250 a0001c0002t0005g0255 |
3 | HG02257.hp2 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1279+8497A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157758358 | |||||||
| chr1:157758409 | C | T | 10 | a0001c0002t0005g0044 a0001c0002t0005g0247 a0001c0002t0005g0248 others(7): Show |
11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1279+8446G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157758409 | |||||||
| chr1:157758442 | A | C | 1 | a0001c0001t0001g0127 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1279+8413T>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157758442 | |||||||
| chr1:157758511 | T | C | 3 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 |
3 | HG02451.hp2 HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1279+8344A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157758511 | |||||||
| chr1:157758525 | C | G | 10 | a0001c0002t0005g0044 a0001c0002t0005g0247 a0001c0002t0005g0248 others(7): Show |
11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1279+8330G>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157758525 | |||||||
| chr1:157758538 | G | A | 10 | a0001c0002t0005g0044 a0001c0002t0005g0247 a0001c0002t0005g0248 others(7): Show |
11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1279+8317C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157758538 | |||||||
| chr1:157758547 | C | T | 1 | a0001c0001t0003g0058 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1279+8308G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157758547 | |||||||
| chr1:157758567 | A | G | 1 | a0001c0004t0005g0256 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1279+8288T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157758567 | |||||||
| chr1:157758661 | T | C | 1 | a0001c0001t0001g0066 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1279+8194A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157758661 | |||||||
| chr1:157758664 | C | T | 3 | a0001c0001t0008g0227 a0001c0001t0008g0245 a0001c0001t0008g0246 |
3 | HG01891.hp1 HG02145.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1279+8191G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157758664 | |||||||
| chr1:157758665 | C | T | 1 | a0001c0001t0001g0066 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1279+8190G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157758665 | |||||||
| chr1:157758667 | A | G | 1 | a0001c0001t0001g0066 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1279+8188T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157758667 | |||||||
| chr1:157758669 | G | T | 1 | a0001c0001t0001g0066 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1279+8186C>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157758669 | |||||||
| chr1:157758671 | A | C | 1 | a0001c0001t0001g0066 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1279+8184T>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157758671 | |||||||
| chr1:157758674 | C | G | 1 | a0001c0001t0001g0066 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1279+8181G>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157758674 | |||||||
| chr1:157758675 | C | T | 1 | a0001c0001t0001g0066 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1279+8180G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157758675 | |||||||
| chr1:157758676 | C | T | 1 | a0001c0001t0001g0066 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1279+8179G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157758676 | |||||||
| chr1:157758679 | G | T | 2 | a0001c0001t0001g0049 a0001c0001t0001g0050 |
2 | HG02486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1279+8176C>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157758679 | |||||||
| chr1:157758680 | C | CA | 45 | a0001c0001t0001g0002 a0001c0001t0001g0028 a0001c0001t0001g0038 others(42): Show |
58 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.1279+8174dupT | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157758680 | |||||||
| chr1:157758680 | C | CAA | 7 | a0001c0001t0001g0145 a0001c0001t0001g0161 a0001c0001t0001g0178 others(4): Show |
7 | HG01123.hp1 HG02145.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1279+8173_1279+817 others(6): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157758680 | |||||||
| chr1:157758680 | CA | C | 25 | a0001c0001t0001g0034 a0001c0001t0001g0049 a0001c0001t0001g0050 others(22): Show |
31 | HG01109.hp1 HG01884.hp2 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.1279+8174delT | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157758680 | |||||||
| chr1:157758773 | A | G | 1 | a0001c0001t0001g0163 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.1279+8082T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157758773 | |||||||
| chr1:157758943 | T | C | 1 | a0001c0001t0001g0159 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1279+7912A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157758943 | |||||||
| chr1:157758957 | A | G | 3 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 |
3 | HG02630.hp1 HG02895.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1279+7898T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157758957 | |||||||
| chr1:157759106 | G | A | 10 | a0001c0002t0005g0044 a0001c0002t0005g0247 a0001c0002t0005g0248 others(7): Show |
11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1279+7749C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157759106 | |||||||
| chr1:157759110 | T | C | 1 | a0001c0001t0001g0216 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1279+7745A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157759110 | |||||||
| chr1:157759302 | A | G | 10 | a0001c0002t0005g0044 a0001c0002t0005g0247 a0001c0002t0005g0248 others(7): Show |
11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1279+7553T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157759302 | |||||||
| chr1:157759345 | C | A | 3 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 |
3 | HG02630.hp1 HG02895.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1279+7510G>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157759345 | |||||||
| chr1:157759470 | C | A | 10 | a0001c0002t0005g0044 a0001c0002t0005g0247 a0001c0002t0005g0248 others(7): Show |
11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1279+7385G>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157759470 | |||||||
| chr1:157759514 | T | A | 10 | a0001c0001t0001g0030 a0001c0001t0001g0110 a0001c0001t0001g0148 others(7): Show |
11 | HG02004.hp2 HG02055.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1279+7341A>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157759514 | |||||||
| chr1:157759565 | C | G | 1 | a0001c0002t0005g0255 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1279+7290G>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157759565 | |||||||
| chr1:157759580 | A | T | 3 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 |
3 | HG02630.hp1 HG02895.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1279+7275T>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157759580 | |||||||
| chr1:157759765 | C | A | 4 | a0001c0001t0001g0042 a0001c0001t0001g0145 a0001c0001t0001g0216 others(1): Show |
5 | HG02723.hp1 HG02922.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1279+7090G>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157759765 | |||||||
| chr1:157759821 | G | A | 10 | a0001c0002t0005g0044 a0001c0002t0005g0247 a0001c0002t0005g0248 others(7): Show |
11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1279+7034C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157759821 | |||||||
| chr1:157759967 | G | A | 1 | a0001c0001t0001g0094 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1279+6888C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157759967 | |||||||
| chr1:157760090 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1279+6765G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760090 | |||||||
| chr1:157760131 | T | C | 10 | a0001c0002t0005g0044 a0001c0002t0005g0247 a0001c0002t0005g0248 others(7): Show |
11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1279+6724A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760131 | |||||||
| chr1:157760238 | T | C | 34 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0013 others(31): Show |
58 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.1279+6617A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760238 | |||||||
| chr1:157760359 | A | G | 2 | a0001c0001t0008g0245 a0001c0001t0008g0246 |
2 | HG01891.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.1279+6496T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760359 | |||||||
| chr1:157760460 | T | TA | 10 | a0001c0002t0005g0044 a0001c0002t0005g0247 a0001c0002t0005g0248 others(7): Show |
11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1279+6394dupT | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760460 | |||||||
| chr1:157760489 | G | A | 5 | a0001c0001t0001g0017 a0001c0001t0001g0045 a0001c0001t0001g0046 others(2): Show |
6 | HG02145.hp1 HG02280.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.1279+6366C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760489 | |||||||
| chr1:157760588 | T | C | 10 | a0001c0002t0005g0044 a0001c0002t0005g0247 a0001c0002t0005g0248 others(7): Show |
11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1279+6267A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760588 | |||||||
| chr1:157760591 | C | T | 1 | a0001c0001t0001g0162 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1279+6264G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760591 | |||||||
| chr1:157760654 | A | AGAAG | 22 | a0001c0001t0001g0017 a0001c0001t0001g0045 a0001c0001t0001g0046 others(19): Show |
27 | HG00140.hp1 HG00423.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.1279+6197_1279+620 others(8): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760654 | |||||||
| chr1:157760654 | A | G | 1 | a0001c0001t0001g0180 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1279+6201T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760654 | |||||||
| chr1:157760654 | AGAAG | A | 10 | a0001c0001t0001g0030 a0001c0001t0001g0110 a0001c0001t0001g0134 others(7): Show |
11 | HG02004.hp2 HG02055.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1279+6197_1279+620 others(8): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760654 | |||||||
| chr1:157760654 | AGAAGGAA others(5): Show |
A | 1 | a0001c0001t0001g0008 | 5 | HG02056.hp1 NA18939.hp1 NA18952.hp2 others(2): Show |
intron_variant | MODIFIER | c.1279+6189_1279+620 others(16): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760654 | |||||||
| chr1:157760658 | G | A | 10 | a0001c0002t0005g0044 a0001c0002t0005g0247 a0001c0002t0005g0248 others(7): Show |
11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1279+6197C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760658 | |||||||
| chr1:157760662 | G | A | 7 | a0001c0002t0005g0044 a0001c0002t0005g0248 a0001c0002t0005g0249 others(4): Show |
8 | HG02622.hp1 HG02818.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1279+6193C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760662 | |||||||
| chr1:157760678 | G | A | 3 | a0001c0001t0001g0149 a0001c0001t0001g0180 a0001c0001t0001g0233 |
3 | HG01981.hp2 HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1279+6177C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760678 | |||||||
| chr1:157760680 | A | AAAGAAAG others(127): Show |
1 | a0001c0001t0002g0204 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1279+6174_1279+617 others(138): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760680 | |||||||
| chr1:157760680 | A | AAAGAAAG others(123): Show |
6 | a0001c0001t0002g0200 a0001c0001t0002g0201 a0001c0001t0002g0202 others(3): Show |
6 | HG00609.hp2 HG00642.hp2 HG00673.hp1 others(3): Show |
intron_variant | MODIFIER | c.1279+6174_1279+617 others(134): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760680 | |||||||
| chr1:157760682 | A | G | 18 | a0001c0001t0001g0072 a0001c0001t0001g0131 a0001c0001t0003g0062 others(15): Show |
19 | HG00140.hp2 HG00408.hp2 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.1279+6173T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760682 | |||||||
| chr1:157760686 | A | G | 7 | a0001c0002t0005g0044 a0001c0002t0005g0248 a0001c0002t0005g0249 others(4): Show |
8 | HG02622.hp1 HG02818.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1279+6169T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760686 | |||||||
| chr1:157760686 | AGAAAGAA others(5): Show |
A | 4 | a0001c0001t0004g0014 a0001c0001t0004g0222 a0001c0001t0004g0223 others(1): Show |
7 | HG02486.hp1 HG02717.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1279+6157_1279+616 others(16): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760686 | |||||||
| chr1:157760690 | AGAAAGAA others(1): Show |
A | 5 | a0001c0001t0004g0217 a0001c0001t0004g0218 a0001c0001t0004g0224 others(2): Show |
6 | HG02055.hp1 HG02886.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1279+6157_1279+616 others(12): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760690 | |||||||
| chr1:157760694 | A | G | 3 | a0001c0001t0001g0002 a0001c0001t0001g0180 a0001c0001t0004g0041 |
4 | HG00280.hp1 HG01981.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.1279+6161T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760694 | |||||||
| chr1:157760694 | AGAAG | A | 4 | a0001c0001t0003g0111 a0001c0001t0008g0227 a0001c0002t0005g0248 others(1): Show |
4 | HG00735.hp1 HG02257.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.1279+6157_1279+616 others(8): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760694 | |||||||
| chr1:157760698 | G | A | 19 | a0001c0001t0001g0002 a0001c0001t0001g0072 a0001c0001t0001g0131 others(16): Show |
20 | HG00140.hp2 HG00408.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.1279+6157C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760698 | |||||||
| chr1:157760698 | G | GAAGAAAG others(7): Show |
1 | a0001c0001t0001g0006 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1279+6156_1279+615 others(18): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760698 | |||||||
| chr1:157760698 | G | GGAAA | 27 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(24): Show |
42 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(39): Show |
intron_variant | MODIFIER | c.1279+6153_1279+615 others(8): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760698 | |||||||
| chr1:157760698 | G | GGAAAGAA others(1): Show |
19 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(16): Show |
30 | HG00408.hp1 HG00735.hp2 HG01123.hp1 others(27): Show |
intron_variant | MODIFIER | c.1279+6149_1279+615 others(12): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760698 | |||||||
| chr1:157760698 | G | GGAAAGAA others(5): Show |
4 | a0001c0001t0001g0003 a0001c0001t0001g0031 a0001c0001t0001g0152 others(1): Show |
4 | HG01175.hp1 HG02559.hp2 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.1279+6145_1279+615 others(16): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760698 | |||||||
| chr1:157760698 | G | GGAAAGAA others(9): Show |
2 | a0001c0001t0001g0001 a0001c0001t0001g0077 |
2 | NA18984.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.1279+6141_1279+615 others(20): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760698 | |||||||
| chr1:157760698 | G | GGAAAGAA others(9): Show |
7 | a0001c0001t0001g0013 a0001c0001t0001g0028 a0001c0001t0009g0141 others(4): Show |
10 | HG00544.hp1 HG01167.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.1279+6156_1279+615 others(20): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760698 | |||||||
| chr1:157760698 | G | GGAAAGAA others(13): Show |
2 | a0001c0001t0001g0028 a0001c0001t0006g0103 |
2 | HG01109.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1279+6156_1279+615 others(24): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760698 | |||||||
| chr1:157760698 | G | GGAAAGAA others(20): Show |
1 | a0002c0003t0001g0043 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1279+6156_1279+615 others(31): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760698 | |||||||
| chr1:157760698 | GGAAA | G | 22 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(19): Show |
28 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(25): Show |
intron_variant | MODIFIER | c.1279+6153_1279+615 others(8): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760698 | |||||||
| chr1:157760698 | GGAAAGAA others(1): Show |
G | 19 | a0001c0001t0001g0018 a0001c0001t0001g0030 a0001c0001t0001g0059 others(16): Show |
20 | HG00099.hp1 HG00733.hp1 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.1279+6149_1279+615 others(12): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760698 | |||||||
| chr1:157760698 | GGAAAGAA others(5): Show |
G | 12 | a0001c0001t0001g0030 a0001c0001t0001g0032 a0001c0001t0001g0052 others(9): Show |
12 | HG01361.hp2 HG02559.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.1279+6145_1279+615 others(16): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760698 | |||||||
| chr1:157760698 | GGAAAGAA others(9): Show |
G | 2 | a0001c0001t0001g0209 a0001c0001t0001g0211 |
2 | HG02055.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1279+6141_1279+615 others(20): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760698 | |||||||
| chr1:157760699 | G | GAAAGAAA others(5): Show |
8 | a0001c0001t0001g0005 a0001c0001t0001g0017 a0001c0001t0001g0082 others(5): Show |
15 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(12): Show |
intron_variant | MODIFIER | c.1279+6155_1279+615 others(16): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760699 | |||||||
| chr1:157760699 | G | T | 2 | a0001c0001t0001g0233 a0001c0001t0004g0221 |
2 | HG02280.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1279+6156C>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760699 | |||||||
| chr1:157760702 | A | AGAAAGAA others(127): Show |
1 | a0001c0001t0002g0199 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1279+6152_1279+615 others(138): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760702 | |||||||
| chr1:157760702 | A | AGAAAGAA others(123): Show |
1 | a0001c0001t0002g0197 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1279+6152_1279+615 others(134): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760702 | |||||||
| chr1:157760702 | A | AGAAAGAA others(119): Show |
1 | a0001c0001t0002g0196 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1279+6152_1279+615 others(130): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760702 | |||||||
| chr1:157760702 | A | AGAAAGAA others(115): Show |
1 | a0001c0001t0002g0243 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1279+6152_1279+615 others(126): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760702 | |||||||
| chr1:157760702 | A | G | 8 | a0001c0001t0001g0072 a0001c0001t0001g0131 a0001c0001t0003g0062 others(5): Show |
8 | HG00140.hp2 HG00408.hp2 HG01516.hp1 others(5): Show |
intron_variant | MODIFIER | c.1279+6153T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760702 | |||||||
| chr1:157760703 | G | GAAAGAAA others(1): Show |
14 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0047 others(11): Show |
19 | HG01106.hp1 HG01255.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.1279+6151_1279+615 others(12): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760703 | |||||||
| chr1:157760703 | G | GAAGGAAA others(1): Show |
2 | a0001c0001t0001g0042 a0001c0001t0001g0145 |
3 | HG02922.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1279+6151_1279+615 others(12): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760703 | |||||||
| chr1:157760703 | G | T | 2 | a0001c0001t0001g0216 a0001c0001t0004g0146 |
2 | HG02723.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1279+6152C>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760703 | |||||||
| chr1:157760706 | A | AGAAATAA others(123): Show |
1 | a0001c0001t0002g0195 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1279+6148_1279+614 others(134): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760706 | |||||||
| chr1:157760706 | A | AGAAATAA others(119): Show |
1 | a0001c0001t0002g0194 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1279+6148_1279+614 others(130): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760706 | |||||||
| chr1:157760706 | A | AGAAATAA others(115): Show |
1 | a0001c0001t0002g0192 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1279+6148_1279+614 others(126): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760706 | |||||||
| chr1:157760706 | A | AGAAATAA others(111): Show |
1 | a0001c0001t0001g0207 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1279+6148_1279+614 others(122): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760706 | |||||||
| chr1:157760706 | A | G | 6 | a0001c0001t0003g0111 a0001c0001t0004g0014 a0001c0001t0004g0222 others(3): Show |
9 | HG00735.hp1 HG02258.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1279+6149T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760706 | |||||||
| chr1:157760707 | G | GAAAT | 27 | a0001c0001t0001g0016 a0001c0001t0001g0023 a0001c0001t0001g0026 others(24): Show |
32 | HG00099.hp2 HG01123.hp2 HG01192.hp2 others(29): Show |
intron_variant | MODIFIER | c.1279+6147_1279+614 others(8): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760707 | |||||||
| chr1:157760707 | G | GAAATAAA others(139): Show |
1 | a0001c0001t0002g0234 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1279+6147_1279+614 others(150): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760707 | |||||||
| chr1:157760707 | G | GAAATAAA others(131): Show |
1 | a0001c0001t0002g0203 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1279+6147_1279+614 others(142): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760707 | |||||||
| chr1:157760707 | G | GAAATAAA others(119): Show |
1 | a0001c0001t0001g0244 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1279+6147_1279+614 others(130): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760707 | |||||||
| chr1:157760707 | G | T | 2 | a0001c0001t0001g0226 a0001c0001t0004g0041 |
3 | HG02109.hp2 HG02615.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1279+6148C>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760707 | |||||||
| chr1:157760711 | G | T | 46 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(43): Show |
73 | HG00140.hp1 HG00423.hp2 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.1279+6144C>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760711 | |||||||
| chr1:157760715 | G | GAAAGAAA others(119): Show |
1 | a0001c0001t0002g0198 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1279+6139_1279+614 others(130): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760715 | |||||||
| chr1:157760715 | G | T | 18 | a0001c0001t0001g0072 a0001c0001t0001g0074 a0001c0001t0001g0081 others(15): Show |
18 | HG00140.hp2 HG00408.hp2 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.1279+6140C>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760715 | |||||||
| chr1:157760719 | G | GAAAGAAA others(115): Show |
1 | a0001c0001t0002g0193 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1279+6135_1279+613 others(126): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760719 | |||||||
| chr1:157760719 | G | T | 24 | a0001c0001t0001g0018 a0001c0001t0001g0059 a0001c0001t0001g0061 others(21): Show |
28 | HG00099.hp1 HG00733.hp1 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.1279+6136C>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760719 | |||||||
| chr1:157760723 | G | T | 7 | a0001c0001t0001g0060 a0001c0001t0001g0083 a0001c0001t0001g0091 others(4): Show |
7 | HG01361.hp2 HG02559.hp1 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.1279+6132C>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760723 | |||||||
| chr1:157760728 | AAAGAAAG others(20): Show |
A | 1 | a0001c0001t0001g0087 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1279+6100_1279+612 others(31): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760728 | |||||||
| chr1:157760731 | GAAAGAAA others(3): Show |
G | 1 | a0001c0001t0001g0099 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1279+6114_1279+612 others(14): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760731 | |||||||
| chr1:157760735 | GAAAGAA | G | 20 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(17): Show |
39 | HG00597.hp2 HG00621.hp2 HG01256.hp2 others(36): Show |
intron_variant | MODIFIER | c.1279+6114_1279+611 others(10): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760735 | |||||||
| chr1:157760743 | GA | G | 3 | a0001c0002t0005g0249 a0001c0002t0005g0253 a0001c0002t0005g0254 |
3 | HG02818.hp1 HG02895.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1279+6111delT | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760743 | |||||||
| chr1:157760746 | AGAAAGAA others(39): Show |
A | 1 | a0001c0002t0005g0247 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1279+6063_1279+610 others(50): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760746 | |||||||
| chr1:157760750 | AGAAAGAA others(35): Show |
A | 1 | a0001c0002t0005g0250 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1279+6063_1279+610 others(46): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760750 | |||||||
| chr1:157760754 | AGAAGAAA others(31): Show |
A | 1 | a0001c0004t0005g0256 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1279+6063_1279+610 others(42): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760754 | |||||||
| chr1:157760756 | AAGAAAGA others(27): Show |
A | 3 | a0001c0002t0005g0249 a0001c0002t0005g0253 a0001c0002t0005g0254 |
3 | HG02818.hp1 HG02895.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1279+6065_1279+609 others(38): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760756 | |||||||
| chr1:157760765 | T | A | 4 | a0001c0002t0005g0044 a0001c0002t0005g0248 a0001c0002t0005g0251 others(1): Show |
5 | HG02257.hp2 HG02622.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1279+6090A>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760765 | |||||||
| chr1:157760769 | AAAAGAAA others(16): Show |
A | 4 | a0001c0002t0005g0044 a0001c0002t0005g0248 a0001c0002t0005g0251 others(1): Show |
5 | HG02257.hp2 HG02622.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1279+6063_1279+608 others(27): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760769 | |||||||
| chr1:157760792 | G | A | 3 | a0001c0002t0005g0249 a0001c0002t0005g0253 a0001c0002t0005g0254 |
3 | HG02818.hp1 HG02895.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1279+6063C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760792 | |||||||
| chr1:157760812 | G | GGGAA | 3 | a0001c0001t0008g0227 a0001c0001t0008g0245 a0001c0001t0008g0246 |
3 | HG01891.hp1 HG02145.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1279+6039_1279+604 others(8): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760812 | |||||||
| chr1:157761066 | G | A | 1 | a0001c0001t0001g0076 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1279+5789C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157761066 | |||||||
| chr1:157761104 | T | C | 1 | a0001c0001t0001g0216 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1279+5751A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157761104 | |||||||
| chr1:157761174 | T | C | 1 | a0001c0001t0001g0233 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1279+5681A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157761174 | |||||||
| chr1:157761195 | C | T | 10 | a0001c0002t0005g0044 a0001c0002t0005g0247 a0001c0002t0005g0248 others(7): Show |
11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1279+5660G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157761195 | |||||||
| chr1:157761199 | T | C | 10 | a0001c0002t0005g0044 a0001c0002t0005g0247 a0001c0002t0005g0248 others(7): Show |
11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1279+5656A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157761199 | |||||||
| chr1:157761245 | G | C | 1 | a0001c0001t0001g0181 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1279+5610C>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157761245 | |||||||
| chr1:157761286 | A | C | 10 | a0001c0002t0005g0044 a0001c0002t0005g0247 a0001c0002t0005g0248 others(7): Show |
11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1279+5569T>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157761286 | |||||||
| chr1:157761396 | G | A | 68 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(65): Show |
92 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(89): Show |
intron_variant | MODIFIER | c.1279+5459C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157761396 | |||||||
| chr1:157761481 | G | A | 1 | a0001c0001t0008g0227 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1279+5374C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157761481 | |||||||
| chr1:157761585 | G | A | 10 | a0001c0002t0005g0044 a0001c0002t0005g0247 a0001c0002t0005g0248 others(7): Show |
11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1279+5270C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157761585 | |||||||
| chr1:157761612 | C | A | 10 | a0001c0002t0005g0044 a0001c0002t0005g0247 a0001c0002t0005g0248 others(7): Show |
11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1279+5243G>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157761612 | |||||||
| chr1:157761623 | CTT | C | 10 | a0001c0002t0005g0044 a0001c0002t0005g0247 a0001c0002t0005g0248 others(7): Show |
11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1279+5230_1279+523 others(6): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157761623 | |||||||
| chr1:157761670 | C | T | 1 | a0001c0001t0008g0227 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1279+5185G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157761670 | |||||||
| chr1:157761680 | A | T | 10 | a0001c0002t0005g0044 a0001c0002t0005g0247 a0001c0002t0005g0248 others(7): Show |
11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1279+5175T>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157761680 | |||||||
| chr1:157761751 | T | C | 1 | a0001c0001t0003g0064 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1279+5104A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157761751 | |||||||
| chr1:157761794 | A | G | 10 | a0001c0002t0005g0044 a0001c0002t0005g0247 a0001c0002t0005g0248 others(7): Show |
11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1279+5061T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157761794 | |||||||
| chr1:157761874 | T | C | 13 | a0001c0001t0008g0227 a0001c0001t0008g0245 a0001c0001t0008g0246 others(10): Show |
14 | HG01891.hp1 HG02145.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1279+4981A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157761874 | |||||||
| chr1:157762301 | A | C | 68 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(65): Show |
92 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(89): Show |
intron_variant | MODIFIER | c.1279+4554T>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157762301 | |||||||
| chr1:157762400 | C | T | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | HG00738.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.1279+4455G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157762400 | |||||||
| chr1:157762470 | G | A | 10 | a0001c0002t0005g0044 a0001c0002t0005g0247 a0001c0002t0005g0248 others(7): Show |
11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1279+4385C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157762470 | |||||||
| chr1:157762571 | G | C | 1 | a0001c0001t0001g0233 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1279+4284C>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157762571 | |||||||
| chr1:157762729 | A | AACAAG | 34 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0013 others(31): Show |
58 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.1279+4125_1279+412 others(9): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157762729 | |||||||
| chr1:157762750 | C | T | 1 | a0001c0001t0001g0190 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1279+4105G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157762750 | |||||||
| chr1:157762773 | G | A | 1 | a0001c0001t0002g0205 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1279+4082C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157762773 | |||||||
| chr1:157762795 | A | G | 1 | a0001c0001t0001g0096 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1279+4060T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157762795 | |||||||
| chr1:157762899 | C | A | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(249): Show |
375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.1279+3956G>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157762899 | |||||||
| chr1:157762925 | G | A | 2 | a0001c0001t0001g0089 a0001c0001t0001g0101 |
2 | HG01361.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.1279+3930C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157762925 | |||||||
| chr1:157762990 | G | T | 1 | a0001c0001t0001g0029 | 2 | HG00099.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.1279+3865C>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157762990 | |||||||
| chr1:157763205 | A | G | 1 | a0001c0001t0001g0241 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1279+3650T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157763205 | |||||||
| chr1:157763235 | T | C | 1 | a0001c0001t0001g0050 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1279+3620A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157763235 | |||||||
| chr1:157763269 | T | C | 1 | a0001c0001t0008g0227 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1279+3586A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157763269 | |||||||
| chr1:157763300 | G | C | 3 | a0001c0002t0005g0247 a0001c0002t0005g0250 a0001c0002t0005g0255 |
3 | HG02257.hp2 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1279+3555C>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157763300 | |||||||
| chr1:157763321 | G | A | 44 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0013 others(41): Show |
69 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.1279+3534C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157763321 | |||||||
| chr1:157763442 | T | A | 44 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0013 others(41): Show |
69 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.1279+3413A>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157763442 | |||||||
| chr1:157763499 | T | A | 3 | a0001c0002t0005g0247 a0001c0002t0005g0250 a0001c0002t0005g0255 |
3 | HG02257.hp2 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1279+3356A>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157763499 | |||||||
| chr1:157763567 | G | T | 2 | a0001c0001t0001g0049 a0001c0001t0001g0050 |
2 | HG02486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1279+3288C>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157763567 | |||||||
| chr1:157763589 | T | G | 44 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0013 others(41): Show |
69 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.1279+3266A>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157763589 | |||||||
| chr1:157763708 | T | C | 1 | a0001c0001t0001g0185 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1279+3147A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157763708 | |||||||
| chr1:157763754 | G | A | 9 | a0001c0002t0005g0044 a0001c0002t0005g0248 a0001c0002t0005g0249 others(6): Show |
10 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.1279+3101C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157763754 | |||||||
| chr1:157763789 | G | A | 5 | a0001c0001t0001g0017 a0001c0001t0001g0045 a0001c0001t0001g0046 others(2): Show |
6 | HG02145.hp1 HG02280.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.1279+3066C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157763789 | |||||||
| chr1:157763978 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1279+2877G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157763978 | |||||||
| chr1:157764016 | C | T | 1 | a0001c0001t0001g0020 | 2 | NA18984.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.1279+2839G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157764016 | |||||||
| chr1:157764025 | A | G | 185 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(182): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.1279+2830T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157764025 | |||||||
| chr1:157764029 | C | CA | 42 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0013 others(39): Show |
69 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.1279+2825dupT | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157764029 | |||||||
| chr1:157764029 | C | CAAAA | 14 | a0001c0001t0006g0022 a0001c0001t0006g0103 a0001c0001t0006g0105 others(11): Show |
16 | HG01109.hp1 HG01891.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.1279+2822_1279+282 others(8): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157764029 | |||||||
| chr1:157764029 | CA | C | 91 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(88): Show |
115 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(112): Show |
intron_variant | MODIFIER | c.1279+2825delT | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157764029 | |||||||
| chr1:157764076 | C | T | 2 | a0001c0001t0008g0245 a0001c0001t0008g0246 |
2 | HG01891.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.1279+2779G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157764076 | |||||||
| chr1:157764155 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1279+2700C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157764155 | |||||||
| chr1:157764166 | C | T | 4 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(1): Show |
4 | HG02451.hp2 HG02615.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1279+2689G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157764166 | |||||||
| chr1:157764171 | T | G | 2 | a0001c0001t0008g0245 a0001c0001t0008g0246 |
2 | HG01891.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.1279+2684A>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157764171 | |||||||
| chr1:157764229 | T | C | 18 | a0001c0001t0006g0022 a0001c0001t0006g0103 a0001c0001t0006g0104 others(15): Show |
20 | HG01109.hp1 HG01891.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.1279+2626A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157764229 | |||||||
| chr1:157764233 | G | GA | 20 | a0001c0001t0006g0022 a0001c0001t0006g0103 a0001c0001t0006g0104 others(17): Show |
22 | HG01109.hp1 HG01891.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.1279+2621dupT | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157764233 | |||||||
| chr1:157764312 | C | G | 1 | a0001c0001t0001g0023 | 2 | NA18952.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.1279+2543G>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157764312 | |||||||
| chr1:157764404 | T | C | 3 | a0001c0001t0001g0042 a0001c0001t0001g0145 a0001c0001t0001g0226 |
4 | HG02922.hp1 HG02970.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1279+2451A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157764404 | |||||||
| chr1:157764480 | A | G | 2 | a0001c0001t0001g0049 a0001c0001t0001g0050 |
2 | HG02486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1279+2375T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157764480 | |||||||
| chr1:157764792 | A | G | 4 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(1): Show |
4 | HG02451.hp2 HG02615.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1279+2063T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157764792 | |||||||
| chr1:157764991 | T | C | 2 | a0001c0001t0008g0245 a0001c0001t0008g0246 |
2 | HG01891.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.1279+1864A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157764991 | |||||||
| chr1:157765117 | C | T | 182 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(179): Show |
237 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.1279+1738G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157765117 | |||||||
| chr1:157765326 | G | A | 34 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0013 others(31): Show |
58 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.1279+1529C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157765326 | |||||||
| chr1:157765450 | G | A | 18 | a0001c0001t0002g0192 a0001c0001t0002g0193 a0001c0001t0002g0194 others(15): Show |
18 | HG00609.hp2 HG00642.hp2 HG00673.hp1 others(15): Show |
intron_variant | MODIFIER | c.1279+1405C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157765450 | |||||||
| chr1:157765560 | G | A | 11 | a0001c0002t0001g0252 a0001c0002t0005g0044 a0001c0002t0005g0247 others(8): Show |
12 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.1279+1295C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157765560 | |||||||
| chr1:157765575 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1279+1280G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157765575 | |||||||
| chr1:157765655 | T | C | 1 | a0001c0001t0001g0096 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1279+1200A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157765655 | |||||||
| chr1:157765737 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1279+1118C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157765737 | |||||||
| chr1:157765820 | T | C | 1 | a0001c0001t0001g0093 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1279+1035A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157765820 | |||||||
| chr1:157765836 | A | C | 13 | a0001c0001t0008g0245 a0001c0001t0008g0246 a0001c0002t0001g0252 others(10): Show |
14 | HG01891.hp1 HG02145.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1279+1019T>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157765836 | |||||||
| chr1:157765917 | A | G | 11 | a0001c0002t0001g0252 a0001c0002t0005g0044 a0001c0002t0005g0247 others(8): Show |
12 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.1279+938T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157765917 | |||||||
| chr1:157765966 | G | C | 2 | a0001c0001t0001g0080 a0001c0001t0001g0081 |
2 | HG01243.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.1279+889C>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157765966 | |||||||
| chr1:157766287 | T | C | 11 | a0001c0002t0001g0252 a0001c0002t0005g0044 a0001c0002t0005g0247 others(8): Show |
12 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.1279+568A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157766287 | |||||||
| chr1:157766308 | A | G | 69 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(66): Show |
92 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(89): Show |
intron_variant | MODIFIER | c.1279+547T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157766308 | |||||||
| chr1:157766332 | G | T | 1 | a0001c0001t0003g0064 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1279+523C>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157766332 | |||||||
| chr1:157766340 | G | A | 1 | a0001c0001t0001g0147 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1279+515C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157766340 | |||||||
| chr1:157766419 | T | C | 11 | a0001c0002t0001g0252 a0001c0002t0005g0044 a0001c0002t0005g0247 others(8): Show |
12 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.1279+436A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157766419 | |||||||
| chr1:157766483 | AT | A | 21 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(18): Show |
38 | HG00597.hp2 HG00621.hp2 HG01256.hp2 others(35): Show |
intron_variant | MODIFIER | c.1279+371delA | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157766483 | |||||||
| chr1:157766484 | T | A | 7 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 others(4): Show |
7 | HG02004.hp2 HG02055.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1279+371A>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157766484 | |||||||
| chr1:157766486 | T | A | 21 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(18): Show |
38 | HG00597.hp2 HG00621.hp2 HG01256.hp2 others(35): Show |
intron_variant | MODIFIER | c.1279+369A>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157766486 | |||||||
| chr1:157766531 | G | A | 2 | a0001c0001t0001g0207 a0001c0001t0001g0244 |
2 | HG03195.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1279+324C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157766531 | |||||||
| chr1:157766641 | C | A | 89 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(86): Show |
114 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.1279+214G>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157766641 | |||||||
| chr1:157766647 | CTA | C | 8 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0208 others(5): Show |
8 | HG02004.hp2 HG02055.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.1279+206_1279+207d others(4): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157766647 | |||||||
| chr1:157766772 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1279+83G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157766772 | |||||||
| chr1:157767122 | C | A | 11 | a0001c0002t0001g0252 a0001c0002t0005g0044 a0001c0002t0005g0247 others(8): Show |
12 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.1162+109G>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 6/11 | chr1 | 157767122 | |||||||
| chr1:157767135 | G | A | 5 | a0001c0001t0004g0014 a0001c0001t0004g0222 a0001c0001t0004g0223 others(2): Show |
8 | HG02486.hp1 HG02717.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1162+96C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 6/11 | chr1 | 157767135 | |||||||
| chr1:157767141 | C | T | 20 | a0001c0001t0001g0207 a0001c0001t0001g0244 a0001c0001t0002g0192 others(17): Show |
20 | HG00609.hp2 HG00642.hp2 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.1162+90G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 6/11 | chr1 | 157767141 | |||||||
| chr1:157767514 | C | T | 5 | a0001c0001t0001g0017 a0001c0001t0001g0045 a0001c0001t0001g0046 others(2): Show |
6 | HG02145.hp1 HG02280.hp2 HG03195.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.884-5G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 5/11 | chr1 | 157767514 | |||||||
| chr1:157767714 | G | A | 183 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(180): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.884-205C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 5/11 | chr1 | 157767714 | |||||||
| chr1:157768073 | G | A | 1 | a0001c0001t0001g0226 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.883+341C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 5/11 | chr1 | 157768073 | |||||||
| chr1:157768093 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.883+321C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 5/11 | chr1 | 157768093 | |||||||
| chr1:157768181 | C | T | 1 | a0001c0001t0001g0063 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.883+233G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 5/11 | chr1 | 157768181 | |||||||
| chr1:157768293 | A | C | 1 | a0001c0001t0003g0062 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.883+121T>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 5/11 | chr1 | 157768293 | |||||||
| chr1:157768304 | G | A | 1 | a0001c0001t0008g0227 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.883+110C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 5/11 | chr1 | 157768304 | |||||||
| chr1:157768403 | G | C | 1 | a0001c0001t0006g0103 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.883+11C>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 5/11 | chr1 | 157768403 | |||||||
| chr1:157768718 | C | G | 1 | a0001c0001t0001g0154 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.596-17G>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 4/11 | chr1 | 157768718 | |||||||
| chr1:157768942 | A | G | 11 | a0001c0002t0001g0252 a0001c0002t0005g0044 a0001c0002t0005g0247 others(8): Show |
12 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.596-241T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 4/11 | chr1 | 157768942 | |||||||
| chr1:157768970 | A | G | 1 | a0001c0001t0001g0153 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.596-269T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 4/11 | chr1 | 157768970 | |||||||
| chr1:157769195 | G | C | 1 | a0001c0001t0001g0134 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.596-494C>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 4/11 | chr1 | 157769195 | |||||||
| chr1:157769244 | T | G | 11 | a0001c0002t0001g0252 a0001c0002t0005g0044 a0001c0002t0005g0247 others(8): Show |
12 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.596-543A>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 4/11 | chr1 | 157769244 | |||||||
| chr1:157769264 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.596-563G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 4/11 | chr1 | 157769264 | |||||||
| chr1:157769489 | G | A | 11 | a0001c0002t0001g0252 a0001c0002t0005g0044 a0001c0002t0005g0247 others(8): Show |
12 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.595+377C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 4/11 | chr1 | 157769489 | |||||||
| chr1:157769497 | G | A | 7 | a0001c0001t0006g0022 a0001c0001t0006g0103 a0001c0001t0006g0104 others(4): Show |
8 | HG01109.hp1 HG01891.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.595+369C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 4/11 | chr1 | 157769497 | |||||||
| chr1:157769716 | C | T | 1 | a0001c0001t0001g0152 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.595+150G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 4/11 | chr1 | 157769716 | |||||||
| chr1:157769841 | C | T | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | HG00639.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.595+25G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 4/11 | chr1 | 157769841 | |||||||
| chr1:157770396 | GTC | G | 165 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(162): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.310+11_310+12delGA | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 3/11 | chr1 | 157770396 | |||||||
| chr1:157770399 | A | G | 165 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(162): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.310+10T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 3/11 | chr1 | 157770399 | |||||||
| chr1:157770704 | G | A | 7 | a0001c0001t0006g0022 a0001c0001t0006g0103 a0001c0001t0006g0104 others(4): Show |
8 | HG01109.hp1 HG01891.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.53-38C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157770704 | |||||||
| chr1:157770999 | G | C | 68 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(65): Show |
91 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(88): Show |
intron_variant | MODIFIER | c.53-333C>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157770999 | |||||||
| chr1:157771007 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.53-341C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157771007 | |||||||
| chr1:157771099 | T | C | 1 | a0001c0001t0001g0190 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.53-433A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157771099 | |||||||
| chr1:157771309 | G | A | 3 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 |
3 | NA18986.hp1 NA19012.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.53-643C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157771309 | |||||||
| chr1:157771361 | T | C | 1 | a0001c0001t0001g0191 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.53-695A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157771361 | |||||||
| chr1:157771447 | T | A | 181 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(178): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.53-781A>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157771447 | |||||||
| chr1:157771528 | A | C | 66 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(63): Show |
89 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(86): Show |
intron_variant | MODIFIER | c.53-862T>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157771528 | |||||||
| chr1:157771890 | A | G | 7 | a0001c0001t0006g0022 a0001c0001t0006g0103 a0001c0001t0006g0104 others(4): Show |
8 | HG01109.hp1 HG01891.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.53-1224T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157771890 | |||||||
| chr1:157771938 | G | A | 1 | a0001c0001t0001g0233 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.53-1272C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157771938 | |||||||
| chr1:157772011 | A | G | 37 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0013 others(34): Show |
62 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.53-1345T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157772011 | |||||||
| chr1:157772028 | T | TTA | 12 | a0001c0001t0001g0135 a0001c0001t0001g0231 a0001c0002t0001g0252 others(9): Show |
13 | HG00280.hp2 HG02071.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.53-1364_53-1363dup others(2): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157772028 | |||||||
| chr1:157772028 | T | TTATA | 54 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(51): Show |
76 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.53-1366_53-1363dup others(4): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157772028 | |||||||
| chr1:157772028 | T | TTATATA | 8 | a0001c0001t0001g0021 a0001c0001t0001g0097 a0001c0001t0001g0098 others(5): Show |
9 | HG01192.hp2 HG01361.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.53-1368_53-1363dup others(6): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157772028 | |||||||
| chr1:157772028 | T | TTATATAT others(1): Show |
6 | a0001c0001t0001g0017 a0001c0001t0001g0045 a0001c0001t0001g0046 others(3): Show |
7 | HG02145.hp1 HG02280.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.53-1370_53-1363dup others(8): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157772028 | |||||||
| chr1:157772028 | T | TTATATAT others(5): Show |
5 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0143 others(2): Show |
5 | HG00741.hp2 HG02647.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.53-1374_53-1363dup others(12): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157772028 | |||||||
| chr1:157772227 | C | A | 11 | a0001c0002t0001g0252 a0001c0002t0005g0044 a0001c0002t0005g0247 others(8): Show |
12 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.53-1561G>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157772227 | |||||||
| chr1:157772427 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.53-1761C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157772427 | |||||||
| chr1:157772447 | A | C | 1 | a0001c0001t0001g0060 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.53-1781T>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157772447 | |||||||
| chr1:157772514 | T | C | 5 | a0001c0001t0001g0017 a0001c0001t0001g0045 a0001c0001t0001g0046 others(2): Show |
6 | HG02145.hp1 HG02280.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.53-1848A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157772514 | |||||||
| chr1:157772563 | C | T | 1 | a0001c0001t0001g0031 | 2 | HG00642.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.53-1897G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157772563 | |||||||
| chr1:157772564 | G | A | 1 | a0001c0001t0002g0234 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.53-1898C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157772564 | |||||||
| chr1:157772738 | A | G | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG02723.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.53-2072T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157772738 | |||||||
| chr1:157772748 | G | A | 1 | a0001c0001t0001g0147 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.53-2082C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157772748 | |||||||
| chr1:157772749 | A | G | 1 | a0001c0001t0001g0147 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.53-2083T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157772749 | |||||||
| chr1:157772826 | T | C | 5 | a0001c0001t0001g0011 a0001c0001t0001g0237 a0001c0001t0001g0238 others(2): Show |
9 | HG00438.hp1 NA18951.hp1 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.53-2160A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157772826 | |||||||
| chr1:157772858 | C | A | 3 | a0001c0002t0001g0252 a0001c0002t0005g0253 a0001c0002t0005g0254 |
3 | HG02818.hp1 HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.53-2192G>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157772858 | |||||||
| chr1:157773037 | C | T | 1 | a0001c0001t0004g0146 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.53-2371G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157773037 | |||||||
| chr1:157773360 | T | A | 1 | a0001c0001t0001g0101 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.52+2415A>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157773360 | |||||||
| chr1:157773553 | T | C | 11 | a0001c0002t0001g0252 a0001c0002t0005g0044 a0001c0002t0005g0247 others(8): Show |
12 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.52+2222A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157773553 | |||||||
| chr1:157773998 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.52+1777T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157773998 | |||||||
| chr1:157774075 | A | G | 5 | a0001c0001t0001g0017 a0001c0001t0001g0045 a0001c0001t0001g0046 others(2): Show |
6 | HG02145.hp1 HG02280.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.52+1700T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157774075 | |||||||
| chr1:157774197 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.52+1578G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157774197 | |||||||
| chr1:157774214 | A | G | 66 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(63): Show |
89 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(86): Show |
intron_variant | MODIFIER | c.52+1561T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157774214 | |||||||
| chr1:157774352 | A | T | 41 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0013 others(38): Show |
66 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(63): Show |
intron_variant | MODIFIER | c.52+1423T>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157774352 | |||||||
| chr1:157774361 | G | A | 1 | a0001c0001t0001g0235 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.52+1414C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157774361 | |||||||
| chr1:157774366 | T | C | 11 | a0001c0002t0001g0252 a0001c0002t0005g0044 a0001c0002t0005g0247 others(8): Show |
12 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.52+1409A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157774366 | |||||||
| chr1:157774431 | T | C | 6 | a0001c0001t0006g0022 a0001c0001t0006g0104 a0001c0001t0006g0105 others(3): Show |
7 | HG01109.hp1 HG01891.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.52+1344A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157774431 | |||||||
| chr1:157774471 | G | C | 6 | a0001c0001t0001g0011 a0001c0001t0001g0236 a0001c0001t0001g0237 others(3): Show |
10 | HG00438.hp1 HG00544.hp2 NA18951.hp1 others(7): Show |
intron_variant | MODIFIER | c.52+1304C>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157774471 | |||||||
| chr1:157774553 | C | T | 5 | a0001c0001t0003g0054 a0001c0001t0003g0055 a0001c0001t0003g0056 others(2): Show |
5 | HG00140.hp1 HG01069.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.52+1222G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157774553 | |||||||
| chr1:157774710 | T | G | 11 | a0001c0002t0001g0252 a0001c0002t0005g0044 a0001c0002t0005g0247 others(8): Show |
12 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.52+1065A>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157774710 | |||||||
| chr1:157774736 | G | A | 1 | a0001c0001t0001g0241 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.52+1039C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157774736 | |||||||
| chr1:157774942 | T | A | 1 | a0001c0001t0001g0102 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.52+833A>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157774942 | |||||||
| chr1:157774968 | A | G | 7 | a0001c0001t0006g0022 a0001c0001t0006g0103 a0001c0001t0006g0104 others(4): Show |
8 | HG01109.hp1 HG01891.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.52+807T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157774968 | |||||||
| chr1:157774977 | A | G | 1 | a0001c0001t0001g0051 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.52+798T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157774977 | |||||||
| chr1:157774990 | A | T | 2 | a0001c0001t0008g0245 a0001c0001t0008g0246 |
2 | HG01891.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.52+785T>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157774990 | |||||||
| chr1:157775058 | C | T | 57 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(54): Show |
79 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(76): Show |
intron_variant | MODIFIER | c.52+717G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157775058 | |||||||
| chr1:157775200 | A | G | 1 | a0001c0001t0001g0053 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.52+575T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157775200 | |||||||
| chr1:157775335 | G | C | 2 | a0001c0001t0008g0245 a0001c0001t0008g0246 |
2 | HG01891.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.52+440C>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157775335 | |||||||
| chr1:157775373 | T | C | 2 | a0002c0003t0001g0043 a0002c0003t0001g0242 |
3 | HG02257.hp1 HG02630.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.52+402A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157775373 | |||||||
| chr1:157775439 | C | A | 1 | a0001c0001t0002g0243 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.52+336G>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157775439 | |||||||
| chr1:157775525 | C | T | 2 | a0001c0001t0008g0245 a0001c0001t0008g0246 |
2 | HG01891.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.52+250G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157775525 | |||||||
| chr1:157775601 | A | G | 2 | a0001c0001t0001g0051 a0001c0001t0001g0052 |
2 | NA18975.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.52+174T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157775601 | |||||||
| chr1:157775952 | G | A | 2 | a0001c0001t0001g0049 a0001c0001t0001g0050 |
2 | HG02486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.32-157C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 1/11 | chr1 | 157775952 | |||||||
| chr1:157775967 | T | A | 1 | a0001c0002t0005g0254 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.32-172A>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 1/11 | chr1 | 157775967 | |||||||
| chr1:157775994 | T | C | 2 | a0001c0001t0008g0245 a0001c0001t0008g0246 |
2 | HG01891.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.32-199A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 1/11 | chr1 | 157775994 | |||||||
| chr1:157776000 | A | T | 2 | a0001c0001t0008g0245 a0001c0001t0008g0246 |
2 | HG01891.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.32-205T>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 1/11 | chr1 | 157776000 | |||||||
| chr1:157776018 | G | A | 11 | a0001c0002t0001g0252 a0001c0002t0005g0044 a0001c0002t0005g0247 others(8): Show |
12 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.32-223C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 1/11 | chr1 | 157776018 | |||||||
| chr1:157776098 | T | C | 1 | a0001c0002t0005g0255 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.32-303A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 1/11 | chr1 | 157776098 | |||||||
| chr1:157776311 | C | T | 2 | a0001c0001t0001g0049 a0001c0001t0001g0050 |
2 | HG02486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.32-516G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 1/11 | chr1 | 157776311 | |||||||
| chr1:157776321 | G | A | 1 | a0001c0001t0001g0244 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.32-526C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 1/11 | chr1 | 157776321 | |||||||
| chr1:157776471 | T | C | 18 | a0001c0001t0001g0017 a0001c0001t0001g0045 a0001c0001t0001g0046 others(15): Show |
20 | HG01891.hp1 HG02145.hp1 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.31+572A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 1/11 | chr1 | 157776471 | |||||||
| chr1:157776637 | C | T | 5 | a0001c0001t0001g0017 a0001c0001t0001g0045 a0001c0001t0001g0046 others(2): Show |
6 | HG02145.hp1 HG02280.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.31+406G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 1/11 | chr1 | 157776637 | |||||||
| chr1:157776789 | A | T | 11 | a0001c0002t0001g0252 a0001c0002t0005g0044 a0001c0002t0005g0247 others(8): Show |
12 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.31+254T>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 1/11 | chr1 | 157776789 | |||||||
| chr1:157776996 | C | A | 1 | a0001c0004t0005g0256 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.31+47G>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 1/11 | chr1 | 157776996 | |||||||
| chr1:157777024 | G | A | 11 | a0001c0002t0001g0252 a0001c0002t0005g0044 a0001c0002t0005g0247 others(8): Show |
12 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.31+19C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 1/11 | chr1 | 157777024 |