Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 503497 |
| ensemblid | ENSG00000204979.8 |
| hgncid | 16674 |
| symbol | MS4A13 |
| name | membrane spanning 4-domains A13 |
| refseq_nuc | NM_001012417.3 |
| refseq_prot | NP_001012417.2 |
| ensembl_nuc | ENST00000378186.7 |
| ensembl_prot | ENSP00000367428.2 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 60515392 |
| end | 60542721 |
| strand | + |
| ver | v1.2 |
| region | chr11:60515392-60542721 |
| region5000 | chr11:60510392-60547721 |
| regionname0 | MS4A13_chr11_60515392_60542721 |
| regionname5000 | MS4A13_chr11_60510392_60547721 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 152 | 300 | 56 | 48 | 148 | 13 | 35 | 116 | MS4A13_chr11_60510392_60547721 | MS4A13 | MIGIF others(147): Show |
chr11 | 60510392 | 60547721 |
| a0002 | 0/1 | 152 | 99 | 14 | 24 | 51 | 2 | 7 | 41 | MS4A13_chr11_60510392_60547721 | MS4A13 | MIGIF others(147): Show |
chr11 | 60510392 | 60547721 |
| a0003 | 1/0 | 152 | 19 | 16 | 1 | 1 | 0 | 0 | 1 | MS4A13_chr11_60510392_60547721 | MS4A13 | MIGIF others(147): Show |
chr11 | 60510392 | 60547721 |
| a0004 | 0/0 | 152 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | MS4A13_chr11_60510392_60547721 | MS4A13 | MIGIF others(147): Show |
chr11 | 60510392 | 60547721 |
| a0005 | 0/0 | 152 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | MIGIF others(147): Show |
chr11 | 60510392 | 60547721 |
| a0006 | 0/0 | 152 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | MIDIF others(147): Show |
chr11 | 60510392 | 60547721 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 456 | 300 | 56 | 48 | 148 | 13 | 35 | MS4A13_chr11_60510392_60547721 | MS4A13 | ATGAT others(451): Show |
chr11 | 60510392 | 60547721 | ||
| a0002c0002 | 0/0 | 456 | 57 | 13 | 19 | 21 | 2 | 2 | MS4A13_chr11_60510392_60547721 | MS4A13 | ATGAT others(451): Show |
chr11 | 60510392 | 60547721 | ||
| a0002c0003 | 0/1 | 456 | 41 | 1 | 5 | 29 | 0 | 5 | MS4A13_chr11_60510392_60547721 | MS4A13 | ATGAT others(451): Show |
chr11 | 60510392 | 60547721 | ||
| a0002c0008 | 0/0 | 456 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | ATGAT others(451): Show |
chr11 | 60510392 | 60547721 | ||
| a0003c0004 | 1/0 | 456 | 18 | 16 | 1 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | ATGAT others(451): Show |
chr11 | 60510392 | 60547721 | ||
| a0003c0007 | 0/0 | 456 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | ATGAT others(451): Show |
chr11 | 60510392 | 60547721 | ||
| a0004c0005 | 0/0 | 456 | 2 | 0 | 0 | 2 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | ATGAT others(451): Show |
chr11 | 60510392 | 60547721 | ||
| a0005c0009 | 0/0 | 456 | 1 | 0 | 0 | 0 | 1 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | ATGAT others(451): Show |
chr11 | 60510392 | 60547721 | ||
| a0006c0006 | 0/0 | 456 | 1 | 0 | 1 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | ATGAT others(451): Show |
chr11 | 60510392 | 60547721 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 949 | 193 | 45 | 23 | 97 | 5 | 23 | MS4A13_chr11_60510392_60547721 | MS4A13 | GTCAC others(944): Show |
chr11 | 60510392 | 60547721 |
| a0001c0001t0002 | 0/0 | 949 | 105 | 10 | 24 | 51 | 8 | 12 | MS4A13_chr11_60510392_60547721 | MS4A13 | GTCAC others(944): Show |
chr11 | 60510392 | 60547721 |
| a0001c0001t0006 | 0/0 | 949 | 1 | 0 | 1 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | GTCAC others(944): Show |
chr11 | 60510392 | 60547721 |
| a0001c0001t0007 | 0/0 | 949 | 1 | 1 | 0 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | GTCAC others(944): Show |
chr11 | 60510392 | 60547721 |
| a0002c0002t0001 | 0/0 | 949 | 33 | 1 | 11 | 19 | 2 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | GTCAC others(944): Show |
chr11 | 60510392 | 60547721 |
| a0002c0002t0003 | 0/0 | 949 | 14 | 7 | 3 | 2 | 0 | 2 | MS4A13_chr11_60510392_60547721 | MS4A13 | GTCAC others(944): Show |
chr11 | 60510392 | 60547721 |
| a0002c0002t0004 | 0/0 | 949 | 9 | 5 | 4 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | GTCAC others(944): Show |
chr11 | 60510392 | 60547721 |
| a0002c0002t0008 | 0/0 | 949 | 1 | 0 | 1 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | GTCAC others(944): Show |
chr11 | 60510392 | 60547721 |
| a0002c0003t0001 | 0/1 | 949 | 41 | 1 | 5 | 29 | 0 | 5 | MS4A13_chr11_60510392_60547721 | MS4A13 | GTCAC others(944): Show |
chr11 | 60510392 | 60547721 |
| a0002c0008t0001 | 0/0 | 949 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | GTCAC others(944): Show |
chr11 | 60510392 | 60547721 |
| a0003c0004t0001 | 1/0 | 949 | 14 | 12 | 1 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | GTCAC others(944): Show |
chr11 | 60510392 | 60547721 |
| a0003c0004t0005 | 0/0 | 949 | 4 | 4 | 0 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | GTCAC others(944): Show |
chr11 | 60510392 | 60547721 |
| a0003c0007t0001 | 0/0 | 949 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | GTCAC others(944): Show |
chr11 | 60510392 | 60547721 |
| a0004c0005t0002 | 0/0 | 949 | 2 | 0 | 0 | 2 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | GTCAC others(944): Show |
chr11 | 60510392 | 60547721 |
| a0005c0009t0001 | 0/0 | 949 | 1 | 0 | 0 | 0 | 1 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | GTCAC others(944): Show |
chr11 | 60510392 | 60547721 |
| a0006c0006t0001 | 0/0 | 949 | 1 | 0 | 1 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | GTCAC others(944): Show |
chr11 | 60510392 | 60547721 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0005 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0046 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0002g0001 | 0/0 | 11 | 0 | 4 | 6 | 1 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0002g0002 | 0/0 | 10 | 1 | 3 | 4 | 1 | 1 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0002g0013 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0002g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0002g0015 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0002g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0002g0040 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0002g0041 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0002g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0002g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0002g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0002g0045 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0002g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0002g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0002g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0002g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0002g0330 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0002g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0002g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0002g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0006g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0001c0001t0007g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0002t0001g0012 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0002t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0002t0001g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0002t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0002t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0002t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0002t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0002t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0002t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0002t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0002t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0002t0003g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0002t0003g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0002t0003g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0002t0003g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0002t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0002t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0002t0003g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0002t0003g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0002t0003g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0002t0003g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0002t0003g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0002t0003g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0002t0003g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0002t0004g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0002t0004g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0002t0004g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0002t0004g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0002t0004g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0002t0004g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0002t0004g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0002t0008g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0003t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0003t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0003t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0003t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0003t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0003t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0003t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0003t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0003t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0003t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0003t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0003t0001g0211 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0003t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0003t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0003t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0003t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0003t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0003t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0003t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0003t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0003t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0003t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0003t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0003t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0003t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0003t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0003t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0003t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0003t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0003t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0003t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0003t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0003t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0003t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0003t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0003t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0003t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0002c0008t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0003c0004t0001g0010 | 1/0 | 3 | 2 | 0 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0003c0004t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0003c0004t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0003c0004t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0003c0004t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0003c0004t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0003c0004t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0003c0004t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0003c0004t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0003c0004t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0003c0004t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0003c0004t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0003c0004t0005g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0003c0004t0005g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0003c0004t0005g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0003c0007t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0004c0005t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0004c0005t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0005c0009t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| a0006c0006t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0001 | EUR | GBR | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0021 | EUR | GBR | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG00280 | hp1 | a0005 | c0009 | t0001 | g0032 | EUR | FIN | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0330 | EUR | FIN | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0132 | EUR | FIN | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0313 | EUR | FIN | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG00408 | hp1 | a0002 | c0003 | t0001 | g0236 | EAS | CHS | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | CHS | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | CHS | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG00423 | hp2 | a0002 | c0002 | t0001 | g0265 | EAS | CHS | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | CHS | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | CHS | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG00544 | hp2 | a0002 | c0002 | t0001 | g0270 | EAS | CHS | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG00558 | hp1 | a0002 | c0002 | t0001 | g0256 | EAS | CHS | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | CHS | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0334 | EAS | CHS | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | CHS | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | CHS | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | CHS | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG00639 | hp1 | a0002 | c0003 | t0001 | g0032 | AMR | PUR | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0324 | AMR | PUR | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0015 | AMR | PUR | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG00642 | hp2 | a0006 | c0006 | t0001 | g0062 | AMR | PUR | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | CHS | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG00673 | hp2 | a0002 | c0002 | t0001 | g0264 | EAS | CHS | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0317 | AMR | PUR | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0290 | AMR | PUR | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG00738 | hp2 | a0001 | c0001 | t0006 | g0282 | AMR | PUR | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG01069 | hp1 | a0002 | c0002 | t0003 | g0058 | AMR | PUR | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG01069 | hp2 | a0002 | c0002 | t0004 | g0037 | AMR | PUR | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG01070 | hp1 | a0002 | c0002 | t0004 | g0037 | AMR | PUR | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG01071 | hp2 | a0002 | c0002 | t0003 | g0059 | AMR | PUR | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG01081 | hp1 | a0002 | c0002 | t0001 | g0039 | AMR | PUR | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG01099 | hp2 | a0002 | c0002 | t0008 | g0257 | AMR | PUR | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0045 | AMR | PUR | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG01167 | hp2 | a0002 | c0003 | t0001 | g0223 | AMR | PUR | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG01168 | hp2 | a0002 | c0002 | t0001 | g0012 | AMR | PUR | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG01169 | hp1 | a0002 | c0002 | t0001 | g0012 | AMR | PUR | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG01169 | hp2 | a0002 | c0003 | t0001 | g0222 | AMR | PUR | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0042 | AMR | PUR | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0253 | AMR | PUR | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG01192 | hp2 | a0002 | c0002 | t0004 | g0249 | AMR | PUR | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG01243 | hp1 | a0003 | c0004 | t0001 | g0175 | AMR | PUR | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0284 | AMR | CLM | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | CLM | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0291 | AMR | CLM | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG01261 | hp2 | a0002 | c0002 | t0001 | g0251 | AMR | CLM | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0335 | AMR | CLM | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | CLM | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0336 | AMR | CLM | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG01361 | hp1 | a0002 | c0002 | t0001 | g0039 | AMR | CLM | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG01361 | hp2 | a0002 | c0002 | t0004 | g0245 | AMR | CLM | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0281 | AMR | CLM | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | CLM | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | CLM | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0040 | EUR | IBS | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG01515 | hp2 | a0002 | c0002 | t0001 | g0250 | EUR | IBS | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG01516 | hp1 | a0002 | c0002 | t0001 | g0012 | EUR | IBS | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0023 | EUR | IBS | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0040 | EUR | IBS | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0023 | EUR | IBS | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | ACB | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG01884 | hp2 | a0003 | c0004 | t0005 | g0029 | AFR | ACB | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | ACB | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG01891 | hp2 | a0003 | c0004 | t0001 | g0174 | AFR | ACB | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG01928 | hp2 | a0002 | c0002 | t0001 | g0260 | AMR | PEL | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0043 | AMR | PEL | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG01952 | hp2 | a0002 | c0003 | t0001 | g0237 | AMR | PEL | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0042 | AMR | PEL | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG01975 | hp2 | a0002 | c0002 | t0001 | g0259 | AMR | PEL | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0286 | AMR | PEL | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG01978 | hp2 | a0002 | c0002 | t0001 | g0278 | AMR | PEL | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG01981 | hp1 | a0002 | c0002 | t0001 | g0261 | AMR | PEL | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0303 | AMR | PEL | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PEL | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | PEL | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0327 | EAS | KHV | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | KHV | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0331 | EAS | KHV | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | KHV | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG02055 | hp1 | a0002 | c0002 | t0003 | g0054 | AFR | ACB | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0328 | AFR | ACB | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0301 | EAS | KHV | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | KHV | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0329 | EAS | KHV | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0323 | EAS | KHV | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | KHV | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG02129 | hp2 | a0002 | c0002 | t0001 | g0269 | EAS | KHV | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG02132 | hp1 | a0002 | c0003 | t0001 | g0210 | EAS | KHV | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | KHV | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG02135 | hp1 | a0002 | c0002 | t0001 | g0254 | EAS | KHV | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | KHV | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0184 | AFR | ACB | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | ACB | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG02155 | hp1 | a0002 | c0002 | t0001 | g0273 | EAS | CDX | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | CDX | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0320 | EAS | CDX | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG02165 | hp2 | a0002 | c0002 | t0001 | g0266 | EAS | CDX | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | ACB | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG02258 | hp2 | a0002 | c0002 | t0003 | g0052 | AFR | ACB | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG02273 | hp1 | a0002 | c0002 | t0001 | g0258 | AMR | PEL | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0043 | AMR | PEL | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | ACB | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG02280 | hp2 | a0003 | c0004 | t0001 | g0172 | AFR | ACB | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG02293 | hp1 | a0002 | c0002 | t0003 | g0048 | AMR | PEL | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0041 | AMR | PEL | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0318 | AMR | PEL | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG02572 | hp1 | a0003 | c0004 | t0001 | g0176 | AFR | GWD | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0187 | AFR | GWD | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG02622 | hp1 | a0003 | c0004 | t0001 | g0177 | AFR | GWD | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG02622 | hp2 | a0003 | c0004 | t0005 | g0029 | AFR | GWD | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | GWD | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG02683 | hp1 | a0002 | c0003 | t0001 | g0207 | SAS | PJL | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0315 | SAS | PJL | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG02698 | hp1 | a0002 | c0003 | t0001 | g0208 | SAS | PJL | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | GWD | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | GWD | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0292 | SAS | PJL | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG02818 | hp1 | a0003 | c0004 | t0001 | g0180 | AFR | GWD | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | GWD | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | GWD | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG02895 | hp1 | a0003 | c0004 | t0001 | g0179 | AFR | GWD | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0190 | AFR | ESN | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | ESN | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG02965 | hp1 | a0003 | c0004 | t0001 | g0173 | AFR | ESN | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ESN | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | ESN | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG02970 | hp2 | a0002 | c0002 | t0003 | g0016 | AFR | ESN | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | ESN | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | ESN | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0332 | SAS | PJL | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0057 | SAS | PJL | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG03041 | hp1 | a0003 | c0004 | t0001 | g0010 | AFR | GWD | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG03041 | hp2 | a0003 | c0004 | t0005 | g0171 | AFR | GWD | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG03098 | hp1 | a0002 | c0003 | t0001 | g0221 | AFR | MSL | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG03098 | hp2 | a0003 | c0004 | t0001 | g0182 | AFR | MSL | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | ESN | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | ESN | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG03195 | hp1 | a0002 | c0002 | t0001 | g0252 | AFR | ESN | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | ESN | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG03209 | hp1 | a0003 | c0004 | t0005 | g0170 | AFR | MSL | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG03209 | hp2 | a0001 | c0001 | t0007 | g0200 | AFR | MSL | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0030 | AFR | MSL | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | MSL | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG03239 | hp1 | a0002 | c0002 | t0003 | g0047 | SAS | PJL | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | MSL | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG03453 | hp2 | a0003 | c0004 | t0001 | g0010 | AFR | MSL | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG03486 | hp1 | a0002 | c0002 | t0004 | g0036 | AFR | MSL | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0191 | AFR | MSL | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0312 | SAS | PJL | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | STU | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0231 | SAS | STU | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0295 | SAS | PJL | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0060 | SAS | PJL | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0302 | SAS | BEB | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG03831 | hp2 | a0002 | c0003 | t0001 | g0225 | SAS | BEB | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0304 | SAS | BEB | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | BEB | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0166 | SAS | BEB | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0230 | SAS | BEB | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | BEB | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | BEB | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0333 | SAS | BEB | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG04184 | hp2 | a0002 | c0003 | t0001 | g0277 | SAS | BEB | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | STU | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | STU | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG04204 | hp1 | a0002 | c0002 | t0003 | g0049 | SAS | STU | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | STU | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | STU | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0041 | SAS | STU | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18522 | hp1 | a0003 | c0004 | t0001 | g0181 | AFR | YRI | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18522 | hp2 | a0002 | c0002 | t0004 | g0036 | AFR | YRI | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | CHB | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | CHB | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18906 | hp1 | a0002 | c0002 | t0004 | g0247 | AFR | YRI | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | YRI | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18939 | hp1 | a0002 | c0003 | t0001 | g0213 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0308 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18941 | hp2 | a0004 | c0005 | t0002 | g0297 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0337 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18943 | hp2 | a0002 | c0003 | t0001 | g0031 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18945 | hp2 | a0002 | c0002 | t0001 | g0267 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18948 | hp1 | a0002 | c0002 | t0001 | g0274 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18948 | hp2 | a0002 | c0003 | t0001 | g0242 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0316 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18951 | hp2 | a0002 | c0002 | t0003 | g0051 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18953 | hp1 | a0004 | c0005 | t0002 | g0287 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18954 | hp2 | a0002 | c0003 | t0001 | g0244 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18956 | hp1 | a0002 | c0003 | t0001 | g0219 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0325 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18960 | hp1 | a0002 | c0003 | t0001 | g0235 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18962 | hp1 | a0002 | c0002 | t0001 | g0255 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18962 | hp2 | a0002 | c0003 | t0001 | g0238 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18963 | hp1 | a0002 | c0003 | t0001 | g0240 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18966 | hp2 | a0002 | c0003 | t0001 | g0218 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0310 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18967 | hp2 | a0002 | c0003 | t0001 | g0212 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18970 | hp1 | a0003 | c0007 | t0001 | g0203 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0305 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18973 | hp2 | a0002 | c0003 | t0001 | g0241 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0322 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0309 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18979 | hp2 | a0002 | c0003 | t0001 | g0204 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18980 | hp2 | a0002 | c0002 | t0001 | g0038 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18984 | hp2 | a0002 | c0003 | t0001 | g0217 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18985 | hp1 | a0002 | c0003 | t0001 | g0033 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0326 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18992 | hp2 | a0002 | c0003 | t0001 | g0205 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18994 | hp1 | a0002 | c0002 | t0001 | g0038 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0321 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0306 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18998 | hp2 | a0002 | c0002 | t0001 | g0276 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA19001 | hp2 | a0002 | c0002 | t0001 | g0275 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA19003 | hp1 | a0002 | c0003 | t0001 | g0220 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA19005 | hp1 | a0002 | c0003 | t0001 | g0011 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0289 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA19007 | hp2 | a0002 | c0008 | t0001 | g0263 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA19009 | hp1 | a0002 | c0002 | t0001 | g0271 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA19009 | hp2 | a0002 | c0003 | t0001 | g0215 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0314 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | LWK | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA19030 | hp2 | a0002 | c0002 | t0003 | g0016 | AFR | LWK | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0185 | AFR | LWK | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | LWK | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA19055 | hp2 | a0002 | c0003 | t0001 | g0226 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA19056 | hp1 | a0002 | c0002 | t0001 | g0268 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA19056 | hp2 | a0002 | c0003 | t0001 | g0031 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA19059 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0338 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA19063 | hp1 | a0002 | c0002 | t0001 | g0262 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0300 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0283 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA19065 | hp2 | a0002 | c0003 | t0001 | g0243 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA19066 | hp2 | a0002 | c0003 | t0001 | g0011 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0307 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0296 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA19072 | hp2 | a0002 | c0003 | t0001 | g0209 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA19074 | hp2 | a0002 | c0003 | t0001 | g0216 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA19077 | hp1 | a0002 | c0002 | t0001 | g0272 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0294 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0299 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA19083 | hp1 | a0002 | c0002 | t0003 | g0050 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA19085 | hp2 | a0002 | c0003 | t0001 | g0214 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA19086 | hp2 | a0002 | c0003 | t0001 | g0011 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA19088 | hp1 | a0002 | c0003 | t0001 | g0033 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0311 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | YRI | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA19240 | hp2 | a0002 | c0002 | t0003 | g0055 | AFR | YRI | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | ASW | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA20129 | hp2 | a0003 | c0004 | t0001 | g0178 | AFR | ASW | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0280 | EUR | TSI | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0046 | EUR | TSI | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | TSI | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0285 | EUR | TSI | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA20905 | hp1 | a0002 | c0003 | t0001 | g0206 | SAS | GIH | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | GIH | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG01123 | hp1 | a0002 | c0003 | t0001 | g0224 | AMR | CLM | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | ACB | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG02109 | hp2 | a0002 | c0002 | t0004 | g0248 | AFR | ACB | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG02486 | hp1 | a0002 | c0002 | t0003 | g0053 | AFR | ACB | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | ACB | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG02559 | hp1 | a0002 | c0002 | t0003 | g0056 | AFR | ACB | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | ACB | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG03471 | hp1 | a0002 | c0002 | t0004 | g0246 | AFR | MSL | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | MSL | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | USA | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0030 | AFR | USA | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0319 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | USA | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0192 | AFR | USA | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | LWK | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | LWK | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| homoSapiens | chm13v2 | a0002 | c0003 | t0001 | g0211 | REF | REF | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| homoSapiens | grch38p0 | a0003 | c0004 | t0001 | g0010 | REF | REF | MS4A13_chr11_60510392_60547721 | MS4A13 | chr11 | 60510392 | 60547721 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:60518091 | G | A | 1 | a0006 | 1 | HG00642.hp2 | missense_variant | MODERATE | c.8G>A | p.Gly3Asp | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/7 | 352/949 | 8/459 | 3/152 | chr11 | 60518091 | |||
| chr11:60518102 | A | G | 5 | a0001 a0002 a0004 others(2): Show |
402 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(399): Show |
missense_variant | MODERATE | c.19A>G | p.Ile7Val | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/7 | 363/949 | 19/459 | 7/152 | chr11 | 60518102 | |||
| chr11:60518154 | C | G | 1 | a0005 | 1 | HG00280.hp1 | missense_variant | MODERATE | c.71C>G | p.Ala24Gly | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/7 | 415/949 | 71/459 | 24/152 | chr11 | 60518154 | |||
| chr11:60518163 | C | T | 1 | a0004 | 2 | NA18941.hp2 NA18953.hp1 |
missense_variant | MODERATE | c.80C>T | p.Thr27Met | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/7 | 424/949 | 80/459 | 27/152 | chr11 | 60518163 | |||
| chr11:60523940 | C | T | 3 | a0001 a0004 a0006 |
303 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(300): Show |
missense_variant | MODERATE | c.173C>T | p.Pro58Leu | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 4/7 | 517/949 | 173/459 | 58/152 | chr11 | 60523940 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:60529388 | T | C | 1 | a0002c0008 | 1 | NA19007.hp2 | synonymous_variant | LOW | c.330T>C | p.Arg110Arg | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/7 | 674/949 | 330/459 | 110/152 | chr11 | 60529388 | |||
| chr11:60529406 | C | T | 3 | a0002c0003 a0003c0007 a0005c0009 |
42 | HG00280.hp1 HG00408.hp1 HG00639.hp1 others(39): Show |
synonymous_variant | LOW | c.348C>T | p.Tyr116Tyr | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/7 | 692/949 | 348/459 | 116/152 | chr11 | 60529406 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:60515405 | G | T | 1 | a0003c0004t0005 | 4 | HG01884.hp2 HG02622.hp2 HG03041.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-331G>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 1/7 | 2679 | chr11 | 60515405 | ||||||
| chr11:60515416 | C | A | 1 | a0001c0001t0006 | 1 | HG00738.hp2 | 5_prime_UTR_variant | MODIFIER | c.-320C>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 1/7 | 2668 | chr11 | 60515416 | ||||||
| chr11:60542603 | G | C | 1 | a0002c0002t0003 | 14 | HG01069.hp1 HG01071.hp2 HG02055.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*28G>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 7/7 | 28 | chr11 | 60542603 | ||||||
| chr11:60542610 | A | T | 3 | a0001c0001t0002 a0001c0001t0006 a0004c0005t0002 |
108 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(105): Show |
3_prime_UTR_variant | MODIFIER | c.*35A>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 7/7 | 35 | chr11 | 60542610 | ||||||
| chr11:60542639 | T | C | 1 | a0001c0001t0007 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*64T>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 7/7 | 64 | chr11 | 60542639 | ||||||
| chr11:60542677 | C | G | 1 | a0002c0002t0008 | 1 | HG01099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*102C>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 7/7 | 102 | chr11 | 60542677 | ||||||
| chr11:60542686 | A | C | 1 | a0002c0002t0004 | 9 | HG01069.hp2 HG01070.hp1 HG01192.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*111A>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 7/7 | 111 | chr11 | 60542686 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:60515688 | C | T | 1 | a0001c0001t0001g0046 | 2 | HG01346.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-129+81C>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 1/6 | chr11 | 60515688 | |||||||
| chr11:60515839 | G | A | 14 | a0001c0001t0002g0057 a0002c0002t0003g0016 a0002c0002t0003g0047 others(11): Show |
15 | HG01069.hp1 HG01071.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.-128-130G>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 1/6 | chr11 | 60515839 | |||||||
| chr11:60515918 | C | G | 2 | a0001c0001t0001g0337 a0001c0001t0001g0338 |
2 | NA18943.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.-128-51C>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 1/6 | chr11 | 60515918 | |||||||
| chr11:60516154 | A | G | 68 | a0001c0001t0001g0335 a0001c0001t0001g0336 a0001c0001t0002g0001 others(65): Show |
99 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.-13+70A>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 2/6 | chr11 | 60516154 | |||||||
| chr11:60516162 | G | T | 1 | a0001c0001t0001g0279 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.-13+78G>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 2/6 | chr11 | 60516162 | |||||||
| chr11:60516195 | GT | G | 130 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(127): Show |
165 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(162): Show |
intron_variant | MODIFIER | c.-13+123delT | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr11 | 60516195 | ||||||
| chr11:60516216 | G | T | 1 | a0001c0001t0001g0166 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-13+132G>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 2/6 | chr11 | 60516216 | |||||||
| chr11:60516434 | T | A | 3 | a0001c0001t0002g0280 a0001c0001t0002g0281 a0001c0001t0006g0282 |
3 | HG00738.hp2 HG01433.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.-13+350T>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 2/6 | chr11 | 60516434 | |||||||
| chr11:60516498 | C | A | 3 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0169 |
3 | HG01243.hp2 HG02922.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-13+414C>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 2/6 | chr11 | 60516498 | |||||||
| chr11:60516557 | G | A | 1 | a0001c0001t0002g0283 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-13+473G>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 2/6 | chr11 | 60516557 | |||||||
| chr11:60516607 | C | T | 2 | a0002c0002t0003g0058 a0002c0002t0003g0059 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-13+523C>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 2/6 | chr11 | 60516607 | |||||||
| chr11:60516777 | A | G | 1 | a0002c0002t0001g0278 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-13+693A>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 2/6 | chr11 | 60516777 | |||||||
| chr11:60517007 | T | TA | 13 | a0002c0002t0003g0016 a0002c0002t0003g0047 a0002c0002t0003g0048 others(10): Show |
14 | HG01069.hp1 HG01071.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.-13+936dupA | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr11 | 60517007 | ||||||
| chr11:60517049 | A | G | 105 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0167 others(102): Show |
118 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.-13+965A>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 2/6 | chr11 | 60517049 | |||||||
| chr11:60517184 | T | TA | 51 | a0002c0002t0001g0012 a0002c0002t0001g0038 a0002c0002t0001g0039 others(48): Show |
58 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.-12-878dupA | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr11 | 60517184 | ||||||
| chr11:60517184 | T | TAA | 53 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0167 others(50): Show |
59 | HG00280.hp1 HG00408.hp1 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.-12-879_-12-878dup others(2): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr11 | 60517184 | ||||||
| chr11:60517207 | A | G | 323 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(320): Show |
403 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(400): Show |
intron_variant | MODIFIER | c.-12-865A>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 2/6 | chr11 | 60517207 | |||||||
| chr11:60517251 | T | G | 7 | a0002c0002t0004g0036 a0002c0002t0004g0037 a0002c0002t0004g0245 others(4): Show |
9 | HG01069.hp2 HG01070.hp1 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.-12-821T>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 2/6 | chr11 | 60517251 | |||||||
| chr11:60517307 | T | C | 1 | a0001c0001t0001g0007 | 3 | HG01496.hp2 HG03688.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.-12-765T>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 2/6 | chr11 | 60517307 | |||||||
| chr11:60517309 | A | C | 133 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(130): Show |
168 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(165): Show |
intron_variant | MODIFIER | c.-12-763A>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 2/6 | chr11 | 60517309 | |||||||
| chr11:60517535 | T | A | 1 | a0001c0001t0001g0061 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-12-537T>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 2/6 | chr11 | 60517535 | |||||||
| chr11:60517745 | C | G | 1 | a0001c0001t0001g0198 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-12-327C>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 2/6 | chr11 | 60517745 | |||||||
| chr11:60517961 | T | C | 4 | a0002c0002t0001g0012 a0002c0002t0001g0250 a0002c0002t0001g0251 others(1): Show |
6 | HG01168.hp2 HG01169.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.-12-111T>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 2/6 | chr11 | 60517961 | |||||||
| chr11:60517962 | G | C | 4 | a0002c0002t0001g0012 a0002c0002t0001g0250 a0002c0002t0001g0251 others(1): Show |
6 | HG01168.hp2 HG01169.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.-12-110G>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 2/6 | chr11 | 60517962 | |||||||
| chr11:60518045 | G | A | 4 | a0002c0002t0001g0012 a0002c0002t0001g0250 a0002c0002t0001g0251 others(1): Show |
6 | HG01168.hp2 HG01169.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.-12-27G>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 2/6 | chr11 | 60518045 | |||||||
| chr11:60518055 | T | G | 105 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0167 others(102): Show |
118 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.-12-17T>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 2/6 | chr11 | 60518055 | |||||||
| chr11:60518330 | C | T | 27 | a0002c0002t0001g0038 a0002c0002t0001g0039 a0002c0002t0001g0253 others(24): Show |
29 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(26): Show |
intron_variant | MODIFIER | c.129+118C>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | chr11 | 60518330 | |||||||
| chr11:60518565 | A | T | 218 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(215): Show |
285 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(282): Show |
intron_variant | MODIFIER | c.129+353A>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | chr11 | 60518565 | |||||||
| chr11:60518566 | C | T | 4 | a0002c0003t0001g0241 a0002c0003t0001g0242 a0002c0003t0001g0243 others(1): Show |
4 | NA18948.hp2 NA18954.hp2 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.129+354C>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | chr11 | 60518566 | |||||||
| chr11:60518911 | G | A | 2 | a0001c0001t0002g0284 a0001c0001t0002g0285 |
2 | HG01255.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.129+699G>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | chr11 | 60518911 | |||||||
| chr11:60519001 | T | G | 1 | a0006c0006t0001g0062 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.129+789T>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | chr11 | 60519001 | |||||||
| chr11:60519177 | CT | C | 47 | a0002c0002t0001g0038 a0002c0002t0001g0039 a0002c0002t0001g0253 others(44): Show |
52 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.129+966delT | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | chr11 | 60519177 | |||||||
| chr11:60519347 | G | A | 3 | a0003c0004t0005g0029 a0003c0004t0005g0170 a0003c0004t0005g0171 |
4 | HG01884.hp2 HG02622.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.129+1135G>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | chr11 | 60519347 | |||||||
| chr11:60519405 | G | GT | 7 | a0001c0001t0001g0165 a0001c0001t0001g0195 a0001c0001t0001g0196 others(4): Show |
7 | HG02559.hp1 HG02602.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.129+1206dupT | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 60519405 | ||||||
| chr11:60519683 | G | T | 1 | a0001c0001t0001g0164 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.129+1471G>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | chr11 | 60519683 | |||||||
| chr11:60519775 | G | T | 1 | a0001c0001t0001g0239 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.129+1563G>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | chr11 | 60519775 | |||||||
| chr11:60519836 | G | A | 3 | a0001c0001t0001g0017 a0001c0001t0001g0063 a0001c0001t0001g0064 |
4 | HG02056.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.129+1624G>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | chr11 | 60519836 | |||||||
| chr11:60520136 | G | A | 1 | a0001c0001t0001g0008 | 3 | HG02615.hp2 HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.129+1924G>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | chr11 | 60520136 | |||||||
| chr11:60520168 | G | T | 4 | a0002c0003t0001g0235 a0002c0003t0001g0236 a0002c0003t0001g0237 others(1): Show |
4 | HG00408.hp1 HG01952.hp2 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.129+1956G>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | chr11 | 60520168 | |||||||
| chr11:60520191 | T | C | 2 | a0001c0001t0001g0065 a0001c0001t0001g0066 |
2 | HG02630.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.129+1979T>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | chr11 | 60520191 | |||||||
| chr11:60520443 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.129+2231C>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | chr11 | 60520443 | |||||||
| chr11:60520463 | A | G | 14 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0167 others(11): Show |
16 | HG01243.hp2 HG01496.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.129+2251A>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | chr11 | 60520463 | |||||||
| chr11:60520493 | C | G | 3 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 |
3 | HG02647.hp2 HG02717.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.129+2281C>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | chr11 | 60520493 | |||||||
| chr11:60520493 | C | T | 1 | a0001c0001t0002g0334 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.129+2281C>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | chr11 | 60520493 | |||||||
| chr11:60520507 | A | G | 2 | a0001c0001t0002g0332 a0001c0001t0002g0333 |
2 | HG03017.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.129+2295A>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | chr11 | 60520507 | |||||||
| chr11:60520707 | G | A | 2 | a0001c0001t0001g0067 a0001c0001t0001g0068 |
2 | HG02602.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.129+2495G>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | chr11 | 60520707 | |||||||
| chr11:60520893 | C | T | 1 | a0001c0001t0001g0162 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.129+2681C>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | chr11 | 60520893 | |||||||
| chr11:60520912 | C | T | 2 | a0001c0001t0001g0161 a0003c0004t0001g0182 |
2 | HG01433.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.129+2700C>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | chr11 | 60520912 | |||||||
| chr11:60520922 | C | T | 1 | a0001c0001t0001g0160 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.129+2710C>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | chr11 | 60520922 | |||||||
| chr11:60521066 | A | G | 6 | a0001c0001t0001g0008 a0001c0001t0001g0028 a0001c0001t0001g0157 others(3): Show |
9 | HG01884.hp1 HG02615.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.130-2831A>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | chr11 | 60521066 | |||||||
| chr11:60521331 | T | G | 16 | a0001c0001t0001g0008 a0001c0001t0001g0028 a0001c0001t0001g0046 others(13): Show |
20 | HG00642.hp2 HG01099.hp1 HG01346.hp2 others(17): Show |
intron_variant | MODIFIER | c.130-2566T>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | chr11 | 60521331 | |||||||
| chr11:60521447 | G | T | 1 | a0001c0001t0001g0076 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.130-2450G>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | chr11 | 60521447 | |||||||
| chr11:60521519 | A | G | 4 | a0002c0002t0001g0012 a0002c0002t0001g0250 a0002c0002t0001g0251 others(1): Show |
6 | HG01168.hp2 HG01169.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.130-2378A>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | chr11 | 60521519 | |||||||
| chr11:60521543 | A | G | 4 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(1): Show |
4 | HG02647.hp2 HG02717.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.130-2354A>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | chr11 | 60521543 | |||||||
| chr11:60521584 | T | G | 95 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0167 others(92): Show |
129 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.130-2313T>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | chr11 | 60521584 | |||||||
| chr11:60521607 | C | T | 1 | a0001c0001t0001g0156 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.130-2290C>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | chr11 | 60521607 | |||||||
| chr11:60521754 | T | C | 4 | a0002c0002t0001g0012 a0002c0002t0001g0250 a0002c0002t0001g0251 others(1): Show |
6 | HG01168.hp2 HG01169.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.130-2143T>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | chr11 | 60521754 | |||||||
| chr11:60521818 | T | C | 89 | a0002c0002t0001g0012 a0002c0002t0001g0038 a0002c0002t0001g0039 others(86): Show |
100 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.130-2079T>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | chr11 | 60521818 | |||||||
| chr11:60522000 | G | T | 89 | a0002c0002t0001g0012 a0002c0002t0001g0038 a0002c0002t0001g0039 others(86): Show |
100 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.130-1897G>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | chr11 | 60522000 | |||||||
| chr11:60522098 | A | G | 1 | a0001c0001t0001g0155 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.130-1799A>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | chr11 | 60522098 | |||||||
| chr11:60522197 | C | CAGAT | 48 | a0001c0001t0001g0035 a0001c0001t0001g0169 a0001c0001t0001g0186 others(45): Show |
62 | HG00323.hp2 HG00558.hp2 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.130-1659_130-1656d others(6): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 60522197 | ||||||
| chr11:60522197 | C | CAGATAGA others(1): Show |
42 | a0001c0001t0001g0034 a0001c0001t0001g0167 a0001c0001t0001g0168 others(39): Show |
58 | HG00099.hp1 HG01123.hp2 HG01175.hp1 others(55): Show |
intron_variant | MODIFIER | c.130-1663_130-1656d others(10): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 60522197 | ||||||
| chr11:60522197 | C | CAGATAGA others(5): Show |
7 | a0001c0001t0002g0013 a0001c0001t0002g0040 a0001c0001t0002g0286 others(4): Show |
10 | HG00735.hp2 HG01515.hp1 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.130-1667_130-1656d others(14): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 60522197 | ||||||
| chr11:60522197 | CAGAT | C | 5 | a0003c0004t0001g0179 a0003c0004t0001g0180 a0003c0004t0001g0181 others(2): Show |
6 | HG01884.hp2 HG02622.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.130-1659_130-1656d others(6): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 60522197 | ||||||
| chr11:60522202 | A | AGAT | 27 | a0002c0002t0001g0038 a0002c0002t0001g0039 a0002c0002t0001g0253 others(24): Show |
29 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(26): Show |
intron_variant | MODIFIER | c.130-1694_130-1692d others(5): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 60522202 | ||||||
| chr11:60522223 | G | GATGTAT | 129 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(126): Show |
164 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(161): Show |
intron_variant | MODIFIER | c.130-1672_130-1671i others(8): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 60522223 | ||||||
| chr11:60522223 | G | GATGTATA others(5): Show |
2 | a0002c0003t0001g0225 a0002c0003t0001g0226 |
2 | HG03831.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.130-1672_130-1671i others(14): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 60522223 | ||||||
| chr11:60522227 | G | GATGTATA others(3): Show |
1 | a0001c0001t0001g0155 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.130-1668_130-1667i others(12): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 60522227 | ||||||
| chr11:60522227 | G | GATGTATA others(7): Show |
4 | a0002c0003t0001g0221 a0002c0003t0001g0222 a0002c0003t0001g0223 others(1): Show |
4 | HG01123.hp1 HG01167.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.130-1668_130-1667i others(16): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 60522227 | ||||||
| chr11:60522227 | G | GATGTATA others(9): Show |
29 | a0002c0003t0001g0011 a0002c0003t0001g0032 a0002c0003t0001g0033 others(26): Show |
32 | HG00280.hp1 HG00408.hp1 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.130-1668_130-1667i others(18): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 60522227 | ||||||
| chr11:60522227 | G | GATGTATA others(11): Show |
1 | a0002c0003t0001g0031 | 2 | NA18943.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.130-1668_130-1667i others(20): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 60522227 | ||||||
| chr11:60522227 | G | T | 131 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(128): Show |
166 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.130-1670G>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | chr11 | 60522227 | |||||||
| chr11:60522231 | G | GATGTATA others(7): Show |
2 | a0001c0001t0001g0066 a0001c0001t0002g0192 |
2 | HG02630.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.130-1664_130-1663i others(16): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 60522231 | ||||||
| chr11:60522231 | G | GATGTATA others(13): Show |
2 | a0002c0003t0001g0204 a0003c0007t0001g0203 |
2 | NA18970.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.130-1664_130-1663i others(22): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 60522231 | ||||||
| chr11:60522231 | G | T | 166 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(163): Show |
205 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.130-1666G>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | chr11 | 60522231 | |||||||
| chr11:60522234 | A | C | 170 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(167): Show |
209 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.130-1663A>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | chr11 | 60522234 | |||||||
| chr11:60522235 | G | GATGTATA others(11): Show |
1 | a0001c0001t0001g0065 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.130-1660_130-1659i others(20): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 60522235 | ||||||
| chr11:60522235 | G | T | 170 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(167): Show |
209 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.130-1662G>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | chr11 | 60522235 | |||||||
| chr11:60522239 | G | GATAGATA others(23): Show |
5 | a0001c0001t0001g0195 a0001c0001t0001g0239 a0001c0001t0002g0280 others(2): Show |
5 | HG01433.hp1 NA19030.hp1 NA19070.hp2 others(2): Show |
intron_variant | MODIFIER | c.130-1656_130-1655i others(32): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 60522239 | ||||||
| chr11:60522239 | G | GATAGATA others(29): Show |
1 | a0002c0002t0001g0253 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.130-1656_130-1655i others(38): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 60522239 | ||||||
| chr11:60522239 | G | GATAGATG others(21): Show |
1 | a0002c0002t0003g0058 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.130-1656_130-1655i others(30): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 60522239 | ||||||
| chr11:60522239 | G | GATAGATG others(19): Show |
6 | a0001c0001t0001g0196 a0001c0001t0001g0198 a0001c0001t0001g0201 others(3): Show |
6 | HG00738.hp2 HG02717.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.130-1656_130-1655i others(28): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 60522239 | ||||||
| chr11:60522239 | G | GATAGATG others(25): Show |
10 | a0002c0002t0001g0038 a0002c0002t0001g0254 a0002c0002t0001g0255 others(7): Show |
11 | HG00558.hp1 HG01099.hp2 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.130-1656_130-1655i others(34): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 60522239 | ||||||
| chr11:60522239 | G | GATGGATG others(21): Show |
1 | a0001c0001t0002g0330 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.130-1655_130-1654i others(30): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 60522239 | ||||||
| chr11:60522239 | G | GATGTATA others(19): Show |
1 | a0002c0002t0003g0049 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.130-1645_130-1644i others(28): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 60522239 | ||||||
| chr11:60522239 | G | GATGTATA others(17): Show |
22 | a0002c0002t0001g0012 a0002c0002t0001g0250 a0002c0002t0001g0251 others(19): Show |
27 | HG01069.hp2 HG01070.hp1 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.130-1645_130-1644i others(26): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 60522239 | ||||||
| chr11:60522239 | G | GATGTATA others(15): Show |
90 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0167 others(87): Show |
123 | HG00099.hp1 HG00323.hp2 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.130-1645_130-1644i others(24): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 60522239 | ||||||
| chr11:60522239 | G | GATGTGTA others(21): Show |
16 | a0002c0002t0001g0039 a0002c0002t0001g0262 a0002c0002t0001g0264 others(13): Show |
17 | HG00423.hp2 HG00544.hp2 HG00673.hp2 others(14): Show |
intron_variant | MODIFIER | c.130-1654_130-1653i others(30): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 60522239 | ||||||
| chr11:60522239 | G | T | 171 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(168): Show |
210 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.130-1658G>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | chr11 | 60522239 | |||||||
| chr11:60522270 | ATATG | A | 3 | a0002c0002t0003g0054 a0002c0002t0003g0055 a0002c0002t0003g0056 |
3 | HG02055.hp1 HG02559.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.130-1621_130-1618d others(6): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 60522270 | ||||||
| chr11:60522357 | T | C | 1 | a0002c0003t0001g0205 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.130-1540T>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | chr11 | 60522357 | |||||||
| chr11:60522359 | C | A | 1 | a0001c0001t0001g0077 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.130-1538C>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | chr11 | 60522359 | |||||||
| chr11:60522363 | C | T | 70 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(67): Show |
76 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.130-1534C>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | chr11 | 60522363 | |||||||
| chr11:60522364 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.130-1533G>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | chr11 | 60522364 | |||||||
| chr11:60522480 | G | A | 36 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0018 others(33): Show |
48 | HG00099.hp2 HG00408.hp2 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.130-1417G>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | chr11 | 60522480 | |||||||
| chr11:60522508 | C | T | 3 | a0003c0004t0005g0029 a0003c0004t0005g0170 a0003c0004t0005g0171 |
4 | HG01884.hp2 HG02622.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.130-1389C>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | chr11 | 60522508 | |||||||
| chr11:60522515 | A | G | 97 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0167 others(94): Show |
131 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.130-1382A>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | chr11 | 60522515 | |||||||
| chr11:60522524 | G | A | 1 | a0002c0002t0001g0262 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.130-1373G>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | chr11 | 60522524 | |||||||
| chr11:60522622 | A | G | 323 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(320): Show |
403 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(400): Show |
intron_variant | MODIFIER | c.130-1275A>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | chr11 | 60522622 | |||||||
| chr11:60522750 | G | T | 89 | a0002c0002t0001g0012 a0002c0002t0001g0038 a0002c0002t0001g0039 others(86): Show |
100 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.130-1147G>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | chr11 | 60522750 | |||||||
| chr11:60522784 | T | C | 174 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(171): Show |
213 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.130-1113T>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | chr11 | 60522784 | |||||||
| chr11:60522875 | C | T | 90 | a0001c0001t0001g0017 a0002c0002t0001g0012 a0002c0002t0001g0038 others(87): Show |
102 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.130-1022C>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | chr11 | 60522875 | |||||||
| chr11:60522879 | T | C | 89 | a0002c0002t0001g0012 a0002c0002t0001g0038 a0002c0002t0001g0039 others(86): Show |
100 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.130-1018T>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | chr11 | 60522879 | |||||||
| chr11:60522904 | C | T | 1 | a0001c0001t0002g0329 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.130-993C>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | chr11 | 60522904 | |||||||
| chr11:60523144 | A | G | 13 | a0002c0002t0003g0016 a0002c0002t0003g0047 a0002c0002t0003g0048 others(10): Show |
14 | HG01069.hp1 HG01071.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.130-753A>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | chr11 | 60523144 | |||||||
| chr11:60523233 | C | T | 1 | a0001c0001t0001g0151 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.130-664C>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | chr11 | 60523233 | |||||||
| chr11:60523368 | C | G | 1 | a0001c0001t0001g0194 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.130-529C>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | chr11 | 60523368 | |||||||
| chr11:60523395 | G | A | 1 | a0002c0002t0001g0254 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.130-502G>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | chr11 | 60523395 | |||||||
| chr11:60523449 | C | A | 1 | a0002c0002t0003g0048 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.130-448C>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | chr11 | 60523449 | |||||||
| chr11:60523487 | A | G | 89 | a0002c0002t0001g0012 a0002c0002t0001g0038 a0002c0002t0001g0039 others(86): Show |
100 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.130-410A>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | chr11 | 60523487 | |||||||
| chr11:60523552 | G | A | 4 | a0002c0002t0001g0012 a0002c0002t0001g0250 a0002c0002t0001g0251 others(1): Show |
6 | HG01168.hp2 HG01169.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.130-345G>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | chr11 | 60523552 | |||||||
| chr11:60523793 | A | C | 1 | a0006c0006t0001g0062 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.130-104A>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | chr11 | 60523793 | |||||||
| chr11:60523843 | T | C | 2 | a0001c0001t0001g0069 a0001c0001t0001g0070 |
2 | HG01099.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.130-54T>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 3/6 | chr11 | 60523843 | |||||||
| chr11:60524031 | G | A | 4 | a0001c0001t0002g0284 a0001c0001t0002g0285 a0001c0001t0002g0291 others(1): Show |
4 | HG00323.hp2 HG01255.hp1 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.186+78G>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 4/6 | chr11 | 60524031 | |||||||
| chr11:60524075 | A | G | 89 | a0002c0002t0001g0012 a0002c0002t0001g0038 a0002c0002t0001g0039 others(86): Show |
100 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.186+122A>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 4/6 | chr11 | 60524075 | |||||||
| chr11:60524130 | T | C | 2 | a0002c0002t0001g0038 a0002c0002t0001g0255 |
3 | NA18962.hp1 NA18980.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.186+177T>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 4/6 | chr11 | 60524130 | |||||||
| chr11:60524136 | A | C | 2 | a0001c0001t0002g0312 a0001c0001t0002g0328 |
2 | HG02055.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.186+183A>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 4/6 | chr11 | 60524136 | |||||||
| chr11:60524213 | T | C | 2 | a0002c0003t0001g0206 a0002c0003t0001g0207 |
2 | HG02683.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.186+260T>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 4/6 | chr11 | 60524213 | |||||||
| chr11:60524378 | T | C | 38 | a0002c0003t0001g0011 a0002c0003t0001g0031 a0002c0003t0001g0032 others(35): Show |
42 | HG00280.hp1 HG00408.hp1 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.186+425T>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 4/6 | chr11 | 60524378 | |||||||
| chr11:60524386 | T | C | 2 | a0002c0002t0003g0054 a0002c0002t0003g0056 |
2 | HG02055.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.186+433T>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 4/6 | chr11 | 60524386 | |||||||
| chr11:60524428 | A | G | 1 | a0001c0001t0001g0150 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.186+475A>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 4/6 | chr11 | 60524428 | |||||||
| chr11:60524573 | T | C | 323 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(320): Show |
403 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(400): Show |
intron_variant | MODIFIER | c.186+620T>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 4/6 | chr11 | 60524573 | |||||||
| chr11:60524661 | A | AT | 7 | a0002c0002t0004g0036 a0002c0002t0004g0037 a0002c0002t0004g0245 others(4): Show |
9 | HG01069.hp2 HG01070.hp1 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.187-546_187-545ins others(1): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 4/6 | chr11 | 60524661 | |||||||
| chr11:60524662 | C | CT | 54 | a0002c0002t0001g0012 a0002c0002t0001g0250 a0002c0002t0001g0251 others(51): Show |
61 | HG00280.hp1 HG00408.hp1 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.187-527dupT | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr11 | 60524662 | ||||||
| chr11:60524662 | C | T | 7 | a0002c0002t0004g0036 a0002c0002t0004g0037 a0002c0002t0004g0245 others(4): Show |
9 | HG01069.hp2 HG01070.hp1 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.187-545C>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 4/6 | chr11 | 60524662 | |||||||
| chr11:60524662 | CT | C | 239 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(236): Show |
307 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(304): Show |
intron_variant | MODIFIER | c.187-527delT | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr11 | 60524662 | ||||||
| chr11:60524662 | CTT | C | 20 | a0001c0001t0001g0022 a0001c0001t0001g0034 a0001c0001t0001g0035 others(17): Show |
23 | HG01243.hp2 HG01496.hp1 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.187-528_187-527del others(2): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr11 | 60524662 | ||||||
| chr11:60524681 | G | A | 9 | a0003c0004t0001g0176 a0003c0004t0001g0177 a0003c0004t0001g0178 others(6): Show |
10 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.187-526G>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 4/6 | chr11 | 60524681 | |||||||
| chr11:60524699 | C | G | 89 | a0002c0002t0001g0012 a0002c0002t0001g0038 a0002c0002t0001g0039 others(86): Show |
100 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.187-508C>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 4/6 | chr11 | 60524699 | |||||||
| chr11:60524732 | G | A | 1 | a0001c0001t0002g0329 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.187-475G>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 4/6 | chr11 | 60524732 | |||||||
| chr11:60524808 | C | T | 1 | a0003c0004t0001g0175 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.187-399C>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 4/6 | chr11 | 60524808 | |||||||
| chr11:60524896 | G | A | 38 | a0002c0003t0001g0011 a0002c0003t0001g0031 a0002c0003t0001g0032 others(35): Show |
42 | HG00280.hp1 HG00408.hp1 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.187-311G>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 4/6 | chr11 | 60524896 | |||||||
| chr11:60525132 | T | G | 1 | a0001c0001t0002g0293 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.187-75T>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 4/6 | chr11 | 60525132 | |||||||
| chr11:60525490 | T | C | 4 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0335 others(1): Show |
4 | HG01346.hp1 HG01358.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.306+164T>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | chr11 | 60525490 | |||||||
| chr11:60525910 | T | TAAAATAT others(308): Show |
45 | a0002c0002t0001g0038 a0002c0002t0001g0039 a0002c0002t0001g0253 others(42): Show |
50 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.306+601_306+602ins others(315): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr11 | 60525910 | ||||||
| chr11:60525910 | T | TAAAATAT others(309): Show |
5 | a0002c0002t0001g0012 a0002c0002t0001g0250 a0002c0002t0001g0251 others(2): Show |
7 | HG00673.hp2 HG01168.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.306+601_306+602ins others(316): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr11 | 60525910 | ||||||
| chr11:60525910 | T | TAAAATAT others(308): Show |
1 | a0002c0002t0001g0276 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.306+601_306+602ins others(315): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr11 | 60525910 | ||||||
| chr11:60525910 | T | TAAAATAT others(308): Show |
37 | a0002c0003t0001g0011 a0002c0003t0001g0031 a0002c0003t0001g0032 others(34): Show |
41 | HG00280.hp1 HG00408.hp1 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.306+601_306+602ins others(315): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr11 | 60525910 | ||||||
| chr11:60525915 | T | TATTAGTG others(308): Show |
1 | a0002c0003t0001g0210 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.306+601_306+602ins others(315): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr11 | 60525915 | ||||||
| chr11:60526230 | T | G | 5 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(2): Show |
5 | HG02572.hp1 HG02647.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.306+904T>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | chr11 | 60526230 | |||||||
| chr11:60526292 | C | T | 4 | a0002c0002t0001g0012 a0002c0002t0001g0250 a0002c0002t0001g0251 others(1): Show |
6 | HG01168.hp2 HG01169.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.306+966C>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | chr11 | 60526292 | |||||||
| chr11:60526361 | G | A | 1 | a0001c0001t0001g0100 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.306+1035G>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | chr11 | 60526361 | |||||||
| chr11:60526373 | A | G | 3 | a0001c0001t0002g0030 a0001c0001t0002g0190 a0001c0001t0002g0191 |
4 | HG02922.hp1 HG03225.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.306+1047A>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | chr11 | 60526373 | |||||||
| chr11:60526711 | C | A | 89 | a0002c0002t0001g0012 a0002c0002t0001g0038 a0002c0002t0001g0039 others(86): Show |
100 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.306+1385C>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | chr11 | 60526711 | |||||||
| chr11:60526740 | C | A | 1 | a0001c0001t0001g0101 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.306+1414C>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | chr11 | 60526740 | |||||||
| chr11:60526898 | G | A | 2 | a0002c0002t0001g0265 a0002c0002t0001g0266 |
2 | HG00423.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.306+1572G>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | chr11 | 60526898 | |||||||
| chr11:60527179 | G | C | 2 | a0001c0001t0001g0193 a0001c0001t0001g0198 |
2 | HG02723.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.306+1853G>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | chr11 | 60527179 | |||||||
| chr11:60527358 | TTCCG | T | 3 | a0001c0001t0001g0008 a0001c0001t0001g0147 a0001c0001t0001g0148 |
5 | HG02004.hp1 HG02615.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.307-2004_307-2001d others(6): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr11 | 60527358 | ||||||
| chr11:60527358 | TTCCGTCT others(1): Show |
T | 3 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0144 |
8 | HG01496.hp2 HG03239.hp2 HG03688.hp1 others(5): Show |
intron_variant | MODIFIER | c.307-2004_307-1997d others(10): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr11 | 60527358 | ||||||
| chr11:60527358 | TTCCGTCT others(3): Show |
T | 1 | a0001c0001t0001g0145 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.307-2004_307-1995d others(12): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr11 | 60527358 | ||||||
| chr11:60527358 | TTCCGTCT others(5): Show |
T | 1 | a0001c0001t0001g0146 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.307-2004_307-1993d others(14): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr11 | 60527358 | ||||||
| chr11:60527361 | C | T | 122 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(119): Show |
149 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.307-2004C>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | chr11 | 60527361 | |||||||
| chr11:60527361 | CGT | C | 21 | a0001c0001t0002g0044 a0001c0001t0002g0191 a0001c0001t0007g0200 others(18): Show |
23 | HG00408.hp1 HG00558.hp2 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.307-2003_307-2002d others(4): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | chr11 | 60527361 | |||||||
| chr11:60527361 | CGTCT | C | 15 | a0001c0001t0001g0231 a0001c0001t0002g0001 a0001c0001t0002g0057 others(12): Show |
16 | HG00099.hp1 HG00597.hp1 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.307-2003_307-2000d others(6): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | chr11 | 60527361 | |||||||
| chr11:60527361 | CGTCTCT | C | 23 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0013 others(20): Show |
30 | HG00639.hp2 HG01106.hp2 HG01255.hp1 others(27): Show |
intron_variant | MODIFIER | c.307-2003_307-1998d others(8): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | chr11 | 60527361 | |||||||
| chr11:60527361 | CGTCTCTC others(1): Show |
C | 27 | a0001c0001t0001g0239 a0001c0001t0002g0001 a0001c0001t0002g0002 others(24): Show |
40 | HG00280.hp2 HG00323.hp2 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.307-2003_307-1996d others(10): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | chr11 | 60527361 | |||||||
| chr11:60527361 | CGTCTCTC others(3): Show |
C | 4 | a0001c0001t0002g0040 a0001c0001t0002g0291 a0001c0001t0002g0304 others(1): Show |
5 | HG01261.hp1 HG01515.hp1 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.307-2003_307-1994d others(12): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | chr11 | 60527361 | |||||||
| chr11:60527361 | CGTCTCTC others(5): Show |
C | 6 | a0001c0001t0001g0195 a0001c0001t0002g0002 a0001c0001t0002g0184 others(3): Show |
6 | HG02145.hp1 NA18955.hp1 NA18989.hp2 others(3): Show |
intron_variant | MODIFIER | c.307-2003_307-1992d others(14): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | chr11 | 60527361 | |||||||
| chr11:60527361 | CGTCTCTC others(7): Show |
C | 2 | a0001c0001t0001g0196 a0001c0001t0001g0197 |
2 | HG02647.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.307-2003_307-1990d others(16): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | chr11 | 60527361 | |||||||
| chr11:60527361 | CGTCTCTC others(9): Show |
C | 2 | a0002c0003t0001g0032 a0005c0009t0001g0032 |
2 | HG00280.hp1 HG00639.hp1 |
intron_variant | MODIFIER | c.307-2003_307-1988d others(18): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | chr11 | 60527361 | |||||||
| chr11:60527362 | G | C | 220 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(217): Show |
258 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(255): Show |
intron_variant | MODIFIER | c.307-2003G>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | chr11 | 60527362 | |||||||
| chr11:60527386 | C | CTGTGTG | 2 | a0002c0002t0004g0037 a0002c0002t0004g0246 |
3 | HG01069.hp2 HG01070.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.307-1978_307-1977i others(8): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr11 | 60527386 | ||||||
| chr11:60527388 | C | G | 7 | a0002c0002t0004g0036 a0002c0002t0004g0037 a0002c0002t0004g0245 others(4): Show |
9 | HG01069.hp2 HG01070.hp1 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.307-1977C>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | chr11 | 60527388 | |||||||
| chr11:60527390 | C | CTG | 3 | a0001c0001t0001g0186 a0001c0001t0001g0228 a0001c0001t0001g0229 |
3 | HG02486.hp2 HG02886.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.307-1974_307-1973i others(4): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr11 | 60527390 | ||||||
| chr11:60527390 | C | G | 10 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0234 others(7): Show |
12 | HG01069.hp2 HG01070.hp1 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.307-1975C>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | chr11 | 60527390 | |||||||
| chr11:60527392 | C | CTG | 3 | a0001c0001t0001g0143 a0001c0001t0001g0232 a0001c0001t0002g0192 |
3 | HG02145.hp2 NA18971.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.307-1972_307-1971i others(4): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr11 | 60527392 | ||||||
| chr11:60527392 | C | G | 19 | a0001c0001t0001g0034 a0001c0001t0001g0167 a0001c0001t0001g0168 others(16): Show |
22 | HG01069.hp2 HG01070.hp1 HG01192.hp2 others(19): Show |
intron_variant | MODIFIER | c.307-1973C>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | chr11 | 60527392 | |||||||
| chr11:60527394 | C | CTGTGTGT others(3): Show |
1 | a0001c0001t0002g0290 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.307-1970_307-1969i others(12): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr11 | 60527394 | ||||||
| chr11:60527394 | C | G | 28 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0066 others(25): Show |
32 | HG01069.hp2 HG01070.hp1 HG01192.hp2 others(29): Show |
intron_variant | MODIFIER | c.307-1971C>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | chr11 | 60527394 | |||||||
| chr11:60527396 | C | CTGTG | 3 | a0001c0001t0001g0027 a0001c0001t0001g0046 a0001c0001t0002g0311 |
5 | HG01346.hp2 NA18975.hp1 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.307-1968_307-1967i others(6): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr11 | 60527396 | ||||||
| chr11:60527396 | C | CTGTGTG | 5 | a0001c0001t0001g0026 a0001c0001t0001g0070 a0001c0001t0001g0138 others(2): Show |
8 | HG00673.hp1 HG01891.hp1 HG02015.hp1 others(5): Show |
intron_variant | MODIFIER | c.307-1968_307-1967i others(8): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr11 | 60527396 | ||||||
| chr11:60527396 | C | CTGTGTGT others(1): Show |
4 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0199 others(1): Show |
4 | HG00438.hp1 NA18947.hp2 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.307-1968_307-1967i others(10): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr11 | 60527396 | ||||||
| chr11:60527396 | C | CTGTGTGT others(3): Show |
5 | a0001c0001t0001g0135 a0001c0001t0002g0308 a0001c0001t0002g0309 others(2): Show |
5 | HG00609.hp1 HG02027.hp1 NA18941.hp1 others(2): Show |
intron_variant | MODIFIER | c.307-1968_307-1967i others(12): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr11 | 60527396 | ||||||
| chr11:60527396 | C | G | 37 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0065 others(34): Show |
42 | HG00438.hp2 HG00735.hp2 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.307-1969C>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | chr11 | 60527396 | |||||||
| chr11:60527398 | C | CTGTGTGT others(1): Show |
4 | a0001c0001t0001g0017 a0001c0001t0001g0130 a0001c0001t0001g0131 others(1): Show |
5 | HG03130.hp1 HG03491.hp1 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.307-1966_307-1965i others(10): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr11 | 60527398 | ||||||
| chr11:60527398 | C | CTGTGTGT others(3): Show |
1 | a0001c0001t0001g0159 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.307-1966_307-1965i others(12): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr11 | 60527398 | ||||||
| chr11:60527398 | C | G | 62 | a0001c0001t0001g0007 a0001c0001t0001g0026 a0001c0001t0001g0027 others(59): Show |
74 | HG00438.hp1 HG00438.hp2 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.307-1967C>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | chr11 | 60527398 | |||||||
| chr11:60527400 | C | CTGTG | 10 | a0001c0001t0001g0020 a0001c0001t0001g0075 a0001c0001t0001g0090 others(7): Show |
11 | HG01981.hp1 HG02300.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.307-1964_307-1963i others(6): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr11 | 60527400 | ||||||
| chr11:60527400 | C | CTGTGTG | 8 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0019 others(5): Show |
18 | HG00408.hp2 HG00738.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.307-1964_307-1963i others(8): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr11 | 60527400 | ||||||
| chr11:60527400 | C | CTGTGTGT others(1): Show |
5 | a0001c0001t0001g0063 a0001c0001t0001g0073 a0001c0001t0001g0085 others(2): Show |
5 | HG02027.hp2 HG03471.hp2 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.307-1964_307-1963i others(10): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr11 | 60527400 | ||||||
| chr11:60527400 | C | CTGTGTGT others(3): Show |
3 | a0001c0001t0001g0072 a0001c0001t0001g0076 a0001c0001t0001g0164 |
3 | HG03195.hp2 HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.307-1964_307-1963i others(12): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr11 | 60527400 | ||||||
| chr11:60527400 | C | CTGTGTGT others(5): Show |
1 | a0001c0001t0001g0028 | 2 | HG02717.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.307-1964_307-1963i others(14): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr11 | 60527400 | ||||||
| chr11:60527400 | C | G | 80 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0021 others(77): Show |
97 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.307-1965C>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | chr11 | 60527400 | |||||||
| chr11:60527402 | C | CTG | 6 | a0001c0001t0001g0067 a0001c0001t0001g0077 a0001c0001t0001g0122 others(3): Show |
6 | HG01071.hp1 HG02015.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.307-1962_307-1961i others(4): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr11 | 60527402 | ||||||
| chr11:60527402 | C | CTGTG | 8 | a0001c0001t0001g0009 a0001c0001t0001g0100 a0001c0001t0001g0120 others(5): Show |
10 | HG03654.hp1 HG03927.hp1 NA18747.hp1 others(7): Show |
intron_variant | MODIFIER | c.307-1962_307-1961i others(6): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr11 | 60527402 | ||||||
| chr11:60527402 | C | CTGTGTG | 6 | a0001c0001t0001g0018 a0001c0001t0001g0084 a0001c0001t0001g0117 others(3): Show |
7 | HG02040.hp1 HG02523.hp1 NA18981.hp1 others(4): Show |
intron_variant | MODIFIER | c.307-1962_307-1961i others(8): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr11 | 60527402 | ||||||
| chr11:60527402 | C | CTGTGTGT others(1): Show |
7 | a0001c0001t0001g0004 a0001c0001t0001g0081 a0001c0001t0001g0082 others(4): Show |
11 | HG00544.hp1 HG00597.hp2 HG00621.hp1 others(8): Show |
intron_variant | MODIFIER | c.307-1962_307-1961i others(10): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr11 | 60527402 | ||||||
| chr11:60527402 | C | CTGTGTGT others(3): Show |
3 | a0001c0001t0001g0114 a0001c0001t0001g0158 a0001c0001t0001g0163 |
3 | HG02970.hp1 HG03540.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.307-1962_307-1961i others(12): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr11 | 60527402 | ||||||
| chr11:60527402 | C | CTGTGTGT others(5): Show |
2 | a0001c0001t0001g0080 a0001c0001t0001g0149 |
2 | NA18959.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.307-1962_307-1961i others(14): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr11 | 60527402 | ||||||
| chr11:60527402 | C | G | 117 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(114): Show |
146 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.307-1963C>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | chr11 | 60527402 | |||||||
| chr11:60527404 | C | CTG | 3 | a0001c0001t0001g0113 a0002c0003t0001g0011 a0003c0007t0001g0203 |
5 | NA18970.hp1 NA18995.hp2 NA19005.hp1 others(2): Show |
intron_variant | MODIFIER | c.307-1960_307-1959i others(4): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr11 | 60527404 | ||||||
| chr11:60527404 | C | CTGTG | 2 | a0001c0001t0001g0024 a0001c0001t0001g0079 |
3 | HG01070.hp2 HG02523.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.307-1960_307-1959i others(6): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr11 | 60527404 | ||||||
| chr11:60527404 | C | CTGTGTG | 3 | a0001c0001t0001g0023 a0002c0002t0001g0260 a0002c0002t0003g0056 |
4 | HG01516.hp2 HG01517.hp2 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.307-1960_307-1959i others(8): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr11 | 60527404 | ||||||
| chr11:60527404 | C | CTGTGTGT others(1): Show |
11 | a0001c0001t0001g0069 a0001c0001t0001g0078 a0001c0001t0001g0110 others(8): Show |
12 | HG01081.hp1 HG01081.hp2 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.307-1960_307-1959i others(10): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr11 | 60527404 | ||||||
| chr11:60527404 | C | CTGTGTGT others(3): Show |
2 | a0002c0002t0001g0278 a0002c0002t0003g0052 |
2 | HG01978.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.307-1960_307-1959i others(12): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr11 | 60527404 | ||||||
| chr11:60527404 | C | CTGTGTGT others(5): Show |
1 | a0001c0001t0001g0279 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.307-1960_307-1959i others(14): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr11 | 60527404 | ||||||
| chr11:60527404 | C | G | 175 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(172): Show |
212 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(209): Show |
intron_variant | MODIFIER | c.307-1961C>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | chr11 | 60527404 | |||||||
| chr11:60527406 | C | CTGTGTGT others(3): Show |
6 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 others(3): Show |
7 | HG01074.hp2 HG01257.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.307-1958_307-1957i others(12): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr11 | 60527406 | ||||||
| chr11:60527406 | C | CTGTGTGT others(5): Show |
1 | a0001c0001t0001g0071 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.307-1958_307-1957i others(14): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr11 | 60527406 | ||||||
| chr11:60527406 | C | CTGTGTGT others(7): Show |
1 | a0001c0001t0001g0336 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.307-1958_307-1957i others(16): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr11 | 60527406 | ||||||
| chr11:60527406 | C | G | 251 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(248): Show |
322 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(319): Show |
intron_variant | MODIFIER | c.307-1959C>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | chr11 | 60527406 | |||||||
| chr11:60527406 | CTCTCTGT others(5): Show |
C | 1 | a0002c0003t0001g0215 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.307-1957_307-1946d others(14): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr11 | 60527406 | ||||||
| chr11:60527408 | C | CTG | 3 | a0002c0003t0001g0206 a0002c0003t0001g0207 a0002c0003t0001g0212 |
3 | HG02683.hp1 NA18967.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.307-1956_307-1955i others(4): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr11 | 60527408 | ||||||
| chr11:60527408 | C | CTGTGTGT others(3): Show |
3 | a0002c0002t0001g0264 a0002c0002t0001g0266 a0002c0002t0001g0275 |
3 | HG00673.hp2 HG02165.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.307-1956_307-1955i others(12): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr11 | 60527408 | ||||||
| chr11:60527408 | C | CTGTGTGT others(5): Show |
6 | a0001c0001t0001g0099 a0001c0001t0001g0104 a0002c0002t0001g0274 others(3): Show |
6 | HG00642.hp2 HG01069.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.307-1956_307-1955i others(14): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr11 | 60527408 | ||||||
| chr11:60527408 | C | CTGTGTGT others(7): Show |
2 | a0002c0002t0001g0255 a0002c0002t0001g0273 |
2 | HG02155.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.307-1956_307-1955i others(16): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr11 | 60527408 | ||||||
| chr11:60527408 | C | CTGTGTGT others(9): Show |
4 | a0001c0001t0001g0098 a0001c0001t0001g0335 a0002c0002t0001g0271 others(1): Show |
4 | HG01346.hp1 HG03492.hp1 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.307-1956_307-1955i others(18): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr11 | 60527408 | ||||||
| chr11:60527408 | C | CTGTGTGT others(11): Show |
1 | a0002c0002t0001g0254 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.307-1956_307-1955i others(20): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr11 | 60527408 | ||||||
| chr11:60527408 | C | G | 277 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(274): Show |
354 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(351): Show |
intron_variant | MODIFIER | c.307-1957C>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | chr11 | 60527408 | |||||||
| chr11:60527410 | C | CTCTCTCT others(15): Show |
1 | a0001c0001t0001g0194 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.307-1954_307-1953i others(24): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr11 | 60527410 | ||||||
| chr11:60527410 | C | CTCTCTCT others(3): Show |
1 | a0003c0004t0001g0172 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.307-1954_307-1953i others(12): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr11 | 60527410 | ||||||
| chr11:60527410 | C | CTCTCTGT others(9): Show |
1 | a0002c0002t0001g0267 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.307-1954_307-1953i others(18): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr11 | 60527410 | ||||||
| chr11:60527410 | C | CTCTCTGT others(17): Show |
1 | a0002c0002t0001g0256 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.307-1954_307-1953i others(26): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr11 | 60527410 | ||||||
| chr11:60527410 | C | CTCTGTGT others(5): Show |
1 | a0002c0002t0003g0048 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.307-1954_307-1953i others(14): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr11 | 60527410 | ||||||
| chr11:60527410 | C | CTCTGTGT others(7): Show |
2 | a0002c0002t0001g0262 a0002c0002t0001g0268 |
2 | NA19056.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.307-1954_307-1953i others(16): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr11 | 60527410 | ||||||
| chr11:60527410 | C | CTCTGTGT others(9): Show |
1 | a0001c0001t0001g0102 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.307-1954_307-1953i others(18): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr11 | 60527410 | ||||||
| chr11:60527410 | C | CTCTGTGT others(11): Show |
2 | a0002c0002t0001g0276 a0002c0002t0003g0050 |
2 | NA18998.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.307-1954_307-1953i others(20): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr11 | 60527410 | ||||||
| chr11:60527410 | C | CTCTGTGT others(13): Show |
1 | a0001c0001t0001g0101 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.307-1954_307-1953i others(22): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr11 | 60527410 | ||||||
| chr11:60527410 | C | CTGTGTGT others(5): Show |
2 | a0002c0002t0001g0265 a0002c0002t0001g0270 |
2 | HG00423.hp2 HG00544.hp2 |
intron_variant | MODIFIER | c.307-1931_307-1920d others(14): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr11 | 60527410 | ||||||
| chr11:60527410 | C | CTGTGTGT others(7): Show |
3 | a0002c0002t0001g0269 a0002c0002t0003g0047 a0002c0008t0001g0263 |
3 | HG02129.hp2 HG03239.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.307-1933_307-1920d others(16): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr11 | 60527410 | ||||||
| chr11:60527410 | C | CTGTGTGT others(9): Show |
1 | a0002c0002t0003g0051 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.307-1935_307-1920d others(18): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr11 | 60527410 | ||||||
| chr11:60527410 | C | G | 302 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(299): Show |
380 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(377): Show |
intron_variant | MODIFIER | c.307-1955C>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | chr11 | 60527410 | |||||||
| chr11:60527410 | CTGTG | C | 3 | a0001c0001t0001g0006 a0001c0001t0001g0103 a0001c0001t0001g0146 |
6 | NA18963.hp2 NA18971.hp1 NA18978.hp2 others(3): Show |
intron_variant | MODIFIER | c.307-1923_307-1920d others(6): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr11 | 60527410 | ||||||
| chr11:60527412 | G | C | 3 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0003c0004t0001g0182 |
3 | HG03098.hp2 HG03239.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.307-1953G>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | chr11 | 60527412 | |||||||
| chr11:60527445 | T | TGTGTGTG others(4): Show |
1 | a0001c0001t0001g0156 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.307-1920_307-1919i others(13): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | chr11 | 60527445 | |||||||
| chr11:60527468 | T | C | 3 | a0001c0001t0001g0008 a0001c0001t0001g0028 a0001c0001t0001g0158 |
5 | HG02615.hp2 HG02717.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.307-1897T>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | chr11 | 60527468 | |||||||
| chr11:60527470 | T | A | 1 | a0002c0002t0001g0267 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.307-1895T>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | chr11 | 60527470 | |||||||
| chr11:60527501 | C | T | 1 | a0001c0001t0001g0199 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.307-1864C>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | chr11 | 60527501 | |||||||
| chr11:60527599 | G | A | 13 | a0002c0002t0003g0016 a0002c0002t0003g0047 a0002c0002t0003g0048 others(10): Show |
14 | HG01069.hp1 HG01071.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.307-1766G>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | chr11 | 60527599 | |||||||
| chr11:60527669 | C | T | 38 | a0002c0003t0001g0011 a0002c0003t0001g0031 a0002c0003t0001g0032 others(35): Show |
42 | HG00280.hp1 HG00408.hp1 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.307-1696C>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | chr11 | 60527669 | |||||||
| chr11:60527697 | A | G | 1 | a0003c0004t0001g0178 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.307-1668A>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | chr11 | 60527697 | |||||||
| chr11:60527729 | C | G | 89 | a0002c0002t0001g0012 a0002c0002t0001g0038 a0002c0002t0001g0039 others(86): Show |
100 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.307-1636C>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | chr11 | 60527729 | |||||||
| chr11:60527761 | A | G | 89 | a0002c0002t0001g0012 a0002c0002t0001g0038 a0002c0002t0001g0039 others(86): Show |
100 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.307-1604A>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | chr11 | 60527761 | |||||||
| chr11:60527772 | G | A | 97 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0167 others(94): Show |
131 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.307-1593G>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | chr11 | 60527772 | |||||||
| chr11:60527859 | A | T | 2 | a0001c0001t0001g0186 a0001c0001t0001g0189 |
2 | HG02886.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.307-1506A>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | chr11 | 60527859 | |||||||
| chr11:60527974 | G | T | 323 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(320): Show |
403 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(400): Show |
intron_variant | MODIFIER | c.307-1391G>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | chr11 | 60527974 | |||||||
| chr11:60528170 | ACT | A | 89 | a0002c0002t0001g0012 a0002c0002t0001g0038 a0002c0002t0001g0039 others(86): Show |
100 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.307-1192_307-1191d others(4): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr11 | 60528170 | ||||||
| chr11:60528417 | C | T | 1 | a0001c0001t0001g0231 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.307-948C>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | chr11 | 60528417 | |||||||
| chr11:60528513 | A | T | 89 | a0002c0002t0001g0012 a0002c0002t0001g0038 a0002c0002t0001g0039 others(86): Show |
100 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.307-852A>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | chr11 | 60528513 | |||||||
| chr11:60528643 | T | G | 3 | a0003c0004t0005g0029 a0003c0004t0005g0170 a0003c0004t0005g0171 |
4 | HG01884.hp2 HG02622.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.307-722T>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | chr11 | 60528643 | |||||||
| chr11:60528812 | C | T | 1 | a0002c0003t0001g0207 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.307-553C>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | chr11 | 60528812 | |||||||
| chr11:60528966 | G | A | 9 | a0001c0001t0002g0014 a0001c0001t0002g0290 a0001c0001t0002g0308 others(6): Show |
11 | HG00735.hp2 HG02015.hp1 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.307-399G>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | chr11 | 60528966 | |||||||
| chr11:60529220 | A | G | 38 | a0002c0003t0001g0011 a0002c0003t0001g0031 a0002c0003t0001g0032 others(35): Show |
42 | HG00280.hp1 HG00408.hp1 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.307-145A>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | chr11 | 60529220 | |||||||
| chr11:60529255 | C | CT | 143 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(140): Show |
179 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(176): Show |
intron_variant | MODIFIER | c.307-90dupT | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr11 | 60529255 | ||||||
| chr11:60529255 | C | CTT | 126 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0034 others(123): Show |
164 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.307-91_307-90dupTT | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr11 | 60529255 | ||||||
| chr11:60529255 | C | CTTT | 10 | a0001c0001t0001g0107 a0001c0001t0001g0193 a0001c0001t0001g0198 others(7): Show |
11 | HG01257.hp2 HG01981.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.307-92_307-90dupTT others(1): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr11 | 60529255 | ||||||
| chr11:60529255 | CT | C | 38 | a0001c0001t0007g0200 a0002c0002t0001g0012 a0002c0002t0001g0250 others(35): Show |
44 | HG00280.hp1 HG00639.hp1 HG01123.hp1 others(41): Show |
intron_variant | MODIFIER | c.307-90delT | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr11 | 60529255 | ||||||
| chr11:60529301 | A | G | 4 | a0002c0002t0001g0012 a0002c0002t0001g0250 a0002c0002t0001g0251 others(1): Show |
6 | HG01168.hp2 HG01169.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.307-64A>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | chr11 | 60529301 | |||||||
| chr11:60529326 | A | G | 1 | a0001c0001t0002g0319 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.307-39A>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | chr11 | 60529326 | |||||||
| chr11:60529350 | GT | G | 4 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0093 others(1): Show |
4 | HG02698.hp2 HG03654.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.307-9delT | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr11 | 60529350 | ||||||
| chr11:60529361 | A | G | 22 | a0001c0001t0001g0017 a0001c0001t0001g0026 a0001c0001t0001g0027 others(19): Show |
25 | HG00323.hp1 HG00438.hp1 HG00609.hp1 others(22): Show |
splice_region_variant&intron_variant | LOW | c.307-4A>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 5/6 | chr11 | 60529361 | |||||||
| chr11:60529521 | A | G | 3 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 |
3 | HG02647.hp2 HG02717.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.402+61A>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60529521 | |||||||
| chr11:60529541 | G | C | 4 | a0003c0004t0001g0177 a0003c0004t0001g0178 a0003c0004t0001g0179 others(1): Show |
4 | HG02622.hp1 HG02895.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.402+81G>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60529541 | |||||||
| chr11:60529617 | T | TAGAA | 89 | a0002c0002t0001g0012 a0002c0002t0001g0038 a0002c0002t0001g0039 others(86): Show |
100 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.402+159_402+160ins others(4): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 60529617 | ||||||
| chr11:60529767 | C | T | 7 | a0002c0002t0004g0036 a0002c0002t0004g0037 a0002c0002t0004g0245 others(4): Show |
9 | HG01069.hp2 HG01070.hp1 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.402+307C>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60529767 | |||||||
| chr11:60529933 | G | A | 13 | a0002c0002t0003g0016 a0002c0002t0003g0047 a0002c0002t0003g0048 others(10): Show |
14 | HG01069.hp1 HG01071.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.402+473G>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60529933 | |||||||
| chr11:60529949 | A | G | 1 | a0001c0001t0001g0023 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.402+489A>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60529949 | |||||||
| chr11:60530245 | G | A | 4 | a0001c0001t0002g0295 a0001c0001t0002g0312 a0001c0001t0002g0315 others(1): Show |
4 | HG02055.hp2 HG02683.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.402+785G>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60530245 | |||||||
| chr11:60530495 | A | C | 132 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(129): Show |
167 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.402+1035A>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60530495 | |||||||
| chr11:60530698 | T | C | 234 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(231): Show |
303 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(300): Show |
intron_variant | MODIFIER | c.402+1238T>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60530698 | |||||||
| chr11:60530699 | G | A | 4 | a0001c0001t0002g0042 a0001c0001t0002g0043 a0001c0001t0002g0286 others(1): Show |
6 | HG01175.hp1 HG01943.hp1 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.402+1239G>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60530699 | |||||||
| chr11:60530826 | G | A | 1 | a0002c0003t0001g0212 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.402+1366G>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60530826 | |||||||
| chr11:60530861 | T | A | 1 | a0001c0001t0007g0200 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.402+1401T>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60530861 | |||||||
| chr11:60530914 | AG | A | 89 | a0002c0002t0001g0012 a0002c0002t0001g0038 a0002c0002t0001g0039 others(86): Show |
100 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.402+1456delG | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 60530914 | ||||||
| chr11:60530916 | G | A | 1 | a0001c0001t0007g0200 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.402+1456G>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60530916 | |||||||
| chr11:60530940 | G | A | 3 | a0001c0001t0001g0009 a0001c0001t0001g0081 a0001c0001t0001g0162 |
5 | NA18957.hp2 NA18964.hp2 NA18991.hp1 others(2): Show |
intron_variant | MODIFIER | c.402+1480G>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60530940 | |||||||
| chr11:60530970 | A | C | 89 | a0002c0002t0001g0012 a0002c0002t0001g0038 a0002c0002t0001g0039 others(86): Show |
100 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.402+1510A>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60530970 | |||||||
| chr11:60530998 | A | G | 3 | a0001c0001t0001g0186 a0001c0001t0001g0188 a0001c0001t0001g0189 |
3 | HG02886.hp1 HG06807.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.402+1538A>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60530998 | |||||||
| chr11:60531068 | T | C | 89 | a0002c0002t0001g0012 a0002c0002t0001g0038 a0002c0002t0001g0039 others(86): Show |
100 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.402+1608T>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60531068 | |||||||
| chr11:60531091 | C | T | 89 | a0002c0002t0001g0012 a0002c0002t0001g0038 a0002c0002t0001g0039 others(86): Show |
100 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.402+1631C>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60531091 | |||||||
| chr11:60531107 | G | C | 27 | a0002c0002t0001g0038 a0002c0002t0001g0039 a0002c0002t0001g0253 others(24): Show |
29 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(26): Show |
intron_variant | MODIFIER | c.402+1647G>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60531107 | |||||||
| chr11:60531187 | A | T | 89 | a0002c0002t0001g0012 a0002c0002t0001g0038 a0002c0002t0001g0039 others(86): Show |
100 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.402+1727A>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60531187 | |||||||
| chr11:60531251 | A | G | 1 | a0001c0001t0001g0128 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.402+1791A>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60531251 | |||||||
| chr11:60531272 | A | G | 89 | a0002c0002t0001g0012 a0002c0002t0001g0038 a0002c0002t0001g0039 others(86): Show |
100 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.402+1812A>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60531272 | |||||||
| chr11:60531314 | A | C | 1 | a0001c0001t0002g0283 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.402+1854A>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60531314 | |||||||
| chr11:60531331 | T | C | 4 | a0001c0001t0001g0018 a0001c0001t0001g0078 a0001c0001t0001g0079 others(1): Show |
5 | NA18944.hp1 NA18966.hp1 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.402+1871T>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60531331 | |||||||
| chr11:60531490 | A | G | 27 | a0002c0002t0001g0038 a0002c0002t0001g0039 a0002c0002t0001g0253 others(24): Show |
29 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(26): Show |
intron_variant | MODIFIER | c.402+2030A>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60531490 | |||||||
| chr11:60531577 | G | A | 1 | a0001c0001t0001g0125 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.402+2117G>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60531577 | |||||||
| chr11:60531656 | C | T | 89 | a0002c0002t0001g0012 a0002c0002t0001g0038 a0002c0002t0001g0039 others(86): Show |
100 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.402+2196C>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60531656 | |||||||
| chr11:60531759 | G | A | 1 | a0001c0001t0002g0313 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.402+2299G>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60531759 | |||||||
| chr11:60531764 | C | T | 1 | a0002c0003t0001g0243 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.402+2304C>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60531764 | |||||||
| chr11:60531806 | T | A | 1 | a0001c0001t0001g0231 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.402+2346T>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60531806 | |||||||
| chr11:60531857 | G | A | 89 | a0002c0002t0001g0012 a0002c0002t0001g0038 a0002c0002t0001g0039 others(86): Show |
100 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.402+2397G>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60531857 | |||||||
| chr11:60531910 | G | C | 1 | a0001c0001t0002g0327 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.402+2450G>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60531910 | |||||||
| chr11:60531998 | T | A | 1 | a0001c0001t0001g0101 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.402+2538T>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60531998 | |||||||
| chr11:60532038 | T | A | 4 | a0002c0002t0001g0012 a0002c0002t0001g0250 a0002c0002t0001g0251 others(1): Show |
6 | HG01168.hp2 HG01169.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.402+2578T>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60532038 | |||||||
| chr11:60532092 | G | A | 1 | a0001c0001t0002g0330 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.402+2632G>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60532092 | |||||||
| chr11:60532150 | G | C | 5 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(2): Show |
5 | HG00609.hp2 HG02155.hp2 NA18943.hp1 others(2): Show |
intron_variant | MODIFIER | c.402+2690G>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60532150 | |||||||
| chr11:60532179 | C | T | 97 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0167 others(94): Show |
131 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.402+2719C>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60532179 | |||||||
| chr11:60532189 | C | G | 1 | a0002c0002t0001g0273 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.402+2729C>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60532189 | |||||||
| chr11:60532196 | G | A | 1 | a0002c0002t0003g0049 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.402+2736G>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60532196 | |||||||
| chr11:60532324 | G | A | 2 | a0002c0002t0003g0058 a0002c0002t0003g0059 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.402+2864G>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60532324 | |||||||
| chr11:60532331 | G | A | 6 | a0001c0001t0002g0283 a0001c0001t0002g0305 a0001c0001t0002g0306 others(3): Show |
6 | HG02165.hp1 NA18950.hp1 NA18973.hp1 others(3): Show |
intron_variant | MODIFIER | c.402+2871G>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60532331 | |||||||
| chr11:60532333 | A | C | 1 | a0002c0002t0001g0278 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.402+2873A>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60532333 | |||||||
| chr11:60532356 | C | T | 1 | a0001c0001t0001g0160 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.402+2896C>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60532356 | |||||||
| chr11:60532365 | T | G | 89 | a0002c0002t0001g0012 a0002c0002t0001g0038 a0002c0002t0001g0039 others(86): Show |
100 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.402+2905T>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60532365 | |||||||
| chr11:60532380 | G | A | 2 | a0002c0002t0001g0012 a0002c0002t0001g0250 |
4 | HG01168.hp2 HG01169.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.402+2920G>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60532380 | |||||||
| chr11:60532412 | G | T | 1 | a0002c0003t0001g0240 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.402+2952G>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60532412 | |||||||
| chr11:60532413 | A | C | 1 | a0002c0003t0001g0240 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.402+2953A>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60532413 | |||||||
| chr11:60532414 | C | G | 1 | a0002c0003t0001g0240 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.402+2954C>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60532414 | |||||||
| chr11:60532415 | G | T | 1 | a0002c0003t0001g0240 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.402+2955G>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60532415 | |||||||
| chr11:60532421 | G | T | 1 | a0002c0003t0001g0240 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.402+2961G>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60532421 | |||||||
| chr11:60532426 | A | C | 1 | a0002c0003t0001g0240 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.402+2966A>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60532426 | |||||||
| chr11:60532432 | T | G | 1 | a0002c0003t0001g0240 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.402+2972T>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60532432 | |||||||
| chr11:60532433 | C | A | 1 | a0002c0003t0001g0240 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.402+2973C>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60532433 | |||||||
| chr11:60532444 | G | T | 1 | a0001c0001t0002g0285 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.402+2984G>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60532444 | |||||||
| chr11:60532457 | T | C | 1 | a0002c0003t0001g0240 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.402+2997T>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60532457 | |||||||
| chr11:60532458 | T | C | 1 | a0002c0003t0001g0240 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.402+2998T>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60532458 | |||||||
| chr11:60532462 | A | T | 1 | a0002c0003t0001g0240 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.402+3002A>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60532462 | |||||||
| chr11:60532463 | C | G | 1 | a0002c0003t0001g0240 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.402+3003C>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60532463 | |||||||
| chr11:60532476 | C | A | 1 | a0002c0003t0001g0240 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.402+3016C>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60532476 | |||||||
| chr11:60532476 | C | T | 2 | a0001c0001t0001g0133 a0001c0001t0001g0161 |
2 | HG01175.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.402+3016C>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60532476 | |||||||
| chr11:60532477 | G | A | 5 | a0001c0001t0001g0165 a0002c0002t0001g0012 a0002c0002t0001g0250 others(2): Show |
7 | HG01168.hp2 HG01169.hp1 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.402+3017G>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60532477 | |||||||
| chr11:60532478 | G | C | 1 | a0002c0003t0001g0240 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.402+3018G>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60532478 | |||||||
| chr11:60532480 | G | T | 1 | a0002c0003t0001g0240 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.402+3020G>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60532480 | |||||||
| chr11:60532482 | A | G | 1 | a0002c0003t0001g0240 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.402+3022A>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60532482 | |||||||
| chr11:60532485 | A | C | 1 | a0002c0003t0001g0240 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.402+3025A>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60532485 | |||||||
| chr11:60532486 | G | T | 1 | a0002c0003t0001g0240 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.402+3026G>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60532486 | |||||||
| chr11:60532488 | A | C | 1 | a0002c0003t0001g0240 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.402+3028A>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60532488 | |||||||
| chr11:60532489 | G | T | 1 | a0002c0003t0001g0240 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.402+3029G>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60532489 | |||||||
| chr11:60532490 | A | T | 1 | a0002c0003t0001g0240 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.402+3030A>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60532490 | |||||||
| chr11:60532492 | T | G | 1 | a0002c0003t0001g0240 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.402+3032T>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60532492 | |||||||
| chr11:60532493 | A | G | 1 | a0002c0003t0001g0240 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.402+3033A>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60532493 | |||||||
| chr11:60532494 | T | C | 1 | a0002c0003t0001g0240 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.402+3034T>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60532494 | |||||||
| chr11:60532495 | A | C | 1 | a0002c0003t0001g0240 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.402+3035A>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60532495 | |||||||
| chr11:60532498 | C | G | 1 | a0002c0003t0001g0240 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.402+3038C>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60532498 | |||||||
| chr11:60532500 | A | G | 1 | a0002c0003t0001g0240 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.402+3040A>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60532500 | |||||||
| chr11:60532501 | C | T | 37 | a0002c0003t0001g0011 a0002c0003t0001g0031 a0002c0003t0001g0032 others(34): Show |
41 | HG00280.hp1 HG00408.hp1 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.402+3041C>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60532501 | |||||||
| chr11:60532504 | C | T | 1 | a0002c0003t0001g0240 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.402+3044C>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60532504 | |||||||
| chr11:60532506 | G | T | 1 | a0002c0003t0001g0240 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.402+3046G>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60532506 | |||||||
| chr11:60532509 | T | A | 1 | a0002c0003t0001g0240 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.402+3049T>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60532509 | |||||||
| chr11:60532512 | G | C | 1 | a0002c0003t0001g0240 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.402+3052G>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60532512 | |||||||
| chr11:60532514 | G | C | 1 | a0002c0003t0001g0240 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.402+3054G>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60532514 | |||||||
| chr11:60532515 | G | T | 1 | a0002c0003t0001g0240 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.402+3055G>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60532515 | |||||||
| chr11:60532517 | T | G | 1 | a0002c0003t0001g0240 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.402+3057T>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60532517 | |||||||
| chr11:60532529 | G | T | 1 | a0002c0003t0001g0240 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.402+3069G>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60532529 | |||||||
| chr11:60532560 | C | G | 323 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(320): Show |
403 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(400): Show |
intron_variant | MODIFIER | c.402+3100C>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60532560 | |||||||
| chr11:60532573 | G | C | 1 | a0003c0004t0001g0182 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.402+3113G>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60532573 | |||||||
| chr11:60532588 | T | C | 89 | a0002c0002t0001g0012 a0002c0002t0001g0038 a0002c0002t0001g0039 others(86): Show |
100 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.402+3128T>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60532588 | |||||||
| chr11:60532600 | C | T | 1 | a0001c0001t0002g0183 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.402+3140C>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60532600 | |||||||
| chr11:60532613 | G | C | 1 | a0001c0001t0002g0305 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.402+3153G>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60532613 | |||||||
| chr11:60532638 | A | G | 1 | a0001c0001t0001g0061 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.402+3178A>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60532638 | |||||||
| chr11:60532669 | C | G | 7 | a0002c0002t0004g0036 a0002c0002t0004g0037 a0002c0002t0004g0245 others(4): Show |
9 | HG01069.hp2 HG01070.hp1 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.402+3209C>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60532669 | |||||||
| chr11:60532704 | C | G | 1 | a0002c0002t0003g0016 | 2 | HG02970.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.402+3244C>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60532704 | |||||||
| chr11:60532784 | T | C | 4 | a0002c0002t0001g0012 a0002c0002t0001g0250 a0002c0002t0001g0251 others(1): Show |
6 | HG01168.hp2 HG01169.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.402+3324T>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60532784 | |||||||
| chr11:60532830 | C | T | 7 | a0002c0002t0004g0036 a0002c0002t0004g0037 a0002c0002t0004g0245 others(4): Show |
9 | HG01069.hp2 HG01070.hp1 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.402+3370C>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60532830 | |||||||
| chr11:60532926 | C | T | 2 | a0002c0002t0001g0251 a0002c0002t0001g0252 |
2 | HG01261.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.402+3466C>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60532926 | |||||||
| chr11:60532928 | G | A | 27 | a0002c0002t0001g0038 a0002c0002t0001g0039 a0002c0002t0001g0253 others(24): Show |
29 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(26): Show |
intron_variant | MODIFIER | c.402+3468G>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60532928 | |||||||
| chr11:60533008 | A | G | 88 | a0002c0002t0001g0012 a0002c0002t0001g0038 a0002c0002t0001g0039 others(85): Show |
99 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.402+3548A>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60533008 | |||||||
| chr11:60533030 | AT | A | 4 | a0002c0002t0001g0012 a0002c0002t0001g0250 a0002c0002t0001g0251 others(1): Show |
6 | HG01168.hp2 HG01169.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.402+3571delT | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60533030 | |||||||
| chr11:60533112 | C | T | 4 | a0002c0002t0001g0012 a0002c0002t0001g0250 a0002c0002t0001g0251 others(1): Show |
6 | HG01168.hp2 HG01169.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.402+3652C>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60533112 | |||||||
| chr11:60533141 | C | A | 2 | a0001c0001t0001g0023 a0001c0001t0001g0144 |
3 | HG01516.hp2 HG01517.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.402+3681C>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60533141 | |||||||
| chr11:60533153 | C | T | 2 | a0001c0001t0001g0153 a0001c0001t0001g0154 |
2 | HG00609.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.402+3693C>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60533153 | |||||||
| chr11:60533212 | T | C | 1 | a0001c0001t0002g0057 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.402+3752T>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60533212 | |||||||
| chr11:60533230 | C | T | 49 | a0002c0002t0001g0038 a0002c0002t0001g0039 a0002c0002t0001g0253 others(46): Show |
54 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.402+3770C>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60533230 | |||||||
| chr11:60533257 | A | G | 323 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(320): Show |
403 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(400): Show |
intron_variant | MODIFIER | c.402+3797A>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60533257 | |||||||
| chr11:60533258 | A | C | 1 | a0001c0001t0001g0112 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.402+3798A>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60533258 | |||||||
| chr11:60533271 | C | T | 89 | a0002c0002t0001g0012 a0002c0002t0001g0038 a0002c0002t0001g0039 others(86): Show |
100 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.402+3811C>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60533271 | |||||||
| chr11:60533283 | A | C | 4 | a0002c0002t0001g0012 a0002c0002t0001g0250 a0002c0002t0001g0251 others(1): Show |
6 | HG01168.hp2 HG01169.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.402+3823A>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60533283 | |||||||
| chr11:60533328 | G | A | 1 | a0001c0001t0002g0184 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.402+3868G>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60533328 | |||||||
| chr11:60533336 | T | A | 1 | a0002c0003t0001g0213 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.402+3876T>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60533336 | |||||||
| chr11:60533356 | C | T | 8 | a0002c0002t0001g0039 a0002c0002t0001g0253 a0002c0002t0001g0258 others(5): Show |
9 | HG01081.hp1 HG01099.hp2 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.402+3896C>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60533356 | |||||||
| chr11:60533357 | A | G | 89 | a0002c0002t0001g0012 a0002c0002t0001g0038 a0002c0002t0001g0039 others(86): Show |
100 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.402+3897A>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60533357 | |||||||
| chr11:60533392 | C | T | 1 | a0001c0001t0001g0194 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.402+3932C>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60533392 | |||||||
| chr11:60533393 | G | A | 8 | a0003c0004t0001g0176 a0003c0004t0001g0177 a0003c0004t0001g0178 others(5): Show |
9 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.402+3933G>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60533393 | |||||||
| chr11:60533424 | A | G | 1 | a0001c0001t0001g0116 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.402+3964A>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60533424 | |||||||
| chr11:60533460 | G | A | 89 | a0002c0002t0001g0012 a0002c0002t0001g0038 a0002c0002t0001g0039 others(86): Show |
100 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.402+4000G>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60533460 | |||||||
| chr11:60533539 | C | T | 4 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(1): Show |
4 | HG02647.hp2 HG02717.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.402+4079C>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60533539 | |||||||
| chr11:60533540 | G | A | 7 | a0002c0002t0004g0036 a0002c0002t0004g0037 a0002c0002t0004g0245 others(4): Show |
9 | HG01069.hp2 HG01070.hp1 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.402+4080G>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60533540 | |||||||
| chr11:60533557 | A | G | 89 | a0002c0002t0001g0012 a0002c0002t0001g0038 a0002c0002t0001g0039 others(86): Show |
100 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.402+4097A>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60533557 | |||||||
| chr11:60533562 | T | G | 89 | a0002c0002t0001g0012 a0002c0002t0001g0038 a0002c0002t0001g0039 others(86): Show |
100 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.402+4102T>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60533562 | |||||||
| chr11:60533563 | G | A | 89 | a0002c0002t0001g0012 a0002c0002t0001g0038 a0002c0002t0001g0039 others(86): Show |
100 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.402+4103G>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60533563 | |||||||
| chr11:60533567 | G | T | 89 | a0002c0002t0001g0012 a0002c0002t0001g0038 a0002c0002t0001g0039 others(86): Show |
100 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.402+4107G>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60533567 | |||||||
| chr11:60533580 | CAAGTTGG others(73): Show |
C | 89 | a0002c0002t0001g0012 a0002c0002t0001g0038 a0002c0002t0001g0039 others(86): Show |
100 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.402+4123_402+4202d others(82): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 60533580 | ||||||
| chr11:60533655 | T | A | 1 | a0001c0001t0001g0003 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.402+4195T>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60533655 | |||||||
| chr11:60533667 | G | C | 1 | a0001c0001t0002g0317 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.402+4207G>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60533667 | |||||||
| chr11:60533672 | C | T | 97 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0167 others(94): Show |
131 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.402+4212C>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60533672 | |||||||
| chr11:60533825 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.402+4365C>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60533825 | |||||||
| chr11:60533839 | C | T | 38 | a0002c0003t0001g0011 a0002c0003t0001g0031 a0002c0003t0001g0032 others(35): Show |
42 | HG00280.hp1 HG00408.hp1 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.402+4379C>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60533839 | |||||||
| chr11:60533877 | G | T | 42 | a0002c0002t0001g0012 a0002c0002t0001g0250 a0002c0002t0001g0251 others(39): Show |
48 | HG00280.hp1 HG00408.hp1 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.402+4417G>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60533877 | |||||||
| chr11:60534023 | C | T | 89 | a0002c0002t0001g0012 a0002c0002t0001g0038 a0002c0002t0001g0039 others(86): Show |
100 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.402+4563C>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60534023 | |||||||
| chr11:60534039 | G | T | 13 | a0002c0002t0003g0016 a0002c0002t0003g0047 a0002c0002t0003g0048 others(10): Show |
14 | HG01069.hp1 HG01071.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.402+4579G>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60534039 | |||||||
| chr11:60534050 | A | G | 3 | a0002c0002t0003g0054 a0002c0002t0003g0055 a0002c0002t0003g0056 |
3 | HG02055.hp1 HG02559.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.402+4590A>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60534050 | |||||||
| chr11:60534057 | G | A | 90 | a0001c0001t0007g0200 a0002c0002t0001g0012 a0002c0002t0001g0038 others(87): Show |
101 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.402+4597G>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60534057 | |||||||
| chr11:60534118 | T | C | 228 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(225): Show |
274 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(271): Show |
intron_variant | MODIFIER | c.402+4658T>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60534118 | |||||||
| chr11:60534128 | C | A | 2 | a0001c0001t0001g0127 a0001c0001t0001g0131 |
2 | HG02027.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.402+4668C>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60534128 | |||||||
| chr11:60534189 | A | G | 1 | a0001c0001t0002g0314 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.402+4729A>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60534189 | |||||||
| chr11:60534316 | G | C | 1 | a0001c0001t0001g0110 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.402+4856G>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60534316 | |||||||
| chr11:60534374 | T | G | 89 | a0002c0002t0001g0012 a0002c0002t0001g0038 a0002c0002t0001g0039 others(86): Show |
100 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.402+4914T>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60534374 | |||||||
| chr11:60534465 | G | A | 4 | a0002c0002t0001g0012 a0002c0002t0001g0250 a0002c0002t0001g0251 others(1): Show |
6 | HG01168.hp2 HG01169.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.402+5005G>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60534465 | |||||||
| chr11:60534489 | T | G | 3 | a0001c0001t0001g0186 a0001c0001t0001g0188 a0001c0001t0001g0189 |
3 | HG02886.hp1 HG06807.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.402+5029T>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60534489 | |||||||
| chr11:60534519 | A | G | 1 | a0002c0003t0001g0226 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.402+5059A>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60534519 | |||||||
| chr11:60534531 | G | C | 1 | a0001c0001t0001g0089 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.402+5071G>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60534531 | |||||||
| chr11:60534555 | C | A | 9 | a0001c0001t0002g0014 a0001c0001t0002g0290 a0001c0001t0002g0308 others(6): Show |
11 | HG00735.hp2 HG02015.hp1 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.402+5095C>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60534555 | |||||||
| chr11:60534627 | C | T | 38 | a0002c0003t0001g0011 a0002c0003t0001g0031 a0002c0003t0001g0032 others(35): Show |
42 | HG00280.hp1 HG00408.hp1 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.402+5167C>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60534627 | |||||||
| chr11:60534634 | G | C | 38 | a0002c0003t0001g0011 a0002c0003t0001g0031 a0002c0003t0001g0032 others(35): Show |
42 | HG00280.hp1 HG00408.hp1 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.402+5174G>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60534634 | |||||||
| chr11:60534668 | C | T | 27 | a0002c0002t0001g0038 a0002c0002t0001g0039 a0002c0002t0001g0253 others(24): Show |
29 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(26): Show |
intron_variant | MODIFIER | c.402+5208C>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60534668 | |||||||
| chr11:60534669 | G | A | 20 | a0002c0002t0003g0016 a0002c0002t0003g0047 a0002c0002t0003g0048 others(17): Show |
23 | HG01069.hp1 HG01069.hp2 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.402+5209G>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60534669 | |||||||
| chr11:60534699 | C | T | 6 | a0001c0001t0001g0021 a0001c0001t0001g0090 a0001c0001t0001g0091 others(3): Show |
7 | HG00099.hp2 HG01943.hp2 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.402+5239C>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60534699 | |||||||
| chr11:60534766 | G | T | 1 | a0001c0001t0001g0149 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.402+5306G>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60534766 | |||||||
| chr11:60534768 | T | G | 1 | a0001c0001t0001g0149 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.402+5308T>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60534768 | |||||||
| chr11:60534780 | T | G | 1 | a0001c0001t0002g0184 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.402+5320T>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60534780 | |||||||
| chr11:60534880 | C | T | 2 | a0003c0004t0001g0177 a0003c0004t0001g0178 |
2 | HG02622.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.402+5420C>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60534880 | |||||||
| chr11:60534881 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.402+5421G>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60534881 | |||||||
| chr11:60534936 | C | A | 1 | a0001c0001t0002g0327 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.402+5476C>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60534936 | |||||||
| chr11:60534958 | G | A | 89 | a0002c0002t0001g0012 a0002c0002t0001g0038 a0002c0002t0001g0039 others(86): Show |
100 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.402+5498G>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60534958 | |||||||
| chr11:60534975 | C | T | 137 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(134): Show |
172 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(169): Show |
intron_variant | MODIFIER | c.402+5515C>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60534975 | |||||||
| chr11:60534977 | A | G | 132 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(129): Show |
167 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.402+5517A>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60534977 | |||||||
| chr11:60535012 | G | T | 4 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(1): Show |
4 | HG02647.hp2 HG02717.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.402+5552G>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60535012 | |||||||
| chr11:60535057 | T | C | 2 | a0001c0001t0001g0065 a0001c0001t0001g0066 |
2 | HG02630.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.402+5597T>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60535057 | |||||||
| chr11:60535129 | C | A | 14 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0167 others(11): Show |
16 | HG01243.hp2 HG01496.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.402+5669C>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60535129 | |||||||
| chr11:60535155 | G | C | 89 | a0002c0002t0001g0012 a0002c0002t0001g0038 a0002c0002t0001g0039 others(86): Show |
100 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.402+5695G>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60535155 | |||||||
| chr11:60535167 | C | T | 92 | a0001c0001t0002g0292 a0001c0001t0002g0302 a0001c0001t0002g0304 others(89): Show |
103 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.402+5707C>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60535167 | |||||||
| chr11:60535168 | A | G | 1 | a0001c0001t0002g0302 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.402+5708A>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60535168 | |||||||
| chr11:60535170 | A | G | 1 | a0001c0001t0002g0302 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.402+5710A>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60535170 | |||||||
| chr11:60535174 | A | C | 1 | a0001c0001t0002g0302 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.402+5714A>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60535174 | |||||||
| chr11:60535246 | G | T | 4 | a0002c0002t0001g0012 a0002c0002t0001g0250 a0002c0002t0001g0251 others(1): Show |
6 | HG01168.hp2 HG01169.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.402+5786G>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60535246 | |||||||
| chr11:60535259 | A | G | 1 | a0001c0001t0001g0068 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.402+5799A>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60535259 | |||||||
| chr11:60535271 | C | T | 38 | a0002c0003t0001g0011 a0002c0003t0001g0031 a0002c0003t0001g0032 others(35): Show |
42 | HG00280.hp1 HG00408.hp1 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.402+5811C>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60535271 | |||||||
| chr11:60535351 | A | G | 1 | a0001c0001t0001g0075 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.402+5891A>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60535351 | |||||||
| chr11:60535384 | T | C | 4 | a0001c0001t0002g0030 a0001c0001t0002g0190 a0001c0001t0002g0191 others(1): Show |
5 | HG02922.hp1 HG03225.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.402+5924T>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60535384 | |||||||
| chr11:60535431 | G | A | 1 | a0001c0001t0001g0017 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.402+5971G>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60535431 | |||||||
| chr11:60535456 | C | G | 89 | a0002c0002t0001g0012 a0002c0002t0001g0038 a0002c0002t0001g0039 others(86): Show |
100 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.402+5996C>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60535456 | |||||||
| chr11:60535458 | G | C | 89 | a0002c0002t0001g0012 a0002c0002t0001g0038 a0002c0002t0001g0039 others(86): Show |
100 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.402+5998G>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60535458 | |||||||
| chr11:60535482 | A | T | 47 | a0002c0002t0001g0038 a0002c0002t0001g0039 a0002c0002t0001g0253 others(44): Show |
52 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.402+6022A>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60535482 | |||||||
| chr11:60535509 | C | A | 1 | a0001c0001t0001g0193 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.402+6049C>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60535509 | |||||||
| chr11:60535541 | CA | C | 9 | a0001c0001t0002g0014 a0001c0001t0002g0290 a0001c0001t0002g0308 others(6): Show |
11 | HG00735.hp2 HG02015.hp1 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.402+6083delA | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 60535541 | ||||||
| chr11:60535588 | C | A | 1 | a0002c0002t0001g0256 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.402+6128C>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60535588 | |||||||
| chr11:60535684 | A | G | 1 | a0003c0004t0001g0182 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.402+6224A>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60535684 | |||||||
| chr11:60535762 | G | A | 1 | a0001c0001t0002g0296 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.402+6302G>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60535762 | |||||||
| chr11:60535763 | CA | C | 4 | a0002c0002t0001g0012 a0002c0002t0001g0250 a0002c0002t0001g0251 others(1): Show |
6 | HG01168.hp2 HG01169.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.402+6308delA | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 60535763 | ||||||
| chr11:60535768 | A | G | 4 | a0002c0002t0001g0012 a0002c0002t0001g0250 a0002c0002t0001g0251 others(1): Show |
6 | HG01168.hp2 HG01169.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.402+6308A>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60535768 | |||||||
| chr11:60535783 | C | A | 1 | a0003c0004t0001g0172 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.402+6323C>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60535783 | |||||||
| chr11:60535792 | C | T | 2 | a0001c0001t0002g0296 a0001c0001t0002g0334 |
2 | HG00597.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.402+6332C>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60535792 | |||||||
| chr11:60535793 | G | A | 1 | a0001c0001t0002g0327 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.402+6333G>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60535793 | |||||||
| chr11:60535794 | A | C | 132 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(129): Show |
167 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.402+6334A>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60535794 | |||||||
| chr11:60535873 | C | T | 1 | a0002c0003t0001g0204 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.402+6413C>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60535873 | |||||||
| chr11:60535874 | G | A | 2 | a0001c0001t0002g0318 a0002c0003t0001g0208 |
2 | HG02300.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.402+6414G>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60535874 | |||||||
| chr11:60535883 | T | C | 1 | a0001c0001t0002g0190 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.402+6423T>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60535883 | |||||||
| chr11:60535883 | T | G | 2 | a0004c0005t0002g0287 a0004c0005t0002g0297 |
2 | NA18941.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.402+6423T>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60535883 | |||||||
| chr11:60535909 | G | A | 1 | a0003c0004t0001g0177 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.402+6449G>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60535909 | |||||||
| chr11:60535976 | C | G | 7 | a0002c0002t0004g0036 a0002c0002t0004g0037 a0002c0002t0004g0245 others(4): Show |
9 | HG01069.hp2 HG01070.hp1 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.402+6516C>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60535976 | |||||||
| chr11:60535990 | A | G | 89 | a0002c0002t0001g0012 a0002c0002t0001g0038 a0002c0002t0001g0039 others(86): Show |
100 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.403-6529A>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60535990 | |||||||
| chr11:60536018 | C | T | 2 | a0003c0004t0001g0174 a0003c0004t0001g0175 |
2 | HG01243.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.403-6501C>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60536018 | |||||||
| chr11:60536038 | G | C | 89 | a0002c0002t0001g0012 a0002c0002t0001g0038 a0002c0002t0001g0039 others(86): Show |
100 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.403-6481G>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60536038 | |||||||
| chr11:60536121 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.403-6398G>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60536121 | |||||||
| chr11:60536138 | C | T | 3 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0109 |
3 | HG01074.hp2 HG01257.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.403-6381C>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60536138 | |||||||
| chr11:60536156 | T | C | 89 | a0002c0002t0001g0012 a0002c0002t0001g0038 a0002c0002t0001g0039 others(86): Show |
100 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.403-6363T>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60536156 | |||||||
| chr11:60536209 | C | G | 38 | a0002c0003t0001g0011 a0002c0003t0001g0031 a0002c0003t0001g0032 others(35): Show |
42 | HG00280.hp1 HG00408.hp1 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.403-6310C>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60536209 | |||||||
| chr11:60536229 | C | G | 89 | a0002c0002t0001g0012 a0002c0002t0001g0038 a0002c0002t0001g0039 others(86): Show |
100 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.403-6290C>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60536229 | |||||||
| chr11:60536250 | T | C | 89 | a0002c0002t0001g0012 a0002c0002t0001g0038 a0002c0002t0001g0039 others(86): Show |
100 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.403-6269T>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60536250 | |||||||
| chr11:60536289 | C | A | 97 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0167 others(94): Show |
131 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.403-6230C>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60536289 | |||||||
| chr11:60536310 | A | C | 1 | a0001c0001t0001g0143 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.403-6209A>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60536310 | |||||||
| chr11:60536327 | T | A | 1 | a0001c0001t0002g0280 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.403-6192T>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60536327 | |||||||
| chr11:60536331 | A | T | 1 | a0003c0004t0005g0171 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.403-6188A>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60536331 | |||||||
| chr11:60536379 | T | C | 323 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(320): Show |
403 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(400): Show |
intron_variant | MODIFIER | c.403-6140T>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60536379 | |||||||
| chr11:60536413 | A | C | 89 | a0002c0002t0001g0012 a0002c0002t0001g0038 a0002c0002t0001g0039 others(86): Show |
100 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.403-6106A>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60536413 | |||||||
| chr11:60536416 | A | C | 89 | a0002c0002t0001g0012 a0002c0002t0001g0038 a0002c0002t0001g0039 others(86): Show |
100 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.403-6103A>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60536416 | |||||||
| chr11:60536471 | A | C | 1 | a0001c0001t0001g0063 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.403-6048A>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60536471 | |||||||
| chr11:60536531 | C | T | 2 | a0001c0001t0001g0111 a0001c0001t0001g0140 |
2 | HG02132.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.403-5988C>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60536531 | |||||||
| chr11:60536558 | C | A | 2 | a0001c0001t0001g0021 a0001c0001t0001g0166 |
3 | HG00099.hp2 HG01943.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.403-5961C>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60536558 | |||||||
| chr11:60536580 | C | T | 89 | a0002c0002t0001g0012 a0002c0002t0001g0038 a0002c0002t0001g0039 others(86): Show |
100 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.403-5939C>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60536580 | |||||||
| chr11:60536657 | C | A | 7 | a0001c0001t0001g0004 a0001c0001t0001g0077 a0001c0001t0001g0097 others(4): Show |
11 | HG00544.hp1 HG00597.hp2 HG00621.hp2 others(8): Show |
intron_variant | MODIFIER | c.403-5862C>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60536657 | |||||||
| chr11:60536687 | T | C | 1 | a0002c0003t0001g0226 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.403-5832T>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60536687 | |||||||
| chr11:60536708 | G | A | 1 | a0001c0001t0001g0035 | 2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.403-5811G>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60536708 | |||||||
| chr11:60536712 | T | C | 89 | a0002c0002t0001g0012 a0002c0002t0001g0038 a0002c0002t0001g0039 others(86): Show |
100 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.403-5807T>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60536712 | |||||||
| chr11:60536743 | G | A | 132 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(129): Show |
167 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.403-5776G>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60536743 | |||||||
| chr11:60536757 | A | C | 1 | a0003c0004t0001g0173 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.403-5762A>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60536757 | |||||||
| chr11:60536843 | A | G | 1 | a0002c0003t0001g0277 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.403-5676A>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60536843 | |||||||
| chr11:60536867 | T | A | 4 | a0002c0002t0001g0012 a0002c0002t0001g0250 a0002c0002t0001g0251 others(1): Show |
6 | HG01168.hp2 HG01169.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.403-5652T>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60536867 | |||||||
| chr11:60536949 | G | T | 1 | a0001c0001t0001g0201 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.403-5570G>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60536949 | |||||||
| chr11:60537161 | C | A | 1 | a0003c0004t0001g0182 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.403-5358C>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60537161 | |||||||
| chr11:60537214 | G | C | 1 | a0001c0001t0002g0280 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.403-5305G>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60537214 | |||||||
| chr11:60537245 | C | T | 1 | a0001c0001t0002g0315 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.403-5274C>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60537245 | |||||||
| chr11:60537248 | C | A | 1 | a0001c0001t0001g0239 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.403-5271C>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60537248 | |||||||
| chr11:60537326 | A | G | 2 | a0001c0001t0001g0115 a0001c0001t0001g0119 |
2 | NA18972.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.403-5193A>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60537326 | |||||||
| chr11:60537337 | AC | A | 13 | a0002c0002t0003g0016 a0002c0002t0003g0047 a0002c0002t0003g0048 others(10): Show |
14 | HG01069.hp1 HG01071.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.403-5181delC | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60537337 | |||||||
| chr11:60537423 | A | G | 1 | a0001c0001t0002g0301 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.403-5096A>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60537423 | |||||||
| chr11:60537557 | A | G | 323 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(320): Show |
403 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(400): Show |
intron_variant | MODIFIER | c.403-4962A>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60537557 | |||||||
| chr11:60537642 | A | G | 2 | a0001c0001t0001g0193 a0001c0001t0001g0198 |
2 | HG02723.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.403-4877A>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60537642 | |||||||
| chr11:60537690 | G | T | 87 | a0002c0002t0001g0012 a0002c0002t0001g0038 a0002c0002t0001g0039 others(84): Show |
98 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.403-4829G>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60537690 | |||||||
| chr11:60537862 | T | A | 3 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0006c0006t0001g0062 |
3 | HG00642.hp2 HG01099.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.403-4657T>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60537862 | |||||||
| chr11:60537962 | G | T | 1 | a0001c0001t0001g0116 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.403-4557G>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60537962 | |||||||
| chr11:60538028 | G | A | 3 | a0001c0001t0001g0035 a0001c0001t0001g0227 a0001c0001t0001g0233 |
4 | HG01496.hp1 HG02647.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.403-4491G>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60538028 | |||||||
| chr11:60538033 | C | T | 1 | a0003c0004t0001g0182 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.403-4486C>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60538033 | |||||||
| chr11:60538077 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.403-4442G>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60538077 | |||||||
| chr11:60538177 | T | TA | 10 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0070 others(7): Show |
10 | HG01891.hp1 HG02040.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.403-4328dupA | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 60538177 | ||||||
| chr11:60538177 | T | TTAA | 26 | a0002c0003t0001g0011 a0002c0003t0001g0032 a0002c0003t0001g0033 others(23): Show |
29 | HG00280.hp1 HG00408.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.403-4342_403-4341i others(5): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60538177 | |||||||
| chr11:60538177 | T | TTAAA | 9 | a0002c0003t0001g0031 a0002c0003t0001g0205 a0002c0003t0001g0210 others(6): Show |
10 | HG01952.hp2 HG02132.hp1 HG03098.hp1 others(7): Show |
intron_variant | MODIFIER | c.403-4342_403-4341i others(6): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60538177 | |||||||
| chr11:60538177 | T | TTAAAA | 40 | a0002c0002t0001g0038 a0002c0002t0001g0039 a0002c0002t0001g0253 others(37): Show |
43 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.403-4342_403-4341i others(7): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60538177 | |||||||
| chr11:60538177 | T | TTAAAAA | 8 | a0002c0002t0003g0058 a0002c0002t0004g0036 a0002c0002t0004g0037 others(5): Show |
10 | HG01069.hp1 HG01069.hp2 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.403-4342_403-4341i others(8): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60538177 | |||||||
| chr11:60538177 | TA | T | 9 | a0001c0001t0001g0006 a0001c0001t0001g0103 a0001c0001t0001g0113 others(6): Show |
12 | HG02280.hp2 HG02886.hp1 HG06807.hp1 others(9): Show |
intron_variant | MODIFIER | c.403-4328delA | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 60538177 | ||||||
| chr11:60538178 | A | T | 1 | a0002c0003t0001g0206 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.403-4341A>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60538178 | |||||||
| chr11:60538192 | C | A | 37 | a0002c0003t0001g0011 a0002c0003t0001g0031 a0002c0003t0001g0032 others(34): Show |
41 | HG00280.hp1 HG00408.hp1 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.403-4327C>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60538192 | |||||||
| chr11:60538193 | G | A | 37 | a0002c0003t0001g0011 a0002c0003t0001g0031 a0002c0003t0001g0032 others(34): Show |
41 | HG00280.hp1 HG00408.hp1 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.403-4326G>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60538193 | |||||||
| chr11:60538226 | A | G | 1 | a0002c0003t0001g0217 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.403-4293A>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60538226 | |||||||
| chr11:60538267 | G | A | 1 | a0001c0001t0001g0007 | 3 | HG01496.hp2 HG03688.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.403-4252G>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60538267 | |||||||
| chr11:60538314 | G | A | 1 | a0001c0001t0007g0200 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.403-4205G>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60538314 | |||||||
| chr11:60538323 | G | C | 1 | a0001c0001t0001g0123 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.403-4196G>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60538323 | |||||||
| chr11:60538350 | G | A | 1 | a0001c0001t0002g0291 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.403-4169G>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60538350 | |||||||
| chr11:60538407 | A | G | 3 | a0001c0001t0001g0186 a0001c0001t0001g0188 a0001c0001t0001g0189 |
3 | HG02886.hp1 HG06807.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.403-4112A>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60538407 | |||||||
| chr11:60538449 | ATATGAGG others(1): Show |
A | 4 | a0002c0002t0001g0012 a0002c0002t0001g0250 a0002c0002t0001g0251 others(1): Show |
6 | HG01168.hp2 HG01169.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.403-4064_403-4057d others(10): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 60538449 | ||||||
| chr11:60538566 | A | T | 2 | a0001c0001t0001g0335 a0001c0001t0001g0336 |
2 | HG01346.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.403-3953A>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60538566 | |||||||
| chr11:60538585 | TA | T | 179 | a0001c0001t0001g0035 a0001c0001t0001g0133 a0001c0001t0001g0161 others(176): Show |
223 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.403-3923delA | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 60538585 | ||||||
| chr11:60538586 | A | T | 3 | a0001c0001t0001g0186 a0001c0001t0001g0188 a0001c0001t0001g0189 |
3 | HG02886.hp1 HG06807.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.403-3933A>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60538586 | |||||||
| chr11:60538599 | G | T | 1 | a0001c0001t0001g0195 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.403-3920G>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60538599 | |||||||
| chr11:60538616 | A | C | 1 | a0001c0001t0001g0193 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.403-3903A>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60538616 | |||||||
| chr11:60538692 | G | T | 7 | a0002c0002t0004g0036 a0002c0002t0004g0037 a0002c0002t0004g0245 others(4): Show |
9 | HG01069.hp2 HG01070.hp1 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.403-3827G>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60538692 | |||||||
| chr11:60538713 | T | C | 323 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(320): Show |
403 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(400): Show |
intron_variant | MODIFIER | c.403-3806T>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60538713 | |||||||
| chr11:60538727 | C | G | 1 | a0002c0003t0001g0220 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.403-3792C>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60538727 | |||||||
| chr11:60538743 | A | G | 1 | a0002c0002t0001g0259 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.403-3776A>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60538743 | |||||||
| chr11:60538828 | G | C | 234 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(231): Show |
303 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(300): Show |
intron_variant | MODIFIER | c.403-3691G>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60538828 | |||||||
| chr11:60539026 | C | A | 1 | a0001c0001t0002g0302 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.403-3493C>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60539026 | |||||||
| chr11:60539061 | C | T | 1 | a0001c0001t0002g0185 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.403-3458C>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60539061 | |||||||
| chr11:60539183 | T | G | 1 | a0001c0001t0002g0308 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.403-3336T>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60539183 | |||||||
| chr11:60539189 | C | CA | 48 | a0002c0002t0001g0038 a0002c0002t0001g0039 a0002c0002t0001g0253 others(45): Show |
53 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.403-3311dupA | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 60539189 | ||||||
| chr11:60539189 | CA | C | 130 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(127): Show |
164 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(161): Show |
intron_variant | MODIFIER | c.403-3311delA | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 60539189 | ||||||
| chr11:60539189 | CAA | C | 76 | a0001c0001t0001g0022 a0001c0001t0001g0034 a0001c0001t0001g0035 others(73): Show |
106 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.403-3312_403-3311d others(4): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 60539189 | ||||||
| chr11:60539189 | CAAA | C | 27 | a0001c0001t0001g0168 a0001c0001t0002g0014 a0001c0001t0002g0030 others(24): Show |
32 | HG00558.hp2 HG00639.hp2 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.403-3313_403-3311d others(5): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 60539189 | ||||||
| chr11:60539294 | G | A | 89 | a0002c0002t0001g0012 a0002c0002t0001g0038 a0002c0002t0001g0039 others(86): Show |
100 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.403-3225G>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60539294 | |||||||
| chr11:60539404 | T | A | 89 | a0002c0002t0001g0012 a0002c0002t0001g0038 a0002c0002t0001g0039 others(86): Show |
100 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.403-3115T>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60539404 | |||||||
| chr11:60539667 | G | A | 1 | a0003c0004t0001g0182 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.403-2852G>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60539667 | |||||||
| chr11:60539701 | C | CA | 53 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0002c0002t0001g0012 others(50): Show |
60 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.403-2809dupA | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 60539701 | ||||||
| chr11:60539701 | C | CAA | 37 | a0002c0003t0001g0011 a0002c0003t0001g0032 a0002c0003t0001g0033 others(34): Show |
40 | HG00280.hp1 HG00408.hp1 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.403-2810_403-2809d others(4): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 60539701 | ||||||
| chr11:60539711 | T | C | 2 | a0001c0001t0002g0295 a0001c0001t0002g0315 |
2 | HG02683.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.403-2808T>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60539711 | |||||||
| chr11:60539744 | C | T | 4 | a0001c0001t0002g0030 a0001c0001t0002g0190 a0001c0001t0002g0191 others(1): Show |
5 | HG02922.hp1 HG03225.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.403-2775C>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60539744 | |||||||
| chr11:60539746 | A | G | 4 | a0002c0002t0001g0012 a0002c0002t0001g0250 a0002c0002t0001g0251 others(1): Show |
6 | HG01168.hp2 HG01169.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.403-2773A>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60539746 | |||||||
| chr11:60539868 | CA | C | 3 | a0002c0002t0003g0054 a0002c0002t0003g0055 a0002c0002t0003g0056 |
3 | HG02055.hp1 HG02559.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.403-2646delA | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 60539868 | ||||||
| chr11:60539917 | A | G | 14 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0167 others(11): Show |
16 | HG01243.hp2 HG01496.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.403-2602A>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60539917 | |||||||
| chr11:60539937 | A | C | 14 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0167 others(11): Show |
16 | HG01243.hp2 HG01496.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.403-2582A>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60539937 | |||||||
| chr11:60540002 | A | T | 1 | a0001c0001t0002g0331 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.403-2517A>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60540002 | |||||||
| chr11:60540123 | C | T | 17 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(14): Show |
26 | NA18944.hp1 NA18946.hp1 NA18947.hp1 others(23): Show |
intron_variant | MODIFIER | c.403-2396C>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60540123 | |||||||
| chr11:60540167 | A | G | 1 | a0001c0001t0001g0202 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.403-2352A>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60540167 | |||||||
| chr11:60540281 | A | G | 1 | a0001c0001t0002g0323 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.403-2238A>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60540281 | |||||||
| chr11:60540473 | G | A | 1 | a0001c0001t0002g0298 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.403-2046G>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60540473 | |||||||
| chr11:60540566 | T | C | 89 | a0002c0002t0001g0012 a0002c0002t0001g0038 a0002c0002t0001g0039 others(86): Show |
100 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.403-1953T>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60540566 | |||||||
| chr11:60540568 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.403-1951G>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60540568 | |||||||
| chr11:60540655 | G | A | 69 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0013 others(66): Show |
100 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.403-1864G>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60540655 | |||||||
| chr11:60540729 | A | T | 89 | a0002c0002t0001g0012 a0002c0002t0001g0038 a0002c0002t0001g0039 others(86): Show |
100 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.403-1790A>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60540729 | |||||||
| chr11:60540762 | C | T | 1 | a0003c0004t0005g0171 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.403-1757C>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60540762 | |||||||
| chr11:60540946 | C | T | 4 | a0002c0002t0001g0012 a0002c0002t0001g0250 a0002c0002t0001g0251 others(1): Show |
6 | HG01168.hp2 HG01169.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.403-1573C>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60540946 | |||||||
| chr11:60540956 | C | CAA | 7 | a0002c0002t0004g0036 a0002c0002t0004g0037 a0002c0002t0004g0245 others(4): Show |
9 | HG01069.hp2 HG01070.hp1 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.403-1549_403-1548d others(4): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 60540956 | ||||||
| chr11:60540956 | CA | C | 153 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(150): Show |
190 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.403-1548delA | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 60540956 | ||||||
| chr11:60540961 | A | G | 1 | a0001c0001t0001g0124 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.403-1558A>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60540961 | |||||||
| chr11:60540998 | G | A | 3 | a0001c0001t0002g0184 a0001c0001t0002g0187 a0001c0001t0007g0200 |
3 | HG02145.hp1 HG02572.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.403-1521G>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60540998 | |||||||
| chr11:60541364 | A | C | 1 | a0001c0001t0002g0284 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.403-1155A>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60541364 | |||||||
| chr11:60541484 | T | C | 128 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(125): Show |
162 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.403-1035T>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60541484 | |||||||
| chr11:60541541 | G | T | 2 | a0001c0001t0002g0289 a0001c0001t0002g0322 |
2 | NA18975.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.403-978G>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60541541 | |||||||
| chr11:60541598 | C | G | 93 | a0001c0001t0001g0018 a0001c0001t0001g0078 a0001c0001t0001g0079 others(90): Show |
105 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.403-921C>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60541598 | |||||||
| chr11:60541965 | G | T | 31 | a0001c0001t0001g0018 a0001c0001t0001g0078 a0001c0001t0001g0079 others(28): Show |
34 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.403-554G>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60541965 | |||||||
| chr11:60542016 | T | G | 323 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(320): Show |
403 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(400): Show |
intron_variant | MODIFIER | c.403-503T>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60542016 | |||||||
| chr11:60542117 | GA | G | 315 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(312): Show |
393 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(390): Show |
intron_variant | MODIFIER | c.403-388delA | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 60542117 | ||||||
| chr11:60542117 | GAA | G | 5 | a0002c0002t0001g0012 a0002c0002t0001g0250 a0002c0002t0001g0251 others(2): Show |
7 | HG01168.hp2 HG01169.hp1 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.403-389_403-388del others(2): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 60542117 | ||||||
| chr11:60542199 | G | A | 1 | a0001c0001t0001g0163 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.403-320G>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60542199 | |||||||
| chr11:60542228 | G | GAAGGAAG others(2): Show |
174 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(171): Show |
214 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.403-289_403-281dup others(9): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 60542228 | ||||||
| chr11:60542252 | GAGAA | G | 32 | a0001c0001t0001g0008 a0001c0001t0001g0028 a0001c0001t0001g0071 others(29): Show |
38 | HG01069.hp1 HG01069.hp2 HG01070.hp1 others(35): Show |
intron_variant | MODIFIER | c.403-253_403-250del others(4): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 60542252 | ||||||
| chr11:60542265 | A | G | 7 | a0002c0002t0004g0036 a0002c0002t0004g0037 a0002c0002t0004g0245 others(4): Show |
9 | HG01069.hp2 HG01070.hp1 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.403-254A>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60542265 | |||||||
| chr11:60542272 | GGAAA | G | 3 | a0001c0001t0001g0137 a0001c0001t0001g0143 a0001c0001t0001g0146 |
3 | HG00438.hp1 NA18971.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.403-236_403-233del others(4): Show |
MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 60542272 | ||||||
| chr11:60542278 | A | G | 1 | a0001c0001t0001g0227 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.403-241A>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60542278 | |||||||
| chr11:60542311 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.403-208G>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60542311 | |||||||
| chr11:60542364 | A | G | 2 | a0001c0001t0002g0321 a0001c0001t0002g0323 |
2 | HG02083.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.403-155A>G | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60542364 | |||||||
| chr11:60542401 | T | A | 1 | a0002c0002t0004g0248 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.403-118T>A | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60542401 | |||||||
| chr11:60542473 | T | C | 1 | a0002c0003t0001g0213 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.403-46T>C | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60542473 | |||||||
| chr11:60542474 | A | T | 323 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(320): Show |
403 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(400): Show |
intron_variant | MODIFIER | c.403-45A>T | MS4A13 | ENSG00000204979.8 | transcript | ENST00000378186.7 | protein_coding | 6/6 | chr11 | 60542474 |