Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 7106 |
| ensemblid | ENSG00000214063.12 |
| hgncid | 11859 |
| symbol | TSPAN4 |
| name | tetraspanin 4 |
| refseq_nuc | NM_003271.5 |
| refseq_prot | NP_003262.1 |
| ensembl_nuc | ENST00000397397.7 |
| ensembl_prot | ENSP00000380552.2 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 842852 |
| end | 867111 |
| strand | + |
| ver | v1.2 |
| region | chr11:842852-867111 |
| region5000 | chr11:837852-872111 |
| regionname0 | TSPAN4_chr11_842852_867111 |
| regionname5000 | TSPAN4_chr11_837852_872111 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 238 | 391 | 88 | 70 | 173 | 16 | 42 | 125 | TSPAN4_chr11_837852_872111 | TSPAN4 | MARAC others(233): Show |
chr11 | 837852 | 872111 |
| a0002 | 0/0 | 238 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | MARAC others(233): Show |
chr11 | 837852 | 872111 |
| a0003 | 0/0 | 238 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | MARAC others(233): Show |
chr11 | 837852 | 872111 |
| a0004 | 0/0 | 238 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TSPAN4_chr11_837852_872111 | TSPAN4 | MARAC others(233): Show |
chr11 | 837852 | 872111 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 714 | 365 | 75 | 63 | 169 | 15 | 42 | TSPAN4_chr11_837852_872111 | TSPAN4 | ATGGC others(709): Show |
chr11 | 837852 | 872111 | ||
| a0001c0002 | 0/0 | 714 | 13 | 8 | 5 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | ATGGC others(709): Show |
chr11 | 837852 | 872111 | ||
| a0001c0003 | 0/0 | 714 | 3 | 1 | 1 | 0 | 1 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | ATGGC others(709): Show |
chr11 | 837852 | 872111 | ||
| a0001c0004 | 0/0 | 714 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | ATGGC others(709): Show |
chr11 | 837852 | 872111 | ||
| a0001c0005 | 1/0 | 714 | 2 | 1 | 0 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | ATGGC others(709): Show |
chr11 | 837852 | 872111 | ||
| a0001c0006 | 0/0 | 714 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | ATGGC others(709): Show |
chr11 | 837852 | 872111 | ||
| a0001c0007 | 0/0 | 714 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | ATGGC others(709): Show |
chr11 | 837852 | 872111 | ||
| a0001c0010 | 0/0 | 714 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | ATGGC others(709): Show |
chr11 | 837852 | 872111 | ||
| a0001c0012 | 0/0 | 714 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | ATGGC others(709): Show |
chr11 | 837852 | 872111 | ||
| a0001c0013 | 0/0 | 714 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | ATGGC others(709): Show |
chr11 | 837852 | 872111 | ||
| a0002c0009 | 0/0 | 714 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | ATGGC others(709): Show |
chr11 | 837852 | 872111 | ||
| a0003c0008 | 0/0 | 714 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | ATGGC others(709): Show |
chr11 | 837852 | 872111 | ||
| a0004c0011 | 0/0 | 714 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | ATGGC others(709): Show |
chr11 | 837852 | 872111 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 1379 | 233 | 45 | 25 | 125 | 6 | 31 | TSPAN4_chr11_837852_872111 | TSPAN4 | GTGTC others(1374): Show |
chr11 | 837852 | 872111 |
| a0001c0001t0002 | 0/0 | 1379 | 105 | 26 | 27 | 39 | 4 | 9 | TSPAN4_chr11_837852_872111 | TSPAN4 | GTGTC others(1374): Show |
chr11 | 837852 | 872111 |
| a0001c0001t0003 | 0/0 | 1379 | 18 | 0 | 10 | 5 | 3 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | GTGTC others(1374): Show |
chr11 | 837852 | 872111 |
| a0001c0001t0004 | 0/0 | 1379 | 2 | 1 | 1 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | GTGTC others(1374): Show |
chr11 | 837852 | 872111 |
| a0001c0001t0005 | 0/0 | 1379 | 2 | 0 | 0 | 0 | 2 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | GTGTC others(1374): Show |
chr11 | 837852 | 872111 |
| a0001c0001t0006 | 0/0 | 1379 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | GTGTC others(1374): Show |
chr11 | 837852 | 872111 |
| a0001c0001t0007 | 0/0 | 1379 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN4_chr11_837852_872111 | TSPAN4 | GTGTC others(1374): Show |
chr11 | 837852 | 872111 |
| a0001c0001t0008 | 0/0 | 1379 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | GTGTC others(1374): Show |
chr11 | 837852 | 872111 |
| a0001c0001t0009 | 0/0 | 1379 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN4_chr11_837852_872111 | TSPAN4 | GTGTC others(1374): Show |
chr11 | 837852 | 872111 |
| a0001c0001t0010 | 0/0 | 1379 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | GTGTC others(1374): Show |
chr11 | 837852 | 872111 |
| a0001c0002t0001 | 0/0 | 1379 | 13 | 8 | 5 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | GTGTC others(1374): Show |
chr11 | 837852 | 872111 |
| a0001c0003t0001 | 0/0 | 1379 | 3 | 1 | 1 | 0 | 1 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | GTGTC others(1374): Show |
chr11 | 837852 | 872111 |
| a0001c0004t0002 | 0/0 | 1379 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | GTGTC others(1374): Show |
chr11 | 837852 | 872111 |
| a0001c0005t0002 | 1/0 | 1379 | 2 | 1 | 0 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | GTGTC others(1374): Show |
chr11 | 837852 | 872111 |
| a0001c0006t0002 | 0/0 | 1379 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | GTGTC others(1374): Show |
chr11 | 837852 | 872111 |
| a0001c0007t0002 | 0/0 | 1379 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | GTGTC others(1374): Show |
chr11 | 837852 | 872111 |
| a0001c0010t0002 | 0/0 | 1379 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | GTGTC others(1374): Show |
chr11 | 837852 | 872111 |
| a0001c0012t0001 | 0/0 | 1379 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | GTGTC others(1374): Show |
chr11 | 837852 | 872111 |
| a0001c0013t0001 | 0/0 | 1379 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | GTGTC others(1374): Show |
chr11 | 837852 | 872111 |
| a0002c0009t0002 | 0/0 | 1379 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | GTGTC others(1374): Show |
chr11 | 837852 | 872111 |
| a0003c0008t0001 | 0/0 | 1379 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | GTGTC others(1374): Show |
chr11 | 837852 | 872111 |
| a0004c0011t0001 | 0/0 | 1379 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | GTGTC others(1374): Show |
chr11 | 837852 | 872111 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0176 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0002g0001 | 0/0 | 9 | 1 | 4 | 3 | 0 | 1 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0002g0004 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0002g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0002g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0002g0009 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0002g0022 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0002g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0002g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0002g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0002g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0003g0005 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0003g0010 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0003g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0003g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0003g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0004g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0005g0002 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0006g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0007g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0008g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0009g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0001t0010g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0002t0001g0013 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0002t0001g0014 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0002t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0002t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0002t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0002t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0002t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0002t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0002t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0003t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0003t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0003t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0004t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0004t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0005t0002g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0005t0002g0317 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0006t0002g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0007t0002g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0010t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0012t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0001c0013t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0002c0009t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0003c0008t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| a0004c0011t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0003 | t0001 | g0283 | EUR | GBR | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0225 | EUR | GBR | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0009 | EUR | FIN | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0173 | EUR | FIN | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0081 | EUR | FIN | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0155 | EUR | FIN | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | CHS | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | CHS | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG00423 | hp2 | a0001 | c0004 | t0002 | g0102 | EAS | CHS | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | CHS | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | CHS | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0266 | EAS | CHS | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | CHS | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | CHS | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0072 | EAS | CHS | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | CHS | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0205 | EAS | CHS | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | CHS | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | CHS | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0080 | AMR | PUR | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0175 | AMR | PUR | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0164 | AMR | PUR | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0049 | AMR | PUR | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0130 | AMR | PUR | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG00741 | hp2 | a0001 | c0001 | t0004 | g0029 | AMR | PUR | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0051 | AMR | PUR | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG01106 | hp2 | a0001 | c0010 | t0002 | g0050 | AMR | PUR | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG01109 | hp2 | a0001 | c0002 | t0001 | g0013 | AMR | PUR | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0005 | AMR | PUR | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0053 | AMR | PUR | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG01168 | hp2 | a0001 | c0003 | t0001 | g0177 | AMR | PUR | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG01175 | hp2 | a0002 | c0009 | t0002 | g0052 | AMR | PUR | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0304 | AMR | PUR | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0123 | AMR | PUR | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0014 | AMR | PUR | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0301 | AMR | PUR | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | CLM | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0151 | AMR | CLM | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0097 | AMR | CLM | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0010 | AMR | CLM | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG01257 | hp2 | a0001 | c0001 | t0003 | g0161 | AMR | CLM | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0118 | AMR | CLM | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | CLM | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | CLM | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0160 | AMR | CLM | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0215 | AMR | CLM | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0048 | AMR | CLM | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0084 | AMR | CLM | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | CLM | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0091 | EUR | IBS | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG01515 | hp2 | a0001 | c0001 | t0005 | g0002 | EUR | IBS | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0033 | EUR | IBS | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0042 | EUR | IBS | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0033 | EUR | IBS | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG01517 | hp2 | a0001 | c0001 | t0005 | g0002 | EUR | IBS | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG01884 | hp1 | a0001 | c0001 | t0004 | g0029 | AFR | ACB | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0013 | AFR | ACB | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0133 | AMR | PEL | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG01928 | hp2 | a0001 | c0001 | t0003 | g0010 | AMR | PEL | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0096 | AMR | PEL | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PEL | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0099 | AMR | PEL | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG01943 | hp2 | a0001 | c0002 | t0001 | g0313 | AMR | PEL | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0120 | AMR | PEL | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG01952 | hp2 | a0001 | c0001 | t0003 | g0010 | AMR | PEL | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0022 | AMR | PEL | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | PEL | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PEL | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0103 | AMR | PEL | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PEL | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0276 | AMR | PEL | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0089 | AMR | PEL | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | KHV | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | KHV | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | KHV | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0132 | AFR | ACB | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | KHV | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | KHV | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | KHV | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02071 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | KHV | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | KHV | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | KHV | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | KHV | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | KHV | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | KHV | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0263 | EAS | KHV | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | KHV | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0311 | EAS | KHV | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | KHV | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02145 | hp1 | a0001 | c0001 | t0008 | g0046 | AFR | ACB | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0312 | AFR | ACB | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | CDX | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | CDX | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | CDX | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | CDX | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0294 | AFR | ACB | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0028 | AFR | ACB | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | ACB | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0107 | AFR | ACB | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02273 | hp1 | a0001 | c0001 | t0003 | g0186 | AMR | PEL | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0098 | AMR | PEL | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | ACB | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | ACB | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0093 | AMR | PEL | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02293 | hp2 | a0003 | c0008 | t0001 | g0207 | AMR | PEL | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0122 | AMR | PEL | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | ACB | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | ACB | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | KHV | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | KHV | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0195 | SAS | PJL | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02615 | hp1 | a0001 | c0002 | t0001 | g0014 | AFR | GWD | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | GWD | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0152 | AFR | GWD | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0216 | AFR | GWD | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | GWD | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0264 | AFR | GWD | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0258 | SAS | PJL | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0288 | SAS | PJL | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0184 | AFR | GWD | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | GWD | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0070 | SAS | PJL | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0273 | SAS | PJL | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0296 | AFR | GWD | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02809 | hp2 | a0001 | c0002 | t0001 | g0013 | AFR | GWD | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | GWD | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0027 | AFR | GWD | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0129 | AFR | GWD | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0028 | AFR | GWD | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | GWD | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02965 | hp1 | a0001 | c0007 | t0002 | g0315 | AFR | ESN | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | ESN | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | ESN | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0153 | AFR | ESN | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | ESN | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0295 | AFR | ESN | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0261 | SAS | PJL | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0109 | SAS | PJL | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | GWD | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG03130 | hp1 | a0001 | c0006 | t0002 | g0034 | AFR | ESN | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG03130 | hp2 | a0001 | c0005 | t0002 | g0316 | AFR | ESN | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG03139 | hp1 | a0001 | c0001 | t0010 | g0234 | AFR | ESN | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | ESN | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | ESN | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | MSL | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0127 | AFR | MSL | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG03225 | hp2 | a0001 | c0001 | t0006 | g0026 | AFR | MSL | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG03239 | hp1 | a0001 | c0001 | t0009 | g0299 | SAS | PJL | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG03239 | hp2 | a0001 | c0001 | t0007 | g0237 | SAS | PJL | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | MSL | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | MSL | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0303 | AFR | MSL | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0314 | AFR | MSL | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | PJL | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0185 | SAS | PJL | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | ESN | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | ESN | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0124 | AFR | GWD | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0150 | AFR | MSL | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0154 | AFR | MSL | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0224 | SAS | PJL | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | STU | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0159 | SAS | STU | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0121 | SAS | PJL | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0275 | SAS | PJL | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0181 | SAS | BEB | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0067 | SAS | BEB | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | BEB | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | BEB | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0291 | SAS | BEB | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | BEB | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0289 | SAS | BEB | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0196 | SAS | BEB | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0297 | SAS | STU | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0191 | SAS | STU | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0088 | SAS | BEB | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | BEB | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0277 | SAS | STU | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0310 | SAS | STU | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | STU | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | STU | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | STU | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0282 | SAS | STU | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | YRI | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA18522 | hp2 | a0001 | c0006 | t0002 | g0034 | AFR | YRI | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA18612 | hp1 | a0001 | c0012 | t0001 | g0040 | EAS | CHB | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | CHB | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0255 | EAS | CHB | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | CHB | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | YRI | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0110 | AFR | YRI | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA18952 | hp1 | a0001 | c0004 | t0002 | g0101 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0125 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA18967 | hp1 | a0001 | c0001 | t0003 | g0071 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA18969 | hp2 | a0001 | c0001 | t0003 | g0112 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA18987 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA18997 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA19030 | hp1 | a0001 | c0003 | t0001 | g0002 | AFR | LWK | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0268 | AFR | LWK | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | LWK | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | LWK | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA19088 | hp1 | a0001 | c0013 | t0001 | g0242 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0300 | AFR | YRI | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0026 | AFR | YRI | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0180 | AFR | ASW | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | ASW | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0134 | EUR | TSI | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0038 | EUR | TSI | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0076 | EUR | TSI | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0022 | EUR | TSI | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0044 | SAS | GIH | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0260 | SAS | GIH | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | ACB | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0292 | AFR | ACB | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | ACB | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02486 | hp2 | a0001 | c0002 | t0001 | g0014 | AFR | ACB | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | ACB | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0069 | AFR | ACB | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | MSL | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0293 | AFR | MSL | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | USA | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0092 | AFR | USA | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA18955 | hp1 | a0004 | c0011 | t0001 | g0236 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | USA | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0027 | AFR | USA | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA21309 | hp1 | a0001 | c0002 | t0001 | g0174 | AFR | LWK | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0307 | AFR | LWK | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0176 | REF | REF | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| homoSapiens | grch38p0 | a0001 | c0005 | t0002 | g0317 | REF | REF | TSPAN4_chr11_837852_872111 | TSPAN4 | chr11 | 837852 | 872111 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:865815 | G | C | 1 | a0003 | 1 | HG02293.hp2 | missense_variant | MODERATE | c.554G>C | p.Trp185Ser | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 7/9 | 735/1379 | 554/717 | 185/238 | chr11 | 865815 | |||
| chr11:865991 | C | T | 1 | a0004 | 1 | NA18955.hp1 | missense_variant | MODERATE | c.638C>T | p.Ala213Val | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 8/9 | 819/1379 | 638/717 | 213/238 | chr11 | 865991 | |||
| chr11:866625 | G | A | 1 | a0002 | 1 | HG01175.hp2 | missense_variant | MODERATE | c.712G>A | p.Ala238Thr | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 9/9 | 893/1379 | 712/717 | 238/238 | chr11 | 866625 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:850319 | C | T | 1 | a0001c0006 | 2 | HG03130.hp1 NA18522.hp2 |
synonymous_variant | LOW | c.15C>T | p.Cys5Cys | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/9 | 196/1379 | 15/717 | 5/238 | chr11 | 850319 | |||
| chr11:862564 | C | T | 1 | a0001c0013 | 1 | NA19088.hp1 | synonymous_variant | LOW | c.78C>T | p.Gly26Gly | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 4/9 | 259/1379 | 78/717 | 26/238 | chr11 | 862564 | |||
| chr11:862652 | T | C | 12 | a0001c0001 a0001c0002 a0001c0003 others(9): Show |
391 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(388): Show |
synonymous_variant | LOW | c.166T>C | p.Leu56Leu | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 4/9 | 347/1379 | 166/717 | 56/238 | chr11 | 862652 | |||
| chr11:864445 | G | C | 1 | a0001c0003 | 3 | HG00140.hp1 HG01168.hp2 NA19030.hp1 |
synonymous_variant | LOW | c.264G>C | p.Leu88Leu | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 5/9 | 445/1379 | 264/717 | 88/238 | chr11 | 864445 | |||
| chr11:864511 | G | A | 1 | a0001c0004 | 2 | HG00423.hp2 NA18952.hp1 |
splice_region_variant&synonymous_variant | LOW | c.330G>A | p.Lys110Lys | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 5/9 | 511/1379 | 330/717 | 110/238 | chr11 | 864511 | |||
| chr11:865560 | C | T | 1 | a0001c0002 | 13 | HG00642.hp2 HG01109.hp2 HG01243.hp1 others(10): Show |
synonymous_variant | LOW | c.378C>T | p.Tyr126Tyr | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 6/9 | 559/1379 | 378/717 | 126/238 | chr11 | 865560 | |||
| chr11:865614 | C | T | 1 | a0001c0012 | 1 | NA18612.hp1 | splice_region_variant&synonymous_variant | LOW | c.432C>T | p.Asp144Asp | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 6/9 | 613/1379 | 432/717 | 144/238 | chr11 | 865614 | |||
| chr11:865798 | G | A | 1 | a0001c0007 | 1 | HG02965.hp1 | synonymous_variant | LOW | c.537G>A | p.Leu179Leu | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 7/9 | 718/1379 | 537/717 | 179/238 | chr11 | 865798 | |||
| chr11:866612 | A | G | 1 | a0001c0010 | 1 | HG01106.hp2 | synonymous_variant | LOW | c.699A>G | p.Ala233Ala | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 9/9 | 880/1379 | 699/717 | 233/238 | chr11 | 866612 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:850303 | G | A | 1 | a0001c0001t0004 | 2 | HG00741.hp2 HG01884.hp1 |
5_prime_UTR_variant | MODIFIER | c.-2G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/9 | 2 | chr11 | 850303 | ||||||
| chr11:866794 | A | G | 13 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(10): Show |
260 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(257): Show |
3_prime_UTR_variant | MODIFIER | c.*164A>G | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 9/9 | 164 | chr11 | 866794 | ||||||
| chr11:866814 | C | T | 1 | a0001c0001t0010 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*184C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 9/9 | 184 | chr11 | 866814 | ||||||
| chr11:866818 | G | A | 1 | a0001c0001t0007 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*188G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 9/9 | 188 | chr11 | 866818 | ||||||
| chr11:866826 | C | G | 1 | a0001c0001t0005 | 2 | HG01515.hp2 HG01517.hp2 |
3_prime_UTR_variant | MODIFIER | c.*196C>G | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 9/9 | 196 | chr11 | 866826 | ||||||
| chr11:866854 | C | T | 1 | a0001c0001t0009 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*224C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 9/9 | 224 | chr11 | 866854 | ||||||
| chr11:866903 | C | T | 1 | a0001c0001t0008 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*273C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 9/9 | 273 | chr11 | 866903 | ||||||
| chr11:866920 | T | G | 1 | a0001c0001t0003 | 18 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*290T>G | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 9/9 | 290 | chr11 | 866920 | ||||||
| chr11:866984 | C | T | 1 | a0001c0001t0006 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*354C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 9/9 | 354 | chr11 | 866984 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:842931 | G | C | 315 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(312): Show |
387 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(384): Show |
intron_variant | MODIFIER | c.-118+16G>C | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 842931 | |||||||
| chr11:842933 | T | A | 1 | a0001c0001t0002g0044 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-118+18T>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 842933 | |||||||
| chr11:842998 | G | A | 2 | a0001c0001t0001g0045 a0001c0001t0008g0046 |
2 | HG02145.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-118+83G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 842998 | |||||||
| chr11:843097 | G | C | 150 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0021 others(147): Show |
183 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(180): Show |
intron_variant | MODIFIER | c.-118+182G>C | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 843097 | |||||||
| chr11:843191 | G | T | 1 | a0001c0001t0001g0311 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-118+276G>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 843191 | |||||||
| chr11:843287 | T | C | 3 | a0001c0001t0001g0312 a0001c0002t0001g0313 a0001c0002t0001g0314 |
3 | HG01943.hp2 HG02145.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-118+372T>C | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 843287 | |||||||
| chr11:843304 | C | T | 1 | a0001c0001t0001g0310 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-118+389C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 843304 | |||||||
| chr11:843312 | T | C | 2 | a0001c0001t0001g0171 a0001c0001t0001g0172 |
2 | NA18991.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.-118+397T>C | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 843312 | |||||||
| chr11:843396 | G | A | 1 | a0001c0007t0002g0315 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-118+481G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 843396 | |||||||
| chr11:843461 | T | C | 145 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0021 others(142): Show |
180 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.-118+546T>C | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 843461 | |||||||
| chr11:843481 | A | G | 3 | a0001c0001t0001g0308 a0001c0001t0001g0309 a0001c0001t0001g0311 |
3 | HG02056.hp1 HG02132.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.-118+566A>G | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 843481 | |||||||
| chr11:843483 | C | T | 1 | a0001c0001t0001g0307 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-118+568C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 843483 | |||||||
| chr11:843486 | G | A | 1 | a0001c0001t0001g0312 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-118+571G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 843486 | |||||||
| chr11:843534 | C | T | 1 | a0001c0006t0002g0034 | 2 | HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-118+619C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 843534 | |||||||
| chr11:843713 | C | CTCCTTGG others(31): Show |
182 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(179): Show |
230 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(227): Show |
intron_variant | MODIFIER | c.-118+815_-118+816i others(40): Show |
TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 843713 | ||||||
| chr11:843713 | C | T | 129 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0016 others(126): Show |
148 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.-118+798C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 843713 | |||||||
| chr11:843880 | G | A | 3 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 |
3 | HG02055.hp2 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-118+965G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 843880 | |||||||
| chr11:843927 | A | G | 199 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(196): Show |
248 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.-118+1012A>G | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 843927 | |||||||
| chr11:843944 | G | A | 2 | a0001c0001t0001g0218 a0001c0001t0001g0219 |
2 | HG01109.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.-118+1029G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 843944 | |||||||
| chr11:843996 | G | A | 6 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(3): Show |
6 | HG01943.hp2 HG02055.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.-118+1081G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 843996 | |||||||
| chr11:844057 | C | G | 178 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(175): Show |
227 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.-118+1142C>G | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 844057 | |||||||
| chr11:844154 | G | T | 1 | a0001c0001t0001g0217 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-118+1239G>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 844154 | |||||||
| chr11:844170 | T | A | 3 | a0001c0001t0001g0179 a0001c0001t0001g0220 a0001c0001t0001g0307 |
3 | HG02615.hp2 HG02976.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-118+1255T>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 844170 | |||||||
| chr11:844235 | A | T | 1 | a0001c0001t0001g0306 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.-118+1320A>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 844235 | |||||||
| chr11:844241 | TG | T | 16 | a0001c0001t0001g0020 a0001c0001t0001g0054 a0001c0001t0001g0060 others(13): Show |
17 | HG00408.hp2 HG00438.hp1 HG00673.hp1 others(14): Show |
intron_variant | MODIFIER | c.-118+1331delG | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 844241 | ||||||
| chr11:844402 | C | T | 1 | a0001c0001t0002g0151 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-118+1487C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 844402 | |||||||
| chr11:844411 | C | T | 2 | a0001c0002t0001g0313 a0001c0002t0001g0314 |
2 | HG01943.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-118+1496C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 844411 | |||||||
| chr11:844422 | C | T | 9 | a0001c0001t0001g0303 a0001c0001t0002g0304 a0001c0001t0008g0046 others(6): Show |
13 | HG01109.hp2 HG01192.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.-118+1507C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 844422 | |||||||
| chr11:844423 | A | G | 10 | a0001c0001t0001g0179 a0001c0001t0001g0303 a0001c0001t0002g0304 others(7): Show |
14 | HG01109.hp2 HG01192.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.-118+1508A>G | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 844423 | |||||||
| chr11:844648 | C | T | 1 | a0001c0001t0001g0307 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-118+1733C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 844648 | |||||||
| chr11:844706 | T | G | 1 | a0001c0001t0001g0221 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-118+1791T>G | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 844706 | |||||||
| chr11:844706 | T | TG | 92 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(89): Show |
108 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.-118+1802dupG | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 844706 | ||||||
| chr11:844715 | G | GT | 25 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0041 others(22): Show |
32 | HG00140.hp1 HG00733.hp1 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.-118+1800_-118+180 others(5): Show |
TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 844715 | |||||||
| chr11:844715 | G | T | 11 | a0001c0001t0001g0170 a0001c0001t0001g0179 a0001c0001t0001g0220 others(8): Show |
11 | HG02109.hp2 HG02257.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.-118+1800G>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 844715 | |||||||
| chr11:844723 | G | C | 1 | a0001c0001t0001g0264 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-118+1808G>C | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 844723 | |||||||
| chr11:844779 | C | T | 2 | a0001c0001t0001g0278 a0001c0001t0002g0263 |
2 | HG02129.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.-118+1864C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 844779 | |||||||
| chr11:844862 | G | C | 315 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(312): Show |
387 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(384): Show |
intron_variant | MODIFIER | c.-118+1947G>C | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 844862 | |||||||
| chr11:844910 | C | T | 1 | a0001c0001t0002g0150 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-118+1995C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 844910 | |||||||
| chr11:844969 | C | T | 314 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(311): Show |
386 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(383): Show |
intron_variant | MODIFIER | c.-118+2054C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 844969 | |||||||
| chr11:845077 | C | G | 124 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0016 others(121): Show |
144 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.-117-2124C>G | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 845077 | |||||||
| chr11:845084 | C | G | 1 | a0001c0002t0001g0180 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-117-2117C>G | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 845084 | |||||||
| chr11:845160 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-117-2041G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 845160 | |||||||
| chr11:845237 | G | A | 1 | a0001c0001t0001g0222 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-117-1964G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 845237 | |||||||
| chr11:845311 | C | T | 317 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(314): Show |
389 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(386): Show |
intron_variant | MODIFIER | c.-117-1890C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 845311 | |||||||
| chr11:845328 | TGTCCTCT others(54): Show |
T | 1 | a0001c0001t0001g0079 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-117-1848_-117-178 others(65): Show |
TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 845328 | ||||||
| chr11:845353 | T | C | 317 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(314): Show |
389 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(386): Show |
intron_variant | MODIFIER | c.-117-1848T>C | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 845353 | |||||||
| chr11:845366 | A | G | 316 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(313): Show |
388 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(385): Show |
intron_variant | MODIFIER | c.-117-1835A>G | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 845366 | |||||||
| chr11:845467 | G | A | 1 | a0001c0001t0001g0223 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-117-1734G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 845467 | |||||||
| chr11:845513 | T | G | 1 | a0001c0001t0002g0080 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-117-1688T>G | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 845513 | |||||||
| chr11:845776 | C | T | 15 | a0001c0001t0001g0038 a0001c0001t0001g0221 a0001c0001t0001g0257 others(12): Show |
16 | HG00642.hp2 HG02004.hp1 HG02647.hp1 others(13): Show |
intron_variant | MODIFIER | c.-117-1425C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 845776 | |||||||
| chr11:845789 | C | T | 79 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(76): Show |
101 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.-117-1412C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 845789 | |||||||
| chr11:845855 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-117-1346G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 845855 | |||||||
| chr11:845916 | C | T | 1 | a0001c0001t0003g0134 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-117-1285C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 845916 | |||||||
| chr11:845991 | G | A | 3 | a0001c0001t0001g0312 a0001c0002t0001g0313 a0001c0002t0001g0314 |
3 | HG01943.hp2 HG02145.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-117-1210G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 845991 | |||||||
| chr11:846004 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-117-1197C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 846004 | |||||||
| chr11:846070 | C | T | 51 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(48): Show |
62 | HG00423.hp1 HG00597.hp2 HG01071.hp1 others(59): Show |
intron_variant | MODIFIER | c.-117-1131C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 846070 | |||||||
| chr11:846172 | C | T | 6 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0254 others(3): Show |
6 | HG02027.hp2 HG02155.hp1 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.-117-1029C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 846172 | |||||||
| chr11:846209 | G | C | 1 | a0001c0001t0001g0279 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-117-992G>C | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 846209 | |||||||
| chr11:846225 | G | A | 2 | a0001c0001t0002g0265 a0001c0001t0002g0266 |
2 | HG00544.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.-117-976G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 846225 | |||||||
| chr11:846238 | G | A | 3 | a0001c0001t0001g0312 a0001c0002t0001g0313 a0001c0002t0001g0314 |
3 | HG01943.hp2 HG02145.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-117-963G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 846238 | |||||||
| chr11:846244 | GGCACCCA others(7): Show |
G | 1 | a0001c0001t0001g0214 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-117-953_-117-940d others(16): Show |
TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 846244 | ||||||
| chr11:846257 | C | T | 1 | a0001c0001t0001g0172 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.-117-944C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 846257 | |||||||
| chr11:846343 | C | T | 2 | a0001c0001t0001g0300 a0001c0001t0001g0301 |
2 | HG01243.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-117-858C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 846343 | |||||||
| chr11:846399 | C | A | 1 | a0001c0001t0001g0235 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-117-802C>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 846399 | |||||||
| chr11:846400 | T | C | 1 | a0001c0001t0001g0235 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-117-801T>C | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 846400 | |||||||
| chr11:846401 | C | A | 1 | a0001c0001t0001g0235 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-117-800C>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 846401 | |||||||
| chr11:846407 | C | T | 1 | a0001c0001t0001g0213 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-117-794C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 846407 | |||||||
| chr11:846408 | A | T | 1 | a0001c0001t0001g0235 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-117-793A>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 846408 | |||||||
| chr11:846424 | G | A | 1 | a0001c0001t0001g0235 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-117-777G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 846424 | |||||||
| chr11:846426 | G | A | 1 | a0001c0001t0001g0235 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-117-775G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 846426 | |||||||
| chr11:846431 | T | C | 1 | a0001c0001t0001g0235 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-117-770T>C | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 846431 | |||||||
| chr11:846436 | T | G | 1 | a0001c0001t0001g0235 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-117-765T>G | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 846436 | |||||||
| chr11:846437 | T | G | 1 | a0001c0001t0001g0235 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-117-764T>G | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 846437 | |||||||
| chr11:846442 | C | G | 1 | a0001c0001t0001g0235 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-117-759C>G | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 846442 | |||||||
| chr11:846444 | T | A | 1 | a0001c0001t0001g0235 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-117-757T>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 846444 | |||||||
| chr11:846448 | C | T | 1 | a0001c0006t0002g0034 | 2 | HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-117-753C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 846448 | |||||||
| chr11:846452 | G | T | 1 | a0001c0001t0001g0235 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-117-749G>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 846452 | |||||||
| chr11:846458 | T | G | 1 | a0001c0001t0001g0235 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-117-743T>G | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 846458 | |||||||
| chr11:846460 | G | A | 1 | a0001c0001t0001g0235 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-117-741G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 846460 | |||||||
| chr11:846461 | A | G | 1 | a0001c0001t0001g0235 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-117-740A>G | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 846461 | |||||||
| chr11:846463 | G | T | 1 | a0001c0001t0001g0235 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-117-738G>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 846463 | |||||||
| chr11:846464 | G | C | 1 | a0001c0001t0001g0235 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-117-737G>C | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 846464 | |||||||
| chr11:846465 | A | T | 1 | a0001c0001t0001g0235 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-117-736A>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 846465 | |||||||
| chr11:846469 | T | A | 1 | a0001c0001t0001g0235 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-117-732T>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 846469 | |||||||
| chr11:846470 | T | C | 1 | a0001c0001t0001g0235 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-117-731T>C | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 846470 | |||||||
| chr11:846474 | T | A | 1 | a0001c0001t0001g0235 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-117-727T>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 846474 | |||||||
| chr11:846477 | C | G | 1 | a0001c0001t0001g0235 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-117-724C>G | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 846477 | |||||||
| chr11:846478 | T | G | 1 | a0001c0001t0001g0235 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-117-723T>G | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 846478 | |||||||
| chr11:846488 | T | A | 1 | a0001c0001t0001g0235 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-117-713T>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 846488 | |||||||
| chr11:846490 | G | C | 1 | a0001c0001t0001g0235 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-117-711G>C | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 846490 | |||||||
| chr11:846492 | T | C | 1 | a0001c0001t0001g0235 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-117-709T>C | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 846492 | |||||||
| chr11:846493 | C | A | 1 | a0001c0001t0001g0235 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-117-708C>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 846493 | |||||||
| chr11:846494 | T | A | 1 | a0001c0001t0001g0235 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-117-707T>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 846494 | |||||||
| chr11:846511 | C | T | 1 | a0001c0001t0001g0075 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-117-690C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 846511 | |||||||
| chr11:846550 | G | A | 3 | a0001c0001t0001g0308 a0001c0001t0001g0309 a0001c0001t0001g0311 |
3 | HG02056.hp1 HG02132.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.-117-651G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 846550 | |||||||
| chr11:846594 | TCCCTGAG others(26): Show |
T | 3 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 |
3 | HG02055.hp2 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-117-604_-117-572d others(35): Show |
TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 846594 | ||||||
| chr11:846636 | C | T | 1 | a0001c0001t0002g0133 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-117-565C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 846636 | |||||||
| chr11:846725 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-117-476G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 846725 | |||||||
| chr11:846743 | T | G | 1 | a0001c0001t0001g0054 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-117-458T>G | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 846743 | |||||||
| chr11:846744 | A | T | 1 | a0001c0001t0001g0054 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-117-457A>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 846744 | |||||||
| chr11:846744 | AG | A | 177 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(174): Show |
225 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(222): Show |
intron_variant | MODIFIER | c.-117-453delG | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 846744 | ||||||
| chr11:846745 | G | A | 1 | a0001c0001t0001g0054 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-117-456G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 846745 | |||||||
| chr11:846842 | A | G | 69 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(66): Show |
80 | HG00423.hp1 HG00544.hp2 HG00597.hp2 others(77): Show |
intron_variant | MODIFIER | c.-117-359A>G | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 1/8 | chr11 | 846842 | |||||||
| chr11:847309 | G | C | 1 | a0001c0001t0001g0078 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-18+9G>C | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 2/8 | chr11 | 847309 | |||||||
| chr11:847314 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-18+14C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 2/8 | chr11 | 847314 | |||||||
| chr11:847338 | G | A | 1 | a0001c0001t0001g0185 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.-18+38G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 2/8 | chr11 | 847338 | |||||||
| chr11:847347 | G | A | 1 | a0001c0001t0002g0082 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-18+47G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 2/8 | chr11 | 847347 | |||||||
| chr11:847436 | G | A | 1 | a0001c0001t0001g0076 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-18+136G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 2/8 | chr11 | 847436 | |||||||
| chr11:847530 | G | T | 4 | a0001c0001t0001g0045 a0001c0001t0001g0224 a0001c0001t0001g0225 others(1): Show |
4 | HG00140.hp2 HG02145.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18+230G>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 2/8 | chr11 | 847530 | |||||||
| chr11:847611 | A | AC | 37 | a0001c0001t0001g0047 a0001c0001t0001g0066 a0001c0001t0001g0073 others(34): Show |
37 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(34): Show |
intron_variant | MODIFIER | c.-18+320dupC | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 847611 | ||||||
| chr11:847613 | C | A | 1 | a0001c0001t0002g0083 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.-18+313C>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 2/8 | chr11 | 847613 | |||||||
| chr11:847618 | C | A | 3 | a0001c0001t0001g0033 a0001c0001t0001g0187 a0001c0001t0003g0186 |
4 | HG01261.hp2 HG01516.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18+318C>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 2/8 | chr11 | 847618 | |||||||
| chr11:847681 | C | T | 1 | a0001c0001t0001g0209 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-18+381C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 2/8 | chr11 | 847681 | |||||||
| chr11:847838 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-18+538C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 2/8 | chr11 | 847838 | |||||||
| chr11:847868 | C | T | 3 | a0001c0001t0003g0130 a0001c0001t0003g0134 a0001c0001t0004g0029 |
4 | HG00738.hp2 HG00741.hp2 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18+568C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 2/8 | chr11 | 847868 | |||||||
| chr11:847905 | G | T | 1 | a0001c0001t0001g0146 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-18+605G>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 2/8 | chr11 | 847905 | |||||||
| chr11:847947 | G | A | 1 | a0001c0001t0002g0084 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-18+647G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 2/8 | chr11 | 847947 | |||||||
| chr11:848055 | T | C | 1 | a0001c0001t0002g0085 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-18+755T>C | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 2/8 | chr11 | 848055 | |||||||
| chr11:848154 | C | T | 1 | a0001c0001t0001g0271 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-18+854C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 2/8 | chr11 | 848154 | |||||||
| chr11:848248 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-18+948C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 2/8 | chr11 | 848248 | |||||||
| chr11:848278 | C | T | 1 | a0001c0001t0001g0217 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-18+978C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 2/8 | chr11 | 848278 | |||||||
| chr11:848314 | G | A | 1 | a0001c0001t0001g0188 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-18+1014G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 2/8 | chr11 | 848314 | |||||||
| chr11:848345 | T | G | 1 | a0001c0001t0001g0078 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-18+1045T>G | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 2/8 | chr11 | 848345 | |||||||
| chr11:848546 | G | A | 317 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(314): Show |
389 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(386): Show |
intron_variant | MODIFIER | c.-18+1246G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 2/8 | chr11 | 848546 | |||||||
| chr11:848674 | C | T | 1 | a0001c0001t0002g0261 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-18+1374C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 2/8 | chr11 | 848674 | |||||||
| chr11:848683 | C | T | 2 | a0001c0001t0002g0028 a0001c0001t0002g0129 |
3 | HG02257.hp2 HG02886.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.-18+1383C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 2/8 | chr11 | 848683 | |||||||
| chr11:849090 | C | G | 311 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(308): Show |
383 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(380): Show |
intron_variant | MODIFIER | c.-17-1198C>G | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 2/8 | chr11 | 849090 | |||||||
| chr11:849111 | C | G | 1 | a0001c0001t0001g0312 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-17-1177C>G | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 2/8 | chr11 | 849111 | |||||||
| chr11:849296 | G | A | 1 | a0001c0001t0002g0086 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-17-992G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 2/8 | chr11 | 849296 | |||||||
| chr11:849419 | C | T | 1 | a0001c0001t0001g0208 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-17-869C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 2/8 | chr11 | 849419 | |||||||
| chr11:849442 | T | C | 4 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0228 others(1): Show |
4 | HG02074.hp2 HG02129.hp1 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.-17-846T>C | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 2/8 | chr11 | 849442 | |||||||
| chr11:849577 | G | C | 312 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(309): Show |
384 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(381): Show |
intron_variant | MODIFIER | c.-17-711G>C | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 2/8 | chr11 | 849577 | |||||||
| chr11:849587 | C | G | 184 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(181): Show |
233 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(230): Show |
intron_variant | MODIFIER | c.-17-701C>G | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 2/8 | chr11 | 849587 | |||||||
| chr11:849636 | G | T | 1 | a0001c0001t0001g0145 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-17-652G>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 2/8 | chr11 | 849636 | |||||||
| chr11:849666 | C | A | 1 | a0001c0001t0001g0217 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-17-622C>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 2/8 | chr11 | 849666 | |||||||
| chr11:849666 | C | CG | 7 | a0001c0001t0001g0047 a0001c0001t0001g0073 a0001c0001t0001g0087 others(4): Show |
7 | HG00544.hp1 HG01433.hp1 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.-17-618dupG | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 849666 | ||||||
| chr11:849687 | G | T | 1 | a0001c0001t0002g0128 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-17-601G>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 2/8 | chr11 | 849687 | |||||||
| chr11:849703 | G | C | 39 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0041 others(36): Show |
46 | HG00140.hp1 HG00733.hp1 HG01074.hp1 others(43): Show |
intron_variant | MODIFIER | c.-17-585G>C | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 2/8 | chr11 | 849703 | |||||||
| chr11:849802 | CGGGGCGG others(8): Show |
C | 1 | a0001c0003t0001g0177 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-17-482_-17-468del others(15): Show |
TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 849802 | ||||||
| chr11:849826 | G | GGCGCGGG others(7): Show |
1 | a0001c0001t0001g0054 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-17-456_-17-443dup others(14): Show |
TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 849826 | ||||||
| chr11:849830 | C | T | 1 | a0001c0001t0001g0045 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-17-458C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 2/8 | chr11 | 849830 | |||||||
| chr11:849843 | G | T | 1 | a0001c0001t0010g0234 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-17-445G>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 2/8 | chr11 | 849843 | |||||||
| chr11:849862 | T | C | 44 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0021 others(41): Show |
52 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.-17-426T>C | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 2/8 | chr11 | 849862 | |||||||
| chr11:849866 | GT | G | 4 | a0001c0001t0001g0045 a0001c0001t0001g0224 a0001c0001t0001g0225 others(1): Show |
4 | HG00140.hp2 HG02145.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-17-420delT | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 849866 | ||||||
| chr11:849876 | C | T | 1 | a0001c0001t0001g0278 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-17-412C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 2/8 | chr11 | 849876 | |||||||
| chr11:849877 | G | A | 1 | a0001c0001t0002g0160 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-17-411G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 2/8 | chr11 | 849877 | |||||||
| chr11:849911 | C | CGCGGGGG others(5): Show |
1 | a0001c0001t0003g0134 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-17-371_-17-360dup others(12): Show |
TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 849911 | ||||||
| chr11:849918 | G | A | 1 | a0001c0007t0002g0315 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-17-370G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 2/8 | chr11 | 849918 | |||||||
| chr11:849959 | C | T | 11 | a0001c0001t0001g0038 a0001c0001t0001g0258 a0001c0001t0001g0259 others(8): Show |
12 | HG02004.hp1 HG02683.hp1 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.-17-329C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 2/8 | chr11 | 849959 | |||||||
| chr11:850021 | CG | C | 80 | a0001c0001t0001g0025 a0001c0001t0001g0054 a0001c0001t0001g0087 others(77): Show |
99 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.-17-264delG | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 850021 | ||||||
| chr11:850024 | G | C | 81 | a0001c0001t0001g0025 a0001c0001t0001g0054 a0001c0001t0001g0087 others(78): Show |
100 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.-17-264G>C | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 2/8 | chr11 | 850024 | |||||||
| chr11:850025 | C | T | 81 | a0001c0001t0001g0025 a0001c0001t0001g0054 a0001c0001t0001g0087 others(78): Show |
100 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.-17-263C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 2/8 | chr11 | 850025 | |||||||
| chr11:850070 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-17-218C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 2/8 | chr11 | 850070 | |||||||
| chr11:850073 | C | T | 1 | a0001c0001t0001g0264 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-17-215C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 2/8 | chr11 | 850073 | |||||||
| chr11:850170 | T | G | 319 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(316): Show |
391 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(388): Show |
intron_variant | MODIFIER | c.-17-118T>G | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 2/8 | chr11 | 850170 | |||||||
| chr11:850199 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-17-89C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 2/8 | chr11 | 850199 | |||||||
| chr11:850207 | C | T | 15 | a0001c0001t0001g0038 a0001c0001t0001g0159 a0001c0001t0001g0221 others(12): Show |
16 | HG00642.hp2 HG02004.hp1 HG02647.hp1 others(13): Show |
intron_variant | MODIFIER | c.-17-81C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 2/8 | chr11 | 850207 | |||||||
| chr11:850396 | G | A | 8 | a0001c0001t0001g0303 a0001c0001t0002g0304 a0001c0002t0001g0013 others(5): Show |
12 | HG01109.hp2 HG01192.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.63+29G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 850396 | |||||||
| chr11:850409 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.63+42G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 850409 | |||||||
| chr11:850607 | G | GCCCCC | 8 | a0001c0001t0001g0303 a0001c0001t0002g0304 a0001c0002t0001g0013 others(5): Show |
12 | HG01109.hp2 HG01192.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.63+240_63+241insCC others(3): Show |
TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 850607 | |||||||
| chr11:850608 | T | C | 1 | a0001c0001t0001g0078 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.63+241T>C | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 850608 | |||||||
| chr11:850610 | C | CCCTCT | 57 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(54): Show |
68 | HG00423.hp1 HG00597.hp2 HG01071.hp1 others(65): Show |
intron_variant | MODIFIER | c.63+263_63+267dupTC others(3): Show |
TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 850610 | ||||||
| chr11:850610 | C | T | 8 | a0001c0001t0001g0303 a0001c0001t0002g0304 a0001c0002t0001g0013 others(5): Show |
12 | HG01109.hp2 HG01192.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.63+243C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 850610 | |||||||
| chr11:850610 | CCCTCTCC others(3): Show |
C | 1 | a0001c0001t0001g0035 | 2 | HG01981.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.63+258_63+267delTC others(8): Show |
TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 850610 | ||||||
| chr11:850662 | C | T | 1 | a0001c0001t0001g0251 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.63+295C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 850662 | |||||||
| chr11:850685 | C | G | 1 | a0001c0001t0001g0078 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.63+318C>G | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 850685 | |||||||
| chr11:850767 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.63+400C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 850767 | |||||||
| chr11:850803 | C | T | 1 | a0001c0001t0001g0065 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.63+436C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 850803 | |||||||
| chr11:850870 | TGCCGCCA others(18): Show |
T | 3 | a0001c0001t0001g0233 a0001c0001t0001g0268 a0001c0001t0010g0234 |
3 | HG02109.hp1 HG03139.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.63+505_63+529delCC others(23): Show |
TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 850870 | ||||||
| chr11:850901 | G | T | 1 | a0001c0001t0001g0289 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.63+534G>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 850901 | |||||||
| chr11:850917 | C | A | 1 | a0001c0001t0001g0191 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.63+550C>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 850917 | |||||||
| chr11:850979 | T | C | 1 | a0004c0011t0001g0236 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.63+612T>C | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 850979 | |||||||
| chr11:850980 | C | T | 1 | a0004c0011t0001g0236 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.63+613C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 850980 | |||||||
| chr11:851141 | C | T | 2 | a0001c0001t0001g0220 a0001c0001t0001g0307 |
2 | HG02976.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.63+774C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 851141 | |||||||
| chr11:851214 | A | G | 5 | a0001c0001t0001g0025 a0001c0001t0002g0048 a0001c0001t0002g0118 others(2): Show |
6 | HG01070.hp2 HG01071.hp2 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+847A>G | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 851214 | |||||||
| chr11:851314 | G | T | 1 | a0001c0001t0001g0251 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.63+947G>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 851314 | |||||||
| chr11:851348 | C | G | 2 | a0001c0001t0001g0220 a0001c0001t0001g0307 |
2 | HG02976.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.63+981C>G | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 851348 | |||||||
| chr11:851513 | G | C | 1 | a0001c0001t0002g0088 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.63+1146G>C | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 851513 | |||||||
| chr11:851524 | G | T | 7 | a0001c0001t0001g0303 a0001c0001t0002g0304 a0001c0002t0001g0013 others(4): Show |
11 | HG01109.hp2 HG01192.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.63+1157G>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 851524 | |||||||
| chr11:851623 | T | A | 137 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0025 others(134): Show |
170 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.63+1256T>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 851623 | |||||||
| chr11:851818 | G | A | 2 | a0001c0001t0002g0055 a0001c0001t0002g0056 |
2 | NA18987.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.63+1451G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 851818 | |||||||
| chr11:851933 | G | T | 1 | a0001c0001t0001g0209 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.63+1566G>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 851933 | |||||||
| chr11:851981 | AG | A | 162 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(159): Show |
201 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.63+1616delG | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 851981 | ||||||
| chr11:851993 | C | T | 1 | a0001c0001t0002g0110 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.63+1626C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 851993 | |||||||
| chr11:852085 | C | T | 10 | a0001c0001t0001g0016 a0001c0001t0001g0156 a0001c0001t0001g0157 others(7): Show |
12 | HG02055.hp2 HG02280.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.63+1718C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 852085 | |||||||
| chr11:852096 | C | T | 2 | a0001c0001t0001g0221 a0001c0001t0001g0257 |
2 | HG02647.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.63+1729C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 852096 | |||||||
| chr11:852097 | C | A | 1 | a0001c0001t0002g0304 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.63+1730C>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 852097 | |||||||
| chr11:852097 | C | G | 91 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(88): Show |
106 | HG00423.hp1 HG00597.hp2 HG00642.hp2 others(103): Show |
intron_variant | MODIFIER | c.63+1730C>G | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 852097 | |||||||
| chr11:852119 | A | G | 4 | a0001c0001t0001g0035 a0001c0001t0001g0183 a0001c0001t0001g0206 others(1): Show |
5 | HG01175.hp1 HG01978.hp1 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+1752A>G | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 852119 | |||||||
| chr11:852154 | G | A | 1 | a0001c0001t0002g0111 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.63+1787G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 852154 | |||||||
| chr11:852167 | G | A | 4 | a0001c0001t0001g0041 a0001c0001t0001g0279 a0001c0001t0001g0280 others(1): Show |
5 | NA18949.hp2 NA18967.hp2 NA19002.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+1800G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 852167 | |||||||
| chr11:852215 | T | G | 52 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(49): Show |
62 | HG00423.hp1 HG00597.hp2 HG01071.hp1 others(59): Show |
intron_variant | MODIFIER | c.63+1848T>G | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 852215 | |||||||
| chr11:852226 | C | T | 2 | a0001c0001t0002g0070 a0001c0001t0002g0109 |
2 | HG02738.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.63+1859C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 852226 | |||||||
| chr11:852270 | C | T | 3 | a0001c0002t0001g0313 a0001c0002t0001g0314 a0001c0007t0002g0315 |
3 | HG01943.hp2 HG02965.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.63+1903C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 852270 | |||||||
| chr11:852298 | A | G | 2 | a0001c0001t0001g0300 a0001c0001t0001g0301 |
2 | HG01243.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.63+1931A>G | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 852298 | |||||||
| chr11:852313 | A | G | 1 | a0001c0001t0001g0250 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.63+1946A>G | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 852313 | |||||||
| chr11:852365 | G | A | 96 | a0001c0001t0001g0087 a0001c0001t0001g0104 a0001c0001t0001g0126 others(93): Show |
121 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.63+1998G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 852365 | |||||||
| chr11:852441 | G | A | 1 | a0001c0001t0002g0055 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.63+2074G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 852441 | |||||||
| chr11:852554 | G | T | 3 | a0001c0001t0001g0232 a0001c0001t0001g0300 a0001c0001t0001g0301 |
3 | HG01243.hp2 HG02451.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.63+2187G>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 852554 | |||||||
| chr11:852679 | G | A | 2 | a0001c0001t0002g0070 a0001c0001t0002g0109 |
2 | HG02738.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.63+2312G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 852679 | |||||||
| chr11:852761 | C | T | 1 | a0001c0001t0001g0230 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.63+2394C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 852761 | |||||||
| chr11:852797 | C | T | 2 | a0001c0001t0001g0078 a0001c0007t0002g0315 |
2 | HG02965.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.63+2430C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 852797 | |||||||
| chr11:852810 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.63+2443C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 852810 | |||||||
| chr11:852818 | CAG | C | 5 | a0001c0001t0001g0045 a0001c0001t0001g0156 a0001c0001t0001g0157 others(2): Show |
5 | HG02055.hp2 HG02818.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+2452_63+2453del others(2): Show |
TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 852818 | |||||||
| chr11:852855 | C | T | 3 | a0001c0001t0002g0048 a0001c0001t0002g0118 a0001c0001t0002g0160 |
3 | HG01261.hp1 HG01358.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.63+2488C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 852855 | |||||||
| chr11:852866 | C | A | 1 | a0001c0001t0003g0123 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.63+2499C>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 852866 | |||||||
| chr11:852867 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.63+2500G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 852867 | |||||||
| chr11:852884 | G | A | 1 | a0001c0001t0001g0193 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.63+2517G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 852884 | |||||||
| chr11:852885 | C | T | 1 | a0001c0001t0001g0217 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.63+2518C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 852885 | |||||||
| chr11:852891 | T | A | 3 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0267 |
3 | HG02040.hp2 HG02056.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.63+2524T>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 852891 | |||||||
| chr11:852900 | A | AC | 179 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(176): Show |
219 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(216): Show |
intron_variant | MODIFIER | c.63+2539dupC | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 852900 | ||||||
| chr11:852900 | A | ACC | 99 | a0001c0001t0001g0060 a0001c0001t0001g0087 a0001c0001t0001g0104 others(96): Show |
123 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.63+2538_63+2539dup others(2): Show |
TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 852900 | ||||||
| chr11:852907 | G | A | 1 | a0001c0001t0001g0025 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.63+2540G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 852907 | |||||||
| chr11:852978 | G | A | 5 | a0001c0001t0001g0045 a0001c0001t0001g0156 a0001c0001t0001g0157 others(2): Show |
5 | HG02055.hp2 HG02818.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+2611G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 852978 | |||||||
| chr11:853050 | G | A | 2 | a0001c0001t0001g0185 a0001c0001t0001g0194 |
2 | HG01081.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.63+2683G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 853050 | |||||||
| chr11:853234 | T | C | 1 | a0001c0007t0002g0315 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.63+2867T>C | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 853234 | |||||||
| chr11:853269 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.63+2902C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 853269 | |||||||
| chr11:853276 | G | A | 1 | a0001c0002t0001g0175 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.63+2909G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 853276 | |||||||
| chr11:853482 | C | T | 1 | a0001c0001t0001g0303 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.63+3115C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 853482 | |||||||
| chr11:853497 | C | T | 2 | a0001c0001t0001g0064 a0001c0007t0002g0315 |
2 | HG02965.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.63+3130C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 853497 | |||||||
| chr11:853546 | T | G | 1 | a0001c0001t0002g0083 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.63+3179T>G | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 853546 | |||||||
| chr11:853747 | T | G | 1 | a0001c0001t0001g0206 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.63+3380T>G | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 853747 | |||||||
| chr11:853760 | C | A | 11 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0228 others(8): Show |
11 | HG01192.hp1 HG01243.hp2 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.63+3393C>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 853760 | |||||||
| chr11:853761 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.63+3394C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 853761 | |||||||
| chr11:853859 | C | T | 1 | a0001c0001t0001g0256 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.63+3492C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 853859 | |||||||
| chr11:853887 | G | A | 7 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0047 others(4): Show |
9 | HG00438.hp2 NA18942.hp2 NA18946.hp2 others(6): Show |
intron_variant | MODIFIER | c.63+3520G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 853887 | |||||||
| chr11:853947 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.63+3580C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 853947 | |||||||
| chr11:853979 | G | A | 1 | a0001c0001t0001g0223 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.63+3612G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 853979 | |||||||
| chr11:853994 | G | A | 1 | a0001c0001t0002g0089 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.63+3627G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 853994 | |||||||
| chr11:854007 | C | T | 1 | a0001c0007t0002g0315 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.63+3640C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 854007 | |||||||
| chr11:854025 | C | T | 1 | a0001c0001t0001g0231 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.63+3658C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 854025 | |||||||
| chr11:854143 | G | A | 1 | a0001c0001t0001g0232 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.63+3776G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 854143 | |||||||
| chr11:854215 | G | A | 1 | a0001c0001t0002g0304 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.63+3848G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 854215 | |||||||
| chr11:854278 | C | G | 1 | a0001c0007t0002g0315 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.63+3911C>G | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 854278 | |||||||
| chr11:854419 | T | G | 1 | a0001c0001t0002g0083 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.63+4052T>G | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 854419 | |||||||
| chr11:854443 | G | A | 1 | a0001c0001t0003g0071 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.63+4076G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 854443 | |||||||
| chr11:854487 | T | C | 1 | a0001c0007t0002g0315 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.63+4120T>C | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 854487 | |||||||
| chr11:854496 | C | CCT | 180 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(177): Show |
227 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.63+4130_63+4131dup others(2): Show |
TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 854496 | ||||||
| chr11:854510 | C | T | 67 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(64): Show |
79 | HG00140.hp2 HG00423.hp1 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.63+4143C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 854510 | |||||||
| chr11:854513 | G | A | 1 | a0001c0007t0002g0315 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.63+4146G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 854513 | |||||||
| chr11:854543 | C | T | 316 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(313): Show |
388 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(385): Show |
intron_variant | MODIFIER | c.63+4176C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 854543 | |||||||
| chr11:854544 | G | A | 1 | a0001c0001t0008g0046 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.63+4177G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 854544 | |||||||
| chr11:854700 | C | G | 1 | a0001c0001t0008g0046 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.63+4333C>G | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 854700 | |||||||
| chr11:854730 | AG | A | 318 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(315): Show |
390 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(387): Show |
intron_variant | MODIFIER | c.63+4368delG | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 854730 | ||||||
| chr11:854967 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.63+4600G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 854967 | |||||||
| chr11:855116 | A | G | 319 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(316): Show |
391 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(388): Show |
intron_variant | MODIFIER | c.63+4749A>G | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 855116 | |||||||
| chr11:855186 | C | G | 6 | a0001c0001t0001g0230 a0001c0002t0001g0013 a0001c0002t0001g0014 others(3): Show |
10 | HG01109.hp2 HG01243.hp1 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.63+4819C>G | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 855186 | |||||||
| chr11:855187 | G | A | 2 | a0001c0001t0001g0156 a0001c0001t0001g0157 |
2 | HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.63+4820G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 855187 | |||||||
| chr11:855214 | T | C | 317 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(314): Show |
389 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(386): Show |
intron_variant | MODIFIER | c.63+4847T>C | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 855214 | |||||||
| chr11:855221 | A | G | 317 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(314): Show |
389 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(386): Show |
intron_variant | MODIFIER | c.63+4854A>G | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 855221 | |||||||
| chr11:855318 | T | C | 193 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(190): Show |
241 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(238): Show |
intron_variant | MODIFIER | c.63+4951T>C | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 855318 | |||||||
| chr11:855372 | A | G | 217 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(214): Show |
268 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(265): Show |
intron_variant | MODIFIER | c.63+5005A>G | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 855372 | |||||||
| chr11:855724 | A | T | 11 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0228 others(8): Show |
12 | HG01243.hp2 HG02074.hp2 HG02129.hp1 others(9): Show |
intron_variant | MODIFIER | c.63+5357A>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 855724 | |||||||
| chr11:855778 | G | A | 5 | a0001c0001t0001g0017 a0001c0001t0001g0163 a0001c0001t0001g0239 others(2): Show |
7 | HG02027.hp1 HG02165.hp1 NA18747.hp2 others(4): Show |
intron_variant | MODIFIER | c.63+5411G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 855778 | |||||||
| chr11:855784 | G | A | 2 | a0001c0001t0002g0026 a0001c0001t0006g0026 |
2 | HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.63+5417G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 855784 | |||||||
| chr11:855790 | G | A | 1 | a0001c0001t0001g0143 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.63+5423G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 855790 | |||||||
| chr11:855877 | C | A | 1 | a0001c0001t0002g0083 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.63+5510C>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 855877 | |||||||
| chr11:855877 | C | G | 1 | a0001c0001t0001g0217 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.63+5510C>G | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 855877 | |||||||
| chr11:855918 | C | T | 2 | a0001c0001t0001g0036 a0001c0001t0001g0208 |
3 | HG01934.hp2 HG01975.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.63+5551C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 855918 | |||||||
| chr11:855935 | A | G | 319 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(316): Show |
391 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(388): Show |
intron_variant | MODIFIER | c.63+5568A>G | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 855935 | |||||||
| chr11:855978 | C | T | 1 | a0001c0001t0002g0106 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.63+5611C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 855978 | |||||||
| chr11:856020 | T | C | 1 | a0001c0001t0003g0155 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.63+5653T>C | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 856020 | |||||||
| chr11:856061 | T | A | 1 | a0001c0001t0002g0083 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.63+5694T>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 856061 | |||||||
| chr11:856198 | T | C | 1 | a0001c0007t0002g0315 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.63+5831T>C | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 856198 | |||||||
| chr11:856319 | C | T | 3 | a0001c0001t0002g0152 a0001c0001t0002g0153 a0001c0001t0002g0154 |
3 | HG02622.hp2 HG02970.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.63+5952C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 856319 | |||||||
| chr11:856320 | G | A | 1 | a0001c0001t0001g0258 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.63+5953G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 856320 | |||||||
| chr11:856329 | CCAGAGAT others(68): Show |
C | 1 | a0001c0007t0002g0315 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.63+5966_63+6040del others(75): Show |
TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 856329 | ||||||
| chr11:856461 | T | C | 7 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0174 others(4): Show |
11 | HG00642.hp2 HG01109.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.64-6089T>C | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 856461 | |||||||
| chr11:856556 | C | CG | 5 | a0001c0001t0001g0138 a0001c0001t0001g0222 a0001c0001t0001g0270 others(2): Show |
5 | NA18946.hp2 NA18949.hp1 NA18949.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-5992dupG | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 856556 | ||||||
| chr11:856557 | G | A | 2 | a0001c0001t0001g0156 a0001c0001t0001g0157 |
2 | HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.64-5993G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 856557 | |||||||
| chr11:856559 | C | G | 318 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(315): Show |
390 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(387): Show |
intron_variant | MODIFIER | c.64-5991C>G | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 856559 | |||||||
| chr11:856639 | C | T | 1 | a0001c0001t0002g0105 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.64-5911C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 856639 | |||||||
| chr11:856799 | T | C | 1 | a0001c0001t0001g0078 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.64-5751T>C | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 856799 | |||||||
| chr11:856890 | G | A | 1 | a0001c0001t0008g0046 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.64-5660G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 856890 | |||||||
| chr11:856971 | A | G | 319 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(316): Show |
391 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(388): Show |
intron_variant | MODIFIER | c.64-5579A>G | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 856971 | |||||||
| chr11:856992 | C | T | 101 | a0001c0001t0001g0087 a0001c0001t0001g0104 a0001c0001t0001g0126 others(98): Show |
125 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.64-5558C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 856992 | |||||||
| chr11:856995 | G | A | 1 | a0001c0001t0003g0161 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.64-5555G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 856995 | |||||||
| chr11:857065 | C | T | 1 | a0001c0001t0001g0179 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.64-5485C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 857065 | |||||||
| chr11:857182 | A | G | 1 | a0001c0001t0001g0281 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.64-5368A>G | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 857182 | |||||||
| chr11:857183 | G | A | 1 | a0001c0001t0001g0281 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.64-5367G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 857183 | |||||||
| chr11:857242 | C | T | 1 | a0001c0001t0001g0238 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.64-5308C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 857242 | |||||||
| chr11:857288 | G | T | 1 | a0001c0001t0001g0137 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.64-5262G>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 857288 | |||||||
| chr11:857311 | G | C | 1 | a0001c0001t0001g0238 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.64-5239G>C | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 857311 | |||||||
| chr11:857312 | C | G | 1 | a0001c0001t0001g0238 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.64-5238C>G | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 857312 | |||||||
| chr11:857345 | G | A | 36 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0025 others(33): Show |
44 | HG00140.hp1 HG00733.hp1 HG01070.hp2 others(41): Show |
intron_variant | MODIFIER | c.64-5205G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 857345 | |||||||
| chr11:857352 | G | C | 1 | a0001c0001t0002g0124 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.64-5198G>C | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 857352 | |||||||
| chr11:857361 | G | A | 9 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0174 others(6): Show |
13 | HG00642.hp2 HG01109.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.64-5189G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 857361 | |||||||
| chr11:857400 | G | GTT | 48 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0025 others(45): Show |
59 | HG00733.hp1 HG01070.hp2 HG01071.hp2 others(56): Show |
intron_variant | MODIFIER | c.64-5131_64-5130dup others(2): Show |
TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 857400 | ||||||
| chr11:857400 | G | GTTT | 192 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0015 others(189): Show |
237 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(234): Show |
intron_variant | MODIFIER | c.64-5132_64-5130dup others(3): Show |
TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 857400 | ||||||
| chr11:857400 | G | GTTTT | 65 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0031 others(62): Show |
76 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.64-5133_64-5130dup others(4): Show |
TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 857400 | ||||||
| chr11:857400 | G | GTTTTT | 12 | a0001c0001t0001g0007 a0001c0001t0001g0179 a0001c0001t0001g0187 others(9): Show |
15 | HG01192.hp1 HG01261.hp2 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.64-5134_64-5130dup others(5): Show |
TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 857400 | ||||||
| chr11:857461 | G | A | 1 | a0002c0009t0002g0052 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.64-5089G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 857461 | |||||||
| chr11:857469 | G | C | 1 | a0001c0007t0002g0315 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.64-5081G>C | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 857469 | |||||||
| chr11:857485 | C | T | 1 | a0001c0001t0001g0214 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.64-5065C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 857485 | |||||||
| chr11:857495 | T | C | 1 | a0001c0001t0001g0246 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.64-5055T>C | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 857495 | |||||||
| chr11:857526 | CT | C | 6 | a0001c0001t0001g0038 a0001c0001t0001g0142 a0001c0001t0001g0258 others(3): Show |
7 | HG02004.hp1 HG02683.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-5023delT | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 857526 | |||||||
| chr11:857537 | C | T | 1 | a0001c0001t0001g0065 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.64-5013C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 857537 | |||||||
| chr11:857602 | C | A | 2 | a0001c0001t0002g0265 a0001c0001t0002g0266 |
2 | HG00544.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.64-4948C>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 857602 | |||||||
| chr11:857604 | C | T | 2 | a0001c0001t0002g0265 a0001c0001t0002g0266 |
2 | HG00544.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.64-4946C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 857604 | |||||||
| chr11:857650 | G | A | 191 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(188): Show |
234 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.64-4900G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 857650 | |||||||
| chr11:857789 | C | T | 58 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(55): Show |
69 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.64-4761C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 857789 | |||||||
| chr11:857819 | G | C | 1 | a0001c0001t0002g0056 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.64-4731G>C | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 857819 | |||||||
| chr11:857820 | C | T | 1 | a0001c0001t0002g0056 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.64-4730C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 857820 | |||||||
| chr11:857840 | T | G | 1 | a0001c0001t0002g0056 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.64-4710T>G | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 857840 | |||||||
| chr11:858078 | G | A | 9 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0228 others(6): Show |
10 | HG02074.hp2 HG02129.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.64-4472G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 858078 | |||||||
| chr11:858097 | G | A | 1 | a0001c0001t0002g0092 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.64-4453G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 858097 | |||||||
| chr11:858138 | G | A | 3 | a0001c0001t0001g0045 a0001c0001t0001g0223 a0001c0001t0008g0046 |
3 | HG02145.hp1 HG02818.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.64-4412G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 858138 | |||||||
| chr11:858232 | T | G | 1 | a0001c0002t0001g0215 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.64-4318T>G | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 858232 | |||||||
| chr11:858314 | C | G | 1 | a0001c0001t0001g0303 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.64-4236C>G | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 858314 | |||||||
| chr11:858332 | T | C | 1 | a0001c0007t0002g0315 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.64-4218T>C | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 858332 | |||||||
| chr11:858394 | A | C | 1 | a0001c0001t0002g0056 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.64-4156A>C | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 858394 | |||||||
| chr11:858400 | G | C | 1 | a0001c0001t0002g0056 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.64-4150G>C | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 858400 | |||||||
| chr11:858408 | T | G | 1 | a0001c0001t0002g0056 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.64-4142T>G | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 858408 | |||||||
| chr11:858410 | A | G | 1 | a0001c0001t0002g0056 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.64-4140A>G | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 858410 | |||||||
| chr11:858411 | T | A | 1 | a0001c0001t0002g0056 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.64-4139T>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 858411 | |||||||
| chr11:858412 | T | G | 1 | a0001c0001t0002g0056 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.64-4138T>G | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 858412 | |||||||
| chr11:858413 | A | T | 2 | a0001c0001t0002g0056 a0001c0007t0002g0315 |
2 | HG02965.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.64-4137A>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 858413 | |||||||
| chr11:858414 | G | A | 1 | a0001c0001t0001g0282 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.64-4136G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 858414 | |||||||
| chr11:858424 | C | T | 102 | a0001c0001t0001g0087 a0001c0001t0001g0104 a0001c0001t0001g0126 others(99): Show |
126 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.64-4126C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 858424 | |||||||
| chr11:858476 | CCACCCTG others(9): Show |
C | 2 | a0001c0004t0002g0101 a0001c0004t0002g0102 |
2 | HG00423.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.64-4059_64-4044del others(16): Show |
TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 858476 | ||||||
| chr11:858559 | AGGCTCAC others(10): Show |
A | 1 | a0001c0001t0002g0092 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.64-3982_64-3966del others(17): Show |
TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 858559 | ||||||
| chr11:858560 | GGCTCACA others(26): Show |
G | 1 | a0001c0001t0001g0226 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.64-3982_64-3950del others(33): Show |
TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 858560 | ||||||
| chr11:858609 | G | A | 1 | a0001c0001t0002g0085 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.64-3941G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 858609 | |||||||
| chr11:858618 | G | A | 2 | a0001c0001t0001g0168 a0001c0001t0001g0169 |
2 | HG02056.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.64-3932G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 858618 | |||||||
| chr11:858634 | G | GCACCCCG others(6): Show |
14 | a0001c0001t0001g0038 a0001c0001t0001g0142 a0001c0001t0001g0217 others(11): Show |
16 | HG00741.hp2 HG01884.hp1 HG02004.hp1 others(13): Show |
intron_variant | MODIFIER | c.64-3910_64-3898dup others(13): Show |
TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 858634 | ||||||
| chr11:858650 | C | T | 1 | a0001c0007t0002g0315 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.64-3900C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 858650 | |||||||
| chr11:858759 | C | T | 315 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(312): Show |
387 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(384): Show |
intron_variant | MODIFIER | c.64-3791C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 858759 | |||||||
| chr11:858806 | C | T | 1 | a0001c0001t0001g0204 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.64-3744C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 858806 | |||||||
| chr11:858820 | G | A | 103 | a0001c0001t0001g0087 a0001c0001t0001g0104 a0001c0001t0001g0126 others(100): Show |
127 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.64-3730G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 858820 | |||||||
| chr11:858904 | ACACGCAC others(9): Show |
A | 1 | a0001c0001t0001g0249 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.64-3635_64-3620del others(16): Show |
TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 858904 | ||||||
| chr11:858905 | C | G | 2 | a0001c0001t0001g0220 a0001c0001t0001g0307 |
2 | HG02976.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.64-3645C>G | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 858905 | |||||||
| chr11:858907 | CGCACCCC others(105): Show |
C | 2 | a0001c0001t0001g0300 a0001c0001t0001g0301 |
2 | HG01243.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.64-3607_64-3496del | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 858907 | ||||||
| chr11:858943 | CCCAACAG others(102): Show |
C | 1 | a0001c0007t0002g0315 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.64-3556_64-3448del | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 858943 | ||||||
| chr11:859035 | C | T | 2 | a0001c0001t0003g0130 a0001c0001t0003g0134 |
2 | HG00738.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.64-3515C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 859035 | |||||||
| chr11:859068 | C | T | 2 | a0001c0001t0001g0228 a0001c0001t0001g0229 |
2 | HG02129.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.64-3482C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 859068 | |||||||
| chr11:859070 | C | T | 1 | a0001c0001t0002g0086 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.64-3480C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 859070 | |||||||
| chr11:859151 | C | T | 1 | a0001c0007t0002g0315 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.64-3399C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 859151 | |||||||
| chr11:859179 | C | T | 1 | a0001c0007t0002g0315 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.64-3371C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 859179 | |||||||
| chr11:859294 | C | G | 1 | a0001c0001t0002g0131 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.64-3256C>G | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 859294 | |||||||
| chr11:859295 | A | C | 1 | a0001c0001t0002g0131 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.64-3255A>C | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 859295 | |||||||
| chr11:859296 | C | A | 1 | a0001c0001t0002g0131 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.64-3254C>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 859296 | |||||||
| chr11:859299 | C | CGGCTCAC others(46): Show |
1 | a0001c0001t0001g0310 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.64-3232_64-3231ins others(53): Show |
TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 859299 | ||||||
| chr11:859299 | C | CGGCTCAC others(45): Show |
19 | a0001c0001t0001g0002 a0001c0001t0001g0025 a0001c0001t0001g0042 others(16): Show |
24 | HG00140.hp1 HG00733.hp1 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.64-3207_64-3156dup others(52): Show |
TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 859299 | ||||||
| chr11:859299 | C | CGGCTCAC others(45): Show |
4 | a0001c0001t0001g0041 a0001c0001t0001g0279 a0001c0001t0001g0280 others(1): Show |
5 | HG03927.hp1 NA18967.hp2 NA19002.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-3239_64-3238ins others(52): Show |
TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 859299 | ||||||
| chr11:859310 | C | T | 1 | a0001c0007t0002g0315 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.64-3240C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 859310 | |||||||
| chr11:859319 | T | C | 5 | a0001c0001t0001g0054 a0001c0001t0001g0235 a0001c0001t0001g0256 others(2): Show |
5 | HG02056.hp1 HG02109.hp2 NA18966.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-3231T>C | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 859319 | |||||||
| chr11:859320 | TTCACACG others(10): Show |
T | 57 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(54): Show |
69 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.64-3199_64-3183del others(17): Show |
TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 859320 | ||||||
| chr11:859320 | TTCACACG others(142): Show |
T | 2 | a0001c0001t0001g0274 a0001c0001t0001g0285 |
2 | HG03516.hp1 NA18946.hp1 |
intron_variant | MODIFIER | c.64-3181_64-3033del | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 859320 | ||||||
| chr11:859321 | TCACACGC others(9): Show |
T | 5 | a0001c0001t0001g0054 a0001c0001t0001g0235 a0001c0001t0001g0256 others(2): Show |
5 | HG02056.hp1 HG02109.hp2 NA18966.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-3228_64-3213del others(16): Show |
TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 859321 | |||||||
| chr11:859330 | C | A | 2 | a0001c0001t0002g0070 a0001c0001t0002g0109 |
2 | HG02738.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.64-3220C>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 859330 | |||||||
| chr11:859337 | C | CTCACACG others(29): Show |
1 | a0001c0001t0001g0290 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.64-3180_64-3179ins others(36): Show |
TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 859337 | ||||||
| chr11:859337 | C | CTCACACG others(28): Show |
6 | a0001c0001t0001g0019 a0001c0001t0001g0140 a0001c0001t0001g0267 others(3): Show |
8 | HG02015.hp1 HG02040.hp2 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.64-3190_64-3156dup others(35): Show |
TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 859337 | ||||||
| chr11:859343 | CGCACCCC others(45): Show |
C | 1 | a0001c0007t0002g0315 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.64-3197_64-3146del others(52): Show |
TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 859343 | ||||||
| chr11:859346 | ACCCCGGG others(11): Show |
A | 1 | a0001c0001t0002g0131 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.64-3199_64-3182del others(18): Show |
TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 859346 | ||||||
| chr11:859346 | ACCCCGGG others(12): Show |
A | 98 | a0001c0001t0001g0087 a0001c0001t0001g0104 a0001c0001t0001g0126 others(95): Show |
122 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.64-3199_64-3181del others(19): Show |
TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 859346 | ||||||
| chr11:859347 | C | CCCCCCTT others(120): Show |
1 | a0001c0001t0002g0059 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.64-3200_64-3199ins others(127): Show |
TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 859347 | ||||||
| chr11:859351 | G | C | 1 | a0001c0001t0002g0059 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.64-3199G>C | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 859351 | |||||||
| chr11:859354 | CTCACACG others(11): Show |
C | 1 | a0001c0001t0001g0204 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.64-3182_64-3165del others(18): Show |
TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 859354 | ||||||
| chr11:859371 | T | C | 98 | a0001c0001t0001g0087 a0001c0001t0001g0104 a0001c0001t0001g0126 others(95): Show |
122 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.64-3179T>C | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 859371 | |||||||
| chr11:859372 | T | C | 1 | a0001c0001t0002g0059 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.64-3178T>C | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 859372 | |||||||
| chr11:859372 | T | G | 1 | a0001c0001t0002g0131 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.64-3178T>G | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 859372 | |||||||
| chr11:859376 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.64-3174C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 859376 | |||||||
| chr11:859388 | G | C | 1 | a0001c0001t0002g0059 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.64-3162G>C | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 859388 | |||||||
| chr11:859388 | GCTCACAT others(25): Show |
G | 2 | a0001c0001t0001g0078 a0001c0001t0001g0257 |
2 | HG02647.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.64-3155_64-3124del others(32): Show |
TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 859388 | ||||||
| chr11:859393 | C | G | 1 | a0001c0001t0002g0068 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.64-3157C>G | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 859393 | |||||||
| chr11:859395 | T | C | 314 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(311): Show |
386 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(383): Show |
intron_variant | MODIFIER | c.64-3155T>C | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 859395 | |||||||
| chr11:859398 | A | ACCCCGGG others(46): Show |
1 | a0001c0001t0001g0281 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.64-3146_64-3145ins others(53): Show |
TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 859398 | ||||||
| chr11:859402 | C | CCCCTTTC others(12): Show |
2 | a0001c0001t0001g0168 a0001c0001t0001g0169 |
2 | HG02056.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.64-3148_64-3147ins others(19): Show |
TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 859402 | |||||||
| chr11:859402 | C | CGGGCTCA others(29): Show |
1 | a0001c0001t0001g0282 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.64-3146_64-3145ins others(36): Show |
TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 859402 | ||||||
| chr11:859404 | G | GCTCACAC others(9): Show |
1 | a0001c0001t0002g0059 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.64-3131_64-3116dup others(16): Show |
TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 859404 | ||||||
| chr11:859409 | C | T | 1 | a0001c0007t0002g0315 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.64-3141C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 859409 | |||||||
| chr11:859410 | A | T | 1 | a0001c0001t0002g0131 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.64-3140A>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 859410 | |||||||
| chr11:859413 | C | T | 149 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(146): Show |
184 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(181): Show |
intron_variant | MODIFIER | c.64-3137C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 859413 | |||||||
| chr11:859418 | CCTCTCAC others(11): Show |
C | 3 | a0001c0001t0001g0232 a0001c0001t0001g0300 a0001c0001t0001g0301 |
3 | HG01243.hp2 HG02451.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.64-3128_64-3111del others(18): Show |
TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 859418 | ||||||
| chr11:859419 | C | G | 3 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0282 |
3 | HG02056.hp2 HG02135.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.64-3131C>G | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 859419 | |||||||
| chr11:859419 | CTCTCACA others(10): Show |
C | 3 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 |
3 | HG02055.hp2 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.64-3130_64-3114del others(17): Show |
TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 859419 | |||||||
| chr11:859420 | T | G | 3 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0282 |
3 | HG02056.hp2 HG02135.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.64-3130T>G | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 859420 | |||||||
| chr11:859420 | TCTCACAC others(9): Show |
T | 144 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0015 others(141): Show |
173 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.64-3115_64-3100del others(16): Show |
TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 859420 | ||||||
| chr11:859420 | TCTCACAC others(41): Show |
T | 1 | a0001c0001t0001g0031 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.64-3113_64-3066del others(48): Show |
TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 859420 | ||||||
| chr11:859422 | TCACACGC others(7): Show |
T | 1 | a0001c0001t0001g0047 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.64-3126_64-3113del others(14): Show |
TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 859422 | ||||||
| chr11:859432 | CCCGGCTC others(22): Show |
C | 1 | a0001c0001t0001g0145 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.64-3115_64-3087del others(29): Show |
TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 859432 | ||||||
| chr11:859434 | CGGCTCAC others(26): Show |
C | 51 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(48): Show |
69 | HG00621.hp2 HG00642.hp2 HG00673.hp1 others(66): Show |
intron_variant | MODIFIER | c.64-3114_64-3082del others(33): Show |
TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 859434 | ||||||
| chr11:859434 | CGGCTCAC others(43): Show |
C | 1 | a0001c0001t0001g0312 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.64-3114_64-3065del others(50): Show |
TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 859434 | ||||||
| chr11:859435 | G | C | 5 | a0001c0001t0001g0078 a0001c0001t0001g0168 a0001c0001t0001g0169 others(2): Show |
5 | HG02056.hp2 HG02135.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.64-3115G>C | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 859435 | |||||||
| chr11:859436 | G | C | 1 | a0001c0001t0001g0281 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.64-3114G>C | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 859436 | |||||||
| chr11:859436 | G | T | 5 | a0001c0001t0001g0078 a0001c0001t0001g0168 a0001c0001t0001g0169 others(2): Show |
5 | HG02056.hp2 HG02135.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.64-3114G>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 859436 | |||||||
| chr11:859447 | CCCCCCTC others(7): Show |
C | 1 | a0001c0001t0001g0281 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.64-3098_64-3085del others(14): Show |
TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 859447 | ||||||
| chr11:859451 | CCTCACAC others(10): Show |
C | 48 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0030 others(45): Show |
56 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(53): Show |
intron_variant | MODIFIER | c.64-3050_64-3034del others(17): Show |
TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 859451 | ||||||
| chr11:859460 | C | T | 1 | a0001c0001t0002g0022 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.64-3090C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 859460 | |||||||
| chr11:859468 | G | C | 51 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(48): Show |
69 | HG00621.hp2 HG00642.hp2 HG00673.hp1 others(66): Show |
intron_variant | MODIFIER | c.64-3082G>C | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 859468 | |||||||
| chr11:859475 | C | T | 2 | a0001c0001t0001g0062 a0001c0001t0001g0064 |
2 | NA19004.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.64-3075C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 859475 | |||||||
| chr11:859484 | G | C | 1 | a0001c0007t0002g0315 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.64-3066G>C | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 859484 | |||||||
| chr11:859485 | G | C | 1 | a0001c0001t0001g0312 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.64-3065G>C | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 859485 | |||||||
| chr11:859485 | G | T | 1 | a0001c0007t0002g0315 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.64-3065G>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 859485 | |||||||
| chr11:859488 | C | T | 1 | a0001c0007t0002g0315 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.64-3062C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 859488 | |||||||
| chr11:859504 | T | C | 1 | a0001c0007t0002g0315 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.64-3046T>C | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 859504 | |||||||
| chr11:859518 | T | G | 1 | a0001c0007t0002g0315 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.64-3032T>G | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 859518 | |||||||
| chr11:859519 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.64-3031C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 859519 | |||||||
| chr11:859521 | T | C | 1 | a0001c0007t0002g0315 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.64-3029T>C | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 859521 | |||||||
| chr11:859532 | C | T | 3 | a0001c0001t0001g0308 a0001c0001t0001g0309 a0001c0001t0001g0311 |
3 | HG02056.hp1 HG02132.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.64-3018C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 859532 | |||||||
| chr11:859579 | C | T | 1 | a0001c0001t0001g0225 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.64-2971C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 859579 | |||||||
| chr11:859670 | C | T | 2 | a0001c0001t0001g0220 a0001c0001t0001g0307 |
2 | HG02976.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.64-2880C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 859670 | |||||||
| chr11:859722 | C | A | 1 | a0001c0001t0001g0228 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.64-2828C>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 859722 | |||||||
| chr11:859827 | C | T | 1 | a0001c0001t0002g0304 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.64-2723C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 859827 | |||||||
| chr11:859837 | A | G | 1 | a0001c0007t0002g0315 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.64-2713A>G | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 859837 | |||||||
| chr11:859891 | G | C | 1 | a0001c0001t0002g0093 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.64-2659G>C | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 859891 | |||||||
| chr11:859915 | C | T | 212 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(209): Show |
260 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(257): Show |
intron_variant | MODIFIER | c.64-2635C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 859915 | |||||||
| chr11:860081 | A | G | 1 | a0001c0007t0002g0315 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.64-2469A>G | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 860081 | |||||||
| chr11:860086 | G | A | 1 | a0001c0001t0002g0131 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.64-2464G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 860086 | |||||||
| chr11:860090 | C | A | 1 | a0001c0001t0002g0131 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.64-2460C>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 860090 | |||||||
| chr11:860107 | G | A | 1 | a0001c0007t0002g0315 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.64-2443G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 860107 | |||||||
| chr11:860190 | T | A | 1 | a0001c0001t0002g0091 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.64-2360T>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 860190 | |||||||
| chr11:860236 | A | G | 1 | a0001c0007t0002g0315 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.64-2314A>G | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 860236 | |||||||
| chr11:860290 | T | C | 1 | a0001c0001t0002g0080 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.64-2260T>C | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 860290 | |||||||
| chr11:860504 | C | A | 1 | a0001c0001t0003g0125 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.64-2046C>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 860504 | |||||||
| chr11:860539 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.64-2011C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 860539 | |||||||
| chr11:860610 | G | A | 1 | a0001c0001t0002g0107 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.64-1940G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 860610 | |||||||
| chr11:860635 | C | T | 2 | a0001c0001t0001g0045 a0001c0001t0008g0046 |
2 | HG02145.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.64-1915C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 860635 | |||||||
| chr11:860825 | C | A | 1 | a0001c0006t0002g0034 | 2 | HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.64-1725C>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 860825 | |||||||
| chr11:860878 | G | A | 1 | a0001c0001t0003g0186 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.64-1672G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 860878 | |||||||
| chr11:860880 | G | A | 1 | a0001c0001t0001g0045 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.64-1670G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 860880 | |||||||
| chr11:860996 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.64-1554C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 860996 | |||||||
| chr11:861098 | G | C | 101 | a0001c0001t0001g0087 a0001c0001t0001g0104 a0001c0001t0002g0001 others(98): Show |
125 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.64-1452G>C | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 861098 | |||||||
| chr11:861108 | G | A | 1 | a0001c0001t0001g0198 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.64-1442G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 861108 | |||||||
| chr11:861434 | T | C | 1 | a0001c0007t0002g0315 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.64-1116T>C | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 861434 | |||||||
| chr11:861440 | T | C | 1 | a0001c0007t0002g0315 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.64-1110T>C | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 861440 | |||||||
| chr11:861487 | T | C | 1 | a0001c0007t0002g0315 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.64-1063T>C | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 861487 | |||||||
| chr11:861500 | T | C | 1 | a0001c0007t0002g0315 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.64-1050T>C | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 861500 | |||||||
| chr11:861501 | G | A | 1 | a0001c0007t0002g0315 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.64-1049G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 861501 | |||||||
| chr11:861503 | G | A | 1 | a0001c0001t0001g0267 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.64-1047G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 861503 | |||||||
| chr11:861509 | A | G | 1 | a0001c0001t0001g0037 | 2 | HG01071.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.64-1041A>G | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 861509 | |||||||
| chr11:861528 | C | T | 1 | a0001c0001t0001g0037 | 2 | HG01071.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.64-1022C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 861528 | |||||||
| chr11:861539 | T | C | 1 | a0001c0001t0001g0037 | 2 | HG01071.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.64-1011T>C | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 861539 | |||||||
| chr11:861568 | T | C | 1 | a0001c0007t0002g0315 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.64-982T>C | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 861568 | |||||||
| chr11:861644 | G | A | 2 | a0001c0001t0001g0078 a0001c0001t0001g0126 |
2 | HG03139.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.64-906G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 861644 | |||||||
| chr11:861711 | C | A | 2 | a0001c0001t0001g0228 a0001c0001t0001g0229 |
2 | HG02129.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.64-839C>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 861711 | |||||||
| chr11:861711 | C | CA | 19 | a0001c0001t0001g0060 a0001c0001t0001g0187 a0001c0001t0001g0199 others(16): Show |
19 | HG00642.hp2 HG01192.hp2 HG01261.hp1 others(16): Show |
intron_variant | MODIFIER | c.64-829dupA | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 861711 | ||||||
| chr11:861721 | A | G | 1 | a0001c0001t0002g0100 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.64-829A>G | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 861721 | |||||||
| chr11:861775 | C | T | 1 | a0001c0001t0002g0266 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.64-775C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 861775 | |||||||
| chr11:861814 | G | A | 100 | a0001c0001t0001g0087 a0001c0001t0001g0104 a0001c0001t0002g0001 others(97): Show |
124 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.64-736G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 861814 | |||||||
| chr11:861852 | G | A | 1 | a0001c0001t0001g0012 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.64-698G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 861852 | |||||||
| chr11:861965 | T | C | 1 | a0001c0007t0002g0315 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.64-585T>C | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 861965 | |||||||
| chr11:861980 | G | A | 1 | a0001c0001t0008g0046 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.64-570G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 861980 | |||||||
| chr11:861982 | T | C | 1 | a0001c0001t0001g0074 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.64-568T>C | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 861982 | |||||||
| chr11:861997 | T | C | 3 | a0001c0001t0001g0015 a0001c0001t0001g0269 a0001c0001t0001g0272 |
5 | HG00423.hp1 NA18951.hp2 NA18995.hp1 others(2): Show |
intron_variant | MODIFIER | c.64-553T>C | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 861997 | |||||||
| chr11:862071 | G | T | 1 | a0001c0001t0002g0131 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.64-479G>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 862071 | |||||||
| chr11:862084 | C | T | 1 | a0001c0001t0002g0304 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.64-466C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 862084 | |||||||
| chr11:862159 | A | G | 1 | a0001c0007t0002g0315 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.64-391A>G | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 862159 | |||||||
| chr11:862184 | C | T | 1 | a0001c0001t0002g0153 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.64-366C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 862184 | |||||||
| chr11:862217 | T | C | 2 | a0001c0001t0001g0078 a0001c0001t0001g0126 |
2 | HG03139.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.64-333T>C | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 862217 | |||||||
| chr11:862236 | GTCCCTTT others(3): Show |
G | 7 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0228 others(4): Show |
7 | HG02074.hp2 HG02129.hp1 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-310_64-301delCT others(8): Show |
TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 862236 | ||||||
| chr11:862312 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.64-238C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 862312 | |||||||
| chr11:862385 | G | A | 1 | a0001c0001t0001g0295 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.64-165G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 862385 | |||||||
| chr11:862404 | C | T | 2 | a0001c0001t0001g0163 a0001c0001t0001g0245 |
2 | HG02165.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.64-146C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 862404 | |||||||
| chr11:862505 | T | C | 73 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(70): Show |
85 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.64-45T>C | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 862505 | |||||||
| chr11:862526 | G | C | 1 | a0001c0001t0001g0195 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.64-24G>C | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 862526 | |||||||
| chr11:862533 | C | A | 1 | a0001c0007t0002g0315 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.64-17C>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 3/8 | chr11 | 862533 | |||||||
| chr11:862802 | C | T | 1 | a0001c0007t0002g0315 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.255+61C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 4/8 | chr11 | 862802 | |||||||
| chr11:862820 | C | T | 1 | a0001c0013t0001g0242 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.255+79C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 4/8 | chr11 | 862820 | |||||||
| chr11:862828 | C | T | 1 | a0001c0005t0002g0316 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.255+87C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 4/8 | chr11 | 862828 | |||||||
| chr11:862830 | C | T | 1 | a0001c0001t0002g0099 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.255+89C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 4/8 | chr11 | 862830 | |||||||
| chr11:862885 | G | A | 2 | a0001c0001t0002g0184 a0001c0006t0002g0034 |
3 | HG02723.hp1 HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.255+144G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 4/8 | chr11 | 862885 | |||||||
| chr11:862933 | G | C | 21 | a0001c0001t0001g0012 a0001c0001t0001g0035 a0001c0001t0001g0181 others(18): Show |
24 | HG00735.hp1 HG00741.hp1 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.255+192G>C | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 4/8 | chr11 | 862933 | |||||||
| chr11:862997 | C | G | 1 | a0001c0001t0003g0072 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.255+256C>G | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 4/8 | chr11 | 862997 | |||||||
| chr11:863029 | A | G | 23 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0060 others(20): Show |
26 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(23): Show |
intron_variant | MODIFIER | c.255+288A>G | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 4/8 | chr11 | 863029 | |||||||
| chr11:863037 | G | A | 13 | a0001c0001t0001g0016 a0001c0001t0001g0045 a0001c0001t0001g0179 others(10): Show |
15 | HG00140.hp2 HG02109.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.255+296G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 4/8 | chr11 | 863037 | |||||||
| chr11:863079 | G | A | 1 | a0001c0001t0001g0303 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.255+338G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 4/8 | chr11 | 863079 | |||||||
| chr11:863172 | G | A | 1 | a0001c0001t0001g0196 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.255+431G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 4/8 | chr11 | 863172 | |||||||
| chr11:863183 | C | T | 6 | a0001c0001t0001g0006 a0001c0001t0001g0192 a0001c0001t0001g0200 others(3): Show |
9 | NA18941.hp1 NA18952.hp2 NA18969.hp1 others(6): Show |
intron_variant | MODIFIER | c.255+442C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 4/8 | chr11 | 863183 | |||||||
| chr11:863335 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.255+594G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 4/8 | chr11 | 863335 | |||||||
| chr11:863379 | C | T | 2 | a0001c0001t0001g0036 a0001c0001t0001g0208 |
3 | HG01934.hp2 HG01975.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.255+638C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 4/8 | chr11 | 863379 | |||||||
| chr11:863380 | G | A | 1 | a0001c0001t0001g0136 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.255+639G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 4/8 | chr11 | 863380 | |||||||
| chr11:863414 | T | C | 1 | a0001c0001t0001g0264 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.255+673T>C | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 4/8 | chr11 | 863414 | |||||||
| chr11:863428 | C | A | 1 | a0001c0001t0001g0163 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.255+687C>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 4/8 | chr11 | 863428 | |||||||
| chr11:863455 | A | G | 1 | a0001c0001t0001g0104 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.255+714A>G | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 4/8 | chr11 | 863455 | |||||||
| chr11:863458 | C | A | 1 | a0001c0001t0001g0247 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.255+717C>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 4/8 | chr11 | 863458 | |||||||
| chr11:863830 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.256-607G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 4/8 | chr11 | 863830 | |||||||
| chr11:863847 | G | A | 3 | a0001c0001t0001g0108 a0001c0001t0001g0114 a0001c0001t0001g0159 |
3 | HG01167.hp2 HG01255.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.256-590G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 4/8 | chr11 | 863847 | |||||||
| chr11:863948 | C | T | 1 | a0001c0001t0001g0143 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.256-489C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 4/8 | chr11 | 863948 | |||||||
| chr11:863974 | T | C | 2 | a0001c0001t0002g0261 a0001c0001t0002g0275 |
2 | HG03017.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.256-463T>C | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 4/8 | chr11 | 863974 | |||||||
| chr11:864051 | C | T | 1 | a0001c0001t0001g0281 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.256-386C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 4/8 | chr11 | 864051 | |||||||
| chr11:864299 | C | T | 2 | a0001c0001t0003g0130 a0001c0001t0003g0134 |
2 | HG00738.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.256-138C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 4/8 | chr11 | 864299 | |||||||
| chr11:864336 | C | A | 1 | a0001c0007t0002g0315 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.256-101C>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 4/8 | chr11 | 864336 | |||||||
| chr11:864376 | T | C | 1 | a0001c0001t0001g0210 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.256-61T>C | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 4/8 | chr11 | 864376 | |||||||
| chr11:864561 | C | G | 3 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 |
3 | HG02055.hp2 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.330+50C>G | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 5/8 | chr11 | 864561 | |||||||
| chr11:864587 | C | G | 1 | a0001c0007t0002g0315 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.330+76C>G | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 5/8 | chr11 | 864587 | |||||||
| chr11:864626 | A | G | 319 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(316): Show |
391 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(388): Show |
intron_variant | MODIFIER | c.330+115A>G | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 5/8 | chr11 | 864626 | |||||||
| chr11:864675 | C | T | 2 | a0001c0001t0001g0039 a0001c0001t0001g0253 |
3 | NA18959.hp1 NA18985.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.330+164C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 5/8 | chr11 | 864675 | |||||||
| chr11:864707 | C | T | 1 | a0001c0001t0001g0303 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.330+196C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 5/8 | chr11 | 864707 | |||||||
| chr11:864835 | C | G | 319 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(316): Show |
391 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(388): Show |
intron_variant | MODIFIER | c.330+324C>G | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 5/8 | chr11 | 864835 | |||||||
| chr11:864893 | C | T | 319 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(316): Show |
391 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(388): Show |
intron_variant | MODIFIER | c.330+382C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 5/8 | chr11 | 864893 | |||||||
| chr11:864903 | G | A | 1 | a0001c0001t0002g0097 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.330+392G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 5/8 | chr11 | 864903 | |||||||
| chr11:864919 | T | C | 1 | a0001c0007t0002g0315 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.330+408T>C | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 5/8 | chr11 | 864919 | |||||||
| chr11:864937 | C | CACA | 319 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(316): Show |
391 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(388): Show |
intron_variant | MODIFIER | c.330+427_330+429dup others(3): Show |
TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr11 | 864937 | ||||||
| chr11:864955 | G | C | 1 | a0001c0001t0001g0045 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.330+444G>C | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 5/8 | chr11 | 864955 | |||||||
| chr11:864969 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.330+458G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 5/8 | chr11 | 864969 | |||||||
| chr11:865257 | G | A | 86 | a0001c0001t0001g0104 a0001c0001t0002g0001 a0001c0001t0002g0004 others(83): Show |
107 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.331-256G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 5/8 | chr11 | 865257 | |||||||
| chr11:865412 | C | T | 1 | a0001c0002t0001g0216 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.331-101C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 5/8 | chr11 | 865412 | |||||||
| chr11:865447 | G | A | 314 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(311): Show |
386 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(383): Show |
intron_variant | MODIFIER | c.331-66G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 5/8 | chr11 | 865447 | |||||||
| chr11:865467 | C | T | 1 | a0001c0001t0002g0086 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.331-46C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 5/8 | chr11 | 865467 | |||||||
| chr11:865495 | C | A | 3 | a0001c0001t0001g0223 a0001c0002t0001g0313 a0001c0002t0001g0314 |
3 | HG01943.hp2 HG02818.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.331-18C>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 5/8 | chr11 | 865495 | |||||||
| chr11:865503 | G | A | 314 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(311): Show |
386 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(383): Show |
intron_variant | MODIFIER | c.331-10G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 5/8 | chr11 | 865503 | |||||||
| chr11:865659 | C | G | 1 | a0001c0001t0003g0155 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.433-35C>G | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 6/8 | chr11 | 865659 | |||||||
| chr11:865673 | C | T | 4 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0228 others(1): Show |
4 | HG02074.hp2 HG02129.hp1 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.433-21C>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 6/8 | chr11 | 865673 | |||||||
| chr11:865897 | G | C | 3 | a0001c0001t0001g0045 a0001c0001t0001g0223 a0001c0001t0008g0046 |
3 | HG02145.hp1 HG02818.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.565-21G>C | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 7/8 | chr11 | 865897 | |||||||
| chr11:865899 | A | G | 2 | a0001c0001t0001g0220 a0001c0001t0001g0307 |
2 | HG02976.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.565-19A>G | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 7/8 | chr11 | 865899 | |||||||
| chr11:866044 | A | G | 319 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(316): Show |
391 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(388): Show |
intron_variant | MODIFIER | c.648+43A>G | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 8/8 | chr11 | 866044 | |||||||
| chr11:866133 | G | A | 1 | a0001c0001t0003g0155 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.648+132G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 8/8 | chr11 | 866133 | |||||||
| chr11:866183 | T | C | 319 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(316): Show |
391 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(388): Show |
intron_variant | MODIFIER | c.648+182T>C | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 8/8 | chr11 | 866183 | |||||||
| chr11:866184 | T | C | 3 | a0001c0001t0003g0130 a0001c0001t0003g0134 a0001c0001t0003g0161 |
3 | HG00738.hp2 HG01257.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.648+183T>C | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 8/8 | chr11 | 866184 | |||||||
| chr11:866250 | A | G | 4 | a0001c0001t0001g0043 a0001c0001t0001g0269 a0001c0001t0001g0305 others(1): Show |
5 | NA18962.hp2 NA18981.hp2 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.648+249A>G | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 8/8 | chr11 | 866250 | |||||||
| chr11:866410 | A | T | 2 | a0001c0001t0002g0094 a0001c0001t0002g0098 |
2 | HG02273.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.649-152A>T | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 8/8 | chr11 | 866410 | |||||||
| chr11:866498 | T | C | 319 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(316): Show |
391 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(388): Show |
intron_variant | MODIFIER | c.649-64T>C | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 8/8 | chr11 | 866498 | |||||||
| chr11:866499 | G | A | 38 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(35): Show |
53 | HG00558.hp2 HG00621.hp2 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.649-63G>A | TSPAN4 | ENSG00000214063.12 | transcript | ENST00000397397.7 | protein_coding | 8/8 | chr11 | 866499 |