Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 23118 |
| ensemblid | ENSG00000055208.20 |
| hgncid | 17075 |
| symbol | TAB2 |
| name | TGF-beta activated kinase 1 (MAP3K7) binding protein 2 |
| refseq_nuc | NM_001292034.3 |
| refseq_prot | NP_001278963.1 |
| ensembl_nuc | ENST00000637181.2 |
| ensembl_prot | ENSP00000490618.1 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 149317712 |
| end | 149411607 |
| strand | + |
| ver | v1.2 |
| region | chr6:149317712-149411607 |
| region5000 | chr6:149312712-149416607 |
| regionname0 | TAB2_chr6_149317712_149411607 |
| regionname5000 | TAB2_chr6_149312712_149416607 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2079 | 275 | 95 | 55 | 85 | 10 | 28 | TAB2_chr6_149312712_149416607 | TAB2 | ATGGC others(2074): Show |
chr6 | 149312712 | 149416607 | ||
| a0001c0002 | 0/0 | 2079 | 84 | 3 | 12 | 61 | 2 | 6 | TAB2_chr6_149312712_149416607 | TAB2 | ATGGC others(2074): Show |
chr6 | 149312712 | 149416607 | ||
| a0001c0003 | 0/0 | 2079 | 2 | 0 | 2 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | ATGGC others(2074): Show |
chr6 | 149312712 | 149416607 | ||
| a0001c0004 | 0/0 | 2079 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | ATGGC others(2074): Show |
chr6 | 149312712 | 149416607 | ||
| a0001c0005 | 0/0 | 2079 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | ATGGC others(2074): Show |
chr6 | 149312712 | 149416607 | ||
| a0001c0006 | 0/0 | 2079 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | ATGGC others(2074): Show |
chr6 | 149312712 | 149416607 | ||
| a0001c0007 | 0/0 | 2079 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | ATGGC others(2074): Show |
chr6 | 149312712 | 149416607 | ||
| a0001c0008 | 0/0 | 2079 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | ATGGC others(2074): Show |
chr6 | 149312712 | 149416607 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4360 | 129 | 39 | 26 | 49 | 5 | 10 | TAB2_chr6_149312712_149416607 | TAB2 | GTCGT others(4355): Show |
chr6 | 149312712 | 149416607 |
| a0001c0001t0003 | 0/1 | 4360 | 61 | 19 | 19 | 10 | 3 | 9 | TAB2_chr6_149312712_149416607 | TAB2 | GTCGT others(4355): Show |
chr6 | 149312712 | 149416607 |
| a0001c0001t0004 | 1/0 | 4363 | 46 | 13 | 7 | 21 | 1 | 3 | TAB2_chr6_149312712_149416607 | TAB2 | GTCGT others(4358): Show |
chr6 | 149312712 | 149416607 |
| a0001c0001t0005 | 0/0 | 4360 | 9 | 3 | 1 | 0 | 0 | 5 | TAB2_chr6_149312712_149416607 | TAB2 | GTCGT others(4355): Show |
chr6 | 149312712 | 149416607 |
| a0001c0001t0007 | 0/0 | 4382 | 5 | 5 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | GTCGT others(4377): Show |
chr6 | 149312712 | 149416607 |
| a0001c0001t0008 | 0/0 | 4360 | 4 | 4 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | GTCGT others(4355): Show |
chr6 | 149312712 | 149416607 |
| a0001c0001t0009 | 0/0 | 4360 | 4 | 4 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | GTCGT others(4355): Show |
chr6 | 149312712 | 149416607 |
| a0001c0001t0010 | 0/0 | 4360 | 3 | 0 | 0 | 3 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | GTCGT others(4355): Show |
chr6 | 149312712 | 149416607 |
| a0001c0001t0011 | 0/0 | 4360 | 3 | 0 | 1 | 0 | 1 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | GTCGT others(4355): Show |
chr6 | 149312712 | 149416607 |
| a0001c0001t0013 | 0/0 | 4360 | 2 | 2 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | GTCGT others(4355): Show |
chr6 | 149312712 | 149416607 |
| a0001c0001t0015 | 0/0 | 4360 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | GTCGT others(4355): Show |
chr6 | 149312712 | 149416607 |
| a0001c0001t0016 | 0/0 | 4348 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | GTCGT others(4343): Show |
chr6 | 149312712 | 149416607 |
| a0001c0001t0017 | 0/0 | 4360 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | GTCGT others(4355): Show |
chr6 | 149312712 | 149416607 |
| a0001c0001t0019 | 0/0 | 4360 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | GTCGT others(4355): Show |
chr6 | 149312712 | 149416607 |
| a0001c0001t0020 | 0/0 | 4363 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | GTCGT others(4358): Show |
chr6 | 149312712 | 149416607 |
| a0001c0001t0021 | 0/0 | 4363 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | GTCGT others(4358): Show |
chr6 | 149312712 | 149416607 |
| a0001c0001t0022 | 0/0 | 4363 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | GTCGT others(4358): Show |
chr6 | 149312712 | 149416607 |
| a0001c0001t0023 | 0/0 | 4382 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | GTCGT others(4377): Show |
chr6 | 149312712 | 149416607 |
| a0001c0001t0024 | 0/0 | 4383 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | GTCGT others(4378): Show |
chr6 | 149312712 | 149416607 |
| a0001c0002t0002 | 0/0 | 4360 | 75 | 3 | 12 | 52 | 2 | 6 | TAB2_chr6_149312712_149416607 | TAB2 | GTCGT others(4355): Show |
chr6 | 149312712 | 149416607 |
| a0001c0002t0006 | 0/0 | 4360 | 5 | 0 | 0 | 5 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | GTCGT others(4355): Show |
chr6 | 149312712 | 149416607 |
| a0001c0002t0012 | 0/0 | 4360 | 2 | 0 | 0 | 2 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | GTCGT others(4355): Show |
chr6 | 149312712 | 149416607 |
| a0001c0002t0014 | 0/0 | 4363 | 2 | 0 | 0 | 2 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | GTCGT others(4358): Show |
chr6 | 149312712 | 149416607 |
| a0001c0003t0001 | 0/0 | 4360 | 2 | 0 | 2 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | GTCGT others(4355): Show |
chr6 | 149312712 | 149416607 |
| a0001c0004t0002 | 0/0 | 4360 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | GTCGT others(4355): Show |
chr6 | 149312712 | 149416607 |
| a0001c0005t0002 | 0/0 | 4360 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | GTCGT others(4355): Show |
chr6 | 149312712 | 149416607 |
| a0001c0006t0004 | 0/0 | 4363 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | GTCGT others(4358): Show |
chr6 | 149312712 | 149416607 |
| a0001c0007t0002 | 0/0 | 4360 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | GTCGT others(4355): Show |
chr6 | 149312712 | 149416607 |
| a0001c0008t0018 | 0/0 | 4360 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | GTCGT others(4355): Show |
chr6 | 149312712 | 149416607 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0354 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0001g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0008 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0306 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0331 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0337 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0003g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0003 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0050 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0004g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0005g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0005g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0005g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0005g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0005g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0005g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0005g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0005g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0005g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0007g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0007g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0007g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0007g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0007g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0008g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0008g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0008g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0008g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0009g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0009g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0009g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0009g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0010g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0010g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0010g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0011g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0011g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0011g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0013g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0013g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0015g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0016g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0017g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0019g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0020g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0021g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0022g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0023g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0001t0024g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0006g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0006g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0006g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0006g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0006g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0012g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0012g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0014g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0002t0014g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0003t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0003t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0004t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0005t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0006t0004g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0007t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| a0001c0008t0018g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0265 | EUR | GBR | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0337 | EUR | GBR | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0142 | EUR | GBR | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0318 | EUR | GBR | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG00423 | hp1 | a0001 | c0002 | t0002 | g0192 | EAS | CHS | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | CHS | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG00558 | hp1 | a0001 | c0002 | t0006 | g0240 | EAS | CHS | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | CHS | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | CHS | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG00597 | hp2 | a0001 | c0002 | t0002 | g0105 | EAS | CHS | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG00609 | hp1 | a0001 | c0002 | t0002 | g0210 | EAS | CHS | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG00609 | hp2 | a0001 | c0001 | t0003 | g0307 | EAS | CHS | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG00621 | hp1 | a0001 | c0002 | t0002 | g0099 | EAS | CHS | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG00621 | hp2 | a0001 | c0002 | t0002 | g0245 | EAS | CHS | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0173 | AMR | PUR | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG00639 | hp2 | a0001 | c0002 | t0002 | g0200 | AMR | PUR | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG00642 | hp1 | a0001 | c0003 | t0001 | g0258 | AMR | PUR | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | CHS | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG00673 | hp2 | a0001 | c0002 | t0002 | g0101 | EAS | CHS | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0291 | AMR | PUR | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG00735 | hp1 | a0001 | c0001 | t0004 | g0069 | AMR | PUR | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG00738 | hp1 | a0001 | c0001 | t0004 | g0068 | AMR | PUR | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0010 | AMR | PUR | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0340 | AMR | PUR | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG00741 | hp2 | a0001 | c0007 | t0002 | g0114 | AMR | PUR | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0286 | AMR | PUR | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01069 | hp2 | a0001 | c0001 | t0004 | g0054 | AMR | PUR | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01070 | hp2 | a0001 | c0001 | t0003 | g0342 | AMR | PUR | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0335 | AMR | PUR | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01071 | hp2 | a0001 | c0001 | t0004 | g0003 | AMR | PUR | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0295 | AMR | PUR | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0293 | AMR | PUR | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0334 | AMR | PUR | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01099 | hp2 | a0001 | c0001 | t0004 | g0043 | AMR | PUR | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0172 | AMR | PUR | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01167 | hp1 | a0001 | c0002 | t0002 | g0229 | AMR | PUR | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0170 | AMR | PUR | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0272 | AMR | PUR | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0317 | AMR | PUR | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01175 | hp1 | a0001 | c0001 | t0021 | g0097 | AMR | PUR | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0321 | AMR | PUR | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0308 | AMR | PUR | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0330 | AMR | PUR | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01243 | hp2 | a0001 | c0001 | t0005 | g0120 | AMR | PUR | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01255 | hp1 | a0001 | c0002 | t0002 | g0239 | AMR | CLM | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0169 | AMR | CLM | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0355 | AMR | CLM | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0345 | AMR | CLM | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01257 | hp1 | a0001 | c0002 | t0002 | g0201 | AMR | CLM | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01257 | hp2 | a0001 | c0001 | t0003 | g0341 | AMR | CLM | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0356 | AMR | CLM | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01258 | hp2 | a0001 | c0002 | t0002 | g0199 | AMR | CLM | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01261 | hp1 | a0001 | c0002 | t0002 | g0109 | AMR | CLM | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | CLM | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01346 | hp2 | a0001 | c0003 | t0001 | g0259 | AMR | CLM | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0353 | AMR | CLM | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | CLM | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0338 | AMR | CLM | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | CLM | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01433 | hp1 | a0001 | c0001 | t0011 | g0140 | AMR | CLM | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01433 | hp2 | a0001 | c0002 | t0002 | g0197 | AMR | CLM | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0301 | AMR | CLM | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0336 | AMR | CLM | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01515 | hp1 | a0001 | c0001 | t0011 | g0139 | EUR | IBS | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01515 | hp2 | a0001 | c0002 | t0002 | g0247 | EUR | IBS | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0284 | EUR | IBS | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01516 | hp2 | a0001 | c0001 | t0004 | g0049 | EUR | IBS | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01517 | hp1 | a0001 | c0002 | t0002 | g0246 | EUR | IBS | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0287 | EUR | IBS | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | ACB | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0329 | AFR | ACB | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01934 | hp1 | a0001 | c0001 | t0004 | g0121 | AMR | PEL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PEL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PEL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01943 | hp2 | a0001 | c0002 | t0002 | g0248 | AMR | PEL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02004 | hp1 | a0001 | c0001 | t0003 | g0174 | AMR | PEL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0283 | AMR | PEL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02015 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | KHV | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02040 | hp1 | a0001 | c0002 | t0002 | g0104 | EAS | KHV | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02040 | hp2 | a0001 | c0001 | t0004 | g0038 | EAS | KHV | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02055 | hp1 | a0001 | c0001 | t0009 | g0084 | AFR | ACB | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | KHV | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02056 | hp2 | a0001 | c0002 | t0006 | g0350 | EAS | KHV | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02080 | hp1 | a0001 | c0008 | t0018 | g0292 | EAS | KHV | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02080 | hp2 | a0001 | c0002 | t0002 | g0220 | EAS | KHV | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02083 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | KHV | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0310 | EAS | KHV | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02129 | hp2 | a0001 | c0002 | t0002 | g0235 | EAS | KHV | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02132 | hp2 | a0001 | c0002 | t0002 | g0100 | EAS | KHV | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0311 | EAS | KHV | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02135 | hp2 | a0001 | c0002 | t0002 | g0112 | EAS | KHV | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02145 | hp2 | a0001 | c0001 | t0009 | g0083 | AFR | ACB | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02148 | hp1 | a0001 | c0002 | t0002 | g0108 | AMR | PEL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | CDX | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02155 | hp2 | a0001 | c0002 | t0002 | g0117 | EAS | CDX | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | ACB | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0316 | AFR | ACB | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02258 | hp1 | a0001 | c0001 | t0004 | g0028 | AFR | ACB | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0299 | AFR | ACB | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0280 | AMR | PEL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02273 | hp2 | a0001 | c0002 | t0002 | g0228 | AMR | PEL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02280 | hp1 | a0001 | c0001 | t0008 | g0165 | AFR | ACB | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0327 | AFR | ACB | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02293 | hp2 | a0001 | c0002 | t0002 | g0217 | AMR | PEL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02300 | hp1 | a0001 | c0002 | t0002 | g0227 | AMR | PEL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0008 | AMR | PEL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0339 | AFR | ACB | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02523 | hp1 | a0001 | c0002 | t0002 | g0244 | EAS | KHV | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02572 | hp2 | a0001 | c0001 | t0009 | g0082 | AFR | GWD | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0277 | SAS | PJL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02602 | hp2 | a0001 | c0001 | t0005 | g0184 | SAS | PJL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02615 | hp1 | a0001 | c0001 | t0004 | g0036 | AFR | GWD | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02615 | hp2 | a0001 | c0001 | t0013 | g0179 | AFR | GWD | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0326 | AFR | GWD | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02630 | hp1 | a0001 | c0001 | t0004 | g0040 | AFR | GWD | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02630 | hp2 | a0001 | c0001 | t0007 | g0078 | AFR | GWD | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0324 | AFR | GWD | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02647 | hp2 | a0001 | c0002 | t0002 | g0098 | AFR | GWD | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02683 | hp1 | a0001 | c0001 | t0005 | g0182 | SAS | PJL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02683 | hp2 | a0001 | c0001 | t0003 | g0344 | SAS | PJL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02698 | hp1 | a0001 | c0002 | t0002 | g0249 | SAS | PJL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02698 | hp2 | a0001 | c0001 | t0004 | g0031 | SAS | PJL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02717 | hp1 | a0001 | c0001 | t0004 | g0185 | AFR | GWD | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02717 | hp2 | a0001 | c0001 | t0008 | g0166 | AFR | GWD | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0261 | SAS | PJL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02735 | hp2 | a0001 | c0002 | t0002 | g0202 | SAS | PJL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | GWD | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02818 | hp1 | a0001 | c0001 | t0005 | g0351 | AFR | GWD | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0186 | AFR | GWD | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0349 | AFR | GWD | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0348 | AFR | GWD | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0175 | AFR | ESN | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | ESN | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02965 | hp1 | a0001 | c0001 | t0004 | g0039 | AFR | ESN | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0333 | AFR | ESN | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0304 | AFR | ESN | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02970 | hp2 | a0001 | c0001 | t0004 | g0030 | AFR | ESN | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0042 | AFR | ESN | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | ESN | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0007 | AFR | GWD | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG03041 | hp2 | a0001 | c0001 | t0004 | g0034 | AFR | GWD | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG03098 | hp1 | a0001 | c0001 | t0005 | g0352 | AFR | MSL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0325 | AFR | MSL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0343 | AFR | ESN | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | ESN | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0297 | AFR | ESN | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG03195 | hp2 | a0001 | c0001 | t0004 | g0037 | AFR | ESN | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG03225 | hp1 | a0001 | c0001 | t0007 | g0080 | AFR | MSL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | MSL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | MSL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG03453 | hp2 | a0001 | c0001 | t0008 | g0026 | AFR | MSL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | MSL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG03486 | hp2 | a0001 | c0001 | t0007 | g0086 | AFR | MSL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG03490 | hp1 | a0001 | c0001 | t0003 | g0006 | SAS | PJL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0346 | SAS | PJL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG03491 | hp2 | a0001 | c0001 | t0003 | g0319 | SAS | PJL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0006 | SAS | PJL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG03516 | hp1 | a0001 | c0001 | t0009 | g0085 | AFR | ESN | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG03516 | hp2 | a0001 | c0001 | t0008 | g0167 | AFR | ESN | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG03579 | hp1 | a0001 | c0001 | t0007 | g0077 | AFR | MSL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | MSL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0176 | SAS | PJL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG03704 | hp2 | a0001 | c0001 | t0005 | g0119 | SAS | PJL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0354 | SAS | PJL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG03710 | hp2 | a0001 | c0002 | t0002 | g0226 | SAS | PJL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG03831 | hp1 | a0001 | c0002 | t0002 | g0118 | SAS | BEB | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0282 | SAS | BEB | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0171 | SAS | BEB | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | BEB | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG03942 | hp1 | a0001 | c0001 | t0004 | g0032 | SAS | BEB | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG03942 | hp2 | a0001 | c0001 | t0005 | g0181 | SAS | BEB | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG04115 | hp1 | a0001 | c0001 | t0005 | g0183 | SAS | STU | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0267 | SAS | STU | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0322 | SAS | BEB | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG04184 | hp2 | a0001 | c0001 | t0011 | g0137 | SAS | BEB | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG04199 | hp1 | a0001 | c0001 | t0004 | g0070 | SAS | STU | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0303 | SAS | STU | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG04204 | hp1 | a0001 | c0002 | t0002 | g0110 | SAS | STU | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0273 | SAS | STU | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0276 | SAS | STU | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG04228 | hp2 | a0001 | c0002 | t0002 | g0111 | SAS | STU | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0298 | AFR | YRI | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | YRI | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | CHB | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18612 | hp2 | a0001 | c0002 | t0002 | g0224 | EAS | CHB | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18906 | hp1 | a0001 | c0001 | t0023 | g0074 | AFR | YRI | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | YRI | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18941 | hp1 | a0001 | c0002 | t0002 | g0208 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18942 | hp1 | a0001 | c0001 | t0004 | g0044 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18942 | hp2 | a0001 | c0002 | t0002 | g0242 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18943 | hp2 | a0001 | c0001 | t0004 | g0045 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18944 | hp1 | a0001 | c0002 | t0002 | g0205 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18944 | hp2 | a0001 | c0001 | t0004 | g0058 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18947 | hp2 | a0001 | c0002 | t0012 | g0195 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18949 | hp1 | a0001 | c0001 | t0015 | g0156 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18949 | hp2 | a0001 | c0001 | t0004 | g0035 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18950 | hp1 | a0001 | c0001 | t0003 | g0312 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18950 | hp2 | a0001 | c0001 | t0004 | g0046 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18952 | hp1 | a0001 | c0002 | t0002 | g0251 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18953 | hp1 | a0001 | c0002 | t0002 | g0203 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18956 | hp2 | a0001 | c0006 | t0004 | g0048 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18957 | hp1 | a0001 | c0002 | t0002 | g0209 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18957 | hp2 | a0001 | c0001 | t0004 | g0057 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18962 | hp1 | a0001 | c0002 | t0006 | g0214 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18962 | hp2 | a0001 | c0001 | t0004 | g0066 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18963 | hp1 | a0001 | c0001 | t0003 | g0315 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18963 | hp2 | a0001 | c0001 | t0004 | g0053 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18964 | hp1 | a0001 | c0002 | t0002 | g0231 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18966 | hp1 | a0001 | c0001 | t0003 | g0332 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18968 | hp1 | a0001 | c0001 | t0004 | g0059 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18973 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18973 | hp2 | a0001 | c0002 | t0014 | g0107 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18975 | hp1 | a0001 | c0001 | t0004 | g0063 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18975 | hp2 | a0001 | c0002 | t0002 | g0116 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18977 | hp1 | a0001 | c0002 | t0002 | g0243 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18977 | hp2 | a0001 | c0001 | t0003 | g0309 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18978 | hp1 | a0001 | c0001 | t0003 | g0314 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18978 | hp2 | a0001 | c0002 | t0002 | g0115 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18979 | hp1 | a0001 | c0002 | t0002 | g0106 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18980 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18985 | hp1 | a0001 | c0002 | t0002 | g0211 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18985 | hp2 | a0001 | c0001 | t0004 | g0052 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18987 | hp1 | a0001 | c0002 | t0002 | g0237 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18989 | hp2 | a0001 | c0002 | t0014 | g0113 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18990 | hp2 | a0001 | c0002 | t0002 | g0213 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18993 | hp2 | a0001 | c0002 | t0002 | g0222 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18994 | hp2 | a0001 | c0002 | t0002 | g0193 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18995 | hp1 | a0001 | c0002 | t0002 | g0212 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18998 | hp1 | a0001 | c0002 | t0002 | g0190 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18999 | hp1 | a0001 | c0001 | t0003 | g0347 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA18999 | hp2 | a0001 | c0002 | t0012 | g0196 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19000 | hp2 | a0001 | c0004 | t0002 | g0221 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19001 | hp1 | a0001 | c0002 | t0002 | g0103 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19001 | hp2 | a0001 | c0001 | t0004 | g0065 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19002 | hp1 | a0001 | c0002 | t0002 | g0230 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19002 | hp2 | a0001 | c0001 | t0010 | g0159 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19004 | hp1 | a0001 | c0002 | t0002 | g0223 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19005 | hp2 | a0001 | c0002 | t0002 | g0102 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19009 | hp1 | a0001 | c0002 | t0002 | g0219 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19009 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19011 | hp1 | a0001 | c0001 | t0003 | g0313 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19011 | hp2 | a0001 | c0002 | t0002 | g0232 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0320 | AFR | LWK | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19030 | hp2 | a0001 | c0001 | t0024 | g0081 | AFR | LWK | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19043 | hp1 | a0001 | c0001 | t0022 | g0178 | AFR | LWK | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19043 | hp2 | a0001 | c0001 | t0016 | g0087 | AFR | LWK | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19059 | hp1 | a0001 | c0002 | t0002 | g0250 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19060 | hp2 | a0001 | c0002 | t0002 | g0234 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19062 | hp1 | a0001 | c0002 | t0006 | g0215 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19063 | hp1 | a0001 | c0002 | t0002 | g0207 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19063 | hp2 | a0001 | c0001 | t0004 | g0062 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19066 | hp1 | a0001 | c0001 | t0004 | g0064 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19067 | hp1 | a0001 | c0001 | t0004 | g0060 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19067 | hp2 | a0001 | c0002 | t0002 | g0236 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19068 | hp1 | a0001 | c0002 | t0006 | g0238 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19070 | hp1 | a0001 | c0002 | t0002 | g0191 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19072 | hp1 | a0001 | c0001 | t0004 | g0056 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19078 | hp1 | a0001 | c0002 | t0002 | g0194 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19078 | hp2 | a0001 | c0001 | t0020 | g0055 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19079 | hp1 | a0001 | c0002 | t0002 | g0241 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19080 | hp1 | a0001 | c0002 | t0002 | g0218 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19080 | hp2 | a0001 | c0001 | t0004 | g0047 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19083 | hp1 | a0001 | c0005 | t0002 | g0233 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19085 | hp2 | a0001 | c0002 | t0002 | g0198 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19086 | hp1 | a0001 | c0002 | t0002 | g0204 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19086 | hp2 | a0001 | c0001 | t0004 | g0051 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19087 | hp2 | a0001 | c0002 | t0002 | g0216 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19088 | hp2 | a0001 | c0001 | t0010 | g0160 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19091 | hp1 | a0001 | c0001 | t0010 | g0158 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19240 | hp1 | a0001 | c0001 | t0019 | g0305 | AFR | YRI | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA19240 | hp2 | a0001 | c0001 | t0017 | g0027 | AFR | YRI | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA20129 | hp1 | a0001 | c0002 | t0002 | g0206 | AFR | ASW | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | ASW | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0256 | EUR | TSI | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0331 | EUR | TSI | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0281 | AMR | CLM | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG01123 | hp2 | a0001 | c0001 | t0004 | g0061 | AMR | CLM | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02109 | hp1 | a0001 | c0001 | t0013 | g0180 | AFR | ACB | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0323 | AFR | ACB | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0328 | AFR | ACB | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG02559 | hp2 | a0001 | c0001 | t0004 | g0029 | AFR | ACB | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | MSL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG03471 | hp2 | a0001 | c0001 | t0004 | g0041 | AFR | MSL | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG06807 | hp1 | a0001 | c0001 | t0007 | g0079 | AFR | USA | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| HG06807 | hp2 | a0001 | c0001 | t0004 | g0033 | AFR | USA | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA20300 | hp1 | a0001 | c0002 | t0002 | g0225 | AFR | USA | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | USA | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA21309 | hp1 | a0001 | c0001 | t0005 | g0252 | AFR | LWK | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | LWK | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0306 | REF | REF | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0004 | g0050 | REF | REF | TAB2_chr6_149312712_149416607 | TAB2 | chr6 | 149312712 | 149416607 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:149370018 | A | G | 1 | a0001c0008 | 1 | HG02080.hp1 | synonymous_variant | LOW | c.21A>G | p.Gln7Gln | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/7 | 414/4363 | 21/2082 | 7/693 | chr6 | 149370018 | |||
| chr6:149378197 | A | G | 1 | a0001c0003 | 2 | HG00642.hp1 HG01346.hp2 |
synonymous_variant | LOW | c.282A>G | p.Gly94Gly | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/7 | 675/4363 | 282/2082 | 94/693 | chr6 | 149378197 | |||
| chr6:149378290 | G | A | 2 | a0001c0004 a0001c0005 |
2 | NA19000.hp2 NA19083.hp1 |
synonymous_variant | LOW | c.375G>A | p.Glu125Glu | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/7 | 768/4363 | 375/2082 | 125/693 | chr6 | 149378290 | |||
| chr6:149378686 | T | C | 1 | a0001c0006 | 1 | NA18956.hp2 | synonymous_variant | LOW | c.771T>C | p.Thr257Thr | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/7 | 1164/4363 | 771/2082 | 257/693 | chr6 | 149378686 | |||
| chr6:149379043 | G | A | 1 | a0001c0007 | 1 | HG00741.hp2 | synonymous_variant | LOW | c.1128G>A | p.Thr376Thr | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/7 | 1521/4363 | 1128/2082 | 376/693 | chr6 | 149379043 | |||
| chr6:149379067 | A | G | 1 | a0001c0005 | 1 | NA19083.hp1 | synonymous_variant | LOW | c.1152A>G | p.Gln384Gln | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/7 | 1545/4363 | 1152/2082 | 384/693 | chr6 | 149379067 | |||
| chr6:149379355 | G | A | 4 | a0001c0002 a0001c0004 a0001c0005 others(1): Show |
87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
synonymous_variant | LOW | c.1440G>A | p.Val480Val | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/7 | 1833/4363 | 1440/2082 | 480/693 | chr6 | 149379355 | |||
| chr6:149409710 | G | A | 4 | a0001c0002 a0001c0004 a0001c0005 others(1): Show |
87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
synonymous_variant | LOW | c.2073G>A | p.Arg691Arg | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 7/7 | 2466/4363 | 2073/2082 | 691/693 | chr6 | 149409710 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:149317834 | A | AGGGGGCT others(15): Show |
2 | a0001c0001t0007 a0001c0001t0023 |
6 | HG02630.hp2 HG03225.hp1 HG03486.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-269_-248dupGGGGCT others(16): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/7 | 52140 | INFO_REALIGN_3_PRIME | chr6 | 149317834 | |||||
| chr6:149317834 | A | AGGGGGCT others(16): Show |
1 | a0001c0001t0024 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-270_-248dupGGGGGC others(17): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/7 | 52140 | INFO_REALIGN_3_PRIME | chr6 | 149317834 | |||||
| chr6:149317891 | G | A | 1 | a0001c0001t0015 | 1 | NA18949.hp1 | 5_prime_UTR_variant | MODIFIER | c.-214G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/7 | 52107 | chr6 | 149317891 | ||||||
| chr6:149317896 | CGGCGGCG others(5): Show |
C | 1 | a0001c0001t0016 | 1 | NA19043.hp2 | 5_prime_UTR_variant | MODIFIER | c.-199_-188delGCTGGC others(6): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/7 | 52081 | INFO_REALIGN_3_PRIME | chr6 | 149317896 | |||||
| chr6:149317962 | AGGC | A | 23 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(20): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
5_prime_UTR_variant | MODIFIER | c.-127_-125delGGC | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/7 | 52018 | INFO_REALIGN_3_PRIME | chr6 | 149317962 | |||||
| chr6:149318000 | G | A | 1 | a0001c0002t0012 | 2 | NA18947.hp2 NA18999.hp2 |
5_prime_UTR_variant | MODIFIER | c.-105G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/7 | 51998 | chr6 | 149318000 | ||||||
| chr6:149410005 | A | C | 2 | a0001c0001t0013 a0001c0001t0022 |
3 | HG02109.hp1 HG02615.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*286A>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 7/7 | 286 | chr6 | 149410005 | ||||||
| chr6:149410309 | A | G | 1 | a0001c0001t0019 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*590A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 7/7 | 590 | chr6 | 149410309 | ||||||
| chr6:149410340 | C | G | 3 | a0001c0001t0003 a0001c0001t0019 a0001c0001t0021 |
62 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*621C>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 7/7 | 621 | chr6 | 149410340 | ||||||
| chr6:149410420 | A | G | 1 | a0001c0001t0011 | 3 | HG01433.hp1 HG01515.hp1 HG04184.hp2 |
3_prime_UTR_variant | MODIFIER | c.*701A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 7/7 | 701 | chr6 | 149410420 | ||||||
| chr6:149410523 | C | A | 2 | a0001c0001t0013 a0001c0001t0022 |
3 | HG02109.hp1 HG02615.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*804C>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 7/7 | 804 | chr6 | 149410523 | ||||||
| chr6:149410655 | G | T | 1 | a0001c0001t0005 | 9 | HG01243.hp2 HG02602.hp2 HG02683.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*936G>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 7/7 | 936 | chr6 | 149410655 | ||||||
| chr6:149410658 | A | G | 4 | a0001c0001t0007 a0001c0001t0009 a0001c0001t0016 others(1): Show |
11 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*939A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 7/7 | 939 | chr6 | 149410658 | ||||||
| chr6:149410658 | A | T | 1 | a0001c0001t0005 | 9 | HG01243.hp2 HG02602.hp2 HG02683.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*939A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 7/7 | 939 | chr6 | 149410658 | ||||||
| chr6:149410767 | C | A | 1 | a0001c0001t0020 | 1 | NA19078.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1048C>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 7/7 | 1048 | chr6 | 149410767 | ||||||
| chr6:149410768 | C | T | 7 | a0001c0002t0002 a0001c0002t0006 a0001c0002t0012 others(4): Show |
87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*1049C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 7/7 | 1049 | chr6 | 149410768 | ||||||
| chr6:149411096 | A | G | 1 | a0001c0002t0006 | 5 | HG00558.hp1 HG02056.hp2 NA18962.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1377A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 7/7 | 1377 | chr6 | 149411096 | ||||||
| chr6:149411383 | C | T | 1 | a0001c0001t0008 | 4 | HG02280.hp1 HG02717.hp2 HG03453.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1664C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 7/7 | 1664 | chr6 | 149411383 | ||||||
| chr6:149411404 | G | A | 1 | a0001c0001t0017 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1685G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 7/7 | 1685 | chr6 | 149411404 | ||||||
| chr6:149411468 | G | A | 1 | a0001c0001t0010 | 3 | NA19002.hp2 NA19088.hp2 NA19091.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1749G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 7/7 | 1749 | chr6 | 149411468 | ||||||
| chr6:149411507 | G | A | 1 | a0001c0008t0018 | 1 | HG02080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1788G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 7/7 | 1788 | chr6 | 149411507 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:149318152 | T | C | 1 | a0001c0001t0001g0009 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-90+137T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149318152 | |||||||
| chr6:149318177 | C | T | 2 | a0001c0001t0001g0355 a0001c0001t0001g0356 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-90+162C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149318177 | |||||||
| chr6:149318264 | G | C | 1 | a0001c0001t0003g0010 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-90+249G>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149318264 | |||||||
| chr6:149318273 | C | CG | 173 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0189 others(170): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.-90+266dupG | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149318273 | ||||||
| chr6:149318276 | G | A | 1 | a0001c0001t0001g0011 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-90+261G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149318276 | |||||||
| chr6:149318278 | G | T | 1 | a0001c0001t0001g0354 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-90+263G>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149318278 | |||||||
| chr6:149318380 | C | G | 2 | a0001c0001t0004g0185 a0001c0001t0004g0186 |
2 | HG02717.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-90+365C>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149318380 | |||||||
| chr6:149318400 | G | A | 15 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(12): Show |
15 | HG00733.hp2 HG02145.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.-90+385G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149318400 | |||||||
| chr6:149318490 | G | T | 3 | a0001c0001t0001g0353 a0001c0001t0001g0355 a0001c0001t0001g0356 |
3 | HG01256.hp1 HG01258.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.-90+475G>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149318490 | |||||||
| chr6:149318616 | A | T | 173 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0011 others(170): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.-90+601A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149318616 | |||||||
| chr6:149318762 | C | T | 1 | a0001c0001t0004g0121 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-90+747C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149318762 | |||||||
| chr6:149318956 | C | T | 1 | a0001c0001t0005g0120 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-90+941C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149318956 | |||||||
| chr6:149319055 | G | A | 1 | a0001c0001t0017g0027 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-90+1040G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149319055 | |||||||
| chr6:149319177 | G | T | 9 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0005g0181 others(6): Show |
9 | HG01243.hp2 HG02602.hp2 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.-90+1162G>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149319177 | |||||||
| chr6:149319366 | G | A | 1 | a0001c0001t0004g0028 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-90+1351G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149319366 | |||||||
| chr6:149319538 | A | T | 290 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(287): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.-90+1523A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149319538 | |||||||
| chr6:149319839 | A | G | 3 | a0001c0001t0013g0179 a0001c0001t0013g0180 a0001c0001t0022g0178 |
3 | HG02109.hp1 HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-90+1824A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149319839 | |||||||
| chr6:149319972 | A | G | 8 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(5): Show |
8 | HG02895.hp1 HG02895.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-90+1957A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149319972 | |||||||
| chr6:149319982 | C | T | 1 | a0001c0001t0001g0177 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-90+1967C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149319982 | |||||||
| chr6:149320047 | G | A | 1 | a0001c0001t0022g0178 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-90+2032G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149320047 | |||||||
| chr6:149320064 | A | T | 85 | a0001c0002t0002g0002 a0001c0002t0002g0098 a0001c0002t0002g0099 others(82): Show |
87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.-90+2049A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149320064 | |||||||
| chr6:149320090 | T | C | 1 | a0001c0002t0002g0190 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-90+2075T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149320090 | |||||||
| chr6:149320136 | G | C | 17 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(14): Show |
17 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.-90+2121G>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149320136 | |||||||
| chr6:149320324 | G | T | 1 | a0001c0001t0001g0005 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-90+2309G>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149320324 | |||||||
| chr6:149320346 | A | G | 9 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0005g0181 others(6): Show |
9 | HG01243.hp2 HG02602.hp2 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.-90+2331A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149320346 | |||||||
| chr6:149320372 | G | A | 1 | a0001c0001t0001g0177 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-90+2357G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149320372 | |||||||
| chr6:149320491 | T | C | 115 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(112): Show |
118 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.-90+2476T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149320491 | |||||||
| chr6:149320501 | ATTTTCCC others(15): Show |
A | 115 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(112): Show |
118 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.-90+2495_-90+2516d others(24): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149320501 | ||||||
| chr6:149320662 | C | G | 1 | a0001c0002t0002g0251 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-90+2647C>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149320662 | |||||||
| chr6:149320672 | A | AT | 60 | a0001c0001t0001g0302 a0001c0001t0003g0006 a0001c0001t0003g0007 others(57): Show |
63 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.-90+2666dupT | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149320672 | ||||||
| chr6:149320683 | A | C | 3 | a0001c0001t0013g0179 a0001c0001t0013g0180 a0001c0001t0022g0178 |
3 | HG02109.hp1 HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-90+2668A>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149320683 | |||||||
| chr6:149320754 | A | G | 2 | a0001c0001t0003g0348 a0001c0001t0003g0349 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-90+2739A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149320754 | |||||||
| chr6:149321471 | A | C | 11 | a0001c0001t0007g0077 a0001c0001t0007g0078 a0001c0001t0007g0079 others(8): Show |
11 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.-90+3456A>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149321471 | |||||||
| chr6:149321536 | C | T | 1 | a0001c0001t0005g0184 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-90+3521C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149321536 | |||||||
| chr6:149321721 | A | G | 3 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 |
3 | HG03209.hp1 HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-90+3706A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149321721 | |||||||
| chr6:149321733 | G | C | 2 | a0001c0001t0001g0256 a0001c0001t0001g0257 |
2 | HG02809.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-90+3718G>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149321733 | |||||||
| chr6:149321953 | A | G | 17 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(14): Show |
17 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.-90+3938A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149321953 | |||||||
| chr6:149322050 | A | T | 1 | a0001c0001t0001g0301 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-90+4035A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149322050 | |||||||
| chr6:149322150 | T | A | 59 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(56): Show |
62 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.-90+4135T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149322150 | |||||||
| chr6:149322151 | G | T | 59 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(56): Show |
62 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.-90+4136G>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149322151 | |||||||
| chr6:149322152 | C | G | 59 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(56): Show |
62 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.-90+4137C>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149322152 | |||||||
| chr6:149322213 | G | A | 3 | a0001c0001t0013g0179 a0001c0001t0013g0180 a0001c0001t0022g0178 |
3 | HG02109.hp1 HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-90+4198G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149322213 | |||||||
| chr6:149322289 | A | G | 18 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(15): Show |
18 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.-90+4274A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149322289 | |||||||
| chr6:149322423 | A | G | 1 | a0001c0001t0003g0347 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-90+4408A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149322423 | |||||||
| chr6:149322467 | G | A | 1 | a0001c0001t0005g0181 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-90+4452G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149322467 | |||||||
| chr6:149322475 | A | G | 1 | a0001c0001t0001g0300 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-90+4460A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149322475 | |||||||
| chr6:149322478 | G | C | 1 | a0001c0001t0001g0018 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-90+4463G>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149322478 | |||||||
| chr6:149322548 | A | G | 2 | a0001c0001t0001g0298 a0001c0001t0001g0299 |
2 | HG02258.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-90+4533A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149322548 | |||||||
| chr6:149322573 | T | C | 59 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(56): Show |
62 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.-90+4558T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149322573 | |||||||
| chr6:149322615 | T | G | 3 | a0001c0001t0001g0260 a0001c0003t0001g0258 a0001c0003t0001g0259 |
3 | HG00642.hp1 HG01261.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.-90+4600T>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149322615 | |||||||
| chr6:149322826 | T | A | 85 | a0001c0002t0002g0002 a0001c0002t0002g0098 a0001c0002t0002g0099 others(82): Show |
87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.-90+4811T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149322826 | |||||||
| chr6:149322924 | A | G | 1 | a0001c0001t0017g0027 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-90+4909A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149322924 | |||||||
| chr6:149322942 | A | G | 1 | a0001c0002t0002g0250 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.-90+4927A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149322942 | |||||||
| chr6:149323203 | T | C | 1 | a0001c0001t0003g0303 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-90+5188T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149323203 | |||||||
| chr6:149323497 | C | T | 1 | a0001c0001t0001g0168 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-90+5482C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149323497 | |||||||
| chr6:149323538 | G | A | 1 | a0001c0001t0001g0122 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-90+5523G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149323538 | |||||||
| chr6:149323562 | G | A | 84 | a0001c0002t0002g0002 a0001c0002t0002g0098 a0001c0002t0002g0099 others(81): Show |
86 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.-90+5547G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149323562 | |||||||
| chr6:149323568 | C | G | 6 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0297 others(3): Show |
6 | HG02280.hp1 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-90+5553C>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149323568 | |||||||
| chr6:149323625 | T | G | 6 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(3): Show |
6 | HG00733.hp2 HG02145.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-90+5610T>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149323625 | |||||||
| chr6:149323648 | G | A | 59 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(56): Show |
62 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.-90+5633G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149323648 | |||||||
| chr6:149323676 | A | C | 2 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
2 | NA18987.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.-90+5661A>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149323676 | |||||||
| chr6:149323742 | A | G | 1 | a0001c0001t0001g0296 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-90+5727A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149323742 | |||||||
| chr6:149323783 | G | A | 1 | a0001c0001t0001g0009 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-90+5768G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149323783 | |||||||
| chr6:149323918 | A | AT | 289 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(286): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.-90+5911dupT | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149323918 | ||||||
| chr6:149324033 | G | C | 1 | a0001c0001t0004g0029 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-90+6018G>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149324033 | |||||||
| chr6:149324280 | C | T | 3 | a0001c0001t0010g0158 a0001c0001t0010g0159 a0001c0001t0010g0160 |
3 | NA19002.hp2 NA19088.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.-90+6265C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149324280 | |||||||
| chr6:149324351 | A | C | 1 | a0001c0001t0004g0070 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-90+6336A>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149324351 | |||||||
| chr6:149324405 | A | G | 3 | a0001c0001t0013g0179 a0001c0001t0013g0180 a0001c0001t0022g0178 |
3 | HG02109.hp1 HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-90+6390A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149324405 | |||||||
| chr6:149324503 | G | T | 1 | a0001c0001t0016g0087 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-90+6488G>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149324503 | |||||||
| chr6:149324685 | A | G | 3 | a0001c0001t0013g0179 a0001c0001t0013g0180 a0001c0001t0022g0178 |
3 | HG02109.hp1 HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-90+6670A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149324685 | |||||||
| chr6:149324713 | G | A | 3 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 |
3 | HG00733.hp2 HG02145.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.-90+6698G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149324713 | |||||||
| chr6:149324826 | C | CT | 71 | a0001c0001t0001g0157 a0001c0001t0003g0006 a0001c0001t0003g0007 others(68): Show |
74 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(71): Show |
intron_variant | MODIFIER | c.-90+6829dupT | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149324826 | ||||||
| chr6:149324826 | C | CTTT | 17 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(14): Show |
17 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.-90+6827_-90+6829d others(5): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149324826 | ||||||
| chr6:149325097 | A | G | 6 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(3): Show |
6 | HG00735.hp2 HG01070.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.-90+7082A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149325097 | |||||||
| chr6:149325172 | C | T | 147 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(144): Show |
152 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.-90+7157C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149325172 | |||||||
| chr6:149325317 | T | C | 1 | a0001c0002t0002g0099 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-90+7302T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149325317 | |||||||
| chr6:149325364 | G | A | 115 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(112): Show |
118 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.-90+7349G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149325364 | |||||||
| chr6:149325385 | A | G | 85 | a0001c0002t0002g0002 a0001c0002t0002g0098 a0001c0002t0002g0099 others(82): Show |
87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.-90+7370A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149325385 | |||||||
| chr6:149325582 | T | C | 1 | a0001c0001t0001g0261 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-90+7567T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149325582 | |||||||
| chr6:149325694 | C | T | 2 | a0001c0002t0002g0248 a0001c0002t0002g0249 |
2 | HG01943.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.-90+7679C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149325694 | |||||||
| chr6:149325795 | A | G | 59 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(56): Show |
62 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.-90+7780A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149325795 | |||||||
| chr6:149325804 | A | G | 59 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(56): Show |
62 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.-90+7789A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149325804 | |||||||
| chr6:149325886 | C | G | 1 | a0001c0001t0003g0346 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-90+7871C>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149325886 | |||||||
| chr6:149325929 | G | A | 1 | a0001c0001t0008g0026 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-90+7914G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149325929 | |||||||
| chr6:149325964 | G | A | 290 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(287): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.-90+7949G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149325964 | |||||||
| chr6:149326236 | A | G | 1 | a0001c0001t0001g0067 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-90+8221A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149326236 | |||||||
| chr6:149326271 | CA | C | 204 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(201): Show |
209 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(206): Show |
intron_variant | MODIFIER | c.-90+8275delA | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149326271 | ||||||
| chr6:149326271 | CAA | C | 10 | a0001c0001t0001g0022 a0001c0001t0005g0119 a0001c0001t0005g0120 others(7): Show |
10 | HG01243.hp2 HG02602.hp2 HG02683.hp1 others(7): Show |
intron_variant | MODIFIER | c.-90+8274_-90+8275d others(4): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149326271 | ||||||
| chr6:149326271 | CAAAAAA | C | 59 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(56): Show |
62 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.-90+8270_-90+8275d others(8): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149326271 | ||||||
| chr6:149326295 | G | A | 1 | a0001c0001t0005g0252 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-90+8280G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149326295 | |||||||
| chr6:149326389 | T | C | 148 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(145): Show |
153 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.-90+8374T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149326389 | |||||||
| chr6:149326397 | T | A | 1 | a0001c0001t0001g0011 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-90+8382T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149326397 | |||||||
| chr6:149326425 | C | G | 6 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0297 others(3): Show |
6 | HG02280.hp1 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-90+8410C>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149326425 | |||||||
| chr6:149326546 | G | A | 1 | a0001c0001t0008g0026 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-90+8531G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149326546 | |||||||
| chr6:149326551 | TA | T | 80 | a0001c0001t0001g0131 a0001c0002t0002g0002 a0001c0002t0002g0098 others(77): Show |
82 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.-90+8537delA | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149326551 | |||||||
| chr6:149326552 | A | T | 5 | a0001c0002t0002g0102 a0001c0002t0002g0104 a0001c0002t0002g0106 others(2): Show |
5 | HG02040.hp1 HG02056.hp2 NA18953.hp1 others(2): Show |
intron_variant | MODIFIER | c.-90+8537A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149326552 | |||||||
| chr6:149326552 | AT | A | 126 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(123): Show |
129 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.-90+8550delT | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149326552 | ||||||
| chr6:149326552 | ATT | A | 75 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(72): Show |
78 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(75): Show |
intron_variant | MODIFIER | c.-90+8549_-90+8550d others(4): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149326552 | ||||||
| chr6:149326567 | A | G | 3 | a0001c0001t0008g0165 a0001c0001t0008g0166 a0001c0001t0008g0167 |
3 | HG02280.hp1 HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-90+8552A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149326567 | |||||||
| chr6:149326622 | A | G | 3 | a0001c0001t0013g0179 a0001c0001t0013g0180 a0001c0001t0022g0178 |
3 | HG02109.hp1 HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-90+8607A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149326622 | |||||||
| chr6:149326667 | C | G | 9 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0005g0181 others(6): Show |
9 | HG01243.hp2 HG02602.hp2 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.-90+8652C>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149326667 | |||||||
| chr6:149326692 | C | T | 1 | a0001c0001t0005g0252 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-90+8677C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149326692 | |||||||
| chr6:149326749 | T | C | 1 | a0001c0002t0002g0192 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-90+8734T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149326749 | |||||||
| chr6:149326752 | T | C | 1 | a0001c0002t0002g0193 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-90+8737T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149326752 | |||||||
| chr6:149326808 | C | T | 147 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(144): Show |
152 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.-90+8793C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149326808 | |||||||
| chr6:149327107 | A | G | 6 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0297 others(3): Show |
6 | HG02280.hp1 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-90+9092A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149327107 | |||||||
| chr6:149327119 | T | C | 8 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(5): Show |
8 | HG02895.hp1 HG02895.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-90+9104T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149327119 | |||||||
| chr6:149327245 | G | A | 84 | a0001c0002t0002g0002 a0001c0002t0002g0098 a0001c0002t0002g0099 others(81): Show |
86 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.-90+9230G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149327245 | |||||||
| chr6:149327260 | AAGAC | A | 3 | a0001c0001t0013g0179 a0001c0001t0013g0180 a0001c0001t0022g0178 |
3 | HG02109.hp1 HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-90+9249_-90+9252d others(6): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149327260 | ||||||
| chr6:149327276 | T | C | 2 | a0001c0001t0004g0031 a0001c0001t0004g0032 |
2 | HG02698.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.-90+9261T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149327276 | |||||||
| chr6:149327304 | T | A | 147 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(144): Show |
152 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.-90+9289T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149327304 | |||||||
| chr6:149327363 | C | T | 1 | a0001c0001t0003g0345 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-90+9348C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149327363 | |||||||
| chr6:149327459 | G | A | 92 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0011 others(89): Show |
93 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.-90+9444G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149327459 | |||||||
| chr6:149327763 | T | A | 85 | a0001c0002t0002g0002 a0001c0002t0002g0098 a0001c0002t0002g0099 others(82): Show |
87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.-90+9748T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149327763 | |||||||
| chr6:149327860 | T | C | 5 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0023 others(2): Show |
5 | HG02895.hp2 HG02897.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.-90+9845T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149327860 | |||||||
| chr6:149328046 | T | G | 1 | a0001c0001t0001g0089 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-90+10031T>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149328046 | |||||||
| chr6:149328128 | C | G | 1 | a0001c0001t0005g0252 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-90+10113C>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149328128 | |||||||
| chr6:149328169 | T | C | 1 | a0001c0001t0005g0252 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-90+10154T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149328169 | |||||||
| chr6:149328254 | A | G | 1 | a0001c0002t0002g0250 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.-90+10239A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149328254 | |||||||
| chr6:149328276 | A | G | 1 | a0001c0001t0003g0344 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-90+10261A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149328276 | |||||||
| chr6:149328293 | C | T | 42 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0010 others(39): Show |
44 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.-90+10278C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149328293 | |||||||
| chr6:149328357 | G | T | 1 | a0001c0001t0005g0252 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-90+10342G>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149328357 | |||||||
| chr6:149328559 | T | C | 1 | a0001c0001t0001g0163 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-90+10544T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149328559 | |||||||
| chr6:149328585 | C | T | 84 | a0001c0002t0002g0002 a0001c0002t0002g0098 a0001c0002t0002g0099 others(81): Show |
86 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.-90+10570C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149328585 | |||||||
| chr6:149328625 | A | C | 6 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0297 others(3): Show |
6 | HG02280.hp1 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-90+10610A>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149328625 | |||||||
| chr6:149328647 | C | T | 3 | a0001c0001t0013g0179 a0001c0001t0013g0180 a0001c0001t0022g0178 |
3 | HG02109.hp1 HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-90+10632C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149328647 | |||||||
| chr6:149328677 | G | C | 1 | a0001c0002t0002g0194 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.-90+10662G>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149328677 | |||||||
| chr6:149328744 | T | C | 289 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(286): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.-90+10729T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149328744 | |||||||
| chr6:149328808 | C | T | 59 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(56): Show |
62 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.-90+10793C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149328808 | |||||||
| chr6:149328964 | G | C | 84 | a0001c0002t0002g0002 a0001c0002t0002g0098 a0001c0002t0002g0099 others(81): Show |
86 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.-90+10949G>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149328964 | |||||||
| chr6:149329024 | A | G | 3 | a0001c0001t0013g0179 a0001c0001t0013g0180 a0001c0001t0022g0178 |
3 | HG02109.hp1 HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-90+11009A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149329024 | |||||||
| chr6:149329030 | A | T | 2 | a0001c0002t0002g0246 a0001c0002t0002g0247 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.-90+11015A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149329030 | |||||||
| chr6:149329248 | G | T | 1 | a0001c0001t0001g0146 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-90+11233G>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149329248 | |||||||
| chr6:149329325 | A | G | 2 | a0001c0002t0002g0248 a0001c0002t0002g0249 |
2 | HG01943.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.-90+11310A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149329325 | |||||||
| chr6:149329344 | TA | T | 289 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(286): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.-90+11331delA | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149329344 | ||||||
| chr6:149329492 | G | A | 1 | a0001c0001t0003g0173 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-90+11477G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149329492 | |||||||
| chr6:149329723 | G | A | 2 | a0001c0001t0004g0033 a0001c0001t0004g0034 |
2 | HG03041.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-90+11708G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149329723 | |||||||
| chr6:149329728 | T | C | 2 | a0001c0001t0005g0182 a0001c0001t0005g0183 |
2 | HG02683.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.-90+11713T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149329728 | |||||||
| chr6:149330070 | G | A | 287 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(284): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.-90+12055G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149330070 | |||||||
| chr6:149330072 | G | GA | 17 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(14): Show |
17 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.-90+12058dupA | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149330072 | ||||||
| chr6:149330095 | C | CT | 84 | a0001c0002t0002g0002 a0001c0002t0002g0098 a0001c0002t0002g0099 others(81): Show |
86 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.-90+12090dupT | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149330095 | ||||||
| chr6:149330128 | G | A | 146 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(143): Show |
151 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.-90+12113G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149330128 | |||||||
| chr6:149330279 | G | A | 2 | a0001c0001t0001g0131 a0001c0001t0015g0156 |
2 | NA18949.hp1 NA19059.hp2 |
intron_variant | MODIFIER | c.-90+12264G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149330279 | |||||||
| chr6:149330637 | T | C | 2 | a0001c0001t0003g0304 a0001c0001t0019g0305 |
2 | HG02970.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-90+12622T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149330637 | |||||||
| chr6:149330927 | G | C | 1 | a0001c0001t0017g0027 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-90+12912G>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149330927 | |||||||
| chr6:149330961 | G | C | 1 | a0001c0001t0022g0178 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-90+12946G>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149330961 | |||||||
| chr6:149331071 | T | C | 3 | a0001c0001t0003g0316 a0001c0001t0003g0317 a0001c0001t0003g0318 |
3 | HG00140.hp2 HG01168.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.-90+13056T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149331071 | |||||||
| chr6:149331148 | G | A | 59 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(56): Show |
62 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.-90+13133G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149331148 | |||||||
| chr6:149331150 | G | A | 84 | a0001c0002t0002g0002 a0001c0002t0002g0098 a0001c0002t0002g0099 others(81): Show |
86 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.-90+13135G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149331150 | |||||||
| chr6:149331222 | C | A | 1 | a0001c0001t0008g0026 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-90+13207C>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149331222 | |||||||
| chr6:149331370 | A | G | 6 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(3): Show |
6 | HG01884.hp2 HG02257.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.-90+13355A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149331370 | |||||||
| chr6:149331469 | G | A | 3 | a0001c0001t0013g0179 a0001c0001t0013g0180 a0001c0001t0022g0178 |
3 | HG02109.hp1 HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-90+13454G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149331469 | |||||||
| chr6:149331599 | C | T | 1 | a0001c0001t0003g0173 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-90+13584C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149331599 | |||||||
| chr6:149331730 | T | A | 1 | a0001c0001t0004g0035 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-90+13715T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149331730 | |||||||
| chr6:149331749 | A | G | 5 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0013g0179 others(2): Show |
5 | HG02109.hp1 HG02615.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.-90+13734A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149331749 | |||||||
| chr6:149331854 | G | A | 2 | a0001c0002t0012g0195 a0001c0002t0012g0196 |
2 | NA18947.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.-90+13839G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149331854 | |||||||
| chr6:149332153 | A | C | 9 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0005g0181 others(6): Show |
9 | HG01243.hp2 HG02602.hp2 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.-90+14138A>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149332153 | |||||||
| chr6:149332288 | G | A | 5 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0134 others(2): Show |
5 | NA18943.hp1 NA18956.hp1 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.-90+14273G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149332288 | |||||||
| chr6:149332379 | A | G | 1 | a0001c0001t0008g0026 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-90+14364A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149332379 | |||||||
| chr6:149332448 | T | C | 1 | a0001c0001t0003g0319 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-90+14433T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149332448 | |||||||
| chr6:149332449 | A | G | 1 | a0001c0001t0001g0155 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-90+14434A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149332449 | |||||||
| chr6:149332615 | G | T | 1 | a0001c0001t0008g0026 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-90+14600G>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149332615 | |||||||
| chr6:149332656 | G | A | 85 | a0001c0002t0002g0002 a0001c0002t0002g0098 a0001c0002t0002g0099 others(82): Show |
87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.-90+14641G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149332656 | |||||||
| chr6:149332662 | G | C | 4 | a0001c0001t0013g0179 a0001c0001t0013g0180 a0001c0001t0017g0027 others(1): Show |
4 | HG02109.hp1 HG02615.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.-90+14647G>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149332662 | |||||||
| chr6:149332667 | A | C | 1 | a0001c0001t0001g0294 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-90+14652A>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149332667 | |||||||
| chr6:149332692 | C | T | 290 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(287): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.-90+14677C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149332692 | |||||||
| chr6:149332694 | G | A | 1 | a0001c0002t0002g0197 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-90+14679G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149332694 | |||||||
| chr6:149332749 | A | C | 1 | a0001c0001t0001g0293 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-90+14734A>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149332749 | |||||||
| chr6:149332898 | T | C | 8 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(5): Show |
8 | HG02895.hp1 HG02895.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-90+14883T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149332898 | |||||||
| chr6:149332899 | A | G | 1 | a0001c0001t0001g0076 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-90+14884A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149332899 | |||||||
| chr6:149332984 | G | A | 59 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(56): Show |
62 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.-90+14969G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149332984 | |||||||
| chr6:149333074 | C | T | 3 | a0001c0001t0010g0158 a0001c0001t0010g0159 a0001c0001t0010g0160 |
3 | NA19002.hp2 NA19088.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.-90+15059C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149333074 | |||||||
| chr6:149333094 | G | A | 3 | a0001c0001t0013g0179 a0001c0001t0013g0180 a0001c0001t0022g0178 |
3 | HG02109.hp1 HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-90+15079G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149333094 | |||||||
| chr6:149333276 | A | G | 1 | a0001c0001t0013g0180 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-90+15261A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149333276 | |||||||
| chr6:149333493 | T | C | 1 | a0001c0001t0001g0132 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-90+15478T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149333493 | |||||||
| chr6:149333708 | A | AGT | 98 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0067 others(95): Show |
102 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.-90+15730_-90+1573 others(6): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149333708 | ||||||
| chr6:149333708 | A | AGTGT | 36 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0257 others(33): Show |
36 | HG00099.hp2 HG00558.hp1 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.-90+15728_-90+1573 others(8): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149333708 | ||||||
| chr6:149333708 | A | AGTGTGT | 9 | a0001c0001t0001g0291 a0001c0001t0003g0008 a0001c0001t0004g0065 others(6): Show |
10 | HG00621.hp1 HG00621.hp2 HG00733.hp1 others(7): Show |
intron_variant | MODIFIER | c.-90+15726_-90+1573 others(10): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149333708 | ||||||
| chr6:149333708 | A | AGTGTGTG others(3): Show |
1 | a0001c0001t0003g0173 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-90+15722_-90+1573 others(14): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149333708 | ||||||
| chr6:149333708 | AGT | A | 29 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(26): Show |
29 | HG00609.hp2 HG00642.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.-90+15730_-90+1573 others(6): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149333708 | ||||||
| chr6:149333708 | AGTGT | A | 29 | a0001c0001t0001g0076 a0001c0001t0001g0147 a0001c0001t0001g0148 others(26): Show |
29 | HG00099.hp1 HG01081.hp1 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.-90+15728_-90+1573 others(8): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149333708 | ||||||
| chr6:149333708 | AGTGTGT | A | 11 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(8): Show |
11 | HG00733.hp2 HG01884.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.-90+15726_-90+1573 others(10): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149333708 | ||||||
| chr6:149333708 | AGTGTGTG others(1): Show |
A | 3 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0262 |
3 | HG02523.hp2 NA19070.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.-90+15724_-90+1573 others(12): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149333708 | ||||||
| chr6:149333708 | AGTGTGTG others(3): Show |
A | 10 | a0001c0001t0001g0001 a0001c0001t0001g0089 a0001c0001t0001g0090 others(7): Show |
12 | HG01243.hp1 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.-90+15722_-90+1573 others(14): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149333708 | ||||||
| chr6:149333741 | G | GTGTGTGT others(13): Show |
2 | a0001c0002t0002g0116 a0001c0002t0002g0117 |
2 | HG02155.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.-90+15731_-90+1573 others(24): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149333741 | ||||||
| chr6:149333749 | A | G | 6 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(3): Show |
6 | HG01884.hp2 HG02257.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.-90+15734A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149333749 | |||||||
| chr6:149333812 | A | G | 85 | a0001c0002t0002g0002 a0001c0002t0002g0098 a0001c0002t0002g0099 others(82): Show |
87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.-90+15797A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149333812 | |||||||
| chr6:149334072 | T | G | 1 | a0001c0001t0005g0181 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-90+16057T>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149334072 | |||||||
| chr6:149334125 | G | A | 17 | a0001c0001t0003g0006 a0001c0001t0003g0169 a0001c0001t0003g0170 others(14): Show |
18 | HG00609.hp2 HG01109.hp1 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.-90+16110G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149334125 | |||||||
| chr6:149334210 | A | C | 1 | a0001c0001t0001g0096 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-90+16195A>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149334210 | |||||||
| chr6:149334300 | A | G | 1 | a0001c0001t0017g0027 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-90+16285A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149334300 | |||||||
| chr6:149334337 | C | T | 290 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(287): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.-90+16322C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149334337 | |||||||
| chr6:149334387 | T | C | 59 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(56): Show |
62 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.-90+16372T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149334387 | |||||||
| chr6:149334422 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-90+16407G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149334422 | |||||||
| chr6:149334462 | T | C | 85 | a0001c0002t0002g0002 a0001c0002t0002g0098 a0001c0002t0002g0099 others(82): Show |
87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.-90+16447T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149334462 | |||||||
| chr6:149334477 | G | C | 9 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0005g0181 others(6): Show |
9 | HG01243.hp2 HG02602.hp2 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.-90+16462G>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149334477 | |||||||
| chr6:149334585 | GAGGATCA others(16): Show |
G | 1 | a0001c0002t0002g0237 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-90+16571_-90+1659 others(27): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149334585 | |||||||
| chr6:149334612 | G | C | 18 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(15): Show |
18 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.-90+16597G>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149334612 | |||||||
| chr6:149334622 | CTA | C | 3 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 |
3 | HG02818.hp2 HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-90+16609_-90+1661 others(6): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149334622 | ||||||
| chr6:149334676 | TA | T | 6 | a0001c0001t0001g0255 a0001c0001t0001g0286 a0001c0001t0001g0287 others(3): Show |
6 | HG01069.hp1 HG01070.hp2 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.-90+16675delA | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149334676 | ||||||
| chr6:149334776 | A | G | 85 | a0001c0002t0002g0002 a0001c0002t0002g0098 a0001c0002t0002g0099 others(82): Show |
87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.-90+16761A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149334776 | |||||||
| chr6:149334824 | G | A | 1 | a0001c0001t0013g0180 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-90+16809G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149334824 | |||||||
| chr6:149334914 | A | G | 85 | a0001c0002t0002g0002 a0001c0002t0002g0098 a0001c0002t0002g0099 others(82): Show |
87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.-90+16899A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149334914 | |||||||
| chr6:149335473 | A | ACCTCCCA others(6): Show |
1 | a0001c0001t0003g0315 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-90+17466_-90+1747 others(17): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149335473 | ||||||
| chr6:149335555 | G | T | 3 | a0001c0001t0013g0179 a0001c0001t0013g0180 a0001c0001t0022g0178 |
3 | HG02109.hp1 HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-90+17540G>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149335555 | |||||||
| chr6:149335558 | G | A | 1 | a0001c0001t0001g0265 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-90+17543G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149335558 | |||||||
| chr6:149335950 | A | G | 59 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(56): Show |
62 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.-90+17935A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149335950 | |||||||
| chr6:149336077 | C | T | 59 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(56): Show |
62 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.-90+18062C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149336077 | |||||||
| chr6:149336079 | G | A | 17 | a0001c0001t0001g0001 a0001c0001t0001g0089 a0001c0001t0001g0090 others(14): Show |
19 | HG01081.hp1 HG01109.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.-90+18064G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149336079 | |||||||
| chr6:149336091 | G | A | 147 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(144): Show |
152 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.-90+18076G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149336091 | |||||||
| chr6:149336142 | G | C | 1 | a0001c0001t0004g0036 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-90+18127G>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149336142 | |||||||
| chr6:149336288 | T | C | 1 | a0001c0001t0004g0033 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-90+18273T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149336288 | |||||||
| chr6:149336291 | A | G | 1 | a0001c0001t0003g0303 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-90+18276A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149336291 | |||||||
| chr6:149336293 | G | C | 1 | a0001c0001t0016g0087 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-90+18278G>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149336293 | |||||||
| chr6:149336635 | G | A | 2 | a0001c0002t0002g0203 a0001c0002t0002g0204 |
2 | NA18953.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.-90+18620G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149336635 | |||||||
| chr6:149336922 | T | TA | 58 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0010 others(55): Show |
60 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.-90+18919dupA | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149336922 | ||||||
| chr6:149336922 | TA | T | 229 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(226): Show |
234 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(231): Show |
intron_variant | MODIFIER | c.-90+18919delA | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149336922 | ||||||
| chr6:149336965 | A | T | 115 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(112): Show |
118 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.-90+18950A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149336965 | |||||||
| chr6:149336982 | A | C | 291 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(288): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.-90+18967A>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149336982 | |||||||
| chr6:149337223 | CTG | C | 88 | a0001c0001t0013g0179 a0001c0001t0013g0180 a0001c0001t0022g0178 others(85): Show |
90 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.-90+19210_-90+1921 others(6): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149337223 | ||||||
| chr6:149337256 | A | ATATTT | 290 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(287): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.-90+19245_-90+1924 others(9): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149337256 | ||||||
| chr6:149337290 | C | CAATT | 303 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(300): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.-90+19277_-90+1927 others(8): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149337290 | ||||||
| chr6:149337658 | C | T | 290 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(287): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.-90+19643C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149337658 | |||||||
| chr6:149337673 | C | T | 1 | a0001c0002t0002g0249 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-90+19658C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149337673 | |||||||
| chr6:149337699 | T | G | 1 | a0001c0001t0003g0006 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-90+19684T>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149337699 | |||||||
| chr6:149337842 | T | G | 147 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(144): Show |
152 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.-90+19827T>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149337842 | |||||||
| chr6:149338020 | T | A | 3 | a0001c0001t0003g0319 a0001c0001t0003g0321 a0001c0001t0003g0322 |
3 | HG01175.hp2 HG03491.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.-90+20005T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149338020 | |||||||
| chr6:149338050 | C | T | 1 | a0001c0001t0001g0290 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-90+20035C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149338050 | |||||||
| chr6:149338060 | A | G | 1 | a0001c0001t0004g0069 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-90+20045A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149338060 | |||||||
| chr6:149338123 | C | T | 1 | a0001c0001t0001g0285 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-90+20108C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149338123 | |||||||
| chr6:149338451 | G | C | 2 | a0001c0001t0001g0268 a0001c0001t0001g0302 |
2 | HG00673.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.-90+20436G>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149338451 | |||||||
| chr6:149338467 | G | T | 6 | a0001c0001t0007g0077 a0001c0001t0007g0078 a0001c0001t0007g0079 others(3): Show |
6 | HG02630.hp2 HG03225.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-90+20452G>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149338467 | |||||||
| chr6:149338512 | T | C | 85 | a0001c0002t0002g0002 a0001c0002t0002g0098 a0001c0002t0002g0099 others(82): Show |
87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.-90+20497T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149338512 | |||||||
| chr6:149338559 | T | TTAAGTTT others(5): Show |
1 | a0001c0002t0002g0237 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-90+20550_-90+2056 others(16): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149338559 | ||||||
| chr6:149338563 | G | T | 18 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(15): Show |
18 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.-90+20548G>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149338563 | |||||||
| chr6:149338873 | T | C | 2 | a0001c0001t0004g0033 a0001c0001t0004g0034 |
2 | HG03041.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-90+20858T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149338873 | |||||||
| chr6:149338889 | A | T | 2 | a0001c0001t0003g0332 a0001c0001t0003g0344 |
2 | HG02683.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.-90+20874A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149338889 | |||||||
| chr6:149338973 | C | T | 59 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(56): Show |
62 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.-90+20958C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149338973 | |||||||
| chr6:149339039 | G | A | 8 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(5): Show |
8 | HG02895.hp1 HG02895.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-90+21024G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149339039 | |||||||
| chr6:149339132 | G | A | 86 | a0001c0001t0008g0026 a0001c0002t0002g0002 a0001c0002t0002g0098 others(83): Show |
88 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.-90+21117G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149339132 | |||||||
| chr6:149339233 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-90+21218C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149339233 | |||||||
| chr6:149339272 | A | G | 8 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(5): Show |
8 | HG02895.hp1 HG02895.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-90+21257A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149339272 | |||||||
| chr6:149339301 | G | A | 59 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(56): Show |
62 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.-90+21286G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149339301 | |||||||
| chr6:149339312 | T | A | 1 | a0001c0001t0001g0011 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-90+21297T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149339312 | |||||||
| chr6:149339362 | C | T | 85 | a0001c0002t0002g0002 a0001c0002t0002g0098 a0001c0002t0002g0099 others(82): Show |
87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.-90+21347C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149339362 | |||||||
| chr6:149339367 | C | CA | 8 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(5): Show |
8 | HG01256.hp1 HG01258.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.-90+21360dupA | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149339367 | ||||||
| chr6:149339376 | T | G | 2 | a0001c0001t0001g0355 a0001c0001t0001g0356 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-90+21361T>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149339376 | |||||||
| chr6:149339385 | GA | G | 85 | a0001c0002t0002g0002 a0001c0002t0002g0098 a0001c0002t0002g0099 others(82): Show |
87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.-90+21378delA | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149339385 | ||||||
| chr6:149339512 | A | G | 3 | a0001c0001t0001g0145 a0001c0001t0001g0284 a0001c0001t0001g0287 |
3 | HG01516.hp1 HG01517.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.-90+21497A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149339512 | |||||||
| chr6:149339585 | TTTTATTT others(5): Show |
T | 105 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(102): Show |
108 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.-90+21582_-90+2159 others(16): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149339585 | ||||||
| chr6:149339589 | A | AT | 12 | a0001c0001t0001g0071 a0001c0001t0007g0077 a0001c0001t0007g0078 others(9): Show |
12 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.-90+21577dupT | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149339589 | ||||||
| chr6:149339590 | T | TTTTA | 5 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0075 others(2): Show |
5 | HG02257.hp1 HG02886.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.-90+21577_-90+2157 others(8): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149339590 | ||||||
| chr6:149339590 | TTTA | T | 59 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(56): Show |
62 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.-90+21578_-90+2158 others(7): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149339590 | ||||||
| chr6:149339590 | TTTATTTA others(4): Show |
T | 6 | a0001c0001t0001g0161 a0001c0001t0001g0293 a0001c0001t0008g0165 others(3): Show |
6 | HG01081.hp2 HG02280.hp1 HG04184.hp2 others(3): Show |
intron_variant | MODIFIER | c.-90+21578_-90+2158 others(15): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149339590 | ||||||
| chr6:149339591 | TTATTTAT others(3): Show |
T | 7 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 others(4): Show |
7 | HG01081.hp1 HG01884.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.-90+21578_-90+2158 others(14): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149339591 | ||||||
| chr6:149339592 | TA | T | 85 | a0001c0002t0002g0002 a0001c0002t0002g0098 a0001c0002t0002g0099 others(82): Show |
87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.-90+21578delA | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149339592 | |||||||
| chr6:149339592 | TATTTATT others(6): Show |
T | 2 | a0001c0001t0001g0131 a0001c0001t0001g0269 |
2 | NA18952.hp2 NA19059.hp2 |
intron_variant | MODIFIER | c.-90+21578_-90+2159 others(17): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149339592 | |||||||
| chr6:149339593 | A | T | 6 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0075 others(3): Show |
6 | HG02257.hp1 HG02886.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.-90+21578A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149339593 | |||||||
| chr6:149339597 | A | T | 77 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(74): Show |
80 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(77): Show |
intron_variant | MODIFIER | c.-90+21582A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149339597 | |||||||
| chr6:149339597 | ATTTATTT others(4): Show |
A | 1 | a0001c0001t0005g0252 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-90+21586_-90+2159 others(15): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149339597 | ||||||
| chr6:149339597 | ATTTATTT others(5): Show |
A | 7 | a0001c0001t0005g0119 a0001c0001t0005g0181 a0001c0001t0005g0182 others(4): Show |
7 | HG02602.hp2 HG02683.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.-90+21586_-90+2159 others(16): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149339597 | ||||||
| chr6:149339601 | A | T | 17 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(14): Show |
17 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.-90+21586A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149339601 | |||||||
| chr6:149339603 | TTA | T | 16 | a0001c0001t0003g0006 a0001c0001t0003g0169 a0001c0001t0003g0170 others(13): Show |
17 | HG00609.hp2 HG01109.hp1 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.-90+21590_-90+2159 others(6): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149339603 | ||||||
| chr6:149339604 | T | TTTTA | 11 | a0001c0001t0007g0077 a0001c0001t0007g0078 a0001c0001t0007g0079 others(8): Show |
11 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.-90+21589_-90+2159 others(8): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149339604 | |||||||
| chr6:149339604 | TA | T | 42 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0010 others(39): Show |
43 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.-90+21590delA | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149339604 | |||||||
| chr6:149339605 | A | AT | 9 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(6): Show |
9 | HG02895.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.-90+21605dupT | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149339605 | ||||||
| chr6:149339605 | A | T | 129 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(126): Show |
132 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.-90+21590A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149339605 | |||||||
| chr6:149339605 | ATT | A | 89 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 others(86): Show |
91 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.-90+21604_-90+2160 others(6): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149339605 | ||||||
| chr6:149339609 | T | A | 1 | a0001c0001t0001g0253 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-90+21594T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149339609 | |||||||
| chr6:149339788 | G | A | 18 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(15): Show |
18 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.-90+21773G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149339788 | |||||||
| chr6:149339844 | C | A | 1 | a0001c0002t0002g0112 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-90+21829C>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149339844 | |||||||
| chr6:149339974 | T | C | 3 | a0001c0001t0013g0179 a0001c0001t0013g0180 a0001c0001t0022g0178 |
3 | HG02109.hp1 HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-90+21959T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149339974 | |||||||
| chr6:149339977 | TAATG | T | 9 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0005g0181 others(6): Show |
9 | HG01243.hp2 HG02602.hp2 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.-90+21963_-90+2196 others(8): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149339977 | |||||||
| chr6:149340017 | C | T | 17 | a0001c0001t0001g0001 a0001c0001t0001g0089 a0001c0001t0001g0090 others(14): Show |
19 | HG01081.hp1 HG01109.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.-90+22002C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149340017 | |||||||
| chr6:149340049 | C | G | 3 | a0001c0001t0010g0158 a0001c0001t0010g0159 a0001c0001t0010g0160 |
3 | NA19002.hp2 NA19088.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.-90+22034C>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149340049 | |||||||
| chr6:149340089 | C | G | 1 | a0001c0001t0003g0173 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-90+22074C>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149340089 | |||||||
| chr6:149340102 | A | G | 59 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(56): Show |
62 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.-90+22087A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149340102 | |||||||
| chr6:149340190 | G | A | 6 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 others(3): Show |
6 | HG01081.hp1 HG01884.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-90+22175G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149340190 | |||||||
| chr6:149340667 | C | G | 2 | a0001c0001t0013g0179 a0001c0001t0013g0180 |
2 | HG02109.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.-90+22652C>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149340667 | |||||||
| chr6:149340693 | A | G | 3 | a0001c0001t0013g0179 a0001c0001t0013g0180 a0001c0001t0022g0178 |
3 | HG02109.hp1 HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-90+22678A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149340693 | |||||||
| chr6:149340868 | A | T | 18 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(15): Show |
18 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.-90+22853A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149340868 | |||||||
| chr6:149341021 | T | C | 1 | a0001c0002t0002g0205 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-90+23006T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149341021 | |||||||
| chr6:149341278 | A | G | 1 | a0001c0001t0004g0036 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-90+23263A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149341278 | |||||||
| chr6:149341354 | C | T | 1 | a0001c0001t0017g0027 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-90+23339C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149341354 | |||||||
| chr6:149341813 | A | G | 85 | a0001c0002t0002g0002 a0001c0002t0002g0098 a0001c0002t0002g0099 others(82): Show |
87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.-90+23798A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149341813 | |||||||
| chr6:149341855 | G | C | 125 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(122): Show |
128 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.-90+23840G>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149341855 | |||||||
| chr6:149341977 | A | G | 1 | a0001c0001t0003g0008 | 2 | HG02300.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-90+23962A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149341977 | |||||||
| chr6:149342044 | A | AT | 143 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(140): Show |
148 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(145): Show |
intron_variant | MODIFIER | c.-90+24031dupT | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149342044 | ||||||
| chr6:149342046 | TA | T | 114 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(111): Show |
117 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(114): Show |
intron_variant | MODIFIER | c.-90+24044delA | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149342046 | ||||||
| chr6:149342047 | A | T | 4 | a0001c0002t0002g0116 a0001c0002t0002g0117 a0001c0002t0002g0206 others(1): Show |
4 | HG02155.hp2 NA18975.hp2 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.-90+24032A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149342047 | |||||||
| chr6:149342240 | G | T | 317 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(314): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.-90+24225G>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149342240 | |||||||
| chr6:149342826 | A | G | 1 | a0001c0002t0002g0244 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-90+24811A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149342826 | |||||||
| chr6:149342995 | A | G | 3 | a0001c0001t0001g0260 a0001c0003t0001g0258 a0001c0003t0001g0259 |
3 | HG00642.hp1 HG01261.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.-90+24980A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149342995 | |||||||
| chr6:149343097 | C | T | 17 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(14): Show |
17 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.-90+25082C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149343097 | |||||||
| chr6:149343276 | T | C | 1 | a0001c0001t0001g0012 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-90+25261T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149343276 | |||||||
| chr6:149343289 | C | T | 1 | a0001c0001t0001g0354 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-90+25274C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149343289 | |||||||
| chr6:149343314 | CA | C | 59 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(56): Show |
62 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.-90+25306delA | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149343314 | ||||||
| chr6:149343404 | G | A | 124 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(121): Show |
127 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.-90+25389G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149343404 | |||||||
| chr6:149343471 | C | CA | 7 | a0001c0001t0001g0011 a0001c0001t0003g0309 a0001c0001t0004g0060 others(4): Show |
7 | HG02109.hp1 HG02135.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.-90+25471dupA | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149343471 | ||||||
| chr6:149343471 | CA | C | 8 | a0001c0001t0001g0154 a0001c0001t0003g0318 a0001c0001t0009g0082 others(5): Show |
8 | HG00140.hp2 HG01070.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.-90+25471delA | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149343471 | ||||||
| chr6:149343532 | G | A | 1 | a0001c0001t0001g0150 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-90+25517G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149343532 | |||||||
| chr6:149343693 | A | G | 290 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(287): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.-90+25678A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149343693 | |||||||
| chr6:149343745 | G | C | 17 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(14): Show |
17 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.-90+25730G>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149343745 | |||||||
| chr6:149344274 | T | C | 1 | a0001c0002t0002g0101 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-89-25635T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149344274 | |||||||
| chr6:149344716 | C | T | 59 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(56): Show |
62 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.-89-25193C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149344716 | |||||||
| chr6:149344801 | C | T | 144 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(141): Show |
149 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(146): Show |
intron_variant | MODIFIER | c.-89-25108C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149344801 | |||||||
| chr6:149344837 | A | G | 1 | a0001c0001t0001g0146 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-89-25072A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149344837 | |||||||
| chr6:149345285 | A | G | 4 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 others(1): Show |
4 | HG01081.hp1 HG01884.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-89-24624A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149345285 | |||||||
| chr6:149345327 | A | G | 1 | a0001c0001t0003g0332 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-89-24582A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149345327 | |||||||
| chr6:149345332 | G | A | 3 | a0001c0001t0013g0179 a0001c0001t0013g0180 a0001c0001t0022g0178 |
3 | HG02109.hp1 HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-89-24577G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149345332 | |||||||
| chr6:149345346 | G | C | 2 | a0001c0001t0003g0176 a0001c0001t0003g0345 |
2 | HG01256.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.-89-24563G>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149345346 | |||||||
| chr6:149345484 | T | A | 59 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(56): Show |
62 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.-89-24425T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149345484 | |||||||
| chr6:149345507 | T | A | 1 | a0001c0002t0002g0198 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.-89-24402T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149345507 | |||||||
| chr6:149345508 | A | G | 298 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(295): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.-89-24401A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149345508 | |||||||
| chr6:149345551 | AAT | A | 85 | a0001c0002t0002g0002 a0001c0002t0002g0098 a0001c0002t0002g0099 others(82): Show |
87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.-89-24355_-89-2435 others(6): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149345551 | ||||||
| chr6:149345841 | G | A | 162 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(159): Show |
167 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.-89-24068G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149345841 | |||||||
| chr6:149345845 | A | G | 2 | a0001c0001t0003g0172 a0001c0001t0003g0308 |
2 | HG01109.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.-89-24064A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149345845 | |||||||
| chr6:149345899 | T | G | 1 | a0001c0002t0002g0194 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.-89-24010T>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149345899 | |||||||
| chr6:149345993 | A | T | 59 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(56): Show |
62 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.-89-23916A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149345993 | |||||||
| chr6:149346112 | A | G | 59 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(56): Show |
62 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.-89-23797A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149346112 | |||||||
| chr6:149346124 | A | C | 85 | a0001c0002t0002g0002 a0001c0002t0002g0098 a0001c0002t0002g0099 others(82): Show |
87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.-89-23785A>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149346124 | |||||||
| chr6:149346253 | C | T | 2 | a0001c0001t0013g0179 a0001c0001t0013g0180 |
2 | HG02109.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.-89-23656C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149346253 | |||||||
| chr6:149346257 | C | CACGCATG others(27): Show |
1 | a0001c0001t0001g0131 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.-89-23651_-89-2361 others(38): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149346257 | ||||||
| chr6:149346260 | G | A | 1 | a0001c0002t0006g0238 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-89-23649G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149346260 | |||||||
| chr6:149346323 | G | A | 1 | a0001c0001t0001g0131 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.-89-23586G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149346323 | |||||||
| chr6:149346374 | A | G | 2 | a0001c0001t0004g0056 a0001c0001t0004g0057 |
2 | NA18957.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.-89-23535A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149346374 | |||||||
| chr6:149346426 | G | A | 3 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0290 |
3 | NA18990.hp1 NA19005.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.-89-23483G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149346426 | |||||||
| chr6:149346448 | C | CT | 126 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(123): Show |
129 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.-89-23439dupT | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149346448 | ||||||
| chr6:149346448 | C | CTT | 8 | a0001c0001t0001g0157 a0001c0001t0001g0163 a0001c0001t0001g0164 others(5): Show |
8 | HG02280.hp1 HG02622.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.-89-23440_-89-2343 others(6): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149346448 | ||||||
| chr6:149346448 | CT | C | 45 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0174 others(42): Show |
47 | HG00140.hp2 HG01099.hp2 HG01168.hp2 others(44): Show |
intron_variant | MODIFIER | c.-89-23439delT | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149346448 | ||||||
| chr6:149346448 | CTT | C | 97 | a0001c0001t0003g0006 a0001c0001t0003g0169 a0001c0001t0003g0170 others(94): Show |
100 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.-89-23440_-89-2343 others(6): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149346448 | ||||||
| chr6:149346448 | CTTT | C | 15 | a0001c0001t0003g0010 a0001c0001t0003g0173 a0001c0001t0003g0176 others(12): Show |
15 | HG00099.hp2 HG00639.hp1 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.-89-23441_-89-2343 others(7): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149346448 | ||||||
| chr6:149346457 | T | G | 9 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0005g0181 others(6): Show |
9 | HG01243.hp2 HG02602.hp2 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.-89-23452T>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149346457 | |||||||
| chr6:149346540 | G | A | 59 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(56): Show |
62 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.-89-23369G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149346540 | |||||||
| chr6:149346667 | T | C | 1 | a0001c0001t0001g0071 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-89-23242T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149346667 | |||||||
| chr6:149346777 | C | T | 4 | a0001c0001t0013g0179 a0001c0001t0013g0180 a0001c0001t0017g0027 others(1): Show |
4 | HG02109.hp1 HG02615.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.-89-23132C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149346777 | |||||||
| chr6:149346833 | C | T | 1 | a0001c0002t0002g0198 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.-89-23076C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149346833 | |||||||
| chr6:149347002 | C | G | 17 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(14): Show |
17 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.-89-22907C>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149347002 | |||||||
| chr6:149347048 | T | A | 4 | a0001c0001t0004g0028 a0001c0001t0004g0029 a0001c0001t0004g0039 others(1): Show |
4 | HG02258.hp1 HG02559.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.-89-22861T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149347048 | |||||||
| chr6:149347076 | T | C | 86 | a0001c0001t0004g0045 a0001c0002t0002g0002 a0001c0002t0002g0098 others(83): Show |
88 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.-89-22833T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149347076 | |||||||
| chr6:149347091 | A | G | 6 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(3): Show |
6 | HG00733.hp2 HG02145.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-89-22818A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149347091 | |||||||
| chr6:149347129 | A | G | 1 | a0001c0001t0001g0094 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-89-22780A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149347129 | |||||||
| chr6:149347369 | T | C | 1 | a0001c0001t0022g0178 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-89-22540T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149347369 | |||||||
| chr6:149347391 | A | G | 85 | a0001c0002t0002g0002 a0001c0002t0002g0098 a0001c0002t0002g0099 others(82): Show |
87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.-89-22518A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149347391 | |||||||
| chr6:149347450 | CAT | C | 9 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0005g0181 others(6): Show |
9 | HG01243.hp2 HG02602.hp2 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.-89-22457_-89-2245 others(6): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149347450 | ||||||
| chr6:149347543 | G | A | 1 | a0001c0002t0014g0113 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-89-22366G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149347543 | |||||||
| chr6:149347851 | T | A | 1 | a0001c0001t0001g0131 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.-89-22058T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149347851 | |||||||
| chr6:149347899 | T | C | 1 | a0001c0001t0001g0131 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.-89-22010T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149347899 | |||||||
| chr6:149347967 | A | C | 1 | a0001c0001t0001g0283 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-89-21942A>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149347967 | |||||||
| chr6:149348046 | A | T | 1 | a0001c0002t0002g0250 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.-89-21863A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149348046 | |||||||
| chr6:149348056 | G | T | 1 | a0001c0002t0002g0250 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.-89-21853G>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149348056 | |||||||
| chr6:149348058 | T | C | 1 | a0001c0002t0002g0250 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.-89-21851T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149348058 | |||||||
| chr6:149348060 | A | G | 1 | a0001c0002t0002g0250 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.-89-21849A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149348060 | |||||||
| chr6:149348062 | G | A | 1 | a0001c0002t0002g0250 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.-89-21847G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149348062 | |||||||
| chr6:149348070 | A | T | 1 | a0001c0002t0002g0250 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.-89-21839A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149348070 | |||||||
| chr6:149348072 | T | A | 1 | a0001c0002t0002g0250 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.-89-21837T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149348072 | |||||||
| chr6:149348088 | T | C | 2 | a0001c0001t0003g0316 a0001c0001t0003g0318 |
2 | HG00140.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.-89-21821T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149348088 | |||||||
| chr6:149348137 | T | A | 317 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(314): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.-89-21772T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149348137 | |||||||
| chr6:149348218 | G | T | 317 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(314): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.-89-21691G>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149348218 | |||||||
| chr6:149348265 | G | A | 290 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(287): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.-89-21644G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149348265 | |||||||
| chr6:149348282 | A | G | 1 | a0001c0002t0002g0235 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-89-21627A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149348282 | |||||||
| chr6:149348291 | G | A | 304 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(301): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.-89-21618G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149348291 | |||||||
| chr6:149348407 | A | G | 1 | a0001c0001t0001g0301 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-89-21502A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149348407 | |||||||
| chr6:149348443 | A | C | 85 | a0001c0002t0002g0002 a0001c0002t0002g0098 a0001c0002t0002g0099 others(82): Show |
87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.-89-21466A>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149348443 | |||||||
| chr6:149348455 | C | T | 1 | a0001c0001t0008g0026 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-89-21454C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149348455 | |||||||
| chr6:149348501 | T | C | 290 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(287): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.-89-21408T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149348501 | |||||||
| chr6:149348614 | G | GA | 95 | a0001c0001t0001g0161 a0001c0001t0005g0119 a0001c0001t0005g0120 others(92): Show |
97 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.-89-21285dupA | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149348614 | ||||||
| chr6:149348715 | G | A | 59 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(56): Show |
62 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.-89-21194G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149348715 | |||||||
| chr6:149348818 | T | G | 1 | a0001c0001t0017g0027 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-89-21091T>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149348818 | |||||||
| chr6:149348857 | G | C | 290 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(287): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.-89-21052G>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149348857 | |||||||
| chr6:149348931 | A | C | 290 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(287): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.-89-20978A>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149348931 | |||||||
| chr6:149348935 | C | T | 17 | a0001c0001t0003g0006 a0001c0001t0003g0169 a0001c0001t0003g0170 others(14): Show |
18 | HG00609.hp2 HG01109.hp1 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.-89-20974C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149348935 | |||||||
| chr6:149348975 | T | TA | 4 | a0001c0001t0013g0179 a0001c0001t0013g0180 a0001c0001t0022g0178 others(1): Show |
4 | HG02109.hp1 HG02615.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.-89-20934_-89-2093 others(5): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149348975 | |||||||
| chr6:149348976 | T | A | 290 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(287): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.-89-20933T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149348976 | |||||||
| chr6:149349042 | A | G | 17 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(14): Show |
17 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.-89-20867A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149349042 | |||||||
| chr6:149349186 | T | C | 290 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(287): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.-89-20723T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149349186 | |||||||
| chr6:149349248 | G | A | 85 | a0001c0002t0002g0002 a0001c0002t0002g0098 a0001c0002t0002g0099 others(82): Show |
87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.-89-20661G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149349248 | |||||||
| chr6:149349378 | C | G | 1 | a0001c0002t0002g0197 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-89-20531C>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149349378 | |||||||
| chr6:149349419 | C | CA | 61 | a0001c0001t0001g0161 a0001c0001t0001g0263 a0001c0001t0001g0264 others(58): Show |
64 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.-89-20472dupA | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149349419 | ||||||
| chr6:149349419 | CA | C | 7 | a0001c0001t0001g0017 a0001c0001t0001g0282 a0001c0001t0004g0066 others(4): Show |
7 | HG01243.hp2 HG03540.hp2 HG03704.hp2 others(4): Show |
intron_variant | MODIFIER | c.-89-20472delA | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149349419 | ||||||
| chr6:149349572 | C | T | 1 | a0001c0001t0004g0062 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-89-20337C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149349572 | |||||||
| chr6:149349607 | TA | T | 17 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(14): Show |
17 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.-89-20301delA | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149349607 | |||||||
| chr6:149349658 | G | A | 17 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(14): Show |
17 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.-89-20251G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149349658 | |||||||
| chr6:149349696 | T | G | 1 | a0001c0001t0001g0131 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.-89-20213T>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149349696 | |||||||
| chr6:149349742 | C | T | 88 | a0001c0001t0013g0179 a0001c0001t0013g0180 a0001c0001t0022g0178 others(85): Show |
90 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.-89-20167C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149349742 | |||||||
| chr6:149349898 | T | C | 1 | a0001c0001t0017g0027 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-89-20011T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149349898 | |||||||
| chr6:149349941 | A | T | 59 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(56): Show |
62 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.-89-19968A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149349941 | |||||||
| chr6:149349980 | A | G | 115 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(112): Show |
118 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.-89-19929A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149349980 | |||||||
| chr6:149350041 | T | C | 147 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(144): Show |
152 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.-89-19868T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149350041 | |||||||
| chr6:149350057 | G | A | 27 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0174 others(24): Show |
29 | HG00140.hp2 HG01168.hp2 HG01175.hp2 others(26): Show |
intron_variant | MODIFIER | c.-89-19852G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149350057 | |||||||
| chr6:149350220 | C | T | 1 | a0001c0002t0002g0208 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-89-19689C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149350220 | |||||||
| chr6:149350224 | G | A | 115 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(112): Show |
118 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.-89-19685G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149350224 | |||||||
| chr6:149350249 | C | T | 59 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(56): Show |
62 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.-89-19660C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149350249 | |||||||
| chr6:149350270 | C | G | 59 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(56): Show |
62 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.-89-19639C>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149350270 | |||||||
| chr6:149350319 | G | A | 2 | a0001c0001t0001g0273 a0001c0001t0001g0301 |
2 | HG01496.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.-89-19590G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149350319 | |||||||
| chr6:149350365 | T | A | 3 | a0001c0001t0013g0179 a0001c0001t0013g0180 a0001c0001t0022g0178 |
3 | HG02109.hp1 HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-89-19544T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149350365 | |||||||
| chr6:149350562 | G | T | 165 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(162): Show |
170 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(167): Show |
intron_variant | MODIFIER | c.-89-19347G>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149350562 | |||||||
| chr6:149350617 | C | CT | 56 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(53): Show |
57 | HG00099.hp2 HG00609.hp2 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.-89-19268dupT | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149350617 | ||||||
| chr6:149350617 | C | CTT | 20 | a0001c0001t0001g0075 a0001c0001t0003g0008 a0001c0001t0003g0171 others(17): Show |
21 | HG00140.hp2 HG01168.hp2 HG01175.hp1 others(18): Show |
intron_variant | MODIFIER | c.-89-19269_-89-1926 others(6): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149350617 | ||||||
| chr6:149350617 | CT | C | 93 | a0001c0001t0001g0090 a0001c0001t0001g0254 a0001c0001t0001g0282 others(90): Show |
95 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.-89-19268delT | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149350617 | ||||||
| chr6:149350617 | CTT | C | 113 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(110): Show |
116 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.-89-19269_-89-1926 others(6): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149350617 | ||||||
| chr6:149350617 | CTTT | C | 8 | a0001c0001t0001g0089 a0001c0001t0001g0131 a0001c0001t0001g0133 others(5): Show |
8 | HG01496.hp1 HG03098.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.-89-19270_-89-1926 others(7): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149350617 | ||||||
| chr6:149350632 | T | C | 1 | a0001c0002t0002g0207 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-89-19277T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149350632 | |||||||
| chr6:149350664 | G | T | 1 | a0001c0001t0008g0026 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-89-19245G>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149350664 | |||||||
| chr6:149350685 | G | A | 3 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0297 |
3 | HG02622.hp2 HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-89-19224G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149350685 | |||||||
| chr6:149350714 | A | G | 8 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0005g0181 others(5): Show |
8 | HG01243.hp2 HG02602.hp2 HG02683.hp1 others(5): Show |
intron_variant | MODIFIER | c.-89-19195A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149350714 | |||||||
| chr6:149350762 | G | A | 3 | a0001c0001t0013g0179 a0001c0001t0013g0180 a0001c0001t0022g0178 |
3 | HG02109.hp1 HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-89-19147G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149350762 | |||||||
| chr6:149350827 | G | A | 9 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0005g0181 others(6): Show |
9 | HG01243.hp2 HG02602.hp2 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.-89-19082G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149350827 | |||||||
| chr6:149350888 | T | C | 1 | a0001c0002t0002g0102 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-89-19021T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149350888 | |||||||
| chr6:149350889 | T | C | 1 | a0001c0001t0001g0018 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-89-19020T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149350889 | |||||||
| chr6:149350993 | T | A | 6 | a0001c0001t0007g0077 a0001c0001t0007g0078 a0001c0001t0007g0079 others(3): Show |
6 | HG02630.hp2 HG03225.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-89-18916T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149350993 | |||||||
| chr6:149351080 | C | A | 1 | a0001c0001t0001g0071 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-89-18829C>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149351080 | |||||||
| chr6:149351130 | GC | G | 85 | a0001c0002t0002g0002 a0001c0002t0002g0098 a0001c0002t0002g0099 others(82): Show |
87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.-89-18776delC | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149351130 | ||||||
| chr6:149351187 | A | G | 27 | a0001c0001t0001g0088 a0001c0001t0001g0123 a0001c0001t0001g0124 others(24): Show |
27 | HG00597.hp1 HG00735.hp2 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.-89-18722A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149351187 | |||||||
| chr6:149351239 | C | G | 125 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(122): Show |
128 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.-89-18670C>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149351239 | |||||||
| chr6:149351261 | C | T | 1 | a0001c0001t0017g0027 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-89-18648C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149351261 | |||||||
| chr6:149351262 | G | A | 3 | a0001c0001t0013g0179 a0001c0001t0013g0180 a0001c0001t0022g0178 |
3 | HG02109.hp1 HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-89-18647G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149351262 | |||||||
| chr6:149351529 | T | C | 85 | a0001c0002t0002g0002 a0001c0002t0002g0098 a0001c0002t0002g0099 others(82): Show |
87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.-89-18380T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149351529 | |||||||
| chr6:149351579 | A | T | 9 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0005g0181 others(6): Show |
9 | HG01243.hp2 HG02602.hp2 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.-89-18330A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149351579 | |||||||
| chr6:149351669 | A | G | 290 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(287): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.-89-18240A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149351669 | |||||||
| chr6:149351705 | A | AAAT | 3 | a0001c0001t0013g0179 a0001c0001t0013g0180 a0001c0001t0022g0178 |
3 | HG02109.hp1 HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-89-18202_-89-1820 others(7): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149351705 | ||||||
| chr6:149351920 | A | G | 1 | a0001c0001t0005g0351 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-89-17989A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149351920 | |||||||
| chr6:149351937 | A | G | 3 | a0001c0001t0013g0179 a0001c0001t0013g0180 a0001c0001t0022g0178 |
3 | HG02109.hp1 HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-89-17972A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149351937 | |||||||
| chr6:149352129 | GT | G | 3 | a0001c0002t0002g0210 a0001c0002t0002g0211 a0001c0002t0002g0212 |
3 | HG00609.hp1 NA18985.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.-89-17778delT | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149352129 | ||||||
| chr6:149352246 | A | C | 1 | a0001c0001t0003g0175 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-89-17663A>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149352246 | |||||||
| chr6:149352455 | C | T | 290 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(287): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.-89-17454C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149352455 | |||||||
| chr6:149352598 | A | G | 2 | a0001c0002t0002g0110 a0001c0002t0002g0111 |
2 | HG04204.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.-89-17311A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149352598 | |||||||
| chr6:149352720 | T | A | 59 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(56): Show |
62 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.-89-17189T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149352720 | |||||||
| chr6:149352728 | G | A | 1 | a0001c0001t0017g0027 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-89-17181G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149352728 | |||||||
| chr6:149352748 | C | T | 8 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0005g0181 others(5): Show |
8 | HG01243.hp2 HG02602.hp2 HG02683.hp1 others(5): Show |
intron_variant | MODIFIER | c.-89-17161C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149352748 | |||||||
| chr6:149352783 | A | C | 1 | a0001c0001t0008g0026 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-89-17126A>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149352783 | |||||||
| chr6:149352920 | G | C | 2 | a0001c0002t0002g0190 a0001c0002t0002g0207 |
2 | NA18998.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.-89-16989G>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149352920 | |||||||
| chr6:149353040 | T | C | 9 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0005g0181 others(6): Show |
9 | HG01243.hp2 HG02602.hp2 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.-89-16869T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149353040 | |||||||
| chr6:149353228 | G | GTGC | 20 | a0001c0001t0001g0001 a0001c0001t0001g0089 a0001c0001t0001g0090 others(17): Show |
22 | HG01081.hp1 HG01109.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.-89-16663_-89-1666 others(7): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149353228 | ||||||
| chr6:149353228 | GTGCTGCT others(22): Show |
G | 1 | a0001c0001t0001g0168 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-89-16664_-89-1663 others(33): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149353228 | ||||||
| chr6:149353306 | C | T | 11 | a0001c0001t0007g0077 a0001c0001t0007g0078 a0001c0001t0007g0079 others(8): Show |
11 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.-89-16603C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149353306 | |||||||
| chr6:149353456 | C | A | 1 | a0001c0002t0002g0213 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-89-16453C>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149353456 | |||||||
| chr6:149353652 | A | G | 2 | a0001c0001t0003g0323 a0001c0001t0003g0333 |
2 | HG02486.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-89-16257A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149353652 | |||||||
| chr6:149353678 | C | T | 59 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(56): Show |
62 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.-89-16231C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149353678 | |||||||
| chr6:149353925 | C | T | 4 | a0001c0001t0003g0335 a0001c0001t0003g0340 a0001c0001t0003g0342 others(1): Show |
4 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.-89-15984C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149353925 | |||||||
| chr6:149353927 | T | C | 2 | a0001c0001t0001g0013 a0001c0001t0001g0014 |
2 | HG02145.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.-89-15982T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149353927 | |||||||
| chr6:149353968 | T | C | 290 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(287): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.-89-15941T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149353968 | |||||||
| chr6:149354136 | T | G | 85 | a0001c0002t0002g0002 a0001c0002t0002g0098 a0001c0002t0002g0099 others(82): Show |
87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.-89-15773T>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149354136 | |||||||
| chr6:149354531 | A | T | 3 | a0001c0002t0002g0203 a0001c0002t0002g0204 a0001c0002t0002g0232 |
3 | NA18953.hp1 NA19011.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.-89-15378A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149354531 | |||||||
| chr6:149354608 | G | A | 1 | a0001c0001t0017g0027 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-89-15301G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149354608 | |||||||
| chr6:149354727 | T | C | 1 | a0001c0001t0017g0027 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-89-15182T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149354727 | |||||||
| chr6:149354755 | T | A | 290 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(287): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.-89-15154T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149354755 | |||||||
| chr6:149354992 | T | C | 6 | a0001c0001t0003g0309 a0001c0001t0003g0310 a0001c0001t0003g0312 others(3): Show |
6 | HG02129.hp1 NA18950.hp1 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.-89-14917T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149354992 | |||||||
| chr6:149355176 | C | T | 1 | a0001c0001t0023g0074 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-89-14733C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149355176 | |||||||
| chr6:149355181 | G | A | 9 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0005g0181 others(6): Show |
9 | HG01243.hp2 HG02602.hp2 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.-89-14728G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149355181 | |||||||
| chr6:149355415 | C | T | 2 | a0001c0001t0004g0033 a0001c0001t0004g0034 |
2 | HG03041.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-89-14494C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149355415 | |||||||
| chr6:149355464 | G | C | 92 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0011 others(89): Show |
93 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.-89-14445G>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149355464 | |||||||
| chr6:149355667 | C | CA | 13 | a0001c0001t0001g0012 a0001c0001t0001g0145 a0001c0001t0001g0270 others(10): Show |
13 | HG00733.hp2 HG02055.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.-89-14225dupA | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149355667 | ||||||
| chr6:149355667 | CA | C | 99 | a0001c0001t0001g0001 a0001c0001t0001g0089 a0001c0001t0001g0090 others(96): Show |
104 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(101): Show |
intron_variant | MODIFIER | c.-89-14225delA | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149355667 | ||||||
| chr6:149355667 | CAA | C | 81 | a0001c0001t0005g0252 a0001c0002t0002g0002 a0001c0002t0002g0098 others(78): Show |
83 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.-89-14226_-89-1422 others(6): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149355667 | ||||||
| chr6:149355860 | C | G | 2 | a0001c0001t0001g0013 a0001c0001t0001g0014 |
2 | HG02145.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.-89-14049C>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149355860 | |||||||
| chr6:149355860 | C | T | 1 | a0001c0001t0001g0272 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-89-14049C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149355860 | |||||||
| chr6:149355955 | CA | C | 8 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0005g0181 others(5): Show |
8 | HG01243.hp2 HG02602.hp2 HG02683.hp1 others(5): Show |
intron_variant | MODIFIER | c.-89-13944delA | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149355955 | ||||||
| chr6:149355965 | A | C | 2 | a0001c0001t0005g0182 a0001c0001t0005g0183 |
2 | HG02683.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.-89-13944A>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149355965 | |||||||
| chr6:149356053 | G | A | 1 | a0001c0001t0008g0026 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-89-13856G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149356053 | |||||||
| chr6:149356097 | C | G | 1 | a0001c0001t0003g0321 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-89-13812C>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149356097 | |||||||
| chr6:149356136 | A | C | 3 | a0001c0001t0008g0165 a0001c0001t0008g0166 a0001c0001t0008g0167 |
3 | HG02280.hp1 HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-89-13773A>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149356136 | |||||||
| chr6:149356324 | C | T | 1 | a0001c0001t0004g0070 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-89-13585C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149356324 | |||||||
| chr6:149356361 | A | G | 59 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(56): Show |
62 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.-89-13548A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149356361 | |||||||
| chr6:149356563 | C | T | 1 | a0001c0001t0004g0058 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-89-13346C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149356563 | |||||||
| chr6:149356594 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-89-13315G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149356594 | |||||||
| chr6:149356678 | G | T | 1 | a0001c0008t0018g0292 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-89-13231G>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149356678 | |||||||
| chr6:149356958 | T | G | 1 | a0001c0001t0001g0017 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-89-12951T>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149356958 | |||||||
| chr6:149357191 | G | T | 59 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(56): Show |
62 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.-89-12718G>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149357191 | |||||||
| chr6:149357230 | A | G | 6 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0297 others(3): Show |
6 | HG02280.hp1 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-89-12679A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149357230 | |||||||
| chr6:149357277 | G | A | 6 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(3): Show |
6 | HG01884.hp2 HG02257.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.-89-12632G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149357277 | |||||||
| chr6:149357286 | T | C | 292 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(289): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.-89-12623T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149357286 | |||||||
| chr6:149357287 | G | C | 1 | a0001c0001t0008g0026 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-89-12622G>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149357287 | |||||||
| chr6:149357298 | C | G | 59 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(56): Show |
62 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.-89-12611C>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149357298 | |||||||
| chr6:149357306 | C | T | 6 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(3): Show |
6 | HG01884.hp2 HG02257.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.-89-12603C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149357306 | |||||||
| chr6:149357323 | G | A | 3 | a0001c0001t0013g0179 a0001c0001t0013g0180 a0001c0001t0022g0178 |
3 | HG02109.hp1 HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-89-12586G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149357323 | |||||||
| chr6:149357354 | T | G | 1 | a0001c0001t0021g0097 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-89-12555T>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149357354 | |||||||
| chr6:149357410 | C | T | 1 | a0001c0001t0005g0181 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-89-12499C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149357410 | |||||||
| chr6:149357411 | G | A | 17 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(14): Show |
17 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.-89-12498G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149357411 | |||||||
| chr6:149357419 | G | GA | 3 | a0001c0001t0013g0179 a0001c0001t0013g0180 a0001c0001t0022g0178 |
3 | HG02109.hp1 HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-89-12489dupA | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357419 | ||||||
| chr6:149357421 | G | A | 146 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(143): Show |
151 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.-89-12488G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149357421 | |||||||
| chr6:149357426 | A | AAC | 7 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(4): Show |
7 | HG00733.hp2 HG02145.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-89-12482_-89-1248 others(6): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357426 | ||||||
| chr6:149357426 | A | C | 1 | a0001c0001t0009g0083 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-89-12483A>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149357426 | |||||||
| chr6:149357428 | A | AC | 4 | a0001c0001t0004g0062 a0001c0001t0007g0077 a0001c0001t0007g0078 others(1): Show |
4 | HG02630.hp2 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.-89-12481_-89-1248 others(5): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149357428 | |||||||
| chr6:149357428 | A | C | 17 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(14): Show |
17 | HG00733.hp2 HG02055.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.-89-12481A>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149357428 | |||||||
| chr6:149357430 | A | AAAAAAAA others(5): Show |
1 | a0001c0002t0002g0226 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-89-12478_-89-1247 others(16): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | ||||||
| chr6:149357430 | A | AAAAAAAA others(4): Show |
1 | a0001c0002t0006g0215 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-89-12478_-89-1247 others(15): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | ||||||
| chr6:149357430 | A | AAAAAAAA others(3): Show |
4 | a0001c0002t0002g0105 a0001c0002t0002g0112 a0001c0002t0002g0209 others(1): Show |
4 | HG00597.hp2 HG00621.hp2 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.-89-12478_-89-1247 others(14): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | ||||||
| chr6:149357430 | A | AAAAAAAA others(5): Show |
15 | a0001c0002t0002g0002 a0001c0002t0002g0108 a0001c0002t0002g0111 others(12): Show |
15 | HG01258.hp2 HG02080.hp2 HG02148.hp1 others(12): Show |
intron_variant | MODIFIER | c.-89-12478_-89-1247 others(16): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | ||||||
| chr6:149357430 | A | AAAAAAAA others(7): Show |
3 | a0001c0002t0002g0110 a0001c0002t0002g0194 a0001c0002t0002g0219 |
3 | HG04204.hp1 NA19009.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.-89-12478_-89-1247 others(18): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | ||||||
| chr6:149357430 | A | AAAAAAAA others(13): Show |
1 | a0001c0001t0003g0324 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-89-12478_-89-1247 others(24): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | ||||||
| chr6:149357430 | A | AAAAAAAA others(4): Show |
31 | a0001c0002t0002g0002 a0001c0002t0002g0098 a0001c0002t0002g0106 others(28): Show |
31 | HG00423.hp1 HG00558.hp1 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.-89-12478_-89-1247 others(15): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | ||||||
| chr6:149357430 | A | AAAAAAAA others(6): Show |
11 | a0001c0002t0002g0002 a0001c0002t0002g0109 a0001c0002t0002g0193 others(8): Show |
11 | HG00609.hp1 HG01255.hp1 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.-89-12478_-89-1247 others(17): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | ||||||
| chr6:149357430 | A | AAAAAAAA others(8): Show |
3 | a0001c0002t0002g0101 a0001c0002t0002g0115 a0001c0002t0002g0190 |
3 | HG00673.hp2 NA18978.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.-89-12478_-89-1247 others(19): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | ||||||
| chr6:149357430 | A | AAAAAAAA others(12): Show |
2 | a0001c0001t0003g0007 a0001c0002t0002g0103 |
3 | HG03041.hp1 NA19001.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-89-12478_-89-1247 others(23): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | ||||||
| chr6:149357430 | A | AAAAAAAA others(3): Show |
1 | a0001c0001t0017g0027 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-89-12478_-89-1247 others(14): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | ||||||
| chr6:149357430 | A | AAAAAAAA others(5): Show |
4 | a0001c0001t0005g0352 a0001c0002t0002g0099 a0001c0002t0002g0212 others(1): Show |
4 | HG00621.hp1 HG02129.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-89-12478_-89-1247 others(16): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | ||||||
| chr6:149357430 | A | AAAAAAAA others(7): Show |
1 | a0001c0001t0005g0183 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-89-12478_-89-1247 others(18): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | ||||||
| chr6:149357430 | A | AAAAAAAA others(9): Show |
1 | a0001c0001t0003g0010 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-89-12478_-89-1247 others(20): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | ||||||
| chr6:149357430 | A | AAAAAAAA others(11): Show |
1 | a0001c0001t0003g0304 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-89-12478_-89-1247 others(22): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | ||||||
| chr6:149357430 | A | AAAAAAAA others(15): Show |
2 | a0001c0001t0003g0325 a0001c0001t0003g0326 |
2 | HG02622.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-89-12478_-89-1247 others(26): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | ||||||
| chr6:149357430 | A | AAAAAAAA others(17): Show |
2 | a0001c0001t0003g0328 a0001c0001t0003g0330 |
2 | HG01192.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.-89-12478_-89-1247 others(28): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | ||||||
| chr6:149357430 | A | AAAAAAAA others(19): Show |
1 | a0001c0001t0003g0320 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-89-12478_-89-1247 others(30): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | ||||||
| chr6:149357430 | A | AAAAAAAA others(21): Show |
1 | a0001c0001t0003g0329 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-89-12478_-89-1247 others(32): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | ||||||
| chr6:149357430 | A | AAAAAAAA others(29): Show |
1 | a0001c0001t0003g0327 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-89-12478_-89-1247 others(40): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | ||||||
| chr6:149357430 | A | AAAAAAAC others(4): Show |
5 | a0001c0002t0002g0100 a0001c0002t0002g0104 a0001c0002t0002g0237 others(2): Show |
5 | HG00741.hp2 HG02040.hp1 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.-89-12478_-89-1247 others(15): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | ||||||
| chr6:149357430 | A | AAAAAAAC others(6): Show |
5 | a0001c0001t0003g0008 a0001c0001t0005g0120 a0001c0001t0005g0184 others(2): Show |
5 | HG01243.hp2 HG02602.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.-89-12478_-89-1247 others(17): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | ||||||
| chr6:149357430 | A | AAAAAAAC others(8): Show |
7 | a0001c0001t0003g0338 a0001c0001t0003g0339 a0001c0001t0003g0341 others(4): Show |
7 | HG01256.hp2 HG01257.hp2 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.-89-12478_-89-1247 others(19): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | ||||||
| chr6:149357430 | A | AAAAAAAC others(10): Show |
12 | a0001c0001t0003g0008 a0001c0001t0003g0172 a0001c0001t0003g0175 others(9): Show |
12 | HG00099.hp2 HG01070.hp2 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.-89-12478_-89-1247 others(21): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | ||||||
| chr6:149357430 | A | AAAAAAAC others(12): Show |
4 | a0001c0001t0003g0173 a0001c0001t0003g0318 a0001c0001t0003g0331 others(1): Show |
4 | HG00140.hp2 HG00639.hp1 HG00741.hp1 others(1): Show |
intron_variant | MODIFIER | c.-89-12478_-89-1247 others(23): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | ||||||
| chr6:149357430 | A | AAAAAAAC others(14): Show |
7 | a0001c0001t0003g0316 a0001c0001t0003g0317 a0001c0001t0003g0321 others(4): Show |
7 | HG01168.hp2 HG01175.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.-89-12478_-89-1247 others(25): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | ||||||
| chr6:149357430 | A | AAAAAAAC others(16): Show |
2 | a0001c0001t0003g0174 a0001c0001t0003g0333 |
2 | HG02004.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-89-12478_-89-1247 others(27): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | ||||||
| chr6:149357430 | A | AAAAAAAC others(18): Show |
1 | a0001c0001t0003g0344 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-89-12478_-89-1247 others(29): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | ||||||
| chr6:149357430 | A | AAAAAACA others(5): Show |
1 | a0001c0002t0002g0203 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-89-12478_-89-1247 others(16): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | ||||||
| chr6:149357430 | A | AAAAAACA others(11): Show |
2 | a0001c0001t0003g0307 a0001c0001t0003g0319 |
2 | HG00609.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.-89-12478_-89-1247 others(22): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | ||||||
| chr6:149357430 | A | AAAAAACA others(13): Show |
1 | a0001c0001t0021g0097 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-89-12478_-89-1247 others(24): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | ||||||
| chr6:149357430 | A | AAAAAACA others(15): Show |
1 | a0001c0001t0003g0343 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-89-12478_-89-1247 others(26): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | ||||||
| chr6:149357430 | A | AAAAACAC others(6): Show |
1 | a0001c0002t0002g0204 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-89-12478_-89-1247 others(17): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | ||||||
| chr6:149357430 | A | AAAAACAC others(8): Show |
1 | a0001c0001t0003g0006 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-89-12478_-89-1247 others(19): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | ||||||
| chr6:149357430 | A | AAAAACAC others(10): Show |
6 | a0001c0001t0003g0006 a0001c0001t0003g0169 a0001c0001t0003g0171 others(3): Show |
6 | HG01255.hp2 HG02129.hp1 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.-89-12478_-89-1247 others(21): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | ||||||
| chr6:149357430 | A | AAAAACAC others(12): Show |
3 | a0001c0001t0003g0309 a0001c0001t0003g0312 a0001c0001t0003g0314 |
3 | NA18950.hp1 NA18977.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.-89-12478_-89-1247 others(23): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | ||||||
| chr6:149357430 | A | AAAAACAC others(14): Show |
1 | a0001c0001t0003g0322 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-89-12478_-89-1247 others(25): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | ||||||
| chr6:149357430 | A | AAAACACA others(11): Show |
1 | a0001c0001t0003g0313 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-89-12478_-89-1247 others(22): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | ||||||
| chr6:149357430 | A | AAACACAC others(6): Show |
1 | a0001c0001t0003g0315 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-89-12478_-89-1247 others(17): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | ||||||
| chr6:149357430 | A | AAACACAC others(8): Show |
1 | a0001c0001t0003g0170 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-89-12478_-89-1247 others(19): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | ||||||
| chr6:149357430 | A | AAACACAC others(10): Show |
1 | a0001c0001t0003g0311 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-89-12478_-89-1247 others(21): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | ||||||
| chr6:149357430 | A | AAC | 27 | a0001c0001t0001g0001 a0001c0001t0001g0067 a0001c0001t0001g0089 others(24): Show |
29 | HG00642.hp1 HG00642.hp2 HG01123.hp1 others(26): Show |
intron_variant | MODIFIER | c.-89-12443_-89-1244 others(6): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | ||||||
| chr6:149357430 | A | AACAC | 9 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 others(6): Show |
9 | HG01081.hp1 HG01099.hp2 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.-89-12445_-89-1244 others(8): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357430 | ||||||
| chr6:149357430 | A | ACAC | 4 | a0001c0001t0001g0094 a0001c0001t0001g0122 a0001c0001t0001g0298 others(1): Show |
4 | HG02258.hp2 NA18522.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-89-12479_-89-1247 others(7): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149357430 | |||||||
| chr6:149357430 | A | ACACACAC others(2): Show |
4 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0076 others(1): Show |
4 | HG02257.hp1 HG02886.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-89-12479_-89-1247 others(13): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149357430 | |||||||
| chr6:149357430 | A | ACACACAC others(6): Show |
1 | a0001c0001t0001g0075 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-89-12479_-89-1247 others(17): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149357430 | |||||||
| chr6:149357430 | A | C | 44 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(41): Show |
44 | HG00733.hp2 HG01496.hp1 HG01884.hp2 others(41): Show |
intron_variant | MODIFIER | c.-89-12479A>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149357430 | |||||||
| chr6:149357432 | C | A | 5 | a0001c0001t0013g0179 a0001c0001t0013g0180 a0001c0001t0022g0178 others(2): Show |
5 | HG01433.hp2 HG02080.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.-89-12477C>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149357432 | |||||||
| chr6:149357434 | C | A | 4 | a0001c0001t0013g0179 a0001c0001t0013g0180 a0001c0001t0022g0178 others(1): Show |
4 | HG01433.hp2 HG02109.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-89-12475C>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149357434 | |||||||
| chr6:149357436 | C | A | 4 | a0001c0001t0013g0179 a0001c0001t0013g0180 a0001c0001t0022g0178 others(1): Show |
4 | HG01433.hp2 HG02109.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-89-12473C>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149357436 | |||||||
| chr6:149357438 | C | A | 4 | a0001c0001t0013g0179 a0001c0001t0013g0180 a0001c0001t0022g0178 others(1): Show |
4 | HG01433.hp2 HG02109.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-89-12471C>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149357438 | |||||||
| chr6:149357440 | C | A | 3 | a0001c0001t0013g0179 a0001c0001t0013g0180 a0001c0001t0022g0178 |
3 | HG02109.hp1 HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-89-12469C>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149357440 | |||||||
| chr6:149357464 | C | T | 16 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(13): Show |
16 | HG01884.hp2 HG02055.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.-89-12445C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149357464 | |||||||
| chr6:149357502 | ACT | A | 59 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(56): Show |
62 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.-89-12404_-89-1240 others(6): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357502 | ||||||
| chr6:149357639 | T | C | 1 | a0001c0002t0014g0113 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-89-12270T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149357639 | |||||||
| chr6:149357708 | C | CT | 10 | a0001c0001t0001g0131 a0001c0001t0001g0136 a0001c0001t0005g0119 others(7): Show |
10 | HG00642.hp2 HG01243.hp2 HG02602.hp2 others(7): Show |
intron_variant | MODIFIER | c.-89-12192dupT | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149357708 | ||||||
| chr6:149357799 | A | G | 2 | a0001c0001t0005g0351 a0001c0001t0005g0352 |
2 | HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-89-12110A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149357799 | |||||||
| chr6:149357921 | G | A | 18 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(15): Show |
18 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.-89-11988G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149357921 | |||||||
| chr6:149358073 | G | A | 8 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(5): Show |
8 | HG02895.hp1 HG02895.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-89-11836G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149358073 | |||||||
| chr6:149358235 | A | G | 147 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(144): Show |
152 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.-89-11674A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149358235 | |||||||
| chr6:149358254 | A | G | 3 | a0001c0001t0007g0077 a0001c0001t0007g0079 a0001c0001t0007g0080 |
3 | HG03225.hp1 HG03579.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-89-11655A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149358254 | |||||||
| chr6:149358329 | TG | T | 18 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(15): Show |
18 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.-89-11579delG | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149358329 | |||||||
| chr6:149358364 | G | A | 1 | a0001c0001t0003g0008 | 2 | HG02300.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-89-11545G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149358364 | |||||||
| chr6:149358640 | C | CTG | 6 | a0001c0001t0004g0046 a0001c0001t0004g0062 a0001c0001t0013g0179 others(3): Show |
6 | HG02109.hp1 HG02615.hp2 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.-89-11237_-89-1123 others(6): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149358640 | ||||||
| chr6:149358640 | C | CTGTG | 7 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(4): Show |
8 | HG00733.hp2 HG01099.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.-89-11239_-89-1123 others(8): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149358640 | ||||||
| chr6:149358640 | C | CTGTGTG | 17 | a0001c0001t0003g0169 a0001c0001t0003g0170 a0001c0001t0003g0307 others(14): Show |
17 | HG00609.hp2 HG01167.hp2 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.-89-11241_-89-1123 others(10): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149358640 | ||||||
| chr6:149358640 | C | CTGTGTGT others(1): Show |
15 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0003g0172 others(12): Show |
15 | HG01109.hp1 HG02055.hp1 HG02129.hp1 others(12): Show |
intron_variant | MODIFIER | c.-89-11243_-89-1123 others(12): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149358640 | ||||||
| chr6:149358640 | C | CTGTGTGT others(3): Show |
4 | a0001c0001t0003g0314 a0001c0001t0003g0333 a0001c0001t0007g0079 others(1): Show |
4 | HG02965.hp2 HG06807.hp1 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.-89-11245_-89-1123 others(14): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149358640 | ||||||
| chr6:149358640 | C | CTGTGTGT others(5): Show |
3 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0003g0321 |
3 | HG01175.hp2 HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-89-11247_-89-1123 others(16): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149358640 | ||||||
| chr6:149358640 | C | CTGTGTGT others(7): Show |
13 | a0001c0001t0001g0071 a0001c0001t0001g0149 a0001c0001t0001g0284 others(10): Show |
14 | HG01243.hp2 HG01516.hp1 HG01517.hp2 others(11): Show |
intron_variant | MODIFIER | c.-89-11249_-89-1123 others(18): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149358640 | ||||||
| chr6:149358640 | C | CTGTGTGT others(9): Show |
14 | a0001c0001t0001g0142 a0001c0001t0001g0144 a0001c0001t0001g0145 others(11): Show |
15 | HG00140.hp1 HG01496.hp1 HG02080.hp1 others(12): Show |
intron_variant | MODIFIER | c.-89-11251_-89-1123 others(20): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149358640 | ||||||
| chr6:149358640 | C | CTGTGTGT others(11): Show |
23 | a0001c0001t0001g0011 a0001c0001t0001g0162 a0001c0001t0001g0260 others(20): Show |
23 | HG00140.hp2 HG00733.hp1 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.-89-11253_-89-1123 others(22): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149358640 | ||||||
| chr6:149358640 | C | CTGTGTGT others(13): Show |
35 | a0001c0001t0001g0093 a0001c0001t0001g0123 a0001c0001t0001g0124 others(32): Show |
35 | HG00099.hp2 HG00735.hp2 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.-89-11255_-89-1123 others(24): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149358640 | ||||||
| chr6:149358640 | C | CTGTGTGT others(15): Show |
36 | a0001c0001t0001g0001 a0001c0001t0001g0126 a0001c0001t0001g0128 others(33): Show |
38 | HG00423.hp2 HG00558.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.-89-11257_-89-1123 others(26): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149358640 | ||||||
| chr6:149358640 | C | CTGTGTGT others(17): Show |
28 | a0001c0001t0001g0009 a0001c0001t0001g0088 a0001c0001t0001g0090 others(25): Show |
28 | HG00597.hp1 HG00642.hp2 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.-89-11259_-89-1123 others(28): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149358640 | ||||||
| chr6:149358640 | C | CTGTGTGT others(19): Show |
32 | a0001c0001t0001g0005 a0001c0001t0001g0089 a0001c0001t0001g0091 others(29): Show |
33 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.-89-11261_-89-1123 others(30): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149358640 | ||||||
| chr6:149358640 | C | CTGTGTGT others(21): Show |
24 | a0001c0001t0001g0125 a0001c0001t0003g0325 a0001c0001t0015g0156 others(21): Show |
24 | HG00639.hp2 HG00741.hp2 HG01257.hp1 others(21): Show |
intron_variant | MODIFIER | c.-89-11263_-89-1123 others(32): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149358640 | ||||||
| chr6:149358640 | C | CTGTGTGT others(23): Show |
12 | a0001c0002t0002g0002 a0001c0002t0002g0105 a0001c0002t0002g0199 others(9): Show |
14 | HG00597.hp2 HG01258.hp2 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.-89-11265_-89-1123 others(34): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149358640 | ||||||
| chr6:149358640 | C | CTGTGTGT others(25): Show |
7 | a0001c0001t0001g0146 a0001c0002t0002g0102 a0001c0002t0002g0198 others(4): Show |
7 | HG00558.hp1 HG00621.hp2 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.-89-11267_-89-1123 others(36): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149358640 | ||||||
| chr6:149358640 | C | CTGTGTGT others(27): Show |
2 | a0001c0001t0001g0138 a0001c0005t0002g0233 |
2 | HG02132.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.-89-11236_-89-1123 others(38): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149358640 | ||||||
| chr6:149358640 | C | CTGTGTGT others(29): Show |
1 | a0001c0002t0002g0208 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-89-11236_-89-1123 others(40): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149358640 | ||||||
| chr6:149358640 | C | CTGTGTGT others(31): Show |
1 | a0001c0002t0002g0210 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-89-11236_-89-1123 others(42): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149358640 | ||||||
| chr6:149358640 | CTG | C | 3 | a0001c0001t0001g0020 a0001c0001t0004g0040 a0001c0002t0002g0192 |
3 | HG00423.hp1 HG02630.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-89-11237_-89-1123 others(6): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149358640 | ||||||
| chr6:149358673 | T | TGTGTGTG others(12): Show |
1 | a0001c0001t0001g0161 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-89-11236_-89-1123 others(23): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149358673 | |||||||
| chr6:149358673 | T | TGTGTGTG others(14): Show |
1 | a0001c0001t0003g0327 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-89-11236_-89-1123 others(25): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149358673 | |||||||
| chr6:149358673 | T | TGTGTGTG others(16): Show |
3 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0002t0002g0111 |
3 | HG02572.hp1 HG04228.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-89-11236_-89-1123 others(27): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149358673 | |||||||
| chr6:149358673 | T | TGTGTGTG others(18): Show |
2 | a0001c0001t0001g0096 a0001c0001t0001g0157 |
2 | HG03579.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.-89-11236_-89-1123 others(29): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149358673 | |||||||
| chr6:149358673 | T | TGTGTGTG others(20): Show |
3 | a0001c0001t0001g0122 a0001c0002t0002g0106 a0001c0002t0002g0234 |
3 | NA18947.hp1 NA18979.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.-89-11236_-89-1123 others(31): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149358673 | |||||||
| chr6:149358673 | T | TGTGTGTG others(22): Show |
1 | a0001c0002t0002g0104 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-89-11236_-89-1123 others(33): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149358673 | |||||||
| chr6:149358673 | T | TGTGTGTG others(24): Show |
1 | a0001c0002t0002g0239 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-89-11236_-89-1123 others(35): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149358673 | |||||||
| chr6:149358674 | T | G | 2 | a0001c0001t0001g0298 a0001c0001t0017g0027 |
2 | NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-89-11235T>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149358674 | |||||||
| chr6:149358675 | T | G | 1 | a0001c0001t0001g0094 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-89-11234T>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149358675 | |||||||
| chr6:149358896 | A | G | 298 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(295): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.-89-11013A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149358896 | |||||||
| chr6:149358927 | T | G | 3 | a0001c0001t0007g0078 a0001c0001t0007g0086 a0001c0001t0024g0081 |
3 | HG02630.hp2 HG03486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-89-10982T>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149358927 | |||||||
| chr6:149359145 | G | C | 4 | a0001c0001t0009g0082 a0001c0001t0009g0083 a0001c0001t0009g0084 others(1): Show |
4 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.-89-10764G>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149359145 | |||||||
| chr6:149359276 | T | C | 2 | a0001c0001t0004g0031 a0001c0001t0004g0032 |
2 | HG02698.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.-89-10633T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149359276 | |||||||
| chr6:149359288 | C | T | 2 | a0001c0002t0002g0220 a0001c0002t0002g0243 |
2 | HG02080.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.-89-10621C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149359288 | |||||||
| chr6:149359307 | A | G | 1 | a0001c0001t0003g0346 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-89-10602A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149359307 | |||||||
| chr6:149359370 | G | A | 6 | a0001c0001t0003g0309 a0001c0001t0003g0310 a0001c0001t0003g0312 others(3): Show |
6 | HG02129.hp1 NA18950.hp1 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.-89-10539G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149359370 | |||||||
| chr6:149359680 | C | T | 11 | a0001c0001t0007g0077 a0001c0001t0007g0078 a0001c0001t0007g0079 others(8): Show |
11 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.-89-10229C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149359680 | |||||||
| chr6:149359682 | C | G | 1 | a0001c0002t0002g0225 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-89-10227C>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149359682 | |||||||
| chr6:149360056 | T | C | 59 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(56): Show |
62 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.-89-9853T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149360056 | |||||||
| chr6:149360100 | G | T | 18 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(15): Show |
18 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.-89-9809G>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149360100 | |||||||
| chr6:149360253 | C | T | 2 | a0001c0001t0001g0187 a0001c0001t0001g0188 |
2 | NA18966.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.-89-9656C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149360253 | |||||||
| chr6:149360381 | C | T | 71 | a0001c0002t0002g0002 a0001c0002t0002g0103 a0001c0002t0002g0105 others(68): Show |
73 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.-89-9528C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149360381 | |||||||
| chr6:149360420 | C | G | 2 | a0001c0001t0004g0185 a0001c0001t0004g0186 |
2 | HG02717.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-89-9489C>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149360420 | |||||||
| chr6:149360432 | A | G | 1 | a0001c0001t0001g0129 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-89-9477A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149360432 | |||||||
| chr6:149360529 | A | G | 1 | a0001c0001t0003g0344 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-89-9380A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149360529 | |||||||
| chr6:149360816 | T | C | 18 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(15): Show |
18 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.-89-9093T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149360816 | |||||||
| chr6:149360944 | A | C | 1 | a0001c0001t0005g0252 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-89-8965A>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149360944 | |||||||
| chr6:149361264 | TTC | T | 3 | a0001c0001t0007g0077 a0001c0001t0007g0079 a0001c0001t0007g0080 |
3 | HG03225.hp1 HG03579.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-89-8642_-89-8641d others(4): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149361264 | ||||||
| chr6:149361703 | C | T | 2 | a0001c0001t0008g0165 a0001c0001t0008g0167 |
2 | HG02280.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-89-8206C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149361703 | |||||||
| chr6:149361828 | T | G | 11 | a0001c0001t0007g0077 a0001c0001t0007g0078 a0001c0001t0007g0079 others(8): Show |
11 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.-89-8081T>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149361828 | |||||||
| chr6:149361884 | G | A | 8 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(5): Show |
8 | HG02895.hp1 HG02895.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-89-8025G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149361884 | |||||||
| chr6:149362087 | C | T | 1 | a0001c0002t0002g0229 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-89-7822C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149362087 | |||||||
| chr6:149362479 | A | G | 1 | a0001c0001t0001g0253 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-89-7430A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149362479 | |||||||
| chr6:149362602 | TA | T | 18 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(15): Show |
18 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.-89-7304delA | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149362602 | ||||||
| chr6:149362646 | T | A | 1 | a0001c0001t0003g0171 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-89-7263T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149362646 | |||||||
| chr6:149362663 | TA | T | 290 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(287): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.-89-7244delA | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149362663 | ||||||
| chr6:149362733 | A | G | 3 | a0001c0002t0006g0214 a0001c0002t0006g0215 a0001c0002t0006g0238 |
3 | NA18962.hp1 NA19062.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.-89-7176A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149362733 | |||||||
| chr6:149363429 | A | G | 1 | a0001c0003t0001g0258 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-89-6480A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149363429 | |||||||
| chr6:149363504 | A | T | 1 | a0001c0002t0002g0098 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-89-6405A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149363504 | |||||||
| chr6:149363655 | G | A | 4 | a0001c0001t0001g0001 a0001c0001t0001g0089 a0001c0001t0001g0093 others(1): Show |
6 | HG02109.hp2 HG02451.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-89-6254G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149363655 | |||||||
| chr6:149363719 | C | T | 3 | a0001c0001t0001g0353 a0001c0001t0001g0355 a0001c0001t0001g0356 |
3 | HG01256.hp1 HG01258.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.-89-6190C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149363719 | |||||||
| chr6:149363734 | G | T | 1 | a0001c0001t0001g0126 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-89-6175G>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149363734 | |||||||
| chr6:149363743 | A | G | 1 | a0001c0001t0001g0018 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-89-6166A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149363743 | |||||||
| chr6:149363769 | C | T | 1 | a0001c0001t0001g0265 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-89-6140C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149363769 | |||||||
| chr6:149363791 | C | T | 1 | a0001c0001t0001g0012 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-89-6118C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149363791 | |||||||
| chr6:149363820 | A | G | 1 | a0001c0001t0005g0252 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-89-6089A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149363820 | |||||||
| chr6:149363941 | G | A | 1 | a0001c0002t0002g0106 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-89-5968G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149363941 | |||||||
| chr6:149364195 | G | A | 2 | a0001c0001t0003g0010 a0001c0001t0003g0336 |
2 | HG00738.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.-89-5714G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149364195 | |||||||
| chr6:149364209 | C | A | 1 | a0001c0002t0002g0226 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-89-5700C>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149364209 | |||||||
| chr6:149364212 | G | C | 1 | a0001c0001t0001g0096 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-89-5697G>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149364212 | |||||||
| chr6:149364451 | T | C | 15 | a0001c0001t0007g0077 a0001c0001t0007g0078 a0001c0001t0007g0079 others(12): Show |
15 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.-89-5458T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149364451 | |||||||
| chr6:149364481 | C | T | 178 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(175): Show |
183 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.-89-5428C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149364481 | |||||||
| chr6:149364488 | A | G | 1 | a0001c0001t0001g0296 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-89-5421A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149364488 | |||||||
| chr6:149364520 | T | C | 1 | a0001c0001t0001g0278 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-89-5389T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149364520 | |||||||
| chr6:149364577 | G | C | 59 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(56): Show |
62 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.-89-5332G>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149364577 | |||||||
| chr6:149364633 | A | G | 2 | a0001c0002t0002g0191 a0001c0002t0002g0224 |
2 | NA18612.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.-89-5276A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149364633 | |||||||
| chr6:149364851 | A | G | 4 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0263 others(1): Show |
4 | NA18969.hp1 NA18987.hp2 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.-89-5058A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149364851 | |||||||
| chr6:149364984 | A | G | 1 | a0001c0001t0017g0027 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-89-4925A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149364984 | |||||||
| chr6:149365049 | T | C | 1 | a0001c0001t0001g0293 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-89-4860T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149365049 | |||||||
| chr6:149365102 | G | T | 1 | a0001c0001t0001g0265 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-89-4807G>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149365102 | |||||||
| chr6:149365124 | T | C | 4 | a0001c0001t0008g0026 a0001c0001t0008g0165 a0001c0001t0008g0166 others(1): Show |
4 | HG02280.hp1 HG02717.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-89-4785T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149365124 | |||||||
| chr6:149365124 | T | G | 3 | a0001c0001t0013g0179 a0001c0001t0013g0180 a0001c0001t0022g0178 |
3 | HG02109.hp1 HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-89-4785T>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149365124 | |||||||
| chr6:149365291 | A | G | 2 | a0001c0001t0003g0304 a0001c0001t0019g0305 |
2 | HG02970.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-89-4618A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149365291 | |||||||
| chr6:149365327 | A | G | 2 | a0001c0001t0001g0268 a0001c0001t0001g0302 |
2 | HG00673.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.-89-4582A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149365327 | |||||||
| chr6:149365353 | A | G | 2 | a0001c0001t0001g0122 a0001c0001t0001g0289 |
2 | HG00423.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.-89-4556A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149365353 | |||||||
| chr6:149365382 | T | G | 112 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(109): Show |
115 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.-89-4527T>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149365382 | |||||||
| chr6:149365455 | A | G | 3 | a0001c0001t0013g0179 a0001c0001t0013g0180 a0001c0001t0022g0178 |
3 | HG02109.hp1 HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-89-4454A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149365455 | |||||||
| chr6:149365561 | T | C | 1 | a0001c0001t0001g0283 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-89-4348T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149365561 | |||||||
| chr6:149365641 | C | A | 1 | a0001c0001t0004g0056 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-89-4268C>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149365641 | |||||||
| chr6:149365826 | C | T | 1 | a0001c0001t0001g0012 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-89-4083C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149365826 | |||||||
| chr6:149365897 | T | C | 1 | a0001c0002t0002g0217 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-89-4012T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149365897 | |||||||
| chr6:149365991 | T | A | 4 | a0001c0001t0008g0026 a0001c0001t0008g0165 a0001c0001t0008g0166 others(1): Show |
4 | HG02280.hp1 HG02717.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-89-3918T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149365991 | |||||||
| chr6:149366342 | A | G | 1 | a0001c0001t0003g0307 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-89-3567A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149366342 | |||||||
| chr6:149366395 | T | G | 2 | a0001c0001t0001g0021 a0001c0001t0001g0022 |
2 | HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-89-3514T>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149366395 | |||||||
| chr6:149366587 | C | A | 1 | a0001c0002t0002g0248 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-89-3322C>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149366587 | |||||||
| chr6:149366607 | A | G | 6 | a0001c0001t0007g0077 a0001c0001t0007g0078 a0001c0001t0007g0079 others(3): Show |
6 | HG02630.hp2 HG03225.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-89-3302A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149366607 | |||||||
| chr6:149366720 | G | A | 1 | a0001c0001t0005g0182 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-89-3189G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149366720 | |||||||
| chr6:149366953 | A | AC | 40 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0010 others(37): Show |
42 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.-89-2956_-89-2955i others(3): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149366953 | |||||||
| chr6:149366954 | A | C | 2 | a0001c0001t0003g0319 a0001c0001t0003g0322 |
2 | HG03491.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.-89-2955A>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149366954 | |||||||
| chr6:149366955 | A | AT | 135 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(132): Show |
138 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(135): Show |
intron_variant | MODIFIER | c.-89-2943dupT | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149366955 | ||||||
| chr6:149366955 | A | T | 40 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0010 others(37): Show |
42 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.-89-2954A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149366955 | |||||||
| chr6:149367060 | A | G | 290 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(287): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.-89-2849A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149367060 | |||||||
| chr6:149367400 | T | A | 2 | a0001c0001t0004g0185 a0001c0001t0004g0186 |
2 | HG02717.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-89-2509T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149367400 | |||||||
| chr6:149367490 | A | C | 59 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(56): Show |
62 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.-89-2419A>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149367490 | |||||||
| chr6:149367578 | C | T | 2 | a0001c0001t0005g0182 a0001c0001t0005g0183 |
2 | HG02683.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.-89-2331C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149367578 | |||||||
| chr6:149368106 | C | A | 1 | a0001c0001t0004g0034 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-89-1803C>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149368106 | |||||||
| chr6:149368170 | T | C | 3 | a0001c0001t0013g0179 a0001c0001t0013g0180 a0001c0001t0022g0178 |
3 | HG02109.hp1 HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-89-1739T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149368170 | |||||||
| chr6:149368196 | T | C | 59 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(56): Show |
62 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.-89-1713T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149368196 | |||||||
| chr6:149368305 | T | C | 4 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 others(1): Show |
4 | HG01081.hp1 HG01884.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-89-1604T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149368305 | |||||||
| chr6:149368321 | A | G | 147 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(144): Show |
152 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.-89-1588A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149368321 | |||||||
| chr6:149368329 | A | G | 2 | a0001c0002t0002g0248 a0001c0002t0002g0249 |
2 | HG01943.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.-89-1580A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149368329 | |||||||
| chr6:149368430 | TACGTATA others(3): Show |
T | 1 | a0001c0001t0008g0026 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-89-1477_-89-1468d others(12): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149368430 | ||||||
| chr6:149368592 | T | C | 1 | a0001c0001t0017g0027 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-89-1317T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149368592 | |||||||
| chr6:149368612 | A | C | 1 | a0001c0001t0001g0015 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-89-1297A>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149368612 | |||||||
| chr6:149368618 | A | G | 1 | a0001c0001t0001g0124 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-89-1291A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149368618 | |||||||
| chr6:149368631 | T | C | 1 | a0001c0001t0017g0027 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-89-1278T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149368631 | |||||||
| chr6:149368645 | T | TTG | 51 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(48): Show |
53 | HG00140.hp2 HG00673.hp1 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.-89-1230_-89-1229d others(4): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149368645 | ||||||
| chr6:149368645 | T | TTGTG | 33 | a0001c0001t0001g0071 a0001c0001t0001g0075 a0001c0001t0001g0076 others(30): Show |
33 | HG00423.hp2 HG00558.hp2 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.-89-1232_-89-1229d others(6): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149368645 | ||||||
| chr6:149368645 | T | TTGTGTG | 17 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0003g0007 others(14): Show |
18 | HG00099.hp2 HG00738.hp2 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.-89-1234_-89-1229d others(8): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149368645 | ||||||
| chr6:149368645 | T | TTGTGTGT others(1): Show |
24 | a0001c0001t0003g0006 a0001c0001t0003g0008 a0001c0001t0003g0169 others(21): Show |
26 | HG00609.hp2 HG00741.hp1 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.-89-1236_-89-1229d others(10): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149368645 | ||||||
| chr6:149368645 | T | TTGTGTGT others(3): Show |
2 | a0001c0001t0003g0174 a0001c0001t0003g0303 |
2 | HG02004.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.-89-1238_-89-1229d others(12): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149368645 | ||||||
| chr6:149368645 | T | TTGTGTGT others(5): Show |
6 | a0001c0001t0003g0309 a0001c0001t0003g0312 a0001c0001t0003g0313 others(3): Show |
6 | HG02109.hp1 HG02615.hp2 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.-89-1240_-89-1229d others(14): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149368645 | ||||||
| chr6:149368645 | T | TTGTGTGT others(7): Show |
1 | a0001c0001t0022g0178 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-89-1242_-89-1229d others(16): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149368645 | ||||||
| chr6:149368645 | TTG | T | 3 | a0001c0001t0001g0268 a0001c0001t0017g0027 a0001c0002t0002g0200 |
3 | HG00639.hp2 NA18989.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-89-1230_-89-1229d others(4): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149368645 | ||||||
| chr6:149368645 | TTGTG | T | 27 | a0001c0001t0001g0004 a0001c0001t0004g0004 a0001c0001t0004g0047 others(24): Show |
27 | HG00609.hp1 HG00673.hp2 HG01257.hp1 others(24): Show |
intron_variant | MODIFIER | c.-89-1232_-89-1229d others(6): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149368645 | ||||||
| chr6:149368645 | TTGTGTG | T | 67 | a0001c0001t0005g0252 a0001c0002t0002g0002 a0001c0002t0002g0098 others(64): Show |
69 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.-89-1234_-89-1229d others(8): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 149368645 | ||||||
| chr6:149368906 | T | A | 1 | a0001c0001t0003g0312 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-89-1003T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149368906 | |||||||
| chr6:149369020 | T | C | 4 | a0001c0001t0008g0026 a0001c0001t0008g0165 a0001c0001t0008g0166 others(1): Show |
4 | HG02280.hp1 HG02717.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-89-889T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149369020 | |||||||
| chr6:149369294 | C | T | 1 | a0001c0001t0005g0119 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-89-615C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149369294 | |||||||
| chr6:149369589 | A | C | 85 | a0001c0002t0002g0002 a0001c0002t0002g0098 a0001c0002t0002g0099 others(82): Show |
87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.-89-320A>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149369589 | |||||||
| chr6:149369601 | A | G | 17 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(14): Show |
17 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.-89-308A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149369601 | |||||||
| chr6:149369671 | G | A | 4 | a0001c0001t0004g0028 a0001c0001t0004g0029 a0001c0001t0004g0039 others(1): Show |
4 | HG02258.hp1 HG02559.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.-89-238G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149369671 | |||||||
| chr6:149369729 | A | C | 3 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 |
3 | HG03209.hp1 HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-89-180A>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149369729 | |||||||
| chr6:149369876 | T | C | 1 | a0001c0001t0001g0270 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-89-33T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 1/6 | chr6 | 149369876 | |||||||
| chr6:149370155 | AT | A | 85 | a0001c0002t0002g0002 a0001c0002t0002g0098 a0001c0002t0002g0099 others(82): Show |
87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.102+58delT | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr6 | 149370155 | ||||||
| chr6:149370219 | T | G | 115 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(112): Show |
118 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.102+120T>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149370219 | |||||||
| chr6:149370254 | C | T | 1 | a0001c0001t0001g0071 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.102+155C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149370254 | |||||||
| chr6:149370316 | G | A | 1 | a0001c0001t0001g0131 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.102+217G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149370316 | |||||||
| chr6:149370466 | A | G | 85 | a0001c0002t0002g0002 a0001c0002t0002g0098 a0001c0002t0002g0099 others(82): Show |
87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.102+367A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149370466 | |||||||
| chr6:149370678 | T | C | 1 | a0001c0001t0001g0091 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.102+579T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149370678 | |||||||
| chr6:149370723 | G | A | 115 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(112): Show |
118 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.102+624G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149370723 | |||||||
| chr6:149370902 | C | A | 59 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(56): Show |
62 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.102+803C>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149370902 | |||||||
| chr6:149370986 | A | C | 1 | a0001c0001t0001g0267 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.102+887A>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149370986 | |||||||
| chr6:149371007 | A | G | 27 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0174 others(24): Show |
29 | HG00140.hp2 HG01168.hp2 HG01175.hp2 others(26): Show |
intron_variant | MODIFIER | c.102+908A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149371007 | |||||||
| chr6:149371054 | AG | A | 9 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0005g0181 others(6): Show |
9 | HG01243.hp2 HG02602.hp2 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.102+956delG | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149371054 | |||||||
| chr6:149371065 | C | CA | 104 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(101): Show |
107 | HG00099.hp1 HG00558.hp2 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.102+991dupA | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr6 | 149371065 | ||||||
| chr6:149371065 | C | CAA | 6 | a0001c0001t0001g0090 a0001c0001t0001g0142 a0001c0001t0001g0155 others(3): Show |
6 | HG00140.hp1 HG00423.hp2 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.102+990_102+991dup others(2): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr6 | 149371065 | ||||||
| chr6:149371065 | C | CAAA | 8 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0005g0252 others(5): Show |
8 | HG01243.hp2 HG02109.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.102+989_102+991dup others(3): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr6 | 149371065 | ||||||
| chr6:149371065 | CA | C | 86 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0021 others(83): Show |
89 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.102+991delA | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr6 | 149371065 | ||||||
| chr6:149371065 | CAA | C | 76 | a0001c0001t0001g0019 a0001c0001t0003g0334 a0001c0002t0002g0002 others(73): Show |
78 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.102+990_102+991del others(2): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr6 | 149371065 | ||||||
| chr6:149371093 | G | A | 144 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(141): Show |
149 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(146): Show |
intron_variant | MODIFIER | c.102+994G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149371093 | |||||||
| chr6:149371097 | G | A | 1 | a0001c0002t0002g0099 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.102+998G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149371097 | |||||||
| chr6:149371108 | A | G | 4 | a0001c0001t0003g0010 a0001c0001t0003g0336 a0001c0001t0003g0338 others(1): Show |
4 | HG00738.hp2 HG01257.hp2 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.102+1009A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149371108 | |||||||
| chr6:149371278 | C | T | 1 | a0001c0001t0004g0068 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.102+1179C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149371278 | |||||||
| chr6:149371721 | A | G | 1 | a0001c0001t0001g0125 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.102+1622A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149371721 | |||||||
| chr6:149371799 | G | A | 162 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(159): Show |
167 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.102+1700G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149371799 | |||||||
| chr6:149371901 | A | G | 1 | a0001c0001t0005g0120 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.102+1802A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149371901 | |||||||
| chr6:149371927 | C | T | 9 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0005g0181 others(6): Show |
9 | HG01243.hp2 HG02602.hp2 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.102+1828C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149371927 | |||||||
| chr6:149372001 | C | G | 59 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(56): Show |
62 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.102+1902C>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149372001 | |||||||
| chr6:149372022 | A | G | 4 | a0001c0001t0013g0179 a0001c0001t0013g0180 a0001c0001t0017g0027 others(1): Show |
4 | HG02109.hp1 HG02615.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.102+1923A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149372022 | |||||||
| chr6:149372131 | G | A | 2 | a0001c0001t0013g0179 a0001c0001t0013g0180 |
2 | HG02109.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.102+2032G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149372131 | |||||||
| chr6:149372131 | G | C | 144 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(141): Show |
149 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(146): Show |
intron_variant | MODIFIER | c.102+2032G>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149372131 | |||||||
| chr6:149372182 | T | A | 1 | a0001c0002t0002g0116 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.102+2083T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149372182 | |||||||
| chr6:149372183 | C | A | 85 | a0001c0002t0002g0002 a0001c0002t0002g0098 a0001c0002t0002g0099 others(82): Show |
87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.102+2084C>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149372183 | |||||||
| chr6:149372263 | A | C | 17 | a0001c0001t0001g0001 a0001c0001t0001g0089 a0001c0001t0001g0090 others(14): Show |
19 | HG01081.hp1 HG01109.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.102+2164A>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149372263 | |||||||
| chr6:149372476 | T | C | 290 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(287): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.102+2377T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149372476 | |||||||
| chr6:149372556 | A | T | 1 | a0001c0001t0003g0344 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.102+2457A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149372556 | |||||||
| chr6:149372648 | C | A | 59 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(56): Show |
62 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.102+2549C>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149372648 | |||||||
| chr6:149373269 | T | A | 1 | a0001c0001t0001g0256 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.102+3170T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149373269 | |||||||
| chr6:149373270 | T | A | 1 | a0001c0001t0001g0256 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.102+3171T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149373270 | |||||||
| chr6:149373271 | T | A | 1 | a0001c0001t0001g0256 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.102+3172T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149373271 | |||||||
| chr6:149373272 | T | A | 1 | a0001c0001t0001g0256 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.102+3173T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149373272 | |||||||
| chr6:149373512 | T | TG | 21 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(18): Show |
21 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.102+3414dupG | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr6 | 149373512 | ||||||
| chr6:149373894 | T | A | 1 | a0001c0001t0005g0181 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.102+3795T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149373894 | |||||||
| chr6:149374051 | C | T | 8 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0005g0181 others(5): Show |
8 | HG01243.hp2 HG02602.hp2 HG02683.hp1 others(5): Show |
intron_variant | MODIFIER | c.102+3952C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149374051 | |||||||
| chr6:149374052 | T | C | 17 | a0001c0001t0003g0006 a0001c0001t0003g0169 a0001c0001t0003g0170 others(14): Show |
18 | HG00609.hp2 HG01109.hp1 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.102+3953T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149374052 | |||||||
| chr6:149374079 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.103-3939G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149374079 | |||||||
| chr6:149374208 | T | C | 59 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(56): Show |
62 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.103-3810T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149374208 | |||||||
| chr6:149374224 | T | C | 1 | a0001c0001t0017g0027 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.103-3794T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149374224 | |||||||
| chr6:149374914 | C | T | 2 | a0001c0001t0001g0021 a0001c0001t0001g0022 |
2 | HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.103-3104C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149374914 | |||||||
| chr6:149375030 | T | C | 59 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(56): Show |
62 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.103-2988T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149375030 | |||||||
| chr6:149375118 | A | G | 6 | a0001c0001t0003g0309 a0001c0001t0003g0310 a0001c0001t0003g0312 others(3): Show |
6 | HG02129.hp1 NA18950.hp1 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.103-2900A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149375118 | |||||||
| chr6:149375139 | T | C | 4 | a0001c0001t0013g0179 a0001c0001t0013g0180 a0001c0001t0017g0027 others(1): Show |
4 | HG02109.hp1 HG02615.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.103-2879T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149375139 | |||||||
| chr6:149375145 | C | T | 11 | a0001c0001t0007g0077 a0001c0001t0007g0078 a0001c0001t0007g0079 others(8): Show |
11 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.103-2873C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149375145 | |||||||
| chr6:149375404 | G | C | 1 | a0001c0001t0004g0066 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.103-2614G>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149375404 | |||||||
| chr6:149375414 | A | G | 1 | a0001c0002t0002g0236 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.103-2604A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149375414 | |||||||
| chr6:149375507 | G | A | 3 | a0001c0002t0006g0214 a0001c0002t0006g0215 a0001c0002t0006g0238 |
3 | NA18962.hp1 NA19062.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.103-2511G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149375507 | |||||||
| chr6:149375841 | G | A | 6 | a0001c0001t0007g0077 a0001c0001t0007g0078 a0001c0001t0007g0079 others(3): Show |
6 | HG02630.hp2 HG03225.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.103-2177G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149375841 | |||||||
| chr6:149375970 | C | G | 59 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(56): Show |
62 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.103-2048C>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149375970 | |||||||
| chr6:149376196 | C | T | 2 | a0001c0002t0002g0248 a0001c0002t0002g0249 |
2 | HG01943.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.103-1822C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149376196 | |||||||
| chr6:149376428 | A | G | 59 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(56): Show |
62 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.103-1590A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149376428 | |||||||
| chr6:149376558 | T | C | 3 | a0001c0001t0013g0179 a0001c0001t0013g0180 a0001c0001t0022g0178 |
3 | HG02109.hp1 HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.103-1460T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149376558 | |||||||
| chr6:149376624 | C | T | 85 | a0001c0002t0002g0002 a0001c0002t0002g0098 a0001c0002t0002g0099 others(82): Show |
87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.103-1394C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149376624 | |||||||
| chr6:149376886 | T | TC | 60 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(57): Show |
63 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.103-1122dupC | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr6 | 149376886 | ||||||
| chr6:149376886 | TC | T | 27 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(24): Show |
27 | HG02145.hp1 HG02155.hp1 HG02258.hp1 others(24): Show |
intron_variant | MODIFIER | c.103-1122delC | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr6 | 149376886 | ||||||
| chr6:149376888 | C | A | 1 | a0001c0002t0002g0099 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.103-1130C>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149376888 | |||||||
| chr6:149376920 | G | A | 6 | a0001c0001t0007g0077 a0001c0001t0007g0078 a0001c0001t0007g0079 others(3): Show |
6 | HG02630.hp2 HG03225.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.103-1098G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149376920 | |||||||
| chr6:149376996 | G | A | 1 | a0001c0001t0005g0252 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.103-1022G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149376996 | |||||||
| chr6:149377067 | CTT | C | 58 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(55): Show |
61 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.103-950_103-949del others(2): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149377067 | |||||||
| chr6:149377070 | A | AT | 10 | a0001c0001t0001g0014 a0001c0001t0001g0072 a0001c0001t0001g0162 others(7): Show |
10 | HG00733.hp1 HG02145.hp1 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.103-931dupT | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr6 | 149377070 | ||||||
| chr6:149377070 | A | ATT | 15 | a0001c0001t0001g0071 a0001c0001t0001g0073 a0001c0001t0001g0075 others(12): Show |
15 | HG01884.hp2 HG02257.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.103-932_103-931dup others(2): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr6 | 149377070 | ||||||
| chr6:149377070 | AT | A | 85 | a0001c0001t0001g0022 a0001c0001t0004g0033 a0001c0001t0013g0180 others(82): Show |
87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.103-931delT | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr6 | 149377070 | ||||||
| chr6:149377071 | T | A | 1 | a0001c0001t0003g0317 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.103-947T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149377071 | |||||||
| chr6:149377143 | C | A | 9 | a0001c0001t0004g0028 a0001c0001t0004g0029 a0001c0001t0004g0030 others(6): Show |
9 | HG02258.hp1 HG02559.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.103-875C>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149377143 | |||||||
| chr6:149377163 | A | G | 147 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(144): Show |
152 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.103-855A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149377163 | |||||||
| chr6:149377163 | A | GGGTTCAC others(471): Show |
5 | a0001c0001t0009g0082 a0001c0001t0009g0083 a0001c0001t0009g0084 others(2): Show |
5 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.103-856_103-855ins others(478): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149377163 | |||||||
| chr6:149377168 | C | T | 6 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(3): Show |
6 | HG01884.hp2 HG02257.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.103-850C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149377168 | |||||||
| chr6:149377245 | T | G | 9 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0005g0181 others(6): Show |
9 | HG01243.hp2 HG02602.hp2 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.103-773T>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149377245 | |||||||
| chr6:149377265 | A | G | 290 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(287): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.103-753A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149377265 | |||||||
| chr6:149377295 | G | A | 1 | a0001c0001t0004g0036 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.103-723G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149377295 | |||||||
| chr6:149377485 | G | T | 1 | a0001c0001t0001g0279 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.103-533G>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149377485 | |||||||
| chr6:149377508 | T | A | 1 | a0001c0001t0017g0027 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.103-510T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149377508 | |||||||
| chr6:149377677 | T | G | 21 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(18): Show |
21 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.103-341T>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149377677 | |||||||
| chr6:149377766 | G | T | 306 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(303): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.103-252G>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149377766 | |||||||
| chr6:149377814 | TAGTC | T | 59 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(56): Show |
62 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.103-201_103-198del others(4): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr6 | 149377814 | ||||||
| chr6:149377873 | A | G | 1 | a0001c0002t0002g0098 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.103-145A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149377873 | |||||||
| chr6:149377880 | A | T | 290 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(287): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.103-138A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 2/6 | chr6 | 149377880 | |||||||
| chr6:149379569 | G | T | 1 | a0001c0001t0004g0060 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1603+51G>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149379569 | |||||||
| chr6:149379669 | G | A | 290 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(287): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.1603+151G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149379669 | |||||||
| chr6:149379733 | T | G | 1 | a0001c0001t0001g0273 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1603+215T>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149379733 | |||||||
| chr6:149379737 | A | T | 59 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(56): Show |
62 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.1603+219A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149379737 | |||||||
| chr6:149379806 | C | G | 59 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(56): Show |
62 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.1603+288C>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149379806 | |||||||
| chr6:149379915 | A | G | 1 | a0001c0001t0003g0344 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1603+397A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149379915 | |||||||
| chr6:149380045 | G | A | 1 | a0001c0001t0001g0300 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1603+527G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149380045 | |||||||
| chr6:149380115 | C | T | 4 | a0001c0001t0008g0026 a0001c0001t0013g0179 a0001c0001t0013g0180 others(1): Show |
4 | HG02109.hp1 HG02615.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1603+597C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149380115 | |||||||
| chr6:149380333 | C | T | 59 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(56): Show |
62 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.1603+815C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149380333 | |||||||
| chr6:149380399 | A | T | 59 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(56): Show |
62 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.1603+881A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149380399 | |||||||
| chr6:149380475 | CTA | C | 146 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(143): Show |
149 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.1603+959_1603+960d others(4): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 149380475 | ||||||
| chr6:149380766 | T | C | 4 | a0001c0001t0013g0179 a0001c0001t0013g0180 a0001c0001t0017g0027 others(1): Show |
4 | HG02109.hp1 HG02615.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1603+1248T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149380766 | |||||||
| chr6:149380857 | T | TTTGCCTT others(2102): Show |
1 | a0001c0001t0003g0320 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1603+1358_1603+135 others(2113): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 149380857 | ||||||
| chr6:149380901 | G | A | 3 | a0001c0001t0003g0316 a0001c0001t0003g0317 a0001c0001t0003g0318 |
3 | HG00140.hp2 HG01168.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.1603+1383G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149380901 | |||||||
| chr6:149380938 | C | G | 21 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(18): Show |
21 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.1603+1420C>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149380938 | |||||||
| chr6:149380990 | C | A | 11 | a0001c0001t0003g0008 a0001c0001t0003g0174 a0001c0001t0003g0316 others(8): Show |
12 | HG00140.hp2 HG01168.hp2 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.1603+1472C>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149380990 | |||||||
| chr6:149381032 | A | G | 1 | a0001c0002t0002g0100 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1603+1514A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149381032 | |||||||
| chr6:149381057 | C | T | 1 | a0001c0002t0006g0240 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1603+1539C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149381057 | |||||||
| chr6:149381090 | C | T | 17 | a0001c0001t0003g0006 a0001c0001t0003g0169 a0001c0001t0003g0170 others(14): Show |
18 | HG00609.hp2 HG01109.hp1 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.1603+1572C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149381090 | |||||||
| chr6:149381110 | G | A | 1 | a0001c0001t0001g0014 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1603+1592G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149381110 | |||||||
| chr6:149381168 | G | A | 1 | a0001c0001t0022g0178 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1603+1650G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149381168 | |||||||
| chr6:149381434 | A | G | 4 | a0001c0001t0013g0179 a0001c0001t0013g0180 a0001c0001t0017g0027 others(1): Show |
4 | HG02109.hp1 HG02615.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1603+1916A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149381434 | |||||||
| chr6:149381514 | A | G | 17 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(14): Show |
17 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.1603+1996A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149381514 | |||||||
| chr6:149381547 | T | A | 1 | a0001c0001t0004g0044 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1603+2029T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149381547 | |||||||
| chr6:149381569 | C | CT | 75 | a0001c0001t0001g0135 a0001c0001t0001g0150 a0001c0001t0001g0264 others(72): Show |
78 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(75): Show |
intron_variant | MODIFIER | c.1603+2073dupT | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 149381569 | ||||||
| chr6:149381569 | C | CTT | 9 | a0001c0001t0003g0309 a0001c0001t0003g0311 a0001c0001t0003g0314 others(6): Show |
9 | HG01891.hp2 HG02135.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.1603+2072_1603+207 others(6): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 149381569 | ||||||
| chr6:149381569 | CT | C | 93 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0012 others(90): Show |
96 | HG00733.hp1 HG00733.hp2 HG00735.hp1 others(93): Show |
intron_variant | MODIFIER | c.1603+2073delT | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 149381569 | ||||||
| chr6:149381569 | CTT | C | 10 | a0001c0001t0007g0077 a0001c0001t0007g0078 a0001c0001t0007g0079 others(7): Show |
10 | HG02055.hp1 HG02145.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1603+2072_1603+207 others(6): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 149381569 | ||||||
| chr6:149381591 | T | G | 1 | a0001c0008t0018g0292 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1603+2073T>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149381591 | |||||||
| chr6:149381591 | T | TG | 68 | a0001c0002t0002g0002 a0001c0002t0002g0103 a0001c0002t0002g0105 others(65): Show |
70 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.1603+2076dupG | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 149381591 | ||||||
| chr6:149381613 | G | A | 1 | a0001c0002t0002g0109 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1603+2095G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149381613 | |||||||
| chr6:149381729 | C | T | 1 | a0001c0001t0004g0058 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1603+2211C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149381729 | |||||||
| chr6:149381743 | T | C | 2 | a0001c0001t0001g0273 a0001c0001t0001g0301 |
2 | HG01496.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1603+2225T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149381743 | |||||||
| chr6:149381762 | A | G | 2 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
2 | NA18987.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.1603+2244A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149381762 | |||||||
| chr6:149381786 | TG | T | 4 | a0001c0001t0013g0179 a0001c0001t0013g0180 a0001c0001t0017g0027 others(1): Show |
4 | HG02109.hp1 HG02615.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1603+2270delG | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 149381786 | ||||||
| chr6:149381812 | A | T | 9 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0005g0181 others(6): Show |
9 | HG01243.hp2 HG02602.hp2 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.1603+2294A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149381812 | |||||||
| chr6:149381999 | C | A | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1603+2481C>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149381999 | |||||||
| chr6:149382307 | C | G | 4 | a0001c0001t0003g0007 a0001c0001t0003g0304 a0001c0001t0003g0324 others(1): Show |
5 | HG02647.hp1 HG02970.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1603+2789C>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149382307 | |||||||
| chr6:149382335 | C | T | 1 | a0001c0001t0017g0027 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1603+2817C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149382335 | |||||||
| chr6:149382412 | A | G | 85 | a0001c0002t0002g0002 a0001c0002t0002g0098 a0001c0002t0002g0099 others(82): Show |
87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1603+2894A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149382412 | |||||||
| chr6:149382597 | GA | G | 13 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0007g0077 others(10): Show |
13 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.1603+3092delA | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 149382597 | ||||||
| chr6:149382640 | A | G | 1 | a0001c0001t0003g0343 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1603+3122A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149382640 | |||||||
| chr6:149382650 | C | T | 2 | a0001c0001t0001g0133 a0001c0001t0001g0134 |
2 | NA18968.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.1603+3132C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149382650 | |||||||
| chr6:149382690 | C | A | 1 | a0001c0002t0014g0113 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1603+3172C>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149382690 | |||||||
| chr6:149382707 | T | C | 1 | a0001c0001t0003g0006 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1603+3189T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149382707 | |||||||
| chr6:149382752 | G | C | 1 | a0001c0002t0002g0098 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1603+3234G>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149382752 | |||||||
| chr6:149382785 | T | A | 85 | a0001c0002t0002g0002 a0001c0002t0002g0098 a0001c0002t0002g0099 others(82): Show |
87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1603+3267T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149382785 | |||||||
| chr6:149382822 | T | C | 1 | a0001c0001t0008g0166 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1603+3304T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149382822 | |||||||
| chr6:149383024 | G | C | 18 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(15): Show |
18 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.1603+3506G>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149383024 | |||||||
| chr6:149383104 | G | A | 59 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(56): Show |
62 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.1603+3586G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149383104 | |||||||
| chr6:149383174 | A | G | 7 | a0001c0001t0003g0320 a0001c0001t0003g0325 a0001c0001t0003g0326 others(4): Show |
7 | HG01192.hp2 HG01891.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1603+3656A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149383174 | |||||||
| chr6:149383356 | T | A | 1 | a0001c0001t0004g0185 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1603+3838T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149383356 | |||||||
| chr6:149383390 | G | A | 290 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(287): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.1603+3872G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149383390 | |||||||
| chr6:149383506 | A | G | 4 | a0001c0001t0008g0026 a0001c0001t0008g0165 a0001c0001t0008g0166 others(1): Show |
4 | HG02280.hp1 HG02717.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1603+3988A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149383506 | |||||||
| chr6:149383616 | A | T | 59 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(56): Show |
62 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.1603+4098A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149383616 | |||||||
| chr6:149383740 | G | A | 8 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(5): Show |
8 | HG02895.hp1 HG02895.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1603+4222G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149383740 | |||||||
| chr6:149383765 | G | C | 168 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(165): Show |
173 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.1603+4247G>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149383765 | |||||||
| chr6:149383875 | A | C | 8 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(5): Show |
8 | HG02895.hp1 HG02895.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1603+4357A>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149383875 | |||||||
| chr6:149383926 | G | A | 3 | a0001c0001t0004g0060 a0001c0001t0004g0064 a0001c0001t0004g0066 |
3 | NA18962.hp2 NA19066.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.1603+4408G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149383926 | |||||||
| chr6:149384226 | A | G | 1 | a0001c0002t0002g0101 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1603+4708A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149384226 | |||||||
| chr6:149384442 | C | T | 21 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(18): Show |
21 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.1603+4924C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149384442 | |||||||
| chr6:149384499 | T | C | 59 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(56): Show |
62 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.1603+4981T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149384499 | |||||||
| chr6:149384793 | A | G | 85 | a0001c0002t0002g0002 a0001c0002t0002g0098 a0001c0002t0002g0099 others(82): Show |
87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1603+5275A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149384793 | |||||||
| chr6:149384795 | C | T | 21 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(18): Show |
21 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.1603+5277C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149384795 | |||||||
| chr6:149384940 | C | CT | 8 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(5): Show |
8 | HG02895.hp1 HG02895.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1603+5427dupT | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 149384940 | ||||||
| chr6:149384949 | A | T | 21 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(18): Show |
21 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.1603+5431A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149384949 | |||||||
| chr6:149385041 | A | G | 4 | a0001c0001t0013g0179 a0001c0001t0013g0180 a0001c0001t0017g0027 others(1): Show |
4 | HG02109.hp1 HG02615.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1603+5523A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149385041 | |||||||
| chr6:149385388 | G | T | 2 | a0001c0001t0005g0182 a0001c0001t0005g0183 |
2 | HG02683.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1603+5870G>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149385388 | |||||||
| chr6:149385418 | T | C | 59 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(56): Show |
62 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.1603+5900T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149385418 | |||||||
| chr6:149385473 | G | A | 1 | a0001c0001t0004g0028 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1603+5955G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149385473 | |||||||
| chr6:149385570 | A | C | 21 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(18): Show |
21 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.1603+6052A>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149385570 | |||||||
| chr6:149385748 | T | C | 1 | a0001c0001t0001g0011 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1603+6230T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149385748 | |||||||
| chr6:149385761 | G | A | 4 | a0001c0001t0013g0179 a0001c0001t0013g0180 a0001c0001t0017g0027 others(1): Show |
4 | HG02109.hp1 HG02615.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1603+6243G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149385761 | |||||||
| chr6:149386152 | A | G | 144 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(141): Show |
149 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(146): Show |
intron_variant | MODIFIER | c.1603+6634A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149386152 | |||||||
| chr6:149386240 | G | A | 6 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(3): Show |
6 | HG01884.hp2 HG02257.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1603+6722G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149386240 | |||||||
| chr6:149386248 | A | G | 1 | a0001c0001t0001g0290 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1603+6730A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149386248 | |||||||
| chr6:149386254 | C | A | 1 | a0001c0001t0003g0325 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1603+6736C>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149386254 | |||||||
| chr6:149386331 | T | C | 4 | a0001c0001t0013g0179 a0001c0001t0013g0180 a0001c0001t0017g0027 others(1): Show |
4 | HG02109.hp1 HG02615.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1603+6813T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149386331 | |||||||
| chr6:149386453 | AC | A | 60 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(57): Show |
63 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.1603+6941delC | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 149386453 | ||||||
| chr6:149386515 | A | G | 85 | a0001c0002t0002g0002 a0001c0002t0002g0098 a0001c0002t0002g0099 others(82): Show |
87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1603+6997A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149386515 | |||||||
| chr6:149386665 | T | G | 1 | a0001c0002t0002g0109 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1603+7147T>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149386665 | |||||||
| chr6:149386668 | T | G | 56 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(53): Show |
57 | HG00733.hp2 HG00735.hp1 HG01069.hp2 others(54): Show |
intron_variant | MODIFIER | c.1603+7150T>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149386668 | |||||||
| chr6:149386706 | C | G | 2 | a0001c0001t0005g0182 a0001c0001t0005g0183 |
2 | HG02683.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1603+7188C>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149386706 | |||||||
| chr6:149386706 | C | T | 1 | a0001c0001t0004g0042 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1603+7188C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149386706 | |||||||
| chr6:149386778 | G | A | 1 | a0001c0001t0017g0027 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1603+7260G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149386778 | |||||||
| chr6:149387029 | C | T | 2 | a0001c0001t0003g0304 a0001c0001t0019g0305 |
2 | HG02970.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1603+7511C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149387029 | |||||||
| chr6:149387232 | T | C | 64 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(61): Show |
65 | HG00733.hp2 HG00735.hp1 HG01069.hp2 others(62): Show |
intron_variant | MODIFIER | c.1603+7714T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149387232 | |||||||
| chr6:149387276 | C | G | 5 | a0001c0001t0001g0266 a0001c0001t0001g0272 a0001c0001t0001g0281 others(2): Show |
5 | HG01069.hp1 HG01123.hp1 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.1603+7758C>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149387276 | |||||||
| chr6:149387288 | C | T | 6 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(3): Show |
6 | HG00733.hp2 HG02145.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1603+7770C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149387288 | |||||||
| chr6:149387405 | A | T | 1 | a0001c0001t0001g0189 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1603+7887A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149387405 | |||||||
| chr6:149387449 | A | G | 1 | a0001c0001t0001g0177 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1603+7931A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149387449 | |||||||
| chr6:149387494 | G | A | 1 | a0001c0001t0008g0026 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1603+7976G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149387494 | |||||||
| chr6:149387631 | A | G | 1 | a0001c0001t0005g0181 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1603+8113A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149387631 | |||||||
| chr6:149387642 | A | T | 1 | a0001c0001t0001g0071 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1603+8124A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149387642 | |||||||
| chr6:149387803 | CT | C | 85 | a0001c0002t0002g0002 a0001c0002t0002g0098 a0001c0002t0002g0099 others(82): Show |
87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1603+8293delT | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 149387803 | ||||||
| chr6:149387973 | G | A | 18 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(15): Show |
18 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.1603+8455G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149387973 | |||||||
| chr6:149388015 | T | C | 1 | a0001c0001t0003g0320 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1603+8497T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149388015 | |||||||
| chr6:149388077 | G | T | 1 | a0001c0002t0002g0112 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1603+8559G>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149388077 | |||||||
| chr6:149388197 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1603+8679C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149388197 | |||||||
| chr6:149388243 | C | T | 1 | a0001c0001t0003g0332 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1603+8725C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149388243 | |||||||
| chr6:149388675 | T | C | 3 | a0001c0002t0002g0218 a0001c0002t0002g0235 a0001c0002t0002g0236 |
3 | HG02129.hp2 NA19067.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.1604-8929T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149388675 | |||||||
| chr6:149388765 | C | T | 1 | a0001c0001t0001g0129 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1604-8839C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149388765 | |||||||
| chr6:149388851 | A | G | 1 | a0001c0002t0002g0116 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1604-8753A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149388851 | |||||||
| chr6:149388954 | C | CT | 18 | a0001c0001t0001g0145 a0001c0001t0001g0257 a0001c0001t0001g0267 others(15): Show |
18 | HG02055.hp1 HG02145.hp2 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.1604-8631dupT | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 149388954 | ||||||
| chr6:149388954 | CT | C | 207 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(204): Show |
213 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(210): Show |
intron_variant | MODIFIER | c.1604-8631delT | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 149388954 | ||||||
| chr6:149389066 | C | T | 85 | a0001c0002t0002g0002 a0001c0002t0002g0098 a0001c0002t0002g0099 others(82): Show |
87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1604-8538C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149389066 | |||||||
| chr6:149389167 | G | A | 1 | a0001c0001t0001g0301 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1604-8437G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149389167 | |||||||
| chr6:149389171 | G | A | 21 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(18): Show |
21 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.1604-8433G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149389171 | |||||||
| chr6:149389261 | T | C | 1 | a0001c0001t0001g0018 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1604-8343T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149389261 | |||||||
| chr6:149389361 | T | C | 144 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(141): Show |
149 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(146): Show |
intron_variant | MODIFIER | c.1604-8243T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149389361 | |||||||
| chr6:149389527 | T | C | 230 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(227): Show |
236 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(233): Show |
intron_variant | MODIFIER | c.1604-8077T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149389527 | |||||||
| chr6:149389645 | C | CA | 35 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0075 others(32): Show |
35 | HG01261.hp1 HG01496.hp1 HG02145.hp2 others(32): Show |
intron_variant | MODIFIER | c.1604-7939dupA | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 149389645 | ||||||
| chr6:149389645 | CA | C | 8 | a0001c0001t0001g0131 a0001c0001t0003g0324 a0001c0001t0008g0026 others(5): Show |
8 | HG02109.hp1 HG02280.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1604-7939delA | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 149389645 | ||||||
| chr6:149389645 | CAA | C | 58 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(55): Show |
61 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.1604-7940_1604-793 others(6): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 149389645 | ||||||
| chr6:149389679 | CT | C | 85 | a0001c0002t0002g0002 a0001c0002t0002g0098 a0001c0002t0002g0099 others(82): Show |
87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1604-7924delT | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149389679 | |||||||
| chr6:149389703 | G | A | 5 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0023 others(2): Show |
5 | HG02895.hp2 HG02897.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1604-7901G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149389703 | |||||||
| chr6:149389712 | C | T | 243 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(240): Show |
249 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(246): Show |
intron_variant | MODIFIER | c.1604-7892C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149389712 | |||||||
| chr6:149389902 | T | G | 1 | a0001c0001t0001g0268 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1604-7702T>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149389902 | |||||||
| chr6:149389905 | A | G | 1 | a0001c0001t0001g0256 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1604-7699A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149389905 | |||||||
| chr6:149389935 | A | G | 5 | a0001c0001t0009g0082 a0001c0001t0009g0083 a0001c0001t0009g0084 others(2): Show |
5 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1604-7669A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149389935 | |||||||
| chr6:149389975 | A | G | 17 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(14): Show |
17 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.1604-7629A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149389975 | |||||||
| chr6:149390141 | T | C | 1 | a0001c0001t0022g0178 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1604-7463T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149390141 | |||||||
| chr6:149390151 | A | G | 1 | a0001c0001t0001g0278 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1604-7453A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149390151 | |||||||
| chr6:149390485 | T | C | 3 | a0001c0001t0007g0078 a0001c0001t0007g0086 a0001c0001t0024g0081 |
3 | HG02630.hp2 HG03486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1604-7119T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149390485 | |||||||
| chr6:149390668 | G | T | 1 | a0001c0001t0008g0026 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1604-6936G>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149390668 | |||||||
| chr6:149390686 | T | C | 1 | a0001c0001t0001g0272 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1604-6918T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149390686 | |||||||
| chr6:149390718 | A | G | 2 | a0001c0001t0013g0179 a0001c0001t0013g0180 |
2 | HG02109.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1604-6886A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149390718 | |||||||
| chr6:149390726 | A | C | 144 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(141): Show |
149 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(146): Show |
intron_variant | MODIFIER | c.1604-6878A>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149390726 | |||||||
| chr6:149390726 | A | T | 119 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0012 others(116): Show |
122 | HG00733.hp2 HG00735.hp1 HG00738.hp1 others(119): Show |
intron_variant | MODIFIER | c.1604-6878A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149390726 | |||||||
| chr6:149390847 | G | C | 85 | a0001c0002t0002g0002 a0001c0002t0002g0098 a0001c0002t0002g0099 others(82): Show |
87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1604-6757G>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149390847 | |||||||
| chr6:149390859 | A | G | 1 | a0001c0002t0002g0236 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1604-6745A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149390859 | |||||||
| chr6:149390902 | C | G | 6 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0297 others(3): Show |
6 | HG02280.hp1 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1604-6702C>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149390902 | |||||||
| chr6:149391274 | A | G | 2 | a0001c0001t0001g0276 a0001c0008t0018g0292 |
2 | HG02080.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1604-6330A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149391274 | |||||||
| chr6:149391282 | C | G | 1 | a0001c0001t0008g0026 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1604-6322C>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149391282 | |||||||
| chr6:149391362 | C | T | 11 | a0001c0001t0007g0077 a0001c0001t0007g0078 a0001c0001t0007g0079 others(8): Show |
11 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1604-6242C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149391362 | |||||||
| chr6:149391409 | T | C | 6 | a0001c0001t0001g0094 a0001c0001t0001g0147 a0001c0001t0001g0148 others(3): Show |
6 | HG01081.hp1 HG01884.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1604-6195T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149391409 | |||||||
| chr6:149391419 | T | C | 3 | a0001c0001t0011g0137 a0001c0001t0011g0139 a0001c0001t0011g0140 |
3 | HG01433.hp1 HG01515.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1604-6185T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149391419 | |||||||
| chr6:149391493 | A | G | 5 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0023 others(2): Show |
5 | HG02895.hp2 HG02897.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1604-6111A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149391493 | |||||||
| chr6:149391563 | G | A | 85 | a0001c0002t0002g0002 a0001c0002t0002g0098 a0001c0002t0002g0099 others(82): Show |
87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1604-6041G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149391563 | |||||||
| chr6:149391689 | G | A | 6 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(3): Show |
6 | HG00733.hp2 HG02145.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1604-5915G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149391689 | |||||||
| chr6:149391800 | G | A | 1 | a0001c0002t0014g0113 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1604-5804G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149391800 | |||||||
| chr6:149391837 | G | C | 1 | a0001c0001t0008g0166 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1604-5767G>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149391837 | |||||||
| chr6:149391954 | T | C | 85 | a0001c0002t0002g0002 a0001c0002t0002g0098 a0001c0002t0002g0099 others(82): Show |
87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1604-5650T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149391954 | |||||||
| chr6:149392113 | C | T | 11 | a0001c0001t0007g0077 a0001c0001t0007g0078 a0001c0001t0007g0079 others(8): Show |
11 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1604-5491C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149392113 | |||||||
| chr6:149392145 | C | CG | 75 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0021 others(72): Show |
75 | HG00597.hp1 HG00673.hp1 HG01070.hp1 others(72): Show |
intron_variant | MODIFIER | c.1604-5452dupG | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 149392145 | ||||||
| chr6:149392156 | G | C | 1 | a0001c0001t0004g0068 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1604-5448G>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149392156 | |||||||
| chr6:149392179 | C | T | 1 | a0001c0001t0001g0267 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1604-5425C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149392179 | |||||||
| chr6:149392248 | C | T | 1 | a0001c0001t0022g0178 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1604-5356C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149392248 | |||||||
| chr6:149392290 | G | A | 1 | a0001c0001t0001g0157 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1604-5314G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149392290 | |||||||
| chr6:149392640 | TTCATTCA others(4): Show |
T | 8 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(5): Show |
8 | HG02895.hp1 HG02895.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1604-4958_1604-494 others(15): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 149392640 | ||||||
| chr6:149392727 | G | A | 59 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(56): Show |
62 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.1604-4877G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149392727 | |||||||
| chr6:149392759 | C | A | 3 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 |
3 | HG00733.hp2 HG02145.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1604-4845C>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149392759 | |||||||
| chr6:149392940 | AAACTCAC | A | 11 | a0001c0001t0007g0077 a0001c0001t0007g0078 a0001c0001t0007g0079 others(8): Show |
11 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1604-4662_1604-465 others(11): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 149392940 | ||||||
| chr6:149392988 | GA | G | 18 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(15): Show |
18 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.1604-4615delA | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149392988 | |||||||
| chr6:149392990 | T | C | 18 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(15): Show |
18 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.1604-4614T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149392990 | |||||||
| chr6:149393013 | C | T | 49 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0253 others(46): Show |
50 | HG00735.hp1 HG00738.hp1 HG01069.hp2 others(47): Show |
intron_variant | MODIFIER | c.1604-4591C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149393013 | |||||||
| chr6:149393026 | A | G | 1 | a0001c0001t0001g0353 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1604-4578A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149393026 | |||||||
| chr6:149393084 | A | T | 1 | a0001c0001t0004g0052 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1604-4520A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149393084 | |||||||
| chr6:149393129 | A | T | 1 | a0001c0001t0001g0125 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1604-4475A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149393129 | |||||||
| chr6:149393183 | C | G | 85 | a0001c0002t0002g0002 a0001c0002t0002g0098 a0001c0002t0002g0099 others(82): Show |
87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1604-4421C>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149393183 | |||||||
| chr6:149393186 | T | C | 59 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(56): Show |
62 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.1604-4418T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149393186 | |||||||
| chr6:149393457 | T | C | 59 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(56): Show |
62 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.1604-4147T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149393457 | |||||||
| chr6:149393468 | C | G | 3 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 |
3 | HG03209.hp1 HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1604-4136C>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149393468 | |||||||
| chr6:149393506 | C | T | 8 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(5): Show |
8 | HG02895.hp1 HG02895.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1604-4098C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149393506 | |||||||
| chr6:149393654 | G | T | 85 | a0001c0002t0002g0002 a0001c0002t0002g0098 a0001c0002t0002g0099 others(82): Show |
87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1604-3950G>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149393654 | |||||||
| chr6:149393718 | G | A | 59 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(56): Show |
62 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.1604-3886G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149393718 | |||||||
| chr6:149393727 | G | C | 1 | a0001c0001t0017g0027 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1604-3877G>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149393727 | |||||||
| chr6:149393798 | TAAGTA | T | 10 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0005g0181 others(7): Show |
10 | HG01243.hp2 HG02602.hp2 HG02683.hp1 others(7): Show |
intron_variant | MODIFIER | c.1604-3802_1604-379 others(9): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 149393798 | ||||||
| chr6:149393821 | A | G | 6 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0092 others(3): Show |
6 | HG01243.hp1 HG01891.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.1604-3783A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149393821 | |||||||
| chr6:149393843 | AT | A | 65 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(62): Show |
66 | HG00733.hp2 HG00735.hp1 HG00738.hp1 others(63): Show |
intron_variant | MODIFIER | c.1604-3754delT | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 149393843 | ||||||
| chr6:149393873 | T | C | 59 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(56): Show |
62 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.1604-3731T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149393873 | |||||||
| chr6:149393969 | G | A | 1 | a0001c0002t0006g0240 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1604-3635G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149393969 | |||||||
| chr6:149394107 | G | GT | 11 | a0001c0001t0007g0077 a0001c0001t0007g0078 a0001c0001t0007g0079 others(8): Show |
11 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1604-3489dupT | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 149394107 | ||||||
| chr6:149394314 | A | C | 1 | a0001c0001t0004g0121 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1604-3290A>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149394314 | |||||||
| chr6:149394436 | G | T | 1 | a0001c0001t0017g0027 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1604-3168G>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149394436 | |||||||
| chr6:149394551 | T | C | 9 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0005g0181 others(6): Show |
9 | HG01243.hp2 HG02602.hp2 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.1604-3053T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149394551 | |||||||
| chr6:149394782 | A | G | 1 | a0001c0001t0008g0026 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1604-2822A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149394782 | |||||||
| chr6:149395036 | A | G | 65 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(62): Show |
66 | HG00733.hp2 HG00735.hp1 HG00738.hp1 others(63): Show |
intron_variant | MODIFIER | c.1604-2568A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149395036 | |||||||
| chr6:149395129 | AT | A | 9 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0005g0181 others(6): Show |
9 | HG01243.hp2 HG02602.hp2 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.1604-2469delT | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 149395129 | ||||||
| chr6:149395167 | A | G | 1 | a0001c0001t0005g0181 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1604-2437A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149395167 | |||||||
| chr6:149395299 | A | G | 1 | a0001c0001t0001g0018 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1604-2305A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149395299 | |||||||
| chr6:149395361 | T | G | 1 | a0001c0001t0008g0026 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1604-2243T>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149395361 | |||||||
| chr6:149395705 | CT | C | 11 | a0001c0001t0001g0133 a0001c0001t0001g0145 a0001c0001t0005g0119 others(8): Show |
11 | HG01243.hp2 HG02602.hp2 HG02683.hp1 others(8): Show |
intron_variant | MODIFIER | c.1604-1888delT | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 149395705 | ||||||
| chr6:149395883 | T | G | 9 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0005g0181 others(6): Show |
9 | HG01243.hp2 HG02602.hp2 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.1604-1721T>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149395883 | |||||||
| chr6:149396110 | C | T | 65 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(62): Show |
66 | HG00733.hp2 HG00735.hp1 HG00738.hp1 others(63): Show |
intron_variant | MODIFIER | c.1604-1494C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149396110 | |||||||
| chr6:149396130 | G | A | 1 | a0001c0002t0002g0230 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1604-1474G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149396130 | |||||||
| chr6:149396183 | A | G | 65 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(62): Show |
66 | HG00733.hp2 HG00735.hp1 HG00738.hp1 others(63): Show |
intron_variant | MODIFIER | c.1604-1421A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149396183 | |||||||
| chr6:149396206 | C | T | 85 | a0001c0002t0002g0002 a0001c0002t0002g0098 a0001c0002t0002g0099 others(82): Show |
87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1604-1398C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149396206 | |||||||
| chr6:149396224 | G | A | 6 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(3): Show |
6 | HG01884.hp2 HG02257.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1604-1380G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149396224 | |||||||
| chr6:149396238 | G | A | 2 | a0001c0002t0002g0116 a0001c0002t0002g0117 |
2 | HG02155.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.1604-1366G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149396238 | |||||||
| chr6:149396289 | A | G | 243 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(240): Show |
249 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(246): Show |
intron_variant | MODIFIER | c.1604-1315A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149396289 | |||||||
| chr6:149396340 | C | A | 178 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(175): Show |
183 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.1604-1264C>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149396340 | |||||||
| chr6:149396393 | A | G | 4 | a0001c0001t0013g0179 a0001c0001t0013g0180 a0001c0001t0017g0027 others(1): Show |
4 | HG02109.hp1 HG02615.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1604-1211A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149396393 | |||||||
| chr6:149396688 | A | G | 1 | a0001c0002t0002g0250 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.1604-916A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149396688 | |||||||
| chr6:149396905 | A | T | 1 | a0001c0001t0003g0175 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1604-699A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149396905 | |||||||
| chr6:149396929 | C | A | 1 | a0001c0001t0003g0343 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1604-675C>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149396929 | |||||||
| chr6:149397004 | A | C | 1 | a0001c0001t0003g0343 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1604-600A>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149397004 | |||||||
| chr6:149397186 | A | G | 1 | a0001c0001t0020g0055 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1604-418A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149397186 | |||||||
| chr6:149397360 | G | A | 1 | a0001c0001t0007g0077 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1604-244G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149397360 | |||||||
| chr6:149397364 | C | T | 1 | a0001c0001t0001g0265 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1604-240C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149397364 | |||||||
| chr6:149397414 | C | T | 2 | a0001c0001t0013g0179 a0001c0001t0013g0180 |
2 | HG02109.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1604-190C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149397414 | |||||||
| chr6:149397441 | CA | C | 14 | a0001c0001t0003g0327 a0001c0001t0004g0062 a0001c0001t0007g0077 others(11): Show |
14 | HG01943.hp2 HG02055.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.1604-148delA | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 149397441 | ||||||
| chr6:149397514 | C | T | 243 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(240): Show |
249 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(246): Show |
intron_variant | MODIFIER | c.1604-90C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 3/6 | chr6 | 149397514 | |||||||
| chr6:149397840 | A | G | 1 | a0001c0001t0001g0071 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1764+76A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 4/6 | chr6 | 149397840 | |||||||
| chr6:149398097 | G | T | 1 | a0001c0001t0004g0049 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1858+35G>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 5/6 | chr6 | 149398097 | |||||||
| chr6:149398102 | T | G | 1 | a0001c0001t0003g0175 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1858+40T>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 5/6 | chr6 | 149398102 | |||||||
| chr6:149398125 | G | A | 1 | a0001c0001t0001g0265 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1858+63G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 5/6 | chr6 | 149398125 | |||||||
| chr6:149398218 | C | A | 1 | a0001c0001t0001g0012 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1858+156C>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 5/6 | chr6 | 149398218 | |||||||
| chr6:149398264 | G | A | 144 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(141): Show |
149 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(146): Show |
intron_variant | MODIFIER | c.1858+202G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 5/6 | chr6 | 149398264 | |||||||
| chr6:149398289 | T | C | 1 | a0001c0001t0003g0175 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1858+227T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 5/6 | chr6 | 149398289 | |||||||
| chr6:149398665 | C | T | 1 | a0001c0001t0013g0179 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1859-439C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 5/6 | chr6 | 149398665 | |||||||
| chr6:149398767 | C | T | 65 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(62): Show |
66 | HG00733.hp2 HG00735.hp1 HG00738.hp1 others(63): Show |
intron_variant | MODIFIER | c.1859-337C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 5/6 | chr6 | 149398767 | |||||||
| chr6:149398795 | AT | A | 4 | a0001c0001t0008g0026 a0001c0001t0008g0165 a0001c0001t0008g0166 others(1): Show |
4 | HG02280.hp1 HG02717.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1859-305delT | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr6 | 149398795 | ||||||
| chr6:149398831 | A | T | 59 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(56): Show |
62 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.1859-273A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 5/6 | chr6 | 149398831 | |||||||
| chr6:149398964 | A | G | 6 | a0001c0001t0001g0136 a0001c0001t0001g0145 a0001c0001t0001g0261 others(3): Show |
6 | HG00642.hp2 HG01516.hp1 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.1859-140A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 5/6 | chr6 | 149398964 | |||||||
| chr6:149398978 | G | C | 4 | a0001c0001t0013g0179 a0001c0001t0013g0180 a0001c0001t0017g0027 others(1): Show |
4 | HG02109.hp1 HG02615.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1859-126G>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 5/6 | chr6 | 149398978 | |||||||
| chr6:149398998 | A | G | 5 | a0001c0001t0003g0169 a0001c0001t0003g0170 a0001c0001t0003g0172 others(2): Show |
5 | HG01109.hp1 HG01167.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.1859-106A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 5/6 | chr6 | 149398998 | |||||||
| chr6:149399056 | T | A | 17 | a0001c0001t0003g0006 a0001c0001t0003g0169 a0001c0001t0003g0170 others(14): Show |
18 | HG00609.hp2 HG01109.hp1 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.1859-48T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 5/6 | chr6 | 149399056 | |||||||
| chr6:149399292 | A | C | 2 | a0001c0001t0001g0021 a0001c0001t0001g0022 |
2 | HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1939+108A>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149399292 | |||||||
| chr6:149399370 | A | G | 2 | a0001c0001t0001g0021 a0001c0001t0001g0022 |
2 | HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1939+186A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149399370 | |||||||
| chr6:149399530 | T | C | 3 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0297 |
3 | HG02622.hp2 HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1939+346T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149399530 | |||||||
| chr6:149399530 | T | TC | 85 | a0001c0001t0001g0128 a0001c0001t0001g0188 a0001c0001t0001g0279 others(82): Show |
87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1939+356dupC | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149399530 | ||||||
| chr6:149399530 | TC | T | 60 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0010 others(57): Show |
62 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.1939+356delC | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149399530 | ||||||
| chr6:149399545 | G | A | 263 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0012 others(260): Show |
271 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(268): Show |
intron_variant | MODIFIER | c.1939+361G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149399545 | |||||||
| chr6:149399706 | A | T | 1 | a0001c0001t0001g0260 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1939+522A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149399706 | |||||||
| chr6:149399710 | A | G | 59 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(56): Show |
62 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.1939+526A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149399710 | |||||||
| chr6:149399822 | A | G | 59 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(56): Show |
62 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.1939+638A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149399822 | |||||||
| chr6:149399888 | A | G | 85 | a0001c0002t0002g0002 a0001c0002t0002g0098 a0001c0002t0002g0099 others(82): Show |
87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1939+704A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149399888 | |||||||
| chr6:149399940 | T | C | 1 | a0001c0002t0006g0238 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1939+756T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149399940 | |||||||
| chr6:149399987 | C | T | 2 | a0001c0001t0001g0256 a0001c0001t0001g0257 |
2 | HG02809.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1939+803C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149399987 | |||||||
| chr6:149400018 | G | A | 1 | a0001c0001t0004g0058 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1939+834G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149400018 | |||||||
| chr6:149400053 | A | C | 1 | a0001c0001t0017g0027 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1939+869A>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149400053 | |||||||
| chr6:149400095 | A | G | 1 | a0001c0001t0005g0182 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1939+911A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149400095 | |||||||
| chr6:149400139 | A | T | 1 | a0001c0001t0003g0315 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1939+955A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149400139 | |||||||
| chr6:149400339 | G | A | 1 | a0001c0002t0002g0118 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1939+1155G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149400339 | |||||||
| chr6:149400355 | T | C | 2 | a0001c0001t0003g0348 a0001c0001t0003g0349 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1939+1171T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149400355 | |||||||
| chr6:149400392 | A | G | 7 | a0001c0001t0003g0320 a0001c0001t0003g0325 a0001c0001t0003g0326 others(4): Show |
7 | HG01192.hp2 HG01891.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1939+1208A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149400392 | |||||||
| chr6:149400543 | G | A | 2 | a0001c0001t0004g0033 a0001c0001t0004g0034 |
2 | HG03041.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1939+1359G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149400543 | |||||||
| chr6:149400554 | G | A | 243 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(240): Show |
249 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(246): Show |
intron_variant | MODIFIER | c.1939+1370G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149400554 | |||||||
| chr6:149400663 | C | T | 2 | a0001c0001t0004g0033 a0001c0001t0004g0034 |
2 | HG03041.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1939+1479C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149400663 | |||||||
| chr6:149400664 | G | A | 1 | a0001c0002t0002g0198 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1939+1480G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149400664 | |||||||
| chr6:149400829 | T | C | 263 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0012 others(260): Show |
271 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(268): Show |
intron_variant | MODIFIER | c.1939+1645T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149400829 | |||||||
| chr6:149400899 | A | G | 5 | a0001c0001t0001g0012 a0001c0001t0008g0026 a0001c0001t0008g0165 others(2): Show |
5 | HG00733.hp2 HG02280.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1939+1715A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149400899 | |||||||
| chr6:149401050 | C | T | 4 | a0001c0001t0005g0181 a0001c0001t0005g0182 a0001c0001t0005g0183 others(1): Show |
4 | HG02602.hp2 HG02683.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.1939+1866C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149401050 | |||||||
| chr6:149401053 | A | C | 60 | a0001c0001t0001g0009 a0001c0001t0003g0006 a0001c0001t0003g0007 others(57): Show |
63 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.1939+1869A>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149401053 | |||||||
| chr6:149401580 | G | A | 1 | a0001c0001t0004g0065 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1939+2396G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149401580 | |||||||
| chr6:149401626 | A | G | 85 | a0001c0002t0002g0002 a0001c0002t0002g0098 a0001c0002t0002g0099 others(82): Show |
87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1939+2442A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149401626 | |||||||
| chr6:149401682 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1939+2498C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149401682 | |||||||
| chr6:149401686 | C | T | 59 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(56): Show |
62 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.1939+2502C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149401686 | |||||||
| chr6:149401753 | G | A | 4 | a0001c0002t0002g0103 a0001c0002t0002g0193 a0001c0002t0002g0230 others(1): Show |
4 | NA18964.hp1 NA18994.hp2 NA19001.hp1 others(1): Show |
intron_variant | MODIFIER | c.1939+2569G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149401753 | |||||||
| chr6:149401801 | A | G | 9 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0005g0181 others(6): Show |
9 | HG01243.hp2 HG02602.hp2 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.1939+2617A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149401801 | |||||||
| chr6:149401998 | TA | T | 139 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0071 others(136): Show |
142 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(139): Show |
intron_variant | MODIFIER | c.1939+2827delA | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149401998 | ||||||
| chr6:149401999 | A | G | 1 | a0001c0001t0001g0265 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1939+2815A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149401999 | |||||||
| chr6:149402249 | G | A | 1 | a0001c0002t0002g0220 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1939+3065G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149402249 | |||||||
| chr6:149402372 | T | G | 1 | a0001c0001t0003g0174 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1939+3188T>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149402372 | |||||||
| chr6:149402412 | A | G | 147 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(144): Show |
152 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.1939+3228A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149402412 | |||||||
| chr6:149402535 | A | G | 1 | a0001c0002t0002g0251 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1939+3351A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149402535 | |||||||
| chr6:149402553 | CTCAAACA others(1): Show |
C | 65 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(62): Show |
66 | HG00733.hp2 HG00735.hp1 HG00738.hp1 others(63): Show |
intron_variant | MODIFIER | c.1939+3370_1939+337 others(12): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149402553 | |||||||
| chr6:149402695 | A | G | 6 | a0001c0001t0007g0077 a0001c0001t0007g0078 a0001c0001t0007g0079 others(3): Show |
6 | HG02630.hp2 HG03225.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1939+3511A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149402695 | |||||||
| chr6:149402776 | C | A | 3 | a0001c0001t0013g0179 a0001c0001t0013g0180 a0001c0001t0022g0178 |
3 | HG02109.hp1 HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1939+3592C>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149402776 | |||||||
| chr6:149402900 | A | C | 9 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0005g0181 others(6): Show |
9 | HG01243.hp2 HG02602.hp2 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.1939+3716A>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149402900 | |||||||
| chr6:149403093 | G | C | 85 | a0001c0002t0002g0002 a0001c0002t0002g0098 a0001c0002t0002g0099 others(82): Show |
87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1939+3909G>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403093 | |||||||
| chr6:149403126 | C | T | 57 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(54): Show |
58 | HG00733.hp2 HG00735.hp1 HG00738.hp1 others(55): Show |
intron_variant | MODIFIER | c.1939+3942C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403126 | |||||||
| chr6:149403234 | TA | T | 6 | a0001c0001t0001g0071 a0001c0001t0001g0089 a0001c0001t0001g0090 others(3): Show |
6 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.1939+4064delA | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403234 | ||||||
| chr6:149403234 | TAA | T | 24 | a0001c0001t0001g0011 a0001c0001t0001g0122 a0001c0001t0001g0123 others(21): Show |
24 | HG01433.hp1 HG02015.hp1 HG02056.hp1 others(21): Show |
intron_variant | MODIFIER | c.1939+4063_1939+406 others(6): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403234 | ||||||
| chr6:149403243 | AAAAAATA others(5): Show |
A | 2 | a0001c0001t0001g0021 a0001c0001t0001g0022 |
2 | HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1939+4061_1939+407 others(16): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403243 | ||||||
| chr6:149403243 | AAAAAATA others(9): Show |
A | 1 | a0001c0001t0001g0276 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1939+4061_1939+407 others(20): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403243 | ||||||
| chr6:149403244 | AAAAATAT others(4): Show |
A | 4 | a0001c0002t0002g0199 a0001c0002t0002g0200 a0001c0002t0002g0201 others(1): Show |
4 | HG00639.hp2 HG01257.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1939+4062_1939+407 others(15): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403244 | ||||||
| chr6:149403244 | AAAAATAT others(8): Show |
A | 2 | a0001c0001t0003g0334 a0001c0001t0003g0339 |
2 | HG01099.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1939+4062_1939+407 others(19): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403244 | ||||||
| chr6:149403245 | A | AATATATA others(3): Show |
1 | a0001c0001t0001g0353 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1939+4062_1939+406 others(14): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403245 | ||||||
| chr6:149403245 | A | AT | 7 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0094 others(4): Show |
7 | HG01243.hp1 HG01891.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1939+4061_1939+406 others(5): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403245 | |||||||
| chr6:149403245 | A | T | 3 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0297 |
3 | HG02622.hp2 HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1939+4061A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403245 | |||||||
| chr6:149403245 | AAAAT | A | 26 | a0001c0001t0001g0075 a0001c0001t0001g0150 a0001c0001t0001g0151 others(23): Show |
26 | HG00099.hp1 HG00733.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.1939+4063_1939+406 others(8): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403245 | ||||||
| chr6:149403246 | AAATATAT others(4): Show |
A | 1 | a0001c0002t0002g0226 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1939+4064_1939+407 others(15): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403246 | ||||||
| chr6:149403246 | AAATATAT others(6): Show |
A | 5 | a0001c0002t0002g0002 a0001c0002t0002g0105 a0001c0002t0002g0109 others(2): Show |
5 | HG00597.hp2 HG01261.hp1 HG02015.hp2 others(2): Show |
intron_variant | MODIFIER | c.1939+4064_1939+407 others(17): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403246 | ||||||
| chr6:149403246 | AAATATAT others(10): Show |
A | 9 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0005g0181 others(6): Show |
9 | HG01243.hp2 HG02602.hp2 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.1939+4064_1939+408 others(21): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403246 | ||||||
| chr6:149403247 | A | AAAAATAT others(4): Show |
1 | a0001c0001t0008g0026 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1939+4064_1939+406 others(15): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403247 | ||||||
| chr6:149403247 | A | ATATATAT others(4): Show |
1 | a0001c0001t0007g0086 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1939+4063_1939+406 others(15): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403247 | |||||||
| chr6:149403247 | A | T | 52 | a0001c0001t0001g0009 a0001c0001t0001g0089 a0001c0001t0001g0090 others(49): Show |
52 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.1939+4063A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403247 | |||||||
| chr6:149403247 | AATATATA others(17): Show |
A | 2 | a0001c0001t0001g0355 a0001c0001t0001g0356 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1939+4077_1939+410 others(28): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403247 | ||||||
| chr6:149403248 | AT | A | 3 | a0001c0001t0001g0073 a0001c0001t0003g0007 a0001c0001t0007g0079 |
3 | HG02257.hp1 HG03041.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1939+4065delT | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403248 | |||||||
| chr6:149403248 | ATATATAT others(4): Show |
A | 6 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(3): Show |
6 | HG01346.hp1 HG01433.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1939+4065_1939+407 others(15): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403248 | |||||||
| chr6:149403248 | ATATATAT others(6): Show |
A | 75 | a0001c0001t0004g0062 a0001c0001t0004g0064 a0001c0001t0004g0066 others(72): Show |
76 | HG00423.hp1 HG00558.hp1 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.1939+4065_1939+407 others(17): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403248 | |||||||
| chr6:149403248 | ATATATAT others(40): Show |
A | 1 | a0001c0001t0017g0027 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1939+4065_1939+411 others(51): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403248 | |||||||
| chr6:149403249 | T | A | 58 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0019 others(55): Show |
60 | HG00609.hp2 HG00733.hp2 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.1939+4065T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403249 | |||||||
| chr6:149403251 | T | A | 4 | a0001c0001t0003g0307 a0001c0001t0004g0033 a0001c0001t0004g0035 others(1): Show |
4 | HG00609.hp2 HG06807.hp2 NA18949.hp2 others(1): Show |
intron_variant | MODIFIER | c.1939+4067T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403251 | |||||||
| chr6:149403263 | T | A | 2 | a0001c0001t0004g0064 a0001c0001t0004g0066 |
2 | NA18962.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.1939+4079T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403263 | |||||||
| chr6:149403263 | T | TACAC | 5 | a0001c0001t0009g0082 a0001c0001t0009g0083 a0001c0001t0009g0084 others(2): Show |
5 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1939+4080_1939+408 others(8): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403263 | ||||||
| chr6:149403265 | T | TACACAC | 3 | a0001c0001t0008g0165 a0001c0001t0008g0166 a0001c0001t0008g0167 |
3 | HG02280.hp1 HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1939+4082_1939+408 others(10): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403265 | ||||||
| chr6:149403265 | TATATATA others(15): Show |
T | 5 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0023 others(2): Show |
5 | HG02895.hp2 HG02897.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1939+4083_1939+410 others(26): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403265 | ||||||
| chr6:149403269 | TATATATA others(13): Show |
T | 2 | a0001c0001t0004g0060 a0001c0002t0002g0115 |
2 | NA18978.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.1939+4087_1939+410 others(24): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403269 | ||||||
| chr6:149403271 | T | C | 37 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0010 others(34): Show |
39 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.1939+4087T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403271 | |||||||
| chr6:149403271 | TATATATA others(9): Show |
T | 3 | a0001c0001t0001g0018 a0001c0001t0004g0041 a0001c0001t0020g0055 |
3 | HG03195.hp1 HG03471.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.1939+4089_1939+410 others(20): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403271 | ||||||
| chr6:149403271 | TATATATA others(11): Show |
T | 38 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(35): Show |
38 | HG00733.hp2 HG00735.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.1939+4089_1939+410 others(22): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403271 | ||||||
| chr6:149403271 | TATATATA others(13): Show |
T | 6 | a0001c0001t0004g0003 a0001c0001t0004g0035 a0001c0001t0004g0038 others(3): Show |
6 | HG02040.hp2 NA18942.hp1 NA18943.hp2 others(3): Show |
intron_variant | MODIFIER | c.1939+4089_1939+410 others(24): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403271 | ||||||
| chr6:149403273 | T | C | 53 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(50): Show |
56 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.1939+4089T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403273 | |||||||
| chr6:149403273 | TATATATA others(9): Show |
T | 3 | a0001c0001t0004g0033 a0001c0001t0004g0036 a0001c0001t0004g0040 |
3 | HG02615.hp1 HG02630.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1939+4091_1939+410 others(20): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403273 | ||||||
| chr6:149403275 | T | A | 3 | a0001c0001t0008g0165 a0001c0001t0008g0166 a0001c0001t0008g0167 |
3 | HG02280.hp1 HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1939+4091T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403275 | |||||||
| chr6:149403275 | T | C | 18 | a0001c0001t0003g0006 a0001c0001t0003g0169 a0001c0001t0003g0170 others(15): Show |
19 | HG00609.hp2 HG01109.hp1 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.1939+4091T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403275 | |||||||
| chr6:149403275 | TATATATA others(9): Show |
T | 3 | a0001c0001t0003g0335 a0001c0001t0003g0340 a0001c0001t0003g0342 |
3 | HG00741.hp1 HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1939+4093_1939+410 others(20): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403275 | ||||||
| chr6:149403277 | T | C | 1 | a0001c0001t0003g0311 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1939+4093T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403277 | |||||||
| chr6:149403281 | T | C | 7 | a0001c0001t0001g0011 a0001c0001t0001g0141 a0001c0001t0001g0266 others(4): Show |
7 | HG01069.hp1 HG01123.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.1939+4097T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403281 | |||||||
| chr6:149403283 | T | C | 53 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(50): Show |
55 | HG00558.hp2 HG00597.hp1 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.1939+4099T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403283 | |||||||
| chr6:149403283 | TACAC | T | 23 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0005g0181 others(20): Show |
24 | HG01243.hp2 HG01261.hp1 HG02015.hp2 others(21): Show |
intron_variant | MODIFIER | c.1939+4109_1939+411 others(8): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403283 | ||||||
| chr6:149403283 | TACACAC | T | 84 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0021 others(81): Show |
84 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.1939+4107_1939+411 others(10): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403283 | ||||||
| chr6:149403285 | C | T | 39 | a0001c0001t0001g0073 a0001c0001t0001g0146 a0001c0001t0001g0163 others(36): Show |
40 | HG00609.hp2 HG01109.hp1 HG01109.hp2 others(37): Show |
intron_variant | MODIFIER | c.1939+4101C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403285 | |||||||
| chr6:149403287 | C | T | 14 | a0001c0001t0003g0311 a0001c0001t0007g0077 a0001c0001t0007g0078 others(11): Show |
14 | HG02055.hp1 HG02135.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.1939+4103C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403287 | |||||||
| chr6:149403289 | C | T | 7 | a0001c0001t0007g0079 a0001c0001t0007g0080 a0001c0001t0008g0165 others(4): Show |
7 | HG02280.hp1 HG02717.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.1939+4105C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403289 | |||||||
| chr6:149403289 | CACACACA others(1): Show |
C | 5 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0075 others(2): Show |
5 | HG01884.hp2 HG02886.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1939+4107_1939+411 others(12): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403289 | ||||||
| chr6:149403291 | C | T | 7 | a0001c0001t0001g0266 a0001c0001t0001g0281 a0001c0001t0001g0283 others(4): Show |
7 | HG01069.hp1 HG01123.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.1939+4107C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403291 | |||||||
| chr6:149403291 | CACACATA others(15): Show |
C | 36 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0010 others(33): Show |
38 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.1939+4113_1939+413 others(26): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403291 | ||||||
| chr6:149403293 | C | T | 31 | a0001c0001t0001g0266 a0001c0001t0001g0272 a0001c0001t0001g0280 others(28): Show |
32 | HG00733.hp1 HG01069.hp1 HG01123.hp1 others(29): Show |
intron_variant | MODIFIER | c.1939+4109C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403293 | |||||||
| chr6:149403293 | CACATATA others(13): Show |
C | 1 | a0001c0001t0003g0345 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1939+4113_1939+413 others(24): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403293 | ||||||
| chr6:149403295 | C | CAT | 3 | a0001c0001t0001g0124 a0001c0001t0001g0131 a0001c0001t0001g0289 |
3 | HG00423.hp2 NA19059.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1939+4129_1939+413 others(6): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403295 | ||||||
| chr6:149403295 | C | T | 223 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(220): Show |
227 | HG00423.hp1 HG00558.hp1 HG00558.hp2 others(224): Show |
intron_variant | MODIFIER | c.1939+4111C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403295 | |||||||
| chr6:149403295 | CAT | C | 3 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0164 |
3 | HG00735.hp2 HG01070.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1939+4129_1939+413 others(6): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403295 | ||||||
| chr6:149403295 | CATATATA others(9): Show |
C | 1 | a0001c0001t0003g0311 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1939+4115_1939+413 others(20): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403295 | ||||||
| chr6:149403295 | CATATATA others(11): Show |
C | 16 | a0001c0001t0003g0006 a0001c0001t0003g0169 a0001c0001t0003g0170 others(13): Show |
17 | HG00609.hp2 HG01109.hp1 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.1939+4113_1939+413 others(22): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403295 | ||||||
| chr6:149403297 | T | A | 1 | a0001c0001t0017g0027 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1939+4113T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403297 | |||||||
| chr6:149403297 | T | C | 2 | a0001c0001t0001g0146 a0001c0001t0001g0353 |
2 | HG01358.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.1939+4113T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403297 | |||||||
| chr6:149403299 | T | A | 1 | a0001c0001t0008g0026 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1939+4115T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403299 | |||||||
| chr6:149403307 | T | C | 5 | a0001c0001t0003g0334 a0001c0001t0003g0335 a0001c0001t0003g0339 others(2): Show |
5 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.1939+4123T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403307 | |||||||
| chr6:149403307 | TATATATA others(17): Show |
T | 1 | a0001c0001t0015g0156 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1939+4131_1939+415 others(28): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403307 | ||||||
| chr6:149403309 | T | C | 5 | a0001c0001t0003g0334 a0001c0001t0003g0335 a0001c0001t0003g0339 others(2): Show |
5 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.1939+4125T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403309 | |||||||
| chr6:149403311 | T | C | 6 | a0001c0001t0003g0334 a0001c0001t0003g0335 a0001c0001t0003g0339 others(3): Show |
6 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.1939+4127T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403311 | |||||||
| chr6:149403313 | T | C | 31 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(28): Show |
31 | HG00140.hp1 HG00733.hp2 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.1939+4129T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403313 | |||||||
| chr6:149403315 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1939+4131C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403315 | |||||||
| chr6:149403319 | C | T | 10 | a0001c0001t0007g0077 a0001c0001t0007g0078 a0001c0001t0007g0079 others(7): Show |
10 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1939+4135C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403319 | |||||||
| chr6:149403321 | C | T | 13 | a0001c0001t0007g0077 a0001c0001t0007g0078 a0001c0001t0007g0079 others(10): Show |
13 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.1939+4137C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403321 | |||||||
| chr6:149403323 | T | C | 1 | a0001c0001t0001g0090 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1939+4139T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403323 | |||||||
| chr6:149403329 | T | TACACACA others(1): Show |
10 | a0001c0001t0007g0077 a0001c0001t0007g0078 a0001c0001t0007g0079 others(7): Show |
10 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1939+4148_1939+414 others(12): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403329 | ||||||
| chr6:149403329 | T | TATACACA others(3): Show |
1 | a0001c0001t0007g0080 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1939+4146_1939+414 others(14): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403329 | ||||||
| chr6:149403329 | T | TATATATA others(5): Show |
1 | a0001c0001t0022g0178 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1939+4146_1939+414 others(16): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403329 | ||||||
| chr6:149403329 | T | TATATATA others(7): Show |
2 | a0001c0001t0013g0179 a0001c0001t0013g0180 |
2 | HG02109.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1939+4146_1939+414 others(18): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403329 | ||||||
| chr6:149403331 | C | CACATAT | 3 | a0001c0001t0008g0165 a0001c0001t0008g0166 a0001c0001t0008g0167 |
3 | HG02280.hp1 HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1939+4148_1939+414 others(10): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403331 | ||||||
| chr6:149403331 | C | T | 3 | a0001c0001t0001g0090 a0001c0001t0001g0278 a0001c0001t0008g0026 |
3 | HG00558.hp2 HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1939+4147C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403331 | |||||||
| chr6:149403333 | T | C | 1 | a0001c0001t0001g0090 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1939+4149T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403333 | |||||||
| chr6:149403337 | TATACACA others(1): Show |
T | 4 | a0001c0001t0003g0344 a0001c0002t0002g0210 a0001c0002t0002g0235 others(1): Show |
4 | HG00609.hp1 HG02129.hp2 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.1939+4155_1939+416 others(12): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403337 | ||||||
| chr6:149403337 | TATACACA others(3): Show |
T | 67 | a0001c0001t0004g0121 a0001c0002t0002g0002 a0001c0002t0002g0103 others(64): Show |
69 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.1939+4155_1939+416 others(14): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403337 | ||||||
| chr6:149403337 | TATACACA others(7): Show |
T | 1 | a0001c0002t0002g0197 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1939+4155_1939+416 others(18): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403337 | ||||||
| chr6:149403339 | TAC | T | 49 | a0001c0001t0001g0005 a0001c0001t0001g0089 a0001c0001t0001g0091 others(46): Show |
50 | HG00140.hp1 HG00423.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.1939+4189_1939+419 others(6): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403339 | ||||||
| chr6:149403339 | TACAC | T | 5 | a0001c0001t0001g0001 a0001c0001t0001g0267 a0001c0001t0001g0286 others(2): Show |
5 | HG00733.hp1 HG01069.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.1939+4187_1939+419 others(8): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403339 | ||||||
| chr6:149403339 | TACACACA others(1): Show |
T | 63 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0297 others(60): Show |
66 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.1939+4183_1939+419 others(12): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403339 | ||||||
| chr6:149403339 | TACACACA others(3): Show |
T | 83 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(80): Show |
84 | HG00621.hp1 HG00673.hp2 HG00733.hp2 others(81): Show |
intron_variant | MODIFIER | c.1939+4181_1939+419 others(14): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403339 | ||||||
| chr6:149403339 | TACACACA others(5): Show |
T | 11 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(8): Show |
11 | HG00609.hp2 HG01099.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.1939+4179_1939+419 others(16): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403339 | ||||||
| chr6:149403341 | C | CAT | 10 | a0001c0001t0007g0077 a0001c0001t0007g0079 a0001c0001t0007g0080 others(7): Show |
10 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1939+4158_1939+415 others(6): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403341 | ||||||
| chr6:149403341 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1939+4157C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403341 | |||||||
| chr6:149403343 | C | T | 14 | a0001c0001t0007g0077 a0001c0001t0007g0078 a0001c0001t0007g0079 others(11): Show |
14 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.1939+4159C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403343 | |||||||
| chr6:149403345 | C | CACATATA others(13): Show |
1 | a0001c0001t0001g0278 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1939+4164_1939+416 others(24): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403345 | ||||||
| chr6:149403345 | C | T | 14 | a0001c0001t0007g0077 a0001c0001t0007g0078 a0001c0001t0007g0079 others(11): Show |
14 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.1939+4161C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403345 | |||||||
| chr6:149403347 | C | T | 14 | a0001c0001t0007g0077 a0001c0001t0007g0078 a0001c0001t0007g0079 others(11): Show |
14 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.1939+4163C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403347 | |||||||
| chr6:149403349 | C | T | 4 | a0001c0001t0007g0078 a0001c0001t0013g0179 a0001c0001t0013g0180 others(1): Show |
4 | HG02109.hp1 HG02615.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1939+4165C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403349 | |||||||
| chr6:149403351 | C | CATATATA others(9): Show |
3 | a0001c0001t0008g0165 a0001c0001t0008g0166 a0001c0001t0008g0167 |
3 | HG02280.hp1 HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1939+4168_1939+416 others(20): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403351 | ||||||
| chr6:149403351 | C | CATATATA others(11): Show |
1 | a0001c0001t0008g0026 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1939+4168_1939+416 others(22): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149403351 | ||||||
| chr6:149403351 | C | T | 10 | a0001c0001t0001g0018 a0001c0001t0005g0119 a0001c0001t0005g0120 others(7): Show |
10 | HG01243.hp2 HG02602.hp2 HG02683.hp1 others(7): Show |
intron_variant | MODIFIER | c.1939+4167C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403351 | |||||||
| chr6:149403353 | C | T | 4 | a0001c0001t0008g0165 a0001c0001t0008g0166 a0001c0001t0008g0167 others(1): Show |
4 | HG02280.hp1 HG02717.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1939+4169C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403353 | |||||||
| chr6:149403395 | G | T | 65 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(62): Show |
66 | HG00733.hp2 HG00735.hp1 HG00738.hp1 others(63): Show |
intron_variant | MODIFIER | c.1939+4211G>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403395 | |||||||
| chr6:149403655 | C | G | 1 | a0001c0002t0002g0110 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1939+4471C>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403655 | |||||||
| chr6:149403736 | G | A | 59 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(56): Show |
62 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.1939+4552G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403736 | |||||||
| chr6:149403761 | G | T | 1 | a0001c0001t0004g0053 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1939+4577G>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403761 | |||||||
| chr6:149403825 | A | G | 18 | a0001c0001t0001g0267 a0001c0001t0003g0006 a0001c0001t0003g0169 others(15): Show |
19 | HG00609.hp2 HG01109.hp1 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.1939+4641A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403825 | |||||||
| chr6:149403970 | A | G | 85 | a0001c0002t0002g0002 a0001c0002t0002g0098 a0001c0002t0002g0099 others(82): Show |
87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1939+4786A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403970 | |||||||
| chr6:149403972 | A | G | 1 | a0001c0003t0001g0258 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1939+4788A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149403972 | |||||||
| chr6:149404126 | A | T | 1 | a0001c0001t0003g0343 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1939+4942A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149404126 | |||||||
| chr6:149404154 | G | A | 178 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(175): Show |
183 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.1939+4970G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149404154 | |||||||
| chr6:149404273 | A | C | 1 | a0001c0001t0005g0119 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1939+5089A>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149404273 | |||||||
| chr6:149404446 | A | G | 85 | a0001c0002t0002g0002 a0001c0002t0002g0098 a0001c0002t0002g0099 others(82): Show |
87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1940-5131A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149404446 | |||||||
| chr6:149404894 | A | T | 1 | a0001c0002t0002g0229 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1940-4683A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149404894 | |||||||
| chr6:149405030 | A | G | 1 | a0001c0001t0003g0303 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1940-4547A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149405030 | |||||||
| chr6:149405222 | T | C | 11 | a0001c0001t0007g0077 a0001c0001t0007g0078 a0001c0001t0007g0079 others(8): Show |
11 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1940-4355T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149405222 | |||||||
| chr6:149405409 | A | G | 21 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(18): Show |
21 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.1940-4168A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149405409 | |||||||
| chr6:149405489 | A | G | 85 | a0001c0002t0002g0002 a0001c0002t0002g0098 a0001c0002t0002g0099 others(82): Show |
87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1940-4088A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149405489 | |||||||
| chr6:149405830 | G | A | 59 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(56): Show |
62 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.1940-3747G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149405830 | |||||||
| chr6:149405928 | G | A | 238 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(235): Show |
244 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(241): Show |
intron_variant | MODIFIER | c.1940-3649G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149405928 | |||||||
| chr6:149406129 | A | T | 1 | a0001c0001t0004g0060 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1940-3448A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149406129 | |||||||
| chr6:149406169 | A | G | 1 | a0001c0001t0005g0181 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1940-3408A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149406169 | |||||||
| chr6:149406209 | T | A | 85 | a0001c0002t0002g0002 a0001c0002t0002g0098 a0001c0002t0002g0099 others(82): Show |
87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1940-3368T>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149406209 | |||||||
| chr6:149406423 | A | G | 2 | a0001c0001t0001g0269 a0001c0001t0001g0274 |
2 | NA18952.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.1940-3154A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149406423 | |||||||
| chr6:149406556 | C | CT | 6 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(3): Show |
6 | HG01884.hp2 HG02257.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1940-3020dupT | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149406556 | ||||||
| chr6:149406585 | G | A | 1 | a0001c0001t0005g0120 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1940-2992G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149406585 | |||||||
| chr6:149406741 | A | G | 4 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 others(1): Show |
4 | HG01081.hp1 HG01884.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1940-2836A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149406741 | |||||||
| chr6:149406860 | G | A | 1 | a0001c0001t0001g0256 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1940-2717G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149406860 | |||||||
| chr6:149407042 | T | C | 85 | a0001c0002t0002g0002 a0001c0002t0002g0098 a0001c0002t0002g0099 others(82): Show |
87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1940-2535T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149407042 | |||||||
| chr6:149407118 | G | C | 243 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(240): Show |
249 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(246): Show |
intron_variant | MODIFIER | c.1940-2459G>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149407118 | |||||||
| chr6:149407258 | CTGAA | C | 6 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(3): Show |
6 | HG01884.hp2 HG02257.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1940-2315_1940-231 others(8): Show |
TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149407258 | ||||||
| chr6:149407277 | A | G | 1 | a0001c0002t0002g0211 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1940-2300A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149407277 | |||||||
| chr6:149407370 | T | C | 1 | a0001c0001t0001g0152 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1940-2207T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149407370 | |||||||
| chr6:149407409 | G | C | 5 | a0001c0001t0009g0082 a0001c0001t0009g0083 a0001c0001t0009g0084 others(2): Show |
5 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1940-2168G>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149407409 | |||||||
| chr6:149407440 | G | A | 2 | a0001c0001t0003g0348 a0001c0001t0003g0349 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1940-2137G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149407440 | |||||||
| chr6:149407498 | A | G | 2 | a0001c0001t0004g0056 a0001c0001t0004g0057 |
2 | NA18957.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.1940-2079A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149407498 | |||||||
| chr6:149407613 | A | G | 59 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(56): Show |
62 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.1940-1964A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149407613 | |||||||
| chr6:149407723 | C | A | 1 | a0001c0001t0008g0166 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1940-1854C>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149407723 | |||||||
| chr6:149407829 | C | T | 1 | a0001c0001t0017g0027 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1940-1748C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149407829 | |||||||
| chr6:149407937 | G | A | 1 | a0001c0001t0001g0122 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1940-1640G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149407937 | |||||||
| chr6:149407944 | G | A | 5 | a0001c0001t0009g0082 a0001c0001t0009g0083 a0001c0001t0009g0084 others(2): Show |
5 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1940-1633G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149407944 | |||||||
| chr6:149407947 | A | G | 2 | a0001c0001t0003g0338 a0001c0001t0003g0341 |
2 | HG01257.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.1940-1630A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149407947 | |||||||
| chr6:149408062 | T | C | 243 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(240): Show |
249 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(246): Show |
intron_variant | MODIFIER | c.1940-1515T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149408062 | |||||||
| chr6:149408142 | C | T | 1 | a0001c0002t0002g0118 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1940-1435C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149408142 | |||||||
| chr6:149408143 | G | C | 1 | a0001c0001t0003g0175 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1940-1434G>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149408143 | |||||||
| chr6:149408146 | G | A | 59 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0008 others(56): Show |
62 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.1940-1431G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149408146 | |||||||
| chr6:149408155 | CA | C | 165 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(162): Show |
170 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(167): Show |
intron_variant | MODIFIER | c.1940-1418delA | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 149408155 | ||||||
| chr6:149408224 | G | C | 1 | a0001c0002t0006g0214 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1940-1353G>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149408224 | |||||||
| chr6:149408237 | A | G | 1 | a0001c0001t0001g0271 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1940-1340A>G | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149408237 | |||||||
| chr6:149408446 | T | C | 1 | a0001c0001t0004g0029 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1940-1131T>C | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149408446 | |||||||
| chr6:149408707 | A | T | 1 | a0001c0001t0022g0178 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1940-870A>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149408707 | |||||||
| chr6:149408824 | C | T | 85 | a0001c0002t0002g0002 a0001c0002t0002g0098 a0001c0002t0002g0099 others(82): Show |
87 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1940-753C>T | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149408824 | |||||||
| chr6:149409418 | G | A | 1 | a0001c0002t0002g0237 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1940-159G>A | TAB2 | ENSG00000055208.20 | transcript | ENST00000637181.2 | protein_coding | 6/6 | chr6 | 149409418 |