Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 10454 |
| ensemblid | ENSG00000100324.14 |
| hgncid | 18157 |
| symbol | TAB1 |
| name | TGF-beta activated kinase 1 (MAP3K7) binding protein 1 |
| refseq_nuc | NM_006116.3 |
| refseq_prot | NP_006107.1 |
| ensembl_nuc | ENST00000216160.11 |
| ensembl_prot | ENSP00000216160.6 |
| mane_status | MANE Select |
| chr | chr22 |
| start | 39399780 |
| end | 39431882 |
| strand | + |
| ver | v1.2 |
| region | chr22:39399780-39431882 |
| region5000 | chr22:39394780-39436882 |
| regionname0 | TAB1_chr22_39399780_39431882 |
| regionname5000 | TAB1_chr22_39394780_39436882 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 504 | 293 | 89 | 62 | 82 | 14 | 44 | 56 | TAB1_chr22_39394780_39436882 | TAB1 | MAAQR others(499): Show |
chr22 | 39394780 | 39436882 |
| a0002 | 0/0 | 504 | 15 | 0 | 0 | 15 | 0 | 0 | 8 | TAB1_chr22_39394780_39436882 | TAB1 | MAAQR others(499): Show |
chr22 | 39394780 | 39436882 |
| a0003 | 0/0 | 504 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | MAAQR others(499): Show |
chr22 | 39394780 | 39436882 |
| a0004 | 0/0 | 504 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | MAAQR others(499): Show |
chr22 | 39394780 | 39436882 |
| a0005 | 0/0 | 504 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | MAAQR others(499): Show |
chr22 | 39394780 | 39436882 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1512 | 279 | 83 | 62 | 74 | 14 | 44 | TAB1_chr22_39394780_39436882 | TAB1 | ATGGC others(1507): Show |
chr22 | 39394780 | 39436882 | ||
| a0001c0002 | 0/0 | 1512 | 10 | 3 | 0 | 7 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | ATGGC others(1507): Show |
chr22 | 39394780 | 39436882 | ||
| a0001c0009 | 0/0 | 1512 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | ATGGC others(1507): Show |
chr22 | 39394780 | 39436882 | ||
| a0001c0010 | 0/0 | 1512 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | ATGGC others(1507): Show |
chr22 | 39394780 | 39436882 | ||
| a0001c0011 | 0/0 | 1512 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | ATGGC others(1507): Show |
chr22 | 39394780 | 39436882 | ||
| a0001c0012 | 0/0 | 1512 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | ATGGC others(1507): Show |
chr22 | 39394780 | 39436882 | ||
| a0002c0003 | 0/0 | 1512 | 8 | 0 | 0 | 8 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | ATGGC others(1507): Show |
chr22 | 39394780 | 39436882 | ||
| a0002c0004 | 0/0 | 1512 | 4 | 0 | 0 | 4 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | ATGGC others(1507): Show |
chr22 | 39394780 | 39436882 | ||
| a0002c0005 | 0/0 | 1512 | 3 | 0 | 0 | 3 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | ATGGC others(1507): Show |
chr22 | 39394780 | 39436882 | ||
| a0003c0006 | 0/0 | 1512 | 2 | 0 | 0 | 2 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | ATGGC others(1507): Show |
chr22 | 39394780 | 39436882 | ||
| a0004c0008 | 0/0 | 1512 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | ATGGC others(1507): Show |
chr22 | 39394780 | 39436882 | ||
| a0005c0007 | 0/0 | 1512 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | ATGGC others(1507): Show |
chr22 | 39394780 | 39436882 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3198 | 219 | 59 | 46 | 70 | 10 | 33 | TAB1_chr22_39394780_39436882 | TAB1 | GCTCC others(3193): Show |
chr22 | 39394780 | 39436882 |
| a0001c0001t0002 | 1/0 | 3198 | 34 | 5 | 15 | 0 | 4 | 9 | TAB1_chr22_39394780_39436882 | TAB1 | GCTCC others(3193): Show |
chr22 | 39394780 | 39436882 |
| a0001c0001t0003 | 0/0 | 3198 | 15 | 14 | 1 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | GCTCC others(3193): Show |
chr22 | 39394780 | 39436882 |
| a0001c0001t0005 | 0/0 | 3198 | 3 | 0 | 0 | 3 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | GCTCC others(3193): Show |
chr22 | 39394780 | 39436882 |
| a0001c0001t0006 | 0/0 | 3198 | 2 | 0 | 0 | 0 | 0 | 2 | TAB1_chr22_39394780_39436882 | TAB1 | GCTCC others(3193): Show |
chr22 | 39394780 | 39436882 |
| a0001c0001t0007 | 0/0 | 3198 | 2 | 2 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | GCTCC others(3193): Show |
chr22 | 39394780 | 39436882 |
| a0001c0001t0009 | 0/0 | 3198 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | GCTCC others(3193): Show |
chr22 | 39394780 | 39436882 |
| a0001c0001t0010 | 0/0 | 3198 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | GCTCC others(3193): Show |
chr22 | 39394780 | 39436882 |
| a0001c0001t0011 | 0/0 | 3198 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | GCTCC others(3193): Show |
chr22 | 39394780 | 39436882 |
| a0001c0001t0013 | 0/0 | 3198 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | GCTCC others(3193): Show |
chr22 | 39394780 | 39436882 |
| a0001c0002t0003 | 0/0 | 3198 | 2 | 2 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | GCTCC others(3193): Show |
chr22 | 39394780 | 39436882 |
| a0001c0002t0004 | 0/0 | 3198 | 7 | 0 | 0 | 7 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | GCTCC others(3193): Show |
chr22 | 39394780 | 39436882 |
| a0001c0002t0012 | 0/0 | 3198 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | GCTCC others(3193): Show |
chr22 | 39394780 | 39436882 |
| a0001c0009t0001 | 0/0 | 3198 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | GCTCC others(3193): Show |
chr22 | 39394780 | 39436882 |
| a0001c0010t0001 | 0/0 | 3198 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | GCTCC others(3193): Show |
chr22 | 39394780 | 39436882 |
| a0001c0011t0001 | 0/0 | 3198 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | GCTCC others(3193): Show |
chr22 | 39394780 | 39436882 |
| a0001c0012t0001 | 0/0 | 3198 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | GCTCC others(3193): Show |
chr22 | 39394780 | 39436882 |
| a0002c0003t0001 | 0/0 | 3198 | 8 | 0 | 0 | 8 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | GCTCC others(3193): Show |
chr22 | 39394780 | 39436882 |
| a0002c0004t0001 | 0/0 | 3198 | 4 | 0 | 0 | 4 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | GCTCC others(3193): Show |
chr22 | 39394780 | 39436882 |
| a0002c0005t0001 | 0/0 | 3198 | 3 | 0 | 0 | 3 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | GCTCC others(3193): Show |
chr22 | 39394780 | 39436882 |
| a0003c0006t0001 | 0/0 | 3198 | 2 | 0 | 0 | 2 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | GCTCC others(3193): Show |
chr22 | 39394780 | 39436882 |
| a0004c0008t0001 | 0/0 | 3198 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | GCTCC others(3193): Show |
chr22 | 39394780 | 39436882 |
| a0005c0007t0008 | 0/0 | 3198 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | GCTCC others(3193): Show |
chr22 | 39394780 | 39436882 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 6 | 0 | 1 | 1 | 1 | 3 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0003 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0004 | 0/0 | 4 | 0 | 1 | 0 | 1 | 2 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0005 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0117 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0002g0001 | 0/0 | 8 | 1 | 3 | 0 | 2 | 2 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0002g0017 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0002g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0002g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0002g0218 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0002g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0003g0006 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0003g0022 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0003g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0003g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0003g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0003g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0003g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0003g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0003g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0003g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0003g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0005g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0005g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0005g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0006g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0007g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0007g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0009g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0010g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0011g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0001t0013g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0002t0003g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0002t0003g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0002t0004g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0002t0004g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0002t0004g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0002t0004g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0002t0004g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0002t0004g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0002t0004g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0002t0012g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0009t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0010t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0011t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0001c0012t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0002c0003t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0002c0003t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0002c0003t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0002c0003t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0002c0003t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0002c0003t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0002c0003t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0002c0003t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0002c0004t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0002c0004t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0002c0004t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0002c0004t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0002c0005t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0002c0005t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0003c0006t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0003c0006t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0004c0008t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| a0005c0007t0008g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0150 | EUR | GBR | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0115 | EUR | GBR | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0207 | EUR | GBR | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0148 | EUR | FIN | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0183 | EUR | FIN | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | CHS | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG00423 | hp2 | a0002 | c0003 | t0001 | g0239 | EAS | CHS | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG00544 | hp1 | a0002 | c0005 | t0001 | g0234 | EAS | CHS | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | CHS | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | CHS | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | CHS | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | CHS | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | CHS | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG00621 | hp1 | a0002 | c0005 | t0001 | g0021 | EAS | CHS | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0208 | AMR | PUR | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0129 | AMR | PUR | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG00673 | hp1 | a0003 | c0006 | t0001 | g0101 | EAS | CHS | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0017 | AMR | PUR | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0018 | AMR | PUR | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0214 | AMR | PUR | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0205 | AMR | PUR | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0206 | AMR | PUR | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0018 | AMR | PUR | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0022 | AMR | PUR | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0210 | AMR | CLM | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | CLM | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | CLM | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | CLM | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | CLM | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0127 | AMR | CLM | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0215 | AMR | CLM | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0209 | AMR | CLM | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | CLM | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0001 | EUR | IBS | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0186 | EUR | IBS | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0001 | EUR | IBS | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0158 | EUR | IBS | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | ACB | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | ACB | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG01891 | hp2 | a0001 | c0009 | t0001 | g0181 | AFR | ACB | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PEL | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PEL | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG02015 | hp2 | a0002 | c0003 | t0001 | g0236 | EAS | KHV | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | KHV | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | KHV | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | KHV | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | KHV | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG02071 | hp2 | a0002 | c0003 | t0001 | g0243 | EAS | KHV | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG02074 | hp2 | a0004 | c0008 | t0001 | g0037 | EAS | KHV | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG02083 | hp1 | a0003 | c0006 | t0001 | g0080 | EAS | KHV | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG02083 | hp2 | a0001 | c0012 | t0001 | g0098 | EAS | KHV | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG02129 | hp1 | a0001 | c0002 | t0004 | g0264 | EAS | KHV | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | KHV | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | KHV | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG02145 | hp1 | a0001 | c0001 | t0009 | g0113 | AFR | ACB | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | ACB | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PEL | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PEL | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | CDX | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | CDX | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | CDX | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CDX | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG02257 | hp1 | a0001 | c0010 | t0001 | g0135 | AFR | ACB | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG02257 | hp2 | a0001 | c0002 | t0012 | g0109 | AFR | ACB | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | ACB | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG02280 | hp1 | a0001 | c0002 | t0003 | g0111 | AFR | ACB | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0254 | AFR | ACB | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PEL | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | ACB | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | ACB | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG02523 | hp1 | a0002 | c0003 | t0001 | g0240 | EAS | KHV | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG02523 | hp2 | a0001 | c0001 | t0013 | g0083 | EAS | KHV | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0249 | AFR | GWD | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | GWD | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | GWD | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0128 | SAS | PJL | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | GWD | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | GWD | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | GWD | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0266 | AFR | GWD | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | GWD | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0106 | AFR | ESN | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG02922 | hp2 | a0001 | c0002 | t0003 | g0110 | AFR | ESN | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | ESN | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | ESN | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0265 | AFR | ESN | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | ESN | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | ESN | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0256 | AFR | ESN | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | GWD | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | MSL | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | MSL | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | ESN | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | ESN | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG03195 | hp1 | a0001 | c0001 | t0010 | g0225 | AFR | ESN | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0250 | AFR | MSL | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | MSL | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0019 | SAS | PJL | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0255 | AFR | MSL | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG03453 | hp2 | a0001 | c0001 | t0011 | g0107 | AFR | MSL | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | MSL | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | MSL | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0019 | SAS | PJL | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0211 | SAS | PJL | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0187 | SAS | PJL | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG03516 | hp2 | a0001 | c0001 | t0007 | g0247 | AFR | ESN | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | GWD | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | MSL | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | MSL | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0216 | SAS | PJL | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG03669 | hp2 | a0001 | c0001 | t0006 | g0009 | SAS | PJL | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | STU | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0017 | SAS | STU | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0213 | SAS | PJL | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | BEB | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | BEB | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | BEB | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | BEB | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | BEB | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | BEB | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | BEB | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | STU | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | STU | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | BEB | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG04184 | hp2 | a0001 | c0001 | t0006 | g0009 | SAS | BEB | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | STU | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0179 | SAS | STU | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | STU | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0055 | SAS | STU | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | YRI | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | YRI | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA18747 | hp1 | a0002 | c0004 | t0001 | g0233 | EAS | CHB | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | CHB | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | YRI | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | YRI | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA18945 | hp2 | a0001 | c0002 | t0004 | g0262 | EAS | JPT | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA18947 | hp2 | a0002 | c0003 | t0001 | g0102 | EAS | JPT | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA18950 | hp2 | a0002 | c0004 | t0001 | g0164 | EAS | JPT | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA18951 | hp1 | a0001 | c0002 | t0004 | g0258 | EAS | JPT | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA18954 | hp1 | a0002 | c0003 | t0001 | g0244 | EAS | JPT | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA18959 | hp2 | a0002 | c0004 | t0001 | g0235 | EAS | JPT | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA18964 | hp2 | a0002 | c0003 | t0001 | g0246 | EAS | JPT | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA18971 | hp2 | a0001 | c0001 | t0005 | g0088 | EAS | JPT | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA18979 | hp1 | a0001 | c0002 | t0004 | g0263 | EAS | JPT | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0248 | AFR | LWK | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | LWK | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0251 | AFR | LWK | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA19043 | hp2 | a0005 | c0007 | t0008 | g0267 | AFR | LWK | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA19055 | hp1 | a0001 | c0002 | t0004 | g0259 | EAS | JPT | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA19056 | hp2 | a0001 | c0001 | t0005 | g0057 | EAS | JPT | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA19060 | hp2 | a0002 | c0003 | t0001 | g0245 | EAS | JPT | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA19066 | hp1 | a0001 | c0002 | t0004 | g0260 | EAS | JPT | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA19068 | hp2 | a0002 | c0005 | t0001 | g0021 | EAS | JPT | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA19070 | hp1 | a0002 | c0004 | t0001 | g0241 | EAS | JPT | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA19090 | hp2 | a0001 | c0001 | t0005 | g0096 | EAS | JPT | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA19091 | hp1 | a0001 | c0002 | t0004 | g0261 | EAS | JPT | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA19240 | hp1 | a0001 | c0001 | t0007 | g0204 | AFR | YRI | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | YRI | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | ASW | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0022 | AFR | ASW | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0217 | EUR | TSI | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0155 | EUR | TSI | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | TSI | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | TSI | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | GIH | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | GIH | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0253 | AFR | ACB | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | ACB | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | ACB | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0252 | AFR | MSL | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | MSL | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0212 | AFR | USA | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | USA | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | USA | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | USA | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA21309 | hp1 | a0001 | c0011 | t0001 | g0120 | AFR | LWK | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | LWK | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0117 | REF | REF | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0218 | REF | REF | TAB1_chr22_39394780_39436882 | TAB1 | chr22 | 39394780 | 39436882 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:39399819 | G | A | 1 | a0005 | 1 | NA19043.hp2 | missense_variant | MODERATE | c.17G>A | p.Arg6Lys | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/11 | 40/3198 | 17/1515 | 6/504 | chr22 | 39399819 | |||
| chr22:39417736 | C | T | 1 | a0003 | 2 | HG00673.hp1 HG02083.hp1 |
missense_variant | MODERATE | c.437C>T | p.Pro146Leu | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 5/11 | 460/3198 | 437/1515 | 146/504 | chr22 | 39417736 | |||
| chr22:39417754 | T | C | 1 | a0002 | 15 | HG00423.hp2 HG00544.hp1 HG00621.hp1 others(12): Show |
missense_variant | MODERATE | c.455T>C | p.Leu152Pro | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 5/11 | 478/3198 | 455/1515 | 152/504 | chr22 | 39417754 | |||
| chr22:39419559 | T | G | 1 | a0004 | 1 | HG02074.hp2 | missense_variant | MODERATE | c.705T>G | p.Cys235Trp | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 7/11 | 728/3198 | 705/1515 | 235/504 | chr22 | 39419559 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:39415584 | C | T | 1 | a0001c0012 | 1 | HG02083.hp2 | synonymous_variant | LOW | c.255C>T | p.Ser85Ser | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 3/11 | 278/3198 | 255/1515 | 85/504 | chr22 | 39415584 | |||
| chr22:39415614 | C | T | 1 | a0001c0011 | 1 | NA21309.hp1 | synonymous_variant | LOW | c.285C>T | p.Ala95Ala | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 3/11 | 308/3198 | 285/1515 | 95/504 | chr22 | 39415614 | |||
| chr22:39417839 | C | T | 1 | a0002c0005 | 3 | HG00544.hp1 HG00621.hp1 NA19068.hp2 |
synonymous_variant | LOW | c.540C>T | p.Val180Val | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 5/11 | 563/3198 | 540/1515 | 180/504 | chr22 | 39417839 | |||
| chr22:39418760 | G | C | 2 | a0002c0004 a0002c0005 |
7 | HG00544.hp1 HG00621.hp1 NA18747.hp1 others(4): Show |
synonymous_variant | LOW | c.579G>C | p.Ser193Ser | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 6/11 | 602/3198 | 579/1515 | 193/504 | chr22 | 39418760 | |||
| chr22:39421881 | G | A | 1 | a0001c0009 | 1 | HG01891.hp2 | synonymous_variant | LOW | c.831G>A | p.Pro277Pro | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 8/11 | 854/3198 | 831/1515 | 277/504 | chr22 | 39421881 | |||
| chr22:39426846 | C | T | 1 | a0001c0002 | 10 | HG02129.hp1 HG02257.hp2 HG02280.hp1 others(7): Show |
synonymous_variant | LOW | c.1065C>T | p.His355His | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 9/11 | 1088/3198 | 1065/1515 | 355/504 | chr22 | 39426846 | |||
| chr22:39430132 | C | T | 1 | a0001c0010 | 1 | HG02257.hp1 | synonymous_variant | LOW | c.1425C>T | p.Asp475Asp | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 11/11 | 1448/3198 | 1425/1515 | 475/504 | chr22 | 39430132 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:39430288 | A | G | 1 | a0001c0001t0013 | 1 | HG02523.hp2 | 3_prime_UTR_variant | MODIFIER | c.*66A>G | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 11/11 | 66 | chr22 | 39430288 | ||||||
| chr22:39430328 | C | G | 1 | a0001c0001t0007 | 2 | HG03516.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*106C>G | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 11/11 | 106 | chr22 | 39430328 | ||||||
| chr22:39430356 | G | A | 2 | a0001c0001t0003 a0001c0002t0003 |
17 | HG01243.hp2 HG02280.hp1 HG02280.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*134G>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 11/11 | 134 | chr22 | 39430356 | ||||||
| chr22:39430389 | T | G | 1 | a0005c0007t0008 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*167T>G | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 11/11 | 167 | chr22 | 39430389 | ||||||
| chr22:39430419 | C | T | 1 | a0001c0002t0012 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*197C>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 11/11 | 197 | chr22 | 39430419 | ||||||
| chr22:39430522 | G | A | 2 | a0001c0001t0007 a0001c0002t0012 |
3 | HG02257.hp2 HG03516.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*300G>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 11/11 | 300 | chr22 | 39430522 | ||||||
| chr22:39430704 | G | A | 1 | a0005c0007t0008 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*482G>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 11/11 | 482 | chr22 | 39430704 | ||||||
| chr22:39430783 | G | A | 17 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0006 others(14): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
3_prime_UTR_variant | MODIFIER | c.*561G>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 11/11 | 561 | chr22 | 39430783 | ||||||
| chr22:39430812 | C | T | 1 | a0001c0001t0005 | 3 | NA18971.hp2 NA19056.hp2 NA19090.hp2 |
3_prime_UTR_variant | MODIFIER | c.*590C>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 11/11 | 590 | chr22 | 39430812 | ||||||
| chr22:39431305 | G | C | 1 | a0001c0001t0006 | 2 | HG03669.hp2 HG04184.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1083G>C | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 11/11 | 1083 | chr22 | 39431305 | ||||||
| chr22:39431313 | G | A | 1 | a0001c0002t0004 | 7 | HG02129.hp1 NA18945.hp2 NA18951.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1091G>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 11/11 | 1091 | chr22 | 39431313 | ||||||
| chr22:39431439 | G | T | 3 | a0001c0001t0003 a0001c0001t0011 a0001c0002t0003 |
18 | HG01243.hp2 HG02280.hp1 HG02280.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1217G>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 11/11 | 1217 | chr22 | 39431439 | ||||||
| chr22:39431548 | G | A | 16 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0006 others(13): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
3_prime_UTR_variant | MODIFIER | c.*1326G>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 11/11 | 1326 | chr22 | 39431548 | ||||||
| chr22:39431551 | G | A | 1 | a0001c0001t0009 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1329G>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 11/11 | 1329 | chr22 | 39431551 | ||||||
| chr22:39431682 | C | T | 1 | a0001c0001t0010 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1460C>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 11/11 | 1460 | chr22 | 39431682 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:39399847 | G | A | 1 | a0001c0001t0001g0023 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.33+12G>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39399847 | |||||||
| chr22:39399932 | A | G | 3 | a0001c0001t0002g0265 a0001c0001t0002g0266 a0005c0007t0008g0267 |
3 | HG02886.hp2 HG02970.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.33+97A>G | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39399932 | |||||||
| chr22:39399967 | C | T | 7 | a0001c0002t0004g0258 a0001c0002t0004g0259 a0001c0002t0004g0260 others(4): Show |
7 | HG02129.hp1 NA18945.hp2 NA18951.hp1 others(4): Show |
intron_variant | MODIFIER | c.33+132C>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39399967 | |||||||
| chr22:39400018 | G | T | 1 | a0001c0001t0001g0257 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.33+183G>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39400018 | |||||||
| chr22:39400019 | C | T | 1 | a0001c0001t0001g0257 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.33+184C>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39400019 | |||||||
| chr22:39400088 | G | A | 5 | a0001c0001t0001g0011 a0001c0001t0001g0024 a0001c0001t0001g0025 others(2): Show |
6 | HG01069.hp2 HG01081.hp1 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.33+253G>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39400088 | |||||||
| chr22:39400092 | T | C | 84 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(81): Show |
99 | HG00099.hp1 HG00423.hp1 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.33+257T>C | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39400092 | |||||||
| chr22:39400265 | C | T | 10 | a0001c0001t0003g0006 a0001c0001t0003g0248 a0001c0001t0003g0249 others(7): Show |
13 | HG02280.hp2 HG02486.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.33+430C>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39400265 | |||||||
| chr22:39400461 | TCTGA | T | 11 | a0001c0001t0003g0006 a0001c0001t0003g0022 a0001c0001t0003g0248 others(8): Show |
15 | HG01243.hp2 HG02280.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.33+630_33+633delAC others(2): Show |
TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr22 | 39400461 | ||||||
| chr22:39400538 | A | G | 1 | a0005c0007t0008g0267 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.33+703A>G | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39400538 | |||||||
| chr22:39400550 | G | A | 2 | a0001c0001t0002g0106 a0001c0001t0011g0107 |
2 | HG02922.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.33+715G>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39400550 | |||||||
| chr22:39400668 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.33+833G>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39400668 | |||||||
| chr22:39400741 | A | G | 11 | a0001c0001t0003g0006 a0001c0001t0003g0022 a0001c0001t0003g0248 others(8): Show |
15 | HG01243.hp2 HG02280.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.33+906A>G | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39400741 | |||||||
| chr22:39400758 | G | A | 2 | a0001c0001t0002g0265 a0001c0001t0002g0266 |
2 | HG02886.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.33+923G>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39400758 | |||||||
| chr22:39400849 | C | G | 1 | a0005c0007t0008g0267 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.33+1014C>G | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39400849 | |||||||
| chr22:39400895 | G | A | 3 | a0001c0002t0003g0110 a0001c0002t0003g0111 a0001c0002t0012g0109 |
3 | HG02257.hp2 HG02280.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.33+1060G>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39400895 | |||||||
| chr22:39400939 | A | G | 3 | a0001c0001t0002g0265 a0001c0001t0002g0266 a0005c0007t0008g0267 |
3 | HG02886.hp2 HG02970.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.33+1104A>G | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39400939 | |||||||
| chr22:39400991 | G | T | 11 | a0001c0001t0003g0006 a0001c0001t0003g0022 a0001c0001t0003g0248 others(8): Show |
15 | HG01243.hp2 HG02280.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.33+1156G>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39400991 | |||||||
| chr22:39401034 | C | CA | 42 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(39): Show |
45 | HG00140.hp1 HG00642.hp1 HG01071.hp1 others(42): Show |
intron_variant | MODIFIER | c.33+1221dupA | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr22 | 39401034 | ||||||
| chr22:39401034 | CA | C | 16 | a0001c0001t0001g0237 a0001c0001t0001g0238 a0001c0001t0001g0242 others(13): Show |
17 | HG00423.hp2 HG00544.hp1 HG00621.hp1 others(14): Show |
intron_variant | MODIFIER | c.33+1221delA | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr22 | 39401034 | ||||||
| chr22:39401034 | CAAA | C | 6 | a0001c0002t0004g0259 a0001c0002t0004g0260 a0001c0002t0004g0261 others(3): Show |
6 | HG02129.hp1 NA18945.hp2 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.33+1219_33+1221del others(3): Show |
TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr22 | 39401034 | ||||||
| chr22:39401056 | AC | A | 16 | a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0219 others(13): Show |
19 | HG01884.hp1 HG01891.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.33+1222delC | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39401056 | |||||||
| chr22:39401057 | C | A | 2 | a0001c0001t0001g0133 a0001c0001t0001g0134 |
2 | HG01175.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.33+1222C>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39401057 | |||||||
| chr22:39401069 | C | T | 2 | a0001c0001t0002g0265 a0001c0001t0002g0266 |
2 | HG02886.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.33+1234C>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39401069 | |||||||
| chr22:39401173 | G | C | 216 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(213): Show |
246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.33+1338G>C | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39401173 | |||||||
| chr22:39401182 | C | G | 1 | a0001c0001t0001g0199 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.33+1347C>G | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39401182 | |||||||
| chr22:39401733 | G | A | 2 | a0001c0001t0001g0130 a0001c0001t0001g0131 |
2 | NA19240.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.33+1898G>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39401733 | |||||||
| chr22:39401774 | G | A | 241 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(238): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.33+1939G>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39401774 | |||||||
| chr22:39401812 | A | T | 3 | a0001c0001t0002g0265 a0001c0001t0002g0266 a0005c0007t0008g0267 |
3 | HG02886.hp2 HG02970.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.33+1977A>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39401812 | |||||||
| chr22:39401925 | G | A | 7 | a0001c0002t0004g0258 a0001c0002t0004g0259 a0001c0002t0004g0260 others(4): Show |
7 | HG02129.hp1 NA18945.hp2 NA18951.hp1 others(4): Show |
intron_variant | MODIFIER | c.33+2090G>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39401925 | |||||||
| chr22:39401982 | T | C | 213 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(210): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.33+2147T>C | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39401982 | |||||||
| chr22:39402023 | TG | T | 5 | a0001c0001t0001g0126 a0001c0001t0001g0200 a0001c0001t0001g0201 others(2): Show |
5 | HG02056.hp1 HG03486.hp1 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.33+2192delG | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr22 | 39402023 | ||||||
| chr22:39402122 | A | G | 49 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0016 others(46): Show |
54 | HG00280.hp2 HG00738.hp2 HG01069.hp2 others(51): Show |
intron_variant | MODIFIER | c.33+2287A>G | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39402122 | |||||||
| chr22:39402174 | G | A | 3 | a0001c0002t0003g0110 a0001c0002t0003g0111 a0001c0002t0012g0109 |
3 | HG02257.hp2 HG02280.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.33+2339G>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39402174 | |||||||
| chr22:39402232 | G | A | 3 | a0001c0001t0002g0017 a0001c0001t0002g0205 a0001c0001t0002g0206 |
4 | HG00738.hp1 HG01167.hp1 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.33+2397G>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39402232 | |||||||
| chr22:39402369 | A | G | 7 | a0001c0002t0004g0258 a0001c0002t0004g0259 a0001c0002t0004g0260 others(4): Show |
7 | HG02129.hp1 NA18945.hp2 NA18951.hp1 others(4): Show |
intron_variant | MODIFIER | c.33+2534A>G | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39402369 | |||||||
| chr22:39402424 | G | T | 213 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(210): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.33+2589G>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39402424 | |||||||
| chr22:39402444 | T | C | 244 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(241): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.33+2609T>C | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39402444 | |||||||
| chr22:39402587 | C | A | 1 | a0005c0007t0008g0267 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.33+2752C>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39402587 | |||||||
| chr22:39402588 | T | A | 1 | a0005c0007t0008g0267 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.33+2753T>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39402588 | |||||||
| chr22:39402625 | T | G | 1 | a0005c0007t0008g0267 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.33+2790T>G | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39402625 | |||||||
| chr22:39402805 | G | A | 1 | a0001c0001t0001g0168 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.33+2970G>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39402805 | |||||||
| chr22:39402860 | G | A | 2 | a0001c0002t0003g0110 a0001c0002t0003g0111 |
2 | HG02280.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.33+3025G>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39402860 | |||||||
| chr22:39402885 | A | G | 1 | a0001c0001t0001g0119 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.33+3050A>G | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39402885 | |||||||
| chr22:39402923 | A | C | 1 | a0005c0007t0008g0267 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.33+3088A>C | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39402923 | |||||||
| chr22:39403104 | C | T | 2 | a0001c0001t0001g0166 a0001c0001t0001g0167 |
2 | HG02895.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.33+3269C>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39403104 | |||||||
| chr22:39403275 | A | G | 1 | a0001c0001t0011g0107 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.33+3440A>G | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39403275 | |||||||
| chr22:39403370 | C | T | 1 | a0001c0001t0001g0027 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.33+3535C>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39403370 | |||||||
| chr22:39403462 | G | A | 1 | a0001c0001t0001g0023 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.33+3627G>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39403462 | |||||||
| chr22:39403520 | G | C | 1 | a0001c0001t0001g0044 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.33+3685G>C | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39403520 | |||||||
| chr22:39403640 | C | CT | 186 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(183): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.33+3821dupT | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr22 | 39403640 | ||||||
| chr22:39403641 | T | C | 2 | a0001c0001t0007g0204 a0001c0001t0007g0247 |
2 | HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.33+3806T>C | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39403641 | |||||||
| chr22:39403729 | C | T | 1 | a0001c0001t0002g0206 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.33+3894C>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39403729 | |||||||
| chr22:39403784 | A | G | 227 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(224): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.33+3949A>G | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39403784 | |||||||
| chr22:39403814 | A | AT | 7 | a0001c0001t0001g0008 a0001c0001t0001g0043 a0001c0001t0001g0099 others(4): Show |
9 | HG00673.hp1 HG00673.hp2 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.33+3990dupT | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr22 | 39403814 | ||||||
| chr22:39403896 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.33+4061G>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39403896 | |||||||
| chr22:39403934 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.33+4099G>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39403934 | |||||||
| chr22:39404393 | G | A | 1 | a0001c0001t0001g0168 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.33+4558G>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39404393 | |||||||
| chr22:39404558 | A | AC | 214 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(211): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.33+4725dupC | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr22 | 39404558 | ||||||
| chr22:39404699 | C | G | 213 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(210): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.33+4864C>G | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39404699 | |||||||
| chr22:39404937 | T | C | 1 | a0002c0004t0001g0233 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.33+5102T>C | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39404937 | |||||||
| chr22:39404987 | C | T | 2 | a0001c0001t0001g0026 a0001c0001t0001g0027 |
2 | HG01069.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.33+5152C>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39404987 | |||||||
| chr22:39405191 | A | G | 1 | a0001c0001t0001g0232 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.33+5356A>G | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39405191 | |||||||
| chr22:39405261 | C | T | 1 | a0001c0012t0001g0098 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.33+5426C>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39405261 | |||||||
| chr22:39405262 | C | T | 3 | a0001c0001t0007g0204 a0001c0001t0007g0247 a0005c0007t0008g0267 |
3 | HG03516.hp2 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.33+5427C>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39405262 | |||||||
| chr22:39405441 | C | T | 1 | a0001c0001t0001g0197 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.33+5606C>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39405441 | |||||||
| chr22:39405473 | C | T | 1 | a0001c0001t0001g0042 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.33+5638C>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39405473 | |||||||
| chr22:39405522 | A | G | 2 | a0001c0001t0002g0265 a0001c0001t0002g0266 |
2 | HG02886.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.33+5687A>G | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39405522 | |||||||
| chr22:39405686 | A | T | 5 | a0001c0001t0001g0126 a0001c0001t0001g0200 a0001c0001t0001g0201 others(2): Show |
5 | HG02056.hp1 HG03486.hp1 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.33+5851A>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39405686 | |||||||
| chr22:39405743 | G | A | 13 | a0001c0001t0002g0018 a0001c0001t0002g0106 a0001c0001t0002g0127 others(10): Show |
14 | HG00140.hp2 HG00639.hp2 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.33+5908G>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39405743 | |||||||
| chr22:39405783 | G | C | 10 | a0001c0001t0007g0204 a0001c0001t0007g0247 a0001c0002t0004g0258 others(7): Show |
10 | HG02129.hp1 HG03516.hp2 NA18945.hp2 others(7): Show |
intron_variant | MODIFIER | c.33+5948G>C | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39405783 | |||||||
| chr22:39405826 | C | T | 1 | a0001c0002t0003g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.33+5991C>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39405826 | |||||||
| chr22:39405987 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.33+6152C>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39405987 | |||||||
| chr22:39406060 | G | A | 1 | a0001c0001t0001g0048 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.33+6225G>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39406060 | |||||||
| chr22:39406065 | CAT | C | 5 | a0001c0001t0001g0126 a0001c0001t0001g0200 a0001c0001t0001g0201 others(2): Show |
5 | HG02056.hp1 HG03486.hp1 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.33+6231_33+6232del others(2): Show |
TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39406065 | |||||||
| chr22:39406071 | G | A | 1 | a0005c0007t0008g0267 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.33+6236G>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39406071 | |||||||
| chr22:39406204 | C | A | 7 | a0001c0002t0004g0258 a0001c0002t0004g0259 a0001c0002t0004g0260 others(4): Show |
7 | HG02129.hp1 NA18945.hp2 NA18951.hp1 others(4): Show |
intron_variant | MODIFIER | c.33+6369C>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39406204 | |||||||
| chr22:39406255 | C | T | 3 | a0001c0001t0001g0118 a0001c0001t0007g0204 a0001c0001t0007g0247 |
3 | HG02602.hp2 HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.33+6420C>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39406255 | |||||||
| chr22:39406354 | G | A | 5 | a0001c0001t0001g0016 a0001c0001t0001g0132 a0001c0001t0001g0170 others(2): Show |
6 | HG01496.hp2 HG02109.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.33+6519G>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39406354 | |||||||
| chr22:39406355 | C | T | 1 | a0001c0001t0001g0196 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.33+6520C>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39406355 | |||||||
| chr22:39406397 | CA | C | 205 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(202): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.33+6583delA | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr22 | 39406397 | ||||||
| chr22:39406397 | CAAA | C | 9 | a0001c0001t0007g0204 a0001c0002t0004g0258 a0001c0002t0004g0259 others(6): Show |
9 | HG02129.hp1 NA18945.hp2 NA18951.hp1 others(6): Show |
intron_variant | MODIFIER | c.33+6581_33+6583del others(3): Show |
TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr22 | 39406397 | ||||||
| chr22:39406417 | A | G | 3 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0105 |
3 | HG01255.hp1 HG01934.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.33+6582A>G | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39406417 | |||||||
| chr22:39406490 | T | C | 4 | a0001c0001t0002g0127 a0001c0001t0002g0207 a0001c0001t0002g0208 others(1): Show |
4 | HG00140.hp2 HG00639.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.33+6655T>C | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39406490 | |||||||
| chr22:39406496 | C | A | 1 | a0001c0001t0001g0174 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.33+6661C>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39406496 | |||||||
| chr22:39406880 | G | A | 6 | a0001c0001t0001g0010 a0001c0001t0001g0133 a0001c0001t0001g0219 others(3): Show |
8 | HG01175.hp2 HG01884.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.33+7045G>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39406880 | |||||||
| chr22:39406925 | G | A | 7 | a0001c0002t0004g0258 a0001c0002t0004g0259 a0001c0002t0004g0260 others(4): Show |
7 | HG02129.hp1 NA18945.hp2 NA18951.hp1 others(4): Show |
intron_variant | MODIFIER | c.33+7090G>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39406925 | |||||||
| chr22:39406928 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.33+7093C>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39406928 | |||||||
| chr22:39407048 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.33+7213G>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39407048 | |||||||
| chr22:39407211 | C | T | 2 | a0001c0001t0002g0106 a0001c0001t0011g0107 |
2 | HG02922.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.33+7376C>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39407211 | |||||||
| chr22:39407385 | C | T | 4 | a0002c0003t0001g0243 a0002c0003t0001g0244 a0002c0003t0001g0245 others(1): Show |
4 | HG02071.hp2 NA18954.hp1 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.33+7550C>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39407385 | |||||||
| chr22:39407394 | T | C | 1 | a0001c0011t0001g0120 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.33+7559T>C | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39407394 | |||||||
| chr22:39407489 | G | GT | 13 | a0001c0001t0001g0126 a0001c0001t0001g0200 a0001c0001t0001g0201 others(10): Show |
13 | HG02056.hp1 HG02129.hp1 HG03486.hp1 others(10): Show |
intron_variant | MODIFIER | c.34-7505dupT | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr22 | 39407489 | ||||||
| chr22:39407544 | C | G | 2 | a0001c0001t0007g0204 a0001c0001t0007g0247 |
2 | HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.34-7462C>G | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39407544 | |||||||
| chr22:39407647 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.34-7359G>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39407647 | |||||||
| chr22:39407737 | G | A | 3 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0105 |
3 | HG01255.hp1 HG01934.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.34-7269G>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39407737 | |||||||
| chr22:39407809 | A | G | 1 | a0001c0001t0001g0165 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.34-7197A>G | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39407809 | |||||||
| chr22:39407811 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.34-7195G>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39407811 | |||||||
| chr22:39407885 | G | T | 1 | a0005c0007t0008g0267 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.34-7121G>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39407885 | |||||||
| chr22:39407985 | A | T | 1 | a0001c0001t0001g0203 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.34-7021A>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39407985 | |||||||
| chr22:39408113 | G | T | 1 | a0001c0001t0001g0041 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.34-6893G>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39408113 | |||||||
| chr22:39408240 | G | A | 1 | a0001c0001t0001g0033 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.34-6766G>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39408240 | |||||||
| chr22:39408320 | A | C | 3 | a0002c0003t0001g0244 a0002c0003t0001g0245 a0002c0003t0001g0246 |
3 | NA18954.hp1 NA18964.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.34-6686A>C | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39408320 | |||||||
| chr22:39408522 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.34-6484G>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39408522 | |||||||
| chr22:39408750 | C | T | 19 | a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0132 others(16): Show |
22 | HG01175.hp2 HG01884.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.34-6256C>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39408750 | |||||||
| chr22:39408791 | G | A | 1 | a0001c0001t0001g0139 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.34-6215G>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39408791 | |||||||
| chr22:39408987 | A | C | 1 | a0001c0001t0001g0173 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.34-6019A>C | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39408987 | |||||||
| chr22:39409601 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.34-5405G>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39409601 | |||||||
| chr22:39409715 | C | A | 1 | a0001c0001t0001g0034 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.34-5291C>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39409715 | |||||||
| chr22:39409732 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.34-5274C>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39409732 | |||||||
| chr22:39409738 | G | A | 2 | a0001c0001t0001g0166 a0001c0001t0001g0167 |
2 | HG02895.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.34-5268G>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39409738 | |||||||
| chr22:39409746 | C | T | 2 | a0001c0001t0007g0204 a0001c0001t0007g0247 |
2 | HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.34-5260C>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39409746 | |||||||
| chr22:39409747 | G | A | 28 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0020 others(25): Show |
32 | HG01175.hp2 HG01884.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.34-5259G>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39409747 | |||||||
| chr22:39409984 | A | G | 5 | a0001c0001t0003g0022 a0001c0001t0003g0252 a0001c0001t0003g0253 others(2): Show |
6 | HG01243.hp2 HG02486.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.34-5022A>G | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39409984 | |||||||
| chr22:39410001 | T | G | 1 | a0001c0002t0012g0109 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.34-5005T>G | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39410001 | |||||||
| chr22:39410111 | TTTC | T | 8 | a0001c0002t0004g0258 a0001c0002t0004g0259 a0001c0002t0004g0260 others(5): Show |
8 | HG02129.hp1 NA18945.hp2 NA18951.hp1 others(5): Show |
intron_variant | MODIFIER | c.34-4886_34-4884del others(3): Show |
TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr22 | 39410111 | ||||||
| chr22:39410126 | G | C | 19 | a0001c0001t0001g0016 a0001c0001t0001g0108 a0001c0001t0001g0121 others(16): Show |
20 | HG01109.hp2 HG01243.hp1 HG01496.hp2 others(17): Show |
intron_variant | MODIFIER | c.34-4880G>C | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39410126 | |||||||
| chr22:39410148 | T | C | 65 | a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0133 others(62): Show |
82 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(79): Show |
intron_variant | MODIFIER | c.34-4858T>C | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39410148 | |||||||
| chr22:39410241 | G | C | 5 | a0001c0001t0001g0126 a0001c0001t0001g0200 a0001c0001t0001g0201 others(2): Show |
5 | HG02056.hp1 HG03486.hp1 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.34-4765G>C | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39410241 | |||||||
| chr22:39410469 | G | C | 2 | a0001c0001t0002g0265 a0001c0001t0002g0266 |
2 | HG02886.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.34-4537G>C | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39410469 | |||||||
| chr22:39410498 | C | CTT | 6 | a0001c0002t0004g0258 a0001c0002t0004g0260 a0001c0002t0004g0261 others(3): Show |
6 | HG02129.hp1 NA18945.hp2 NA18951.hp1 others(3): Show |
intron_variant | MODIFIER | c.34-4495_34-4494dup others(2): Show |
TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr22 | 39410498 | ||||||
| chr22:39410498 | CT | C | 127 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(124): Show |
149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.34-4494delT | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr22 | 39410498 | ||||||
| chr22:39410674 | AAAAT | A | 3 | a0001c0001t0001g0146 a0001c0001t0002g0265 a0001c0001t0002g0266 |
3 | HG02886.hp2 HG02970.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.34-4320_34-4317del others(4): Show |
TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr22 | 39410674 | ||||||
| chr22:39410827 | C | T | 1 | a0001c0001t0001g0092 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.34-4179C>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39410827 | |||||||
| chr22:39410932 | C | T | 3 | a0001c0001t0001g0125 a0001c0001t0001g0172 a0001c0001t0001g0195 |
3 | HG02622.hp2 NA18522.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.34-4074C>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39410932 | |||||||
| chr22:39411065 | G | A | 1 | a0005c0007t0008g0267 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.34-3941G>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39411065 | |||||||
| chr22:39411138 | A | G | 2 | a0001c0001t0001g0130 a0001c0001t0001g0131 |
2 | NA19240.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.34-3868A>G | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39411138 | |||||||
| chr22:39411196 | A | G | 1 | a0001c0001t0001g0182 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.34-3810A>G | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39411196 | |||||||
| chr22:39411226 | C | T | 7 | a0001c0002t0004g0258 a0001c0002t0004g0259 a0001c0002t0004g0260 others(4): Show |
7 | HG02129.hp1 NA18945.hp2 NA18951.hp1 others(4): Show |
intron_variant | MODIFIER | c.34-3780C>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39411226 | |||||||
| chr22:39411531 | G | A | 5 | a0001c0001t0001g0126 a0001c0001t0001g0200 a0001c0001t0001g0201 others(2): Show |
5 | HG02056.hp1 HG03486.hp1 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.34-3475G>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39411531 | |||||||
| chr22:39411911 | T | C | 4 | a0001c0001t0001g0114 a0001c0001t0001g0130 a0001c0001t0001g0131 others(1): Show |
4 | HG02559.hp2 HG06807.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.34-3095T>C | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39411911 | |||||||
| chr22:39412028 | A | ATTGTT | 6 | a0001c0001t0007g0204 a0001c0001t0007g0247 a0001c0002t0003g0110 others(3): Show |
6 | HG02257.hp2 HG02280.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.34-2956_34-2952dup others(5): Show |
TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr22 | 39412028 | ||||||
| chr22:39412028 | ATTGTT | A | 4 | a0001c0001t0001g0016 a0001c0001t0001g0170 a0001c0001t0001g0171 others(1): Show |
5 | HG01496.hp2 HG02109.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.34-2956_34-2952del others(5): Show |
TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr22 | 39412028 | ||||||
| chr22:39412066 | C | T | 1 | a0001c0001t0001g0132 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.34-2940C>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39412066 | |||||||
| chr22:39412168 | T | C | 1 | a0001c0001t0001g0033 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.34-2838T>C | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39412168 | |||||||
| chr22:39412200 | C | A | 1 | a0001c0001t0001g0114 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.34-2806C>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39412200 | |||||||
| chr22:39412200 | C | T | 1 | a0001c0001t0001g0242 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.34-2806C>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39412200 | |||||||
| chr22:39412329 | T | C | 1 | a0001c0012t0001g0098 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.34-2677T>C | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39412329 | |||||||
| chr22:39412351 | A | G | 1 | a0001c0001t0001g0097 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.34-2655A>G | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39412351 | |||||||
| chr22:39412396 | G | C | 5 | a0001c0001t0001g0003 a0001c0001t0001g0061 a0001c0001t0001g0062 others(2): Show |
9 | HG00558.hp1 HG00597.hp1 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.34-2610G>C | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39412396 | |||||||
| chr22:39412415 | G | A | 8 | a0001c0002t0004g0258 a0001c0002t0004g0259 a0001c0002t0004g0260 others(5): Show |
8 | HG02129.hp1 NA18945.hp2 NA18951.hp1 others(5): Show |
intron_variant | MODIFIER | c.34-2591G>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39412415 | |||||||
| chr22:39412484 | TCA | T | 16 | a0001c0001t0001g0016 a0001c0001t0001g0108 a0001c0001t0001g0121 others(13): Show |
17 | HG01109.hp2 HG01243.hp1 HG01496.hp2 others(14): Show |
intron_variant | MODIFIER | c.34-2519_34-2518del others(2): Show |
TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr22 | 39412484 | ||||||
| chr22:39412630 | T | C | 8 | a0001c0002t0004g0258 a0001c0002t0004g0259 a0001c0002t0004g0260 others(5): Show |
8 | HG02129.hp1 NA18945.hp2 NA18951.hp1 others(5): Show |
intron_variant | MODIFIER | c.34-2376T>C | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39412630 | |||||||
| chr22:39412661 | A | G | 2 | a0001c0001t0001g0058 a0001c0001t0001g0091 |
2 | HG02040.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.34-2345A>G | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39412661 | |||||||
| chr22:39412681 | C | T | 1 | a0001c0001t0002g0206 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.34-2325C>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39412681 | |||||||
| chr22:39412797 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.34-2209C>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39412797 | |||||||
| chr22:39412838 | T | C | 1 | a0001c0001t0001g0199 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.34-2168T>C | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39412838 | |||||||
| chr22:39412892 | C | CT | 151 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(148): Show |
173 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.34-2092dupT | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr22 | 39412892 | ||||||
| chr22:39412892 | C | CTT | 21 | a0001c0001t0001g0063 a0001c0001t0001g0097 a0001c0001t0001g0114 others(18): Show |
22 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(19): Show |
intron_variant | MODIFIER | c.34-2093_34-2092dup others(2): Show |
TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr22 | 39412892 | ||||||
| chr22:39412892 | CTTT | C | 8 | a0001c0002t0004g0258 a0001c0002t0004g0259 a0001c0002t0004g0260 others(5): Show |
8 | HG02129.hp1 NA18945.hp2 NA18951.hp1 others(5): Show |
intron_variant | MODIFIER | c.34-2094_34-2092del others(3): Show |
TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr22 | 39412892 | ||||||
| chr22:39412908 | TTTTTTTG others(10): Show |
T | 1 | a0001c0001t0001g0199 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.34-2091_34-2075del others(17): Show |
TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr22 | 39412908 | ||||||
| chr22:39413116 | A | G | 8 | a0001c0002t0004g0258 a0001c0002t0004g0259 a0001c0002t0004g0260 others(5): Show |
8 | HG02129.hp1 NA18945.hp2 NA18951.hp1 others(5): Show |
intron_variant | MODIFIER | c.34-1890A>G | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39413116 | |||||||
| chr22:39413349 | C | T | 3 | a0001c0001t0001g0016 a0001c0001t0001g0170 a0001c0001t0001g0171 |
4 | HG01496.hp2 HG02109.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.34-1657C>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39413349 | |||||||
| chr22:39413420 | AT | A | 7 | a0001c0001t0001g0029 a0001c0001t0001g0058 a0001c0001t0001g0126 others(4): Show |
7 | HG02056.hp1 HG03486.hp1 NA18963.hp1 others(4): Show |
intron_variant | MODIFIER | c.34-1573delT | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr22 | 39413420 | ||||||
| chr22:39413544 | G | A | 3 | a0001c0002t0003g0110 a0001c0002t0003g0111 a0001c0002t0012g0109 |
3 | HG02257.hp2 HG02280.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.34-1462G>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39413544 | |||||||
| chr22:39413617 | G | A | 3 | a0001c0002t0003g0110 a0001c0002t0003g0111 a0001c0002t0012g0109 |
3 | HG02257.hp2 HG02280.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.34-1389G>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39413617 | |||||||
| chr22:39413664 | G | A | 2 | a0001c0001t0001g0035 a0001c0001t0001g0064 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.34-1342G>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39413664 | |||||||
| chr22:39413778 | G | A | 2 | a0001c0001t0001g0179 a0001c0001t0001g0180 |
2 | HG02602.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.34-1228G>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39413778 | |||||||
| chr22:39413815 | G | C | 245 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(242): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.34-1191G>C | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39413815 | |||||||
| chr22:39413829 | G | A | 7 | a0001c0002t0004g0258 a0001c0002t0004g0259 a0001c0002t0004g0260 others(4): Show |
7 | HG02129.hp1 NA18945.hp2 NA18951.hp1 others(4): Show |
intron_variant | MODIFIER | c.34-1177G>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39413829 | |||||||
| chr22:39413961 | C | T | 8 | a0001c0002t0004g0258 a0001c0002t0004g0259 a0001c0002t0004g0260 others(5): Show |
8 | HG02129.hp1 NA18945.hp2 NA18951.hp1 others(5): Show |
intron_variant | MODIFIER | c.34-1045C>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39413961 | |||||||
| chr22:39413989 | C | T | 3 | a0001c0002t0003g0110 a0001c0002t0003g0111 a0001c0002t0012g0109 |
3 | HG02257.hp2 HG02280.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.34-1017C>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39413989 | |||||||
| chr22:39414002 | A | G | 1 | a0001c0001t0001g0032 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.34-1004A>G | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39414002 | |||||||
| chr22:39414374 | C | T | 228 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(225): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.34-632C>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39414374 | |||||||
| chr22:39414397 | G | A | 1 | a0001c0001t0001g0231 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.34-609G>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39414397 | |||||||
| chr22:39414544 | T | TGCAGATG others(4): Show |
1 | a0005c0007t0008g0267 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.34-460_34-450dupCA others(9): Show |
TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr22 | 39414544 | ||||||
| chr22:39414967 | C | T | 3 | a0001c0001t0001g0163 a0001c0001t0001g0166 a0001c0001t0001g0167 |
3 | HG02615.hp2 HG02895.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.34-39C>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 1/10 | chr22 | 39414967 | |||||||
| chr22:39415180 | T | A | 1 | a0001c0001t0001g0067 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.170+38T>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 2/10 | chr22 | 39415180 | |||||||
| chr22:39415308 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.170+166C>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 2/10 | chr22 | 39415308 | |||||||
| chr22:39415338 | T | C | 3 | a0001c0002t0003g0110 a0001c0002t0003g0111 a0001c0002t0012g0109 |
3 | HG02257.hp2 HG02280.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.171-162T>C | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 2/10 | chr22 | 39415338 | |||||||
| chr22:39415375 | G | A | 1 | a0005c0007t0008g0267 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.171-125G>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 2/10 | chr22 | 39415375 | |||||||
| chr22:39415388 | C | T | 6 | a0001c0001t0001g0010 a0001c0001t0001g0133 a0001c0001t0001g0219 others(3): Show |
8 | HG01175.hp2 HG01884.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.171-112C>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 2/10 | chr22 | 39415388 | |||||||
| chr22:39415480 | C | G | 1 | a0001c0001t0003g0256 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.171-20C>G | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 2/10 | chr22 | 39415480 | |||||||
| chr22:39415682 | A | T | 3 | a0001c0001t0001g0031 a0001c0001t0001g0066 a0001c0001t0001g0093 |
3 | NA18968.hp2 NA18981.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.324+29A>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 3/10 | chr22 | 39415682 | |||||||
| chr22:39415836 | G | A | 1 | a0001c0001t0001g0068 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.324+183G>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 3/10 | chr22 | 39415836 | |||||||
| chr22:39416066 | C | T | 1 | a0001c0001t0002g0019 | 2 | HG03239.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.324+413C>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 3/10 | chr22 | 39416066 | |||||||
| chr22:39416067 | G | A | 7 | a0001c0002t0004g0258 a0001c0002t0004g0259 a0001c0002t0004g0260 others(4): Show |
7 | HG02129.hp1 NA18945.hp2 NA18951.hp1 others(4): Show |
intron_variant | MODIFIER | c.324+414G>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 3/10 | chr22 | 39416067 | |||||||
| chr22:39416109 | A | C | 1 | a0001c0001t0001g0136 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.324+456A>C | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 3/10 | chr22 | 39416109 | |||||||
| chr22:39416128 | G | C | 8 | a0001c0002t0004g0258 a0001c0002t0004g0259 a0001c0002t0004g0260 others(5): Show |
8 | HG02129.hp1 NA18945.hp2 NA18951.hp1 others(5): Show |
intron_variant | MODIFIER | c.324+475G>C | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 3/10 | chr22 | 39416128 | |||||||
| chr22:39416202 | C | G | 2 | a0001c0001t0001g0145 a0001c0001t0009g0113 |
2 | HG02145.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.324+549C>G | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 3/10 | chr22 | 39416202 | |||||||
| chr22:39416304 | T | C | 1 | a0001c0001t0002g0206 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.325-487T>C | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 3/10 | chr22 | 39416304 | |||||||
| chr22:39416404 | T | G | 245 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(242): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.325-387T>G | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 3/10 | chr22 | 39416404 | |||||||
| chr22:39416550 | T | C | 1 | a0001c0001t0001g0103 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.325-241T>C | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 3/10 | chr22 | 39416550 | |||||||
| chr22:39416764 | C | G | 3 | a0001c0002t0003g0110 a0001c0002t0003g0111 a0001c0002t0012g0109 |
3 | HG02257.hp2 HG02280.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.325-27C>G | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 3/10 | chr22 | 39416764 | |||||||
| chr22:39416786 | C | T | 7 | a0001c0002t0004g0258 a0001c0002t0004g0259 a0001c0002t0004g0260 others(4): Show |
7 | HG02129.hp1 NA18945.hp2 NA18951.hp1 others(4): Show |
splice_region_variant&intron_variant | LOW | c.325-5C>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 3/10 | chr22 | 39416786 | |||||||
| chr22:39416952 | T | C | 1 | a0005c0007t0008g0267 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.411+75T>C | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 4/10 | chr22 | 39416952 | |||||||
| chr22:39416981 | C | A | 257 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(254): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.411+104C>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 4/10 | chr22 | 39416981 | |||||||
| chr22:39417157 | C | G | 1 | a0001c0001t0001g0105 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.411+280C>G | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 4/10 | chr22 | 39417157 | |||||||
| chr22:39417186 | C | T | 12 | a0001c0001t0003g0006 a0001c0001t0003g0022 a0001c0001t0003g0248 others(9): Show |
16 | HG01243.hp2 HG02280.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.411+309C>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 4/10 | chr22 | 39417186 | |||||||
| chr22:39417245 | G | GAGCT | 3 | a0001c0002t0003g0110 a0001c0002t0003g0111 a0001c0002t0012g0109 |
3 | HG02257.hp2 HG02280.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.411+369_411+372dup others(4): Show |
TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr22 | 39417245 | ||||||
| chr22:39417323 | C | G | 1 | a0001c0001t0001g0160 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.412-388C>G | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 4/10 | chr22 | 39417323 | |||||||
| chr22:39417348 | T | C | 6 | a0001c0001t0001g0050 a0001c0001t0001g0069 a0001c0001t0001g0070 others(3): Show |
6 | HG01099.hp2 HG02040.hp1 HG02129.hp2 others(3): Show |
intron_variant | MODIFIER | c.412-363T>C | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 4/10 | chr22 | 39417348 | |||||||
| chr22:39417480 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.412-231C>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 4/10 | chr22 | 39417480 | |||||||
| chr22:39417514 | T | G | 8 | a0001c0002t0004g0258 a0001c0002t0004g0259 a0001c0002t0004g0260 others(5): Show |
8 | HG02129.hp1 NA18945.hp2 NA18951.hp1 others(5): Show |
intron_variant | MODIFIER | c.412-197T>G | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 4/10 | chr22 | 39417514 | |||||||
| chr22:39417668 | T | C | 1 | a0001c0001t0001g0062 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.412-43T>C | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 4/10 | chr22 | 39417668 | |||||||
| chr22:39417943 | C | G | 2 | a0001c0001t0001g0089 a0001c0001t0001g0090 |
2 | HG02135.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.550+94C>G | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 5/10 | chr22 | 39417943 | |||||||
| chr22:39418032 | C | T | 1 | a0005c0007t0008g0267 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.550+183C>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 5/10 | chr22 | 39418032 | |||||||
| chr22:39418044 | C | T | 3 | a0001c0001t0005g0057 a0001c0001t0005g0088 a0001c0001t0005g0096 |
3 | NA18971.hp2 NA19056.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.550+195C>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 5/10 | chr22 | 39418044 | |||||||
| chr22:39418147 | A | G | 1 | a0001c0001t0001g0200 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.550+298A>G | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 5/10 | chr22 | 39418147 | |||||||
| chr22:39418284 | G | A | 1 | a0001c0001t0001g0124 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.550+435G>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 5/10 | chr22 | 39418284 | |||||||
| chr22:39418288 | C | T | 1 | a0001c0001t0001g0124 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.550+439C>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 5/10 | chr22 | 39418288 | |||||||
| chr22:39418326 | A | G | 1 | a0005c0007t0008g0267 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.551-406A>G | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 5/10 | chr22 | 39418326 | |||||||
| chr22:39418440 | A | C | 17 | a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0133 others(14): Show |
20 | HG01175.hp2 HG01884.hp1 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.551-292A>C | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 5/10 | chr22 | 39418440 | |||||||
| chr22:39418548 | A | G | 1 | a0005c0007t0008g0267 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.551-184A>G | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 5/10 | chr22 | 39418548 | |||||||
| chr22:39418562 | G | C | 1 | a0001c0001t0001g0114 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.551-170G>C | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 5/10 | chr22 | 39418562 | |||||||
| chr22:39418608 | C | A | 7 | a0001c0001t0002g0018 a0001c0001t0002g0128 a0001c0001t0002g0210 others(4): Show |
8 | HG01070.hp2 HG01081.hp2 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.551-124C>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 5/10 | chr22 | 39418608 | |||||||
| chr22:39418925 | G | A | 1 | a0001c0001t0001g0094 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.664+80G>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 6/10 | chr22 | 39418925 | |||||||
| chr22:39419012 | G | GAACTTA | 7 | a0001c0002t0004g0258 a0001c0002t0004g0259 a0001c0002t0004g0260 others(4): Show |
7 | HG02129.hp1 NA18945.hp2 NA18951.hp1 others(4): Show |
intron_variant | MODIFIER | c.664+169_664+174dup others(6): Show |
TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr22 | 39419012 | ||||||
| chr22:39419190 | C | G | 1 | a0001c0001t0002g0214 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.665-329C>G | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 6/10 | chr22 | 39419190 | |||||||
| chr22:39419514 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG02559.hp1 | splice_region_variant&intron_variant | LOW | c.665-5C>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 6/10 | chr22 | 39419514 | |||||||
| chr22:39419641 | G | A | 4 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0166 others(1): Show |
4 | HG00639.hp1 HG02615.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.776+11G>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 7/10 | chr22 | 39419641 | |||||||
| chr22:39419646 | G | A | 3 | a0001c0001t0005g0057 a0001c0001t0005g0088 a0001c0001t0005g0096 |
3 | NA18971.hp2 NA19056.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.776+16G>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 7/10 | chr22 | 39419646 | |||||||
| chr22:39419968 | T | TGAG | 245 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(242): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.776+339_776+341dup others(3): Show |
TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr22 | 39419968 | ||||||
| chr22:39420278 | A | G | 2 | a0001c0001t0002g0265 a0001c0001t0002g0266 |
2 | HG02886.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.776+648A>G | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 7/10 | chr22 | 39420278 | |||||||
| chr22:39420505 | G | A | 8 | a0001c0002t0004g0258 a0001c0002t0004g0259 a0001c0002t0004g0260 others(5): Show |
8 | HG02129.hp1 NA18945.hp2 NA18951.hp1 others(5): Show |
intron_variant | MODIFIER | c.776+875G>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 7/10 | chr22 | 39420505 | |||||||
| chr22:39420563 | C | T | 3 | a0001c0001t0001g0067 a0001c0001t0001g0087 a0001c0001t0001g0125 |
3 | HG01975.hp2 NA18971.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.776+933C>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 7/10 | chr22 | 39420563 | |||||||
| chr22:39420606 | G | A | 2 | a0001c0001t0002g0265 a0001c0001t0002g0266 |
2 | HG02886.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.776+976G>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 7/10 | chr22 | 39420606 | |||||||
| chr22:39420669 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.776+1039C>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 7/10 | chr22 | 39420669 | |||||||
| chr22:39420775 | C | CTG | 39 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0029 others(36): Show |
51 | HG00140.hp1 HG00423.hp2 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.777-1010_777-1009d others(4): Show |
TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr22 | 39420775 | ||||||
| chr22:39420775 | C | CTGTG | 50 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0020 others(47): Show |
56 | HG00140.hp2 HG00639.hp2 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.777-1012_777-1009d others(6): Show |
TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr22 | 39420775 | ||||||
| chr22:39420775 | C | CTGTGTG | 59 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0011 others(56): Show |
65 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.777-1014_777-1009d others(8): Show |
TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr22 | 39420775 | ||||||
| chr22:39420775 | C | CTGTGTGT others(1): Show |
42 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(39): Show |
53 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.777-1016_777-1009d others(10): Show |
TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr22 | 39420775 | ||||||
| chr22:39420775 | C | CTGTGTGT others(3): Show |
13 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0016 others(10): Show |
16 | HG00544.hp2 HG00558.hp1 HG01516.hp2 others(13): Show |
intron_variant | MODIFIER | c.777-1018_777-1009d others(12): Show |
TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr22 | 39420775 | ||||||
| chr22:39420775 | C | CTGTGTGT others(5): Show |
2 | a0001c0001t0001g0176 a0001c0012t0001g0098 |
2 | HG02083.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.777-1020_777-1009d others(14): Show |
TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr22 | 39420775 | ||||||
| chr22:39420775 | CTG | C | 21 | a0001c0001t0001g0065 a0001c0001t0001g0084 a0001c0001t0001g0126 others(18): Show |
25 | HG00544.hp1 HG00621.hp1 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.777-1010_777-1009d others(4): Show |
TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr22 | 39420775 | ||||||
| chr22:39420775 | CTGTG | C | 4 | a0001c0001t0001g0085 a0001c0001t0003g0250 a0001c0001t0003g0251 others(1): Show |
4 | HG01168.hp2 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.777-1012_777-1009d others(6): Show |
TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr22 | 39420775 | ||||||
| chr22:39420775 | CTGTGTG | C | 4 | a0001c0001t0001g0200 a0001c0001t0001g0202 a0002c0003t0001g0102 others(1): Show |
4 | HG03486.hp1 NA18947.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.777-1014_777-1009d others(8): Show |
TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr22 | 39420775 | ||||||
| chr22:39420775 | CTGTGTGT others(1): Show |
C | 3 | a0001c0001t0001g0073 a0001c0001t0001g0086 a0001c0001t0001g0112 |
3 | HG01099.hp2 HG03688.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.777-1016_777-1009d others(10): Show |
TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr22 | 39420775 | ||||||
| chr22:39420777 | G | C | 1 | a0001c0001t0001g0137 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.777-1050G>C | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 7/10 | chr22 | 39420777 | |||||||
| chr22:39420818 | T | TGTGTG | 4 | a0001c0001t0001g0139 a0001c0001t0001g0142 a0001c0001t0001g0188 others(1): Show |
4 | HG01361.hp1 HG01361.hp2 HG02074.hp2 others(1): Show |
intron_variant | MODIFIER | c.777-1009_777-1008i others(7): Show |
TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 7/10 | chr22 | 39420818 | |||||||
| chr22:39420818 | T | TGTGTGTG others(6): Show |
1 | a0001c0001t0001g0034 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.777-1009_777-1008i others(15): Show |
TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 7/10 | chr22 | 39420818 | |||||||
| chr22:39420819 | T | G | 13 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0108 others(10): Show |
13 | HG00280.hp2 HG01069.hp2 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.777-1008T>G | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 7/10 | chr22 | 39420819 | |||||||
| chr22:39420823 | C | T | 11 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0108 others(8): Show |
11 | HG01069.hp2 HG01358.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.777-1004C>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 7/10 | chr22 | 39420823 | |||||||
| chr22:39420853 | G | A | 1 | a0001c0001t0001g0049 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.777-974G>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 7/10 | chr22 | 39420853 | |||||||
| chr22:39420874 | GTC | G | 3 | a0001c0001t0001g0227 a0001c0001t0003g0255 a0001c0002t0012g0109 |
3 | HG02257.hp2 HG02965.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.777-945_777-944del others(2): Show |
TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr22 | 39420874 | ||||||
| chr22:39420878 | CTCTCTGT others(15): Show |
C | 1 | a0005c0007t0008g0267 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.777-947_777-926del others(22): Show |
TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr22 | 39420878 | ||||||
| chr22:39420880 | C | CTGTG | 8 | a0001c0001t0003g0006 a0001c0001t0003g0248 a0001c0001t0003g0249 others(5): Show |
11 | HG02280.hp2 HG02572.hp2 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.777-946_777-945ins others(4): Show |
TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr22 | 39420880 | ||||||
| chr22:39420880 | C | CTGTGTGT others(3): Show |
1 | a0001c0001t0003g0022 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.777-946_777-945ins others(10): Show |
TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr22 | 39420880 | ||||||
| chr22:39420880 | CTCTGTGT others(3): Show |
C | 1 | a0001c0001t0001g0170 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.777-945_777-936del others(10): Show |
TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr22 | 39420880 | ||||||
| chr22:39420882 | C | CTCTGTGT others(3): Show |
1 | a0001c0001t0001g0177 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.777-944_777-943ins others(10): Show |
TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr22 | 39420882 | ||||||
| chr22:39420882 | C | CTCTGTGT others(7): Show |
2 | a0001c0001t0001g0176 a0001c0001t0001g0178 |
2 | NA18906.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.777-944_777-943ins others(14): Show |
TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr22 | 39420882 | ||||||
| chr22:39420882 | C | CTG | 53 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(50): Show |
62 | HG00741.hp1 HG01074.hp2 HG01168.hp1 others(59): Show |
intron_variant | MODIFIER | c.777-901_777-900dup others(2): Show |
TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr22 | 39420882 | ||||||
| chr22:39420882 | C | CTGTG | 22 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0023 others(19): Show |
22 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(19): Show |
intron_variant | MODIFIER | c.777-903_777-900dup others(4): Show |
TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr22 | 39420882 | ||||||
| chr22:39420882 | C | CTGTGTG | 28 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0025 others(25): Show |
32 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(29): Show |
intron_variant | MODIFIER | c.777-905_777-900dup others(6): Show |
TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr22 | 39420882 | ||||||
| chr22:39420882 | C | CTGTGTGT others(1): Show |
10 | a0001c0001t0001g0024 a0001c0001t0001g0163 a0001c0001t0001g0186 others(7): Show |
10 | HG00423.hp2 HG01169.hp2 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.777-907_777-900dup others(8): Show |
TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr22 | 39420882 | ||||||
| chr22:39420882 | C | CTGTGTGT others(3): Show |
5 | a0001c0001t0001g0162 a0001c0001t0001g0187 a0001c0001t0001g0200 others(2): Show |
5 | HG00639.hp1 HG02015.hp2 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.777-909_777-900dup others(10): Show |
TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr22 | 39420882 | ||||||
| chr22:39420882 | C | CTGTGTGT others(9): Show |
1 | a0002c0005t0001g0021 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.777-915_777-900dup others(16): Show |
TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr22 | 39420882 | ||||||
| chr22:39420882 | C | G | 15 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0003g0006 others(12): Show |
19 | HG01243.hp2 HG02280.hp1 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.777-945C>G | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 7/10 | chr22 | 39420882 | |||||||
| chr22:39420882 | CTG | C | 14 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0085 others(11): Show |
15 | HG00741.hp2 HG01109.hp2 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.777-901_777-900del others(2): Show |
TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr22 | 39420882 | ||||||
| chr22:39420882 | CTGTG | C | 16 | a0001c0001t0001g0007 a0001c0001t0001g0058 a0001c0001t0001g0063 others(13): Show |
17 | HG00140.hp2 HG00597.hp1 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.777-903_777-900del others(4): Show |
TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr22 | 39420882 | ||||||
| chr22:39420882 | CTGTGTGT others(3): Show |
C | 3 | a0001c0001t0001g0016 a0001c0001t0001g0171 a0001c0011t0001g0120 |
4 | HG01496.hp2 HG02109.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.777-909_777-900del others(10): Show |
TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr22 | 39420882 | ||||||
| chr22:39420882 | CTGTGTGT others(15): Show |
C | 7 | a0001c0002t0004g0258 a0001c0002t0004g0259 a0001c0002t0004g0260 others(4): Show |
7 | HG02129.hp1 NA18945.hp2 NA18951.hp1 others(4): Show |
intron_variant | MODIFIER | c.777-921_777-900del others(22): Show |
TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr22 | 39420882 | ||||||
| chr22:39420900 | G | C | 1 | a0001c0001t0001g0231 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.777-927G>C | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 7/10 | chr22 | 39420900 | |||||||
| chr22:39420903 | T | G | 1 | a0001c0001t0001g0094 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.777-924T>G | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 7/10 | chr22 | 39420903 | |||||||
| chr22:39420917 | T | A | 2 | a0001c0001t0001g0036 a0001c0001t0001g0074 |
2 | HG00544.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.777-910T>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 7/10 | chr22 | 39420917 | |||||||
| chr22:39420927 | T | TGTG | 3 | a0001c0001t0001g0068 a0001c0001t0001g0139 a0001c0001t0001g0149 |
3 | HG01361.hp1 HG03927.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.777-900_777-899ins others(3): Show |
TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 7/10 | chr22 | 39420927 | |||||||
| chr22:39420927 | T | TGTGTGTG others(4): Show |
1 | a0002c0003t0001g0243 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.777-900_777-899ins others(11): Show |
TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 7/10 | chr22 | 39420927 | |||||||
| chr22:39420928 | T | G | 4 | a0001c0001t0001g0148 a0001c0001t0001g0155 a0001c0001t0001g0183 others(1): Show |
4 | HG00280.hp1 HG00280.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.777-899T>G | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 7/10 | chr22 | 39420928 | |||||||
| chr22:39420967 | ACCCAGGT others(19): Show |
A | 13 | a0001c0001t0002g0208 a0001c0001t0003g0251 a0001c0001t0007g0204 others(10): Show |
13 | HG00639.hp2 HG02129.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.777-785_777-760del others(26): Show |
TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr22 | 39420967 | ||||||
| chr22:39421012 | C | A | 80 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(77): Show |
95 | HG00099.hp1 HG00423.hp1 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.777-815C>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 7/10 | chr22 | 39421012 | |||||||
| chr22:39421012 | C | G | 133 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(130): Show |
148 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.777-815C>G | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 7/10 | chr22 | 39421012 | |||||||
| chr22:39421042 | C | T | 1 | a0001c0001t0001g0048 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.777-785C>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 7/10 | chr22 | 39421042 | |||||||
| chr22:39421055 | T | G | 1 | a0002c0005t0001g0234 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.777-772T>G | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 7/10 | chr22 | 39421055 | |||||||
| chr22:39421138 | C | G | 2 | a0001c0001t0002g0265 a0001c0001t0002g0266 |
2 | HG02886.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.777-689C>G | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 7/10 | chr22 | 39421138 | |||||||
| chr22:39421156 | T | G | 7 | a0001c0002t0004g0258 a0001c0002t0004g0259 a0001c0002t0004g0260 others(4): Show |
7 | HG02129.hp1 NA18945.hp2 NA18951.hp1 others(4): Show |
intron_variant | MODIFIER | c.777-671T>G | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 7/10 | chr22 | 39421156 | |||||||
| chr22:39421225 | A | G | 1 | a0001c0001t0002g0127 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.777-602A>G | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 7/10 | chr22 | 39421225 | |||||||
| chr22:39421308 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.777-519G>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 7/10 | chr22 | 39421308 | |||||||
| chr22:39421619 | T | G | 3 | a0001c0001t0001g0011 a0001c0001t0001g0024 a0001c0001t0001g0025 |
4 | HG01081.hp1 HG01167.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.777-208T>G | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 7/10 | chr22 | 39421619 | |||||||
| chr22:39421747 | A | G | 1 | a0001c0001t0001g0144 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.777-80A>G | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 7/10 | chr22 | 39421747 | |||||||
| chr22:39422295 | A | G | 1 | a0001c0001t0001g0049 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.921+324A>G | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 8/10 | chr22 | 39422295 | |||||||
| chr22:39422400 | C | CT | 27 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0036 others(24): Show |
29 | HG01175.hp1 HG01884.hp1 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.921+455dupT | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr22 | 39422400 | ||||||
| chr22:39422400 | C | CTTTT | 8 | a0001c0001t0002g0018 a0001c0001t0002g0127 a0001c0001t0002g0128 others(5): Show |
9 | HG00140.hp2 HG00639.hp2 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.921+452_921+455dup others(4): Show |
TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr22 | 39422400 | ||||||
| chr22:39422400 | CT | C | 30 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0001g0026 others(27): Show |
34 | HG01069.hp2 HG01243.hp2 HG01257.hp2 others(31): Show |
intron_variant | MODIFIER | c.921+455delT | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr22 | 39422400 | ||||||
| chr22:39422466 | T | C | 1 | a0001c0001t0001g0223 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.921+495T>C | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 8/10 | chr22 | 39422466 | |||||||
| chr22:39422686 | C | T | 7 | a0001c0002t0004g0258 a0001c0002t0004g0259 a0001c0002t0004g0260 others(4): Show |
7 | HG02129.hp1 NA18945.hp2 NA18951.hp1 others(4): Show |
intron_variant | MODIFIER | c.921+715C>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 8/10 | chr22 | 39422686 | |||||||
| chr22:39422693 | G | A | 2 | a0001c0001t0002g0265 a0001c0001t0002g0266 |
2 | HG02886.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.921+722G>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 8/10 | chr22 | 39422693 | |||||||
| chr22:39422722 | G | A | 7 | a0001c0002t0004g0258 a0001c0002t0004g0259 a0001c0002t0004g0260 others(4): Show |
7 | HG02129.hp1 NA18945.hp2 NA18951.hp1 others(4): Show |
intron_variant | MODIFIER | c.921+751G>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 8/10 | chr22 | 39422722 | |||||||
| chr22:39422749 | G | A | 5 | a0001c0001t0003g0022 a0001c0001t0003g0252 a0001c0001t0003g0253 others(2): Show |
6 | HG01243.hp2 HG02486.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.921+778G>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 8/10 | chr22 | 39422749 | |||||||
| chr22:39422788 | A | G | 7 | a0001c0002t0004g0258 a0001c0002t0004g0259 a0001c0002t0004g0260 others(4): Show |
7 | HG02129.hp1 NA18945.hp2 NA18951.hp1 others(4): Show |
intron_variant | MODIFIER | c.921+817A>G | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 8/10 | chr22 | 39422788 | |||||||
| chr22:39422978 | C | CT | 17 | a0001c0001t0001g0093 a0001c0001t0001g0176 a0001c0001t0001g0177 others(14): Show |
21 | HG01243.hp2 HG01884.hp2 HG02280.hp2 others(18): Show |
intron_variant | MODIFIER | c.921+1025dupT | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr22 | 39422978 | ||||||
| chr22:39422978 | CT | C | 10 | a0001c0001t0001g0038 a0001c0001t0001g0051 a0001c0001t0001g0065 others(7): Show |
10 | HG01069.hp1 HG02735.hp1 HG03041.hp1 others(7): Show |
intron_variant | MODIFIER | c.921+1025delT | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr22 | 39422978 | ||||||
| chr22:39422978 | CTT | C | 7 | a0001c0002t0004g0258 a0001c0002t0004g0259 a0001c0002t0004g0260 others(4): Show |
7 | HG02129.hp1 NA18945.hp2 NA18951.hp1 others(4): Show |
intron_variant | MODIFIER | c.921+1024_921+1025d others(4): Show |
TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr22 | 39422978 | ||||||
| chr22:39422996 | T | A | 1 | a0001c0001t0001g0149 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.921+1025T>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 8/10 | chr22 | 39422996 | |||||||
| chr22:39423003 | T | C | 245 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(242): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.921+1032T>C | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 8/10 | chr22 | 39423003 | |||||||
| chr22:39423044 | G | C | 245 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(242): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.921+1073G>C | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 8/10 | chr22 | 39423044 | |||||||
| chr22:39423194 | C | T | 1 | a0005c0007t0008g0267 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.921+1223C>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 8/10 | chr22 | 39423194 | |||||||
| chr22:39423519 | C | T | 1 | a0001c0001t0003g0255 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.921+1548C>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 8/10 | chr22 | 39423519 | |||||||
| chr22:39423584 | A | G | 8 | a0001c0002t0004g0258 a0001c0002t0004g0259 a0001c0002t0004g0260 others(5): Show |
8 | HG02129.hp1 NA18945.hp2 NA18951.hp1 others(5): Show |
intron_variant | MODIFIER | c.921+1613A>G | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 8/10 | chr22 | 39423584 | |||||||
| chr22:39423755 | C | T | 1 | a0001c0001t0001g0050 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.921+1784C>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 8/10 | chr22 | 39423755 | |||||||
| chr22:39423757 | G | GTAGCATA others(3821): Show |
1 | a0001c0002t0004g0260 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.921+1789_921+1790i others(3830): Show |
TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr22 | 39423757 | ||||||
| chr22:39423757 | G | GTAGCATA others(3788): Show |
1 | a0001c0002t0004g0258 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.921+1789_921+1790i others(3797): Show |
TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr22 | 39423757 | ||||||
| chr22:39423757 | G | GTAGCATA others(3755): Show |
1 | a0001c0002t0004g0259 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.921+1789_921+1790i others(3764): Show |
TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr22 | 39423757 | ||||||
| chr22:39423757 | G | GTAGCATA others(3755): Show |
1 | a0001c0002t0004g0261 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.921+1789_921+1790i others(3764): Show |
TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr22 | 39423757 | ||||||
| chr22:39423757 | G | GTAGCATA others(3623): Show |
1 | a0001c0002t0004g0263 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.921+1789_921+1790i others(3632): Show |
TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr22 | 39423757 | ||||||
| chr22:39423757 | G | GTAGCATA others(3953): Show |
1 | a0001c0002t0004g0264 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.921+1789_921+1790i others(3962): Show |
TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr22 | 39423757 | ||||||
| chr22:39423757 | G | GTAGCGTA others(1181): Show |
1 | a0005c0007t0008g0267 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.921+1789_921+1790i others(1190): Show |
TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr22 | 39423757 | ||||||
| chr22:39423761 | T | C | 6 | a0001c0002t0004g0258 a0001c0002t0004g0259 a0001c0002t0004g0260 others(3): Show |
6 | NA18945.hp2 NA18951.hp1 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.921+1790T>C | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 8/10 | chr22 | 39423761 | |||||||
| chr22:39423762 | G | A | 1 | a0001c0002t0004g0262 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.921+1791G>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 8/10 | chr22 | 39423762 | |||||||
| chr22:39423766 | A | G | 7 | a0001c0002t0004g0258 a0001c0002t0004g0259 a0001c0002t0004g0260 others(4): Show |
7 | HG02129.hp1 NA18951.hp1 NA18979.hp1 others(4): Show |
intron_variant | MODIFIER | c.921+1795A>G | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 8/10 | chr22 | 39423766 | |||||||
| chr22:39423773 | G | C | 1 | a0001c0002t0004g0262 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.921+1802G>C | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 8/10 | chr22 | 39423773 | |||||||
| chr22:39423794 | T | C | 1 | a0001c0002t0004g0262 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.921+1823T>C | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 8/10 | chr22 | 39423794 | |||||||
| chr22:39423799 | A | G | 7 | a0001c0002t0004g0258 a0001c0002t0004g0259 a0001c0002t0004g0260 others(4): Show |
7 | HG02129.hp1 NA18951.hp1 NA18979.hp1 others(4): Show |
intron_variant | MODIFIER | c.921+1828A>G | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 8/10 | chr22 | 39423799 | |||||||
| chr22:39423806 | C | G | 22 | a0001c0001t0002g0265 a0001c0001t0002g0266 a0001c0001t0003g0006 others(19): Show |
25 | HG00673.hp1 HG02083.hp1 HG02129.hp1 others(22): Show |
intron_variant | MODIFIER | c.921+1835C>G | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 8/10 | chr22 | 39423806 | |||||||
| chr22:39423827 | T | C | 1 | a0001c0002t0004g0262 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.921+1856T>C | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 8/10 | chr22 | 39423827 | |||||||
| chr22:39423832 | A | ATTGTAAG others(3755): Show |
1 | a0001c0002t0004g0262 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.921+1867_921+1868i others(3764): Show |
TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr22 | 39423832 | ||||||
| chr22:39423832 | A | G | 7 | a0001c0002t0004g0258 a0001c0002t0004g0259 a0001c0002t0004g0260 others(4): Show |
7 | HG02129.hp1 NA18951.hp1 NA18979.hp1 others(4): Show |
intron_variant | MODIFIER | c.921+1861A>G | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 8/10 | chr22 | 39423832 | |||||||
| chr22:39423839 | C | G | 7 | a0001c0002t0004g0258 a0001c0002t0004g0259 a0001c0002t0004g0260 others(4): Show |
7 | HG02129.hp1 NA18945.hp2 NA18951.hp1 others(4): Show |
intron_variant | MODIFIER | c.921+1868C>G | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 8/10 | chr22 | 39423839 | |||||||
| chr22:39423865 | A | G | 8 | a0001c0002t0004g0258 a0001c0002t0004g0259 a0001c0002t0004g0260 others(5): Show |
8 | HG02129.hp1 NA18945.hp2 NA18951.hp1 others(5): Show |
intron_variant | MODIFIER | c.921+1894A>G | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 8/10 | chr22 | 39423865 | |||||||
| chr22:39423872 | C | G | 7 | a0001c0002t0004g0258 a0001c0002t0004g0259 a0001c0002t0004g0260 others(4): Show |
7 | HG02129.hp1 NA18945.hp2 NA18951.hp1 others(4): Show |
intron_variant | MODIFIER | c.921+1901C>G | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 8/10 | chr22 | 39423872 | |||||||
| chr22:39423898 | A | G | 9 | a0001c0001t0001g0203 a0001c0002t0004g0258 a0001c0002t0004g0259 others(6): Show |
9 | HG02056.hp1 HG02129.hp1 NA18945.hp2 others(6): Show |
intron_variant | MODIFIER | c.921+1927A>G | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 8/10 | chr22 | 39423898 | |||||||
| chr22:39423905 | C | G | 7 | a0001c0002t0004g0258 a0001c0002t0004g0259 a0001c0002t0004g0260 others(4): Show |
7 | NA18945.hp2 NA18951.hp1 NA18979.hp1 others(4): Show |
intron_variant | MODIFIER | c.921+1934C>G | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 8/10 | chr22 | 39423905 | |||||||
| chr22:39423938 | C | G | 8 | a0001c0002t0004g0258 a0001c0002t0004g0259 a0001c0002t0004g0260 others(5): Show |
8 | HG02129.hp1 NA18945.hp2 NA18951.hp1 others(5): Show |
intron_variant | MODIFIER | c.921+1967C>G | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 8/10 | chr22 | 39423938 | |||||||
| chr22:39423964 | A | G | 227 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(224): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.921+1993A>G | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 8/10 | chr22 | 39423964 | |||||||
| chr22:39423994 | A | G | 7 | a0001c0002t0004g0258 a0001c0002t0004g0259 a0001c0002t0004g0260 others(4): Show |
7 | HG02129.hp1 NA18945.hp2 NA18951.hp1 others(4): Show |
intron_variant | MODIFIER | c.921+2023A>G | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 8/10 | chr22 | 39423994 | |||||||
| chr22:39424000 | A | C | 8 | a0001c0002t0004g0258 a0001c0002t0004g0259 a0001c0002t0004g0260 others(5): Show |
8 | HG02129.hp1 NA18945.hp2 NA18951.hp1 others(5): Show |
intron_variant | MODIFIER | c.921+2029A>C | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 8/10 | chr22 | 39424000 | |||||||
| chr22:39424138 | C | T | 1 | a0005c0007t0008g0267 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.921+2167C>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 8/10 | chr22 | 39424138 | |||||||
| chr22:39424324 | C | T | 1 | a0001c0001t0003g0252 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.921+2353C>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 8/10 | chr22 | 39424324 | |||||||
| chr22:39424438 | C | CT | 18 | a0001c0001t0001g0093 a0001c0001t0001g0134 a0001c0001t0001g0190 others(15): Show |
18 | HG01106.hp1 HG01192.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.922-2241dupT | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr22 | 39424438 | ||||||
| chr22:39424438 | CT | C | 26 | a0001c0001t0001g0028 a0001c0001t0001g0050 a0001c0001t0001g0052 others(23): Show |
26 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(23): Show |
intron_variant | MODIFIER | c.922-2241delT | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr22 | 39424438 | ||||||
| chr22:39424548 | C | A | 1 | a0001c0001t0001g0200 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.922-2155C>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 8/10 | chr22 | 39424548 | |||||||
| chr22:39424597 | A | G | 1 | a0005c0007t0008g0267 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.922-2106A>G | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 8/10 | chr22 | 39424597 | |||||||
| chr22:39424739 | C | T | 17 | a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0132 others(14): Show |
20 | HG01175.hp2 HG01884.hp1 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.922-1964C>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 8/10 | chr22 | 39424739 | |||||||
| chr22:39424795 | G | T | 7 | a0001c0001t0002g0265 a0001c0001t0002g0266 a0001c0001t0007g0204 others(4): Show |
7 | HG02257.hp2 HG02280.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.922-1908G>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 8/10 | chr22 | 39424795 | |||||||
| chr22:39424825 | T | C | 2 | a0001c0001t0001g0140 a0001c0001t0001g0143 |
2 | HG02109.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.922-1878T>C | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 8/10 | chr22 | 39424825 | |||||||
| chr22:39424880 | A | G | 233 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(230): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.922-1823A>G | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 8/10 | chr22 | 39424880 | |||||||
| chr22:39424917 | A | G | 1 | a0001c0001t0013g0083 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.922-1786A>G | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 8/10 | chr22 | 39424917 | |||||||
| chr22:39425092 | GCTGGGCG others(38): Show |
G | 1 | a0001c0001t0001g0118 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.922-1610_922-1566d others(47): Show |
TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 8/10 | chr22 | 39425092 | |||||||
| chr22:39425144 | G | A | 15 | a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0133 others(12): Show |
18 | HG01175.hp2 HG01884.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.922-1559G>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 8/10 | chr22 | 39425144 | |||||||
| chr22:39425162 | C | T | 1 | a0001c0001t0001g0172 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.922-1541C>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 8/10 | chr22 | 39425162 | |||||||
| chr22:39425218 | C | CA | 18 | a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0026 others(15): Show |
21 | HG01069.hp2 HG01175.hp2 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.922-1470dupA | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr22 | 39425218 | ||||||
| chr22:39425218 | CA | C | 6 | a0001c0001t0001g0126 a0001c0001t0001g0201 a0001c0001t0001g0202 others(3): Show |
6 | HG02056.hp1 HG02280.hp2 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.922-1470delA | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr22 | 39425218 | ||||||
| chr22:39425314 | T | C | 244 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(241): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.922-1389T>C | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 8/10 | chr22 | 39425314 | |||||||
| chr22:39425321 | T | G | 1 | a0001c0001t0001g0069 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.922-1382T>G | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 8/10 | chr22 | 39425321 | |||||||
| chr22:39425412 | A | G | 5 | a0001c0001t0001g0126 a0001c0001t0001g0200 a0001c0001t0001g0201 others(2): Show |
5 | HG02056.hp1 HG03486.hp1 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.922-1291A>G | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 8/10 | chr22 | 39425412 | |||||||
| chr22:39425428 | A | G | 5 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0192 others(2): Show |
5 | HG02135.hp2 HG02155.hp2 NA18953.hp1 others(2): Show |
intron_variant | MODIFIER | c.922-1275A>G | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 8/10 | chr22 | 39425428 | |||||||
| chr22:39425531 | A | G | 233 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(230): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.922-1172A>G | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 8/10 | chr22 | 39425531 | |||||||
| chr22:39425636 | A | G | 245 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(242): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.922-1067A>G | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 8/10 | chr22 | 39425636 | |||||||
| chr22:39425642 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.922-1061C>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 8/10 | chr22 | 39425642 | |||||||
| chr22:39425695 | C | T | 1 | a0001c0001t0001g0124 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.922-1008C>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 8/10 | chr22 | 39425695 | |||||||
| chr22:39425708 | G | A | 52 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(49): Show |
63 | HG00099.hp1 HG00544.hp2 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.922-995G>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 8/10 | chr22 | 39425708 | |||||||
| chr22:39425841 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.922-862C>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 8/10 | chr22 | 39425841 | |||||||
| chr22:39425873 | C | CT | 11 | a0001c0001t0001g0066 a0001c0001t0001g0136 a0001c0001t0002g0106 others(8): Show |
11 | HG02074.hp2 HG02559.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.922-813dupT | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr22 | 39425873 | ||||||
| chr22:39425993 | G | A | 2 | a0001c0001t0001g0153 a0001c0001t0001g0154 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.922-710G>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 8/10 | chr22 | 39425993 | |||||||
| chr22:39426090 | C | T | 1 | a0001c0001t0001g0151 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.922-613C>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 8/10 | chr22 | 39426090 | |||||||
| chr22:39426111 | A | G | 218 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(215): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.922-592A>G | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 8/10 | chr22 | 39426111 | |||||||
| chr22:39426140 | C | T | 2 | a0001c0001t0007g0204 a0001c0001t0007g0247 |
2 | HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.922-563C>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 8/10 | chr22 | 39426140 | |||||||
| chr22:39426141 | A | G | 2 | a0001c0001t0007g0204 a0001c0001t0007g0247 |
2 | HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.922-562A>G | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 8/10 | chr22 | 39426141 | |||||||
| chr22:39426154 | C | T | 7 | a0001c0002t0004g0258 a0001c0002t0004g0259 a0001c0002t0004g0260 others(4): Show |
7 | HG02129.hp1 NA18945.hp2 NA18951.hp1 others(4): Show |
intron_variant | MODIFIER | c.922-549C>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 8/10 | chr22 | 39426154 | |||||||
| chr22:39426425 | CGTATTCA others(15): Show |
C | 2 | a0001c0001t0001g0147 a0001c0001t0001g0230 |
2 | HG03139.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.922-275_922-254del others(22): Show |
TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr22 | 39426425 | ||||||
| chr22:39426456 | C | T | 1 | a0001c0001t0001g0049 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.922-247C>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 8/10 | chr22 | 39426456 | |||||||
| chr22:39426624 | T | A | 1 | a0001c0001t0002g0211 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.922-79T>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 8/10 | chr22 | 39426624 | |||||||
| chr22:39426648 | T | C | 2 | a0001c0001t0001g0023 a0001c0001t0001g0221 |
2 | HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.922-55T>C | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 8/10 | chr22 | 39426648 | |||||||
| chr22:39426933 | T | C | 1 | a0001c0001t0001g0078 | 1 | NA19064.hp2 | splice_region_variant&intron_variant | LOW | c.1144+8T>C | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 9/10 | chr22 | 39426933 | |||||||
| chr22:39426944 | C | G | 1 | a0001c0001t0001g0168 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1144+19C>G | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 9/10 | chr22 | 39426944 | |||||||
| chr22:39426967 | C | T | 2 | a0001c0001t0001g0237 a0001c0001t0001g0238 |
2 | HG01109.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1144+42C>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 9/10 | chr22 | 39426967 | |||||||
| chr22:39427010 | A | G | 220 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(217): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.1144+85A>G | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 9/10 | chr22 | 39427010 | |||||||
| chr22:39427217 | C | T | 6 | a0001c0001t0002g0018 a0001c0001t0002g0128 a0001c0001t0002g0210 others(3): Show |
7 | HG01070.hp2 HG01192.hp2 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.1144+292C>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 9/10 | chr22 | 39427217 | |||||||
| chr22:39427426 | G | A | 2 | a0001c0001t0002g0265 a0001c0001t0002g0266 |
2 | HG02886.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1144+501G>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 9/10 | chr22 | 39427426 | |||||||
| chr22:39427435 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1144+510G>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 9/10 | chr22 | 39427435 | |||||||
| chr22:39427611 | C | T | 1 | a0005c0007t0008g0267 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1145-410C>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 9/10 | chr22 | 39427611 | |||||||
| chr22:39427618 | G | T | 1 | a0001c0001t0001g0180 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1145-403G>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 9/10 | chr22 | 39427618 | |||||||
| chr22:39427625 | C | T | 12 | a0001c0001t0007g0204 a0001c0001t0007g0247 a0001c0002t0003g0110 others(9): Show |
12 | HG02129.hp1 HG02257.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.1145-396C>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 9/10 | chr22 | 39427625 | |||||||
| chr22:39427677 | A | G | 1 | a0001c0001t0001g0202 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1145-344A>G | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 9/10 | chr22 | 39427677 | |||||||
| chr22:39427904 | G | A | 1 | a0001c0001t0001g0032 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1145-117G>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 9/10 | chr22 | 39427904 | |||||||
| chr22:39428445 | C | T | 238 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(235): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.1307+262C>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 10/10 | chr22 | 39428445 | |||||||
| chr22:39428638 | CA | C | 7 | a0001c0002t0004g0258 a0001c0002t0004g0259 a0001c0002t0004g0260 others(4): Show |
7 | HG02129.hp1 NA18945.hp2 NA18951.hp1 others(4): Show |
intron_variant | MODIFIER | c.1307+456delA | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 10/10 | chr22 | 39428638 | |||||||
| chr22:39428702 | T | G | 246 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(243): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.1307+519T>G | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 10/10 | chr22 | 39428702 | |||||||
| chr22:39428776 | A | G | 24 | a0001c0001t0001g0014 a0001c0001t0001g0020 a0001c0001t0001g0141 others(21): Show |
30 | HG01243.hp2 HG01891.hp1 HG02280.hp2 others(27): Show |
intron_variant | MODIFIER | c.1307+593A>G | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 10/10 | chr22 | 39428776 | |||||||
| chr22:39429014 | G | A | 5 | a0001c0002t0004g0258 a0001c0002t0004g0260 a0001c0002t0004g0262 others(2): Show |
5 | HG02129.hp1 NA18945.hp2 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.1307+831G>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 10/10 | chr22 | 39429014 | |||||||
| chr22:39429020 | T | C | 5 | a0001c0002t0004g0258 a0001c0002t0004g0260 a0001c0002t0004g0262 others(2): Show |
5 | HG02129.hp1 NA18945.hp2 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.1307+837T>C | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 10/10 | chr22 | 39429020 | |||||||
| chr22:39429185 | G | A | 1 | a0001c0001t0001g0202 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1308-830G>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 10/10 | chr22 | 39429185 | |||||||
| chr22:39429317 | T | G | 221 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(218): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.1308-698T>G | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 10/10 | chr22 | 39429317 | |||||||
| chr22:39429374 | C | G | 3 | a0001c0002t0003g0110 a0001c0002t0003g0111 a0001c0002t0012g0109 |
3 | HG02257.hp2 HG02280.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1308-641C>G | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 10/10 | chr22 | 39429374 | |||||||
| chr22:39429427 | C | T | 1 | a0003c0006t0001g0101 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1308-588C>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 10/10 | chr22 | 39429427 | |||||||
| chr22:39429487 | A | T | 218 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(215): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.1308-528A>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 10/10 | chr22 | 39429487 | |||||||
| chr22:39429620 | G | T | 3 | a0001c0001t0001g0237 a0001c0001t0001g0238 a0001c0001t0001g0242 |
3 | HG01109.hp1 HG02647.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1308-395G>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 10/10 | chr22 | 39429620 | |||||||
| chr22:39429626 | C | T | 8 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0134 others(5): Show |
8 | HG02145.hp2 HG02965.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.1308-389C>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 10/10 | chr22 | 39429626 | |||||||
| chr22:39429702 | G | A | 1 | a0001c0001t0013g0083 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1308-313G>A | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 10/10 | chr22 | 39429702 | |||||||
| chr22:39429921 | G | T | 1 | a0001c0001t0001g0175 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1308-94G>T | TAB1 | ENSG00000100324.14 | transcript | ENST00000216160.11 | protein_coding | 10/10 | chr22 | 39429921 |