Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 7248 |
| ensemblid | ENSG00000165699.15 |
| hgncid | 12362 |
| symbol | TSC1 |
| name | TSC complex subunit 1 |
| refseq_nuc | NM_000368.5 |
| refseq_prot | NP_000359.1 |
| ensembl_nuc | ENST00000298552.9 |
| ensembl_prot | ENSP00000298552.3 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 132891349 |
| end | 132944616 |
| strand | - |
| ver | v1.2 |
| region | chr9:132891349-132944616 |
| region5000 | chr9:132886349-132949616 |
| regionname0 | TSC1_chr9_132891349_132944616 |
| regionname5000 | TSC1_chr9_132886349_132949616 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1164 | 277 | 61 | 51 | 133 | 6 | 24 | 100 | TSC1_chr9_132886349_132949616 | TSC1 | MAQQA others(1159): Show |
chr9 | 132886349 | 132949616 |
| a0002 | 0/0 | 1164 | 42 | 22 | 4 | 12 | 2 | 2 | 9 | TSC1_chr9_132886349_132949616 | TSC1 | MAQQA others(1159): Show |
chr9 | 132886349 | 132949616 |
| a0003 | 0/0 | 1164 | 9 | 0 | 9 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | MAQQA others(1159): Show |
chr9 | 132886349 | 132949616 |
| a0004 | 0/0 | 1164 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | MAQQA others(1159): Show |
chr9 | 132886349 | 132949616 |
| a0005 | 0/0 | 1164 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | MAQQA others(1159): Show |
chr9 | 132886349 | 132949616 |
| a0006 | 0/0 | 1164 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | MAQQA others(1159): Show |
chr9 | 132886349 | 132949616 |
| a0007 | 0/0 | 1164 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | MAQQA others(1159): Show |
chr9 | 132886349 | 132949616 |
| a0008 | 0/0 | 1164 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | MAQQA others(1159): Show |
chr9 | 132886349 | 132949616 |
| a0009 | 0/0 | 1164 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | MAQQA others(1159): Show |
chr9 | 132886349 | 132949616 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 3492 | 234 | 53 | 36 | 114 | 6 | 24 | TSC1_chr9_132886349_132949616 | TSC1 | ATGGC others(3487): Show |
chr9 | 132886349 | 132949616 | ||
| a0001c0003 | 0/1 | 3492 | 17 | 4 | 8 | 4 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | ATGGC others(3487): Show |
chr9 | 132886349 | 132949616 | ||
| a0001c0004 | 0/0 | 3492 | 9 | 0 | 0 | 9 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | ATGGC others(3487): Show |
chr9 | 132886349 | 132949616 | ||
| a0001c0006 | 0/0 | 3492 | 8 | 0 | 7 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | ATGGC others(3487): Show |
chr9 | 132886349 | 132949616 | ||
| a0001c0007 | 0/0 | 3492 | 4 | 4 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | ATGGC others(3487): Show |
chr9 | 132886349 | 132949616 | ||
| a0001c0008 | 0/0 | 3492 | 3 | 0 | 0 | 3 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | ATGGC others(3487): Show |
chr9 | 132886349 | 132949616 | ||
| a0001c0015 | 0/0 | 3492 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | ATGGC others(3487): Show |
chr9 | 132886349 | 132949616 | ||
| a0001c0018 | 0/0 | 3492 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | ATGGC others(3487): Show |
chr9 | 132886349 | 132949616 | ||
| a0002c0002 | 0/0 | 3492 | 39 | 19 | 4 | 12 | 2 | 2 | TSC1_chr9_132886349_132949616 | TSC1 | ATGGC others(3487): Show |
chr9 | 132886349 | 132949616 | ||
| a0002c0009 | 0/0 | 3492 | 2 | 2 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | ATGGC others(3487): Show |
chr9 | 132886349 | 132949616 | ||
| a0002c0013 | 0/0 | 3492 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | ATGGC others(3487): Show |
chr9 | 132886349 | 132949616 | ||
| a0003c0005 | 0/0 | 3492 | 9 | 0 | 9 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | ATGGC others(3487): Show |
chr9 | 132886349 | 132949616 | ||
| a0004c0011 | 0/0 | 3492 | 2 | 2 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | ATGGC others(3487): Show |
chr9 | 132886349 | 132949616 | ||
| a0005c0010 | 0/0 | 3492 | 2 | 2 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | ATGGC others(3487): Show |
chr9 | 132886349 | 132949616 | ||
| a0006c0012 | 0/0 | 3492 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | ATGGC others(3487): Show |
chr9 | 132886349 | 132949616 | ||
| a0007c0017 | 0/0 | 3492 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | ATGGC others(3487): Show |
chr9 | 132886349 | 132949616 | ||
| a0008c0014 | 0/0 | 3492 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | ATGGC others(3487): Show |
chr9 | 132886349 | 132949616 | ||
| a0009c0016 | 0/0 | 3492 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | ATGGC others(3487): Show |
chr9 | 132886349 | 132949616 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 8597 | 86 | 6 | 17 | 52 | 2 | 9 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8592): Show |
chr9 | 132886349 | 132949616 |
| a0001c0001t0002 | 1/0 | 8598 | 25 | 1 | 2 | 19 | 0 | 2 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8593): Show |
chr9 | 132886349 | 132949616 |
| a0001c0001t0003 | 0/0 | 8598 | 10 | 0 | 0 | 8 | 2 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8593): Show |
chr9 | 132886349 | 132949616 |
| a0001c0001t0004 | 0/0 | 8598 | 8 | 0 | 2 | 6 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8593): Show |
chr9 | 132886349 | 132949616 |
| a0001c0001t0005 | 0/0 | 8598 | 5 | 4 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8593): Show |
chr9 | 132886349 | 132949616 |
| a0001c0001t0006 | 0/0 | 8598 | 5 | 5 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8593): Show |
chr9 | 132886349 | 132949616 |
| a0001c0001t0007 | 0/0 | 8599 | 5 | 5 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8594): Show |
chr9 | 132886349 | 132949616 |
| a0001c0001t0008 | 0/0 | 8596 | 6 | 0 | 0 | 5 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8591): Show |
chr9 | 132886349 | 132949616 |
| a0001c0001t0010 | 0/0 | 8598 | 5 | 0 | 0 | 4 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8593): Show |
chr9 | 132886349 | 132949616 |
| a0001c0001t0011 | 0/0 | 8598 | 4 | 4 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8593): Show |
chr9 | 132886349 | 132949616 |
| a0001c0001t0012 | 0/0 | 8598 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8593): Show |
chr9 | 132886349 | 132949616 |
| a0001c0001t0013 | 0/0 | 8598 | 2 | 2 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8593): Show |
chr9 | 132886349 | 132949616 |
| a0001c0001t0015 | 0/0 | 8599 | 3 | 3 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8594): Show |
chr9 | 132886349 | 132949616 |
| a0001c0001t0016 | 0/0 | 8599 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8594): Show |
chr9 | 132886349 | 132949616 |
| a0001c0001t0017 | 0/0 | 8597 | 3 | 0 | 1 | 0 | 1 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8592): Show |
chr9 | 132886349 | 132949616 |
| a0001c0001t0018 | 0/0 | 8597 | 3 | 0 | 2 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8592): Show |
chr9 | 132886349 | 132949616 |
| a0001c0001t0019 | 0/0 | 8598 | 3 | 3 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8593): Show |
chr9 | 132886349 | 132949616 |
| a0001c0001t0020 | 0/0 | 8599 | 2 | 1 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8594): Show |
chr9 | 132886349 | 132949616 |
| a0001c0001t0021 | 0/0 | 8598 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8593): Show |
chr9 | 132886349 | 132949616 |
| a0001c0001t0022 | 0/0 | 8596 | 2 | 2 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8591): Show |
chr9 | 132886349 | 132949616 |
| a0001c0001t0023 | 0/0 | 8597 | 2 | 0 | 1 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8592): Show |
chr9 | 132886349 | 132949616 |
| a0001c0001t0024 | 0/0 | 8597 | 2 | 0 | 0 | 0 | 0 | 2 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8592): Show |
chr9 | 132886349 | 132949616 |
| a0001c0001t0025 | 0/0 | 8597 | 2 | 0 | 0 | 2 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8592): Show |
chr9 | 132886349 | 132949616 |
| a0001c0001t0027 | 0/0 | 8598 | 2 | 2 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8593): Show |
chr9 | 132886349 | 132949616 |
| a0001c0001t0028 | 0/0 | 8598 | 2 | 0 | 0 | 1 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8593): Show |
chr9 | 132886349 | 132949616 |
| a0001c0001t0033 | 0/0 | 8599 | 2 | 1 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8594): Show |
chr9 | 132886349 | 132949616 |
| a0001c0001t0034 | 0/0 | 8599 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8594): Show |
chr9 | 132886349 | 132949616 |
| a0001c0001t0036 | 0/0 | 8598 | 2 | 0 | 0 | 2 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8593): Show |
chr9 | 132886349 | 132949616 |
| a0001c0001t0037 | 0/0 | 8598 | 2 | 2 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8593): Show |
chr9 | 132886349 | 132949616 |
| a0001c0001t0039 | 0/0 | 8598 | 2 | 0 | 0 | 0 | 1 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8593): Show |
chr9 | 132886349 | 132949616 |
| a0001c0001t0040 | 0/0 | 8598 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8593): Show |
chr9 | 132886349 | 132949616 |
| a0001c0001t0041 | 0/0 | 8600 | 2 | 2 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8595): Show |
chr9 | 132886349 | 132949616 |
| a0001c0001t0042 | 0/0 | 8597 | 2 | 0 | 0 | 1 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8592): Show |
chr9 | 132886349 | 132949616 |
| a0001c0001t0044 | 0/0 | 8597 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8592): Show |
chr9 | 132886349 | 132949616 |
| a0001c0001t0045 | 0/0 | 8598 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8593): Show |
chr9 | 132886349 | 132949616 |
| a0001c0001t0046 | 0/0 | 8597 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8592): Show |
chr9 | 132886349 | 132949616 |
| a0001c0001t0047 | 0/0 | 8597 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8592): Show |
chr9 | 132886349 | 132949616 |
| a0001c0001t0048 | 0/0 | 8597 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8592): Show |
chr9 | 132886349 | 132949616 |
| a0001c0001t0049 | 0/0 | 8597 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8592): Show |
chr9 | 132886349 | 132949616 |
| a0001c0001t0050 | 0/0 | 8597 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8592): Show |
chr9 | 132886349 | 132949616 |
| a0001c0001t0051 | 0/0 | 8597 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8592): Show |
chr9 | 132886349 | 132949616 |
| a0001c0001t0052 | 0/0 | 8597 | 1 | 0 | 0 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8592): Show |
chr9 | 132886349 | 132949616 |
| a0001c0001t0053 | 0/0 | 8597 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8592): Show |
chr9 | 132886349 | 132949616 |
| a0001c0001t0054 | 0/0 | 8596 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8591): Show |
chr9 | 132886349 | 132949616 |
| a0001c0001t0055 | 0/0 | 8598 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8593): Show |
chr9 | 132886349 | 132949616 |
| a0001c0001t0056 | 0/0 | 8597 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8592): Show |
chr9 | 132886349 | 132949616 |
| a0001c0001t0061 | 0/0 | 8598 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8593): Show |
chr9 | 132886349 | 132949616 |
| a0001c0001t0062 | 0/0 | 8599 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8594): Show |
chr9 | 132886349 | 132949616 |
| a0001c0001t0063 | 0/0 | 8597 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8592): Show |
chr9 | 132886349 | 132949616 |
| a0001c0001t0068 | 0/0 | 8597 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8592): Show |
chr9 | 132886349 | 132949616 |
| a0001c0001t0071 | 0/0 | 8598 | 1 | 0 | 0 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8593): Show |
chr9 | 132886349 | 132949616 |
| a0001c0001t0078 | 0/0 | 8599 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8594): Show |
chr9 | 132886349 | 132949616 |
| a0001c0001t0082 | 0/0 | 8599 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8594): Show |
chr9 | 132886349 | 132949616 |
| a0001c0001t0083 | 0/0 | 8600 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8595): Show |
chr9 | 132886349 | 132949616 |
| a0001c0001t0085 | 0/0 | 8597 | 1 | 0 | 0 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8592): Show |
chr9 | 132886349 | 132949616 |
| a0001c0001t0088 | 0/0 | 8598 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8593): Show |
chr9 | 132886349 | 132949616 |
| a0001c0001t0090 | 0/0 | 8600 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8595): Show |
chr9 | 132886349 | 132949616 |
| a0001c0001t0091 | 0/0 | 8598 | 1 | 0 | 0 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8593): Show |
chr9 | 132886349 | 132949616 |
| a0001c0001t0092 | 0/0 | 8598 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8593): Show |
chr9 | 132886349 | 132949616 |
| a0001c0001t0094 | 0/0 | 8598 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8593): Show |
chr9 | 132886349 | 132949616 |
| a0001c0001t0095 | 0/0 | 8599 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8594): Show |
chr9 | 132886349 | 132949616 |
| a0001c0001t0096 | 0/0 | 8598 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8593): Show |
chr9 | 132886349 | 132949616 |
| a0001c0001t0099 | 0/0 | 8598 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8593): Show |
chr9 | 132886349 | 132949616 |
| a0001c0003t0009 | 0/0 | 8598 | 3 | 0 | 1 | 2 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8593): Show |
chr9 | 132886349 | 132949616 |
| a0001c0003t0011 | 0/0 | 8598 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8593): Show |
chr9 | 132886349 | 132949616 |
| a0001c0003t0030 | 0/0 | 8597 | 2 | 2 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8592): Show |
chr9 | 132886349 | 132949616 |
| a0001c0003t0031 | 0/0 | 8598 | 2 | 0 | 2 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8593): Show |
chr9 | 132886349 | 132949616 |
| a0001c0003t0035 | 0/0 | 8598 | 2 | 0 | 2 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8593): Show |
chr9 | 132886349 | 132949616 |
| a0001c0003t0060 | 0/0 | 8598 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8593): Show |
chr9 | 132886349 | 132949616 |
| a0001c0003t0076 | 0/0 | 8598 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8593): Show |
chr9 | 132886349 | 132949616 |
| a0001c0003t0077 | 0/0 | 8599 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8594): Show |
chr9 | 132886349 | 132949616 |
| a0001c0003t0079 | 0/0 | 8600 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8595): Show |
chr9 | 132886349 | 132949616 |
| a0001c0003t0081 | 0/0 | 8598 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8593): Show |
chr9 | 132886349 | 132949616 |
| a0001c0003t0084 | 0/1 | 8598 | 1 | 0 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8593): Show |
chr9 | 132886349 | 132949616 |
| a0001c0003t0097 | 0/0 | 8598 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8593): Show |
chr9 | 132886349 | 132949616 |
| a0001c0004t0003 | 0/0 | 8598 | 6 | 0 | 0 | 6 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8593): Show |
chr9 | 132886349 | 132949616 |
| a0001c0004t0010 | 0/0 | 8598 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8593): Show |
chr9 | 132886349 | 132949616 |
| a0001c0004t0021 | 0/0 | 8598 | 2 | 0 | 0 | 2 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8593): Show |
chr9 | 132886349 | 132949616 |
| a0001c0006t0002 | 0/0 | 8598 | 7 | 0 | 6 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8593): Show |
chr9 | 132886349 | 132949616 |
| a0001c0006t0020 | 0/0 | 8599 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8594): Show |
chr9 | 132886349 | 132949616 |
| a0001c0007t0005 | 0/0 | 8598 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8593): Show |
chr9 | 132886349 | 132949616 |
| a0001c0007t0006 | 0/0 | 8598 | 2 | 2 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8593): Show |
chr9 | 132886349 | 132949616 |
| a0001c0007t0064 | 0/0 | 8598 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8593): Show |
chr9 | 132886349 | 132949616 |
| a0001c0008t0009 | 0/0 | 8598 | 2 | 0 | 0 | 2 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8593): Show |
chr9 | 132886349 | 132949616 |
| a0001c0008t0089 | 0/0 | 8598 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8593): Show |
chr9 | 132886349 | 132949616 |
| a0001c0015t0003 | 0/0 | 8598 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8593): Show |
chr9 | 132886349 | 132949616 |
| a0001c0018t0009 | 0/0 | 8598 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8593): Show |
chr9 | 132886349 | 132949616 |
| a0002c0002t0003 | 0/0 | 8598 | 3 | 3 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8593): Show |
chr9 | 132886349 | 132949616 |
| a0002c0002t0005 | 0/0 | 8598 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8593): Show |
chr9 | 132886349 | 132949616 |
| a0002c0002t0012 | 0/0 | 8598 | 3 | 0 | 0 | 3 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8593): Show |
chr9 | 132886349 | 132949616 |
| a0002c0002t0013 | 0/0 | 8598 | 1 | 0 | 0 | 0 | 1 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8593): Show |
chr9 | 132886349 | 132949616 |
| a0002c0002t0014 | 0/0 | 8598 | 4 | 4 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8593): Show |
chr9 | 132886349 | 132949616 |
| a0002c0002t0016 | 0/0 | 8599 | 2 | 0 | 0 | 2 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8594): Show |
chr9 | 132886349 | 132949616 |
| a0002c0002t0026 | 0/0 | 8598 | 2 | 0 | 0 | 2 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8593): Show |
chr9 | 132886349 | 132949616 |
| a0002c0002t0029 | 0/0 | 8597 | 2 | 2 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8592): Show |
chr9 | 132886349 | 132949616 |
| a0002c0002t0032 | 0/0 | 8597 | 2 | 2 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8592): Show |
chr9 | 132886349 | 132949616 |
| a0002c0002t0034 | 0/0 | 8599 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8594): Show |
chr9 | 132886349 | 132949616 |
| a0002c0002t0038 | 0/0 | 8597 | 2 | 2 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8592): Show |
chr9 | 132886349 | 132949616 |
| a0002c0002t0040 | 0/0 | 8598 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8593): Show |
chr9 | 132886349 | 132949616 |
| a0002c0002t0057 | 0/0 | 8599 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8594): Show |
chr9 | 132886349 | 132949616 |
| a0002c0002t0058 | 0/0 | 8599 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8594): Show |
chr9 | 132886349 | 132949616 |
| a0002c0002t0059 | 0/0 | 8598 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8593): Show |
chr9 | 132886349 | 132949616 |
| a0002c0002t0065 | 0/0 | 8598 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8593): Show |
chr9 | 132886349 | 132949616 |
| a0002c0002t0066 | 0/0 | 8599 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8594): Show |
chr9 | 132886349 | 132949616 |
| a0002c0002t0067 | 0/0 | 8599 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8594): Show |
chr9 | 132886349 | 132949616 |
| a0002c0002t0069 | 0/0 | 8598 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8593): Show |
chr9 | 132886349 | 132949616 |
| a0002c0002t0070 | 0/0 | 8598 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8593): Show |
chr9 | 132886349 | 132949616 |
| a0002c0002t0072 | 0/0 | 8598 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8593): Show |
chr9 | 132886349 | 132949616 |
| a0002c0002t0073 | 0/0 | 8598 | 1 | 0 | 0 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8593): Show |
chr9 | 132886349 | 132949616 |
| a0002c0002t0074 | 0/0 | 8598 | 1 | 0 | 0 | 0 | 1 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8593): Show |
chr9 | 132886349 | 132949616 |
| a0002c0002t0075 | 0/0 | 8599 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8594): Show |
chr9 | 132886349 | 132949616 |
| a0002c0002t0080 | 0/0 | 8597 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8592): Show |
chr9 | 132886349 | 132949616 |
| a0002c0002t0086 | 0/0 | 8598 | 1 | 0 | 0 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8593): Show |
chr9 | 132886349 | 132949616 |
| a0002c0002t0098 | 0/0 | 8599 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8594): Show |
chr9 | 132886349 | 132949616 |
| a0002c0009t0093 | 0/0 | 8600 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8595): Show |
chr9 | 132886349 | 132949616 |
| a0002c0009t0100 | 0/0 | 8600 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8595): Show |
chr9 | 132886349 | 132949616 |
| a0002c0013t0087 | 0/0 | 8599 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8594): Show |
chr9 | 132886349 | 132949616 |
| a0003c0005t0001 | 0/0 | 8597 | 8 | 0 | 8 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8592): Show |
chr9 | 132886349 | 132949616 |
| a0003c0005t0004 | 0/0 | 8598 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8593): Show |
chr9 | 132886349 | 132949616 |
| a0004c0011t0007 | 0/0 | 8599 | 2 | 2 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8594): Show |
chr9 | 132886349 | 132949616 |
| a0005c0010t0043 | 0/0 | 8597 | 2 | 2 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8592): Show |
chr9 | 132886349 | 132949616 |
| a0006c0012t0013 | 0/0 | 8598 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8593): Show |
chr9 | 132886349 | 132949616 |
| a0007c0017t0001 | 0/0 | 8597 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8592): Show |
chr9 | 132886349 | 132949616 |
| a0008c0014t0001 | 0/0 | 8597 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8592): Show |
chr9 | 132886349 | 132949616 |
| a0009c0016t0001 | 0/0 | 8597 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | GTACG others(8592): Show |
chr9 | 132886349 | 132949616 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 10 | 0 | 4 | 3 | 0 | 3 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0001g0017 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0001g0018 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0001g0020 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0002g0007 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0002g0011 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0002g0084 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0003g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0003g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0003g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0004g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0004g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0004g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0004g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0004g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0004g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0004g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0004g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0005g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0005g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0005g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0005g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0005g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0006g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0006g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0006g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0006g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0006g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0007g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0007g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0007g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0007g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0007g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0008g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0008g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0008g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0008g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0008g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0008g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0010g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0010g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0010g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0010g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0010g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0011g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0011g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0011g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0011g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0012g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0013g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0013g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0015g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0015g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0015g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0016g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0017g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0017g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0017g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0018g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0018g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0018g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0019g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0019g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0019g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0020g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0020g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0021g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0022g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0022g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0023g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0023g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0024g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0024g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0025g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0025g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0027g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0027g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0028g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0028g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0033g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0033g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0034g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0036g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0037g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0037g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0039g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0039g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0040g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0041g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0041g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0042g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0042g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0044g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0045g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0046g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0047g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0048g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0049g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0050g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0051g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0052g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0053g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0054g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0055g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0056g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0061g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0062g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0063g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0068g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0071g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0078g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0082g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0083g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0085g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0088g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0090g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0091g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0092g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0094g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0095g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0096g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0001t0099g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0003t0009g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0003t0009g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0003t0009g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0003t0011g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0003t0030g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0003t0030g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0003t0031g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0003t0031g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0003t0035g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0003t0035g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0003t0060g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0003t0076g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0003t0077g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0003t0079g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0003t0081g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0003t0084g0283 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0003t0097g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0004t0003g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0004t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0004t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0004t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0004t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0004t0010g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0004t0021g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0004t0021g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0006t0002g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0006t0002g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0006t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0006t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0006t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0006t0020g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0007t0005g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0007t0006g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0007t0006g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0007t0064g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0008t0009g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0008t0009g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0008t0089g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0015t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0001c0018t0009g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0002c0002t0003g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0002c0002t0003g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0002c0002t0003g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0002c0002t0005g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0002c0002t0012g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0002c0002t0012g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0002c0002t0012g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0002c0002t0013g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0002c0002t0014g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0002c0002t0014g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0002c0002t0014g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0002c0002t0014g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0002c0002t0016g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0002c0002t0016g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0002c0002t0026g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0002c0002t0026g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0002c0002t0029g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0002c0002t0029g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0002c0002t0032g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0002c0002t0034g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0002c0002t0038g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0002c0002t0038g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0002c0002t0040g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0002c0002t0057g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0002c0002t0058g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0002c0002t0059g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0002c0002t0065g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0002c0002t0066g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0002c0002t0067g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0002c0002t0069g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0002c0002t0070g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0002c0002t0072g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0002c0002t0073g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0002c0002t0074g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0002c0002t0075g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0002c0002t0080g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0002c0002t0086g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0002c0002t0098g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0002c0009t0093g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0002c0009t0100g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0002c0013t0087g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0003c0005t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0003c0005t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0003c0005t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0003c0005t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0003c0005t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0003c0005t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0003c0005t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0003c0005t0004g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0004c0011t0007g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0005c0010t0043g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0005c0010t0043g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0006c0012t0013g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0007c0017t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0008c0014t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| a0009c0016t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0019 | EUR | FIN | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG00280 | hp2 | a0001 | c0001 | t0017 | g0079 | EUR | FIN | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG00323 | hp1 | a0002 | c0002 | t0074 | g0265 | EUR | FIN | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0229 | EUR | FIN | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG00408 | hp2 | a0001 | c0001 | t0025 | g0073 | EAS | CHS | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | CHS | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | CHS | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG00438 | hp1 | a0002 | c0002 | t0016 | g0242 | EAS | CHS | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG00438 | hp2 | a0001 | c0004 | t0003 | g0104 | EAS | CHS | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG00544 | hp1 | a0001 | c0004 | t0021 | g0050 | EAS | CHS | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | CHS | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG00558 | hp2 | a0002 | c0002 | t0065 | g0244 | EAS | CHS | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | CHS | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG00621 | hp2 | a0001 | c0004 | t0003 | g0063 | EAS | CHS | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG00639 | hp1 | a0002 | c0002 | t0072 | g0241 | AMR | PUR | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | CHS | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | CHS | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG00733 | hp2 | a0001 | c0001 | t0088 | g0219 | AMR | PUR | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG00735 | hp1 | a0001 | c0001 | t0082 | g0289 | AMR | PUR | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG00738 | hp2 | a0001 | c0006 | t0002 | g0012 | AMR | PUR | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG00741 | hp1 | a0001 | c0001 | t0017 | g0062 | AMR | PUR | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG00741 | hp2 | a0003 | c0005 | t0001 | g0159 | AMR | PUR | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG01071 | hp2 | a0001 | c0001 | t0047 | g0166 | AMR | PUR | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG01074 | hp1 | a0001 | c0003 | t0035 | g0299 | AMR | PUR | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG01074 | hp2 | a0003 | c0005 | t0001 | g0016 | AMR | PUR | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG01081 | hp1 | a0002 | c0002 | t0066 | g0291 | AMR | PUR | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG01099 | hp1 | a0003 | c0005 | t0001 | g0162 | AMR | PUR | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG01099 | hp2 | a0001 | c0001 | t0023 | g0181 | AMR | PUR | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG01106 | hp1 | a0001 | c0001 | t0055 | g0116 | AMR | PUR | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG01109 | hp1 | a0002 | c0002 | t0040 | g0128 | AMR | PUR | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0054 | AMR | PUR | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG01167 | hp1 | a0001 | c0001 | t0005 | g0216 | AMR | PUR | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG01168 | hp1 | a0003 | c0005 | t0001 | g0167 | AMR | PUR | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG01169 | hp2 | a0003 | c0005 | t0001 | g0178 | AMR | PUR | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG01175 | hp1 | a0001 | c0003 | t0035 | g0297 | AMR | PUR | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG01175 | hp2 | a0001 | c0001 | t0099 | g0112 | AMR | PUR | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG01192 | hp1 | a0001 | c0003 | t0031 | g0300 | AMR | PUR | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG01192 | hp2 | a0001 | c0001 | t0049 | g0171 | AMR | PUR | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG01255 | hp2 | a0002 | c0002 | t0005 | g0261 | AMR | CLM | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG01256 | hp1 | a0001 | c0001 | t0018 | g0237 | AMR | CLM | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | CLM | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG01258 | hp1 | a0001 | c0001 | t0018 | g0236 | AMR | CLM | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG01361 | hp1 | a0001 | c0001 | t0061 | g0110 | AMR | CLM | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG01433 | hp1 | a0001 | c0001 | t0083 | g0264 | AMR | CLM | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG01433 | hp2 | a0001 | c0003 | t0009 | g0276 | AMR | CLM | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG01516 | hp1 | a0001 | c0001 | t0039 | g0218 | EUR | IBS | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0194 | EUR | IBS | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG01891 | hp1 | a0002 | c0002 | t0080 | g0270 | AFR | ACB | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG01891 | hp2 | a0001 | c0001 | t0007 | g0025 | AFR | ACB | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG01928 | hp1 | a0003 | c0005 | t0001 | g0016 | AMR | PEL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG01928 | hp2 | a0001 | c0006 | t0002 | g0035 | AMR | PEL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG01934 | hp1 | a0003 | c0005 | t0001 | g0168 | AMR | PEL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG01934 | hp2 | a0001 | c0006 | t0002 | g0008 | AMR | PEL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG01952 | hp1 | a0003 | c0005 | t0001 | g0169 | AMR | PEL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG01952 | hp2 | a0001 | c0003 | t0076 | g0280 | AMR | PEL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG01978 | hp1 | a0001 | c0003 | t0079 | g0296 | AMR | PEL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG01978 | hp2 | a0001 | c0006 | t0020 | g0111 | AMR | PEL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG01981 | hp1 | a0001 | c0001 | t0004 | g0145 | AMR | PEL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG01981 | hp2 | a0003 | c0005 | t0004 | g0175 | AMR | PEL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG01993 | hp1 | a0001 | c0003 | t0081 | g0268 | AMR | PEL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG01993 | hp2 | a0001 | c0006 | t0002 | g0048 | AMR | PEL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG02004 | hp2 | a0001 | c0006 | t0002 | g0012 | AMR | PEL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | KHV | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG02027 | hp2 | a0001 | c0008 | t0009 | g0275 | EAS | KHV | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG02040 | hp2 | a0001 | c0004 | t0021 | g0069 | EAS | KHV | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG02055 | hp1 | a0001 | c0007 | t0064 | g0294 | AFR | ACB | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG02056 | hp2 | a0001 | c0004 | t0003 | g0051 | EAS | KHV | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG02071 | hp2 | a0001 | c0001 | t0050 | g0193 | EAS | KHV | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | KHV | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | KHV | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | KHV | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG02080 | hp2 | a0001 | c0008 | t0089 | g0287 | EAS | KHV | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG02129 | hp1 | a0001 | c0008 | t0009 | g0094 | EAS | KHV | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG02129 | hp2 | a0002 | c0002 | t0069 | g0243 | EAS | KHV | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG02132 | hp2 | a0001 | c0004 | t0003 | g0052 | EAS | KHV | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG02145 | hp1 | a0001 | c0001 | t0006 | g0200 | AFR | ACB | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG02145 | hp2 | a0001 | c0001 | t0005 | g0214 | AFR | ACB | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | CDX | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | CDX | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG02257 | hp1 | a0002 | c0002 | t0014 | g0247 | AFR | ACB | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG02258 | hp1 | a0002 | c0002 | t0029 | g0269 | AFR | ACB | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG02258 | hp2 | a0001 | c0001 | t0053 | g0117 | AFR | ACB | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG02273 | hp1 | a0001 | c0003 | t0031 | g0298 | AMR | PEL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG02273 | hp2 | a0001 | c0001 | t0004 | g0138 | AMR | PEL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG02280 | hp1 | a0002 | c0002 | t0014 | g0250 | AFR | ACB | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG02280 | hp2 | a0001 | c0001 | t0011 | g0030 | AFR | ACB | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PEL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG02293 | hp2 | a0001 | c0006 | t0002 | g0008 | AMR | PEL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG02451 | hp1 | a0002 | c0002 | t0003 | g0251 | AFR | ACB | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG02451 | hp2 | a0001 | c0001 | t0006 | g0195 | AFR | ACB | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG02572 | hp1 | a0002 | c0002 | t0038 | g0302 | AFR | GWD | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG02572 | hp2 | a0001 | c0001 | t0056 | g0118 | AFR | GWD | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG02602 | hp2 | a0001 | c0001 | t0039 | g0217 | SAS | PJL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG02615 | hp1 | a0001 | c0003 | t0030 | g0274 | AFR | GWD | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG02615 | hp2 | a0001 | c0001 | t0011 | g0089 | AFR | GWD | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG02630 | hp1 | a0002 | c0002 | t0014 | g0248 | AFR | GWD | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG02630 | hp2 | a0002 | c0002 | t0038 | g0301 | AFR | GWD | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG02647 | hp1 | a0001 | c0001 | t0005 | g0033 | AFR | GWD | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0075 | AFR | GWD | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG02723 | hp1 | a0002 | c0002 | t0032 | g0021 | AFR | GWD | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG02723 | hp2 | a0001 | c0001 | t0068 | g0273 | AFR | GWD | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG02735 | hp1 | a0001 | c0001 | t0028 | g0065 | SAS | PJL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG02735 | hp2 | a0002 | c0002 | t0073 | g0240 | SAS | PJL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG02738 | hp1 | a0001 | c0001 | t0091 | g0098 | SAS | PJL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG02809 | hp1 | a0001 | c0001 | t0005 | g0215 | AFR | GWD | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG02809 | hp2 | a0002 | c0002 | t0032 | g0021 | AFR | GWD | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG02818 | hp1 | a0001 | c0003 | t0060 | g0278 | AFR | GWD | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG02818 | hp2 | a0001 | c0001 | t0015 | g0272 | AFR | GWD | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG02886 | hp1 | a0001 | c0001 | t0034 | g0024 | AFR | GWD | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG02886 | hp2 | a0001 | c0001 | t0019 | g0080 | AFR | GWD | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG02895 | hp1 | a0001 | c0001 | t0062 | g0031 | AFR | GWD | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG02895 | hp2 | a0002 | c0002 | t0003 | g0254 | AFR | GWD | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG02896 | hp1 | a0001 | c0001 | t0011 | g0114 | AFR | GWD | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG02896 | hp2 | a0004 | c0011 | t0007 | g0005 | AFR | GWD | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG02897 | hp1 | a0004 | c0011 | t0007 | g0005 | AFR | GWD | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG02897 | hp2 | a0002 | c0002 | t0003 | g0253 | AFR | GWD | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG02965 | hp1 | a0001 | c0001 | t0041 | g0113 | AFR | ESN | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG02965 | hp2 | a0001 | c0001 | t0015 | g0036 | AFR | ESN | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG02970 | hp1 | a0001 | c0001 | t0015 | g0037 | AFR | ESN | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG02970 | hp2 | a0001 | c0001 | t0027 | g0227 | AFR | ESN | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG02976 | hp1 | a0001 | c0001 | t0090 | g0074 | AFR | ESN | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG02976 | hp2 | a0002 | c0002 | t0029 | g0271 | AFR | ESN | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG03017 | hp1 | a0001 | c0001 | t0071 | g0091 | SAS | PJL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG03041 | hp1 | a0001 | c0007 | t0006 | g0198 | AFR | GWD | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG03041 | hp2 | a0001 | c0001 | t0054 | g0115 | AFR | GWD | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG03098 | hp1 | a0001 | c0001 | t0007 | g0101 | AFR | MSL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG03098 | hp2 | a0001 | c0001 | t0027 | g0226 | AFR | MSL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG03130 | hp1 | a0002 | c0002 | t0014 | g0249 | AFR | ESN | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG03130 | hp2 | a0001 | c0001 | t0011 | g0108 | AFR | ESN | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG03139 | hp1 | a0001 | c0001 | t0005 | g0034 | AFR | ESN | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG03139 | hp2 | a0001 | c0003 | t0077 | g0282 | AFR | ESN | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG03195 | hp1 | a0001 | c0001 | t0041 | g0081 | AFR | ESN | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG03195 | hp2 | a0001 | c0001 | t0022 | g0221 | AFR | ESN | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG03209 | hp1 | a0005 | c0010 | t0043 | g0224 | AFR | MSL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG03209 | hp2 | a0001 | c0003 | t0030 | g0279 | AFR | MSL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG03225 | hp1 | a0001 | c0001 | t0019 | g0058 | AFR | MSL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG03225 | hp2 | a0001 | c0007 | t0005 | g0231 | AFR | MSL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG03453 | hp1 | a0002 | c0002 | t0067 | g0290 | AFR | MSL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG03453 | hp2 | a0001 | c0001 | t0019 | g0097 | AFR | MSL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG03491 | hp1 | a0001 | c0001 | t0008 | g0160 | SAS | PJL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG03491 | hp2 | a0001 | c0001 | t0042 | g0053 | SAS | PJL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG03516 | hp1 | a0001 | c0001 | t0033 | g0023 | AFR | ESN | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG03516 | hp2 | a0001 | c0001 | t0006 | g0201 | AFR | ESN | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG03540 | hp1 | a0001 | c0001 | t0006 | g0196 | AFR | GWD | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG03540 | hp2 | a0001 | c0001 | t0037 | g0032 | AFR | GWD | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG03579 | hp1 | a0001 | c0001 | t0037 | g0090 | AFR | MSL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG03579 | hp2 | a0002 | c0002 | t0098 | g0235 | AFR | MSL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG03669 | hp1 | a0001 | c0001 | t0017 | g0078 | SAS | PJL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG03669 | hp2 | a0001 | c0001 | t0024 | g0188 | SAS | PJL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | STU | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | STU | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG03704 | hp1 | a0001 | c0001 | t0024 | g0202 | SAS | PJL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG03704 | hp2 | a0001 | c0001 | t0018 | g0092 | SAS | PJL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG03710 | hp1 | a0001 | c0001 | t0010 | g0059 | SAS | PJL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0007 | SAS | BEB | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0203 | SAS | BEB | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG04115 | hp1 | a0002 | c0002 | t0086 | g0260 | SAS | STU | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0172 | SAS | STU | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0103 | SAS | STU | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG04204 | hp2 | a0001 | c0001 | t0052 | g0152 | SAS | STU | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA18522 | hp1 | a0002 | c0002 | t0034 | g0292 | AFR | YRI | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA18522 | hp2 | a0002 | c0009 | t0100 | g0304 | AFR | YRI | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA18747 | hp1 | a0001 | c0001 | t0025 | g0040 | EAS | CHB | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | CHB | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA18906 | hp1 | a0001 | c0001 | t0007 | g0043 | AFR | YRI | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA18906 | hp2 | a0001 | c0001 | t0044 | g0222 | AFR | YRI | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA18939 | hp2 | a0001 | c0001 | t0036 | g0006 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA18941 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA18942 | hp1 | a0001 | c0001 | t0042 | g0064 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA18943 | hp1 | a0001 | c0003 | t0097 | g0284 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA18943 | hp2 | a0001 | c0001 | t0045 | g0057 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA18944 | hp1 | a0001 | c0001 | t0023 | g0140 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA18945 | hp2 | a0001 | c0003 | t0009 | g0281 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA18946 | hp1 | a0001 | c0001 | t0016 | g0228 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA18948 | hp1 | a0001 | c0001 | t0008 | g0134 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA18948 | hp2 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA18960 | hp1 | a0001 | c0001 | t0008 | g0133 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA18960 | hp2 | a0001 | c0001 | t0008 | g0210 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA18961 | hp1 | a0001 | c0001 | t0010 | g0086 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA18961 | hp2 | a0001 | c0001 | t0008 | g0165 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA18962 | hp2 | a0001 | c0001 | t0008 | g0163 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA18963 | hp2 | a0001 | c0001 | t0048 | g0027 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA18965 | hp1 | a0001 | c0015 | t0003 | g0099 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA18965 | hp2 | a0001 | c0003 | t0011 | g0277 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA18966 | hp1 | a0001 | c0001 | t0004 | g0179 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA18966 | hp2 | a0002 | c0002 | t0012 | g0266 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA18972 | hp1 | a0001 | c0001 | t0003 | g0044 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA18973 | hp2 | a0001 | c0001 | t0028 | g0085 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA18977 | hp1 | a0001 | c0001 | t0003 | g0066 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA18977 | hp2 | a0001 | c0001 | t0004 | g0174 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA18979 | hp2 | a0007 | c0017 | t0001 | g0205 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA18982 | hp1 | a0001 | c0018 | t0009 | g0285 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA18984 | hp1 | a0001 | c0001 | t0092 | g0046 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA18987 | hp1 | a0001 | c0001 | t0096 | g0056 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA18987 | hp2 | a0008 | c0014 | t0001 | g0122 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA18991 | hp1 | a0001 | c0001 | t0004 | g0147 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA18991 | hp2 | a0001 | c0001 | t0095 | g0083 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA18993 | hp2 | a0001 | c0001 | t0010 | g0049 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA18994 | hp1 | a0001 | c0001 | t0020 | g0082 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA18994 | hp2 | a0002 | c0002 | t0058 | g0259 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA18997 | hp1 | a0001 | c0001 | t0004 | g0131 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA18997 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA19000 | hp2 | a0001 | c0001 | t0004 | g0208 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA19003 | hp2 | a0002 | c0002 | t0026 | g0246 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA19006 | hp1 | a0002 | c0002 | t0012 | g0267 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA19009 | hp1 | a0001 | c0003 | t0009 | g0288 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA19010 | hp1 | a0001 | c0004 | t0010 | g0100 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA19011 | hp2 | a0001 | c0001 | t0021 | g0071 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA19030 | hp1 | a0001 | c0001 | t0022 | g0220 | AFR | LWK | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA19030 | hp2 | a0002 | c0013 | t0087 | g0293 | AFR | LWK | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA19043 | hp1 | a0001 | c0001 | t0006 | g0197 | AFR | LWK | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA19043 | hp2 | a0001 | c0001 | t0013 | g0029 | AFR | LWK | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA19054 | hp1 | a0001 | c0004 | t0003 | g0010 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA19063 | hp1 | a0001 | c0001 | t0004 | g0141 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA19063 | hp2 | a0001 | c0001 | t0003 | g0107 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA19064 | hp1 | a0001 | c0001 | t0012 | g0088 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA19064 | hp2 | a0002 | c0002 | t0016 | g0245 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA19065 | hp1 | a0002 | c0002 | t0070 | g0263 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA19074 | hp1 | a0002 | c0002 | t0026 | g0258 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA19074 | hp2 | a0001 | c0001 | t0036 | g0006 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA19081 | hp2 | a0009 | c0016 | t0001 | g0146 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA19082 | hp1 | a0002 | c0002 | t0075 | g0262 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA19084 | hp2 | a0001 | c0006 | t0002 | g0105 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA19085 | hp2 | a0001 | c0001 | t0094 | g0055 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA19086 | hp1 | a0001 | c0001 | t0010 | g0230 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA19087 | hp1 | a0001 | c0001 | t0010 | g0087 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA19088 | hp2 | a0002 | c0002 | t0012 | g0255 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA19089 | hp1 | a0001 | c0004 | t0003 | g0010 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA19090 | hp2 | a0001 | c0001 | t0040 | g0070 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA19240 | hp1 | a0002 | c0002 | t0059 | g0252 | AFR | YRI | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA19240 | hp2 | a0002 | c0002 | t0057 | g0026 | AFR | YRI | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ASW | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA20129 | hp2 | a0001 | c0001 | t0020 | g0207 | AFR | ASW | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA20752 | hp1 | a0002 | c0002 | t0013 | g0257 | EUR | TSI | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0295 | EUR | TSI | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA20905 | hp2 | a0001 | c0001 | t0085 | g0076 | SAS | GIH | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG01123 | hp1 | a0001 | c0001 | t0033 | g0286 | AMR | CLM | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG01123 | hp2 | a0001 | c0001 | t0051 | g0156 | AMR | CLM | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG02486 | hp1 | a0002 | c0009 | t0093 | g0303 | AFR | ACB | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG02486 | hp2 | a0006 | c0012 | t0013 | g0256 | AFR | ACB | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | ACB | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG02559 | hp2 | a0001 | c0001 | t0007 | g0038 | AFR | ACB | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG03471 | hp1 | a0001 | c0001 | t0078 | g0135 | AFR | MSL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG03471 | hp2 | a0001 | c0001 | t0063 | g0039 | AFR | MSL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG06807 | hp1 | a0005 | c0010 | t0043 | g0225 | AFR | USA | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| HG06807 | hp2 | a0001 | c0001 | t0007 | g0041 | AFR | USA | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA18955 | hp2 | a0001 | c0001 | t0046 | g0186 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA20300 | hp1 | a0001 | c0007 | t0006 | g0199 | AFR | USA | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | USA | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | LWK | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| NA21309 | hp2 | a0001 | c0001 | t0013 | g0047 | AFR | LWK | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| homoSapiens | chm13v2 | a0001 | c0003 | t0084 | g0283 | REF | REF | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0084 | REF | REF | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:132897540 | G | C | 1 | a0008 | 1 | NA18987.hp2 | missense_variant | MODERATE | c.2696C>G | p.Thr899Ser | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 21/23 | 2913/8598 | 2696/3495 | 899/1164 | chr9 | 132897540 | |||
| chr9:132905618 | G | C | 1 | a0009 | 1 | NA19081.hp2 | missense_variant | MODERATE | c.1960C>G | p.Gln654Glu | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 15/23 | 2177/8598 | 1960/3495 | 654/1164 | chr9 | 132905618 | |||
| chr9:132905818 | T | C | 1 | a0003 | 9 | HG00741.hp2 HG01074.hp2 HG01099.hp1 others(6): Show |
missense_variant | MODERATE | c.1760A>G | p.Lys587Arg | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 15/23 | 1977/8598 | 1760/3495 | 587/1164 | chr9 | 132905818 | |||
| chr9:132906827 | G | A | 1 | a0005 | 2 | HG03209.hp1 HG06807.hp1 |
missense_variant | MODERATE | c.1342C>T | p.Pro448Ser | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 14/23 | 1559/8598 | 1342/3495 | 448/1164 | chr9 | 132906827 | |||
| chr9:132910584 | G | A | 1 | a0007 | 1 | NA18979.hp2 | missense_variant | MODERATE | c.1250C>T | p.Thr417Ile | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/23 | 1467/8598 | 1250/3495 | 417/1164 | chr9 | 132910584 | |||
| chr9:132911517 | A | G | 2 | a0002 a0006 |
43 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(40): Show |
missense_variant | MODERATE | c.965T>C | p.Met322Thr | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 10/23 | 1182/8598 | 965/3495 | 322/1164 | chr9 | 132911517 | |||
| chr9:132921430 | T | A | 1 | a0004 | 2 | HG02896.hp2 HG02897.hp1 |
missense_variant | MODERATE | c.670A>T | p.Met224Leu | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/23 | 887/8598 | 670/3495 | 224/1164 | chr9 | 132921430 | |||
| chr9:132925604 | A | C | 1 | a0006 | 1 | HG02486.hp2 | missense_variant | MODERATE | c.346T>G | p.Leu116Val | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 5/23 | 563/8598 | 346/3495 | 116/1164 | chr9 | 132925604 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:132896406 | G | A | 1 | a0001c0006 | 8 | HG00738.hp2 HG01928.hp2 HG01934.hp2 others(5): Show |
synonymous_variant | LOW | c.3324C>T | p.Gly1108Gly | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 3541/8598 | 3324/3495 | 1108/1164 | chr9 | 132896406 | |||
| chr9:132896448 | C | T | 2 | a0001c0007 a0002c0009 |
6 | HG02055.hp1 HG02486.hp1 HG03041.hp1 others(3): Show |
synonymous_variant | LOW | c.3282G>A | p.Glu1094Glu | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 3499/8598 | 3282/3495 | 1094/1164 | chr9 | 132896448 | |||
| chr9:132897330 | G | A | 3 | a0001c0003 a0001c0008 a0001c0018 |
20 | HG01074.hp1 HG01175.hp1 HG01192.hp1 others(17): Show |
synonymous_variant | LOW | c.2829C>T | p.Ala943Ala | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 22/23 | 3046/8598 | 2829/3495 | 943/1164 | chr9 | 132897330 | |||
| chr9:132904418 | G | A | 1 | a0001c0015 | 1 | NA18965.hp1 | synonymous_variant | LOW | c.2034C>T | p.His678His | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 16/23 | 2251/8598 | 2034/3495 | 678/1164 | chr9 | 132904418 | |||
| chr9:132905852 | A | G | 1 | a0001c0004 | 9 | HG00438.hp2 HG00544.hp1 HG00621.hp2 others(6): Show |
synonymous_variant | LOW | c.1726T>C | p.Leu576Leu | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 15/23 | 1943/8598 | 1726/3495 | 576/1164 | chr9 | 132905852 | |||
| chr9:132905877 | C | T | 1 | a0002c0013 | 1 | NA19030.hp2 | synonymous_variant | LOW | c.1701G>A | p.Ala567Ala | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 15/23 | 1918/8598 | 1701/3495 | 567/1164 | chr9 | 132905877 | |||
| chr9:132906834 | T | C | 4 | a0002c0002 a0002c0009 a0002c0013 others(1): Show |
43 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(40): Show |
splice_region_variant&synonymous_variant | LOW | c.1335A>G | p.Glu445Glu | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 14/23 | 1552/8598 | 1335/3495 | 445/1164 | chr9 | 132906834 | |||
| chr9:132921864 | A | G | 1 | a0001c0008 | 3 | HG02027.hp2 HG02080.hp2 HG02129.hp1 |
synonymous_variant | LOW | c.618T>C | p.His206His | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 7/23 | 835/8598 | 618/3495 | 206/1164 | chr9 | 132921864 | |||
| chr9:132925680 | G | A | 1 | a0001c0018 | 1 | NA18982.hp1 | synonymous_variant | LOW | c.270C>T | p.Leu90Leu | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 5/23 | 487/8598 | 270/3495 | 90/1164 | chr9 | 132925680 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:132891472 | A | G | 3 | a0001c0001t0019 a0001c0001t0041 a0001c0001t0090 |
6 | HG02886.hp2 HG02965.hp1 HG02976.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4763T>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 4763 | chr9 | 132891472 | ||||||
| chr9:132891637 | C | T | 1 | a0001c0001t0049 | 1 | HG01192.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4598G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 4598 | chr9 | 132891637 | ||||||
| chr9:132891798 | C | T | 27 | a0001c0001t0006 a0001c0001t0012 a0001c0001t0024 others(24): Show |
43 | HG00735.hp1 HG01074.hp1 HG01081.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*4437G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 4437 | chr9 | 132891798 | ||||||
| chr9:132891981 | C | T | 1 | a0001c0001t0048 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4254G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 4254 | chr9 | 132891981 | ||||||
| chr9:132892086 | T | C | 1 | a0002c0002t0067 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4149A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 4149 | chr9 | 132892086 | ||||||
| chr9:132892178 | C | T | 1 | a0001c0001t0068 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4057G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 4057 | chr9 | 132892178 | ||||||
| chr9:132892283 | T | C | 1 | a0001c0001t0027 | 2 | HG02970.hp2 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3952A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 3952 | chr9 | 132892283 | ||||||
| chr9:132892356 | C | A | 1 | a0001c0001t0050 | 1 | HG02071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3879G>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 3879 | chr9 | 132892356 | ||||||
| chr9:132892393 | T | G | 1 | a0002c0002t0073 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3842A>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 3842 | chr9 | 132892393 | ||||||
| chr9:132892506 | C | A | 2 | a0001c0003t0060 a0005c0010t0043 |
3 | HG02818.hp1 HG03209.hp1 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3729G>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 3729 | chr9 | 132892506 | ||||||
| chr9:132892556 | C | T | 85 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(82): Show |
237 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(234): Show |
3_prime_UTR_variant | MODIFIER | c.*3679G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 3679 | chr9 | 132892556 | ||||||
| chr9:132892669 | C | T | 1 | a0001c0001t0023 | 2 | HG01099.hp2 NA18944.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3566G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 3566 | chr9 | 132892669 | ||||||
| chr9:132892697 | T | C | 1 | a0001c0001t0056 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3538A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 3538 | chr9 | 132892697 | ||||||
| chr9:132893361 | C | T | 1 | a0002c0002t0057 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2874G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 2874 | chr9 | 132893361 | ||||||
| chr9:132893363 | C | T | 1 | a0001c0001t0047 | 1 | HG01071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2872G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 2872 | chr9 | 132893363 | ||||||
| chr9:132893502 | T | C | 1 | a0002c0002t0057 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2733A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 2733 | chr9 | 132893502 | ||||||
| chr9:132893527 | C | G | 2 | a0002c0002t0029 a0002c0002t0080 |
3 | HG01891.hp1 HG02258.hp1 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2708G>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 2708 | chr9 | 132893527 | ||||||
| chr9:132893584 | C | A | 2 | a0002c0002t0014 a0002c0002t0074 |
5 | HG00323.hp1 HG02257.hp1 HG02280.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2651G>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 2651 | chr9 | 132893584 | ||||||
| chr9:132893607 | C | G | 1 | a0001c0001t0088 | 1 | HG00733.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2628G>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 2628 | chr9 | 132893607 | ||||||
| chr9:132893677 | T | C | 4 | a0001c0001t0022 a0001c0001t0044 a0001c0001t0054 others(1): Show |
6 | HG02723.hp1 HG02809.hp2 HG03041.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2558A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 2558 | chr9 | 132893677 | ||||||
| chr9:132893717 | C | T | 1 | a0001c0001t0036 | 2 | NA18939.hp2 NA19074.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2518G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 2518 | chr9 | 132893717 | ||||||
| chr9:132893774 | C | T | 2 | a0002c0002t0057 a0002c0013t0087 |
2 | NA19030.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2461G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 2461 | chr9 | 132893774 | ||||||
| chr9:132893798 | C | T | 2 | a0002c0002t0066 a0002c0002t0067 |
2 | HG01081.hp1 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2437G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 2437 | chr9 | 132893798 | ||||||
| chr9:132893817 | C | T | 5 | a0001c0001t0053 a0001c0001t0082 a0001c0001t0083 others(2): Show |
5 | HG00735.hp1 HG01081.hp1 HG01433.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2418G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 2418 | chr9 | 132893817 | ||||||
| chr9:132893881 | T | C | 1 | a0002c0013t0087 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2354A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 2354 | chr9 | 132893881 | ||||||
| chr9:132894126 | G | A | 1 | a0002c0002t0057 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2109C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 2109 | chr9 | 132894126 | ||||||
| chr9:132894301 | T | C | 23 | a0001c0001t0006 a0001c0001t0015 a0001c0001t0016 others(20): Show |
37 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*1934A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 1934 | chr9 | 132894301 | ||||||
| chr9:132894333 | A | C | 1 | a0001c0007t0064 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1902T>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 1902 | chr9 | 132894333 | ||||||
| chr9:132894450 | T | C | 2 | a0001c0001t0007 a0004c0011t0007 |
7 | HG01891.hp2 HG02559.hp2 HG02896.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1785A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 1785 | chr9 | 132894450 | ||||||
| chr9:132894686 | G | A | 1 | a0002c0002t0070 | 1 | NA19065.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1549C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 1549 | chr9 | 132894686 | ||||||
| chr9:132894693 | T | TA | 25 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0015 others(22): Show |
42 | HG00438.hp1 HG00735.hp1 HG01081.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*1541dupT | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 1541 | chr9 | 132894693 | ||||||
| chr9:132894693 | T | TAA | 6 | a0001c0001t0041 a0001c0001t0083 a0001c0001t0090 others(3): Show |
7 | HG01433.hp1 HG01978.hp1 HG02486.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1540_*1541dupTT | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 1541 | chr9 | 132894693 | ||||||
| chr9:132894693 | TA | T | 14 | a0001c0001t0008 a0001c0001t0017 a0001c0001t0018 others(11): Show |
29 | HG00280.hp2 HG00741.hp1 HG01256.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*1541delT | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 1541 | chr9 | 132894693 | ||||||
| chr9:132894728 | C | T | 91 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(88): Show |
249 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(246): Show |
3_prime_UTR_variant | MODIFIER | c.*1507G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 1507 | chr9 | 132894728 | ||||||
| chr9:132894747 | G | A | 23 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0008 others(20): Show |
131 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(128): Show |
3_prime_UTR_variant | MODIFIER | c.*1488C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 1488 | chr9 | 132894747 | ||||||
| chr9:132894748 | G | A | 7 | a0001c0001t0006 a0001c0001t0015 a0001c0001t0055 others(4): Show |
14 | HG01081.hp1 HG01106.hp1 HG02145.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1487C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 1487 | chr9 | 132894748 | ||||||
| chr9:132894767 | G | A | 1 | a0001c0001t0051 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1468C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 1468 | chr9 | 132894767 | ||||||
| chr9:132894863 | A | C | 48 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0015 others(45): Show |
75 | HG00280.hp2 HG00558.hp2 HG00735.hp1 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*1372T>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 1372 | chr9 | 132894863 | ||||||
| chr9:132894913 | G | A | 53 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0006 others(50): Show |
173 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(170): Show |
3_prime_UTR_variant | MODIFIER | c.*1322C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 1322 | chr9 | 132894913 | ||||||
| chr9:132894960 | A | C | 86 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(83): Show |
227 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(224): Show |
3_prime_UTR_variant | MODIFIER | c.*1275T>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 1275 | chr9 | 132894960 | ||||||
| chr9:132895183 | C | T | 1 | a0002c0002t0058 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1052G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 1052 | chr9 | 132895183 | ||||||
| chr9:132895394 | G | A | 2 | a0001c0001t0022 a0001c0001t0044 |
3 | HG03195.hp2 NA18906.hp2 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*841C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 841 | chr9 | 132895394 | ||||||
| chr9:132895553 | G | A | 7 | a0001c0001t0022 a0001c0001t0044 a0001c0001t0053 others(4): Show |
9 | HG01106.hp1 HG02258.hp2 HG02572.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*682C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 682 | chr9 | 132895553 | ||||||
| chr9:132895736 | G | A | 1 | a0001c0001t0052 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*499C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 499 | chr9 | 132895736 | ||||||
| chr9:132895830 | T | C | 1 | a0001c0003t0097 | 1 | NA18943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*405A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 405 | chr9 | 132895830 | ||||||
| chr9:132895859 | G | A | 7 | a0001c0001t0022 a0001c0001t0044 a0001c0001t0053 others(4): Show |
9 | HG01106.hp1 HG02258.hp2 HG02572.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*376C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 376 | chr9 | 132895859 | ||||||
| chr9:132895939 | G | C | 1 | a0002c0002t0098 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*296C>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 296 | chr9 | 132895939 | ||||||
| chr9:132895940 | G | T | 1 | a0002c0002t0057 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*295C>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 295 | chr9 | 132895940 | ||||||
| chr9:132895945 | GA | G | 25 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0008 others(22): Show |
134 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(131): Show |
3_prime_UTR_variant | MODIFIER | c.*289delT | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 289 | chr9 | 132895945 | ||||||
| chr9:132896030 | C | T | 1 | a0001c0001t0045 | 1 | NA18943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*205G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 205 | chr9 | 132896030 | ||||||
| chr9:132896037 | A | G | 2 | a0001c0001t0022 a0001c0001t0044 |
3 | HG03195.hp2 NA18906.hp2 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*198T>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 198 | chr9 | 132896037 | ||||||
| chr9:132935051 | G | A | 1 | a0005c0010t0043 | 2 | HG03209.hp1 HG06807.hp1 |
5_prime_UTR_variant | MODIFIER | c.-99C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/23 | 6179 | chr9 | 132935051 | ||||||
| chr9:132935081 | T | A | 1 | a0001c0001t0099 | 1 | HG01175.hp2 | 5_prime_UTR_variant | MODIFIER | c.-129A>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/23 | 6209 | chr9 | 132935081 | ||||||
| chr9:132935082 | G | C | 1 | a0002c0009t0100 | 1 | NA18522.hp2 | 5_prime_UTR_variant | MODIFIER | c.-130C>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/23 | 6210 | chr9 | 132935082 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:132896797 | C | G | 9 | a0001c0001t0022g0220 a0001c0001t0022g0221 a0001c0001t0044g0222 others(6): Show |
9 | HG01106.hp1 HG02258.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.2976-43G>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 22/22 | chr9 | 132896797 | |||||||
| chr9:132896804 | C | T | 1 | a0001c0001t0001g0126 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2976-50G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 22/22 | chr9 | 132896804 | |||||||
| chr9:132896808 | C | T | 3 | a0001c0001t0053g0117 a0001c0001t0055g0116 a0001c0001t0056g0118 |
3 | HG01106.hp1 HG02258.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.2976-54G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 22/22 | chr9 | 132896808 | |||||||
| chr9:132897057 | C | A | 5 | a0001c0001t0053g0117 a0001c0001t0055g0116 a0001c0001t0056g0118 others(2): Show |
5 | HG01106.hp1 HG02258.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.2975+127G>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 22/22 | chr9 | 132897057 | |||||||
| chr9:132897083 | T | C | 9 | a0001c0001t0022g0220 a0001c0001t0022g0221 a0001c0001t0044g0222 others(6): Show |
9 | HG01106.hp1 HG02258.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.2975+101A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 22/22 | chr9 | 132897083 | |||||||
| chr9:132897372 | T | C | 1 | a0001c0001t0002g0054 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2814-27A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 21/22 | chr9 | 132897372 | |||||||
| chr9:132897613 | G | GA | 9 | a0001c0001t0001g0132 a0001c0001t0001g0150 a0001c0001t0001g0154 others(6): Show |
9 | HG01106.hp1 HG01167.hp2 NA18946.hp2 others(6): Show |
splice_region_variant&intron_variant | LOW | c.2626-4dupT | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 20/22 | chr9 | 132897613 | |||||||
| chr9:132897613 | G | GAA | 127 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(124): Show |
147 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(144): Show |
splice_region_variant&intron_variant | LOW | c.2626-5_2626-4dupTT | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 20/22 | chr9 | 132897613 | |||||||
| chr9:132897613 | GA | G | 11 | a0001c0001t0002g0072 a0001c0001t0010g0049 a0001c0001t0042g0053 others(8): Show |
11 | HG01891.hp1 HG02015.hp1 HG02258.hp1 others(8): Show |
splice_region_variant&intron_variant | LOW | c.2626-4delT | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 20/22 | chr9 | 132897613 | |||||||
| chr9:132897657 | T | C | 1 | a0002c0013t0087g0293 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2626-47A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 20/22 | chr9 | 132897657 | |||||||
| chr9:132897727 | C | T | 50 | a0001c0001t0005g0033 a0001c0001t0005g0034 a0001c0001t0006g0195 others(47): Show |
51 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.2626-117G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 20/22 | chr9 | 132897727 | |||||||
| chr9:132897777 | C | T | 31 | a0002c0002t0003g0251 a0002c0002t0003g0253 a0002c0002t0003g0254 others(28): Show |
31 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(28): Show |
intron_variant | MODIFIER | c.2626-167G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 20/22 | chr9 | 132897777 | |||||||
| chr9:132897840 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2626-230C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 20/22 | chr9 | 132897840 | |||||||
| chr9:132898021 | ACAAT | A | 4 | a0001c0007t0005g0231 a0001c0007t0064g0294 a0002c0009t0093g0303 others(1): Show |
4 | HG02055.hp1 HG02486.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2626-415_2626-412d others(6): Show |
TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 20/22 | chr9 | 132898021 | |||||||
| chr9:132898028 | A | G | 1 | a0001c0001t0048g0027 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.2626-418T>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 20/22 | chr9 | 132898028 | |||||||
| chr9:132898106 | C | T | 4 | a0002c0002t0029g0269 a0002c0002t0029g0271 a0002c0002t0034g0292 others(1): Show |
4 | HG01891.hp1 HG02258.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.2626-496G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 20/22 | chr9 | 132898106 | |||||||
| chr9:132898184 | A | G | 2 | a0001c0001t0027g0226 a0001c0001t0027g0227 |
2 | HG02970.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2626-574T>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 20/22 | chr9 | 132898184 | |||||||
| chr9:132898411 | T | C | 1 | a0001c0001t0085g0076 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2626-801A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 20/22 | chr9 | 132898411 | |||||||
| chr9:132898419 | T | C | 2 | a0001c0001t0082g0289 a0001c0001t0083g0264 |
2 | HG00735.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.2626-809A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 20/22 | chr9 | 132898419 | |||||||
| chr9:132898453 | C | G | 1 | a0001c0004t0003g0051 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2626-843G>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 20/22 | chr9 | 132898453 | |||||||
| chr9:132898672 | T | C | 103 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(100): Show |
124 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.2626-1062A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 20/22 | chr9 | 132898672 | |||||||
| chr9:132898673 | G | A | 1 | a0001c0001t0001g0185 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.2626-1063C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 20/22 | chr9 | 132898673 | |||||||
| chr9:132898777 | T | C | 61 | a0001c0001t0001g0017 a0001c0001t0005g0033 a0001c0001t0005g0034 others(58): Show |
63 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.2626-1167A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 20/22 | chr9 | 132898777 | |||||||
| chr9:132898969 | C | T | 20 | a0001c0001t0005g0033 a0001c0001t0005g0034 a0001c0001t0006g0195 others(17): Show |
21 | HG01081.hp1 HG01891.hp1 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.2626-1359G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 20/22 | chr9 | 132898969 | |||||||
| chr9:132898970 | G | A | 1 | a0002c0002t0057g0026 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2626-1360C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 20/22 | chr9 | 132898970 | |||||||
| chr9:132899149 | T | A | 54 | a0001c0001t0005g0033 a0001c0001t0005g0034 a0001c0001t0006g0195 others(51): Show |
55 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.2626-1539A>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 20/22 | chr9 | 132899149 | |||||||
| chr9:132899184 | C | A | 3 | a0001c0001t0053g0117 a0001c0001t0056g0118 a0002c0002t0057g0026 |
3 | HG02258.hp2 HG02572.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2625+1531G>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 20/22 | chr9 | 132899184 | |||||||
| chr9:132899218 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2625+1497C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 20/22 | chr9 | 132899218 | |||||||
| chr9:132899301 | C | T | 1 | a0002c0002t0003g0251 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2625+1414G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 20/22 | chr9 | 132899301 | |||||||
| chr9:132899330 | A | G | 1 | a0001c0001t0078g0135 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2625+1385T>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 20/22 | chr9 | 132899330 | |||||||
| chr9:132899361 | T | C | 53 | a0001c0001t0005g0033 a0001c0001t0005g0034 a0001c0001t0006g0195 others(50): Show |
54 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.2625+1354A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 20/22 | chr9 | 132899361 | |||||||
| chr9:132899454 | C | T | 1 | a0001c0001t0001g0164 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2625+1261G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 20/22 | chr9 | 132899454 | |||||||
| chr9:132899816 | C | A | 167 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(164): Show |
189 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.2625+899G>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 20/22 | chr9 | 132899816 | |||||||
| chr9:132900040 | A | C | 53 | a0001c0001t0005g0033 a0001c0001t0005g0034 a0001c0001t0006g0195 others(50): Show |
54 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.2625+675T>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 20/22 | chr9 | 132900040 | |||||||
| chr9:132900051 | T | C | 2 | a0005c0010t0043g0224 a0005c0010t0043g0225 |
2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2625+664A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 20/22 | chr9 | 132900051 | |||||||
| chr9:132900143 | T | C | 53 | a0001c0001t0005g0033 a0001c0001t0005g0034 a0001c0001t0006g0195 others(50): Show |
54 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.2625+572A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 20/22 | chr9 | 132900143 | |||||||
| chr9:132900168 | C | T | 1 | a0002c0002t0086g0260 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2625+547G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 20/22 | chr9 | 132900168 | |||||||
| chr9:132900234 | G | A | 1 | a0001c0001t0033g0286 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2625+481C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 20/22 | chr9 | 132900234 | |||||||
| chr9:132900323 | A | G | 1 | a0002c0002t0072g0241 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2625+392T>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 20/22 | chr9 | 132900323 | |||||||
| chr9:132900331 | G | GA | 53 | a0001c0001t0005g0033 a0001c0001t0005g0034 a0001c0001t0006g0195 others(50): Show |
54 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.2625+383dupT | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 20/22 | chr9 | 132900331 | |||||||
| chr9:132900530 | T | C | 1 | a0002c0002t0098g0235 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2625+185A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 20/22 | chr9 | 132900530 | |||||||
| chr9:132900640 | T | A | 4 | a0002c0002t0029g0269 a0002c0002t0029g0271 a0002c0002t0034g0292 others(1): Show |
4 | HG01891.hp1 HG02258.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.2625+75A>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 20/22 | chr9 | 132900640 | |||||||
| chr9:132900647 | C | T | 102 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(99): Show |
123 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.2625+68G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 20/22 | chr9 | 132900647 | |||||||
| chr9:132900890 | A | G | 2 | a0003c0005t0001g0167 a0003c0005t0001g0178 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2503-53T>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 19/22 | chr9 | 132900890 | |||||||
| chr9:132900954 | C | A | 53 | a0001c0001t0005g0033 a0001c0001t0005g0034 a0001c0001t0006g0195 others(50): Show |
54 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.2503-117G>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 19/22 | chr9 | 132900954 | |||||||
| chr9:132900980 | C | T | 1 | a0001c0007t0005g0231 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2503-143G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 19/22 | chr9 | 132900980 | |||||||
| chr9:132901066 | G | A | 7 | a0001c0003t0009g0281 a0001c0003t0009g0288 a0001c0003t0011g0277 others(4): Show |
7 | HG02027.hp2 HG02080.hp2 HG02129.hp1 others(4): Show |
intron_variant | MODIFIER | c.2503-229C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 19/22 | chr9 | 132901066 | |||||||
| chr9:132901169 | C | T | 2 | a0001c0007t0005g0231 a0001c0007t0064g0294 |
2 | HG02055.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2503-332G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 19/22 | chr9 | 132901169 | |||||||
| chr9:132901225 | G | A | 1 | a0001c0001t0023g0140 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.2502+364C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 19/22 | chr9 | 132901225 | |||||||
| chr9:132901458 | G | A | 30 | a0002c0002t0003g0251 a0002c0002t0003g0253 a0002c0002t0003g0254 others(27): Show |
30 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.2502+131C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 19/22 | chr9 | 132901458 | |||||||
| chr9:132901538 | T | C | 34 | a0001c0001t0002g0238 a0001c0001t0003g0002 a0001c0001t0003g0028 others(31): Show |
38 | HG00323.hp2 HG00438.hp2 HG00544.hp1 others(35): Show |
intron_variant | MODIFIER | c.2502+51A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 19/22 | chr9 | 132901538 | |||||||
| chr9:132901734 | A | G | 53 | a0001c0001t0005g0033 a0001c0001t0005g0034 a0001c0001t0006g0195 others(50): Show |
54 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.2392-35T>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 18/22 | chr9 | 132901734 | |||||||
| chr9:132901882 | A | G | 7 | a0001c0003t0009g0281 a0001c0003t0009g0288 a0001c0003t0011g0277 others(4): Show |
7 | HG02027.hp2 HG02080.hp2 HG02129.hp1 others(4): Show |
intron_variant | MODIFIER | c.2392-183T>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 18/22 | chr9 | 132901882 | |||||||
| chr9:132901921 | G | A | 1 | a0001c0001t0099g0112 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2392-222C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 18/22 | chr9 | 132901921 | |||||||
| chr9:132902009 | G | A | 2 | a0001c0001t0001g0130 a0001c0001t0008g0134 |
2 | NA18948.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.2392-310C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 18/22 | chr9 | 132902009 | |||||||
| chr9:132902064 | T | C | 53 | a0001c0001t0005g0033 a0001c0001t0005g0034 a0001c0001t0006g0195 others(50): Show |
54 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.2392-365A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 18/22 | chr9 | 132902064 | |||||||
| chr9:132902241 | T | C | 1 | a0001c0007t0005g0231 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2391+364A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 18/22 | chr9 | 132902241 | |||||||
| chr9:132902324 | T | A | 14 | a0001c0001t0002g0009 a0001c0001t0002g0042 a0001c0001t0002g0060 others(11): Show |
15 | HG00408.hp2 HG00423.hp1 HG00673.hp1 others(12): Show |
intron_variant | MODIFIER | c.2391+281A>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 18/22 | chr9 | 132902324 | |||||||
| chr9:132902406 | T | C | 1 | a0001c0001t0002g0068 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2391+199A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 18/22 | chr9 | 132902406 | |||||||
| chr9:132902451 | T | C | 2 | a0002c0009t0093g0303 a0002c0009t0100g0304 |
2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2391+154A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 18/22 | chr9 | 132902451 | |||||||
| chr9:132902571 | C | T | 5 | a0001c0001t0033g0023 a0001c0001t0033g0286 a0001c0001t0034g0024 others(2): Show |
5 | HG00735.hp1 HG01123.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.2391+34G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 18/22 | chr9 | 132902571 | |||||||
| chr9:132903130 | G | A | 2 | a0002c0009t0093g0303 a0002c0009t0100g0304 |
2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2209-343C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 17/22 | chr9 | 132903130 | |||||||
| chr9:132903257 | T | C | 1 | a0002c0002t0034g0292 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2208+394A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 17/22 | chr9 | 132903257 | |||||||
| chr9:132903318 | G | A | 2 | a0005c0010t0043g0224 a0005c0010t0043g0225 |
2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2208+333C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 17/22 | chr9 | 132903318 | |||||||
| chr9:132903440 | C | T | 30 | a0002c0002t0003g0251 a0002c0002t0003g0253 a0002c0002t0003g0254 others(27): Show |
30 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.2208+211G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 17/22 | chr9 | 132903440 | |||||||
| chr9:132903480 | T | C | 4 | a0001c0001t0001g0019 a0001c0001t0001g0194 a0001c0001t0001g0206 others(1): Show |
5 | HG00280.hp1 HG01071.hp2 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.2208+171A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 17/22 | chr9 | 132903480 | |||||||
| chr9:132903559 | T | C | 1 | a0001c0006t0002g0048 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.2208+92A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 17/22 | chr9 | 132903559 | |||||||
| chr9:132904143 | T | C | 53 | a0001c0001t0005g0033 a0001c0001t0005g0034 a0001c0001t0006g0195 others(50): Show |
54 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.2041+268A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 16/22 | chr9 | 132904143 | |||||||
| chr9:132904147 | T | A | 1 | a0001c0001t0078g0135 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2041+264A>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 16/22 | chr9 | 132904147 | |||||||
| chr9:132904294 | G | A | 1 | a0001c0001t0090g0074 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2041+117C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 16/22 | chr9 | 132904294 | |||||||
| chr9:132904619 | TACACTGG | T | 42 | a0002c0002t0003g0251 a0002c0002t0003g0253 a0002c0002t0003g0254 others(39): Show |
43 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.1998-172_1998-166d others(9): Show |
TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 15/22 | chr9 | 132904619 | |||||||
| chr9:132904637 | A | C | 1 | a0001c0001t0001g0120 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1998-183T>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 15/22 | chr9 | 132904637 | |||||||
| chr9:132904756 | G | A | 1 | a0001c0001t0039g0218 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1998-302C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 15/22 | chr9 | 132904756 | |||||||
| chr9:132904836 | C | A | 1 | a0001c0001t0002g0068 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1998-382G>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 15/22 | chr9 | 132904836 | |||||||
| chr9:132904901 | A | G | 301 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(298): Show |
333 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(330): Show |
intron_variant | MODIFIER | c.1998-447T>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 15/22 | chr9 | 132904901 | |||||||
| chr9:132904981 | T | C | 1 | a0001c0001t0003g0045 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1998-527A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 15/22 | chr9 | 132904981 | |||||||
| chr9:132905183 | A | AAAT | 42 | a0002c0002t0003g0251 a0002c0002t0003g0253 a0002c0002t0003g0254 others(39): Show |
43 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.1997+395_1997+397d others(5): Show |
TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 15/22 | chr9 | 132905183 | |||||||
| chr9:132905425 | A | G | 1 | a0001c0001t0055g0116 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1997+156T>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 15/22 | chr9 | 132905425 | |||||||
| chr9:132905448 | T | C | 2 | a0001c0001t0027g0226 a0001c0001t0027g0227 |
2 | HG02970.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1997+133A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 15/22 | chr9 | 132905448 | |||||||
| chr9:132906176 | G | A | 42 | a0002c0002t0003g0251 a0002c0002t0003g0253 a0002c0002t0003g0254 others(39): Show |
43 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.1439-37C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 14/22 | chr9 | 132906176 | |||||||
| chr9:132906263 | C | T | 1 | a0002c0013t0087g0293 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1439-124G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 14/22 | chr9 | 132906263 | |||||||
| chr9:132906322 | G | C | 42 | a0002c0002t0003g0251 a0002c0002t0003g0253 a0002c0002t0003g0254 others(39): Show |
43 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.1439-183C>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 14/22 | chr9 | 132906322 | |||||||
| chr9:132906348 | C | G | 25 | a0001c0001t0033g0023 a0001c0001t0033g0286 a0001c0001t0034g0024 others(22): Show |
25 | HG00735.hp1 HG01074.hp1 HG01123.hp1 others(22): Show |
intron_variant | MODIFIER | c.1439-209G>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 14/22 | chr9 | 132906348 | |||||||
| chr9:132906461 | A | G | 3 | a0001c0001t0053g0117 a0001c0001t0055g0116 a0001c0001t0056g0118 |
3 | HG01106.hp1 HG02258.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1438+270T>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 14/22 | chr9 | 132906461 | |||||||
| chr9:132906548 | C | CA | 20 | a0001c0001t0001g0125 a0001c0001t0001g0170 a0001c0001t0001g0234 others(17): Show |
20 | HG00733.hp2 HG01192.hp1 HG01192.hp2 others(17): Show |
intron_variant | MODIFIER | c.1438+182dupT | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 14/22 | chr9 | 132906548 | |||||||
| chr9:132906548 | CA | C | 37 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0028g0065 others(34): Show |
38 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.1438+182delT | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 14/22 | chr9 | 132906548 | |||||||
| chr9:132906590 | A | G | 1 | a0001c0001t0078g0135 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1438+141T>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 14/22 | chr9 | 132906590 | |||||||
| chr9:132906639 | C | A | 42 | a0002c0002t0003g0251 a0002c0002t0003g0253 a0002c0002t0003g0254 others(39): Show |
43 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.1438+92G>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 14/22 | chr9 | 132906639 | |||||||
| chr9:132906890 | G | C | 30 | a0002c0002t0003g0251 a0002c0002t0003g0253 a0002c0002t0003g0254 others(27): Show |
30 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.1334-55C>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 13/22 | chr9 | 132906890 | |||||||
| chr9:132907037 | T | C | 1 | a0001c0001t0001g0149 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1334-202A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 13/22 | chr9 | 132907037 | |||||||
| chr9:132907092 | G | A | 42 | a0002c0002t0003g0251 a0002c0002t0003g0253 a0002c0002t0003g0254 others(39): Show |
43 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.1333+209C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 13/22 | chr9 | 132907092 | |||||||
| chr9:132907114 | T | C | 5 | a0001c0001t0033g0023 a0001c0001t0033g0286 a0001c0001t0034g0024 others(2): Show |
5 | HG00735.hp1 HG01123.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.1333+187A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 13/22 | chr9 | 132907114 | |||||||
| chr9:132907382 | A | G | 1 | a0001c0001t0001g0233 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1264-12T>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132907382 | |||||||
| chr9:132907520 | G | A | 1 | a0002c0002t0057g0026 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1264-150C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132907520 | |||||||
| chr9:132907543 | G | A | 1 | a0001c0001t0001g0233 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1264-173C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132907543 | |||||||
| chr9:132907560 | G | GC | 42 | a0002c0002t0003g0251 a0002c0002t0003g0253 a0002c0002t0003g0254 others(39): Show |
43 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.1264-191dupG | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132907560 | |||||||
| chr9:132907581 | C | T | 30 | a0002c0002t0003g0251 a0002c0002t0003g0253 a0002c0002t0003g0254 others(27): Show |
30 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.1264-211G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132907581 | |||||||
| chr9:132907663 | T | C | 2 | a0001c0001t0001g0143 a0001c0001t0048g0027 |
2 | NA18963.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.1264-293A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132907663 | |||||||
| chr9:132907765 | C | T | 9 | a0001c0001t0001g0121 a0001c0001t0001g0182 a0001c0001t0001g0183 others(6): Show |
9 | HG02015.hp2 HG02071.hp1 NA18942.hp2 others(6): Show |
intron_variant | MODIFIER | c.1264-395G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132907765 | |||||||
| chr9:132907807 | C | A | 2 | a0001c0001t0027g0226 a0001c0001t0027g0227 |
2 | HG02970.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1264-437G>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132907807 | |||||||
| chr9:132907813 | G | A | 2 | a0001c0001t0002g0042 a0001c0001t0002g0077 |
2 | NA18980.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.1264-443C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132907813 | |||||||
| chr9:132907918 | C | A | 42 | a0002c0002t0003g0251 a0002c0002t0003g0253 a0002c0002t0003g0254 others(39): Show |
43 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.1264-548G>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132907918 | |||||||
| chr9:132908052 | A | G | 1 | a0001c0001t0001g0234 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1264-682T>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132908052 | |||||||
| chr9:132908137 | T | TTTTG | 42 | a0002c0002t0003g0251 a0002c0002t0003g0253 a0002c0002t0003g0254 others(39): Show |
43 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.1264-768_1264-767i others(6): Show |
TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132908137 | |||||||
| chr9:132908262 | C | T | 42 | a0002c0002t0003g0251 a0002c0002t0003g0253 a0002c0002t0003g0254 others(39): Show |
43 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.1264-892G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132908262 | |||||||
| chr9:132908327 | A | G | 42 | a0002c0002t0003g0251 a0002c0002t0003g0253 a0002c0002t0003g0254 others(39): Show |
43 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.1264-957T>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132908327 | |||||||
| chr9:132908367 | G | A | 42 | a0002c0002t0003g0251 a0002c0002t0003g0253 a0002c0002t0003g0254 others(39): Show |
43 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.1264-997C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132908367 | |||||||
| chr9:132908375 | C | T | 2 | a0001c0001t0004g0147 a0001c0001t0004g0179 |
2 | NA18966.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.1264-1005G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132908375 | |||||||
| chr9:132908607 | A | C | 1 | a0001c0001t0018g0092 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1264-1237T>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132908607 | |||||||
| chr9:132908695 | C | T | 1 | a0001c0001t0063g0039 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1264-1325G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132908695 | |||||||
| chr9:132908782 | A | C | 114 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(111): Show |
135 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.1264-1412T>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132908782 | |||||||
| chr9:132908864 | G | A | 2 | a0002c0009t0093g0303 a0002c0009t0100g0304 |
2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1264-1494C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132908864 | |||||||
| chr9:132908901 | C | CT | 8 | a0001c0001t0001g0126 a0001c0001t0001g0157 a0001c0001t0001g0191 others(5): Show |
8 | HG00544.hp1 HG02145.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.1264-1532dupA | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132908901 | |||||||
| chr9:132908901 | C | CTTTTTTT others(3): Show |
2 | a0002c0009t0093g0303 a0002c0009t0100g0304 |
2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1264-1541_1264-153 others(14): Show |
TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132908901 | |||||||
| chr9:132908901 | C | CTTTTTTT others(5): Show |
2 | a0002c0002t0013g0257 a0006c0012t0013g0256 |
2 | HG02486.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1264-1543_1264-153 others(16): Show |
TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132908901 | |||||||
| chr9:132908901 | C | CTTTTTTT others(6): Show |
1 | a0002c0002t0005g0261 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1264-1544_1264-153 others(17): Show |
TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132908901 | |||||||
| chr9:132908901 | C | CTTTTTTT others(8): Show |
1 | a0002c0002t0066g0291 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1264-1546_1264-153 others(19): Show |
TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132908901 | |||||||
| chr9:132908901 | C | CTTTTTTT others(9): Show |
1 | a0002c0002t0067g0290 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1264-1547_1264-153 others(20): Show |
TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132908901 | |||||||
| chr9:132908901 | C | CTTTTTTT others(10): Show |
1 | a0001c0001t0027g0226 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1264-1548_1264-153 others(21): Show |
TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132908901 | |||||||
| chr9:132908901 | C | CTTTTTTT others(11): Show |
1 | a0002c0002t0098g0235 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1264-1532_1264-153 others(22): Show |
TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132908901 | |||||||
| chr9:132908901 | C | CTTTTTTT others(12): Show |
2 | a0001c0001t0027g0227 a0002c0002t0057g0026 |
2 | HG02970.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1264-1532_1264-153 others(23): Show |
TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132908901 | |||||||
| chr9:132908901 | C | CTTTTTTT others(14): Show |
1 | a0002c0002t0032g0021 | 2 | HG02723.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1264-1532_1264-153 others(25): Show |
TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132908901 | |||||||
| chr9:132908901 | C | CTTTTTTT others(16): Show |
4 | a0002c0002t0003g0251 a0002c0002t0012g0266 a0002c0002t0012g0267 others(1): Show |
4 | HG02451.hp1 NA18966.hp2 NA19006.hp1 others(1): Show |
intron_variant | MODIFIER | c.1264-1532_1264-153 others(27): Show |
TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132908901 | |||||||
| chr9:132908901 | C | CTTTTTTT others(17): Show |
4 | a0002c0002t0016g0245 a0002c0002t0059g0252 a0002c0002t0075g0262 others(1): Show |
4 | HG04115.hp1 NA19064.hp2 NA19082.hp1 others(1): Show |
intron_variant | MODIFIER | c.1264-1532_1264-153 others(28): Show |
TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132908901 | |||||||
| chr9:132908901 | C | CTTTTTTT others(18): Show |
3 | a0002c0002t0016g0242 a0002c0002t0026g0246 a0002c0002t0065g0244 |
3 | HG00438.hp1 HG00558.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1264-1532_1264-153 others(29): Show |
TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132908901 | |||||||
| chr9:132908901 | C | CTTTTTTT others(19): Show |
2 | a0002c0002t0040g0128 a0002c0002t0069g0243 |
2 | HG01109.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.1264-1532_1264-153 others(30): Show |
TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132908901 | |||||||
| chr9:132908901 | C | CTTTTTTT others(20): Show |
2 | a0002c0002t0073g0240 a0005c0010t0043g0225 |
2 | HG02735.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1264-1532_1264-153 others(31): Show |
TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132908901 | |||||||
| chr9:132908901 | C | CTTTTTTT others(21): Show |
3 | a0002c0002t0003g0254 a0002c0002t0058g0259 a0005c0010t0043g0224 |
3 | HG02895.hp2 HG03209.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.1264-1532_1264-153 others(32): Show |
TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132908901 | |||||||
| chr9:132908901 | C | CTTTTTTT others(22): Show |
2 | a0002c0002t0003g0253 a0002c0002t0014g0249 |
2 | HG02897.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1264-1532_1264-153 others(33): Show |
TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132908901 | |||||||
| chr9:132908901 | C | CTTTTTTT others(23): Show |
4 | a0002c0002t0012g0255 a0002c0002t0014g0247 a0002c0002t0014g0248 others(1): Show |
4 | HG00323.hp1 HG02257.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1264-1532_1264-153 others(34): Show |
TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132908901 | |||||||
| chr9:132908901 | C | CTTTTTTT others(24): Show |
1 | a0002c0002t0038g0302 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1264-1532_1264-153 others(35): Show |
TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132908901 | |||||||
| chr9:132908901 | C | CTTTTTTT others(25): Show |
1 | a0002c0002t0038g0301 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1264-1532_1264-153 others(36): Show |
TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132908901 | |||||||
| chr9:132908901 | C | CTTTTTTT others(26): Show |
1 | a0002c0002t0014g0250 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1264-1532_1264-153 others(37): Show |
TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132908901 | |||||||
| chr9:132909193 | C | T | 1 | a0002c0002t0014g0248 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1263+1378G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132909193 | |||||||
| chr9:132909248 | C | T | 2 | a0001c0001t0010g0049 a0001c0001t0010g0086 |
2 | NA18961.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.1263+1323G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132909248 | |||||||
| chr9:132909473 | T | C | 2 | a0001c0001t0017g0062 a0001c0001t0017g0078 |
2 | HG00741.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.1263+1098A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132909473 | |||||||
| chr9:132910136 | C | CA | 7 | a0001c0001t0001g0170 a0001c0001t0002g0060 a0001c0006t0002g0105 others(4): Show |
7 | HG03209.hp1 HG06807.hp1 NA18981.hp1 others(4): Show |
intron_variant | MODIFIER | c.1263+434dupT | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132910136 | |||||||
| chr9:132910179 | T | C | 30 | a0002c0002t0003g0251 a0002c0002t0003g0253 a0002c0002t0003g0254 others(27): Show |
30 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.1263+392A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132910179 | |||||||
| chr9:132910256 | G | A | 4 | a0002c0002t0032g0021 a0002c0002t0066g0291 a0002c0002t0067g0290 others(1): Show |
5 | HG01081.hp1 HG02723.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1263+315C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132910256 | |||||||
| chr9:132910265 | C | T | 2 | a0001c0001t0015g0036 a0001c0001t0015g0037 |
2 | HG02965.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1263+306G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132910265 | |||||||
| chr9:132910301 | C | CA | 24 | a0001c0001t0001g0125 a0001c0001t0001g0150 a0001c0001t0001g0158 others(21): Show |
24 | HG00621.hp2 HG00673.hp2 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.1263+269dupT | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132910301 | |||||||
| chr9:132910301 | CA | C | 39 | a0001c0001t0001g0148 a0001c0001t0042g0064 a0002c0002t0003g0251 others(36): Show |
40 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(37): Show |
intron_variant | MODIFIER | c.1263+269delT | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132910301 | |||||||
| chr9:132910465 | C | T | 4 | a0001c0001t0011g0089 a0001c0001t0011g0108 a0001c0001t0011g0114 others(1): Show |
4 | HG02615.hp2 HG02896.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1263+106G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132910465 | |||||||
| chr9:132910725 | T | C | 42 | a0002c0002t0003g0251 a0002c0002t0003g0253 a0002c0002t0003g0254 others(39): Show |
43 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.1142-33A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 11/22 | chr9 | 132910725 | |||||||
| chr9:132910939 | C | T | 4 | a0001c0001t0022g0220 a0001c0001t0022g0221 a0001c0001t0044g0222 others(1): Show |
4 | HG03041.hp2 HG03195.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1141+63G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 11/22 | chr9 | 132910939 | |||||||
| chr9:132911187 | A | G | 2 | a0001c0001t0001g0017 a0001c0001t0049g0171 |
3 | HG00733.hp1 HG01192.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1030-74T>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 10/22 | chr9 | 132911187 | |||||||
| chr9:132911625 | T | TA | 6 | a0001c0001t0001g0158 a0001c0001t0002g0060 a0001c0001t0082g0289 others(3): Show |
6 | HG00735.hp1 HG01175.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.914-58dupT | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 9/22 | chr9 | 132911625 | |||||||
| chr9:132911625 | TA | T | 173 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0013 others(170): Show |
201 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.914-58delT | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 9/22 | chr9 | 132911625 | |||||||
| chr9:132911625 | TAA | T | 39 | a0001c0001t0001g0123 a0001c0001t0001g0137 a0001c0001t0001g0150 others(36): Show |
40 | HG00733.hp2 HG01099.hp1 HG01099.hp2 others(37): Show |
intron_variant | MODIFIER | c.914-59_914-58delTT | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 9/22 | chr9 | 132911625 | |||||||
| chr9:132911625 | TAAAAA | T | 6 | a0002c0002t0029g0269 a0002c0002t0029g0271 a0002c0002t0032g0021 others(3): Show |
7 | HG01891.hp1 HG02258.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.914-62_914-58delTT others(3): Show |
TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 9/22 | chr9 | 132911625 | |||||||
| chr9:132911625 | TAAAAAA | T | 30 | a0002c0002t0003g0253 a0002c0002t0003g0254 a0002c0002t0005g0261 others(27): Show |
30 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.914-63_914-58delTT others(4): Show |
TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 9/22 | chr9 | 132911625 | |||||||
| chr9:132911625 | TAAAAAAA others(5): Show |
T | 1 | a0001c0001t0054g0115 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.914-69_914-58delTT others(10): Show |
TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 9/22 | chr9 | 132911625 | |||||||
| chr9:132911625 | TAAAAAAA others(10): Show |
T | 1 | a0002c0002t0057g0026 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.914-74_914-58delTT others(15): Show |
TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 9/22 | chr9 | 132911625 | |||||||
| chr9:132911769 | C | G | 4 | a0001c0001t0022g0220 a0001c0001t0022g0221 a0001c0001t0044g0222 others(1): Show |
4 | HG03041.hp2 HG03195.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.914-201G>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 9/22 | chr9 | 132911769 | |||||||
| chr9:132911912 | C | T | 1 | a0001c0001t0001g0161 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.914-344G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 9/22 | chr9 | 132911912 | |||||||
| chr9:132911926 | T | C | 1 | a0001c0001t0012g0088 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.913+356A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 9/22 | chr9 | 132911926 | |||||||
| chr9:132911927 | G | C | 1 | a0001c0001t0001g0191 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.913+355C>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 9/22 | chr9 | 132911927 | |||||||
| chr9:132912094 | C | T | 1 | a0001c0007t0005g0231 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.913+188G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 9/22 | chr9 | 132912094 | |||||||
| chr9:132912840 | G | A | 30 | a0002c0002t0003g0251 a0002c0002t0003g0253 a0002c0002t0003g0254 others(27): Show |
30 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.738-383C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132912840 | |||||||
| chr9:132912885 | G | A | 42 | a0002c0002t0003g0251 a0002c0002t0003g0253 a0002c0002t0003g0254 others(39): Show |
43 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.738-428C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132912885 | |||||||
| chr9:132912900 | T | C | 41 | a0002c0002t0003g0251 a0002c0002t0003g0253 a0002c0002t0003g0254 others(38): Show |
42 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.738-443A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132912900 | |||||||
| chr9:132913006 | C | T | 25 | a0001c0001t0033g0023 a0001c0001t0033g0286 a0001c0001t0034g0024 others(22): Show |
25 | HG00735.hp1 HG01074.hp1 HG01123.hp1 others(22): Show |
intron_variant | MODIFIER | c.738-549G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132913006 | |||||||
| chr9:132913125 | T | A | 1 | a0002c0002t0012g0267 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.738-668A>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132913125 | |||||||
| chr9:132913310 | G | A | 1 | a0001c0007t0006g0199 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.738-853C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132913310 | |||||||
| chr9:132913330 | C | T | 2 | a0001c0001t0027g0226 a0001c0001t0027g0227 |
2 | HG02970.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.738-873G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132913330 | |||||||
| chr9:132913548 | C | T | 1 | a0001c0001t0008g0160 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.738-1091G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132913548 | |||||||
| chr9:132913587 | G | A | 4 | a0001c0001t0022g0220 a0001c0001t0022g0221 a0001c0001t0044g0222 others(1): Show |
4 | HG03041.hp2 HG03195.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.738-1130C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132913587 | |||||||
| chr9:132913686 | C | T | 3 | a0001c0001t0006g0196 a0001c0001t0006g0200 a0001c0001t0006g0201 |
3 | HG02145.hp1 HG03516.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.738-1229G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132913686 | |||||||
| chr9:132913688 | C | T | 1 | a0002c0002t0057g0026 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.738-1231G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132913688 | |||||||
| chr9:132913818 | T | C | 1 | a0001c0001t0078g0135 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.738-1361A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132913818 | |||||||
| chr9:132913825 | C | CA | 41 | a0001c0001t0001g0121 a0001c0001t0001g0139 a0001c0001t0001g0150 others(38): Show |
41 | HG00438.hp2 HG00621.hp1 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.738-1369dupT | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132913825 | |||||||
| chr9:132913825 | CA | C | 11 | a0001c0003t0097g0284 a0002c0002t0029g0269 a0002c0002t0032g0021 others(8): Show |
12 | HG01081.hp1 HG01891.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.738-1369delT | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132913825 | |||||||
| chr9:132913844 | A | AAAAAAAA others(5): Show |
1 | a0002c0009t0093g0303 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.738-1388_738-1387i others(14): Show |
TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132913844 | |||||||
| chr9:132913844 | A | AAAAAAAA others(4): Show |
1 | a0002c0009t0100g0304 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.738-1388_738-1387i others(13): Show |
TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132913844 | |||||||
| chr9:132913855 | A | C | 2 | a0002c0009t0093g0303 a0002c0009t0100g0304 |
2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.738-1398T>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132913855 | |||||||
| chr9:132913873 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.738-1416C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132913873 | |||||||
| chr9:132913891 | G | GT | 55 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0042 others(52): Show |
58 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.738-1435dupA | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132913891 | |||||||
| chr9:132913891 | G | T | 2 | a0001c0003t0009g0276 a0002c0002t0057g0026 |
2 | HG01433.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.738-1434C>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132913891 | |||||||
| chr9:132913891 | GT | G | 128 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(125): Show |
148 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(145): Show |
intron_variant | MODIFIER | c.738-1435delA | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132913891 | |||||||
| chr9:132913896 | T | G | 29 | a0001c0001t0001g0119 a0001c0001t0001g0129 a0001c0001t0001g0130 others(26): Show |
30 | HG00423.hp2 HG00621.hp1 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.738-1439A>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132913896 | |||||||
| chr9:132913897 | T | G | 90 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(87): Show |
109 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(106): Show |
intron_variant | MODIFIER | c.738-1440A>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132913897 | |||||||
| chr9:132913900 | T | G | 4 | a0002c0002t0029g0269 a0002c0002t0029g0271 a0002c0002t0034g0292 others(1): Show |
4 | HG01891.hp1 HG02258.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.738-1443A>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132913900 | |||||||
| chr9:132913902 | T | G | 1 | a0001c0001t0078g0135 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.738-1445A>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132913902 | |||||||
| chr9:132913903 | T | G | 3 | a0001c0001t0001g0232 a0002c0009t0093g0303 a0002c0009t0100g0304 |
3 | HG00673.hp2 HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.738-1446A>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132913903 | |||||||
| chr9:132913917 | T | A | 31 | a0002c0002t0003g0251 a0002c0002t0003g0253 a0002c0002t0003g0254 others(28): Show |
31 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(28): Show |
intron_variant | MODIFIER | c.738-1460A>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132913917 | |||||||
| chr9:132913945 | C | A | 4 | a0002c0002t0014g0247 a0002c0002t0014g0248 a0002c0002t0014g0249 others(1): Show |
4 | HG02257.hp1 HG02280.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.738-1488G>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132913945 | |||||||
| chr9:132914232 | G | A | 4 | a0002c0002t0003g0251 a0002c0002t0003g0253 a0002c0002t0003g0254 others(1): Show |
4 | HG02451.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.738-1775C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132914232 | |||||||
| chr9:132914326 | A | C | 3 | a0001c0001t0053g0117 a0001c0001t0055g0116 a0001c0001t0056g0118 |
3 | HG01106.hp1 HG02258.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.738-1869T>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132914326 | |||||||
| chr9:132914442 | A | G | 2 | a0002c0002t0003g0253 a0002c0002t0003g0254 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.738-1985T>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132914442 | |||||||
| chr9:132914514 | T | C | 1 | a0001c0001t0024g0202 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.738-2057A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132914514 | |||||||
| chr9:132914665 | T | G | 2 | a0001c0001t0024g0188 a0001c0001t0024g0202 |
2 | HG03669.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.738-2208A>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132914665 | |||||||
| chr9:132914703 | C | A | 2 | a0001c0001t0001g0189 a0001c0001t0001g0190 |
2 | HG02071.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.738-2246G>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132914703 | |||||||
| chr9:132914703 | C | CA | 12 | a0001c0001t0001g0136 a0001c0001t0005g0214 a0001c0001t0005g0215 others(9): Show |
12 | HG01167.hp1 HG02145.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.738-2247dupT | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132914703 | |||||||
| chr9:132914703 | C | CAA | 8 | a0001c0001t0018g0092 a0001c0001t0018g0236 a0001c0001t0018g0237 others(5): Show |
8 | HG00733.hp2 HG01256.hp1 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.738-2248_738-2247d others(4): Show |
TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132914703 | |||||||
| chr9:132914703 | C | T | 3 | a0001c0001t0001g0121 a0001c0001t0001g0183 a0001c0001t0001g0191 |
3 | NA18952.hp2 NA18963.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.738-2246G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132914703 | |||||||
| chr9:132914703 | CA | C | 60 | a0001c0001t0027g0226 a0001c0001t0027g0227 a0001c0001t0033g0023 others(57): Show |
60 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.738-2247delT | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132914703 | |||||||
| chr9:132914752 | C | T | 1 | a0001c0001t0056g0118 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.738-2295G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132914752 | |||||||
| chr9:132914911 | C | T | 1 | a0001c0001t0001g0209 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.738-2454G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132914911 | |||||||
| chr9:132915089 | C | T | 2 | a0001c0007t0005g0231 a0001c0007t0064g0294 |
2 | HG02055.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.738-2632G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132915089 | |||||||
| chr9:132915109 | C | G | 1 | a0001c0001t0001g0157 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.738-2652G>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132915109 | |||||||
| chr9:132915169 | A | G | 1 | a0001c0001t0051g0156 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.738-2712T>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132915169 | |||||||
| chr9:132915176 | C | G | 1 | a0001c0001t0001g0239 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.738-2719G>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132915176 | |||||||
| chr9:132915256 | G | A | 1 | a0002c0002t0057g0026 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.738-2799C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132915256 | |||||||
| chr9:132915551 | C | T | 2 | a0002c0009t0093g0303 a0002c0009t0100g0304 |
2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.738-3094G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132915551 | |||||||
| chr9:132915598 | T | G | 1 | a0001c0001t0018g0092 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.738-3141A>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132915598 | |||||||
| chr9:132915716 | G | A | 118 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(115): Show |
139 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.738-3259C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132915716 | |||||||
| chr9:132916095 | C | A | 2 | a0002c0009t0093g0303 a0002c0009t0100g0304 |
2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.738-3638G>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132916095 | |||||||
| chr9:132916227 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.738-3770C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132916227 | |||||||
| chr9:132916436 | TA | T | 42 | a0002c0002t0003g0251 a0002c0002t0003g0253 a0002c0002t0003g0254 others(39): Show |
43 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.738-3980delT | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132916436 | |||||||
| chr9:132916654 | G | A | 1 | a0001c0001t0071g0091 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.738-4197C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132916654 | |||||||
| chr9:132916679 | T | C | 4 | a0002c0002t0032g0021 a0002c0002t0066g0291 a0002c0002t0067g0290 others(1): Show |
5 | HG01081.hp1 HG02723.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.738-4222A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132916679 | |||||||
| chr9:132916870 | G | A | 1 | a0002c0002t0098g0235 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.738-4413C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132916870 | |||||||
| chr9:132916870 | G | C | 2 | a0002c0009t0093g0303 a0002c0009t0100g0304 |
2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.738-4413C>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132916870 | |||||||
| chr9:132916878 | T | C | 1 | a0001c0001t0005g0033 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.738-4421A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132916878 | |||||||
| chr9:132916971 | C | T | 2 | a0002c0009t0093g0303 a0002c0009t0100g0304 |
2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.737+4392G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132916971 | |||||||
| chr9:132917026 | G | A | 1 | a0001c0001t0056g0118 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.737+4337C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132917026 | |||||||
| chr9:132917142 | T | C | 1 | a0001c0001t0004g0174 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.737+4221A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132917142 | |||||||
| chr9:132917320 | C | T | 1 | a0001c0001t0033g0286 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.737+4043G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132917320 | |||||||
| chr9:132917393 | C | T | 101 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(98): Show |
122 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.737+3970G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132917393 | |||||||
| chr9:132917464 | G | T | 1 | a0003c0005t0004g0175 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.737+3899C>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132917464 | |||||||
| chr9:132917526 | T | G | 1 | a0001c0001t0071g0091 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.737+3837A>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132917526 | |||||||
| chr9:132917574 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.737+3789G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132917574 | |||||||
| chr9:132917584 | C | T | 1 | a0001c0001t0002g0238 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.737+3779G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132917584 | |||||||
| chr9:132917648 | T | A | 163 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(160): Show |
184 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.737+3715A>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132917648 | |||||||
| chr9:132918388 | G | C | 1 | a0002c0002t0086g0260 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.737+2975C>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132918388 | |||||||
| chr9:132918437 | C | G | 3 | a0002c0002t0032g0021 a0002c0002t0066g0291 a0002c0002t0067g0290 |
4 | HG01081.hp1 HG02723.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.737+2926G>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132918437 | |||||||
| chr9:132918464 | C | T | 1 | a0001c0001t0013g0047 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.737+2899G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132918464 | |||||||
| chr9:132918746 | G | A | 1 | a0001c0001t0018g0092 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.737+2617C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132918746 | |||||||
| chr9:132918790 | G | A | 1 | a0001c0001t0056g0118 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.737+2573C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132918790 | |||||||
| chr9:132918818 | G | A | 1 | a0002c0002t0057g0026 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.737+2545C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132918818 | |||||||
| chr9:132918897 | A | G | 2 | a0002c0009t0093g0303 a0002c0009t0100g0304 |
2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.737+2466T>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132918897 | |||||||
| chr9:132918907 | G | A | 1 | a0002c0002t0057g0026 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.737+2456C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132918907 | |||||||
| chr9:132919180 | G | A | 2 | a0005c0010t0043g0224 a0005c0010t0043g0225 |
2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.737+2183C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132919180 | |||||||
| chr9:132919326 | A | G | 1 | a0002c0002t0057g0026 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.737+2037T>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132919326 | |||||||
| chr9:132919530 | T | C | 1 | a0002c0002t0034g0292 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.737+1833A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132919530 | |||||||
| chr9:132919697 | C | G | 5 | a0001c0001t0033g0023 a0001c0001t0033g0286 a0001c0001t0034g0024 others(2): Show |
5 | HG00735.hp1 HG01123.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.737+1666G>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132919697 | |||||||
| chr9:132920064 | C | A | 2 | a0002c0002t0003g0253 a0002c0002t0003g0254 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.737+1299G>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132920064 | |||||||
| chr9:132920250 | A | C | 1 | a0001c0001t0003g0044 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.737+1113T>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132920250 | |||||||
| chr9:132920287 | C | CAGA | 4 | a0001c0001t0005g0033 a0001c0001t0005g0034 a0001c0001t0037g0032 others(1): Show |
4 | HG02647.hp1 HG02895.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.737+1075_737+1076i others(5): Show |
TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132920287 | |||||||
| chr9:132920397 | G | A | 1 | a0001c0001t0005g0034 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.737+966C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132920397 | |||||||
| chr9:132920484 | A | G | 1 | a0002c0002t0074g0265 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.737+879T>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132920484 | |||||||
| chr9:132920745 | G | A | 2 | a0001c0001t0015g0036 a0001c0001t0015g0037 |
2 | HG02965.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.737+618C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132920745 | |||||||
| chr9:132920795 | C | T | 44 | a0001c0001t0027g0226 a0001c0001t0027g0227 a0002c0002t0003g0251 others(41): Show |
45 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.737+568G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132920795 | |||||||
| chr9:132920802 | A | G | 2 | a0002c0009t0093g0303 a0002c0009t0100g0304 |
2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.737+561T>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132920802 | |||||||
| chr9:132920858 | C | G | 2 | a0002c0009t0093g0303 a0002c0009t0100g0304 |
2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.737+505G>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132920858 | |||||||
| chr9:132920862 | G | T | 4 | a0001c0001t0015g0036 a0001c0001t0015g0037 a0001c0001t0015g0272 others(1): Show |
4 | HG02818.hp2 HG02965.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.737+501C>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132920862 | |||||||
| chr9:132920893 | G | A | 1 | a0001c0001t0078g0135 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.737+470C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132920893 | |||||||
| chr9:132920972 | C | T | 2 | a0002c0009t0093g0303 a0002c0009t0100g0304 |
2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.737+391G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132920972 | |||||||
| chr9:132921080 | T | C | 1 | a0002c0002t0074g0265 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.737+283A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132921080 | |||||||
| chr9:132921114 | G | A | 1 | a0002c0002t0070g0263 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.737+249C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132921114 | |||||||
| chr9:132921130 | G | A | 3 | a0002c0002t0029g0269 a0002c0002t0029g0271 a0002c0002t0080g0270 |
3 | HG01891.hp1 HG02258.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.737+233C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132921130 | |||||||
| chr9:132921221 | A | C | 1 | a0002c0013t0087g0293 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.737+142T>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132921221 | |||||||
| chr9:132921235 | T | C | 1 | a0001c0001t0015g0272 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.737+128A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132921235 | |||||||
| chr9:132921544 | T | C | 2 | a0002c0009t0093g0303 a0002c0009t0100g0304 |
2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.664-108A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 7/22 | chr9 | 132921544 | |||||||
| chr9:132921562 | G | A | 2 | a0002c0009t0093g0303 a0002c0009t0100g0304 |
2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.664-126C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 7/22 | chr9 | 132921562 | |||||||
| chr9:132922067 | T | G | 1 | a0001c0001t0002g0093 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.509-94A>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 6/22 | chr9 | 132922067 | |||||||
| chr9:132922073 | A | G | 2 | a0002c0009t0093g0303 a0002c0009t0100g0304 |
2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.509-100T>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 6/22 | chr9 | 132922073 | |||||||
| chr9:132922203 | T | C | 1 | a0002c0002t0098g0235 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.509-230A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 6/22 | chr9 | 132922203 | |||||||
| chr9:132922268 | A | G | 1 | a0001c0001t0036g0006 | 2 | NA18939.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.509-295T>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 6/22 | chr9 | 132922268 | |||||||
| chr9:132922324 | G | A | 2 | a0002c0009t0093g0303 a0002c0009t0100g0304 |
2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.509-351C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 6/22 | chr9 | 132922324 | |||||||
| chr9:132922607 | C | T | 11 | a0001c0001t0005g0033 a0001c0001t0005g0034 a0001c0001t0006g0195 others(8): Show |
11 | HG02145.hp1 HG02451.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.509-634G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 6/22 | chr9 | 132922607 | |||||||
| chr9:132922750 | G | A | 1 | a0001c0001t0003g0295 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.508+598C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 6/22 | chr9 | 132922750 | |||||||
| chr9:132922803 | A | G | 1 | a0002c0002t0034g0292 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.508+545T>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 6/22 | chr9 | 132922803 | |||||||
| chr9:132922952 | C | T | 1 | a0001c0001t0001g0020 | 2 | HG01106.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.508+396G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 6/22 | chr9 | 132922952 | |||||||
| chr9:132922995 | G | A | 2 | a0001c0001t0055g0116 a0001c0001t0056g0118 |
2 | HG01106.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.508+353C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 6/22 | chr9 | 132922995 | |||||||
| chr9:132923051 | C | T | 2 | a0002c0009t0093g0303 a0002c0009t0100g0304 |
2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.508+297G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 6/22 | chr9 | 132923051 | |||||||
| chr9:132923055 | C | T | 1 | a0002c0002t0098g0235 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.508+293G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 6/22 | chr9 | 132923055 | |||||||
| chr9:132923120 | C | A | 4 | a0001c0001t0022g0220 a0001c0001t0022g0221 a0001c0001t0044g0222 others(1): Show |
4 | HG03041.hp2 HG03195.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.508+228G>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 6/22 | chr9 | 132923120 | |||||||
| chr9:132923120 | C | T | 1 | a0001c0003t0030g0274 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.508+228G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 6/22 | chr9 | 132923120 | |||||||
| chr9:132923249 | A | G | 1 | a0001c0001t0061g0110 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.508+99T>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 6/22 | chr9 | 132923249 | |||||||
| chr9:132923334 | G | A | 1 | a0002c0002t0012g0255 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.508+14C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 6/22 | chr9 | 132923334 | |||||||
| chr9:132923611 | C | T | 2 | a0002c0009t0093g0303 a0002c0009t0100g0304 |
2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.364-119G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 5/22 | chr9 | 132923611 | |||||||
| chr9:132923905 | TGTTA | T | 4 | a0002c0002t0029g0269 a0002c0002t0029g0271 a0002c0002t0034g0292 others(1): Show |
4 | HG01891.hp1 HG02258.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.364-417_364-414del others(4): Show |
TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 5/22 | chr9 | 132923905 | |||||||
| chr9:132923912 | T | TA | 8 | a0001c0001t0006g0195 a0001c0001t0006g0197 a0001c0001t0006g0200 others(5): Show |
8 | HG01106.hp1 HG02145.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.364-421dupT | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 5/22 | chr9 | 132923912 | |||||||
| chr9:132924061 | A | AAT | 188 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(185): Show |
210 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.364-571_364-570dup others(2): Show |
TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 5/22 | chr9 | 132924061 | |||||||
| chr9:132924299 | T | C | 1 | a0001c0003t0097g0284 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.364-807A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 5/22 | chr9 | 132924299 | |||||||
| chr9:132924309 | T | C | 1 | a0002c0002t0057g0026 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.364-817A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 5/22 | chr9 | 132924309 | |||||||
| chr9:132924389 | G | A | 26 | a0001c0001t0001g0137 a0001c0001t0033g0023 a0001c0001t0033g0286 others(23): Show |
26 | HG00735.hp1 HG01074.hp1 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.364-897C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 5/22 | chr9 | 132924389 | |||||||
| chr9:132924530 | G | T | 190 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(187): Show |
212 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.364-1038C>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 5/22 | chr9 | 132924530 | |||||||
| chr9:132924542 | A | C | 3 | a0001c0001t0053g0117 a0001c0007t0005g0231 a0001c0007t0064g0294 |
3 | HG02055.hp1 HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.363+1045T>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 5/22 | chr9 | 132924542 | |||||||
| chr9:132924547 | A | G | 1 | a0002c0002t0032g0021 | 2 | HG02723.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.363+1040T>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 5/22 | chr9 | 132924547 | |||||||
| chr9:132924554 | T | C | 2 | a0005c0010t0043g0224 a0005c0010t0043g0225 |
2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.363+1033A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 5/22 | chr9 | 132924554 | |||||||
| chr9:132924617 | A | G | 44 | a0001c0001t0027g0226 a0001c0001t0027g0227 a0002c0002t0003g0251 others(41): Show |
45 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.363+970T>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 5/22 | chr9 | 132924617 | |||||||
| chr9:132924938 | C | T | 5 | a0001c0001t0003g0044 a0001c0001t0003g0045 a0001c0001t0003g0107 others(2): Show |
5 | NA18951.hp1 NA18965.hp1 NA18972.hp1 others(2): Show |
intron_variant | MODIFIER | c.363+649G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 5/22 | chr9 | 132924938 | |||||||
| chr9:132925249 | T | C | 1 | a0002c0002t0098g0235 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.363+338A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 5/22 | chr9 | 132925249 | |||||||
| chr9:132925375 | C | T | 2 | a0002c0009t0093g0303 a0002c0009t0100g0304 |
2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.363+212G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 5/22 | chr9 | 132925375 | |||||||
| chr9:132925801 | G | C | 1 | a0001c0001t0001g0180 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.211-62C>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 4/22 | chr9 | 132925801 | |||||||
| chr9:132926025 | A | G | 2 | a0002c0002t0066g0291 a0002c0002t0067g0290 |
2 | HG01081.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.211-286T>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 4/22 | chr9 | 132926025 | |||||||
| chr9:132926073 | A | C | 1 | a0001c0001t0001g0022 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.211-334T>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 4/22 | chr9 | 132926073 | |||||||
| chr9:132926494 | C | T | 1 | a0001c0001t0099g0112 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.210+707G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 4/22 | chr9 | 132926494 | |||||||
| chr9:132926572 | G | A | 2 | a0001c0001t0027g0226 a0001c0001t0027g0227 |
2 | HG02970.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.210+629C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 4/22 | chr9 | 132926572 | |||||||
| chr9:132926644 | C | T | 2 | a0002c0009t0093g0303 a0002c0009t0100g0304 |
2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.210+557G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 4/22 | chr9 | 132926644 | |||||||
| chr9:132926685 | CT | C | 103 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(100): Show |
124 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.210+515delA | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 4/22 | chr9 | 132926685 | |||||||
| chr9:132926689 | T | G | 44 | a0001c0001t0027g0226 a0001c0001t0027g0227 a0002c0002t0003g0251 others(41): Show |
45 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.210+512A>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 4/22 | chr9 | 132926689 | |||||||
| chr9:132926703 | A | G | 8 | a0001c0001t0001g0020 a0001c0001t0001g0153 a0001c0001t0001g0154 others(5): Show |
9 | HG01099.hp2 HG01106.hp2 HG01167.hp2 others(6): Show |
intron_variant | MODIFIER | c.210+498T>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 4/22 | chr9 | 132926703 | |||||||
| chr9:132926777 | C | T | 2 | a0002c0009t0093g0303 a0002c0009t0100g0304 |
2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.210+424G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 4/22 | chr9 | 132926777 | |||||||
| chr9:132926799 | T | C | 1 | a0001c0001t0061g0110 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.210+402A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 4/22 | chr9 | 132926799 | |||||||
| chr9:132926911 | A | G | 113 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(110): Show |
134 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.210+290T>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 4/22 | chr9 | 132926911 | |||||||
| chr9:132927168 | C | T | 1 | a0001c0001t0061g0110 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.210+33G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 4/22 | chr9 | 132927168 | |||||||
| chr9:132927452 | T | G | 30 | a0002c0002t0003g0251 a0002c0002t0003g0253 a0002c0002t0003g0254 others(27): Show |
30 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.107-148A>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 3/22 | chr9 | 132927452 | |||||||
| chr9:132927521 | C | CT | 114 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(111): Show |
134 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.107-218dupA | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 3/22 | chr9 | 132927521 | |||||||
| chr9:132927521 | C | CTT | 14 | a0001c0001t0001g0139 a0001c0001t0001g0151 a0001c0001t0001g0232 others(11): Show |
15 | HG00673.hp2 HG01255.hp2 HG02056.hp1 others(12): Show |
intron_variant | MODIFIER | c.107-219_107-218dup others(2): Show |
TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 3/22 | chr9 | 132927521 | |||||||
| chr9:132927521 | C | CTTT | 25 | a0001c0001t0027g0227 a0002c0002t0003g0251 a0002c0002t0003g0253 others(22): Show |
25 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(22): Show |
intron_variant | MODIFIER | c.107-220_107-218dup others(3): Show |
TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 3/22 | chr9 | 132927521 | |||||||
| chr9:132927521 | C | CTTTT | 10 | a0001c0001t0027g0226 a0002c0002t0012g0266 a0002c0002t0029g0269 others(7): Show |
10 | HG00639.hp1 HG01081.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.107-221_107-218dup others(4): Show |
TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 3/22 | chr9 | 132927521 | |||||||
| chr9:132927683 | C | T | 1 | a0001c0001t0055g0116 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.107-379G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 3/22 | chr9 | 132927683 | |||||||
| chr9:132927772 | G | A | 21 | a0001c0001t0001g0137 a0001c0003t0009g0276 a0001c0003t0009g0281 others(18): Show |
21 | HG01074.hp1 HG01175.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.107-468C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 3/22 | chr9 | 132927772 | |||||||
| chr9:132927779 | C | A | 3 | a0001c0001t0053g0117 a0001c0001t0055g0116 a0001c0001t0056g0118 |
3 | HG01106.hp1 HG02258.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.107-475G>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 3/22 | chr9 | 132927779 | |||||||
| chr9:132927845 | C | T | 1 | a0001c0001t0078g0135 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.107-541G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 3/22 | chr9 | 132927845 | |||||||
| chr9:132927922 | C | A | 1 | a0002c0002t0057g0026 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.107-618G>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 3/22 | chr9 | 132927922 | |||||||
| chr9:132928134 | G | A | 3 | a0001c0001t0001g0191 a0002c0002t0038g0301 a0002c0002t0038g0302 |
3 | HG02572.hp1 HG02630.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.106+633C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 3/22 | chr9 | 132928134 | |||||||
| chr9:132928369 | A | C | 2 | a0002c0009t0093g0303 a0002c0009t0100g0304 |
2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.106+398T>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 3/22 | chr9 | 132928369 | |||||||
| chr9:132928580 | C | A | 2 | a0005c0010t0043g0224 a0005c0010t0043g0225 |
2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.106+187G>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 3/22 | chr9 | 132928580 | |||||||
| chr9:132928597 | C | G | 1 | a0002c0002t0012g0266 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.106+170G>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 3/22 | chr9 | 132928597 | |||||||
| chr9:132928679 | A | T | 1 | a0001c0001t0001g0180 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.106+88T>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 3/22 | chr9 | 132928679 | |||||||
| chr9:132928752 | T | C | 10 | a0001c0001t0001g0013 a0001c0001t0001g0119 a0001c0001t0001g0120 others(7): Show |
11 | HG00558.hp1 NA18952.hp1 NA18984.hp2 others(8): Show |
intron_variant | MODIFIER | c.106+15A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 3/22 | chr9 | 132928752 | |||||||
| chr9:132929039 | G | A | 1 | a0001c0001t0054g0115 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-80-87C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/22 | chr9 | 132929039 | |||||||
| chr9:132929161 | C | T | 1 | a0001c0001t0006g0195 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-80-209G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/22 | chr9 | 132929161 | |||||||
| chr9:132929187 | T | G | 2 | a0001c0001t0001g0177 a0003c0005t0001g0178 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.-80-235A>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/22 | chr9 | 132929187 | |||||||
| chr9:132929322 | T | G | 1 | a0001c0001t0002g0095 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-80-370A>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/22 | chr9 | 132929322 | |||||||
| chr9:132929331 | C | T | 1 | a0002c0002t0032g0021 | 2 | HG02723.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.-80-379G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/22 | chr9 | 132929331 | |||||||
| chr9:132929348 | T | C | 113 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(110): Show |
134 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.-80-396A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/22 | chr9 | 132929348 | |||||||
| chr9:132929355 | TC | T | 4 | a0001c0001t0003g0229 a0001c0001t0003g0295 a0001c0001t0010g0230 others(1): Show |
4 | HG00323.hp2 NA18946.hp1 NA19086.hp1 others(1): Show |
intron_variant | MODIFIER | c.-80-404delG | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/22 | chr9 | 132929355 | |||||||
| chr9:132929522 | G | A | 30 | a0002c0002t0003g0251 a0002c0002t0003g0253 a0002c0002t0003g0254 others(27): Show |
30 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.-80-570C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/22 | chr9 | 132929522 | |||||||
| chr9:132929760 | A | AC | 7 | a0001c0001t0006g0195 a0001c0001t0006g0196 a0001c0001t0006g0197 others(4): Show |
7 | HG02145.hp1 HG02451.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.-80-809_-80-808ins others(1): Show |
TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/22 | chr9 | 132929760 | |||||||
| chr9:132930220 | A | C | 37 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(34): Show |
42 | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.-80-1268T>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/22 | chr9 | 132930220 | |||||||
| chr9:132930587 | C | CA | 99 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(96): Show |
120 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.-80-1636dupT | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/22 | chr9 | 132930587 | |||||||
| chr9:132930587 | C | CAA | 66 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0180 others(63): Show |
66 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-1637_-80-1636d others(4): Show |
TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/22 | chr9 | 132930587 | |||||||
| chr9:132930587 | C | CAAA | 12 | a0001c0001t0001g0192 a0001c0001t0001g0212 a0001c0001t0006g0200 others(9): Show |
12 | HG02145.hp1 HG02572.hp1 HG02970.hp2 others(9): Show |
intron_variant | MODIFIER | c.-80-1638_-80-1636d others(5): Show |
TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/22 | chr9 | 132930587 | |||||||
| chr9:132930920 | T | G | 1 | a0002c0002t0086g0260 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-80-1968A>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/22 | chr9 | 132930920 | |||||||
| chr9:132930971 | A | G | 1 | a0001c0001t0025g0040 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-80-2019T>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/22 | chr9 | 132930971 | |||||||
| chr9:132930980 | C | A | 1 | a0001c0001t0078g0135 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-80-2028G>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/22 | chr9 | 132930980 | |||||||
| chr9:132931261 | G | A | 1 | a0001c0001t0002g0109 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-80-2309C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/22 | chr9 | 132931261 | |||||||
| chr9:132931384 | G | A | 4 | a0002c0002t0029g0269 a0002c0002t0029g0271 a0002c0002t0034g0292 others(1): Show |
4 | HG01891.hp1 HG02258.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-80-2432C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/22 | chr9 | 132931384 | |||||||
| chr9:132931475 | T | C | 4 | a0001c0001t0022g0220 a0001c0001t0022g0221 a0001c0001t0044g0222 others(1): Show |
4 | HG03041.hp2 HG03195.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.-80-2523A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/22 | chr9 | 132931475 | |||||||
| chr9:132931606 | G | A | 1 | a0001c0001t0050g0193 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-80-2654C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/22 | chr9 | 132931606 | |||||||
| chr9:132931761 | G | C | 1 | a0002c0002t0005g0261 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-80-2809C>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/22 | chr9 | 132931761 | |||||||
| chr9:132932013 | C | G | 1 | a0001c0001t0063g0039 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-81+3020G>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/22 | chr9 | 132932013 | |||||||
| chr9:132932027 | C | T | 1 | a0002c0013t0087g0293 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-81+3006G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/22 | chr9 | 132932027 | |||||||
| chr9:132932358 | A | G | 1 | a0002c0002t0032g0021 | 2 | HG02723.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.-81+2675T>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/22 | chr9 | 132932358 | |||||||
| chr9:132932430 | G | A | 1 | a0001c0001t0034g0024 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-81+2603C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/22 | chr9 | 132932430 | |||||||
| chr9:132932593 | T | G | 1 | a0001c0001t0001g0194 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-81+2440A>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/22 | chr9 | 132932593 | |||||||
| chr9:132932635 | G | T | 1 | a0002c0013t0087g0293 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-81+2398C>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/22 | chr9 | 132932635 | |||||||
| chr9:132933010 | G | A | 4 | a0001c0001t0005g0033 a0001c0001t0005g0034 a0001c0001t0037g0032 others(1): Show |
4 | HG02647.hp1 HG02895.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-81+2023C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/22 | chr9 | 132933010 | |||||||
| chr9:132933444 | GT | G | 35 | a0002c0002t0003g0251 a0002c0002t0003g0253 a0002c0002t0003g0254 others(32): Show |
36 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.-81+1588delA | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/22 | chr9 | 132933444 | |||||||
| chr9:132933471 | T | C | 30 | a0002c0002t0003g0251 a0002c0002t0003g0253 a0002c0002t0003g0254 others(27): Show |
30 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.-81+1562A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/22 | chr9 | 132933471 | |||||||
| chr9:132933474 | C | T | 102 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(99): Show |
123 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.-81+1559G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/22 | chr9 | 132933474 | |||||||
| chr9:132933513 | G | A | 1 | a0001c0001t0024g0202 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-81+1520C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/22 | chr9 | 132933513 | |||||||
| chr9:132933682 | G | A | 2 | a0001c0001t0082g0289 a0001c0001t0083g0264 |
2 | HG00735.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.-81+1351C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/22 | chr9 | 132933682 | |||||||
| chr9:132933998 | T | C | 2 | a0002c0002t0070g0263 a0002c0002t0075g0262 |
2 | NA19065.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.-81+1035A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/22 | chr9 | 132933998 | |||||||
| chr9:132934008 | T | C | 2 | a0001c0001t0001g0203 a0001c0001t0001g0239 |
2 | HG02080.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.-81+1025A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/22 | chr9 | 132934008 | |||||||
| chr9:132934194 | C | A | 1 | a0002c0002t0098g0235 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-81+839G>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/22 | chr9 | 132934194 | |||||||
| chr9:132934329 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-81+704G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/22 | chr9 | 132934329 | |||||||
| chr9:132934466 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-81+567G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/22 | chr9 | 132934466 | |||||||
| chr9:132934557 | G | A | 1 | a0001c0001t0061g0110 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-81+476C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/22 | chr9 | 132934557 | |||||||
| chr9:132934861 | T | G | 1 | a0001c0006t0020g0111 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-81+172A>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/22 | chr9 | 132934861 | |||||||
| chr9:132934947 | G | A | 1 | a0002c0002t0012g0266 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-81+86C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/22 | chr9 | 132934947 | |||||||
| chr9:132935112 | T | C | 2 | a0002c0009t0093g0303 a0002c0009t0100g0304 |
2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-143-17A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132935112 | |||||||
| chr9:132935209 | C | G | 1 | a0002c0002t0057g0026 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-143-114G>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132935209 | |||||||
| chr9:132935250 | C | T | 2 | a0002c0009t0093g0303 a0002c0009t0100g0304 |
2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-143-155G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132935250 | |||||||
| chr9:132935552 | T | C | 2 | a0002c0009t0093g0303 a0002c0009t0100g0304 |
2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-143-457A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132935552 | |||||||
| chr9:132935623 | G | C | 4 | a0001c0001t0053g0117 a0001c0001t0054g0115 a0001c0001t0055g0116 others(1): Show |
4 | HG01106.hp1 HG02258.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.-143-528C>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132935623 | |||||||
| chr9:132935664 | C | T | 2 | a0001c0001t0007g0038 a0004c0011t0007g0005 |
3 | HG02559.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-143-569G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132935664 | |||||||
| chr9:132935714 | C | T | 2 | a0002c0009t0093g0303 a0002c0009t0100g0304 |
2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-143-619G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132935714 | |||||||
| chr9:132935771 | C | T | 1 | a0001c0001t0078g0135 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-143-676G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132935771 | |||||||
| chr9:132935870 | A | C | 1 | a0002c0013t0087g0293 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-143-775T>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132935870 | |||||||
| chr9:132935882 | C | T | 7 | a0001c0001t0001g0014 a0001c0001t0001g0130 a0001c0001t0001g0132 others(4): Show |
8 | HG02165.hp2 NA18946.hp2 NA18948.hp1 others(5): Show |
intron_variant | MODIFIER | c.-143-787G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132935882 | |||||||
| chr9:132936041 | C | A | 1 | a0001c0001t0001g0204 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-143-946G>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132936041 | |||||||
| chr9:132936396 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-143-1301G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132936396 | |||||||
| chr9:132936423 | T | C | 1 | a0001c0001t0001g0020 | 2 | HG01106.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.-143-1328A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132936423 | |||||||
| chr9:132936550 | T | C | 3 | a0001c0001t0053g0117 a0001c0001t0055g0116 a0001c0001t0056g0118 |
3 | HG01106.hp1 HG02258.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.-143-1455A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132936550 | |||||||
| chr9:132936892 | G | A | 3 | a0002c0002t0032g0021 a0002c0002t0066g0291 a0002c0002t0067g0290 |
4 | HG01081.hp1 HG02723.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.-143-1797C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132936892 | |||||||
| chr9:132937028 | C | G | 1 | a0002c0002t0040g0128 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-143-1933G>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132937028 | |||||||
| chr9:132937100 | G | A | 1 | a0002c0002t0057g0026 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-143-2005C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132937100 | |||||||
| chr9:132937173 | G | A | 2 | a0002c0002t0066g0291 a0002c0002t0067g0290 |
2 | HG01081.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-143-2078C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132937173 | |||||||
| chr9:132937181 | C | A | 2 | a0002c0009t0093g0303 a0002c0009t0100g0304 |
2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-143-2086G>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132937181 | |||||||
| chr9:132937181 | C | G | 29 | a0002c0002t0003g0251 a0002c0002t0003g0253 a0002c0002t0003g0254 others(26): Show |
29 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(26): Show |
intron_variant | MODIFIER | c.-143-2086G>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132937181 | |||||||
| chr9:132937304 | G | A | 1 | a0001c0001t0041g0113 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-143-2209C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132937304 | |||||||
| chr9:132937335 | C | T | 2 | a0001c0001t0015g0036 a0001c0001t0015g0037 |
2 | HG02965.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-143-2240G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132937335 | |||||||
| chr9:132937336 | G | C | 66 | a0001c0001t0033g0023 a0001c0001t0033g0286 a0001c0001t0034g0024 others(63): Show |
67 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.-143-2241C>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132937336 | |||||||
| chr9:132937439 | G | A | 3 | a0001c0001t0005g0214 a0001c0001t0005g0215 a0001c0001t0005g0216 |
3 | HG01167.hp1 HG02145.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.-143-2344C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132937439 | |||||||
| chr9:132937592 | A | T | 2 | a0005c0010t0043g0224 a0005c0010t0043g0225 |
2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-143-2497T>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132937592 | |||||||
| chr9:132937614 | C | T | 59 | a0001c0001t0033g0023 a0001c0001t0033g0286 a0001c0001t0034g0024 others(56): Show |
60 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.-143-2519G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132937614 | |||||||
| chr9:132937692 | G | A | 2 | a0002c0009t0093g0303 a0002c0009t0100g0304 |
2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-143-2597C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132937692 | |||||||
| chr9:132937800 | C | T | 2 | a0002c0009t0093g0303 a0002c0009t0100g0304 |
2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-143-2705G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132937800 | |||||||
| chr9:132937941 | C | T | 1 | a0001c0006t0002g0035 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-143-2846G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132937941 | |||||||
| chr9:132938071 | T | C | 2 | a0001c0001t0053g0117 a0001c0001t0056g0118 |
2 | HG02258.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.-143-2976A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132938071 | |||||||
| chr9:132938251 | T | C | 1 | a0007c0017t0001g0205 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-143-3156A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132938251 | |||||||
| chr9:132938330 | G | A | 1 | a0002c0013t0087g0293 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-143-3235C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132938330 | |||||||
| chr9:132938534 | G | A | 2 | a0005c0010t0043g0224 a0005c0010t0043g0225 |
2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-143-3439C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132938534 | |||||||
| chr9:132938701 | C | T | 1 | a0001c0003t0081g0268 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-143-3606G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132938701 | |||||||
| chr9:132938744 | C | A | 1 | a0001c0001t0001g0206 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-143-3649G>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132938744 | |||||||
| chr9:132938825 | T | C | 1 | a0001c0001t0011g0114 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-143-3730A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132938825 | |||||||
| chr9:132938879 | G | A | 1 | a0002c0013t0087g0293 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-143-3784C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132938879 | |||||||
| chr9:132938994 | A | G | 2 | a0002c0009t0093g0303 a0002c0009t0100g0304 |
2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-143-3899T>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132938994 | |||||||
| chr9:132939296 | G | T | 29 | a0002c0002t0003g0251 a0002c0002t0003g0253 a0002c0002t0003g0254 others(26): Show |
29 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(26): Show |
intron_variant | MODIFIER | c.-143-4201C>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132939296 | |||||||
| chr9:132939882 | T | C | 193 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(190): Show |
215 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.-144+4661A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132939882 | |||||||
| chr9:132939933 | C | T | 10 | a0001c0001t0001g0013 a0001c0001t0001g0119 a0001c0001t0001g0120 others(7): Show |
11 | HG00558.hp1 NA18952.hp1 NA18984.hp2 others(8): Show |
intron_variant | MODIFIER | c.-144+4610G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132939933 | |||||||
| chr9:132940087 | T | G | 115 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(112): Show |
136 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.-144+4456A>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132940087 | |||||||
| chr9:132940239 | TA | T | 8 | a0001c0001t0005g0033 a0001c0001t0005g0034 a0001c0001t0011g0030 others(5): Show |
8 | HG02280.hp2 HG02486.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.-144+4303delT | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132940239 | |||||||
| chr9:132940485 | T | G | 1 | a0001c0001t0020g0207 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-144+4058A>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132940485 | |||||||
| chr9:132940533 | T | C | 1 | a0002c0002t0074g0265 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-144+4010A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132940533 | |||||||
| chr9:132940753 | T | A | 5 | a0001c0001t0001g0209 a0001c0001t0001g0211 a0001c0001t0001g0212 others(2): Show |
5 | NA18941.hp2 NA18960.hp2 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.-144+3790A>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132940753 | |||||||
| chr9:132940878 | C | A | 1 | a0001c0007t0064g0294 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-144+3665G>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132940878 | |||||||
| chr9:132941217 | T | C | 1 | a0001c0001t0002g0213 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-144+3326A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132941217 | |||||||
| chr9:132941232 | G | A | 3 | a0001c0001t0005g0214 a0001c0001t0005g0215 a0001c0001t0005g0216 |
3 | HG01167.hp1 HG02145.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.-144+3311C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132941232 | |||||||
| chr9:132941234 | A | G | 2 | a0005c0010t0043g0224 a0005c0010t0043g0225 |
2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-144+3309T>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132941234 | |||||||
| chr9:132941498 | A | G | 70 | a0001c0001t0027g0226 a0001c0001t0027g0227 a0001c0001t0033g0023 others(67): Show |
71 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.-144+3045T>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132941498 | |||||||
| chr9:132941512 | A | C | 1 | a0001c0001t0003g0028 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-144+3031T>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132941512 | |||||||
| chr9:132941923 | C | T | 1 | a0001c0001t0048g0027 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-144+2620G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132941923 | |||||||
| chr9:132941969 | C | T | 2 | a0002c0009t0093g0303 a0002c0009t0100g0304 |
2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-144+2574G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132941969 | |||||||
| chr9:132942390 | T | G | 3 | a0001c0001t0039g0217 a0001c0001t0039g0218 a0001c0001t0088g0219 |
3 | HG00733.hp2 HG01516.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.-144+2153A>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132942390 | |||||||
| chr9:132942406 | G | A | 3 | a0001c0001t0022g0220 a0001c0001t0022g0221 a0001c0001t0044g0222 |
3 | HG03195.hp2 NA18906.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-144+2137C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132942406 | |||||||
| chr9:132942467 | T | C | 1 | a0002c0002t0012g0266 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-144+2076A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132942467 | |||||||
| chr9:132942571 | T | C | 1 | a0001c0001t0001g0223 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-144+1972A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132942571 | |||||||
| chr9:132943231 | T | TA | 63 | a0001c0001t0003g0229 a0001c0001t0003g0295 a0001c0001t0010g0230 others(60): Show |
63 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.-144+1311dupT | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132943231 | |||||||
| chr9:132943231 | T | TAA | 7 | a0001c0003t0031g0298 a0001c0003t0031g0300 a0001c0003t0035g0297 others(4): Show |
8 | HG01074.hp1 HG01175.hp1 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.-144+1310_-144+131 others(6): Show |
TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132943231 | |||||||
| chr9:132943275 | C | CTTCAGTA others(16): Show |
1 | a0002c0002t0057g0026 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-144+1245_-144+126 others(27): Show |
TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132943275 | |||||||
| chr9:132943294 | T | C | 2 | a0001c0001t0001g0232 a0001c0001t0001g0233 |
2 | HG00673.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.-144+1249A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132943294 | |||||||
| chr9:132943316 | T | A | 1 | a0001c0001t0001g0234 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-144+1227A>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132943316 | |||||||
| chr9:132943317 | T | A | 1 | a0001c0001t0001g0234 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-144+1226A>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132943317 | |||||||
| chr9:132943424 | C | A | 1 | a0002c0002t0032g0021 | 2 | HG02723.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.-144+1119G>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132943424 | |||||||
| chr9:132943511 | C | G | 1 | a0001c0001t0007g0025 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-144+1032G>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132943511 | |||||||
| chr9:132943522 | G | C | 2 | a0002c0009t0093g0303 a0002c0009t0100g0304 |
2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-144+1021C>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132943522 | |||||||
| chr9:132943625 | T | C | 1 | a0002c0002t0098g0235 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-144+918A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132943625 | |||||||
| chr9:132943733 | C | A | 2 | a0001c0001t0018g0236 a0001c0001t0018g0237 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-144+810G>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132943733 | |||||||
| chr9:132943791 | A | C | 2 | a0002c0009t0093g0303 a0002c0009t0100g0304 |
2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-144+752T>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132943791 | |||||||
| chr9:132943980 | C | T | 2 | a0002c0009t0093g0303 a0002c0009t0100g0304 |
2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-144+563G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132943980 | |||||||
| chr9:132944033 | G | T | 32 | a0001c0001t0001g0239 a0001c0001t0002g0238 a0001c0001t0083g0264 others(29): Show |
32 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.-144+510C>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132944033 | |||||||
| chr9:132944097 | T | C | 2 | a0002c0002t0038g0301 a0002c0002t0038g0302 |
2 | HG02572.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.-144+446A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132944097 | |||||||
| chr9:132944192 | G | T | 2 | a0001c0001t0033g0023 a0001c0001t0034g0024 |
2 | HG02886.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-144+351C>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132944192 | |||||||
| chr9:132944194 | G | A | 65 | a0001c0001t0001g0239 a0001c0001t0002g0238 a0001c0001t0003g0295 others(62): Show |
66 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.-144+349C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132944194 | |||||||
| chr9:132944373 | G | A | 2 | a0002c0009t0093g0303 a0002c0009t0100g0304 |
2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-144+170C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132944373 | |||||||
| chr9:132944441 | C | G | 1 | a0001c0001t0001g0022 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-144+102G>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132944441 |