Item | Value |
---|---|
geneid | 27283 |
ensemblid | ENSG00000137251.16 |
hgncid | 14599 |
symbol | TINAG |
name | tubulointerstitial nephritis antigen |
refseq_nuc | NM_014464.4 |
refseq_prot | NP_055279.3 |
ensembl_nuc | ENST00000259782.9 |
ensembl_prot | ENSP00000259782.4 |
mane_status | MANE Select |
chr | chr6 |
start | 54308441 |
end | 54390142 |
strand | + |
ver | v1.2 |
region | chr6:54308441-54390142 |
region5000 | chr6:54303441-54395142 |
regionname0 | TINAG_chr6_54308441_54390142 |
regionname5000 | TINAG_chr6_54303441_54395142 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 476 | 178 | 42 | 33 | 86 | 5 | 11 | 70 | TINAG_chr6_54303441_54395142 | TINAG | MWTGY others(471): Show |
chr6 | 54303441 | 54395142 |
a0002 | 0/0 | 476 | 64 | 8 | 2 | 49 | 0 | 5 | 42 | TINAG_chr6_54303441_54395142 | TINAG | MWTGY others(471): Show |
chr6 | 54303441 | 54395142 |
a0003 | 1/0 | 476 | 62 | 11 | 17 | 21 | 1 | 11 | 18 | TINAG_chr6_54303441_54395142 | TINAG | MWTGY others(471): Show |
chr6 | 54303441 | 54395142 |
a0004 | 0/0 | 476 | 17 | 1 | 4 | 8 | 2 | 2 | 5 | TINAG_chr6_54303441_54395142 | TINAG | MWTGY others(471): Show |
chr6 | 54303441 | 54395142 |
a0005 | 0/0 | 476 | 13 | 5 | 2 | 1 | 1 | 4 | 1 | TINAG_chr6_54303441_54395142 | TINAG | MWTGY others(471): Show |
chr6 | 54303441 | 54395142 |
a0006 | 0/0 | 476 | 6 | 1 | 2 | 0 | 2 | 1 | 0 | TINAG_chr6_54303441_54395142 | TINAG | MWTGY others(471): Show |
chr6 | 54303441 | 54395142 |
a0007 | 0/0 | 476 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | MWAGY others(471): Show |
chr6 | 54303441 | 54395142 |
a0008 | 0/0 | 476 | 3 | 1 | 2 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | MWAGY others(471): Show |
chr6 | 54303441 | 54395142 |
a0009 | 0/0 | 476 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | MWTGY others(471): Show |
chr6 | 54303441 | 54395142 |
a0010 | 0/0 | 476 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | MWTGY others(471): Show |
chr6 | 54303441 | 54395142 |
a0011 | 0/0 | 476 | 2 | 0 | 0 | 0 | 1 | 1 | 0 | TINAG_chr6_54303441_54395142 | TINAG | MWTGY others(471): Show |
chr6 | 54303441 | 54395142 |
a0012 | 0/0 | 476 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | MWTGY others(471): Show |
chr6 | 54303441 | 54395142 |
a0013 | 0/0 | 476 | 2 | 1 | 0 | 1 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | MWTGY others(471): Show |
chr6 | 54303441 | 54395142 |
a0014 | 0/0 | 476 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | MWTGY others(471): Show |
chr6 | 54303441 | 54395142 |
a0015 | 0/0 | 476 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | MWTGY others(471): Show |
chr6 | 54303441 | 54395142 |
a0016 | 0/0 | 476 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | MWTGY others(471): Show |
chr6 | 54303441 | 54395142 |
a0017 | 0/0 | 476 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | MWAGY others(471): Show |
chr6 | 54303441 | 54395142 |
a0018 | 0/0 | 476 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | MWTGY others(471): Show |
chr6 | 54303441 | 54395142 |
a0019 | 0/0 | 476 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | MWTGY others(471): Show |
chr6 | 54303441 | 54395142 |
a0020 | 0/0 | 476 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | MWTGY others(471): Show |
chr6 | 54303441 | 54395142 |
a0021 | 0/0 | 476 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | MWAGY others(471): Show |
chr6 | 54303441 | 54395142 |
a0022 | 0/0 | 476 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TINAG_chr6_54303441_54395142 | TINAG | MWTGY others(471): Show |
chr6 | 54303441 | 54395142 |
a0023 | 0/0 | 476 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | MWTGY others(471): Show |
chr6 | 54303441 | 54395142 |
a0024 | 0/0 | 476 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | MWTGY others(471): Show |
chr6 | 54303441 | 54395142 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1428 | 176 | 40 | 33 | 86 | 5 | 11 | TINAG_chr6_54303441_54395142 | TINAG | ATGTG others(1423): Show |
chr6 | 54303441 | 54395142 | ||
a0001c0010 | 0/0 | 1428 | 2 | 2 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | ATGTG others(1423): Show |
chr6 | 54303441 | 54395142 | ||
a0002c0002 | 0/0 | 1428 | 64 | 8 | 2 | 49 | 0 | 5 | TINAG_chr6_54303441_54395142 | TINAG | ATGTG others(1423): Show |
chr6 | 54303441 | 54395142 | ||
a0003c0003 | 1/0 | 1428 | 62 | 11 | 17 | 21 | 1 | 11 | TINAG_chr6_54303441_54395142 | TINAG | ATGTG others(1423): Show |
chr6 | 54303441 | 54395142 | ||
a0004c0004 | 0/0 | 1428 | 16 | 0 | 4 | 8 | 2 | 2 | TINAG_chr6_54303441_54395142 | TINAG | ATGTG others(1423): Show |
chr6 | 54303441 | 54395142 | ||
a0004c0021 | 0/0 | 1428 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | ATGTG others(1423): Show |
chr6 | 54303441 | 54395142 | ||
a0005c0005 | 0/0 | 1428 | 13 | 5 | 2 | 1 | 1 | 4 | TINAG_chr6_54303441_54395142 | TINAG | ATGTG others(1423): Show |
chr6 | 54303441 | 54395142 | ||
a0006c0006 | 0/0 | 1428 | 6 | 1 | 2 | 0 | 2 | 1 | TINAG_chr6_54303441_54395142 | TINAG | ATGTG others(1423): Show |
chr6 | 54303441 | 54395142 | ||
a0007c0007 | 0/0 | 1428 | 6 | 6 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | ATGTG others(1423): Show |
chr6 | 54303441 | 54395142 | ||
a0008c0008 | 0/0 | 1428 | 3 | 1 | 2 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | ATGTG others(1423): Show |
chr6 | 54303441 | 54395142 | ||
a0009c0016 | 0/0 | 1428 | 2 | 1 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | ATGTG others(1423): Show |
chr6 | 54303441 | 54395142 | ||
a0010c0013 | 0/0 | 1428 | 2 | 1 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | ATGTG others(1423): Show |
chr6 | 54303441 | 54395142 | ||
a0011c0011 | 0/0 | 1428 | 2 | 0 | 0 | 0 | 1 | 1 | TINAG_chr6_54303441_54395142 | TINAG | ATGTG others(1423): Show |
chr6 | 54303441 | 54395142 | ||
a0012c0009 | 0/0 | 1428 | 2 | 2 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | ATGTG others(1423): Show |
chr6 | 54303441 | 54395142 | ||
a0013c0012 | 0/0 | 1428 | 2 | 1 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | ATGTG others(1423): Show |
chr6 | 54303441 | 54395142 | ||
a0014c0014 | 0/0 | 1428 | 2 | 2 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | ATGTG others(1423): Show |
chr6 | 54303441 | 54395142 | ||
a0015c0015 | 0/0 | 1428 | 2 | 2 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | ATGTG others(1423): Show |
chr6 | 54303441 | 54395142 | ||
a0016c0017 | 0/0 | 1428 | 2 | 2 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | ATGTG others(1423): Show |
chr6 | 54303441 | 54395142 | ||
a0017c0018 | 0/0 | 1428 | 2 | 2 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | ATGTG others(1423): Show |
chr6 | 54303441 | 54395142 | ||
a0018c0024 | 0/0 | 1428 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | ATGTG others(1423): Show |
chr6 | 54303441 | 54395142 | ||
a0019c0022 | 0/0 | 1428 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | ATGTG others(1423): Show |
chr6 | 54303441 | 54395142 | ||
a0020c0019 | 0/0 | 1428 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | ATGTG others(1423): Show |
chr6 | 54303441 | 54395142 | ||
a0021c0026 | 0/0 | 1428 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | ATGTG others(1423): Show |
chr6 | 54303441 | 54395142 | ||
a0022c0023 | 0/0 | 1428 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | ATGTG others(1423): Show |
chr6 | 54303441 | 54395142 | ||
a0023c0020 | 0/0 | 1428 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | ATGTG others(1423): Show |
chr6 | 54303441 | 54395142 | ||
a0024c0025 | 0/0 | 1428 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | ATGTG others(1423): Show |
chr6 | 54303441 | 54395142 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 1758 | 176 | 40 | 33 | 86 | 5 | 11 | TINAG_chr6_54303441_54395142 | TINAG | GTTCA others(1753): Show |
chr6 | 54303441 | 54395142 |
a0001c0010t0001 | 0/0 | 1758 | 2 | 2 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | GTTCA others(1753): Show |
chr6 | 54303441 | 54395142 |
a0002c0002t0001 | 0/0 | 1758 | 64 | 8 | 2 | 49 | 0 | 5 | TINAG_chr6_54303441_54395142 | TINAG | GTTCA others(1753): Show |
chr6 | 54303441 | 54395142 |
a0003c0003t0001 | 1/0 | 1758 | 62 | 11 | 17 | 21 | 1 | 11 | TINAG_chr6_54303441_54395142 | TINAG | GTTCA others(1753): Show |
chr6 | 54303441 | 54395142 |
a0004c0004t0001 | 0/0 | 1758 | 16 | 0 | 4 | 8 | 2 | 2 | TINAG_chr6_54303441_54395142 | TINAG | GTTCA others(1753): Show |
chr6 | 54303441 | 54395142 |
a0004c0021t0004 | 0/0 | 1758 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | GTTCA others(1753): Show |
chr6 | 54303441 | 54395142 |
a0005c0005t0001 | 0/0 | 1758 | 13 | 5 | 2 | 1 | 1 | 4 | TINAG_chr6_54303441_54395142 | TINAG | GTTCA others(1753): Show |
chr6 | 54303441 | 54395142 |
a0006c0006t0001 | 0/0 | 1758 | 5 | 0 | 2 | 0 | 2 | 1 | TINAG_chr6_54303441_54395142 | TINAG | GTTCA others(1753): Show |
chr6 | 54303441 | 54395142 |
a0006c0006t0002 | 0/0 | 1758 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | GTTCA others(1753): Show |
chr6 | 54303441 | 54395142 |
a0007c0007t0001 | 0/0 | 1758 | 6 | 6 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | GTTCA others(1753): Show |
chr6 | 54303441 | 54395142 |
a0008c0008t0002 | 0/0 | 1758 | 3 | 1 | 2 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | GTTCA others(1753): Show |
chr6 | 54303441 | 54395142 |
a0009c0016t0001 | 0/0 | 1758 | 2 | 1 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | GTTCA others(1753): Show |
chr6 | 54303441 | 54395142 |
a0010c0013t0001 | 0/0 | 1758 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | GTTCA others(1753): Show |
chr6 | 54303441 | 54395142 |
a0010c0013t0002 | 0/0 | 1758 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | GTTCA others(1753): Show |
chr6 | 54303441 | 54395142 |
a0011c0011t0001 | 0/0 | 1758 | 2 | 0 | 0 | 0 | 1 | 1 | TINAG_chr6_54303441_54395142 | TINAG | GTTCA others(1753): Show |
chr6 | 54303441 | 54395142 |
a0012c0009t0001 | 0/0 | 1758 | 2 | 2 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | GTTCA others(1753): Show |
chr6 | 54303441 | 54395142 |
a0013c0012t0001 | 0/0 | 1758 | 2 | 1 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | GTTCA others(1753): Show |
chr6 | 54303441 | 54395142 |
a0014c0014t0003 | 0/0 | 1758 | 2 | 2 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | GTTCA others(1753): Show |
chr6 | 54303441 | 54395142 |
a0015c0015t0001 | 0/0 | 1758 | 2 | 2 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | GTTCA others(1753): Show |
chr6 | 54303441 | 54395142 |
a0016c0017t0001 | 0/0 | 1758 | 2 | 2 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | GTTCA others(1753): Show |
chr6 | 54303441 | 54395142 |
a0017c0018t0001 | 0/0 | 1758 | 2 | 2 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | GTTCA others(1753): Show |
chr6 | 54303441 | 54395142 |
a0018c0024t0001 | 0/0 | 1758 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | GTTCA others(1753): Show |
chr6 | 54303441 | 54395142 |
a0019c0022t0001 | 0/0 | 1758 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | GTTCA others(1753): Show |
chr6 | 54303441 | 54395142 |
a0020c0019t0001 | 0/0 | 1758 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | GTTCA others(1753): Show |
chr6 | 54303441 | 54395142 |
a0021c0026t0001 | 0/0 | 1758 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | GTTCA others(1753): Show |
chr6 | 54303441 | 54395142 |
a0022c0023t0001 | 0/0 | 1758 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | GTTCA others(1753): Show |
chr6 | 54303441 | 54395142 |
a0023c0020t0001 | 0/0 | 1758 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | GTTCA others(1753): Show |
chr6 | 54303441 | 54395142 |
a0024c0025t0001 | 0/0 | 1758 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | GTTCA others(1753): Show |
chr6 | 54303441 | 54395142 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0226 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0010t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0001c0010t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0002c0002t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0002c0002t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0002c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0002c0002t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0002c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0002c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0002c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0002c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0002c0002t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0002c0002t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0002c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0002c0002t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0002c0002t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0002c0002t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0002c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0002c0002t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0002c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0002c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0002c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0002c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0002c0002t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0002c0002t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0002c0002t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0002c0002t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0002c0002t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0002c0002t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0002c0002t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0002c0002t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0002c0002t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0002c0002t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0002c0002t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0002c0002t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0002c0002t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0002c0002t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0002c0002t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0002c0002t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0002c0002t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0002c0002t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0002c0002t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0002c0002t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0002c0002t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0002c0002t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0002c0002t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0002c0002t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0002c0002t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0002c0002t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0002c0002t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0002c0002t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0002c0002t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0002c0002t0001g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0002c0002t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0002c0002t0001g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0002c0002t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0002c0002t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0002c0002t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0002c0002t0001g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0002c0002t0001g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0003c0003t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0003c0003t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0003c0003t0001g0005 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0003c0003t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0003c0003t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0003c0003t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0003c0003t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0003c0003t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0003c0003t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0003c0003t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0003c0003t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0003c0003t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0003c0003t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0003c0003t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0003c0003t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0003c0003t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0003c0003t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0003c0003t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0003c0003t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0003c0003t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0003c0003t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0003c0003t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0003c0003t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0003c0003t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0003c0003t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0003c0003t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0003c0003t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0003c0003t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0003c0003t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0003c0003t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0003c0003t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0003c0003t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0003c0003t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0003c0003t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0003c0003t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0003c0003t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0003c0003t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0003c0003t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0003c0003t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0003c0003t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0003c0003t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0003c0003t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0003c0003t0001g0059 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0003c0003t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0003c0003t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0003c0003t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0003c0003t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0003c0003t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0003c0003t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0003c0003t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0003c0003t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0003c0003t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0003c0003t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0003c0003t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0003c0003t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0003c0003t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0003c0003t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0003c0003t0001g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0004c0004t0001g0002 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0004c0004t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0004c0004t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0004c0004t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0004c0004t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0004c0004t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0004c0004t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0004c0004t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0004c0004t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0004c0004t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0004c0004t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0004c0004t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0004c0004t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0004c0004t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0004c0021t0004g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0005c0005t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0005c0005t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0005c0005t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0005c0005t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0005c0005t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0005c0005t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0005c0005t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0005c0005t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0005c0005t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0005c0005t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0005c0005t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0005c0005t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0005c0005t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0006c0006t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0006c0006t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0006c0006t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0006c0006t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0006c0006t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0006c0006t0002g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0007c0007t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0007c0007t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0007c0007t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0007c0007t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0007c0007t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0007c0007t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0008c0008t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0008c0008t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0008c0008t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0009c0016t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0009c0016t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0010c0013t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0010c0013t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0011c0011t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0011c0011t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0012c0009t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0012c0009t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0013c0012t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0013c0012t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0014c0014t0003g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0014c0014t0003g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0015c0015t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0015c0015t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0016c0017t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0016c0017t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0017c0018t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0017c0018t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0018c0024t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0019c0022t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0020c0019t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0021c0026t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0022c0023t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0023c0020t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
a0024c0025t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0005 | c0005 | t0001 | g0268 | EUR | GBR | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0123 | EUR | GBR | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG00140 | hp1 | a0006 | c0006 | t0001 | g0247 | EUR | GBR | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG00140 | hp2 | a0003 | c0003 | t0001 | g0044 | EUR | GBR | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG00280 | hp1 | a0006 | c0006 | t0001 | g0125 | EUR | FIN | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0151 | EUR | FIN | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | CHS | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG00408 | hp2 | a0018 | c0024 | t0001 | g0017 | EAS | CHS | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | CHS | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG00438 | hp2 | a0004 | c0004 | t0001 | g0195 | EAS | CHS | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | CHS | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | CHS | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG00621 | hp1 | a0003 | c0003 | t0001 | g0019 | EAS | CHS | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | CHS | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG00639 | hp1 | a0003 | c0003 | t0001 | g0004 | AMR | PUR | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG00639 | hp2 | a0004 | c0004 | t0001 | g0200 | AMR | PUR | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG00642 | hp1 | a0003 | c0003 | t0001 | g0055 | AMR | PUR | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG00642 | hp2 | a0002 | c0002 | t0001 | g0145 | AMR | PUR | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG00673 | hp1 | a0019 | c0022 | t0001 | g0172 | EAS | CHS | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | CHS | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | PUR | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG00735 | hp2 | a0009 | c0016 | t0001 | g0240 | AMR | PUR | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG00738 | hp1 | a0003 | c0003 | t0001 | g0004 | AMR | PUR | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG01069 | hp1 | a0008 | c0008 | t0002 | g0078 | AMR | PUR | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG01070 | hp1 | a0003 | c0003 | t0001 | g0054 | AMR | PUR | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG01081 | hp1 | a0003 | c0003 | t0001 | g0016 | AMR | PUR | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG01081 | hp2 | a0004 | c0004 | t0001 | g0197 | AMR | PUR | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG01099 | hp1 | a0004 | c0004 | t0001 | g0196 | AMR | PUR | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG01109 | hp1 | a0006 | c0006 | t0001 | g0146 | AMR | PUR | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG01109 | hp2 | a0003 | c0003 | t0001 | g0028 | AMR | PUR | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0296 | AMR | PUR | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG01169 | hp1 | a0006 | c0006 | t0001 | g0166 | AMR | PUR | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG01175 | hp1 | a0003 | c0003 | t0001 | g0030 | AMR | PUR | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG01192 | hp1 | a0003 | c0003 | t0001 | g0026 | AMR | PUR | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG01243 | hp1 | a0008 | c0008 | t0002 | g0079 | AMR | PUR | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | CLM | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG01255 | hp2 | a0003 | c0003 | t0001 | g0053 | AMR | CLM | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG01257 | hp2 | a0003 | c0003 | t0001 | g0003 | AMR | CLM | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG01258 | hp2 | a0010 | c0013 | t0001 | g0303 | AMR | CLM | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG01261 | hp1 | a0003 | c0003 | t0001 | g0357 | AMR | CLM | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG01358 | hp1 | a0005 | c0005 | t0001 | g0271 | AMR | CLM | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | CLM | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG01361 | hp1 | a0003 | c0003 | t0001 | g0006 | AMR | CLM | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG01361 | hp2 | a0005 | c0005 | t0001 | g0270 | AMR | CLM | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | CLM | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG01496 | hp2 | a0003 | c0003 | t0001 | g0003 | AMR | CLM | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0111 | EUR | IBS | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG01515 | hp2 | a0011 | c0011 | t0001 | g0048 | EUR | IBS | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG01516 | hp1 | a0004 | c0004 | t0001 | g0002 | EUR | IBS | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0156 | EUR | IBS | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG01517 | hp1 | a0004 | c0004 | t0001 | g0002 | EUR | IBS | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0112 | EUR | IBS | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG01884 | hp1 | a0007 | c0007 | t0001 | g0080 | AFR | ACB | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | ACB | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG01891 | hp1 | a0007 | c0007 | t0001 | g0084 | AFR | ACB | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0289 | AFR | ACB | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG01928 | hp1 | a0004 | c0004 | t0001 | g0002 | AMR | PEL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG01928 | hp2 | a0003 | c0003 | t0001 | g0035 | AMR | PEL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | PEL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG01952 | hp1 | a0003 | c0003 | t0001 | g0006 | AMR | PEL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | PEL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PEL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | PEL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PEL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | KHV | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG02055 | hp1 | a0005 | c0005 | t0001 | g0267 | AFR | ACB | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG02055 | hp2 | a0007 | c0007 | t0001 | g0083 | AFR | ACB | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG02056 | hp1 | a0003 | c0003 | t0001 | g0020 | EAS | KHV | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG02056 | hp2 | a0002 | c0002 | t0001 | g0345 | EAS | KHV | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | KHV | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG02071 | hp2 | a0020 | c0019 | t0001 | g0211 | EAS | KHV | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG02074 | hp1 | a0004 | c0004 | t0001 | g0202 | EAS | KHV | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | KHV | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | KHV | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG02083 | hp1 | a0002 | c0002 | t0001 | g0298 | EAS | KHV | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG02135 | hp1 | a0004 | c0004 | t0001 | g0076 | EAS | KHV | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG02135 | hp2 | a0003 | c0003 | t0001 | g0050 | EAS | KHV | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | ACB | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG02145 | hp2 | a0009 | c0016 | t0001 | g0241 | AFR | ACB | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | PEL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | CDX | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | CDX | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0285 | AFR | ACB | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | ACB | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | ACB | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | ACB | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | PEL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG02273 | hp2 | a0003 | c0003 | t0001 | g0005 | AMR | PEL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG02280 | hp2 | a0003 | c0003 | t0001 | g0068 | AFR | ACB | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0300 | AMR | PEL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PEL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | ACB | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG02451 | hp2 | a0005 | c0005 | t0001 | g0264 | AFR | ACB | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG02523 | hp1 | a0002 | c0002 | t0001 | g0321 | EAS | KHV | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG02523 | hp2 | a0002 | c0002 | t0001 | g0118 | EAS | KHV | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0282 | AFR | GWD | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG02602 | hp1 | a0003 | c0003 | t0001 | g0043 | SAS | PJL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG02615 | hp1 | a0012 | c0009 | t0001 | g0208 | AFR | GWD | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG02615 | hp2 | a0007 | c0007 | t0001 | g0081 | AFR | GWD | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG02622 | hp1 | a0002 | c0002 | t0001 | g0293 | AFR | GWD | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG02630 | hp2 | a0002 | c0002 | t0001 | g0284 | AFR | GWD | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG02647 | hp1 | a0002 | c0002 | t0001 | g0301 | AFR | GWD | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG02647 | hp2 | a0001 | c0010 | t0001 | g0309 | AFR | GWD | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG02683 | hp1 | a0003 | c0003 | t0001 | g0045 | SAS | PJL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG02698 | hp1 | a0006 | c0006 | t0001 | g0193 | SAS | PJL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG02717 | hp1 | a0002 | c0002 | t0001 | g0013 | AFR | GWD | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG02717 | hp2 | a0005 | c0005 | t0001 | g0272 | AFR | GWD | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG02738 | hp1 | a0002 | c0002 | t0001 | g0189 | SAS | PJL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG02738 | hp2 | a0004 | c0004 | t0001 | g0203 | SAS | PJL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG02809 | hp1 | a0003 | c0003 | t0001 | g0066 | AFR | GWD | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG02809 | hp2 | a0013 | c0012 | t0001 | g0069 | AFR | GWD | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG02818 | hp1 | a0003 | c0003 | t0001 | g0064 | AFR | GWD | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | GWD | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0292 | AFR | GWD | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG02895 | hp1 | a0003 | c0003 | t0001 | g0071 | AFR | GWD | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG02895 | hp2 | a0003 | c0003 | t0001 | g0062 | AFR | GWD | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG02897 | hp1 | a0003 | c0003 | t0001 | g0063 | AFR | GWD | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | GWD | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0288 | AFR | ESN | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | ESN | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | ESN | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | ESN | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG02970 | hp1 | a0014 | c0014 | t0003 | g0276 | AFR | ESN | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG02970 | hp2 | a0005 | c0005 | t0001 | g0263 | AFR | ESN | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0287 | AFR | ESN | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG02976 | hp2 | a0002 | c0002 | t0001 | g0013 | AFR | ESN | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG03017 | hp1 | a0005 | c0005 | t0001 | g0269 | SAS | PJL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG03017 | hp2 | a0003 | c0003 | t0001 | g0060 | SAS | PJL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG03041 | hp1 | a0008 | c0008 | t0002 | g0072 | AFR | GWD | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG03041 | hp2 | a0007 | c0007 | t0001 | g0086 | AFR | GWD | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | MSL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | MSL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG03130 | hp1 | a0015 | c0015 | t0001 | g0280 | AFR | ESN | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG03130 | hp2 | a0003 | c0003 | t0001 | g0067 | AFR | ESN | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG03139 | hp1 | a0003 | c0003 | t0001 | g0065 | AFR | ESN | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | ESN | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | ESN | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | ESN | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | MSL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG03209 | hp2 | a0005 | c0005 | t0001 | g0278 | AFR | MSL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG03225 | hp1 | a0016 | c0017 | t0001 | g0275 | AFR | MSL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0310 | AFR | MSL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG03453 | hp1 | a0010 | c0013 | t0002 | g0058 | AFR | MSL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG03453 | hp2 | a0015 | c0015 | t0001 | g0279 | AFR | MSL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | MSL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0254 | AFR | MSL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG03491 | hp2 | a0004 | c0004 | t0001 | g0192 | SAS | PJL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG03492 | hp2 | a0002 | c0002 | t0001 | g0117 | SAS | PJL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG03516 | hp1 | a0004 | c0021 | t0004 | g0201 | AFR | ESN | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG03516 | hp2 | a0003 | c0003 | t0001 | g0243 | AFR | ESN | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0260 | AFR | GWD | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0308 | AFR | GWD | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG03579 | hp1 | a0002 | c0002 | t0001 | g0294 | AFR | MSL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG03579 | hp2 | a0003 | c0003 | t0001 | g0070 | AFR | MSL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG03654 | hp1 | a0002 | c0002 | t0001 | g0311 | SAS | PJL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG03654 | hp2 | a0003 | c0003 | t0001 | g0046 | SAS | PJL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG03669 | hp1 | a0003 | c0003 | t0001 | g0163 | SAS | PJL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG03669 | hp2 | a0005 | c0005 | t0001 | g0239 | SAS | PJL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG03704 | hp1 | a0005 | c0005 | t0001 | g0266 | SAS | PJL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG03704 | hp2 | a0022 | c0023 | t0001 | g0042 | SAS | PJL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG03710 | hp2 | a0003 | c0003 | t0001 | g0052 | SAS | PJL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG03831 | hp1 | a0002 | c0002 | t0001 | g0350 | SAS | BEB | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | BEB | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0227 | SAS | BEB | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG03834 | hp2 | a0005 | c0005 | t0001 | g0265 | SAS | BEB | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | BEB | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG03927 | hp2 | a0003 | c0003 | t0001 | g0057 | SAS | BEB | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG03942 | hp1 | a0003 | c0003 | t0001 | g0039 | SAS | BEB | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG03942 | hp2 | a0011 | c0011 | t0001 | g0040 | SAS | BEB | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG04115 | hp1 | a0003 | c0003 | t0001 | g0056 | SAS | STU | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG04115 | hp2 | a0002 | c0002 | t0001 | g0259 | SAS | STU | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | STU | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG04204 | hp2 | a0003 | c0003 | t0001 | g0047 | SAS | STU | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | CHB | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18612 | hp2 | a0002 | c0002 | t0001 | g0335 | EAS | CHB | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18747 | hp1 | a0002 | c0002 | t0001 | g0074 | EAS | CHB | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18747 | hp2 | a0002 | c0002 | t0001 | g0305 | EAS | CHB | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | YRI | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18906 | hp2 | a0023 | c0020 | t0001 | g0291 | AFR | YRI | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18939 | hp1 | a0002 | c0002 | t0001 | g0348 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18941 | hp2 | a0003 | c0003 | t0001 | g0036 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18942 | hp1 | a0002 | c0002 | t0001 | g0344 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18943 | hp2 | a0002 | c0002 | t0001 | g0332 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18944 | hp1 | a0002 | c0002 | t0001 | g0336 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18944 | hp2 | a0003 | c0003 | t0001 | g0034 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18945 | hp1 | a0002 | c0002 | t0001 | g0349 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18946 | hp1 | a0002 | c0002 | t0001 | g0150 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18947 | hp2 | a0002 | c0002 | t0001 | g0246 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18948 | hp2 | a0002 | c0002 | t0001 | g0324 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18949 | hp1 | a0002 | c0002 | t0001 | g0339 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18949 | hp2 | a0005 | c0005 | t0001 | g0273 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18951 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18952 | hp1 | a0002 | c0002 | t0001 | g0323 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18952 | hp2 | a0003 | c0003 | t0001 | g0031 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18953 | hp1 | a0002 | c0002 | t0001 | g0098 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18953 | hp2 | a0003 | c0003 | t0001 | g0022 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18959 | hp1 | a0003 | c0003 | t0001 | g0061 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18962 | hp1 | a0002 | c0002 | t0001 | g0238 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18963 | hp2 | a0002 | c0002 | t0001 | g0354 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18964 | hp2 | a0003 | c0003 | t0001 | g0032 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18966 | hp2 | a0004 | c0004 | t0001 | g0171 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18967 | hp1 | a0003 | c0003 | t0001 | g0025 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18967 | hp2 | a0002 | c0002 | t0001 | g0314 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18969 | hp1 | a0003 | c0003 | t0001 | g0018 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18971 | hp1 | a0002 | c0002 | t0001 | g0353 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18972 | hp1 | a0002 | c0002 | t0001 | g0351 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18975 | hp2 | a0002 | c0002 | t0001 | g0149 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18977 | hp1 | a0002 | c0002 | t0001 | g0341 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18978 | hp2 | a0002 | c0002 | t0001 | g0356 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18980 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18982 | hp2 | a0003 | c0003 | t0001 | g0304 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18985 | hp1 | a0002 | c0002 | t0001 | g0095 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18988 | hp1 | a0002 | c0002 | t0001 | g0347 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18988 | hp2 | a0004 | c0004 | t0001 | g0198 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18989 | hp2 | a0004 | c0004 | t0001 | g0180 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18991 | hp2 | a0002 | c0002 | t0001 | g0342 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18992 | hp1 | a0004 | c0004 | t0001 | g0199 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18992 | hp2 | a0002 | c0002 | t0001 | g0337 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18997 | hp1 | a0002 | c0002 | t0001 | g0346 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18999 | hp1 | a0002 | c0002 | t0001 | g0327 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18999 | hp2 | a0003 | c0003 | t0001 | g0021 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA19002 | hp2 | a0002 | c0002 | t0001 | g0338 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA19003 | hp2 | a0002 | c0002 | t0001 | g0331 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA19009 | hp2 | a0003 | c0003 | t0001 | g0037 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA19010 | hp1 | a0002 | c0002 | t0001 | g0358 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | LWK | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA19030 | hp2 | a0002 | c0002 | t0001 | g0252 | AFR | LWK | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA19054 | hp1 | a0024 | c0025 | t0001 | g0262 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA19054 | hp2 | a0002 | c0002 | t0001 | g0355 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA19055 | hp2 | a0002 | c0002 | t0001 | g0307 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA19058 | hp1 | a0002 | c0002 | t0001 | g0306 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA19058 | hp2 | a0003 | c0003 | t0001 | g0027 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA19059 | hp1 | a0003 | c0003 | t0001 | g0033 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA19059 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA19060 | hp2 | a0003 | c0003 | t0001 | g0023 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA19064 | hp2 | a0002 | c0002 | t0001 | g0334 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA19065 | hp2 | a0013 | c0012 | t0001 | g0206 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA19066 | hp1 | a0003 | c0003 | t0001 | g0051 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA19068 | hp2 | a0003 | c0003 | t0001 | g0005 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA19070 | hp2 | a0002 | c0002 | t0001 | g0326 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA19074 | hp1 | a0004 | c0004 | t0001 | g0170 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA19076 | hp1 | a0002 | c0002 | t0001 | g0343 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA19077 | hp2 | a0002 | c0002 | t0001 | g0329 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA19080 | hp1 | a0003 | c0003 | t0001 | g0049 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA19083 | hp1 | a0002 | c0002 | t0001 | g0322 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA19086 | hp1 | a0002 | c0002 | t0001 | g0325 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA19088 | hp1 | a0002 | c0002 | t0001 | g0328 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA19091 | hp1 | a0002 | c0002 | t0001 | g0313 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA19091 | hp2 | a0003 | c0003 | t0001 | g0024 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA19240 | hp1 | a0007 | c0007 | t0001 | g0085 | AFR | YRI | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA19240 | hp2 | a0006 | c0006 | t0002 | g0295 | AFR | YRI | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | ASW | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0281 | AFR | ASW | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | GIH | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA20905 | hp2 | a0003 | c0003 | t0001 | g0015 | SAS | GIH | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG01123 | hp1 | a0003 | c0003 | t0001 | g0041 | AMR | CLM | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG01123 | hp2 | a0002 | c0002 | t0001 | g0352 | AMR | CLM | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG02109 | hp1 | a0012 | c0009 | t0001 | g0209 | AFR | ACB | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | ACB | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG02559 | hp1 | a0021 | c0026 | t0001 | g0082 | AFR | ACB | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0283 | AFR | ACB | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG03471 | hp1 | a0002 | c0002 | t0001 | g0251 | AFR | MSL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG03471 | hp2 | a0017 | c0018 | t0001 | g0087 | AFR | MSL | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | USA | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
HG06807 | hp2 | a0017 | c0018 | t0001 | g0242 | AFR | USA | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18955 | hp1 | a0002 | c0002 | t0001 | g0333 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA20300 | hp1 | a0003 | c0003 | t0001 | g0029 | AFR | USA | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA20300 | hp2 | a0001 | c0010 | t0001 | g0244 | AFR | USA | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA21309 | hp1 | a0014 | c0014 | t0003 | g0277 | AFR | LWK | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
NA21309 | hp2 | a0016 | c0017 | t0001 | g0274 | AFR | LWK | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0226 | REF | REF | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
homoSapiens | grch38p0 | a0003 | c0003 | t0001 | g0059 | REF | REF | TINAG_chr6_54303441_54395142 | TINAG | chr6 | 54303441 | 54395142 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:54308557 | A | G | 4 | a0007 a0008 a0017 others(1): Show |
12 | HG01069.hp1 HG01243.hp1 HG01884.hp1 others(9): Show |
missense_variant | MODERATE | c.7A>G | p.Thr3Ala | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/11 | 117/1758 | 7/1431 | 3/476 | chr6 | 54308557 | |||
chr6:54308615 | A | G | 6 | a0005 a0009 a0014 others(3): Show |
22 | HG00099.hp1 HG00735.hp2 HG01358.hp1 others(19): Show |
missense_variant | MODERATE | c.65A>G | p.Gln22Arg | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/11 | 175/1758 | 65/1431 | 22/476 | chr6 | 54308615 | |||
chr6:54308623 | T | G | 1 | a0012 | 2 | HG02109.hp1 HG02615.hp1 |
missense_variant | MODERATE | c.73T>G | p.Ser25Ala | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/11 | 183/1758 | 73/1431 | 25/476 | chr6 | 54308623 | |||
chr6:54308786 | C | T | 1 | a0018 | 1 | HG00408.hp2 | missense_variant | MODERATE | c.236C>T | p.Ala79Val | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/11 | 346/1758 | 236/1431 | 79/476 | chr6 | 54308786 | |||
chr6:54308875 | C | G | 1 | a0024 | 1 | NA19054.hp1 | missense_variant | MODERATE | c.325C>G | p.Pro109Ala | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/11 | 435/1758 | 325/1431 | 109/476 | chr6 | 54308875 | |||
chr6:54321349 | T | C | 14 | a0001 a0002 a0004 others(11): Show |
285 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(282): Show |
missense_variant | MODERATE | c.472T>C | p.Ser158Pro | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/11 | 582/1758 | 472/1431 | 158/476 | chr6 | 54321349 | |||
chr6:54326888 | C | T | 8 | a0004 a0007 a0008 others(5): Show |
33 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(30): Show |
missense_variant | MODERATE | c.596C>T | p.Pro199Leu | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/11 | 706/1758 | 596/1431 | 199/476 | chr6 | 54326888 | |||
chr6:54349787 | G | A | 1 | a0020 | 1 | HG02071.hp2 | missense_variant | MODERATE | c.971G>A | p.Ser324Asn | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 7/11 | 1081/1758 | 971/1431 | 324/476 | chr6 | 54349787 | |||
chr6:54354528 | G | A | 6 | a0004 a0006 a0008 others(3): Show |
32 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(29): Show |
missense_variant | MODERATE | c.1142G>A | p.Arg381His | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/11 | 1252/1758 | 1142/1431 | 381/476 | chr6 | 54354528 | |||
chr6:54354623 | G | A | 2 | a0007 a0023 |
7 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(4): Show |
missense_variant | MODERATE | c.1237G>A | p.Val413Ile | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/11 | 1347/1758 | 1237/1431 | 413/476 | chr6 | 54354623 | |||
chr6:54389791 | A | C | 4 | a0002 a0013 a0016 others(1): Show |
69 | HG00642.hp2 HG01123.hp2 HG02056.hp2 others(66): Show |
missense_variant&splice_region_variant | MODERATE | c.1297A>C | p.Ile433Leu | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 11/11 | 1407/1758 | 1297/1431 | 433/476 | chr6 | 54389791 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:54347440 | C | T | 1 | a0001c0010 | 2 | HG02647.hp2 NA20300.hp2 |
synonymous_variant | LOW | c.822C>T | p.Ile274Ile | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 6/11 | 932/1758 | 822/1431 | 274/476 | chr6 | 54347440 | |||
chr6:54389910 | T | C | 1 | a0004c0021 | 1 | HG03516.hp1 | synonymous_variant | LOW | c.1416T>C | p.Ser472Ser | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 11/11 | 1526/1758 | 1416/1431 | 472/476 | chr6 | 54389910 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:54390001 | G | A | 1 | a0004c0021t0004 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*76G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 11/11 | 76 | chr6 | 54390001 | ||||||
chr6:54390016 | T | G | 1 | a0014c0014t0003 | 2 | HG02970.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*91T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 11/11 | 91 | chr6 | 54390016 | ||||||
chr6:54390062 | C | T | 3 | a0006c0006t0002 a0008c0008t0002 a0010c0013t0002 |
5 | HG01069.hp1 HG01243.hp1 HG03041.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*137C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 11/11 | 137 | chr6 | 54390062 | ||||||
chr6:54390130 | G | T | 1 | a0004c0021t0004 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*205G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 11/11 | 205 | chr6 | 54390130 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:54309091 | A | G | 62 | a0001c0001t0001g0297 a0001c0001t0001g0299 a0001c0001t0001g0300 others(59): Show |
62 | HG01123.hp2 HG01258.hp2 HG01261.hp1 others(59): Show |
intron_variant | MODIFIER | c.355+186A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54309091 | |||||||
chr6:54309329 | A | C | 296 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(293): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.355+424A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54309329 | |||||||
chr6:54309844 | C | CA | 193 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(190): Show |
205 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.355+955dupA | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 54309844 | ||||||
chr6:54309844 | C | CAA | 6 | a0001c0001t0001g0073 a0001c0001t0001g0075 a0001c0001t0001g0077 others(3): Show |
6 | HG01358.hp2 HG02135.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.355+954_355+955dup others(2): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 54309844 | ||||||
chr6:54309844 | CA | C | 51 | a0001c0001t0001g0014 a0001c0001t0001g0257 a0001c0001t0001g0258 others(48): Show |
53 | HG00099.hp1 HG00741.hp1 HG01167.hp2 others(50): Show |
intron_variant | MODIFIER | c.355+955delA | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 54309844 | ||||||
chr6:54309885 | CA | C | 11 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0230 others(8): Show |
11 | HG00438.hp1 HG00735.hp1 HG01934.hp2 others(8): Show |
intron_variant | MODIFIER | c.355+982delA | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 54309885 | ||||||
chr6:54309920 | G | A | 1 | a0001c0001t0001g0257 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.355+1015G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54309920 | |||||||
chr6:54309941 | C | T | 1 | a0001c0001t0001g0227 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.355+1036C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54309941 | |||||||
chr6:54310018 | T | G | 4 | a0001c0001t0001g0258 a0001c0001t0001g0260 a0001c0001t0001g0261 others(1): Show |
4 | HG03098.hp2 HG03195.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.355+1113T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54310018 | |||||||
chr6:54310074 | TCCGTGTG others(4): Show |
T | 2 | a0001c0001t0001g0014 a0001c0001t0001g0296 |
3 | HG00741.hp1 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.355+1170_355+1180d others(13): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54310074 | |||||||
chr6:54310075 | C | T | 1 | a0001c0001t0001g0281 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.355+1170C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54310075 | |||||||
chr6:54310076 | C | CCGTGTGT others(4): Show |
1 | a0001c0001t0001g0281 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.355+1171_355+1172i others(13): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54310076 | |||||||
chr6:54310076 | C | CGT | 8 | a0001c0001t0001g0219 a0001c0001t0001g0245 a0001c0001t0001g0257 others(5): Show |
8 | HG01258.hp2 HG01261.hp1 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.355+1201_355+1202d others(4): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 54310076 | ||||||
chr6:54310076 | C | CGTGT | 13 | a0001c0001t0001g0075 a0001c0001t0001g0160 a0001c0001t0001g0162 others(10): Show |
13 | HG01884.hp2 HG01891.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.355+1199_355+1202d others(6): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 54310076 | ||||||
chr6:54310076 | C | CGTGTGT | 41 | a0001c0001t0001g0012 a0001c0001t0001g0077 a0001c0001t0001g0108 others(38): Show |
45 | HG00408.hp2 HG00621.hp1 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.355+1197_355+1202d others(8): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 54310076 | ||||||
chr6:54310076 | C | CGTGTGTG others(1): Show |
98 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0073 others(95): Show |
103 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.355+1195_355+1202d others(10): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 54310076 | ||||||
chr6:54310076 | C | CGTGTGTG others(3): Show |
52 | a0001c0001t0001g0007 a0001c0001t0001g0092 a0001c0001t0001g0093 others(49): Show |
55 | HG00280.hp1 HG00558.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.355+1193_355+1202d others(12): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 54310076 | ||||||
chr6:54310076 | C | CGTGTGTG others(5): Show |
19 | a0001c0001t0001g0091 a0001c0001t0001g0107 a0001c0001t0001g0205 others(16): Show |
19 | HG00099.hp1 HG00735.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.355+1191_355+1202d others(14): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 54310076 | ||||||
chr6:54310076 | C | CGTGTGTG others(7): Show |
12 | a0001c0001t0001g0194 a0002c0002t0001g0074 a0004c0021t0004g0201 others(9): Show |
12 | HG02145.hp2 HG03017.hp1 HG03130.hp1 others(9): Show |
intron_variant | MODIFIER | c.355+1189_355+1202d others(16): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 54310076 | ||||||
chr6:54310076 | C | CGTGTGTG others(9): Show |
7 | a0005c0005t0001g0271 a0007c0007t0001g0080 a0007c0007t0001g0081 others(4): Show |
7 | HG01358.hp1 HG01884.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.355+1187_355+1202d others(18): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 54310076 | ||||||
chr6:54310076 | C | CGTGTGTG others(13): Show |
1 | a0007c0007t0001g0086 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.355+1183_355+1202d others(22): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 54310076 | ||||||
chr6:54310076 | CGTGTGTG others(1): Show |
C | 3 | a0001c0001t0001g0009 a0001c0001t0001g0158 a0001c0001t0001g0159 |
4 | HG02280.hp1 HG02572.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.355+1195_355+1202d others(10): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 54310076 | ||||||
chr6:54310087 | G | C | 2 | a0001c0001t0001g0014 a0001c0001t0001g0296 |
3 | HG00741.hp1 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.355+1182G>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54310087 | |||||||
chr6:54310088 | T | C | 2 | a0001c0001t0001g0014 a0001c0001t0001g0296 |
3 | HG00741.hp1 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.355+1183T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54310088 | |||||||
chr6:54310108 | A | T | 7 | a0001c0001t0001g0225 a0001c0001t0001g0253 a0001c0001t0001g0254 others(4): Show |
7 | HG02080.hp2 HG02257.hp2 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.355+1203A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54310108 | |||||||
chr6:54310163 | G | A | 2 | a0008c0008t0002g0078 a0008c0008t0002g0079 |
2 | HG01069.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.355+1258G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54310163 | |||||||
chr6:54310205 | C | T | 2 | a0001c0001t0001g0012 a0001c0001t0001g0224 |
3 | NA19010.hp2 NA19059.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.355+1300C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54310205 | |||||||
chr6:54310265 | T | C | 43 | a0001c0001t0001g0014 a0001c0001t0001g0253 a0001c0001t0001g0254 others(40): Show |
44 | HG00099.hp1 HG00735.hp2 HG00741.hp1 others(41): Show |
intron_variant | MODIFIER | c.355+1360T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54310265 | |||||||
chr6:54310422 | T | C | 1 | a0001c0001t0001g0088 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.355+1517T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54310422 | |||||||
chr6:54310478 | CTCTCTTT others(19): Show |
C | 1 | a0001c0001t0001g0223 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.355+1593_355+1618d others(28): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 54310478 | ||||||
chr6:54310480 | C | T | 1 | a0001c0001t0001g0184 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.355+1575C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54310480 | |||||||
chr6:54310492 | TTTC | T | 158 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(155): Show |
167 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.355+1593_355+1595d others(5): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 54310492 | ||||||
chr6:54310496 | TTC | T | 11 | a0007c0007t0001g0080 a0007c0007t0001g0081 a0007c0007t0001g0083 others(8): Show |
11 | HG01069.hp1 HG01243.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.355+1593_355+1594d others(4): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 54310496 | ||||||
chr6:54310567 | CCT | C | 3 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 |
3 | NA18994.hp1 NA19083.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.355+1669_355+1670d others(4): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 54310567 | ||||||
chr6:54310601 | TTCTC | T | 5 | a0001c0001t0001g0292 a0002c0002t0001g0013 a0002c0002t0001g0293 others(2): Show |
6 | HG02622.hp1 HG02717.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.355+1704_355+1707d others(6): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 54310601 | ||||||
chr6:54310622 | CCCTT | C | 78 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0285 others(75): Show |
79 | HG01123.hp2 HG01258.hp2 HG01261.hp1 others(76): Show |
intron_variant | MODIFIER | c.355+1729_355+1732d others(6): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 54310622 | ||||||
chr6:54310642 | CTCTT | C | 4 | a0001c0001t0001g0258 a0001c0001t0001g0260 a0001c0001t0001g0261 others(1): Show |
4 | HG03098.hp2 HG03195.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.355+1745_355+1748d others(6): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 54310642 | ||||||
chr6:54310658 | CTTTTTCT others(58): Show |
C | 19 | a0002c0002t0001g0251 a0002c0002t0001g0252 a0005c0005t0001g0239 others(16): Show |
19 | HG00099.hp1 HG00735.hp2 HG01358.hp1 others(16): Show |
intron_variant | MODIFIER | c.355+1778_355+1842d others(67): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 54310658 | ||||||
chr6:54310715 | CCTCTTTC others(25): Show |
C | 1 | a0006c0006t0002g0295 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.355+1830_355+1861d others(34): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 54310715 | ||||||
chr6:54310754 | CTTT | C | 12 | a0007c0007t0001g0080 a0007c0007t0001g0081 a0007c0007t0001g0083 others(9): Show |
12 | HG01069.hp1 HG01243.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.355+1853_355+1855d others(5): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 54310754 | ||||||
chr6:54310759 | T | C | 2 | a0001c0001t0001g0245 a0023c0020t0001g0291 |
2 | HG02258.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.355+1854T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54310759 | |||||||
chr6:54310776 | C | T | 3 | a0001c0001t0001g0014 a0001c0001t0001g0281 a0001c0001t0001g0296 |
4 | HG00741.hp1 HG01167.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.355+1871C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54310776 | |||||||
chr6:54310815 | CCT | C | 12 | a0001c0001t0001g0011 a0001c0001t0001g0210 a0001c0001t0001g0212 others(9): Show |
13 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(10): Show |
intron_variant | MODIFIER | c.355+1913_355+1914d others(4): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 54310815 | ||||||
chr6:54310815 | CCTCTTTC others(3): Show |
C | 2 | a0001c0001t0001g0245 a0023c0020t0001g0291 |
2 | HG02258.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.355+1921_355+1930d others(12): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 54310815 | ||||||
chr6:54310838 | TC | T | 2 | a0001c0001t0001g0014 a0001c0001t0001g0296 |
3 | HG00741.hp1 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.355+1934delC | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54310838 | |||||||
chr6:54310839 | C | T | 1 | a0001c0001t0001g0281 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.355+1934C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54310839 | |||||||
chr6:54310856 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.355+1951G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54310856 | |||||||
chr6:54310865 | TTC | T | 11 | a0001c0001t0001g0011 a0001c0001t0001g0210 a0001c0001t0001g0212 others(8): Show |
12 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.355+1964_355+1965d others(4): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 54310865 | ||||||
chr6:54310870 | T | C | 2 | a0001c0001t0001g0090 a0001c0001t0001g0091 |
2 | NA18945.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.355+1965T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54310870 | |||||||
chr6:54310873 | CT | C | 11 | a0001c0001t0001g0011 a0001c0001t0001g0210 a0001c0001t0001g0212 others(8): Show |
12 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.355+1975delT | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 54310873 | ||||||
chr6:54310874 | T | C | 1 | a0001c0001t0001g0220 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.355+1969T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54310874 | |||||||
chr6:54310887 | C | G | 3 | a0001c0001t0001g0014 a0001c0001t0001g0281 a0001c0001t0001g0296 |
4 | HG00741.hp1 HG01167.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.355+1982C>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54310887 | |||||||
chr6:54310907 | C | CTTTCTT | 294 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(291): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.355+2007_355+2008i others(8): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 54310907 | ||||||
chr6:54311107 | G | T | 78 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0285 others(75): Show |
79 | HG01123.hp2 HG01258.hp2 HG01261.hp1 others(76): Show |
intron_variant | MODIFIER | c.355+2202G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54311107 | |||||||
chr6:54311218 | C | T | 2 | a0001c0001t0001g0245 a0023c0020t0001g0291 |
2 | HG02258.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.355+2313C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54311218 | |||||||
chr6:54311221 | G | A | 1 | a0003c0003t0001g0037 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.355+2316G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54311221 | |||||||
chr6:54311385 | T | G | 1 | a0002c0002t0001g0298 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.355+2480T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54311385 | |||||||
chr6:54311401 | T | C | 5 | a0001c0001t0001g0292 a0002c0002t0001g0013 a0002c0002t0001g0293 others(2): Show |
6 | HG02622.hp1 HG02717.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.355+2496T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54311401 | |||||||
chr6:54311429 | C | T | 48 | a0001c0001t0001g0014 a0001c0001t0001g0254 a0001c0001t0001g0255 others(45): Show |
49 | HG00099.hp1 HG00735.hp2 HG00741.hp1 others(46): Show |
intron_variant | MODIFIER | c.355+2524C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54311429 | |||||||
chr6:54311516 | A | G | 3 | a0005c0005t0001g0278 a0015c0015t0001g0279 a0015c0015t0001g0280 |
3 | HG03130.hp1 HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.355+2611A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54311516 | |||||||
chr6:54311551 | C | A | 2 | a0001c0001t0001g0254 a0001c0001t0001g0255 |
2 | HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.355+2646C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54311551 | |||||||
chr6:54311551 | C | G | 1 | a0001c0001t0001g0077 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.355+2646C>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54311551 | |||||||
chr6:54311692 | C | T | 56 | a0001c0001t0001g0014 a0001c0001t0001g0207 a0001c0001t0001g0254 others(53): Show |
58 | HG00099.hp1 HG00735.hp2 HG00741.hp1 others(55): Show |
intron_variant | MODIFIER | c.355+2787C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54311692 | |||||||
chr6:54311693 | C | T | 56 | a0001c0001t0001g0014 a0001c0001t0001g0207 a0001c0001t0001g0254 others(53): Show |
58 | HG00099.hp1 HG00735.hp2 HG00741.hp1 others(55): Show |
intron_variant | MODIFIER | c.355+2788C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54311693 | |||||||
chr6:54311744 | C | A | 37 | a0001c0001t0001g0014 a0001c0001t0001g0092 a0001c0001t0001g0207 others(34): Show |
39 | HG00099.hp1 HG00735.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.355+2839C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54311744 | |||||||
chr6:54311767 | A | T | 12 | a0001c0001t0001g0011 a0001c0001t0001g0210 a0001c0001t0001g0212 others(9): Show |
13 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(10): Show |
intron_variant | MODIFIER | c.355+2862A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54311767 | |||||||
chr6:54311975 | A | T | 1 | a0001c0001t0001g0261 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.355+3070A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54311975 | |||||||
chr6:54312053 | GTTTGTTT | G | 3 | a0001c0001t0001g0007 a0001c0001t0001g0093 a0001c0001t0001g0094 |
4 | HG03491.hp1 HG03492.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.355+3165_355+3171d others(9): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 54312053 | ||||||
chr6:54312072 | T | G | 1 | a0001c0001t0001g0088 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.355+3167T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54312072 | |||||||
chr6:54312290 | C | G | 3 | a0001c0001t0001g0014 a0001c0001t0001g0260 a0001c0001t0001g0296 |
4 | HG00741.hp1 HG01167.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.355+3385C>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54312290 | |||||||
chr6:54312321 | T | C | 1 | a0001c0001t0001g0220 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.355+3416T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54312321 | |||||||
chr6:54312322 | A | T | 1 | a0001c0001t0001g0220 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.355+3417A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54312322 | |||||||
chr6:54312378 | A | G | 3 | a0001c0001t0001g0007 a0001c0001t0001g0093 a0001c0001t0001g0094 |
4 | HG03491.hp1 HG03492.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.355+3473A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54312378 | |||||||
chr6:54312421 | A | G | 2 | a0001c0001t0001g0245 a0023c0020t0001g0291 |
2 | HG02258.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.355+3516A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54312421 | |||||||
chr6:54312515 | A | T | 55 | a0001c0001t0001g0297 a0001c0001t0001g0308 a0001c0001t0001g0310 others(52): Show |
55 | HG01123.hp2 HG02056.hp2 HG02071.hp1 others(52): Show |
intron_variant | MODIFIER | c.355+3610A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54312515 | |||||||
chr6:54312529 | A | G | 2 | a0003c0003t0001g0062 a0003c0003t0001g0063 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.355+3624A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54312529 | |||||||
chr6:54312590 | A | G | 1 | a0002c0002t0001g0355 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.355+3685A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54312590 | |||||||
chr6:54312605 | G | A | 303 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(300): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.355+3700G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54312605 | |||||||
chr6:54312607 | C | A | 100 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0012 others(97): Show |
105 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.355+3702C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54312607 | |||||||
chr6:54312750 | T | C | 3 | a0004c0004t0001g0170 a0004c0004t0001g0171 a0019c0022t0001g0172 |
3 | HG00673.hp1 NA18966.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.355+3845T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54312750 | |||||||
chr6:54312794 | A | G | 213 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(210): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.355+3889A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54312794 | |||||||
chr6:54312894 | A | G | 17 | a0001c0001t0001g0011 a0001c0001t0001g0014 a0001c0001t0001g0210 others(14): Show |
19 | HG00741.hp1 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.355+3989A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54312894 | |||||||
chr6:54313014 | G | A | 9 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0285 others(6): Show |
9 | HG01891.hp2 HG02257.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.355+4109G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54313014 | |||||||
chr6:54313108 | A | T | 2 | a0015c0015t0001g0279 a0015c0015t0001g0280 |
2 | HG03130.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.355+4203A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54313108 | |||||||
chr6:54313151 | T | G | 110 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0012 others(107): Show |
115 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.355+4246T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54313151 | |||||||
chr6:54313223 | T | C | 1 | a0004c0004t0001g0180 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.355+4318T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54313223 | |||||||
chr6:54313304 | G | A | 1 | a0017c0018t0001g0087 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.355+4399G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54313304 | |||||||
chr6:54313350 | C | A | 1 | a0002c0002t0001g0095 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.355+4445C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54313350 | |||||||
chr6:54313420 | T | C | 3 | a0001c0001t0001g0007 a0001c0001t0001g0093 a0001c0001t0001g0094 |
4 | HG03491.hp1 HG03492.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.355+4515T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54313420 | |||||||
chr6:54313431 | G | T | 10 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0285 others(7): Show |
10 | HG01891.hp2 HG02257.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.355+4526G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54313431 | |||||||
chr6:54313477 | A | G | 55 | a0001c0001t0001g0297 a0001c0001t0001g0308 a0001c0001t0001g0310 others(52): Show |
55 | HG01123.hp2 HG02056.hp2 HG02071.hp1 others(52): Show |
intron_variant | MODIFIER | c.355+4572A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54313477 | |||||||
chr6:54313489 | A | G | 110 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0012 others(107): Show |
115 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.355+4584A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54313489 | |||||||
chr6:54313536 | G | A | 2 | a0001c0001t0001g0245 a0023c0020t0001g0291 |
2 | HG02258.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.355+4631G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54313536 | |||||||
chr6:54313543 | CTCATTCA | C | 55 | a0001c0001t0001g0297 a0001c0001t0001g0308 a0001c0001t0001g0310 others(52): Show |
55 | HG01123.hp2 HG02056.hp2 HG02071.hp1 others(52): Show |
intron_variant | MODIFIER | c.355+4640_355+4646d others(9): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 54313543 | ||||||
chr6:54313546 | A | T | 1 | a0001c0001t0001g0124 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.355+4641A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54313546 | |||||||
chr6:54313551 | T | A | 55 | a0001c0001t0001g0297 a0001c0001t0001g0308 a0001c0001t0001g0310 others(52): Show |
55 | HG01123.hp2 HG02056.hp2 HG02071.hp1 others(52): Show |
intron_variant | MODIFIER | c.355+4646T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54313551 | |||||||
chr6:54313595 | T | C | 1 | a0002c0002t0001g0305 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.355+4690T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54313595 | |||||||
chr6:54313623 | C | T | 1 | a0002c0002t0001g0298 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.355+4718C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54313623 | |||||||
chr6:54313640 | C | T | 203 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(200): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.355+4735C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54313640 | |||||||
chr6:54313755 | T | G | 55 | a0001c0001t0001g0297 a0001c0001t0001g0308 a0001c0001t0001g0310 others(52): Show |
55 | HG01123.hp2 HG02056.hp2 HG02071.hp1 others(52): Show |
intron_variant | MODIFIER | c.355+4850T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54313755 | |||||||
chr6:54313853 | A | G | 206 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(203): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.355+4948A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54313853 | |||||||
chr6:54313920 | G | A | 3 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0183 |
3 | NA18972.hp2 NA19012.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.355+5015G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54313920 | |||||||
chr6:54314024 | A | G | 134 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0012 others(131): Show |
139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
intron_variant | MODIFIER | c.355+5119A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54314024 | |||||||
chr6:54314041 | G | C | 1 | a0014c0014t0003g0276 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.355+5136G>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54314041 | |||||||
chr6:54314064 | A | C | 110 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0012 others(107): Show |
115 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.355+5159A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54314064 | |||||||
chr6:54314242 | T | C | 57 | a0001c0001t0001g0096 a0001c0001t0001g0297 a0001c0001t0001g0308 others(54): Show |
57 | HG01123.hp2 HG02056.hp2 HG02071.hp1 others(54): Show |
intron_variant | MODIFIER | c.355+5337T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54314242 | |||||||
chr6:54314271 | C | G | 9 | a0003c0003t0001g0064 a0003c0003t0001g0065 a0003c0003t0001g0066 others(6): Show |
9 | HG02280.hp2 HG02809.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.355+5366C>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54314271 | |||||||
chr6:54314358 | A | G | 2 | a0002c0002t0001g0353 a0002c0002t0001g0354 |
2 | NA18963.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.355+5453A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54314358 | |||||||
chr6:54314584 | C | A | 2 | a0015c0015t0001g0279 a0015c0015t0001g0280 |
2 | HG03130.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.355+5679C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54314584 | |||||||
chr6:54314595 | A | T | 2 | a0015c0015t0001g0279 a0015c0015t0001g0280 |
2 | HG03130.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.355+5690A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54314595 | |||||||
chr6:54314605 | C | T | 5 | a0001c0001t0001g0014 a0001c0001t0001g0258 a0001c0001t0001g0260 others(2): Show |
6 | HG00741.hp1 HG01167.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.355+5700C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54314605 | |||||||
chr6:54314606 | G | A | 35 | a0001c0001t0001g0010 a0001c0001t0001g0090 a0001c0001t0001g0091 others(32): Show |
37 | HG00438.hp1 HG00558.hp2 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.355+5701G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54314606 | |||||||
chr6:54314638 | T | C | 3 | a0001c0001t0001g0014 a0001c0001t0001g0260 a0001c0001t0001g0296 |
4 | HG00741.hp1 HG01167.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.355+5733T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54314638 | |||||||
chr6:54314704 | G | A | 55 | a0001c0001t0001g0297 a0001c0001t0001g0308 a0001c0001t0001g0310 others(52): Show |
55 | HG01123.hp2 HG02056.hp2 HG02071.hp1 others(52): Show |
intron_variant | MODIFIER | c.355+5799G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54314704 | |||||||
chr6:54314740 | T | G | 33 | a0001c0001t0001g0194 a0001c0001t0001g0204 a0001c0001t0001g0205 others(30): Show |
35 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.355+5835T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54314740 | |||||||
chr6:54314754 | G | T | 9 | a0003c0003t0001g0064 a0003c0003t0001g0065 a0003c0003t0001g0066 others(6): Show |
9 | HG02280.hp2 HG02809.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.356-5825G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54314754 | |||||||
chr6:54314800 | A | G | 55 | a0001c0001t0001g0297 a0001c0001t0001g0308 a0001c0001t0001g0310 others(52): Show |
55 | HG01123.hp2 HG02056.hp2 HG02071.hp1 others(52): Show |
intron_variant | MODIFIER | c.356-5779A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54314800 | |||||||
chr6:54314842 | G | A | 1 | a0017c0018t0001g0087 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.356-5737G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54314842 | |||||||
chr6:54314950 | T | A | 1 | a0004c0004t0001g0192 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.356-5629T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54314950 | |||||||
chr6:54314972 | A | T | 10 | a0001c0001t0001g0011 a0001c0001t0001g0210 a0001c0001t0001g0212 others(7): Show |
11 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.356-5607A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54314972 | |||||||
chr6:54314976 | T | G | 63 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(60): Show |
63 | HG01123.hp2 HG02056.hp2 HG02071.hp1 others(60): Show |
intron_variant | MODIFIER | c.356-5603T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54314976 | |||||||
chr6:54315057 | G | A | 110 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0012 others(107): Show |
115 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.356-5522G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54315057 | |||||||
chr6:54315183 | G | T | 1 | a0001c0001t0001g0257 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.356-5396G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54315183 | |||||||
chr6:54315211 | G | A | 24 | a0001c0001t0001g0245 a0003c0003t0001g0243 a0003c0003t0001g0357 others(21): Show |
24 | HG00099.hp1 HG00735.hp2 HG01261.hp1 others(21): Show |
intron_variant | MODIFIER | c.356-5368G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54315211 | |||||||
chr6:54315330 | T | C | 294 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(291): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.356-5249T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54315330 | |||||||
chr6:54315386 | A | T | 1 | a0003c0003t0001g0243 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.356-5193A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54315386 | |||||||
chr6:54315455 | G | A | 1 | a0002c0002t0001g0301 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.356-5124G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54315455 | |||||||
chr6:54315463 | G | A | 33 | a0001c0001t0001g0194 a0001c0001t0001g0204 a0001c0001t0001g0205 others(30): Show |
35 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.356-5116G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54315463 | |||||||
chr6:54315547 | A | G | 1 | a0002c0002t0001g0301 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.356-5032A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54315547 | |||||||
chr6:54315644 | T | G | 1 | a0006c0006t0001g0193 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.356-4935T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54315644 | |||||||
chr6:54315683 | A | G | 25 | a0003c0003t0001g0003 a0003c0003t0001g0004 a0003c0003t0001g0016 others(22): Show |
27 | HG00408.hp2 HG00621.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.356-4896A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54315683 | |||||||
chr6:54315687 | A | G | 1 | a0002c0002t0001g0352 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.356-4892A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54315687 | |||||||
chr6:54315691 | A | G | 1 | a0003c0003t0001g0243 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.356-4888A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54315691 | |||||||
chr6:54315692 | G | T | 1 | a0003c0003t0001g0243 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.356-4887G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54315692 | |||||||
chr6:54315693 | T | A | 1 | a0003c0003t0001g0243 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.356-4886T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54315693 | |||||||
chr6:54315693 | T | TA | 201 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(198): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.356-4879dupA | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 54315693 | ||||||
chr6:54315723 | C | T | 10 | a0001c0001t0001g0011 a0001c0001t0001g0210 a0001c0001t0001g0212 others(7): Show |
11 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.356-4856C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54315723 | |||||||
chr6:54315927 | A | G | 20 | a0001c0001t0001g0011 a0001c0001t0001g0210 a0001c0001t0001g0212 others(17): Show |
21 | HG01891.hp2 HG02027.hp1 HG02071.hp2 others(18): Show |
intron_variant | MODIFIER | c.356-4652A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54315927 | |||||||
chr6:54315955 | G | A | 110 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0012 others(107): Show |
115 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.356-4624G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54315955 | |||||||
chr6:54316163 | G | A | 68 | a0001c0001t0001g0010 a0001c0001t0001g0090 a0001c0001t0001g0091 others(65): Show |
72 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.356-4416G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54316163 | |||||||
chr6:54316298 | T | G | 294 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(291): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.356-4281T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54316298 | |||||||
chr6:54316318 | T | C | 10 | a0001c0001t0001g0011 a0001c0001t0001g0210 a0001c0001t0001g0212 others(7): Show |
11 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.356-4261T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54316318 | |||||||
chr6:54316490 | C | A | 206 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(203): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.356-4089C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54316490 | |||||||
chr6:54316541 | G | T | 3 | a0002c0002t0001g0349 a0002c0002t0001g0350 a0002c0002t0001g0351 |
3 | HG03831.hp1 NA18945.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.356-4038G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54316541 | |||||||
chr6:54316562 | C | A | 1 | a0001c0001t0001g0257 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.356-4017C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54316562 | |||||||
chr6:54316595 | C | A | 2 | a0001c0001t0001g0038 a0001c0001t0001g0097 |
2 | HG03831.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.356-3984C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54316595 | |||||||
chr6:54316678 | A | G | 2 | a0001c0001t0001g0178 a0001c0001t0001g0179 |
2 | HG02258.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.356-3901A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54316678 | |||||||
chr6:54316732 | T | A | 1 | a0001c0001t0001g0256 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.356-3847T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54316732 | |||||||
chr6:54316906 | A | G | 1 | a0003c0003t0001g0060 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.356-3673A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54316906 | |||||||
chr6:54317057 | A | G | 1 | a0014c0014t0003g0277 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.356-3522A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54317057 | |||||||
chr6:54317084 | G | A | 206 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(203): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.356-3495G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54317084 | |||||||
chr6:54317149 | T | C | 1 | a0003c0003t0001g0243 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.356-3430T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54317149 | |||||||
chr6:54317198 | T | C | 1 | a0001c0001t0001g0257 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.356-3381T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54317198 | |||||||
chr6:54317233 | G | A | 2 | a0002c0002t0001g0306 a0002c0002t0001g0356 |
2 | NA18978.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.356-3346G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54317233 | |||||||
chr6:54317241 | GCTCT | G | 24 | a0001c0001t0001g0245 a0003c0003t0001g0243 a0003c0003t0001g0357 others(21): Show |
24 | HG00099.hp1 HG00735.hp2 HG01261.hp1 others(21): Show |
intron_variant | MODIFIER | c.356-3333_356-3330d others(6): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 54317241 | ||||||
chr6:54317341 | C | T | 1 | a0001c0010t0001g0244 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.356-3238C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54317341 | |||||||
chr6:54317376 | AGAGG | A | 12 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0230 others(9): Show |
12 | HG00438.hp1 HG00735.hp1 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.356-3200_356-3197d others(6): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 54317376 | ||||||
chr6:54317393 | G | A | 56 | a0001c0001t0001g0297 a0001c0001t0001g0308 a0001c0001t0001g0310 others(53): Show |
56 | HG01123.hp2 HG02056.hp2 HG02071.hp1 others(53): Show |
intron_variant | MODIFIER | c.356-3186G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54317393 | |||||||
chr6:54317401 | G | A | 1 | a0001c0001t0001g0257 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.356-3178G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54317401 | |||||||
chr6:54317433 | G | A | 294 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(291): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.356-3146G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54317433 | |||||||
chr6:54317505 | T | C | 223 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(220): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.356-3074T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54317505 | |||||||
chr6:54317557 | T | C | 293 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(290): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.356-3022T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54317557 | |||||||
chr6:54317561 | C | T | 1 | a0017c0018t0001g0242 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.356-3018C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54317561 | |||||||
chr6:54317568 | G | A | 10 | a0001c0001t0001g0011 a0001c0001t0001g0210 a0001c0001t0001g0212 others(7): Show |
11 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.356-3011G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54317568 | |||||||
chr6:54317620 | A | G | 1 | a0003c0003t0001g0036 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.356-2959A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54317620 | |||||||
chr6:54317728 | A | C | 2 | a0014c0014t0003g0276 a0014c0014t0003g0277 |
2 | HG02970.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.356-2851A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54317728 | |||||||
chr6:54317838 | A | G | 9 | a0002c0002t0001g0305 a0002c0002t0001g0341 a0002c0002t0001g0342 others(6): Show |
9 | HG02056.hp2 NA18747.hp2 NA18939.hp1 others(6): Show |
intron_variant | MODIFIER | c.356-2741A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54317838 | |||||||
chr6:54317844 | G | A | 3 | a0001c0001t0001g0014 a0001c0001t0001g0260 a0001c0001t0001g0296 |
4 | HG00741.hp1 HG01167.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.356-2735G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54317844 | |||||||
chr6:54318058 | C | T | 1 | a0001c0001t0001g0168 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.356-2521C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54318058 | |||||||
chr6:54318341 | C | G | 2 | a0014c0014t0003g0276 a0014c0014t0003g0277 |
2 | HG02970.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.356-2238C>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54318341 | |||||||
chr6:54318366 | G | A | 1 | a0017c0018t0001g0087 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.356-2213G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54318366 | |||||||
chr6:54318500 | A | G | 1 | a0017c0018t0001g0242 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.356-2079A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54318500 | |||||||
chr6:54318518 | C | T | 35 | a0001c0001t0001g0010 a0001c0001t0001g0090 a0001c0001t0001g0091 others(32): Show |
36 | HG00438.hp1 HG00558.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.356-2061C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54318518 | |||||||
chr6:54318529 | T | C | 1 | a0017c0018t0001g0087 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.356-2050T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54318529 | |||||||
chr6:54318641 | C | T | 187 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(184): Show |
197 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.356-1938C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54318641 | |||||||
chr6:54318686 | T | G | 349 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(346): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.356-1893T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54318686 | |||||||
chr6:54319025 | C | T | 33 | a0001c0001t0001g0194 a0001c0001t0001g0204 a0001c0001t0001g0205 others(30): Show |
35 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.356-1554C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54319025 | |||||||
chr6:54319058 | C | G | 1 | a0002c0002t0001g0301 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.356-1521C>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54319058 | |||||||
chr6:54319085 | T | C | 104 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0012 others(101): Show |
109 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.356-1494T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54319085 | |||||||
chr6:54319092 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.356-1487C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54319092 | |||||||
chr6:54319171 | G | A | 2 | a0002c0002t0001g0306 a0002c0002t0001g0356 |
2 | NA18978.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.356-1408G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54319171 | |||||||
chr6:54319197 | T | G | 8 | a0002c0002t0001g0259 a0007c0007t0001g0080 a0007c0007t0001g0081 others(5): Show |
8 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.356-1382T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54319197 | |||||||
chr6:54319258 | T | A | 1 | a0001c0001t0001g0099 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.356-1321T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54319258 | |||||||
chr6:54319405 | G | A | 2 | a0014c0014t0003g0276 a0014c0014t0003g0277 |
2 | HG02970.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.356-1174G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54319405 | |||||||
chr6:54319412 | C | T | 184 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(181): Show |
193 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.356-1167C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54319412 | |||||||
chr6:54319499 | A | T | 1 | a0001c0001t0001g0099 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.356-1080A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54319499 | |||||||
chr6:54319655 | G | A | 1 | a0001c0001t0001g0260 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.356-924G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54319655 | |||||||
chr6:54319840 | T | C | 5 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0102 others(2): Show |
5 | HG00741.hp2 HG01099.hp2 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.356-739T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54319840 | |||||||
chr6:54319893 | C | T | 64 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(61): Show |
64 | HG01123.hp2 HG02056.hp2 HG02071.hp1 others(61): Show |
intron_variant | MODIFIER | c.356-686C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54319893 | |||||||
chr6:54319897 | G | A | 7 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(4): Show |
7 | HG03471.hp1 HG03486.hp2 HG06807.hp1 others(4): Show |
intron_variant | MODIFIER | c.356-682G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54319897 | |||||||
chr6:54319898 | C | A | 7 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(4): Show |
7 | HG03471.hp1 HG03486.hp2 HG06807.hp1 others(4): Show |
intron_variant | MODIFIER | c.356-681C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54319898 | |||||||
chr6:54319996 | A | G | 1 | a0001c0001t0001g0340 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.356-583A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54319996 | |||||||
chr6:54320000 | GT | G | 50 | a0003c0003t0001g0003 a0003c0003t0001g0004 a0003c0003t0001g0005 others(47): Show |
54 | HG00140.hp2 HG00408.hp2 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.356-576delT | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 54320000 | ||||||
chr6:54320082 | T | C | 1 | a0001c0001t0001g0090 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.356-497T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54320082 | |||||||
chr6:54320085 | A | G | 57 | a0001c0001t0001g0297 a0001c0001t0001g0308 a0001c0001t0001g0310 others(54): Show |
57 | HG01123.hp2 HG02056.hp2 HG02071.hp1 others(54): Show |
intron_variant | MODIFIER | c.356-494A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54320085 | |||||||
chr6:54320519 | T | G | 5 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0178 others(2): Show |
5 | HG02258.hp2 HG02897.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.356-60T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 1/10 | chr6 | 54320519 | |||||||
chr6:54320703 | A | G | 1 | a0013c0012t0001g0069 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.419+61A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 2/10 | chr6 | 54320703 | |||||||
chr6:54320720 | C | A | 1 | a0001c0001t0001g0210 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.419+78C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 2/10 | chr6 | 54320720 | |||||||
chr6:54320724 | A | T | 1 | a0002c0002t0001g0298 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.419+82A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 2/10 | chr6 | 54320724 | |||||||
chr6:54320745 | A | G | 2 | a0001c0001t0001g0165 a0006c0006t0001g0166 |
2 | HG01169.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.419+103A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 2/10 | chr6 | 54320745 | |||||||
chr6:54320804 | T | C | 1 | a0007c0007t0001g0080 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.419+162T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 2/10 | chr6 | 54320804 | |||||||
chr6:54320891 | G | T | 116 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0012 others(113): Show |
122 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.419+249G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 2/10 | chr6 | 54320891 | |||||||
chr6:54320907 | C | G | 9 | a0003c0003t0001g0064 a0003c0003t0001g0065 a0003c0003t0001g0066 others(6): Show |
9 | HG02280.hp2 HG02809.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.419+265C>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 2/10 | chr6 | 54320907 | |||||||
chr6:54320917 | A | G | 4 | a0001c0001t0001g0245 a0001c0001t0001g0258 a0001c0001t0001g0261 others(1): Show |
4 | HG02258.hp1 HG03098.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.419+275A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 2/10 | chr6 | 54320917 | |||||||
chr6:54320947 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.419+305G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 2/10 | chr6 | 54320947 | |||||||
chr6:54320994 | C | T | 10 | a0001c0001t0001g0011 a0001c0001t0001g0210 a0001c0001t0001g0212 others(7): Show |
11 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.420-303C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 2/10 | chr6 | 54320994 | |||||||
chr6:54321002 | C | T | 1 | a0001c0001t0001g0164 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.420-295C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 2/10 | chr6 | 54321002 | |||||||
chr6:54321066 | G | A | 261 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(258): Show |
271 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.420-231G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 2/10 | chr6 | 54321066 | |||||||
chr6:54321072 | G | A | 1 | a0002c0002t0001g0307 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.420-225G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 2/10 | chr6 | 54321072 | |||||||
chr6:54321091 | T | G | 1 | a0001c0001t0001g0227 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.420-206T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 2/10 | chr6 | 54321091 | |||||||
chr6:54321103 | G | C | 69 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0285 others(66): Show |
69 | HG01123.hp2 HG01891.hp2 HG02056.hp2 others(66): Show |
intron_variant | MODIFIER | c.420-194G>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 2/10 | chr6 | 54321103 | |||||||
chr6:54321226 | T | C | 108 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0012 others(105): Show |
113 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.420-71T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 2/10 | chr6 | 54321226 | |||||||
chr6:54321257 | T | A | 1 | a0024c0025t0001g0262 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.420-40T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 2/10 | chr6 | 54321257 | |||||||
chr6:54321412 | T | C | 2 | a0001c0001t0001g0254 a0001c0001t0001g0255 |
2 | HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.509+26T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54321412 | |||||||
chr6:54321457 | G | A | 3 | a0001c0001t0001g0007 a0001c0001t0001g0093 a0001c0001t0001g0094 |
4 | HG03491.hp1 HG03492.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.509+71G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54321457 | |||||||
chr6:54321512 | A | C | 2 | a0001c0001t0001g0217 a0001c0001t0001g0218 |
2 | NA18941.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.509+126A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54321512 | |||||||
chr6:54321764 | T | C | 90 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0038 others(87): Show |
94 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.509+378T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54321764 | |||||||
chr6:54321830 | G | A | 3 | a0001c0001t0001g0007 a0001c0001t0001g0093 a0001c0001t0001g0094 |
4 | HG03491.hp1 HG03492.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.509+444G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54321830 | |||||||
chr6:54321877 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.509+491C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54321877 | |||||||
chr6:54321982 | G | A | 1 | a0020c0019t0001g0211 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.509+596G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54321982 | |||||||
chr6:54321986 | C | G | 1 | a0001c0010t0001g0244 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.509+600C>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54321986 | |||||||
chr6:54322135 | T | C | 1 | a0003c0003t0001g0039 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.509+749T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54322135 | |||||||
chr6:54322201 | A | G | 273 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(270): Show |
285 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.509+815A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54322201 | |||||||
chr6:54322272 | C | A | 1 | a0005c0005t0001g0263 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.509+886C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54322272 | |||||||
chr6:54322333 | C | CA | 51 | a0001c0001t0001g0011 a0001c0001t0001g0014 a0001c0001t0001g0105 others(48): Show |
55 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.509+957dupA | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr6 | 54322333 | ||||||
chr6:54322337 | A | C | 67 | a0001c0001t0001g0297 a0001c0001t0001g0308 a0001c0001t0001g0310 others(64): Show |
67 | HG01123.hp2 HG02056.hp2 HG02071.hp1 others(64): Show |
intron_variant | MODIFIER | c.509+951A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54322337 | |||||||
chr6:54322343 | A | AG | 6 | a0001c0001t0001g0207 a0001c0001t0001g0292 a0002c0002t0001g0013 others(3): Show |
7 | HG02622.hp1 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.509+957_509+958ins others(1): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54322343 | |||||||
chr6:54322367 | C | A | 2 | a0008c0008t0002g0078 a0008c0008t0002g0079 |
2 | HG01069.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.509+981C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54322367 | |||||||
chr6:54322388 | T | G | 108 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0012 others(105): Show |
113 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.509+1002T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54322388 | |||||||
chr6:54322447 | C | T | 3 | a0002c0002t0001g0013 a0002c0002t0001g0293 a0002c0002t0001g0294 |
4 | HG02622.hp1 HG02717.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.509+1061C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54322447 | |||||||
chr6:54322496 | A | G | 1 | a0003c0003t0001g0035 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.509+1110A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54322496 | |||||||
chr6:54322684 | C | T | 5 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(2): Show |
5 | HG03471.hp1 HG03486.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.509+1298C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54322684 | |||||||
chr6:54322806 | A | C | 11 | a0001c0001t0001g0014 a0001c0001t0001g0207 a0001c0001t0001g0245 others(8): Show |
13 | HG00741.hp1 HG01167.hp2 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.509+1420A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54322806 | |||||||
chr6:54322844 | A | C | 1 | a0001c0001t0001g0281 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.509+1458A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54322844 | |||||||
chr6:54322860 | G | A | 6 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 others(3): Show |
6 | HG01167.hp1 HG01243.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.509+1474G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54322860 | |||||||
chr6:54322995 | C | A | 9 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0285 others(6): Show |
9 | HG01891.hp2 HG02257.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.509+1609C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54322995 | |||||||
chr6:54323100 | A | T | 2 | a0014c0014t0003g0276 a0014c0014t0003g0277 |
2 | HG02970.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.509+1714A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54323100 | |||||||
chr6:54323251 | A | G | 1 | a0001c0001t0001g0156 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.509+1865A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54323251 | |||||||
chr6:54323290 | A | G | 9 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(6): Show |
9 | HG03098.hp2 HG03195.hp2 HG03471.hp1 others(6): Show |
intron_variant | MODIFIER | c.509+1904A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54323290 | |||||||
chr6:54323384 | C | G | 3 | a0001c0001t0001g0007 a0001c0001t0001g0093 a0001c0001t0001g0094 |
4 | HG03491.hp1 HG03492.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.509+1998C>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54323384 | |||||||
chr6:54323585 | C | T | 10 | a0001c0001t0001g0011 a0001c0001t0001g0210 a0001c0001t0001g0212 others(7): Show |
11 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.509+2199C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54323585 | |||||||
chr6:54323680 | G | A | 1 | a0002c0002t0001g0301 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.509+2294G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54323680 | |||||||
chr6:54323693 | C | A | 35 | a0001c0001t0001g0010 a0001c0001t0001g0090 a0001c0001t0001g0091 others(32): Show |
36 | HG00438.hp1 HG00558.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.509+2307C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54323693 | |||||||
chr6:54323703 | C | T | 33 | a0001c0001t0001g0194 a0001c0001t0001g0204 a0001c0001t0001g0205 others(30): Show |
35 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.509+2317C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54323703 | |||||||
chr6:54323756 | C | A | 6 | a0001c0001t0001g0207 a0001c0001t0001g0292 a0002c0002t0001g0013 others(3): Show |
7 | HG02622.hp1 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.509+2370C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54323756 | |||||||
chr6:54323793 | G | A | 50 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0090 others(47): Show |
52 | HG00438.hp1 HG00558.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.509+2407G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54323793 | |||||||
chr6:54324086 | A | G | 10 | a0001c0001t0001g0011 a0001c0001t0001g0210 a0001c0001t0001g0212 others(7): Show |
11 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.509+2700A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54324086 | |||||||
chr6:54324177 | T | A | 56 | a0001c0001t0001g0297 a0001c0001t0001g0308 a0001c0001t0001g0310 others(53): Show |
56 | HG01123.hp2 HG02056.hp2 HG02071.hp1 others(53): Show |
intron_variant | MODIFIER | c.510-2625T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54324177 | |||||||
chr6:54324194 | T | G | 1 | a0002c0002t0001g0301 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.510-2608T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54324194 | |||||||
chr6:54324281 | G | T | 1 | a0001c0001t0001g0155 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.510-2521G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54324281 | |||||||
chr6:54324424 | T | A | 1 | a0001c0001t0001g0282 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.510-2378T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54324424 | |||||||
chr6:54324620 | C | T | 53 | a0001c0001t0001g0297 a0001c0001t0001g0312 a0001c0001t0001g0315 others(50): Show |
53 | HG01123.hp2 HG02056.hp2 HG02071.hp1 others(50): Show |
intron_variant | MODIFIER | c.510-2182C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54324620 | |||||||
chr6:54324636 | T | G | 37 | a0001c0001t0001g0010 a0001c0001t0001g0090 a0001c0001t0001g0091 others(34): Show |
38 | HG00438.hp1 HG00558.hp2 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.510-2166T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54324636 | |||||||
chr6:54324672 | C | G | 56 | a0001c0001t0001g0297 a0001c0001t0001g0308 a0001c0001t0001g0310 others(53): Show |
56 | HG01123.hp2 HG02056.hp2 HG02071.hp1 others(53): Show |
intron_variant | MODIFIER | c.510-2130C>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54324672 | |||||||
chr6:54324678 | G | C | 1 | a0011c0011t0001g0040 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.510-2124G>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54324678 | |||||||
chr6:54324807 | T | C | 3 | a0001c0001t0001g0014 a0001c0001t0001g0260 a0001c0001t0001g0296 |
4 | HG00741.hp1 HG01167.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.510-1995T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54324807 | |||||||
chr6:54324884 | C | T | 2 | a0014c0014t0003g0276 a0014c0014t0003g0277 |
2 | HG02970.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.510-1918C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54324884 | |||||||
chr6:54324934 | A | G | 2 | a0012c0009t0001g0208 a0012c0009t0001g0209 |
2 | HG02109.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.510-1868A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54324934 | |||||||
chr6:54324946 | A | G | 11 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0285 others(8): Show |
11 | HG01891.hp2 HG02257.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.510-1856A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54324946 | |||||||
chr6:54325275 | A | C | 2 | a0001c0001t0001g0154 a0001c0001t0001g0155 |
2 | HG01192.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.510-1527A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54325275 | |||||||
chr6:54325276 | G | A | 2 | a0001c0010t0001g0244 a0017c0018t0001g0242 |
2 | HG06807.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.510-1526G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54325276 | |||||||
chr6:54325470 | A | G | 2 | a0001c0001t0001g0258 a0001c0001t0001g0261 |
2 | HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.510-1332A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54325470 | |||||||
chr6:54325506 | G | A | 2 | a0001c0001t0001g0245 a0023c0020t0001g0291 |
2 | HG02258.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.510-1296G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54325506 | |||||||
chr6:54325513 | A | G | 1 | a0017c0018t0001g0087 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.510-1289A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54325513 | |||||||
chr6:54325658 | A | G | 218 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(215): Show |
225 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.510-1144A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54325658 | |||||||
chr6:54325698 | C | T | 3 | a0001c0001t0001g0088 a0001c0001t0001g0152 a0001c0001t0001g0153 |
3 | NA18963.hp1 NA18966.hp1 NA18997.hp2 |
intron_variant | MODIFIER | c.510-1104C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54325698 | |||||||
chr6:54325739 | C | T | 1 | a0001c0001t0001g0191 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.510-1063C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54325739 | |||||||
chr6:54325801 | CTTA | C | 9 | a0002c0002t0001g0331 a0002c0002t0001g0332 a0002c0002t0001g0333 others(6): Show |
9 | NA18612.hp2 NA18943.hp2 NA18944.hp1 others(6): Show |
intron_variant | MODIFIER | c.510-998_510-996del others(3): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr6 | 54325801 | ||||||
chr6:54325954 | C | T | 2 | a0014c0014t0003g0276 a0014c0014t0003g0277 |
2 | HG02970.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.510-848C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54325954 | |||||||
chr6:54325956 | A | G | 1 | a0017c0018t0001g0087 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.510-846A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54325956 | |||||||
chr6:54326085 | C | G | 10 | a0007c0007t0001g0080 a0007c0007t0001g0081 a0007c0007t0001g0083 others(7): Show |
10 | HG01069.hp1 HG01243.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.510-717C>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54326085 | |||||||
chr6:54326140 | A | G | 10 | a0001c0001t0001g0011 a0001c0001t0001g0210 a0001c0001t0001g0212 others(7): Show |
11 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.510-662A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54326140 | |||||||
chr6:54326147 | T | A | 272 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(269): Show |
283 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.510-655T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54326147 | |||||||
chr6:54326214 | TTTA | T | 3 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 |
3 | NA18962.hp2 NA18991.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.510-578_510-576del others(3): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr6 | 54326214 | ||||||
chr6:54326350 | A | C | 1 | a0001c0001t0001g0151 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.510-452A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54326350 | |||||||
chr6:54326390 | C | G | 1 | a0017c0018t0001g0242 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.510-412C>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54326390 | |||||||
chr6:54326492 | T | G | 3 | a0001c0001t0001g0007 a0001c0001t0001g0093 a0001c0001t0001g0094 |
4 | HG03491.hp1 HG03492.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.510-310T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54326492 | |||||||
chr6:54326565 | G | A | 112 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0012 others(109): Show |
116 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.510-237G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54326565 | |||||||
chr6:54326655 | A | G | 1 | a0001c0001t0001g0256 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.510-147A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54326655 | |||||||
chr6:54326736 | T | C | 1 | a0017c0018t0001g0087 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.510-66T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 3/10 | chr6 | 54326736 | |||||||
chr6:54326956 | T | C | 2 | a0001c0001t0001g0245 a0023c0020t0001g0291 |
2 | HG02258.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.624+40T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54326956 | |||||||
chr6:54327167 | G | A | 3 | a0001c0001t0001g0256 a0014c0014t0003g0276 a0014c0014t0003g0277 |
3 | HG02970.hp1 NA19030.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.624+251G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54327167 | |||||||
chr6:54327172 | T | A | 275 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(272): Show |
287 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(284): Show |
intron_variant | MODIFIER | c.624+256T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54327172 | |||||||
chr6:54327210 | A | G | 48 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0090 others(45): Show |
50 | HG00438.hp1 HG00558.hp2 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.624+294A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54327210 | |||||||
chr6:54327232 | G | T | 10 | a0001c0001t0001g0011 a0001c0001t0001g0210 a0001c0001t0001g0212 others(7): Show |
11 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.624+316G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54327232 | |||||||
chr6:54327264 | T | C | 38 | a0001c0001t0001g0010 a0001c0001t0001g0090 a0001c0001t0001g0091 others(35): Show |
39 | HG00438.hp1 HG00558.hp2 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.624+348T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54327264 | |||||||
chr6:54327449 | G | A | 3 | a0001c0001t0001g0014 a0001c0001t0001g0260 a0001c0001t0001g0296 |
4 | HG00741.hp1 HG01167.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.624+533G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54327449 | |||||||
chr6:54327463 | A | G | 2 | a0014c0014t0003g0276 a0014c0014t0003g0277 |
2 | HG02970.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.624+547A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54327463 | |||||||
chr6:54327520 | G | T | 1 | a0011c0011t0001g0040 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.624+604G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54327520 | |||||||
chr6:54327557 | G | GT | 6 | a0001c0001t0001g0245 a0001c0001t0001g0256 a0002c0002t0001g0339 others(3): Show |
6 | HG02258.hp1 HG02970.hp1 NA18906.hp2 others(3): Show |
intron_variant | MODIFIER | c.624+651dupT | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 54327557 | ||||||
chr6:54327575 | C | T | 3 | a0002c0002t0001g0251 a0002c0002t0001g0252 a0010c0013t0001g0303 |
3 | HG01258.hp2 HG03471.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.624+659C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54327575 | |||||||
chr6:54327675 | C | T | 1 | a0017c0018t0001g0087 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.624+759C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54327675 | |||||||
chr6:54327891 | C | A | 2 | a0014c0014t0003g0276 a0014c0014t0003g0277 |
2 | HG02970.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.624+975C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54327891 | |||||||
chr6:54327997 | C | G | 1 | a0002c0002t0001g0355 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.624+1081C>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54327997 | |||||||
chr6:54328068 | C | A | 112 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0012 others(109): Show |
116 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.624+1152C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54328068 | |||||||
chr6:54328145 | G | T | 3 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0250 |
3 | HG02258.hp2 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.624+1229G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54328145 | |||||||
chr6:54328176 | G | A | 1 | a0017c0018t0001g0087 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.624+1260G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54328176 | |||||||
chr6:54328233 | C | T | 1 | a0013c0012t0001g0206 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.624+1317C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54328233 | |||||||
chr6:54328274 | C | G | 1 | a0001c0001t0001g0256 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.624+1358C>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54328274 | |||||||
chr6:54328370 | G | A | 306 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(303): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.624+1454G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54328370 | |||||||
chr6:54328431 | A | T | 114 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0090 others(111): Show |
118 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(115): Show |
intron_variant | MODIFIER | c.624+1515A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54328431 | |||||||
chr6:54328592 | C | G | 31 | a0004c0004t0001g0002 a0004c0004t0001g0076 a0004c0004t0001g0170 others(28): Show |
33 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.624+1676C>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54328592 | |||||||
chr6:54328607 | G | A | 4 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0002c0002t0001g0251 others(1): Show |
4 | HG03471.hp1 HG03486.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.624+1691G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54328607 | |||||||
chr6:54328622 | T | A | 2 | a0001c0001t0001g0245 a0023c0020t0001g0291 |
2 | HG02258.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.624+1706T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54328622 | |||||||
chr6:54328674 | C | T | 1 | a0001c0001t0001g0190 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.624+1758C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54328674 | |||||||
chr6:54328797 | A | G | 108 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0090 others(105): Show |
112 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(109): Show |
intron_variant | MODIFIER | c.624+1881A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54328797 | |||||||
chr6:54328835 | A | G | 2 | a0001c0001t0001g0245 a0023c0020t0001g0291 |
2 | HG02258.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.624+1919A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54328835 | |||||||
chr6:54328928 | T | C | 1 | a0004c0004t0001g0170 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.624+2012T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54328928 | |||||||
chr6:54328932 | T | C | 1 | a0001c0001t0001g0256 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.624+2016T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54328932 | |||||||
chr6:54328957 | A | G | 1 | a0001c0010t0001g0244 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.624+2041A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54328957 | |||||||
chr6:54328973 | G | A | 1 | a0002c0002t0001g0341 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.624+2057G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54328973 | |||||||
chr6:54329007 | C | T | 10 | a0001c0001t0001g0011 a0001c0001t0001g0210 a0001c0001t0001g0212 others(7): Show |
11 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.624+2091C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54329007 | |||||||
chr6:54329022 | C | T | 10 | a0001c0001t0001g0011 a0001c0001t0001g0210 a0001c0001t0001g0212 others(7): Show |
11 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.624+2106C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54329022 | |||||||
chr6:54329024 | A | G | 1 | a0001c0001t0001g0256 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.624+2108A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54329024 | |||||||
chr6:54329032 | C | A | 1 | a0004c0004t0001g0195 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.624+2116C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54329032 | |||||||
chr6:54329060 | A | G | 2 | a0014c0014t0003g0276 a0014c0014t0003g0277 |
2 | HG02970.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.624+2144A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54329060 | |||||||
chr6:54329062 | C | A | 144 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0090 others(141): Show |
150 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(147): Show |
intron_variant | MODIFIER | c.624+2146C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54329062 | |||||||
chr6:54329114 | A | T | 1 | a0001c0001t0001g0147 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.624+2198A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54329114 | |||||||
chr6:54329120 | A | G | 1 | a0003c0003t0001g0056 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.624+2204A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54329120 | |||||||
chr6:54329143 | G | A | 1 | a0002c0002t0001g0293 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.624+2227G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54329143 | |||||||
chr6:54329303 | G | A | 4 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0002c0002t0001g0251 others(1): Show |
4 | HG03471.hp1 HG03486.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.624+2387G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54329303 | |||||||
chr6:54329364 | C | T | 2 | a0015c0015t0001g0279 a0015c0015t0001g0280 |
2 | HG03130.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.624+2448C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54329364 | |||||||
chr6:54329407 | T | C | 1 | a0001c0001t0001g0256 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.624+2491T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54329407 | |||||||
chr6:54329650 | A | G | 10 | a0001c0001t0001g0011 a0001c0001t0001g0210 a0001c0001t0001g0212 others(7): Show |
11 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.624+2734A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54329650 | |||||||
chr6:54329709 | G | T | 1 | a0022c0023t0001g0042 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.624+2793G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54329709 | |||||||
chr6:54329727 | C | T | 3 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0175 |
3 | HG02451.hp1 HG02886.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.624+2811C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54329727 | |||||||
chr6:54329854 | G | A | 2 | a0001c0001t0001g0258 a0001c0001t0001g0261 |
2 | HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.624+2938G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54329854 | |||||||
chr6:54329895 | AG | A | 10 | a0001c0001t0001g0011 a0001c0001t0001g0210 a0001c0001t0001g0212 others(7): Show |
11 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.624+2983delG | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 54329895 | ||||||
chr6:54329904 | A | G | 4 | a0003c0003t0001g0068 a0003c0003t0001g0070 a0003c0003t0001g0071 others(1): Show |
4 | HG02280.hp2 HG02895.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.624+2988A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54329904 | |||||||
chr6:54329947 | A | C | 1 | a0001c0001t0001g0292 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.624+3031A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54329947 | |||||||
chr6:54330106 | G | C | 287 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(284): Show |
299 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.624+3190G>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54330106 | |||||||
chr6:54330112 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.624+3196C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54330112 | |||||||
chr6:54330116 | C | T | 10 | a0001c0001t0001g0011 a0001c0001t0001g0210 a0001c0001t0001g0212 others(7): Show |
11 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.624+3200C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54330116 | |||||||
chr6:54330232 | C | G | 1 | a0001c0001t0001g0256 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.624+3316C>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54330232 | |||||||
chr6:54330264 | A | G | 31 | a0004c0004t0001g0002 a0004c0004t0001g0076 a0004c0004t0001g0170 others(28): Show |
33 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.624+3348A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54330264 | |||||||
chr6:54330330 | C | G | 1 | a0001c0001t0001g0256 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.624+3414C>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54330330 | |||||||
chr6:54330339 | C | T | 3 | a0014c0014t0003g0276 a0014c0014t0003g0277 a0017c0018t0001g0087 |
3 | HG02970.hp1 HG03471.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.624+3423C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54330339 | |||||||
chr6:54330395 | C | T | 1 | a0004c0004t0001g0076 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.624+3479C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54330395 | |||||||
chr6:54330422 | A | C | 1 | a0004c0004t0001g0192 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.624+3506A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54330422 | |||||||
chr6:54330465 | G | A | 2 | a0014c0014t0003g0276 a0014c0014t0003g0277 |
2 | HG02970.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.624+3549G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54330465 | |||||||
chr6:54330576 | G | T | 1 | a0003c0003t0001g0034 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.624+3660G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54330576 | |||||||
chr6:54330588 | C | T | 2 | a0003c0003t0001g0067 a0009c0016t0001g0240 |
2 | HG00735.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.624+3672C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54330588 | |||||||
chr6:54330703 | C | T | 1 | a0020c0019t0001g0211 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.624+3787C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54330703 | |||||||
chr6:54330704 | G | A | 1 | a0013c0012t0001g0206 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.624+3788G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54330704 | |||||||
chr6:54330772 | A | T | 1 | a0001c0001t0001g0099 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.624+3856A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54330772 | |||||||
chr6:54330805 | C | G | 3 | a0001c0001t0001g0007 a0001c0001t0001g0093 a0001c0001t0001g0094 |
4 | HG03491.hp1 HG03492.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.624+3889C>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54330805 | |||||||
chr6:54330932 | C | T | 1 | a0001c0001t0001g0256 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.624+4016C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54330932 | |||||||
chr6:54330974 | C | A | 1 | a0002c0002t0001g0117 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.624+4058C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54330974 | |||||||
chr6:54330999 | C | T | 1 | a0001c0001t0001g0207 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.624+4083C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54330999 | |||||||
chr6:54331035 | G | A | 1 | a0002c0002t0001g0246 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.624+4119G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54331035 | |||||||
chr6:54331045 | C | T | 111 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0090 others(108): Show |
115 | HG00438.hp1 HG00558.hp2 HG00735.hp1 others(112): Show |
intron_variant | MODIFIER | c.624+4129C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54331045 | |||||||
chr6:54331087 | C | A | 1 | a0001c0001t0001g0190 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.624+4171C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54331087 | |||||||
chr6:54331131 | A | G | 2 | a0014c0014t0003g0276 a0014c0014t0003g0277 |
2 | HG02970.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.624+4215A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54331131 | |||||||
chr6:54331208 | A | G | 4 | a0001c0001t0001g0007 a0001c0001t0001g0093 a0001c0001t0001g0094 others(1): Show |
5 | HG03471.hp2 HG03491.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.624+4292A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54331208 | |||||||
chr6:54331263 | C | T | 31 | a0004c0004t0001g0002 a0004c0004t0001g0076 a0004c0004t0001g0170 others(28): Show |
33 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.624+4347C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54331263 | |||||||
chr6:54331342 | A | G | 1 | a0002c0002t0001g0301 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.624+4426A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54331342 | |||||||
chr6:54331366 | A | G | 31 | a0004c0004t0001g0002 a0004c0004t0001g0076 a0004c0004t0001g0170 others(28): Show |
33 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.624+4450A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54331366 | |||||||
chr6:54331392 | C | T | 2 | a0014c0014t0003g0276 a0014c0014t0003g0277 |
2 | HG02970.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.624+4476C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54331392 | |||||||
chr6:54331393 | G | A | 1 | a0002c0002t0001g0311 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.624+4477G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54331393 | |||||||
chr6:54331496 | A | G | 32 | a0004c0004t0001g0002 a0004c0004t0001g0076 a0004c0004t0001g0170 others(29): Show |
34 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.624+4580A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54331496 | |||||||
chr6:54331497 | T | G | 1 | a0007c0007t0001g0081 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.624+4581T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54331497 | |||||||
chr6:54331501 | A | G | 3 | a0001c0001t0001g0007 a0001c0001t0001g0093 a0001c0001t0001g0094 |
4 | HG03491.hp1 HG03492.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.624+4585A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54331501 | |||||||
chr6:54331505 | T | C | 10 | a0001c0001t0001g0011 a0001c0001t0001g0210 a0001c0001t0001g0212 others(7): Show |
11 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.624+4589T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54331505 | |||||||
chr6:54331771 | T | TA | 158 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0014 others(155): Show |
165 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(162): Show |
intron_variant | MODIFIER | c.624+4858dupA | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 54331771 | ||||||
chr6:54331820 | A | G | 7 | a0001c0001t0001g0282 a0001c0001t0001g0285 a0001c0001t0001g0286 others(4): Show |
7 | HG01891.hp2 HG02257.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.624+4904A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54331820 | |||||||
chr6:54332057 | G | C | 31 | a0004c0004t0001g0002 a0004c0004t0001g0076 a0004c0004t0001g0170 others(28): Show |
33 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.624+5141G>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54332057 | |||||||
chr6:54332117 | C | T | 1 | a0017c0018t0001g0242 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.624+5201C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54332117 | |||||||
chr6:54332138 | A | G | 1 | a0006c0006t0001g0146 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.624+5222A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54332138 | |||||||
chr6:54332300 | C | T | 3 | a0001c0001t0001g0014 a0001c0001t0001g0260 a0001c0001t0001g0296 |
4 | HG00741.hp1 HG01167.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.624+5384C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54332300 | |||||||
chr6:54332301 | C | T | 2 | a0001c0001t0001g0245 a0023c0020t0001g0291 |
2 | HG02258.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.624+5385C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54332301 | |||||||
chr6:54332339 | A | T | 2 | a0016c0017t0001g0274 a0016c0017t0001g0275 |
2 | HG03225.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.624+5423A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54332339 | |||||||
chr6:54332374 | T | G | 2 | a0001c0001t0001g0245 a0023c0020t0001g0291 |
2 | HG02258.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.624+5458T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54332374 | |||||||
chr6:54332411 | C | T | 7 | a0001c0001t0001g0014 a0001c0001t0001g0254 a0001c0001t0001g0255 others(4): Show |
8 | HG00741.hp1 HG01167.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.624+5495C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54332411 | |||||||
chr6:54332552 | G | A | 2 | a0001c0001t0001g0258 a0001c0001t0001g0261 |
2 | HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.624+5636G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54332552 | |||||||
chr6:54332579 | C | T | 2 | a0001c0001t0001g0245 a0023c0020t0001g0291 |
2 | HG02258.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.624+5663C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54332579 | |||||||
chr6:54332618 | G | A | 3 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0175 |
3 | HG02451.hp1 HG02886.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.624+5702G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54332618 | |||||||
chr6:54332636 | G | A | 112 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0012 others(109): Show |
116 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.624+5720G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54332636 | |||||||
chr6:54332682 | A | C | 1 | a0004c0004t0001g0203 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.624+5766A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54332682 | |||||||
chr6:54332751 | G | A | 2 | a0001c0001t0001g0245 a0023c0020t0001g0291 |
2 | HG02258.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.624+5835G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54332751 | |||||||
chr6:54333062 | G | C | 108 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0012 others(105): Show |
112 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.624+6146G>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54333062 | |||||||
chr6:54333368 | C | A | 1 | a0017c0018t0001g0087 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.624+6452C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54333368 | |||||||
chr6:54333462 | T | A | 2 | a0001c0001t0001g0245 a0023c0020t0001g0291 |
2 | HG02258.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.624+6546T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54333462 | |||||||
chr6:54333485 | G | A | 36 | a0001c0001t0001g0010 a0001c0001t0001g0090 a0001c0001t0001g0091 others(33): Show |
37 | HG00438.hp1 HG00558.hp2 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.624+6569G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54333485 | |||||||
chr6:54333494 | C | T | 2 | a0016c0017t0001g0274 a0016c0017t0001g0275 |
2 | HG03225.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.624+6578C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54333494 | |||||||
chr6:54333513 | T | C | 2 | a0001c0001t0001g0258 a0001c0001t0001g0261 |
2 | HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.624+6597T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54333513 | |||||||
chr6:54333544 | C | A | 68 | a0001c0001t0001g0207 a0001c0001t0001g0254 a0001c0001t0001g0255 others(65): Show |
70 | HG01123.hp2 HG02056.hp2 HG02071.hp1 others(67): Show |
intron_variant | MODIFIER | c.624+6628C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54333544 | |||||||
chr6:54333565 | T | A | 158 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0014 others(155): Show |
165 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(162): Show |
intron_variant | MODIFIER | c.624+6649T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54333565 | |||||||
chr6:54333619 | A | T | 158 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0014 others(155): Show |
165 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(162): Show |
intron_variant | MODIFIER | c.624+6703A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54333619 | |||||||
chr6:54333626 | A | T | 298 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(295): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.624+6710A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54333626 | |||||||
chr6:54333649 | A | G | 33 | a0001c0001t0001g0010 a0001c0001t0001g0090 a0001c0001t0001g0091 others(30): Show |
34 | HG00438.hp1 HG00558.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.624+6733A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54333649 | |||||||
chr6:54333669 | T | C | 1 | a0003c0003t0001g0043 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.624+6753T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54333669 | |||||||
chr6:54333764 | C | T | 1 | a0002c0002t0001g0189 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.624+6848C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54333764 | |||||||
chr6:54333884 | G | T | 10 | a0002c0002t0001g0301 a0003c0003t0001g0064 a0003c0003t0001g0065 others(7): Show |
10 | HG02280.hp2 HG02647.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.624+6968G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54333884 | |||||||
chr6:54333894 | CA | C | 7 | a0001c0001t0001g0014 a0001c0001t0001g0254 a0001c0001t0001g0255 others(4): Show |
8 | HG00741.hp1 HG01167.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.624+6983delA | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 54333894 | ||||||
chr6:54333980 | T | A | 1 | a0001c0001t0001g0119 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.624+7064T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54333980 | |||||||
chr6:54334122 | C | T | 31 | a0004c0004t0001g0002 a0004c0004t0001g0076 a0004c0004t0001g0170 others(28): Show |
33 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.624+7206C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54334122 | |||||||
chr6:54334211 | G | A | 1 | a0005c0005t0001g0264 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.624+7295G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54334211 | |||||||
chr6:54334320 | A | G | 160 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0014 others(157): Show |
167 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(164): Show |
intron_variant | MODIFIER | c.624+7404A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54334320 | |||||||
chr6:54334433 | AG | A | 10 | a0001c0001t0001g0011 a0001c0001t0001g0210 a0001c0001t0001g0212 others(7): Show |
11 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.624+7518delG | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54334433 | |||||||
chr6:54334504 | A | C | 1 | a0001c0001t0001g0190 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.624+7588A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54334504 | |||||||
chr6:54334511 | T | C | 1 | a0001c0010t0001g0244 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.624+7595T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54334511 | |||||||
chr6:54334521 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.624+7605G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54334521 | |||||||
chr6:54334764 | G | A | 3 | a0001c0001t0001g0007 a0001c0001t0001g0093 a0001c0001t0001g0094 |
4 | HG03491.hp1 HG03492.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.624+7848G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54334764 | |||||||
chr6:54334784 | T | C | 37 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0002c0002t0001g0098 others(34): Show |
39 | HG00438.hp2 HG00639.hp2 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.624+7868T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54334784 | |||||||
chr6:54334948 | T | G | 1 | a0001c0001t0001g0250 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.624+8032T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54334948 | |||||||
chr6:54334982 | T | C | 125 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(122): Show |
131 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.624+8066T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54334982 | |||||||
chr6:54335077 | C | T | 3 | a0001c0001t0001g0007 a0001c0001t0001g0093 a0001c0001t0001g0094 |
4 | HG03491.hp1 HG03492.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.625-8149C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54335077 | |||||||
chr6:54335078 | G | T | 7 | a0001c0001t0001g0282 a0001c0001t0001g0285 a0001c0001t0001g0286 others(4): Show |
7 | HG01891.hp2 HG02257.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.625-8148G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54335078 | |||||||
chr6:54335417 | T | C | 1 | a0001c0001t0001g0256 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.625-7809T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54335417 | |||||||
chr6:54335463 | T | C | 1 | a0001c0001t0001g0073 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.625-7763T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54335463 | |||||||
chr6:54335539 | A | G | 9 | a0002c0002t0001g0301 a0007c0007t0001g0080 a0007c0007t0001g0081 others(6): Show |
9 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.625-7687A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54335539 | |||||||
chr6:54335560 | A | G | 1 | a0001c0001t0001g0147 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.625-7666A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54335560 | |||||||
chr6:54335561 | A | G | 13 | a0001c0001t0001g0100 a0001c0001t0001g0102 a0001c0001t0001g0103 others(10): Show |
15 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.625-7665A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54335561 | |||||||
chr6:54335628 | C | A | 3 | a0003c0003t0001g0043 a0003c0003t0001g0046 a0003c0003t0001g0047 |
3 | HG02602.hp1 HG03654.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.625-7598C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54335628 | |||||||
chr6:54335649 | A | C | 1 | a0002c0002t0001g0117 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.625-7577A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54335649 | |||||||
chr6:54335736 | C | T | 68 | a0001c0001t0001g0207 a0001c0001t0001g0308 a0001c0001t0001g0310 others(65): Show |
70 | HG00642.hp2 HG01123.hp2 HG02056.hp2 others(67): Show |
intron_variant | MODIFIER | c.625-7490C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54335736 | |||||||
chr6:54335764 | G | C | 1 | a0001c0001t0001g0312 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.625-7462G>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54335764 | |||||||
chr6:54335987 | G | T | 68 | a0001c0001t0001g0207 a0001c0001t0001g0308 a0001c0001t0001g0310 others(65): Show |
70 | HG00642.hp2 HG01123.hp2 HG02056.hp2 others(67): Show |
intron_variant | MODIFIER | c.625-7239G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54335987 | |||||||
chr6:54336028 | G | A | 18 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0093 others(15): Show |
20 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(17): Show |
intron_variant | MODIFIER | c.625-7198G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54336028 | |||||||
chr6:54336051 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.625-7175G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54336051 | |||||||
chr6:54336091 | G | A | 2 | a0001c0001t0001g0177 a0001c0001t0001g0281 |
2 | HG02897.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.625-7135G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54336091 | |||||||
chr6:54336316 | T | C | 29 | a0004c0004t0001g0002 a0004c0004t0001g0076 a0004c0004t0001g0170 others(26): Show |
31 | HG00140.hp1 HG00438.hp2 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.625-6910T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54336316 | |||||||
chr6:54336408 | A | T | 2 | a0001c0001t0001g0254 a0001c0001t0001g0255 |
2 | HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.625-6818A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54336408 | |||||||
chr6:54336411 | G | T | 3 | a0001c0001t0001g0007 a0001c0001t0001g0093 a0001c0001t0001g0094 |
4 | HG03491.hp1 HG03492.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.625-6815G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54336411 | |||||||
chr6:54336529 | A | T | 9 | a0001c0001t0001g0011 a0001c0001t0001g0210 a0001c0001t0001g0212 others(6): Show |
10 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.625-6697A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54336529 | |||||||
chr6:54336569 | T | A | 1 | a0004c0004t0001g0195 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.625-6657T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54336569 | |||||||
chr6:54336601 | T | C | 1 | a0002c0002t0001g0321 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.625-6625T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54336601 | |||||||
chr6:54336772 | C | T | 1 | a0001c0001t0001g0191 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.625-6454C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54336772 | |||||||
chr6:54336792 | C | T | 1 | a0001c0001t0001g0143 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.625-6434C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54336792 | |||||||
chr6:54336845 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.625-6381C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54336845 | |||||||
chr6:54336846 | G | A | 5 | a0001c0001t0001g0245 a0001c0010t0001g0244 a0001c0010t0001g0309 others(2): Show |
5 | HG02258.hp1 HG02647.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.625-6380G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54336846 | |||||||
chr6:54336912 | G | A | 46 | a0001c0001t0001g0009 a0001c0001t0001g0075 a0001c0001t0001g0090 others(43): Show |
47 | HG00558.hp2 HG00735.hp1 HG01884.hp2 others(44): Show |
intron_variant | MODIFIER | c.625-6314G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54336912 | |||||||
chr6:54336931 | A | C | 1 | a0001c0001t0001g0216 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.625-6295A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54336931 | |||||||
chr6:54337015 | T | A | 1 | a0003c0003t0001g0243 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.625-6211T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54337015 | |||||||
chr6:54337027 | A | C | 8 | a0001c0001t0001g0007 a0001c0001t0001g0093 a0001c0001t0001g0094 others(5): Show |
9 | HG02258.hp1 HG02647.hp2 HG03471.hp2 others(6): Show |
intron_variant | MODIFIER | c.625-6199A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54337027 | |||||||
chr6:54337127 | AT | A | 15 | a0001c0001t0001g0011 a0001c0001t0001g0073 a0001c0001t0001g0122 others(12): Show |
16 | HG00099.hp2 HG00140.hp2 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.625-6090delT | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 54337127 | ||||||
chr6:54337159 | G | C | 1 | a0003c0003t0001g0049 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.625-6067G>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54337159 | |||||||
chr6:54337200 | TTAAAG | T | 3 | a0001c0001t0001g0007 a0001c0001t0001g0093 a0001c0001t0001g0094 |
4 | HG03491.hp1 HG03492.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.625-6022_625-6018d others(7): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 54337200 | ||||||
chr6:54337212 | T | C | 1 | a0010c0013t0002g0058 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.625-6014T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54337212 | |||||||
chr6:54337240 | A | G | 1 | a0002c0002t0001g0329 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.625-5986A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54337240 | |||||||
chr6:54337246 | A | AT | 16 | a0001c0001t0001g0090 a0001c0001t0001g0116 a0001c0001t0001g0162 others(13): Show |
16 | HG00735.hp2 HG01175.hp1 HG01978.hp2 others(13): Show |
intron_variant | MODIFIER | c.625-5956dupT | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 54337246 | ||||||
chr6:54337246 | A | ATTTT | 6 | a0001c0001t0001g0011 a0001c0001t0001g0210 a0001c0001t0001g0214 others(3): Show |
7 | HG02074.hp2 NA18941.hp1 NA18948.hp1 others(4): Show |
intron_variant | MODIFIER | c.625-5959_625-5956d others(6): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 54337246 | ||||||
chr6:54337246 | AT | A | 140 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0012 others(137): Show |
146 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.625-5956delT | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 54337246 | ||||||
chr6:54337246 | ATT | A | 30 | a0001c0001t0001g0122 a0001c0001t0001g0173 a0001c0001t0001g0174 others(27): Show |
30 | HG01069.hp2 HG01884.hp1 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.625-5957_625-5956d others(4): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 54337246 | ||||||
chr6:54337333 | A | T | 47 | a0001c0001t0001g0009 a0001c0001t0001g0075 a0001c0001t0001g0090 others(44): Show |
48 | HG00558.hp2 HG00735.hp1 HG01884.hp2 others(45): Show |
intron_variant | MODIFIER | c.625-5893A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54337333 | |||||||
chr6:54337421 | T | A | 1 | a0001c0001t0001g0215 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.625-5805T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54337421 | |||||||
chr6:54337459 | G | T | 1 | a0017c0018t0001g0242 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.625-5767G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54337459 | |||||||
chr6:54337490 | G | A | 1 | a0003c0003t0001g0064 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.625-5736G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54337490 | |||||||
chr6:54337496 | C | T | 29 | a0004c0004t0001g0002 a0004c0004t0001g0076 a0004c0004t0001g0170 others(26): Show |
31 | HG00140.hp1 HG00438.hp2 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.625-5730C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54337496 | |||||||
chr6:54337626 | A | G | 7 | a0007c0007t0001g0080 a0007c0007t0001g0081 a0007c0007t0001g0083 others(4): Show |
7 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.625-5600A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54337626 | |||||||
chr6:54337726 | G | A | 1 | a0014c0014t0003g0277 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.625-5500G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54337726 | |||||||
chr6:54337767 | A | G | 2 | a0001c0001t0001g0119 a0001c0001t0001g0137 |
2 | HG01496.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.625-5459A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54337767 | |||||||
chr6:54337954 | G | A | 1 | a0006c0006t0001g0247 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.625-5272G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54337954 | |||||||
chr6:54338056 | C | T | 4 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 others(1): Show |
4 | HG01884.hp2 HG02145.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.625-5170C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54338056 | |||||||
chr6:54338272 | A | G | 3 | a0001c0001t0001g0256 a0015c0015t0001g0279 a0015c0015t0001g0280 |
3 | HG03130.hp1 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.625-4954A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54338272 | |||||||
chr6:54338284 | A | T | 1 | a0002c0002t0001g0189 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.625-4942A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54338284 | |||||||
chr6:54338313 | A | G | 8 | a0001c0001t0001g0007 a0001c0001t0001g0093 a0001c0001t0001g0094 others(5): Show |
9 | HG02258.hp1 HG02647.hp2 HG03471.hp2 others(6): Show |
intron_variant | MODIFIER | c.625-4913A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54338313 | |||||||
chr6:54338391 | A | G | 1 | a0017c0018t0001g0087 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.625-4835A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54338391 | |||||||
chr6:54338473 | G | T | 3 | a0001c0001t0001g0256 a0015c0015t0001g0279 a0015c0015t0001g0280 |
3 | HG03130.hp1 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.625-4753G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54338473 | |||||||
chr6:54338487 | C | T | 75 | a0001c0001t0001g0207 a0001c0001t0001g0308 a0001c0001t0001g0310 others(72): Show |
77 | HG00642.hp2 HG01123.hp2 HG01884.hp1 others(74): Show |
intron_variant | MODIFIER | c.625-4739C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54338487 | |||||||
chr6:54338497 | G | A | 5 | a0006c0006t0002g0295 a0008c0008t0002g0072 a0008c0008t0002g0078 others(2): Show |
5 | HG01069.hp1 HG01243.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.625-4729G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54338497 | |||||||
chr6:54338598 | T | C | 128 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0014 others(125): Show |
135 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(132): Show |
intron_variant | MODIFIER | c.625-4628T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54338598 | |||||||
chr6:54338656 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.625-4570G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54338656 | |||||||
chr6:54338692 | C | T | 1 | a0005c0005t0001g0264 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.625-4534C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54338692 | |||||||
chr6:54338719 | C | CA | 38 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0014 others(35): Show |
41 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(38): Show |
intron_variant | MODIFIER | c.625-4483dupA | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 54338719 | ||||||
chr6:54338719 | CA | C | 31 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0101 others(28): Show |
31 | HG01993.hp1 HG02055.hp2 HG02080.hp2 others(28): Show |
intron_variant | MODIFIER | c.625-4483delA | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 54338719 | ||||||
chr6:54338719 | CAA | C | 73 | a0001c0010t0001g0244 a0001c0010t0001g0309 a0002c0002t0001g0008 others(70): Show |
77 | HG00642.hp2 HG01123.hp2 HG01516.hp1 others(74): Show |
intron_variant | MODIFIER | c.625-4484_625-4483d others(4): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 54338719 | ||||||
chr6:54338719 | CAAA | C | 31 | a0001c0001t0001g0310 a0002c0002t0001g0337 a0004c0004t0001g0076 others(28): Show |
31 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(28): Show |
intron_variant | MODIFIER | c.625-4485_625-4483d others(5): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 54338719 | ||||||
chr6:54338781 | T | C | 4 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0187 others(1): Show |
4 | NA18947.hp1 NA19002.hp1 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.625-4445T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54338781 | |||||||
chr6:54338800 | T | A | 1 | a0001c0001t0001g0147 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.625-4426T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54338800 | |||||||
chr6:54338839 | G | T | 1 | a0002c0002t0001g0328 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.625-4387G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54338839 | |||||||
chr6:54338842 | C | T | 11 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0292 others(8): Show |
11 | HG02280.hp2 HG02809.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.625-4384C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54338842 | |||||||
chr6:54338910 | A | G | 7 | a0001c0001t0001g0282 a0001c0001t0001g0285 a0001c0001t0001g0286 others(4): Show |
7 | HG01891.hp2 HG02257.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.625-4316A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54338910 | |||||||
chr6:54338939 | A | T | 2 | a0001c0010t0001g0244 a0001c0010t0001g0309 |
2 | HG02647.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.625-4287A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54338939 | |||||||
chr6:54338953 | C | T | 1 | a0017c0018t0001g0242 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.625-4273C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54338953 | |||||||
chr6:54338998 | A | G | 2 | a0003c0003t0001g0062 a0003c0003t0001g0063 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.625-4228A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54338998 | |||||||
chr6:54339140 | C | T | 5 | a0001c0001t0001g0089 a0001c0001t0001g0142 a0001c0001t0001g0156 others(2): Show |
5 | HG01070.hp2 HG01123.hp1 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.625-4086C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54339140 | |||||||
chr6:54339205 | A | T | 1 | a0001c0001t0001g0260 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.625-4021A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54339205 | |||||||
chr6:54339241 | T | C | 3 | a0001c0001t0001g0007 a0001c0001t0001g0093 a0001c0001t0001g0094 |
4 | HG03491.hp1 HG03492.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.625-3985T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54339241 | |||||||
chr6:54339327 | T | C | 9 | a0001c0001t0001g0011 a0001c0001t0001g0210 a0001c0001t0001g0212 others(6): Show |
10 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.625-3899T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54339327 | |||||||
chr6:54339549 | G | A | 2 | a0015c0015t0001g0279 a0015c0015t0001g0280 |
2 | HG03130.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.625-3677G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54339549 | |||||||
chr6:54339554 | G | C | 1 | a0001c0010t0001g0244 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.625-3672G>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54339554 | |||||||
chr6:54339564 | G | T | 3 | a0001c0001t0001g0007 a0001c0001t0001g0093 a0001c0001t0001g0094 |
4 | HG03491.hp1 HG03492.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.625-3662G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54339564 | |||||||
chr6:54339799 | C | T | 3 | a0001c0001t0001g0014 a0001c0001t0001g0296 a0003c0003t0001g0243 |
4 | HG00741.hp1 HG01167.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.625-3427C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54339799 | |||||||
chr6:54339851 | T | G | 1 | a0001c0001t0001g0283 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.625-3375T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54339851 | |||||||
chr6:54339903 | G | A | 53 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0014 others(50): Show |
58 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.625-3323G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54339903 | |||||||
chr6:54340222 | T | C | 2 | a0014c0014t0003g0276 a0014c0014t0003g0277 |
2 | HG02970.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.625-3004T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54340222 | |||||||
chr6:54340225 | T | C | 3 | a0001c0001t0001g0256 a0015c0015t0001g0279 a0015c0015t0001g0280 |
3 | HG03130.hp1 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.625-3001T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54340225 | |||||||
chr6:54340266 | G | C | 2 | a0001c0001t0001g0014 a0001c0001t0001g0296 |
3 | HG00741.hp1 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.625-2960G>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54340266 | |||||||
chr6:54340323 | T | A | 1 | a0017c0018t0001g0087 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.625-2903T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54340323 | |||||||
chr6:54340366 | G | A | 5 | a0001c0001t0001g0245 a0001c0010t0001g0244 a0001c0010t0001g0309 others(2): Show |
5 | HG02258.hp1 HG02647.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.625-2860G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54340366 | |||||||
chr6:54340395 | C | CA | 48 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0075 others(45): Show |
52 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.625-2817dupA | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 54340395 | ||||||
chr6:54340395 | CA | C | 6 | a0001c0001t0001g0014 a0001c0001t0001g0097 a0001c0001t0001g0296 others(3): Show |
7 | HG00741.hp1 HG01167.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.625-2817delA | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 54340395 | ||||||
chr6:54340529 | C | T | 3 | a0001c0001t0001g0256 a0015c0015t0001g0279 a0015c0015t0001g0280 |
3 | HG03130.hp1 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.625-2697C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54340529 | |||||||
chr6:54340553 | T | C | 30 | a0004c0004t0001g0002 a0004c0004t0001g0076 a0004c0004t0001g0170 others(27): Show |
32 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.625-2673T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54340553 | |||||||
chr6:54340696 | A | G | 1 | a0001c0001t0001g0113 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.625-2530A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54340696 | |||||||
chr6:54340761 | A | G | 5 | a0006c0006t0002g0295 a0008c0008t0002g0072 a0008c0008t0002g0078 others(2): Show |
5 | HG01069.hp1 HG01243.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.625-2465A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54340761 | |||||||
chr6:54340964 | C | T | 82 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0038 others(79): Show |
84 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.625-2262C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54340964 | |||||||
chr6:54341007 | A | G | 1 | a0001c0001t0001g0256 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.625-2219A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54341007 | |||||||
chr6:54341073 | A | G | 76 | a0001c0001t0001g0207 a0001c0001t0001g0308 a0001c0001t0001g0310 others(73): Show |
78 | HG00642.hp2 HG01123.hp2 HG01884.hp1 others(75): Show |
intron_variant | MODIFIER | c.625-2153A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54341073 | |||||||
chr6:54341148 | C | G | 1 | a0003c0003t0001g0055 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.625-2078C>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54341148 | |||||||
chr6:54341426 | T | C | 1 | a0003c0003t0001g0060 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.625-1800T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54341426 | |||||||
chr6:54341459 | T | A | 1 | a0003c0003t0001g0050 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.625-1767T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54341459 | |||||||
chr6:54341468 | C | A | 30 | a0004c0004t0001g0002 a0004c0004t0001g0076 a0004c0004t0001g0170 others(27): Show |
32 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.625-1758C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54341468 | |||||||
chr6:54341479 | C | A | 1 | a0003c0003t0001g0051 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.625-1747C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54341479 | |||||||
chr6:54341559 | T | TC | 30 | a0004c0004t0001g0002 a0004c0004t0001g0076 a0004c0004t0001g0170 others(27): Show |
32 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.625-1663dupC | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 54341559 | ||||||
chr6:54341779 | C | T | 30 | a0004c0004t0001g0002 a0004c0004t0001g0076 a0004c0004t0001g0170 others(27): Show |
32 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.625-1447C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54341779 | |||||||
chr6:54341789 | G | C | 2 | a0014c0014t0003g0276 a0014c0014t0003g0277 |
2 | HG02970.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.625-1437G>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54341789 | |||||||
chr6:54341791 | C | A | 9 | a0001c0001t0001g0011 a0001c0001t0001g0210 a0001c0001t0001g0212 others(6): Show |
10 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.625-1435C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54341791 | |||||||
chr6:54341851 | T | A | 3 | a0001c0001t0001g0014 a0001c0001t0001g0296 a0003c0003t0001g0243 |
4 | HG00741.hp1 HG01167.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.625-1375T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54341851 | |||||||
chr6:54341875 | T | C | 9 | a0001c0001t0001g0011 a0001c0001t0001g0210 a0001c0001t0001g0212 others(6): Show |
10 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.625-1351T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54341875 | |||||||
chr6:54341915 | A | G | 2 | a0001c0001t0001g0258 a0001c0001t0001g0261 |
2 | HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.625-1311A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54341915 | |||||||
chr6:54342033 | A | C | 1 | a0002c0002t0001g0298 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.625-1193A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54342033 | |||||||
chr6:54342044 | A | T | 4 | a0001c0001t0001g0077 a0001c0001t0001g0134 a0001c0001t0001g0135 others(1): Show |
4 | NA18959.hp2 NA19064.hp1 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.625-1182A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54342044 | |||||||
chr6:54342062 | G | GGT | 9 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0093 others(6): Show |
11 | HG00741.hp1 HG01167.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.625-1144_625-1143d others(4): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 54342062 | ||||||
chr6:54342062 | G | GGTGTGTG others(1): Show |
29 | a0004c0004t0001g0002 a0004c0004t0001g0076 a0004c0004t0001g0170 others(26): Show |
31 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(28): Show |
intron_variant | MODIFIER | c.625-1150_625-1143d others(10): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 54342062 | ||||||
chr6:54342062 | GGT | G | 11 | a0001c0001t0001g0011 a0001c0001t0001g0210 a0001c0001t0001g0212 others(8): Show |
12 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.625-1144_625-1143d others(4): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 54342062 | ||||||
chr6:54342066 | T | G | 1 | a0001c0001t0001g0245 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.625-1160T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54342066 | |||||||
chr6:54342082 | T | A | 26 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0120 others(23): Show |
26 | HG00558.hp2 HG00735.hp1 HG01934.hp2 others(23): Show |
intron_variant | MODIFIER | c.625-1144T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54342082 | |||||||
chr6:54342090 | C | T | 272 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(269): Show |
282 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.625-1136C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54342090 | |||||||
chr6:54342096 | C | T | 3 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0175 |
3 | HG02451.hp1 HG02886.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.625-1130C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54342096 | |||||||
chr6:54342132 | T | C | 5 | a0001c0001t0001g0245 a0001c0010t0001g0244 a0001c0010t0001g0309 others(2): Show |
5 | HG02258.hp1 HG02647.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.625-1094T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54342132 | |||||||
chr6:54342361 | C | CT | 17 | a0001c0001t0001g0007 a0001c0001t0001g0093 a0001c0001t0001g0094 others(14): Show |
18 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.625-850dupT | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 54342361 | ||||||
chr6:54342564 | T | A | 3 | a0001c0001t0001g0007 a0001c0001t0001g0093 a0001c0001t0001g0094 |
4 | HG03491.hp1 HG03492.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.625-662T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54342564 | |||||||
chr6:54342568 | C | G | 1 | a0002c0002t0001g0074 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.625-658C>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54342568 | |||||||
chr6:54342634 | C | T | 2 | a0014c0014t0003g0276 a0014c0014t0003g0277 |
2 | HG02970.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.625-592C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54342634 | |||||||
chr6:54342822 | T | G | 5 | a0001c0001t0001g0014 a0001c0001t0001g0296 a0003c0003t0001g0243 others(2): Show |
6 | HG00741.hp1 HG01167.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.625-404T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54342822 | |||||||
chr6:54342833 | T | A | 3 | a0001c0001t0001g0256 a0015c0015t0001g0279 a0015c0015t0001g0280 |
3 | HG03130.hp1 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.625-393T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54342833 | |||||||
chr6:54342840 | A | C | 17 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0093 others(14): Show |
19 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(16): Show |
intron_variant | MODIFIER | c.625-386A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54342840 | |||||||
chr6:54342906 | T | A | 1 | a0001c0001t0001g0212 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.625-320T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54342906 | |||||||
chr6:54342916 | C | A | 1 | a0005c0005t0001g0268 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.625-310C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54342916 | |||||||
chr6:54342930 | A | T | 3 | a0001c0001t0001g0007 a0001c0001t0001g0093 a0001c0001t0001g0094 |
4 | HG03491.hp1 HG03492.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.625-296A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54342930 | |||||||
chr6:54342947 | A | C | 9 | a0001c0001t0001g0011 a0001c0001t0001g0210 a0001c0001t0001g0212 others(6): Show |
10 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.625-279A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54342947 | |||||||
chr6:54342969 | T | C | 9 | a0001c0001t0001g0011 a0001c0001t0001g0210 a0001c0001t0001g0212 others(6): Show |
10 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.625-257T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54342969 | |||||||
chr6:54343001 | T | C | 76 | a0001c0001t0001g0207 a0001c0001t0001g0308 a0001c0001t0001g0310 others(73): Show |
78 | HG00642.hp2 HG01123.hp2 HG01884.hp1 others(75): Show |
intron_variant | MODIFIER | c.625-225T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54343001 | |||||||
chr6:54343096 | T | C | 2 | a0001c0010t0001g0244 a0001c0010t0001g0309 |
2 | HG02647.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.625-130T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54343096 | |||||||
chr6:54343113 | T | C | 3 | a0001c0001t0001g0007 a0001c0001t0001g0093 a0001c0001t0001g0094 |
4 | HG03491.hp1 HG03492.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.625-113T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54343113 | |||||||
chr6:54343161 | G | A | 1 | a0001c0001t0001g0126 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.625-65G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 4/10 | chr6 | 54343161 | |||||||
chr6:54343374 | C | T | 3 | a0001c0001t0001g0014 a0001c0001t0001g0296 a0003c0003t0001g0243 |
4 | HG00741.hp1 HG01167.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.748+25C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54343374 | |||||||
chr6:54343442 | T | C | 75 | a0001c0001t0001g0207 a0001c0001t0001g0308 a0001c0001t0001g0310 others(72): Show |
77 | HG00642.hp2 HG01123.hp2 HG01884.hp1 others(74): Show |
intron_variant | MODIFIER | c.748+93T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54343442 | |||||||
chr6:54343483 | G | T | 2 | a0016c0017t0001g0274 a0016c0017t0001g0275 |
2 | HG03225.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.748+134G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54343483 | |||||||
chr6:54343495 | C | A | 30 | a0004c0004t0001g0002 a0004c0004t0001g0076 a0004c0004t0001g0170 others(27): Show |
32 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.748+146C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54343495 | |||||||
chr6:54343527 | C | A | 7 | a0007c0007t0001g0080 a0007c0007t0001g0081 a0007c0007t0001g0083 others(4): Show |
7 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.748+178C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54343527 | |||||||
chr6:54343533 | G | GT | 42 | a0001c0001t0001g0007 a0001c0001t0001g0093 a0001c0001t0001g0094 others(39): Show |
45 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.748+196dupT | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr6 | 54343533 | ||||||
chr6:54343533 | G | GTT | 6 | a0001c0001t0001g0014 a0001c0001t0001g0245 a0001c0001t0001g0296 others(3): Show |
7 | HG00741.hp1 HG01167.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.748+195_748+196dup others(2): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr6 | 54343533 | ||||||
chr6:54343533 | GT | G | 68 | a0002c0002t0001g0008 a0002c0002t0001g0013 a0002c0002t0001g0074 others(65): Show |
70 | HG00099.hp1 HG00642.hp2 HG01123.hp2 others(67): Show |
intron_variant | MODIFIER | c.748+196delT | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr6 | 54343533 | ||||||
chr6:54343555 | T | C | 76 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0038 others(73): Show |
78 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(75): Show |
intron_variant | MODIFIER | c.748+206T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54343555 | |||||||
chr6:54343575 | G | A | 3 | a0001c0001t0001g0007 a0001c0001t0001g0093 a0001c0001t0001g0094 |
4 | HG03491.hp1 HG03492.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.748+226G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54343575 | |||||||
chr6:54343620 | A | G | 2 | a0002c0002t0001g0238 a0002c0002t0001g0355 |
2 | NA18962.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.748+271A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54343620 | |||||||
chr6:54343632 | G | A | 5 | a0001c0001t0001g0014 a0001c0001t0001g0296 a0003c0003t0001g0243 others(2): Show |
6 | HG00741.hp1 HG01167.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.748+283G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54343632 | |||||||
chr6:54343657 | G | T | 1 | a0001c0001t0001g0186 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.748+308G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54343657 | |||||||
chr6:54343673 | A | T | 1 | a0002c0002t0001g0324 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.748+324A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54343673 | |||||||
chr6:54343712 | C | T | 3 | a0001c0001t0001g0256 a0015c0015t0001g0279 a0015c0015t0001g0280 |
3 | HG03130.hp1 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.748+363C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54343712 | |||||||
chr6:54343731 | C | T | 1 | a0003c0003t0001g0066 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.748+382C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54343731 | |||||||
chr6:54343740 | T | C | 54 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0014 others(51): Show |
59 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.748+391T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54343740 | |||||||
chr6:54343751 | AAC | A | 75 | a0001c0001t0001g0207 a0001c0001t0001g0308 a0001c0001t0001g0310 others(72): Show |
77 | HG00642.hp2 HG01123.hp2 HG01884.hp1 others(74): Show |
intron_variant | MODIFIER | c.748+404_748+405del others(2): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr6 | 54343751 | ||||||
chr6:54343793 | C | A | 3 | a0001c0001t0001g0256 a0015c0015t0001g0279 a0015c0015t0001g0280 |
3 | HG03130.hp1 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.748+444C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54343793 | |||||||
chr6:54343843 | G | A | 3 | a0001c0001t0001g0007 a0001c0001t0001g0093 a0001c0001t0001g0094 |
4 | HG03491.hp1 HG03492.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.748+494G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54343843 | |||||||
chr6:54344433 | T | C | 1 | a0001c0001t0001g0138 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.748+1084T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54344433 | |||||||
chr6:54344646 | T | C | 9 | a0001c0001t0001g0011 a0001c0001t0001g0210 a0001c0001t0001g0212 others(6): Show |
10 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.748+1297T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54344646 | |||||||
chr6:54344677 | G | A | 3 | a0001c0001t0001g0256 a0015c0015t0001g0279 a0015c0015t0001g0280 |
3 | HG03130.hp1 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.748+1328G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54344677 | |||||||
chr6:54344806 | G | T | 18 | a0001c0001t0001g0092 a0001c0001t0001g0177 a0001c0001t0001g0281 others(15): Show |
18 | HG00099.hp1 HG01261.hp1 HG01358.hp1 others(15): Show |
intron_variant | MODIFIER | c.748+1457G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54344806 | |||||||
chr6:54344915 | G | A | 2 | a0014c0014t0003g0276 a0014c0014t0003g0277 |
2 | HG02970.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.748+1566G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54344915 | |||||||
chr6:54344931 | T | TA | 3 | a0001c0001t0001g0007 a0001c0001t0001g0093 a0001c0001t0001g0094 |
4 | HG03491.hp1 HG03492.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.748+1583dupA | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr6 | 54344931 | ||||||
chr6:54345030 | A | G | 1 | a0017c0018t0001g0242 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.748+1681A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54345030 | |||||||
chr6:54345093 | A | G | 1 | a0001c0001t0001g0297 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.748+1744A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54345093 | |||||||
chr6:54345343 | C | T | 55 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0014 others(52): Show |
60 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.748+1994C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54345343 | |||||||
chr6:54345418 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.749-1949C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54345418 | |||||||
chr6:54345517 | T | C | 3 | a0001c0001t0001g0007 a0001c0001t0001g0093 a0001c0001t0001g0094 |
4 | HG03491.hp1 HG03492.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.749-1850T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54345517 | |||||||
chr6:54345527 | A | G | 9 | a0001c0001t0001g0011 a0001c0001t0001g0210 a0001c0001t0001g0212 others(6): Show |
10 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.749-1840A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54345527 | |||||||
chr6:54345634 | C | T | 212 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0011 others(209): Show |
221 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.749-1733C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54345634 | |||||||
chr6:54345712 | G | C | 3 | a0001c0001t0001g0256 a0015c0015t0001g0279 a0015c0015t0001g0280 |
3 | HG03130.hp1 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.749-1655G>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54345712 | |||||||
chr6:54345727 | G | A | 3 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0175 |
3 | HG02451.hp1 HG02886.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.749-1640G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54345727 | |||||||
chr6:54345940 | A | G | 7 | a0007c0007t0001g0080 a0007c0007t0001g0081 a0007c0007t0001g0083 others(4): Show |
7 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.749-1427A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54345940 | |||||||
chr6:54345945 | AT | A | 8 | a0001c0001t0001g0007 a0001c0001t0001g0093 a0001c0001t0001g0094 others(5): Show |
9 | HG02258.hp1 HG02647.hp2 HG03471.hp2 others(6): Show |
intron_variant | MODIFIER | c.749-1421delT | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54345945 | |||||||
chr6:54346012 | G | A | 1 | a0001c0001t0001g0256 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.749-1355G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54346012 | |||||||
chr6:54346208 | A | G | 20 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0093 others(17): Show |
22 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(19): Show |
intron_variant | MODIFIER | c.749-1159A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54346208 | |||||||
chr6:54346259 | G | A | 2 | a0004c0004t0001g0196 a0004c0004t0001g0197 |
2 | HG01081.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.749-1108G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54346259 | |||||||
chr6:54346528 | GTA | G | 3 | a0001c0001t0001g0007 a0001c0001t0001g0093 a0001c0001t0001g0094 |
4 | HG03491.hp1 HG03492.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.749-830_749-829del others(2): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr6 | 54346528 | ||||||
chr6:54346565 | A | G | 2 | a0001c0001t0001g0014 a0001c0001t0001g0296 |
3 | HG00741.hp1 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.749-802A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54346565 | |||||||
chr6:54346576 | T | C | 12 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0181 others(9): Show |
12 | HG00558.hp2 NA18947.hp1 NA18969.hp2 others(9): Show |
intron_variant | MODIFIER | c.749-791T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54346576 | |||||||
chr6:54346576 | T | G | 1 | a0001c0001t0001g0316 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.749-791T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54346576 | |||||||
chr6:54346607 | C | T | 3 | a0001c0001t0001g0256 a0015c0015t0001g0279 a0015c0015t0001g0280 |
3 | HG03130.hp1 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.749-760C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54346607 | |||||||
chr6:54346610 | CAGTT | C | 4 | a0001c0001t0001g0077 a0001c0001t0001g0134 a0001c0001t0001g0135 others(1): Show |
4 | NA18959.hp2 NA19064.hp1 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.749-753_749-750del others(4): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr6 | 54346610 | ||||||
chr6:54346652 | T | C | 8 | a0001c0001t0001g0007 a0001c0001t0001g0093 a0001c0001t0001g0094 others(5): Show |
9 | HG02258.hp1 HG02647.hp2 HG03471.hp2 others(6): Show |
intron_variant | MODIFIER | c.749-715T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54346652 | |||||||
chr6:54346732 | T | A | 3 | a0001c0001t0001g0256 a0015c0015t0001g0279 a0015c0015t0001g0280 |
3 | HG03130.hp1 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.749-635T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54346732 | |||||||
chr6:54346781 | A | T | 9 | a0001c0001t0001g0011 a0001c0001t0001g0210 a0001c0001t0001g0212 others(6): Show |
10 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.749-586A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54346781 | |||||||
chr6:54346820 | C | A | 46 | a0001c0001t0001g0009 a0001c0001t0001g0075 a0001c0001t0001g0090 others(43): Show |
47 | HG00558.hp2 HG00735.hp1 HG01884.hp2 others(44): Show |
intron_variant | MODIFIER | c.749-547C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54346820 | |||||||
chr6:54347325 | C | T | 1 | a0001c0001t0001g0289 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.749-42C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54347325 | |||||||
chr6:54347326 | G | A | 1 | a0001c0001t0001g0253 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.749-41G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 5/10 | chr6 | 54347326 | |||||||
chr6:54347586 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.899+69T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 6/10 | chr6 | 54347586 | |||||||
chr6:54347591 | C | T | 9 | a0001c0001t0001g0011 a0001c0001t0001g0210 a0001c0001t0001g0212 others(6): Show |
10 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.899+74C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 6/10 | chr6 | 54347591 | |||||||
chr6:54347774 | G | A | 1 | a0017c0018t0001g0242 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.899+257G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 6/10 | chr6 | 54347774 | |||||||
chr6:54347816 | A | C | 1 | a0001c0001t0001g0010 | 2 | NA18986.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.899+299A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 6/10 | chr6 | 54347816 | |||||||
chr6:54347972 | C | A | 1 | a0017c0018t0001g0087 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.899+455C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 6/10 | chr6 | 54347972 | |||||||
chr6:54348088 | G | T | 3 | a0001c0001t0001g0256 a0015c0015t0001g0279 a0015c0015t0001g0280 |
3 | HG03130.hp1 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.899+571G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 6/10 | chr6 | 54348088 | |||||||
chr6:54348166 | C | T | 82 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0038 others(79): Show |
84 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.899+649C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 6/10 | chr6 | 54348166 | |||||||
chr6:54348207 | G | A | 17 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0093 others(14): Show |
19 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(16): Show |
intron_variant | MODIFIER | c.899+690G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 6/10 | chr6 | 54348207 | |||||||
chr6:54348215 | T | C | 1 | a0001c0001t0001g0144 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.899+698T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 6/10 | chr6 | 54348215 | |||||||
chr6:54348220 | T | G | 132 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0014 others(129): Show |
139 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.899+703T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 6/10 | chr6 | 54348220 | |||||||
chr6:54348269 | C | T | 66 | a0001c0001t0001g0207 a0002c0002t0001g0008 a0002c0002t0001g0013 others(63): Show |
68 | HG00642.hp2 HG01123.hp2 HG02056.hp2 others(65): Show |
intron_variant | MODIFIER | c.899+752C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 6/10 | chr6 | 54348269 | |||||||
chr6:54348398 | A | C | 3 | a0001c0001t0001g0256 a0015c0015t0001g0279 a0015c0015t0001g0280 |
3 | HG03130.hp1 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.899+881A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 6/10 | chr6 | 54348398 | |||||||
chr6:54348739 | CATATGAA others(5): Show |
C | 1 | a0002c0002t0001g0306 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.900-975_900-964del others(12): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 54348739 | ||||||
chr6:54348816 | T | C | 2 | a0002c0002t0001g0117 a0002c0002t0001g0189 |
2 | HG02738.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.900-900T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 6/10 | chr6 | 54348816 | |||||||
chr6:54348996 | T | G | 3 | a0001c0001t0001g0256 a0015c0015t0001g0279 a0015c0015t0001g0280 |
3 | HG03130.hp1 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.900-720T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 6/10 | chr6 | 54348996 | |||||||
chr6:54349004 | T | C | 76 | a0001c0001t0001g0207 a0001c0001t0001g0308 a0001c0001t0001g0310 others(73): Show |
78 | HG00642.hp2 HG01123.hp2 HG01884.hp1 others(75): Show |
intron_variant | MODIFIER | c.900-712T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 6/10 | chr6 | 54349004 | |||||||
chr6:54349087 | T | C | 81 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0038 others(78): Show |
83 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.900-629T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 6/10 | chr6 | 54349087 | |||||||
chr6:54349106 | C | A | 2 | a0001c0001t0001g0014 a0001c0001t0001g0296 |
3 | HG00741.hp1 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.900-610C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 6/10 | chr6 | 54349106 | |||||||
chr6:54349107 | A | T | 2 | a0001c0001t0001g0014 a0001c0001t0001g0296 |
3 | HG00741.hp1 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.900-609A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 6/10 | chr6 | 54349107 | |||||||
chr6:54349240 | A | T | 3 | a0002c0002t0001g0251 a0002c0002t0001g0252 a0002c0002t0001g0284 |
3 | HG02630.hp2 HG03471.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.900-476A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 6/10 | chr6 | 54349240 | |||||||
chr6:54349335 | T | C | 76 | a0001c0001t0001g0207 a0001c0001t0001g0308 a0001c0001t0001g0310 others(73): Show |
78 | HG00642.hp2 HG01123.hp2 HG01884.hp1 others(75): Show |
intron_variant | MODIFIER | c.900-381T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 6/10 | chr6 | 54349335 | |||||||
chr6:54349394 | G | A | 1 | a0017c0018t0001g0242 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.900-322G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 6/10 | chr6 | 54349394 | |||||||
chr6:54349395 | G | T | 2 | a0014c0014t0003g0276 a0014c0014t0003g0277 |
2 | HG02970.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.900-321G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 6/10 | chr6 | 54349395 | |||||||
chr6:54349672 | A | T | 1 | a0002c0002t0001g0301 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.900-44A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 6/10 | chr6 | 54349672 | |||||||
chr6:54349674 | T | A | 1 | a0002c0002t0001g0321 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.900-42T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 6/10 | chr6 | 54349674 | |||||||
chr6:54349677 | C | T | 3 | a0001c0001t0001g0007 a0001c0001t0001g0093 a0001c0001t0001g0094 |
4 | HG03491.hp1 HG03492.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.900-39C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 6/10 | chr6 | 54349677 | |||||||
chr6:54349685 | T | A | 3 | a0001c0001t0001g0014 a0001c0001t0001g0296 a0003c0003t0001g0243 |
4 | HG00741.hp1 HG01167.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.900-31T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 6/10 | chr6 | 54349685 | |||||||
chr6:54349694 | C | T | 3 | a0001c0001t0001g0256 a0015c0015t0001g0279 a0015c0015t0001g0280 |
3 | HG03130.hp1 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.900-22C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 6/10 | chr6 | 54349694 | |||||||
chr6:54349981 | A | T | 53 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0014 others(50): Show |
58 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.1080+85A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 7/10 | chr6 | 54349981 | |||||||
chr6:54350086 | G | A | 3 | a0001c0001t0001g0007 a0001c0001t0001g0093 a0001c0001t0001g0094 |
4 | HG03491.hp1 HG03492.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.1080+190G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 7/10 | chr6 | 54350086 | |||||||
chr6:54350130 | A | C | 8 | a0001c0001t0001g0007 a0001c0001t0001g0093 a0001c0001t0001g0094 others(5): Show |
9 | HG02258.hp1 HG02647.hp2 HG03471.hp2 others(6): Show |
intron_variant | MODIFIER | c.1080+234A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 7/10 | chr6 | 54350130 | |||||||
chr6:54350162 | A | G | 13 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0258 others(10): Show |
13 | HG02280.hp2 HG02809.hp1 HG02818.hp1 others(10): Show |
intron_variant | MODIFIER | c.1080+266A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 7/10 | chr6 | 54350162 | |||||||
chr6:54350218 | C | CT | 82 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0038 others(79): Show |
84 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.1080+328dupT | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr6 | 54350218 | ||||||
chr6:54350366 | T | C | 3 | a0001c0001t0001g0256 a0015c0015t0001g0279 a0015c0015t0001g0280 |
3 | HG03130.hp1 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1080+470T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 7/10 | chr6 | 54350366 | |||||||
chr6:54350391 | A | T | 1 | a0001c0001t0001g0113 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1080+495A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 7/10 | chr6 | 54350391 | |||||||
chr6:54350420 | T | A | 2 | a0001c0001t0001g0285 a0001c0001t0001g0286 |
2 | HG02257.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1080+524T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 7/10 | chr6 | 54350420 | |||||||
chr6:54350451 | A | G | 2 | a0001c0001t0001g0014 a0001c0001t0001g0296 |
3 | HG00741.hp1 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1080+555A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 7/10 | chr6 | 54350451 | |||||||
chr6:54350488 | A | G | 2 | a0001c0010t0001g0244 a0001c0010t0001g0309 |
2 | HG02647.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1080+592A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 7/10 | chr6 | 54350488 | |||||||
chr6:54350530 | C | T | 3 | a0001c0001t0001g0014 a0001c0001t0001g0296 a0003c0003t0001g0243 |
4 | HG00741.hp1 HG01167.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.1080+634C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 7/10 | chr6 | 54350530 | |||||||
chr6:54350645 | C | A | 1 | a0001c0001t0001g0257 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1081-707C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 7/10 | chr6 | 54350645 | |||||||
chr6:54350645 | C | G | 3 | a0001c0001t0001g0256 a0015c0015t0001g0279 a0015c0015t0001g0280 |
3 | HG03130.hp1 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1081-707C>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 7/10 | chr6 | 54350645 | |||||||
chr6:54350705 | T | C | 4 | a0001c0001t0001g0245 a0001c0010t0001g0244 a0001c0010t0001g0309 others(1): Show |
4 | HG02258.hp1 HG02647.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1081-647T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 7/10 | chr6 | 54350705 | |||||||
chr6:54350743 | T | C | 1 | a0020c0019t0001g0211 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1081-609T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 7/10 | chr6 | 54350743 | |||||||
chr6:54350758 | C | T | 7 | a0007c0007t0001g0080 a0007c0007t0001g0081 a0007c0007t0001g0083 others(4): Show |
7 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.1081-594C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 7/10 | chr6 | 54350758 | |||||||
chr6:54350771 | G | A | 2 | a0004c0004t0001g0195 a0004c0004t0001g0198 |
2 | HG00438.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.1081-581G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 7/10 | chr6 | 54350771 | |||||||
chr6:54350912 | T | C | 213 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0011 others(210): Show |
222 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.1081-440T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 7/10 | chr6 | 54350912 | |||||||
chr6:54350997 | A | G | 9 | a0001c0001t0001g0011 a0001c0001t0001g0210 a0001c0001t0001g0212 others(6): Show |
10 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1081-355A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 7/10 | chr6 | 54350997 | |||||||
chr6:54351075 | C | T | 1 | a0001c0001t0001g0207 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1081-277C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 7/10 | chr6 | 54351075 | |||||||
chr6:54351129 | A | G | 1 | a0001c0001t0001g0245 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1081-223A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 7/10 | chr6 | 54351129 | |||||||
chr6:54351139 | G | C | 53 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0014 others(50): Show |
58 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.1081-213G>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 7/10 | chr6 | 54351139 | |||||||
chr6:54351418 | G | T | 2 | a0001c0001t0001g0012 a0001c0001t0001g0224 |
3 | NA19010.hp2 NA19059.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.1126+21G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 8/10 | chr6 | 54351418 | |||||||
chr6:54351472 | G | A | 1 | a0001c0001t0001g0257 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1126+75G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 8/10 | chr6 | 54351472 | |||||||
chr6:54351513 | C | T | 1 | a0001c0001t0001g0156 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1126+116C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 8/10 | chr6 | 54351513 | |||||||
chr6:54351607 | C | G | 3 | a0001c0001t0001g0014 a0001c0001t0001g0296 a0003c0003t0001g0243 |
4 | HG00741.hp1 HG01167.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.1126+210C>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 8/10 | chr6 | 54351607 | |||||||
chr6:54351772 | A | G | 1 | a0001c0001t0001g0297 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1126+375A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 8/10 | chr6 | 54351772 | |||||||
chr6:54351810 | G | A | 2 | a0008c0008t0002g0078 a0008c0008t0002g0079 |
2 | HG01069.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.1126+413G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 8/10 | chr6 | 54351810 | |||||||
chr6:54352049 | A | G | 1 | a0012c0009t0001g0209 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1126+652A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 8/10 | chr6 | 54352049 | |||||||
chr6:54352062 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1126+665T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 8/10 | chr6 | 54352062 | |||||||
chr6:54352064 | T | A | 55 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0014 others(52): Show |
60 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.1126+667T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 8/10 | chr6 | 54352064 | |||||||
chr6:54352111 | G | A | 9 | a0001c0001t0001g0011 a0001c0001t0001g0210 a0001c0001t0001g0212 others(6): Show |
10 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1126+714G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 8/10 | chr6 | 54352111 | |||||||
chr6:54352169 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1126+772C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 8/10 | chr6 | 54352169 | |||||||
chr6:54352291 | G | A | 3 | a0001c0001t0001g0014 a0001c0001t0001g0296 a0003c0003t0001g0243 |
4 | HG00741.hp1 HG01167.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.1126+894G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 8/10 | chr6 | 54352291 | |||||||
chr6:54352635 | A | C | 2 | a0001c0001t0001g0119 a0001c0001t0001g0137 |
2 | HG01496.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.1126+1238A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 8/10 | chr6 | 54352635 | |||||||
chr6:54352720 | G | GT | 6 | a0001c0001t0001g0007 a0001c0001t0001g0093 a0001c0001t0001g0094 others(3): Show |
7 | HG02258.hp1 HG03471.hp2 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.1126+1333dupT | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr6 | 54352720 | ||||||
chr6:54352780 | A | G | 9 | a0001c0001t0001g0011 a0001c0001t0001g0210 a0001c0001t0001g0212 others(6): Show |
10 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1126+1383A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 8/10 | chr6 | 54352780 | |||||||
chr6:54352949 | G | A | 3 | a0001c0001t0001g0256 a0015c0015t0001g0279 a0015c0015t0001g0280 |
3 | HG03130.hp1 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1126+1552G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 8/10 | chr6 | 54352949 | |||||||
chr6:54352989 | C | T | 2 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
2 | HG03710.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1127-1524C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 8/10 | chr6 | 54352989 | |||||||
chr6:54353014 | G | A | 3 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 |
3 | NA18959.hp2 NA19064.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.1127-1499G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 8/10 | chr6 | 54353014 | |||||||
chr6:54353170 | C | T | 1 | a0001c0001t0001g0207 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1127-1343C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 8/10 | chr6 | 54353170 | |||||||
chr6:54353246 | A | T | 1 | a0001c0001t0001g0161 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1127-1267A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 8/10 | chr6 | 54353246 | |||||||
chr6:54353373 | C | T | 1 | a0006c0006t0001g0125 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1127-1140C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 8/10 | chr6 | 54353373 | |||||||
chr6:54353526 | A | C | 9 | a0001c0001t0001g0011 a0001c0001t0001g0210 a0001c0001t0001g0212 others(6): Show |
10 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1127-987A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 8/10 | chr6 | 54353526 | |||||||
chr6:54353602 | G | T | 2 | a0001c0001t0001g0119 a0001c0001t0001g0137 |
2 | HG01496.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.1127-911G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 8/10 | chr6 | 54353602 | |||||||
chr6:54353634 | A | G | 9 | a0001c0001t0001g0011 a0001c0001t0001g0210 a0001c0001t0001g0212 others(6): Show |
10 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1127-879A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 8/10 | chr6 | 54353634 | |||||||
chr6:54353673 | T | C | 1 | a0017c0018t0001g0087 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1127-840T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 8/10 | chr6 | 54353673 | |||||||
chr6:54353755 | T | C | 1 | a0001c0001t0001g0207 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1127-758T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 8/10 | chr6 | 54353755 | |||||||
chr6:54353776 | G | A | 1 | a0001c0001t0001g0194 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1127-737G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 8/10 | chr6 | 54353776 | |||||||
chr6:54353863 | C | G | 1 | a0004c0021t0004g0201 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1127-650C>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 8/10 | chr6 | 54353863 | |||||||
chr6:54353877 | G | C | 7 | a0003c0003t0001g0018 a0003c0003t0001g0019 a0003c0003t0001g0020 others(4): Show |
7 | HG00621.hp1 HG02056.hp1 NA18944.hp2 others(4): Show |
intron_variant | MODIFIER | c.1127-636G>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 8/10 | chr6 | 54353877 | |||||||
chr6:54354111 | A | C | 1 | a0010c0013t0001g0303 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1127-402A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 8/10 | chr6 | 54354111 | |||||||
chr6:54354117 | A | G | 30 | a0004c0004t0001g0002 a0004c0004t0001g0076 a0004c0004t0001g0170 others(27): Show |
32 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.1127-396A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 8/10 | chr6 | 54354117 | |||||||
chr6:54354270 | G | A | 5 | a0006c0006t0002g0295 a0008c0008t0002g0072 a0008c0008t0002g0078 others(2): Show |
5 | HG01069.hp1 HG01243.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1127-243G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 8/10 | chr6 | 54354270 | |||||||
chr6:54354385 | A | G | 1 | a0001c0001t0001g0128 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1127-128A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 8/10 | chr6 | 54354385 | |||||||
chr6:54354492 | T | C | 30 | a0004c0004t0001g0002 a0004c0004t0001g0076 a0004c0004t0001g0170 others(27): Show |
32 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.1127-21T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 8/10 | chr6 | 54354492 | |||||||
chr6:54354716 | A | C | 1 | a0007c0007t0001g0085 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1250+80A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54354716 | |||||||
chr6:54354757 | T | C | 9 | a0001c0001t0001g0011 a0001c0001t0001g0210 a0001c0001t0001g0212 others(6): Show |
10 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1250+121T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54354757 | |||||||
chr6:54354823 | G | T | 4 | a0003c0003t0001g0064 a0003c0003t0001g0065 a0003c0003t0001g0066 others(1): Show |
4 | HG02809.hp1 HG02818.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1250+187G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54354823 | |||||||
chr6:54354958 | G | A | 10 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0093 others(7): Show |
12 | HG00741.hp1 HG01167.hp2 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.1250+322G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54354958 | |||||||
chr6:54354972 | G | T | 2 | a0014c0014t0003g0276 a0014c0014t0003g0277 |
2 | HG02970.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1250+336G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54354972 | |||||||
chr6:54355263 | T | C | 1 | a0003c0003t0001g0243 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1250+627T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54355263 | |||||||
chr6:54355352 | A | C | 1 | a0001c0001t0001g0135 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1250+716A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54355352 | |||||||
chr6:54355385 | A | G | 11 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0292 others(8): Show |
11 | HG02280.hp2 HG02809.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1250+749A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54355385 | |||||||
chr6:54355397 | T | G | 76 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0038 others(73): Show |
78 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(75): Show |
intron_variant | MODIFIER | c.1250+761T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54355397 | |||||||
chr6:54355398 | G | T | 29 | a0002c0002t0001g0008 a0002c0002t0001g0095 a0002c0002t0001g0098 others(26): Show |
30 | HG02056.hp2 HG03831.hp1 NA18612.hp2 others(27): Show |
intron_variant | MODIFIER | c.1250+762G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54355398 | |||||||
chr6:54355445 | C | T | 63 | a0002c0002t0001g0008 a0002c0002t0001g0013 a0002c0002t0001g0074 others(60): Show |
65 | HG00642.hp2 HG01123.hp2 HG02056.hp2 others(62): Show |
intron_variant | MODIFIER | c.1250+809C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54355445 | |||||||
chr6:54355448 | A | G | 2 | a0001c0001t0001g0132 a0001c0001t0001g0133 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1250+812A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54355448 | |||||||
chr6:54355466 | T | G | 2 | a0001c0001t0001g0132 a0001c0001t0001g0133 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1250+830T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54355466 | |||||||
chr6:54355500 | C | G | 1 | a0001c0001t0001g0010 | 2 | NA18986.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.1250+864C>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54355500 | |||||||
chr6:54355522 | G | A | 8 | a0001c0001t0001g0257 a0007c0007t0001g0080 a0007c0007t0001g0081 others(5): Show |
8 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.1250+886G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54355522 | |||||||
chr6:54355597 | A | G | 30 | a0004c0004t0001g0002 a0004c0004t0001g0076 a0004c0004t0001g0170 others(27): Show |
32 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.1250+961A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54355597 | |||||||
chr6:54355617 | G | A | 3 | a0001c0001t0001g0007 a0001c0001t0001g0093 a0001c0001t0001g0094 |
4 | HG03491.hp1 HG03492.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.1250+981G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54355617 | |||||||
chr6:54355714 | C | CGT | 14 | a0001c0001t0001g0110 a0001c0001t0001g0119 a0001c0001t0001g0147 others(11): Show |
14 | HG01496.hp1 HG01515.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.1250+1109_1250+111 others(6): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54355714 | ||||||
chr6:54355714 | C | CGTGT | 26 | a0001c0001t0001g0088 a0001c0001t0001g0128 a0001c0001t0001g0134 others(23): Show |
26 | HG02109.hp1 HG02109.hp2 HG02280.hp2 others(23): Show |
intron_variant | MODIFIER | c.1250+1107_1250+111 others(8): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54355714 | ||||||
chr6:54355714 | C | CGTGTGT | 57 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0073 others(54): Show |
59 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.1250+1105_1250+111 others(10): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54355714 | ||||||
chr6:54355714 | C | CGTGTGTG others(1): Show |
11 | a0001c0001t0001g0038 a0001c0001t0001g0097 a0001c0001t0001g0105 others(8): Show |
11 | HG01261.hp2 HG01934.hp1 HG02683.hp2 others(8): Show |
intron_variant | MODIFIER | c.1250+1103_1250+111 others(12): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54355714 | ||||||
chr6:54355714 | C | CGTGTGTG others(3): Show |
7 | a0001c0001t0001g0011 a0001c0001t0001g0210 a0001c0001t0001g0212 others(4): Show |
8 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(5): Show |
intron_variant | MODIFIER | c.1250+1101_1250+111 others(14): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54355714 | ||||||
chr6:54355714 | CGT | C | 87 | a0001c0001t0001g0007 a0001c0001t0001g0113 a0001c0001t0001g0186 others(84): Show |
90 | HG00438.hp2 HG00642.hp2 HG01069.hp1 others(87): Show |
intron_variant | MODIFIER | c.1250+1109_1250+111 others(6): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54355714 | ||||||
chr6:54355714 | CGTGT | C | 5 | a0001c0010t0001g0244 a0001c0010t0001g0309 a0002c0002t0001g0259 others(2): Show |
5 | HG02647.hp2 HG02970.hp1 HG04115.hp2 others(2): Show |
intron_variant | MODIFIER | c.1250+1107_1250+111 others(8): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54355714 | ||||||
chr6:54355714 | CGTGTGTG others(5): Show |
C | 1 | a0002c0002t0001g0189 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1250+1099_1250+111 others(16): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54355714 | ||||||
chr6:54355764 | C | T | 11 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0292 others(8): Show |
11 | HG02280.hp2 HG02809.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1250+1128C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54355764 | |||||||
chr6:54355765 | C | T | 11 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0292 others(8): Show |
11 | HG02280.hp2 HG02809.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1250+1129C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54355765 | |||||||
chr6:54355897 | T | C | 3 | a0001c0001t0001g0007 a0001c0001t0001g0093 a0001c0001t0001g0094 |
4 | HG03491.hp1 HG03492.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.1250+1261T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54355897 | |||||||
chr6:54355915 | T | C | 9 | a0001c0001t0001g0011 a0001c0001t0001g0210 a0001c0001t0001g0212 others(6): Show |
10 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1250+1279T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54355915 | |||||||
chr6:54355937 | T | G | 2 | a0014c0014t0003g0276 a0014c0014t0003g0277 |
2 | HG02970.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1250+1301T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54355937 | |||||||
chr6:54356261 | G | T | 5 | a0006c0006t0002g0295 a0008c0008t0002g0072 a0008c0008t0002g0078 others(2): Show |
5 | HG01069.hp1 HG01243.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1250+1625G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54356261 | |||||||
chr6:54356306 | G | A | 1 | a0001c0001t0001g0126 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1250+1670G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54356306 | |||||||
chr6:54356307 | A | G | 6 | a0001c0001t0001g0282 a0001c0001t0001g0285 a0001c0001t0001g0286 others(3): Show |
6 | HG02257.hp1 HG02572.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1250+1671A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54356307 | |||||||
chr6:54356420 | C | G | 30 | a0004c0004t0001g0002 a0004c0004t0001g0076 a0004c0004t0001g0170 others(27): Show |
32 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.1250+1784C>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54356420 | |||||||
chr6:54356432 | G | A | 1 | a0003c0003t0001g0243 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1250+1796G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54356432 | |||||||
chr6:54356435 | G | A | 2 | a0012c0009t0001g0208 a0012c0009t0001g0209 |
2 | HG02109.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1250+1799G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54356435 | |||||||
chr6:54356527 | A | T | 30 | a0004c0004t0001g0002 a0004c0004t0001g0076 a0004c0004t0001g0170 others(27): Show |
32 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.1250+1891A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54356527 | |||||||
chr6:54356657 | A | C | 2 | a0014c0014t0003g0276 a0014c0014t0003g0277 |
2 | HG02970.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1250+2021A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54356657 | |||||||
chr6:54356674 | G | A | 1 | a0003c0003t0001g0243 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1250+2038G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54356674 | |||||||
chr6:54356687 | G | A | 51 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0093 others(48): Show |
55 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.1250+2051G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54356687 | |||||||
chr6:54356847 | T | C | 1 | a0004c0004t0001g0196 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1250+2211T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54356847 | |||||||
chr6:54356888 | C | T | 2 | a0001c0001t0001g0119 a0001c0001t0001g0137 |
2 | HG01496.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.1250+2252C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54356888 | |||||||
chr6:54356918 | T | TA | 265 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(262): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.1250+2293dupA | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54356918 | ||||||
chr6:54357008 | G | C | 9 | a0001c0001t0001g0011 a0001c0001t0001g0210 a0001c0001t0001g0212 others(6): Show |
10 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1250+2372G>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54357008 | |||||||
chr6:54357015 | A | G | 1 | a0003c0003t0001g0016 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1250+2379A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54357015 | |||||||
chr6:54357089 | A | G | 82 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0038 others(79): Show |
84 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.1250+2453A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54357089 | |||||||
chr6:54357129 | T | G | 2 | a0014c0014t0003g0276 a0014c0014t0003g0277 |
2 | HG02970.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1250+2493T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54357129 | |||||||
chr6:54357311 | G | T | 2 | a0015c0015t0001g0279 a0015c0015t0001g0280 |
2 | HG03130.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1250+2675G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54357311 | |||||||
chr6:54357616 | C | G | 1 | a0005c0005t0001g0267 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1250+2980C>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54357616 | |||||||
chr6:54357670 | G | A | 9 | a0001c0001t0001g0011 a0001c0001t0001g0210 a0001c0001t0001g0212 others(6): Show |
10 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1250+3034G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54357670 | |||||||
chr6:54357834 | G | A | 2 | a0006c0006t0001g0146 a0006c0006t0001g0247 |
2 | HG00140.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.1250+3198G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54357834 | |||||||
chr6:54357955 | G | A | 1 | a0004c0021t0004g0201 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1250+3319G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54357955 | |||||||
chr6:54358059 | G | A | 1 | a0003c0003t0001g0027 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1250+3423G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54358059 | |||||||
chr6:54358126 | T | G | 1 | a0017c0018t0001g0242 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1250+3490T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54358126 | |||||||
chr6:54358156 | G | A | 1 | a0001c0001t0001g0256 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1250+3520G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54358156 | |||||||
chr6:54358218 | C | T | 1 | a0001c0001t0001g0281 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1250+3582C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54358218 | |||||||
chr6:54358340 | C | A | 9 | a0001c0001t0001g0011 a0001c0001t0001g0210 a0001c0001t0001g0212 others(6): Show |
10 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1250+3704C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54358340 | |||||||
chr6:54358534 | C | CA | 92 | a0001c0001t0001g0077 a0001c0001t0001g0173 a0001c0001t0001g0174 others(89): Show |
94 | HG00642.hp2 HG01081.hp1 HG01123.hp2 others(91): Show |
intron_variant | MODIFIER | c.1250+3915dupA | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54358534 | ||||||
chr6:54358534 | C | CAAA | 10 | a0001c0001t0001g0011 a0001c0001t0001g0093 a0001c0001t0001g0094 others(7): Show |
11 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.1250+3913_1250+391 others(7): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54358534 | ||||||
chr6:54358534 | CA | C | 33 | a0001c0001t0001g0122 a0001c0001t0001g0177 a0001c0001t0001g0227 others(30): Show |
35 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(32): Show |
intron_variant | MODIFIER | c.1250+3915delA | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54358534 | ||||||
chr6:54358578 | C | T | 1 | a0003c0003t0001g0029 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1250+3942C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54358578 | |||||||
chr6:54358654 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1250+4018C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54358654 | |||||||
chr6:54358702 | A | C | 3 | a0002c0002t0001g0251 a0002c0002t0001g0252 a0002c0002t0001g0284 |
3 | HG02630.hp2 HG03471.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1250+4066A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54358702 | |||||||
chr6:54358729 | G | T | 3 | a0004c0004t0001g0002 a0004c0004t0001g0192 a0004c0004t0001g0200 |
5 | HG00639.hp2 HG01516.hp1 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.1250+4093G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54358729 | |||||||
chr6:54358796 | T | C | 1 | a0001c0001t0001g0256 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1250+4160T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54358796 | |||||||
chr6:54358801 | A | G | 11 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0292 others(8): Show |
11 | HG02280.hp2 HG02809.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1250+4165A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54358801 | |||||||
chr6:54358858 | G | C | 2 | a0015c0015t0001g0279 a0015c0015t0001g0280 |
2 | HG03130.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1250+4222G>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54358858 | |||||||
chr6:54358867 | T | C | 2 | a0001c0010t0001g0244 a0001c0010t0001g0309 |
2 | HG02647.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1250+4231T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54358867 | |||||||
chr6:54359067 | G | T | 30 | a0002c0002t0001g0008 a0002c0002t0001g0095 a0002c0002t0001g0098 others(27): Show |
31 | HG02056.hp2 HG02523.hp1 HG03831.hp1 others(28): Show |
intron_variant | MODIFIER | c.1250+4431G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54359067 | |||||||
chr6:54359415 | C | T | 2 | a0014c0014t0003g0276 a0014c0014t0003g0277 |
2 | HG02970.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1250+4779C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54359415 | |||||||
chr6:54359451 | C | A | 1 | a0001c0001t0001g0245 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1250+4815C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54359451 | |||||||
chr6:54359969 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1250+5333G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54359969 | |||||||
chr6:54360056 | AAGG | A | 9 | a0001c0001t0001g0011 a0001c0001t0001g0210 a0001c0001t0001g0212 others(6): Show |
10 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1250+5425_1250+542 others(7): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54360056 | ||||||
chr6:54360079 | C | T | 1 | a0001c0001t0001g0141 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1250+5443C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54360079 | |||||||
chr6:54360162 | A | G | 1 | a0001c0001t0001g0207 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1250+5526A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54360162 | |||||||
chr6:54360169 | T | G | 34 | a0001c0001t0001g0245 a0001c0010t0001g0244 a0001c0010t0001g0309 others(31): Show |
36 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(33): Show |
intron_variant | MODIFIER | c.1250+5533T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54360169 | |||||||
chr6:54360211 | A | G | 1 | a0001c0010t0001g0244 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1250+5575A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54360211 | |||||||
chr6:54360233 | T | TC | 37 | a0001c0001t0001g0007 a0001c0001t0001g0093 a0001c0001t0001g0094 others(34): Show |
40 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.1250+5603dupC | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54360233 | ||||||
chr6:54360294 | G | T | 1 | a0001c0001t0001g0207 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1250+5658G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54360294 | |||||||
chr6:54360435 | A | C | 3 | a0004c0004t0001g0002 a0004c0004t0001g0192 a0004c0004t0001g0200 |
5 | HG00639.hp2 HG01516.hp1 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.1250+5799A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54360435 | |||||||
chr6:54360566 | AT | A | 3 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 |
3 | NA19012.hp1 NA19080.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.1250+5932delT | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54360566 | ||||||
chr6:54360609 | T | C | 1 | a0017c0018t0001g0242 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1250+5973T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54360609 | |||||||
chr6:54360708 | C | T | 2 | a0014c0014t0003g0276 a0014c0014t0003g0277 |
2 | HG02970.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1250+6072C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54360708 | |||||||
chr6:54360754 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1250+6118C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54360754 | |||||||
chr6:54360839 | G | GTTTTTTT others(6): Show |
1 | a0001c0001t0001g0310 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1250+6204_1250+620 others(17): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54360839 | ||||||
chr6:54360841 | G | GT | 28 | a0001c0001t0001g0100 a0001c0001t0001g0102 a0001c0001t0001g0104 others(25): Show |
30 | HG00639.hp1 HG00642.hp1 HG00673.hp2 others(27): Show |
intron_variant | MODIFIER | c.1250+6236dupT | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54360841 | ||||||
chr6:54360841 | G | GTT | 9 | a0001c0001t0001g0103 a0001c0001t0001g0126 a0001c0001t0001g0223 others(6): Show |
9 | HG00741.hp2 HG01109.hp2 HG01978.hp2 others(6): Show |
intron_variant | MODIFIER | c.1250+6235_1250+623 others(6): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54360841 | ||||||
chr6:54360841 | G | GTTTTTTT others(3): Show |
3 | a0001c0001t0001g0142 a0001c0001t0001g0257 a0002c0002t0001g0344 |
3 | HG01993.hp2 HG02109.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.1250+6227_1250+623 others(14): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54360841 | ||||||
chr6:54360841 | G | GTTTTTTT others(4): Show |
11 | a0002c0002t0001g0008 a0002c0002t0001g0095 a0002c0002t0001g0307 others(8): Show |
12 | HG02056.hp2 NA18945.hp1 NA18951.hp2 others(9): Show |
intron_variant | MODIFIER | c.1250+6226_1250+623 others(15): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54360841 | ||||||
chr6:54360841 | G | GTTTTTTT others(5): Show |
19 | a0001c0001t0001g0308 a0002c0002t0001g0149 a0002c0002t0001g0150 others(16): Show |
19 | HG02523.hp1 HG03540.hp2 NA18612.hp2 others(16): Show |
intron_variant | MODIFIER | c.1250+6225_1250+623 others(16): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54360841 | ||||||
chr6:54360841 | G | GTTTTTTT others(6): Show |
7 | a0001c0001t0001g0088 a0001c0001t0001g0124 a0001c0001t0001g0174 others(4): Show |
7 | HG01934.hp1 HG02451.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1250+6224_1250+623 others(17): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54360841 | ||||||
chr6:54360841 | G | GTTTTTTT others(7): Show |
13 | a0001c0001t0001g0010 a0001c0001t0001g0106 a0001c0001t0001g0107 others(10): Show |
14 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(11): Show |
intron_variant | MODIFIER | c.1250+6223_1250+623 others(18): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54360841 | ||||||
chr6:54360841 | G | GTTTTTTT others(8): Show |
14 | a0001c0001t0001g0012 a0001c0001t0001g0038 a0001c0001t0001g0099 others(11): Show |
15 | HG00438.hp1 HG00738.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.1250+6222_1250+623 others(19): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54360841 | ||||||
chr6:54360841 | G | GTTTTTTT others(9): Show |
8 | a0001c0001t0001g0110 a0001c0001t0001g0136 a0001c0001t0001g0302 others(5): Show |
8 | HG02109.hp1 HG02698.hp2 NA18747.hp1 others(5): Show |
intron_variant | MODIFIER | c.1250+6221_1250+623 others(20): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54360841 | ||||||
chr6:54360841 | G | GTTTTTTT others(10): Show |
4 | a0002c0002t0001g0306 a0002c0002t0001g0311 a0002c0002t0001g0323 others(1): Show |
4 | HG03654.hp1 HG03669.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.1250+6220_1250+623 others(21): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54360841 | ||||||
chr6:54360841 | G | GTTTTTTT others(11): Show |
14 | a0001c0001t0001g0169 a0001c0001t0001g0176 a0001c0001t0001g0215 others(11): Show |
15 | HG01433.hp1 HG02165.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.1250+6219_1250+623 others(22): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54360841 | ||||||
chr6:54360841 | G | GTTTTTTT others(12): Show |
14 | a0001c0001t0001g0073 a0001c0001t0001g0097 a0001c0001t0001g0111 others(11): Show |
14 | HG00280.hp2 HG00642.hp2 HG01358.hp2 others(11): Show |
intron_variant | MODIFIER | c.1250+6218_1250+623 others(23): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54360841 | ||||||
chr6:54360841 | G | GTTTTTTT others(13): Show |
13 | a0001c0001t0001g0112 a0001c0001t0001g0128 a0001c0001t0001g0132 others(10): Show |
13 | HG00621.hp2 HG01123.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.1250+6217_1250+623 others(24): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54360841 | ||||||
chr6:54360841 | G | GTTTTTTT others(14): Show |
6 | a0001c0001t0001g0108 a0001c0001t0001g0133 a0001c0001t0001g0297 others(3): Show |
6 | HG01258.hp1 HG02300.hp1 HG02300.hp2 others(3): Show |
intron_variant | MODIFIER | c.1250+6216_1250+623 others(25): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54360841 | ||||||
chr6:54360841 | G | GTTTTTTT others(15): Show |
6 | a0001c0001t0001g0109 a0001c0001t0001g0168 a0001c0001t0001g0286 others(3): Show |
6 | HG01167.hp1 HG01891.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.1250+6215_1250+623 others(26): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54360841 | ||||||
chr6:54360841 | G | GTTTTTTT others(16): Show |
2 | a0001c0001t0001g0285 a0002c0002t0001g0284 |
2 | HG02257.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1250+6214_1250+623 others(27): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54360841 | ||||||
chr6:54360841 | G | GTTTTTTT others(17): Show |
1 | a0007c0007t0001g0085 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1250+6213_1250+623 others(28): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54360841 | ||||||
chr6:54360841 | G | GTTTTTTT others(18): Show |
1 | a0023c0020t0001g0291 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1250+6212_1250+623 others(29): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54360841 | ||||||
chr6:54360841 | G | GTTTTTTT others(20): Show |
1 | a0007c0007t0001g0081 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1250+6210_1250+623 others(31): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54360841 | ||||||
chr6:54360841 | G | T | 1 | a0001c0001t0001g0310 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1250+6205G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54360841 | |||||||
chr6:54360841 | GT | G | 32 | a0001c0001t0001g0014 a0001c0001t0001g0075 a0001c0001t0001g0091 others(29): Show |
33 | HG00558.hp1 HG00735.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.1250+6236delT | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54360841 | ||||||
chr6:54360841 | GTT | G | 48 | a0001c0001t0001g0009 a0001c0001t0001g0090 a0001c0001t0001g0158 others(45): Show |
49 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.1250+6235_1250+623 others(6): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54360841 | ||||||
chr6:54360841 | GTTT | G | 17 | a0001c0001t0001g0316 a0003c0003t0001g0050 a0004c0004t0001g0002 others(14): Show |
19 | HG00140.hp1 HG00639.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.1250+6234_1250+623 others(7): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54360841 | ||||||
chr6:54360841 | GTTTTTTT others(3): Show |
G | 3 | a0001c0001t0001g0154 a0014c0014t0003g0276 a0014c0014t0003g0277 |
3 | HG01192.hp2 HG02970.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1250+6227_1250+623 others(14): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54360841 | ||||||
chr6:54360841 | GTTTTTTT others(5): Show |
G | 2 | a0001c0001t0001g0077 a0020c0019t0001g0211 |
2 | HG02071.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1250+6225_1250+623 others(16): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54360841 | ||||||
chr6:54360841 | GTTTTTTT others(6): Show |
G | 8 | a0001c0001t0001g0011 a0001c0001t0001g0210 a0001c0001t0001g0212 others(5): Show |
9 | HG02027.hp1 HG02074.hp2 HG02080.hp1 others(6): Show |
intron_variant | MODIFIER | c.1250+6224_1250+623 others(17): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54360841 | ||||||
chr6:54360841 | GTTTTTTT others(8): Show |
G | 1 | a0001c0001t0001g0129 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1250+6222_1250+623 others(19): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54360841 | ||||||
chr6:54360841 | GTTTTTTT others(11): Show |
G | 7 | a0001c0001t0001g0245 a0001c0001t0001g0256 a0001c0010t0001g0244 others(4): Show |
7 | HG02258.hp1 HG02647.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.1250+6219_1250+623 others(22): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54360841 | ||||||
chr6:54360852 | T | A | 2 | a0005c0005t0001g0273 a0024c0025t0001g0262 |
2 | NA18949.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.1250+6216T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54360852 | |||||||
chr6:54360861 | T | A | 2 | a0005c0005t0001g0273 a0024c0025t0001g0262 |
2 | NA18949.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.1250+6225T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54360861 | |||||||
chr6:54360872 | T | TTTTTTTT others(10): Show |
1 | a0002c0002t0001g0246 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1250+6236_1250+623 others(21): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54360872 | |||||||
chr6:54361146 | C | T | 1 | a0001c0001t0001g0287 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1250+6510C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54361146 | |||||||
chr6:54361159 | C | T | 1 | a0003c0003t0001g0056 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1250+6523C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54361159 | |||||||
chr6:54361369 | A | G | 3 | a0001c0001t0001g0155 a0001c0001t0001g0165 a0001c0001t0001g0176 |
3 | HG01261.hp2 HG02683.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1250+6733A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54361369 | |||||||
chr6:54361475 | AC | A | 34 | a0001c0001t0001g0245 a0001c0010t0001g0244 a0001c0010t0001g0309 others(31): Show |
36 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(33): Show |
intron_variant | MODIFIER | c.1250+6840delC | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54361475 | |||||||
chr6:54361515 | A | G | 1 | a0001c0001t0001g0179 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1250+6879A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54361515 | |||||||
chr6:54361541 | C | A | 1 | a0001c0001t0001g0207 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1250+6905C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54361541 | |||||||
chr6:54361542 | T | C | 53 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0093 others(50): Show |
57 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.1250+6906T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54361542 | |||||||
chr6:54361566 | G | A | 1 | a0001c0001t0001g0310 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1250+6930G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54361566 | |||||||
chr6:54361623 | G | C | 1 | a0003c0003t0001g0243 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1250+6987G>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54361623 | |||||||
chr6:54361801 | A | T | 1 | a0001c0001t0001g0302 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1250+7165A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54361801 | |||||||
chr6:54361806 | A | G | 8 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0230 others(5): Show |
8 | HG00735.hp1 HG01934.hp2 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.1250+7170A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54361806 | |||||||
chr6:54362009 | T | C | 1 | a0001c0001t0001g0318 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1250+7373T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54362009 | |||||||
chr6:54362017 | T | A | 1 | a0001c0001t0001g0260 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1250+7381T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54362017 | |||||||
chr6:54362120 | G | T | 1 | a0003c0003t0001g0067 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1250+7484G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54362120 | |||||||
chr6:54362169 | G | T | 1 | a0001c0001t0001g0207 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1250+7533G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54362169 | |||||||
chr6:54362174 | A | T | 1 | a0017c0018t0001g0242 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1250+7538A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54362174 | |||||||
chr6:54362229 | T | A | 1 | a0003c0003t0001g0243 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1250+7593T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54362229 | |||||||
chr6:54362342 | G | C | 77 | a0001c0001t0001g0285 a0001c0001t0001g0286 a0001c0001t0001g0308 others(74): Show |
79 | HG00642.hp2 HG01123.hp2 HG01884.hp1 others(76): Show |
intron_variant | MODIFIER | c.1250+7706G>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54362342 | |||||||
chr6:54362365 | T | C | 9 | a0001c0001t0001g0011 a0001c0001t0001g0210 a0001c0001t0001g0212 others(6): Show |
10 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1250+7729T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54362365 | |||||||
chr6:54362624 | T | C | 1 | a0001c0001t0001g0154 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1250+7988T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54362624 | |||||||
chr6:54362786 | G | A | 77 | a0001c0001t0001g0285 a0001c0001t0001g0286 a0001c0001t0001g0308 others(74): Show |
79 | HG00642.hp2 HG01123.hp2 HG01884.hp1 others(76): Show |
intron_variant | MODIFIER | c.1250+8150G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54362786 | |||||||
chr6:54362805 | G | A | 76 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0038 others(73): Show |
78 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(75): Show |
intron_variant | MODIFIER | c.1250+8169G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54362805 | |||||||
chr6:54362822 | A | G | 34 | a0001c0001t0001g0245 a0001c0010t0001g0244 a0001c0010t0001g0309 others(31): Show |
36 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(33): Show |
intron_variant | MODIFIER | c.1250+8186A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54362822 | |||||||
chr6:54362856 | C | A | 1 | a0001c0001t0001g0194 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1250+8220C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54362856 | |||||||
chr6:54362863 | T | C | 1 | a0001c0001t0001g0308 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1250+8227T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54362863 | |||||||
chr6:54362893 | G | T | 5 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0175 others(2): Show |
5 | HG02109.hp1 HG02451.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1250+8257G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54362893 | |||||||
chr6:54363051 | C | A | 3 | a0001c0001t0001g0007 a0001c0001t0001g0093 a0001c0001t0001g0094 |
4 | HG03491.hp1 HG03492.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.1250+8415C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54363051 | |||||||
chr6:54363123 | G | C | 1 | a0002c0002t0001g0246 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1250+8487G>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54363123 | |||||||
chr6:54363129 | A | T | 1 | a0017c0018t0001g0087 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1250+8493A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54363129 | |||||||
chr6:54363193 | T | C | 46 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0093 others(43): Show |
50 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.1250+8557T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54363193 | |||||||
chr6:54363354 | T | A | 46 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0093 others(43): Show |
50 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.1250+8718T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54363354 | |||||||
chr6:54363364 | G | C | 2 | a0001c0001t0001g0245 a0017c0018t0001g0087 |
2 | HG02258.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1250+8728G>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54363364 | |||||||
chr6:54363451 | A | C | 2 | a0002c0002t0001g0353 a0002c0002t0001g0354 |
2 | NA18963.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.1250+8815A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54363451 | |||||||
chr6:54363482 | G | A | 1 | a0005c0005t0001g0273 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1250+8846G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54363482 | |||||||
chr6:54363493 | G | A | 1 | a0003c0003t0001g0243 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1250+8857G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54363493 | |||||||
chr6:54363533 | T | C | 6 | a0001c0001t0001g0256 a0003c0003t0001g0243 a0014c0014t0003g0276 others(3): Show |
6 | HG02970.hp1 HG03130.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.1250+8897T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54363533 | |||||||
chr6:54363540 | C | A | 1 | a0002c0002t0001g0321 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1250+8904C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54363540 | |||||||
chr6:54363548 | T | C | 1 | a0001c0001t0001g0256 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1250+8912T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54363548 | |||||||
chr6:54363612 | C | T | 1 | a0001c0001t0001g0090 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1250+8976C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54363612 | |||||||
chr6:54363615 | G | A | 213 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0011 others(210): Show |
221 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.1250+8979G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54363615 | |||||||
chr6:54363619 | C | CA | 94 | a0001c0001t0001g0077 a0001c0001t0001g0114 a0001c0001t0001g0130 others(91): Show |
96 | HG00099.hp1 HG00438.hp1 HG00642.hp2 others(93): Show |
intron_variant | MODIFIER | c.1250+8999dupA | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54363619 | ||||||
chr6:54363619 | CA | C | 58 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0094 others(55): Show |
63 | HG00140.hp1 HG00280.hp1 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.1250+8999delA | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54363619 | ||||||
chr6:54363664 | G | C | 1 | a0003c0003t0001g0243 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1250+9028G>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54363664 | |||||||
chr6:54363710 | C | G | 9 | a0001c0001t0001g0011 a0001c0001t0001g0210 a0001c0001t0001g0212 others(6): Show |
10 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1250+9074C>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54363710 | |||||||
chr6:54363832 | C | T | 2 | a0004c0004t0001g0076 a0004c0004t0001g0202 |
2 | HG02074.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.1250+9196C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54363832 | |||||||
chr6:54364044 | G | A | 2 | a0002c0002t0001g0301 a0013c0012t0001g0069 |
2 | HG02647.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1250+9408G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54364044 | |||||||
chr6:54364044 | G | T | 1 | a0001c0001t0001g0310 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1250+9408G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54364044 | |||||||
chr6:54364125 | A | G | 213 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0011 others(210): Show |
221 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.1250+9489A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54364125 | |||||||
chr6:54364493 | A | G | 2 | a0001c0001t0001g0155 a0001c0001t0001g0165 |
2 | HG01261.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.1250+9857A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54364493 | |||||||
chr6:54364585 | T | C | 1 | a0011c0011t0001g0048 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1250+9949T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54364585 | |||||||
chr6:54364724 | C | G | 1 | a0001c0001t0001g0283 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1250+10088C>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54364724 | |||||||
chr6:54364726 | A | G | 2 | a0001c0001t0001g0228 a0001c0001t0001g0229 |
2 | NA18612.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.1250+10090A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54364726 | |||||||
chr6:54364769 | T | G | 1 | a0002c0002t0001g0344 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1250+10133T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54364769 | |||||||
chr6:54364771 | T | G | 1 | a0002c0002t0001g0344 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1250+10135T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54364771 | |||||||
chr6:54364772 | C | A | 1 | a0002c0002t0001g0344 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1250+10136C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54364772 | |||||||
chr6:54365051 | TTCATGCT others(3): Show |
T | 1 | a0007c0007t0001g0081 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1250+10417_1250+10 others(16): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54365051 | ||||||
chr6:54365086 | A | T | 2 | a0001c0001t0001g0258 a0001c0001t0001g0261 |
2 | HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1250+10450A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54365086 | |||||||
chr6:54365160 | C | T | 1 | a0006c0006t0002g0295 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1250+10524C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54365160 | |||||||
chr6:54365206 | A | G | 2 | a0015c0015t0001g0279 a0015c0015t0001g0280 |
2 | HG03130.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1250+10570A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54365206 | |||||||
chr6:54365250 | C | T | 1 | a0001c0001t0001g0233 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1250+10614C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54365250 | |||||||
chr6:54365383 | C | T | 1 | a0003c0003t0001g0243 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1250+10747C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54365383 | |||||||
chr6:54365418 | G | A | 4 | a0001c0001t0001g0256 a0003c0003t0001g0243 a0015c0015t0001g0279 others(1): Show |
4 | HG03130.hp1 HG03453.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1250+10782G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54365418 | |||||||
chr6:54365479 | T | C | 1 | a0003c0003t0001g0050 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1250+10843T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54365479 | |||||||
chr6:54365495 | G | A | 3 | a0001c0001t0001g0007 a0001c0001t0001g0093 a0001c0001t0001g0094 |
4 | HG03491.hp1 HG03492.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.1250+10859G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54365495 | |||||||
chr6:54365516 | C | T | 4 | a0001c0001t0001g0245 a0001c0010t0001g0244 a0001c0010t0001g0309 others(1): Show |
4 | HG02258.hp1 HG02647.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1250+10880C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54365516 | |||||||
chr6:54365554 | C | A | 1 | a0003c0003t0001g0243 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1250+10918C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54365554 | |||||||
chr6:54365724 | T | A | 37 | a0001c0001t0001g0007 a0001c0001t0001g0093 a0001c0001t0001g0094 others(34): Show |
40 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.1250+11088T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54365724 | |||||||
chr6:54365766 | T | G | 2 | a0001c0001t0001g0308 a0001c0001t0001g0310 |
2 | HG03225.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1250+11130T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54365766 | |||||||
chr6:54365833 | G | A | 1 | a0001c0001t0001g0177 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1250+11197G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54365833 | |||||||
chr6:54365844 | C | A | 1 | a0004c0004t0001g0180 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1250+11208C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54365844 | |||||||
chr6:54365861 | T | A | 9 | a0001c0001t0001g0011 a0001c0001t0001g0210 a0001c0001t0001g0212 others(6): Show |
10 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1250+11225T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54365861 | |||||||
chr6:54365905 | C | A | 1 | a0016c0017t0001g0274 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1250+11269C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54365905 | |||||||
chr6:54365905 | C | G | 1 | a0004c0021t0004g0201 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1250+11269C>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54365905 | |||||||
chr6:54365982 | T | A | 9 | a0001c0001t0001g0011 a0001c0001t0001g0210 a0001c0001t0001g0212 others(6): Show |
10 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1250+11346T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54365982 | |||||||
chr6:54366091 | A | T | 37 | a0001c0001t0001g0007 a0001c0001t0001g0093 a0001c0001t0001g0094 others(34): Show |
40 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.1250+11455A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54366091 | |||||||
chr6:54366138 | A | C | 1 | a0017c0018t0001g0242 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1250+11502A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54366138 | |||||||
chr6:54366246 | G | T | 37 | a0001c0001t0001g0007 a0001c0001t0001g0093 a0001c0001t0001g0094 others(34): Show |
40 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.1250+11610G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54366246 | |||||||
chr6:54366254 | A | ATG | 122 | a0001c0001t0001g0011 a0001c0001t0001g0194 a0001c0001t0001g0210 others(119): Show |
127 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.1250+11641_1250+11 others(8): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54366254 | ||||||
chr6:54366254 | A | ATGTG | 5 | a0001c0001t0001g0310 a0002c0002t0001g0118 a0002c0002t0001g0327 others(2): Show |
5 | HG00735.hp2 HG02145.hp2 HG02523.hp2 others(2): Show |
intron_variant | MODIFIER | c.1250+11639_1250+11 others(10): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54366254 | ||||||
chr6:54366288 | G | C | 3 | a0001c0001t0001g0007 a0001c0001t0001g0093 a0001c0001t0001g0094 |
4 | HG03491.hp1 HG03492.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.1250+11652G>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54366288 | |||||||
chr6:54366520 | C | G | 2 | a0001c0001t0001g0014 a0001c0001t0001g0296 |
3 | HG00741.hp1 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1250+11884C>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54366520 | |||||||
chr6:54366690 | G | A | 66 | a0002c0002t0001g0008 a0002c0002t0001g0013 a0002c0002t0001g0074 others(63): Show |
68 | HG00642.hp2 HG01123.hp2 HG02056.hp2 others(65): Show |
intron_variant | MODIFIER | c.1250+12054G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54366690 | |||||||
chr6:54366759 | A | G | 1 | a0003c0003t0001g0066 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1250+12123A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54366759 | |||||||
chr6:54366773 | G | A | 1 | a0003c0003t0001g0243 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1250+12137G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54366773 | |||||||
chr6:54366891 | G | A | 1 | a0004c0021t0004g0201 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1250+12255G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54366891 | |||||||
chr6:54366956 | A | C | 1 | a0001c0001t0001g0257 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1250+12320A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54366956 | |||||||
chr6:54367073 | A | G | 1 | a0001c0001t0001g0256 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1250+12437A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54367073 | |||||||
chr6:54367206 | C | T | 1 | a0001c0001t0001g0077 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1250+12570C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54367206 | |||||||
chr6:54367214 | A | G | 1 | a0001c0001t0001g0183 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1250+12578A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54367214 | |||||||
chr6:54367240 | T | C | 1 | a0011c0011t0001g0040 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1250+12604T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54367240 | |||||||
chr6:54367406 | A | C | 1 | a0001c0001t0001g0207 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1250+12770A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54367406 | |||||||
chr6:54367406 | A | G | 8 | a0001c0001t0001g0073 a0001c0001t0001g0122 a0001c0001t0001g0123 others(5): Show |
8 | HG00099.hp2 HG00140.hp2 HG01069.hp2 others(5): Show |
intron_variant | MODIFIER | c.1250+12770A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54367406 | |||||||
chr6:54367440 | G | T | 64 | a0002c0002t0001g0008 a0002c0002t0001g0013 a0002c0002t0001g0074 others(61): Show |
66 | HG00642.hp2 HG01123.hp2 HG02056.hp2 others(63): Show |
intron_variant | MODIFIER | c.1250+12804G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54367440 | |||||||
chr6:54367453 | G | A | 1 | a0017c0018t0001g0087 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1250+12817G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54367453 | |||||||
chr6:54367597 | G | A | 1 | a0001c0001t0001g0256 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1251-12929G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54367597 | |||||||
chr6:54367873 | G | A | 34 | a0001c0001t0001g0245 a0001c0010t0001g0244 a0001c0010t0001g0309 others(31): Show |
36 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(33): Show |
intron_variant | MODIFIER | c.1251-12653G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54367873 | |||||||
chr6:54367905 | G | C | 3 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0312 |
3 | NA18955.hp2 NA19000.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.1251-12621G>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54367905 | |||||||
chr6:54368020 | A | G | 4 | a0007c0007t0001g0080 a0007c0007t0001g0084 a0007c0007t0001g0085 others(1): Show |
4 | HG01884.hp1 HG01891.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1251-12506A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54368020 | |||||||
chr6:54368049 | G | A | 29 | a0004c0004t0001g0002 a0004c0004t0001g0076 a0004c0004t0001g0170 others(26): Show |
31 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(28): Show |
intron_variant | MODIFIER | c.1251-12477G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54368049 | |||||||
chr6:54368080 | G | A | 4 | a0001c0001t0001g0256 a0003c0003t0001g0243 a0015c0015t0001g0279 others(1): Show |
4 | HG03130.hp1 HG03453.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1251-12446G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54368080 | |||||||
chr6:54368112 | TA | T | 11 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0292 others(8): Show |
11 | HG02280.hp2 HG02809.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1251-12411delA | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54368112 | ||||||
chr6:54368330 | A | T | 3 | a0003c0003t0001g0070 a0003c0003t0001g0071 a0005c0005t0001g0278 |
3 | HG02895.hp1 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1251-12196A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54368330 | |||||||
chr6:54368359 | A | C | 1 | a0004c0021t0004g0201 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1251-12167A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54368359 | |||||||
chr6:54368464 | T | C | 1 | a0017c0018t0001g0242 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1251-12062T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54368464 | |||||||
chr6:54368605 | T | C | 1 | a0003c0003t0001g0243 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1251-11921T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54368605 | |||||||
chr6:54368739 | TA | T | 9 | a0001c0001t0001g0011 a0001c0001t0001g0210 a0001c0001t0001g0212 others(6): Show |
10 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1251-11781delA | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54368739 | ||||||
chr6:54368755 | A | G | 1 | a0001c0001t0001g0225 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1251-11771A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54368755 | |||||||
chr6:54368960 | A | G | 2 | a0016c0017t0001g0274 a0016c0017t0001g0275 |
2 | HG03225.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1251-11566A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54368960 | |||||||
chr6:54368975 | T | C | 3 | a0001c0001t0001g0007 a0001c0001t0001g0093 a0001c0001t0001g0094 |
4 | HG03491.hp1 HG03492.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.1251-11551T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54368975 | |||||||
chr6:54369055 | G | A | 3 | a0001c0001t0001g0007 a0001c0001t0001g0093 a0001c0001t0001g0094 |
4 | HG03491.hp1 HG03492.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.1251-11471G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54369055 | |||||||
chr6:54369093 | G | T | 1 | a0002c0002t0001g0311 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1251-11433G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54369093 | |||||||
chr6:54369105 | T | G | 1 | a0001c0001t0001g0215 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1251-11421T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54369105 | |||||||
chr6:54369311 | A | G | 1 | a0004c0021t0004g0201 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1251-11215A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54369311 | |||||||
chr6:54369532 | T | A | 1 | a0003c0003t0001g0243 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1251-10994T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54369532 | |||||||
chr6:54369606 | C | T | 52 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0093 others(49): Show |
56 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.1251-10920C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54369606 | |||||||
chr6:54369656 | C | A | 4 | a0001c0001t0001g0256 a0003c0003t0001g0243 a0015c0015t0001g0279 others(1): Show |
4 | HG03130.hp1 HG03453.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1251-10870C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54369656 | |||||||
chr6:54369676 | A | G | 11 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0292 others(8): Show |
11 | HG02280.hp2 HG02809.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1251-10850A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54369676 | |||||||
chr6:54369780 | A | G | 2 | a0014c0014t0003g0276 a0014c0014t0003g0277 |
2 | HG02970.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1251-10746A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54369780 | |||||||
chr6:54369815 | A | T | 1 | a0001c0001t0001g0126 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1251-10711A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54369815 | |||||||
chr6:54369833 | T | C | 1 | a0007c0007t0001g0081 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1251-10693T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54369833 | |||||||
chr6:54370071 | T | C | 9 | a0001c0001t0001g0285 a0001c0001t0001g0286 a0007c0007t0001g0080 others(6): Show |
9 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.1251-10455T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54370071 | |||||||
chr6:54370086 | A | G | 3 | a0001c0001t0001g0007 a0001c0001t0001g0093 a0001c0001t0001g0094 |
4 | HG03491.hp1 HG03492.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.1251-10440A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54370086 | |||||||
chr6:54370131 | G | T | 6 | a0001c0001t0001g0001 a0001c0001t0001g0096 a0001c0001t0001g0138 others(3): Show |
8 | HG02083.hp2 NA18939.hp2 NA18946.hp2 others(5): Show |
intron_variant | MODIFIER | c.1251-10395G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54370131 | |||||||
chr6:54370193 | A | G | 6 | a0001c0001t0001g0256 a0003c0003t0001g0243 a0014c0014t0003g0276 others(3): Show |
6 | HG02970.hp1 HG03130.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.1251-10333A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54370193 | |||||||
chr6:54370544 | A | G | 6 | a0001c0001t0001g0256 a0003c0003t0001g0243 a0014c0014t0003g0276 others(3): Show |
6 | HG02970.hp1 HG03130.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.1251-9982A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54370544 | |||||||
chr6:54370738 | G | A | 9 | a0001c0001t0001g0011 a0001c0001t0001g0210 a0001c0001t0001g0212 others(6): Show |
10 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1251-9788G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54370738 | |||||||
chr6:54370819 | T | C | 34 | a0001c0001t0001g0245 a0001c0010t0001g0244 a0001c0010t0001g0309 others(31): Show |
36 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(33): Show |
intron_variant | MODIFIER | c.1251-9707T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54370819 | |||||||
chr6:54370847 | A | G | 3 | a0001c0001t0001g0185 a0001c0001t0001g0191 a0001c0001t0001g0219 |
3 | HG00558.hp2 NA18980.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.1251-9679A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54370847 | |||||||
chr6:54370883 | G | T | 2 | a0001c0001t0001g0178 a0001c0001t0001g0179 |
2 | HG02258.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1251-9643G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54370883 | |||||||
chr6:54370983 | G | T | 1 | a0001c0001t0001g0205 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1251-9543G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54370983 | |||||||
chr6:54371024 | C | A | 34 | a0001c0001t0001g0245 a0001c0010t0001g0244 a0001c0010t0001g0309 others(31): Show |
36 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(33): Show |
intron_variant | MODIFIER | c.1251-9502C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54371024 | |||||||
chr6:54371105 | G | A | 1 | a0003c0003t0001g0163 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1251-9421G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54371105 | |||||||
chr6:54371110 | C | CTG | 82 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0038 others(79): Show |
84 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.1251-9388_1251-938 others(6): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54371110 | ||||||
chr6:54371110 | C | CTGTG | 17 | a0001c0001t0001g0073 a0001c0001t0001g0077 a0001c0001t0001g0122 others(14): Show |
17 | HG00099.hp2 HG00140.hp2 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.1251-9390_1251-938 others(8): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54371110 | ||||||
chr6:54371110 | C | CTGTGTGT others(3): Show |
1 | a0004c0021t0004g0201 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1251-9396_1251-938 others(14): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54371110 | ||||||
chr6:54371110 | CTG | C | 44 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0094 others(41): Show |
49 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.1251-9388_1251-938 others(6): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54371110 | ||||||
chr6:54371110 | CTGTG | C | 10 | a0001c0001t0001g0093 a0001c0001t0001g0207 a0001c0001t0001g0308 others(7): Show |
10 | HG00408.hp2 HG01069.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.1251-9390_1251-938 others(8): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54371110 | ||||||
chr6:54371148 | GAGAA | G | 66 | a0002c0002t0001g0008 a0002c0002t0001g0013 a0002c0002t0001g0074 others(63): Show |
68 | HG00642.hp2 HG01123.hp2 HG02056.hp2 others(65): Show |
intron_variant | MODIFIER | c.1251-9373_1251-937 others(8): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54371148 | ||||||
chr6:54371213 | A | T | 1 | a0003c0003t0001g0051 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1251-9313A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54371213 | |||||||
chr6:54371214 | G | T | 1 | a0003c0003t0001g0051 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1251-9312G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54371214 | |||||||
chr6:54371224 | C | T | 3 | a0001c0001t0001g0007 a0001c0001t0001g0093 a0001c0001t0001g0094 |
4 | HG03491.hp1 HG03492.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.1251-9302C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54371224 | |||||||
chr6:54371271 | G | A | 34 | a0001c0001t0001g0245 a0001c0010t0001g0244 a0001c0010t0001g0309 others(31): Show |
36 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(33): Show |
intron_variant | MODIFIER | c.1251-9255G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54371271 | |||||||
chr6:54371304 | C | T | 1 | a0001c0001t0001g0260 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1251-9222C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54371304 | |||||||
chr6:54371343 | A | C | 4 | a0001c0001t0001g0245 a0001c0010t0001g0244 a0001c0010t0001g0309 others(1): Show |
4 | HG02258.hp1 HG02647.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1251-9183A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54371343 | |||||||
chr6:54371435 | C | T | 1 | a0006c0006t0001g0146 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1251-9091C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54371435 | |||||||
chr6:54371522 | T | C | 1 | a0005c0005t0001g0278 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1251-9004T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54371522 | |||||||
chr6:54371556 | T | C | 29 | a0004c0004t0001g0002 a0004c0004t0001g0076 a0004c0004t0001g0170 others(26): Show |
31 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(28): Show |
intron_variant | MODIFIER | c.1251-8970T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54371556 | |||||||
chr6:54371599 | A | G | 2 | a0001c0001t0001g0258 a0001c0001t0001g0261 |
2 | HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1251-8927A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54371599 | |||||||
chr6:54371599 | A | T | 1 | a0001c0001t0001g0207 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1251-8927A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54371599 | |||||||
chr6:54371641 | G | C | 1 | a0001c0001t0001g0256 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1251-8885G>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54371641 | |||||||
chr6:54371684 | G | A | 1 | a0001c0001t0001g0127 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1251-8842G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54371684 | |||||||
chr6:54371701 | T | C | 1 | a0001c0001t0001g0184 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1251-8825T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54371701 | |||||||
chr6:54371981 | G | GT | 38 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0090 others(35): Show |
41 | HG00621.hp1 HG01167.hp1 HG01175.hp1 others(38): Show |
intron_variant | MODIFIER | c.1251-8518dupT | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54371981 | ||||||
chr6:54371981 | G | GTT | 69 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0012 others(66): Show |
72 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.1251-8519_1251-851 others(6): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54371981 | ||||||
chr6:54371981 | G | GTTT | 21 | a0001c0001t0001g0073 a0001c0001t0001g0123 a0001c0001t0001g0129 others(18): Show |
21 | HG00099.hp2 HG00438.hp1 HG00673.hp2 others(18): Show |
intron_variant | MODIFIER | c.1251-8520_1251-851 others(7): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54371981 | ||||||
chr6:54371981 | GT | G | 8 | a0001c0001t0001g0141 a0001c0001t0001g0227 a0001c0001t0001g0296 others(5): Show |
8 | HG01070.hp1 HG01167.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1251-8518delT | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54371981 | ||||||
chr6:54371981 | GTTT | G | 26 | a0004c0004t0001g0002 a0004c0004t0001g0076 a0004c0004t0001g0170 others(23): Show |
28 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.1251-8520_1251-851 others(7): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54371981 | ||||||
chr6:54371981 | GTTTTTT | G | 72 | a0001c0001t0001g0245 a0001c0001t0001g0285 a0001c0001t0001g0286 others(69): Show |
74 | HG00642.hp2 HG01123.hp2 HG01884.hp1 others(71): Show |
intron_variant | MODIFIER | c.1251-8523_1251-851 others(10): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54371981 | ||||||
chr6:54371986 | T | TTTTTTTT others(14): Show |
1 | a0004c0021t0004g0201 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1251-8532_1251-853 others(25): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54371986 | ||||||
chr6:54371987 | T | G | 2 | a0014c0014t0003g0276 a0014c0014t0003g0277 |
2 | HG02970.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1251-8539T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54371987 | |||||||
chr6:54371996 | T | G | 2 | a0014c0014t0003g0276 a0014c0014t0003g0277 |
2 | HG02970.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1251-8530T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54371996 | |||||||
chr6:54372025 | C | T | 3 | a0001c0001t0001g0245 a0003c0003t0001g0243 a0017c0018t0001g0087 |
3 | HG02258.hp1 HG03471.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1251-8501C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54372025 | |||||||
chr6:54372145 | C | A | 1 | a0005c0005t0001g0265 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1251-8381C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54372145 | |||||||
chr6:54372189 | A | C | 82 | a0001c0001t0001g0207 a0001c0001t0001g0245 a0001c0001t0001g0256 others(79): Show |
84 | HG00642.hp2 HG01123.hp2 HG01884.hp1 others(81): Show |
intron_variant | MODIFIER | c.1251-8337A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54372189 | |||||||
chr6:54372239 | A | C | 1 | a0001c0001t0001g0207 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1251-8287A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54372239 | |||||||
chr6:54372268 | A | G | 1 | a0003c0003t0001g0060 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1251-8258A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54372268 | |||||||
chr6:54372284 | G | A | 2 | a0001c0010t0001g0244 a0001c0010t0001g0309 |
2 | HG02647.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1251-8242G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54372284 | |||||||
chr6:54372641 | G | A | 77 | a0001c0001t0001g0285 a0001c0001t0001g0286 a0001c0001t0001g0308 others(74): Show |
79 | HG00642.hp2 HG01123.hp2 HG01884.hp1 others(76): Show |
intron_variant | MODIFIER | c.1251-7885G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54372641 | |||||||
chr6:54372668 | C | T | 216 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0011 others(213): Show |
224 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.1251-7858C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54372668 | |||||||
chr6:54372696 | C | T | 1 | a0003c0003t0001g0243 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1251-7830C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54372696 | |||||||
chr6:54372697 | G | A | 2 | a0003c0003t0001g0039 a0003c0003t0001g0060 |
2 | HG03017.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1251-7829G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54372697 | |||||||
chr6:54372723 | CATACATA others(27): Show |
C | 16 | a0001c0001t0001g0092 a0001c0001t0001g0177 a0001c0001t0001g0281 others(13): Show |
16 | HG00099.hp1 HG01261.hp1 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.1251-7799_1251-776 others(38): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54372723 | ||||||
chr6:54372727 | C | CAT | 12 | a0001c0001t0001g0104 a0001c0001t0001g0141 a0001c0001t0001g0187 others(9): Show |
12 | HG00408.hp2 HG00621.hp1 HG00738.hp1 others(9): Show |
intron_variant | MODIFIER | c.1251-7755_1251-775 others(6): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54372727 | ||||||
chr6:54372727 | C | CATAT | 7 | a0001c0001t0001g0191 a0003c0003t0001g0004 a0003c0003t0001g0005 others(4): Show |
7 | HG00639.hp1 HG01255.hp2 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.1251-7757_1251-775 others(8): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54372727 | ||||||
chr6:54372727 | C | CATATAT | 6 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0003c0003t0001g0003 others(3): Show |
6 | HG00741.hp2 HG01099.hp2 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.1251-7759_1251-775 others(10): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54372727 | ||||||
chr6:54372727 | C | CATATATA others(3): Show |
1 | a0003c0003t0001g0015 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1251-7763_1251-775 others(14): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54372727 | ||||||
chr6:54372727 | CAT | C | 18 | a0001c0001t0001g0096 a0001c0001t0001g0121 a0001c0001t0001g0140 others(15): Show |
18 | HG00642.hp1 HG01109.hp2 HG01952.hp1 others(15): Show |
intron_variant | MODIFIER | c.1251-7755_1251-775 others(6): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54372727 | ||||||
chr6:54372727 | CATAT | C | 5 | a0001c0001t0001g0101 a0001c0001t0001g0114 a0001c0001t0001g0115 others(2): Show |
5 | HG01993.hp1 HG02080.hp2 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.1251-7757_1251-775 others(8): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54372727 | ||||||
chr6:54372727 | CATATATA others(3): Show |
C | 7 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0186 others(4): Show |
7 | HG02027.hp2 HG02257.hp2 HG06807.hp2 others(4): Show |
intron_variant | MODIFIER | c.1251-7763_1251-775 others(14): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54372727 | ||||||
chr6:54372727 | CATATATA others(5): Show |
C | 14 | a0001c0001t0001g0075 a0001c0001t0001g0093 a0001c0001t0001g0094 others(11): Show |
14 | HG00735.hp1 HG01934.hp2 HG01952.hp2 others(11): Show |
intron_variant | MODIFIER | c.1251-7765_1251-775 others(16): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54372727 | ||||||
chr6:54372727 | CATATATA others(7): Show |
C | 12 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0158 others(9): Show |
14 | HG01884.hp2 HG01891.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.1251-7767_1251-775 others(18): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54372727 | ||||||
chr6:54372727 | CATATATA others(9): Show |
C | 11 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0207 others(8): Show |
11 | HG02258.hp2 HG02559.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1251-7769_1251-775 others(20): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54372727 | ||||||
chr6:54372727 | CATATATA others(11): Show |
C | 107 | a0001c0001t0001g0285 a0001c0001t0001g0286 a0001c0001t0001g0308 others(104): Show |
111 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.1251-7771_1251-775 others(22): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54372727 | ||||||
chr6:54372727 | CATATATA others(13): Show |
C | 6 | a0001c0001t0001g0155 a0001c0001t0001g0165 a0001c0001t0001g0249 others(3): Show |
6 | HG01261.hp2 HG02109.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.1251-7773_1251-775 others(24): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54372727 | ||||||
chr6:54372727 | CATATATA others(15): Show |
C | 76 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0038 others(73): Show |
78 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(75): Show |
intron_variant | MODIFIER | c.1251-7775_1251-775 others(26): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54372727 | ||||||
chr6:54372727 | CATATATA others(17): Show |
C | 9 | a0001c0001t0001g0011 a0001c0001t0001g0210 a0001c0001t0001g0212 others(6): Show |
10 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1251-7777_1251-775 others(28): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54372727 | ||||||
chr6:54372727 | CATATATA others(21): Show |
C | 1 | a0001c0001t0001g0176 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1251-7781_1251-775 others(32): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54372727 | ||||||
chr6:54372730 | ATATATAT others(8): Show |
A | 1 | a0003c0003t0001g0063 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1251-7795_1251-778 others(19): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54372730 | |||||||
chr6:54372731 | T | C | 1 | a0001c0001t0001g0001 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1251-7795T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54372731 | |||||||
chr6:54372733 | T | C | 1 | a0003c0003t0001g0028 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1251-7793T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54372733 | |||||||
chr6:54372747 | TATATATA others(8): Show |
T | 1 | a0003c0003t0001g0065 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1251-7778_1251-776 others(19): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54372747 | |||||||
chr6:54372749 | TATATATA others(6): Show |
T | 4 | a0001c0001t0001g0258 a0001c0001t0001g0261 a0003c0003t0001g0064 others(1): Show |
4 | HG02818.hp1 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1251-7776_1251-776 others(17): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54372749 | |||||||
chr6:54372751 | TATATATA others(4): Show |
T | 5 | a0003c0003t0001g0066 a0003c0003t0001g0068 a0003c0003t0001g0070 others(2): Show |
5 | HG02280.hp2 HG02809.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1251-7774_1251-776 others(15): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54372751 | |||||||
chr6:54372761 | T | C | 1 | a0001c0001t0001g0207 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1251-7765T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54372761 | |||||||
chr6:54372763 | T | C | 38 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0207 others(35): Show |
40 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.1251-7763T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54372763 | |||||||
chr6:54372765 | T | C | 134 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0093 others(131): Show |
140 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(137): Show |
intron_variant | MODIFIER | c.1251-7761T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54372765 | |||||||
chr6:54372767 | T | C | 134 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0093 others(131): Show |
140 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(137): Show |
intron_variant | MODIFIER | c.1251-7759T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54372767 | |||||||
chr6:54372769 | T | C | 134 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0093 others(131): Show |
140 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(137): Show |
intron_variant | MODIFIER | c.1251-7757T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54372769 | |||||||
chr6:54372771 | T | C | 135 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0093 others(132): Show |
141 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(138): Show |
intron_variant | MODIFIER | c.1251-7755T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54372771 | |||||||
chr6:54372778 | A | G | 134 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0093 others(131): Show |
140 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(137): Show |
intron_variant | MODIFIER | c.1251-7748A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54372778 | |||||||
chr6:54372854 | T | C | 1 | a0001c0001t0001g0176 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1251-7672T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54372854 | |||||||
chr6:54372920 | A | G | 1 | a0001c0001t0001g0109 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1251-7606A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54372920 | |||||||
chr6:54372946 | TA | T | 6 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0232 others(3): Show |
6 | HG00735.hp1 HG01934.hp2 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.1251-7575delA | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54372946 | ||||||
chr6:54373035 | G | A | 78 | a0001c0001t0001g0285 a0001c0001t0001g0286 a0001c0001t0001g0308 others(75): Show |
80 | HG00642.hp2 HG01123.hp2 HG01884.hp1 others(77): Show |
intron_variant | MODIFIER | c.1251-7491G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54373035 | |||||||
chr6:54373052 | C | T | 12 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0093 others(9): Show |
14 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(11): Show |
intron_variant | MODIFIER | c.1251-7474C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54373052 | |||||||
chr6:54373210 | T | TTTA | 216 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0011 others(213): Show |
224 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.1251-7315_1251-731 others(7): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54373210 | ||||||
chr6:54373395 | C | T | 1 | a0004c0004t0001g0199 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1251-7131C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54373395 | |||||||
chr6:54373415 | A | T | 3 | a0001c0001t0001g0212 a0001c0001t0001g0214 a0001c0001t0001g0216 |
3 | HG02027.hp1 HG02074.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.1251-7111A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54373415 | |||||||
chr6:54373620 | C | T | 1 | a0002c0002t0001g0074 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1251-6906C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54373620 | |||||||
chr6:54373724 | C | T | 1 | a0001c0001t0001g0237 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1251-6802C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54373724 | |||||||
chr6:54373765 | A | T | 1 | a0017c0018t0001g0242 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1251-6761A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54373765 | |||||||
chr6:54373893 | C | G | 2 | a0014c0014t0003g0276 a0014c0014t0003g0277 |
2 | HG02970.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1251-6633C>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54373893 | |||||||
chr6:54374053 | T | A | 1 | a0001c0001t0001g0245 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1251-6473T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54374053 | |||||||
chr6:54374064 | T | C | 31 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0250 others(28): Show |
33 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.1251-6462T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54374064 | |||||||
chr6:54374110 | T | C | 1 | a0001c0001t0001g0256 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1251-6416T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54374110 | |||||||
chr6:54374129 | T | C | 1 | a0003c0003t0001g0044 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1251-6397T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54374129 | |||||||
chr6:54374171 | T | C | 1 | a0010c0013t0001g0303 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1251-6355T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54374171 | |||||||
chr6:54374215 | C | T | 2 | a0014c0014t0003g0276 a0014c0014t0003g0277 |
2 | HG02970.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1251-6311C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54374215 | |||||||
chr6:54374257 | T | C | 91 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0093 others(88): Show |
95 | HG00642.hp2 HG01123.hp2 HG01884.hp1 others(92): Show |
intron_variant | MODIFIER | c.1251-6269T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54374257 | |||||||
chr6:54374334 | G | A | 2 | a0001c0001t0001g0258 a0001c0001t0001g0261 |
2 | HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1251-6192G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54374334 | |||||||
chr6:54374348 | A | G | 2 | a0001c0010t0001g0244 a0001c0010t0001g0309 |
2 | HG02647.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1251-6178A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54374348 | |||||||
chr6:54374365 | C | A | 3 | a0004c0004t0001g0002 a0004c0004t0001g0192 a0004c0004t0001g0200 |
5 | HG00639.hp2 HG01516.hp1 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.1251-6161C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54374365 | |||||||
chr6:54374411 | T | C | 36 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0207 others(33): Show |
38 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(35): Show |
intron_variant | MODIFIER | c.1251-6115T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54374411 | |||||||
chr6:54374452 | G | A | 91 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0093 others(88): Show |
95 | HG00642.hp2 HG01123.hp2 HG01884.hp1 others(92): Show |
intron_variant | MODIFIER | c.1251-6074G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54374452 | |||||||
chr6:54374507 | C | G | 12 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0093 others(9): Show |
14 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(11): Show |
intron_variant | MODIFIER | c.1251-6019C>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54374507 | |||||||
chr6:54374711 | T | C | 2 | a0001c0010t0001g0244 a0001c0010t0001g0309 |
2 | HG02647.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1251-5815T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54374711 | |||||||
chr6:54374904 | G | GT | 9 | a0001c0001t0001g0285 a0001c0001t0001g0286 a0007c0007t0001g0080 others(6): Show |
9 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.1251-5614dupT | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54374904 | ||||||
chr6:54374987 | G | T | 1 | a0001c0001t0001g0219 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1251-5539G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54374987 | |||||||
chr6:54375032 | A | G | 1 | a0003c0003t0001g0243 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1251-5494A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54375032 | |||||||
chr6:54375250 | C | T | 216 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0011 others(213): Show |
224 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.1251-5276C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54375250 | |||||||
chr6:54375267 | G | A | 1 | a0004c0004t0001g0203 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1251-5259G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54375267 | |||||||
chr6:54375383 | G | A | 2 | a0001c0001t0001g0308 a0001c0001t0001g0310 |
2 | HG03225.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1251-5143G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54375383 | |||||||
chr6:54375493 | T | A | 1 | a0001c0001t0001g0161 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1251-5033T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54375493 | |||||||
chr6:54375555 | A | G | 2 | a0003c0003t0001g0039 a0003c0003t0001g0060 |
2 | HG03017.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1251-4971A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54375555 | |||||||
chr6:54375571 | C | T | 1 | a0004c0021t0004g0201 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1251-4955C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54375571 | |||||||
chr6:54375843 | T | C | 1 | a0001c0001t0001g0100 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1251-4683T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54375843 | |||||||
chr6:54375878 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1251-4648C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54375878 | |||||||
chr6:54375907 | G | T | 1 | a0003c0003t0001g0243 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1251-4619G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54375907 | |||||||
chr6:54375918 | C | T | 2 | a0002c0002t0001g0238 a0002c0002t0001g0355 |
2 | NA18962.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.1251-4608C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54375918 | |||||||
chr6:54375936 | C | T | 2 | a0014c0014t0003g0276 a0014c0014t0003g0277 |
2 | HG02970.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1251-4590C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54375936 | |||||||
chr6:54375974 | C | T | 1 | a0001c0010t0001g0244 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1251-4552C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54375974 | |||||||
chr6:54376017 | A | G | 2 | a0003c0003t0001g0039 a0003c0003t0001g0060 |
2 | HG03017.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1251-4509A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54376017 | |||||||
chr6:54376112 | T | C | 1 | a0017c0018t0001g0242 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1251-4414T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54376112 | |||||||
chr6:54376245 | A | G | 6 | a0002c0002t0001g0008 a0002c0002t0001g0149 a0002c0002t0001g0326 others(3): Show |
7 | NA18951.hp2 NA18963.hp2 NA18971.hp1 others(4): Show |
intron_variant | MODIFIER | c.1251-4281A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54376245 | |||||||
chr6:54376317 | A | G | 4 | a0001c0010t0001g0244 a0001c0010t0001g0309 a0014c0014t0003g0276 others(1): Show |
4 | HG02647.hp2 HG02970.hp1 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.1251-4209A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54376317 | |||||||
chr6:54376565 | T | C | 2 | a0008c0008t0002g0078 a0008c0008t0002g0079 |
2 | HG01069.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.1251-3961T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54376565 | |||||||
chr6:54376688 | A | T | 2 | a0001c0001t0001g0256 a0017c0018t0001g0242 |
2 | HG06807.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1251-3838A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54376688 | |||||||
chr6:54376751 | C | T | 2 | a0001c0001t0001g0245 a0017c0018t0001g0087 |
2 | HG02258.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1251-3775C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54376751 | |||||||
chr6:54376786 | G | T | 2 | a0001c0001t0001g0256 a0017c0018t0001g0242 |
2 | HG06807.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1251-3740G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54376786 | |||||||
chr6:54376795 | T | A | 82 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0038 others(79): Show |
84 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.1251-3731T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54376795 | |||||||
chr6:54376831 | A | G | 3 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0250 |
3 | HG02258.hp2 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1251-3695A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54376831 | |||||||
chr6:54376883 | T | C | 2 | a0014c0014t0003g0276 a0014c0014t0003g0277 |
2 | HG02970.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1251-3643T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54376883 | |||||||
chr6:54376955 | G | A | 4 | a0003c0003t0001g0068 a0003c0003t0001g0070 a0003c0003t0001g0071 others(1): Show |
4 | HG02280.hp2 HG02895.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1251-3571G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54376955 | |||||||
chr6:54376985 | C | T | 1 | a0003c0003t0001g0020 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1251-3541C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54376985 | |||||||
chr6:54377117 | T | C | 29 | a0004c0004t0001g0002 a0004c0004t0001g0076 a0004c0004t0001g0170 others(26): Show |
31 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(28): Show |
intron_variant | MODIFIER | c.1251-3409T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54377117 | |||||||
chr6:54377373 | A | G | 130 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0093 others(127): Show |
136 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(133): Show |
intron_variant | MODIFIER | c.1251-3153A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54377373 | |||||||
chr6:54377387 | T | C | 1 | a0001c0001t0001g0221 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1251-3139T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54377387 | |||||||
chr6:54377443 | C | T | 3 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0175 |
3 | HG02451.hp1 HG02886.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1251-3083C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54377443 | |||||||
chr6:54377454 | A | G | 1 | a0017c0018t0001g0087 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1251-3072A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54377454 | |||||||
chr6:54377513 | G | GAAAT | 48 | a0001c0001t0001g0092 a0001c0001t0001g0177 a0001c0001t0001g0250 others(45): Show |
50 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(47): Show |
intron_variant | MODIFIER | c.1251-2994_1251-299 others(8): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54377513 | ||||||
chr6:54377531 | A | T | 1 | a0002c0002t0001g0336 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1251-2995A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54377531 | |||||||
chr6:54377661 | A | G | 1 | a0001c0001t0001g0256 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1251-2865A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54377661 | |||||||
chr6:54377702 | A | G | 1 | a0003c0003t0001g0243 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1251-2824A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54377702 | |||||||
chr6:54377883 | T | C | 1 | a0004c0021t0004g0201 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1251-2643T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54377883 | |||||||
chr6:54377947 | G | T | 4 | a0001c0001t0001g0282 a0001c0001t0001g0287 a0001c0001t0001g0288 others(1): Show |
4 | HG02572.hp2 HG02922.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1251-2579G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54377947 | |||||||
chr6:54377967 | A | AT | 6 | a0001c0001t0001g0038 a0001c0001t0001g0097 a0001c0001t0001g0302 others(3): Show |
6 | HG02647.hp2 HG03831.hp2 HG04204.hp1 others(3): Show |
intron_variant | MODIFIER | c.1251-2549dupT | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54377967 | ||||||
chr6:54378107 | T | C | 1 | a0007c0007t0001g0086 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1251-2419T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54378107 | |||||||
chr6:54378226 | T | A | 2 | a0002c0002t0001g0013 a0002c0002t0001g0293 |
3 | HG02622.hp1 HG02717.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1251-2300T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54378226 | |||||||
chr6:54378233 | A | T | 1 | a0004c0021t0004g0201 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1251-2293A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54378233 | |||||||
chr6:54378253 | T | C | 1 | a0007c0007t0001g0080 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1251-2273T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54378253 | |||||||
chr6:54378354 | G | A | 4 | a0002c0002t0001g0342 a0002c0002t0001g0346 a0002c0002t0001g0347 others(1): Show |
4 | NA18939.hp1 NA18988.hp1 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.1251-2172G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54378354 | |||||||
chr6:54378385 | C | T | 1 | a0002c0002t0001g0118 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1251-2141C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54378385 | |||||||
chr6:54378429 | A | G | 2 | a0016c0017t0001g0274 a0016c0017t0001g0275 |
2 | HG03225.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1251-2097A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54378429 | |||||||
chr6:54378443 | T | C | 2 | a0003c0003t0001g0024 a0003c0003t0001g0025 |
2 | NA18967.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1251-2083T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54378443 | |||||||
chr6:54378604 | G | A | 84 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0038 others(81): Show |
86 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.1251-1922G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54378604 | |||||||
chr6:54378607 | C | T | 1 | a0001c0001t0001g0140 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1251-1919C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54378607 | |||||||
chr6:54378817 | C | T | 1 | a0001c0001t0001g0168 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1251-1709C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54378817 | |||||||
chr6:54378896 | A | T | 1 | a0001c0001t0001g0121 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1251-1630A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54378896 | |||||||
chr6:54379123 | T | C | 1 | a0001c0001t0001g0207 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1251-1403T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54379123 | |||||||
chr6:54379200 | A | G | 88 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0038 others(85): Show |
90 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.1251-1326A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54379200 | |||||||
chr6:54379256 | G | A | 1 | a0001c0001t0001g0092 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1251-1270G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54379256 | |||||||
chr6:54379330 | A | G | 77 | a0001c0001t0001g0285 a0001c0001t0001g0286 a0001c0001t0001g0308 others(74): Show |
79 | HG00642.hp2 HG01123.hp2 HG01884.hp1 others(76): Show |
intron_variant | MODIFIER | c.1251-1196A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54379330 | |||||||
chr6:54379394 | A | G | 88 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0093 others(85): Show |
92 | HG00642.hp2 HG01123.hp2 HG01884.hp1 others(89): Show |
intron_variant | MODIFIER | c.1251-1132A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54379394 | |||||||
chr6:54379414 | G | A | 1 | a0002c0002t0001g0325 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1251-1112G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54379414 | |||||||
chr6:54379516 | C | T | 2 | a0001c0001t0001g0119 a0001c0001t0001g0137 |
2 | HG01496.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.1251-1010C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54379516 | |||||||
chr6:54379762 | T | A | 2 | a0015c0015t0001g0279 a0015c0015t0001g0280 |
2 | HG03130.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1251-764T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54379762 | |||||||
chr6:54379785 | T | A | 14 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0186 others(11): Show |
14 | HG00735.hp1 HG01934.hp2 HG01952.hp2 others(11): Show |
intron_variant | MODIFIER | c.1251-741T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54379785 | |||||||
chr6:54379829 | G | A | 86 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0038 others(83): Show |
88 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.1251-697G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54379829 | |||||||
chr6:54379986 | G | A | 2 | a0014c0014t0003g0276 a0014c0014t0003g0277 |
2 | HG02970.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1251-540G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54379986 | |||||||
chr6:54380034 | G | A | 1 | a0003c0003t0001g0243 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1251-492G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54380034 | |||||||
chr6:54380034 | G | T | 1 | a0003c0003t0001g0070 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1251-492G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54380034 | |||||||
chr6:54380167 | C | T | 4 | a0003c0003t0001g0064 a0003c0003t0001g0065 a0003c0003t0001g0066 others(1): Show |
4 | HG02809.hp1 HG02818.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1251-359C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54380167 | |||||||
chr6:54380177 | T | C | 10 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0093 others(7): Show |
12 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.1251-349T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54380177 | |||||||
chr6:54380267 | T | TC | 85 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0038 others(82): Show |
87 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.1251-258dupC | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 54380267 | ||||||
chr6:54380381 | G | A | 1 | a0004c0021t0004g0201 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1251-145G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54380381 | |||||||
chr6:54380472 | A | G | 15 | a0001c0001t0001g0092 a0001c0001t0001g0177 a0001c0001t0001g0281 others(12): Show |
15 | HG00099.hp1 HG01261.hp1 HG01358.hp1 others(12): Show |
intron_variant | MODIFIER | c.1251-54A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54380472 | |||||||
chr6:54380484 | C | T | 1 | a0001c0001t0001g0256 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1251-42C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 9/10 | chr6 | 54380484 | |||||||
chr6:54380594 | A | T | 1 | a0009c0016t0001g0240 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1296+23A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54380594 | |||||||
chr6:54380650 | T | C | 3 | a0002c0002t0001g0251 a0002c0002t0001g0252 a0002c0002t0001g0284 |
3 | HG02630.hp2 HG03471.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1296+79T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54380650 | |||||||
chr6:54380667 | C | T | 1 | a0001c0001t0001g0225 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1296+96C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54380667 | |||||||
chr6:54380705 | G | A | 90 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0093 others(87): Show |
94 | HG00642.hp2 HG01123.hp2 HG01884.hp1 others(91): Show |
intron_variant | MODIFIER | c.1296+134G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54380705 | |||||||
chr6:54380892 | A | G | 1 | a0002c0002t0001g0341 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1296+321A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54380892 | |||||||
chr6:54380894 | A | G | 31 | a0001c0001t0001g0100 a0001c0001t0001g0102 a0001c0001t0001g0103 others(28): Show |
33 | HG00408.hp2 HG00621.hp1 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.1296+323A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54380894 | |||||||
chr6:54380963 | T | C | 3 | a0001c0001t0001g0256 a0004c0021t0004g0201 a0017c0018t0001g0242 |
3 | HG03516.hp1 HG06807.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1296+392T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54380963 | |||||||
chr6:54380980 | G | GAT | 23 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0093 others(20): Show |
25 | HG01884.hp1 HG01891.hp1 HG02027.hp1 others(22): Show |
intron_variant | MODIFIER | c.1296+422_1296+423d others(4): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr6 | 54380980 | ||||||
chr6:54380980 | G | GATAT | 66 | a0002c0002t0001g0008 a0002c0002t0001g0013 a0002c0002t0001g0074 others(63): Show |
68 | HG00642.hp2 HG01123.hp2 HG02056.hp2 others(65): Show |
intron_variant | MODIFIER | c.1296+420_1296+423d others(6): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr6 | 54380980 | ||||||
chr6:54381006 | A | G | 2 | a0015c0015t0001g0279 a0015c0015t0001g0280 |
2 | HG03130.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1296+435A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54381006 | |||||||
chr6:54381042 | A | G | 1 | a0005c0005t0001g0270 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1296+471A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54381042 | |||||||
chr6:54381059 | C | T | 93 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0093 others(90): Show |
97 | HG00642.hp2 HG01123.hp2 HG01884.hp1 others(94): Show |
intron_variant | MODIFIER | c.1296+488C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54381059 | |||||||
chr6:54381094 | G | T | 98 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0093 others(95): Show |
102 | HG00642.hp2 HG01123.hp2 HG01884.hp1 others(99): Show |
intron_variant | MODIFIER | c.1296+523G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54381094 | |||||||
chr6:54381103 | T | C | 1 | a0003c0003t0001g0243 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1296+532T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54381103 | |||||||
chr6:54381110 | A | ATATGTAA others(51): Show |
1 | a0001c0001t0001g0256 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1296+550_1296+551i others(60): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr6 | 54381110 | ||||||
chr6:54381122 | C | T | 132 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0093 others(129): Show |
138 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.1296+551C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54381122 | |||||||
chr6:54381170 | CT | C | 79 | a0001c0001t0001g0285 a0001c0001t0001g0286 a0001c0001t0001g0308 others(76): Show |
81 | HG00642.hp2 HG01123.hp2 HG01884.hp1 others(78): Show |
intron_variant | MODIFIER | c.1296+609delT | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr6 | 54381170 | ||||||
chr6:54381358 | CT | C | 260 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(257): Show |
269 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.1296+794delT | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr6 | 54381358 | ||||||
chr6:54381384 | C | T | 1 | a0008c0008t0002g0072 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1296+813C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54381384 | |||||||
chr6:54381408 | A | G | 2 | a0001c0010t0001g0244 a0001c0010t0001g0309 |
2 | HG02647.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1296+837A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54381408 | |||||||
chr6:54381685 | T | G | 3 | a0003c0003t0001g0022 a0003c0003t0001g0023 a0003c0003t0001g0036 |
3 | NA18941.hp2 NA18953.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.1296+1114T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54381685 | |||||||
chr6:54381721 | T | G | 1 | a0004c0021t0004g0201 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1296+1150T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54381721 | |||||||
chr6:54381727 | A | G | 2 | a0015c0015t0001g0279 a0015c0015t0001g0280 |
2 | HG03130.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1296+1156A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54381727 | |||||||
chr6:54381761 | T | C | 1 | a0012c0009t0001g0208 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1296+1190T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54381761 | |||||||
chr6:54381789 | G | A | 1 | a0010c0013t0001g0303 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1296+1218G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54381789 | |||||||
chr6:54381854 | A | G | 1 | a0001c0001t0001g0099 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1296+1283A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54381854 | |||||||
chr6:54381866 | T | A | 5 | a0006c0006t0002g0295 a0008c0008t0002g0072 a0008c0008t0002g0078 others(2): Show |
5 | HG01069.hp1 HG01243.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1296+1295T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54381866 | |||||||
chr6:54381867 | C | T | 1 | a0001c0001t0001g0230 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1296+1296C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54381867 | |||||||
chr6:54381915 | T | A | 33 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0250 others(30): Show |
35 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(32): Show |
intron_variant | MODIFIER | c.1296+1344T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54381915 | |||||||
chr6:54381967 | A | T | 78 | a0001c0001t0001g0285 a0001c0001t0001g0286 a0001c0001t0001g0308 others(75): Show |
80 | HG00642.hp2 HG01123.hp2 HG01884.hp1 others(77): Show |
intron_variant | MODIFIER | c.1296+1396A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54381967 | |||||||
chr6:54382025 | G | A | 3 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0300 |
3 | HG01515.hp1 HG01517.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.1296+1454G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54382025 | |||||||
chr6:54382114 | C | T | 1 | a0004c0021t0004g0201 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1296+1543C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54382114 | |||||||
chr6:54382198 | T | C | 1 | a0009c0016t0001g0241 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1296+1627T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54382198 | |||||||
chr6:54382254 | T | G | 4 | a0014c0014t0003g0276 a0014c0014t0003g0277 a0015c0015t0001g0279 others(1): Show |
4 | HG02970.hp1 HG03130.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1296+1683T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54382254 | |||||||
chr6:54382382 | G | T | 1 | a0001c0001t0001g0282 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1296+1811G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54382382 | |||||||
chr6:54382482 | A | C | 10 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0093 others(7): Show |
12 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.1296+1911A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54382482 | |||||||
chr6:54382489 | C | T | 1 | a0002c0002t0001g0335 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1296+1918C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54382489 | |||||||
chr6:54382536 | T | C | 1 | a0001c0001t0001g0245 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1296+1965T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54382536 | |||||||
chr6:54382669 | A | C | 98 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0093 others(95): Show |
102 | HG00642.hp2 HG01123.hp2 HG01884.hp1 others(99): Show |
intron_variant | MODIFIER | c.1296+2098A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54382669 | |||||||
chr6:54382743 | A | G | 4 | a0014c0014t0003g0276 a0014c0014t0003g0277 a0015c0015t0001g0279 others(1): Show |
4 | HG02970.hp1 HG03130.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1296+2172A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54382743 | |||||||
chr6:54382751 | T | A | 2 | a0012c0009t0001g0208 a0012c0009t0001g0209 |
2 | HG02109.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1296+2180T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54382751 | |||||||
chr6:54382771 | G | T | 94 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0093 others(91): Show |
98 | HG00642.hp2 HG01123.hp2 HG01884.hp1 others(95): Show |
intron_variant | MODIFIER | c.1296+2200G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54382771 | |||||||
chr6:54382886 | G | C | 2 | a0015c0015t0001g0279 a0015c0015t0001g0280 |
2 | HG03130.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1296+2315G>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54382886 | |||||||
chr6:54383063 | G | A | 1 | a0005c0005t0001g0270 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1296+2492G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54383063 | |||||||
chr6:54383157 | A | G | 1 | a0001c0001t0001g0183 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1296+2586A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54383157 | |||||||
chr6:54383370 | T | C | 15 | a0001c0001t0001g0092 a0001c0001t0001g0177 a0001c0001t0001g0281 others(12): Show |
15 | HG00099.hp1 HG01261.hp1 HG01358.hp1 others(12): Show |
intron_variant | MODIFIER | c.1296+2799T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54383370 | |||||||
chr6:54383384 | T | C | 1 | a0001c0001t0001g0283 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1296+2813T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54383384 | |||||||
chr6:54383416 | A | G | 1 | a0004c0021t0004g0201 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1296+2845A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54383416 | |||||||
chr6:54383504 | C | T | 2 | a0001c0010t0001g0244 a0001c0010t0001g0309 |
2 | HG02647.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1296+2933C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54383504 | |||||||
chr6:54383881 | C | G | 4 | a0014c0014t0003g0276 a0014c0014t0003g0277 a0015c0015t0001g0279 others(1): Show |
4 | HG02970.hp1 HG03130.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1296+3310C>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54383881 | |||||||
chr6:54384001 | C | T | 7 | a0001c0001t0001g0011 a0001c0001t0001g0210 a0001c0001t0001g0212 others(4): Show |
8 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(5): Show |
intron_variant | MODIFIER | c.1296+3430C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54384001 | |||||||
chr6:54384009 | A | T | 83 | a0001c0001t0001g0285 a0001c0001t0001g0286 a0001c0001t0001g0308 others(80): Show |
85 | HG00642.hp2 HG01123.hp2 HG01884.hp1 others(82): Show |
intron_variant | MODIFIER | c.1296+3438A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54384009 | |||||||
chr6:54384016 | C | T | 1 | a0001c0001t0001g0257 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1296+3445C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54384016 | |||||||
chr6:54384098 | C | T | 79 | a0001c0001t0001g0285 a0001c0001t0001g0286 a0001c0001t0001g0308 others(76): Show |
81 | HG00642.hp2 HG01123.hp2 HG01884.hp1 others(78): Show |
intron_variant | MODIFIER | c.1296+3527C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54384098 | |||||||
chr6:54384255 | T | C | 2 | a0001c0001t0001g0177 a0001c0001t0001g0281 |
2 | HG02897.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1296+3684T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54384255 | |||||||
chr6:54384284 | G | A | 33 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0250 others(30): Show |
35 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(32): Show |
intron_variant | MODIFIER | c.1296+3713G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54384284 | |||||||
chr6:54384314 | G | T | 2 | a0004c0004t0001g0192 a0004c0004t0001g0200 |
2 | HG00639.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.1296+3743G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54384314 | |||||||
chr6:54384417 | G | A | 3 | a0001c0010t0001g0244 a0001c0010t0001g0309 a0002c0002t0001g0350 |
3 | HG02647.hp2 HG03831.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1296+3846G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54384417 | |||||||
chr6:54384480 | T | C | 2 | a0001c0001t0001g0113 a0005c0005t0001g0239 |
2 | HG01243.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.1296+3909T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54384480 | |||||||
chr6:54384646 | T | C | 2 | a0014c0014t0003g0276 a0014c0014t0003g0277 |
2 | HG02970.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1296+4075T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54384646 | |||||||
chr6:54384839 | T | C | 1 | a0001c0001t0001g0207 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1296+4268T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54384839 | |||||||
chr6:54384871 | A | G | 79 | a0001c0001t0001g0285 a0001c0001t0001g0286 a0001c0001t0001g0308 others(76): Show |
81 | HG00642.hp2 HG01123.hp2 HG01884.hp1 others(78): Show |
intron_variant | MODIFIER | c.1296+4300A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54384871 | |||||||
chr6:54384956 | A | G | 1 | a0003c0003t0001g0046 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1296+4385A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54384956 | |||||||
chr6:54385031 | A | G | 1 | a0005c0005t0001g0264 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1296+4460A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54385031 | |||||||
chr6:54385056 | A | G | 1 | a0001c0001t0001g0257 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1296+4485A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54385056 | |||||||
chr6:54385070 | T | C | 4 | a0014c0014t0003g0276 a0014c0014t0003g0277 a0015c0015t0001g0279 others(1): Show |
4 | HG02970.hp1 HG03130.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1296+4499T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54385070 | |||||||
chr6:54385226 | G | T | 4 | a0014c0014t0003g0276 a0014c0014t0003g0277 a0015c0015t0001g0279 others(1): Show |
4 | HG02970.hp1 HG03130.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1297-4565G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54385226 | |||||||
chr6:54385296 | G | T | 1 | a0001c0001t0001g0215 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1297-4495G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54385296 | |||||||
chr6:54385359 | T | G | 2 | a0001c0010t0001g0244 a0001c0010t0001g0309 |
2 | HG02647.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1297-4432T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54385359 | |||||||
chr6:54385480 | G | GA | 113 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(110): Show |
116 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.1297-4301dupA | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr6 | 54385480 | ||||||
chr6:54385480 | GA | G | 46 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0250 others(43): Show |
48 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.1297-4301delA | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr6 | 54385480 | ||||||
chr6:54385674 | A | G | 2 | a0002c0002t0001g0145 a0002c0002t0001g0352 |
2 | HG00642.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.1297-4117A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54385674 | |||||||
chr6:54385704 | G | A | 2 | a0002c0002t0001g0313 a0002c0002t0001g0314 |
2 | NA18967.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1297-4087G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54385704 | |||||||
chr6:54385778 | A | C | 1 | a0004c0021t0004g0201 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1297-4013A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54385778 | |||||||
chr6:54385801 | T | C | 1 | a0021c0026t0001g0082 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1297-3990T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54385801 | |||||||
chr6:54385879 | A | AT | 111 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(108): Show |
116 | HG00140.hp1 HG00621.hp1 HG00639.hp2 others(113): Show |
intron_variant | MODIFIER | c.1297-3887dupT | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr6 | 54385879 | ||||||
chr6:54385879 | A | ATT | 66 | a0001c0001t0001g0009 a0001c0001t0001g0090 a0001c0001t0001g0091 others(63): Show |
67 | HG00280.hp1 HG00438.hp2 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.1297-3888_1297-388 others(6): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr6 | 54385879 | ||||||
chr6:54385879 | A | ATTT | 18 | a0001c0001t0001g0075 a0001c0001t0001g0162 a0001c0001t0001g0194 others(15): Show |
18 | HG00642.hp2 HG01243.hp1 HG01934.hp2 others(15): Show |
intron_variant | MODIFIER | c.1297-3889_1297-388 others(7): Show |
TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr6 | 54385879 | ||||||
chr6:54385879 | AT | A | 6 | a0001c0001t0001g0184 a0001c0001t0001g0217 a0001c0001t0001g0245 others(3): Show |
6 | HG02258.hp1 HG03471.hp2 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.1297-3887delT | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr6 | 54385879 | ||||||
chr6:54385880 | T | A | 1 | a0004c0021t0004g0201 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1297-3911T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54385880 | |||||||
chr6:54386040 | C | A | 1 | a0001c0001t0001g0207 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1297-3751C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54386040 | |||||||
chr6:54386063 | C | T | 100 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0093 others(97): Show |
104 | HG00642.hp2 HG01123.hp2 HG01884.hp1 others(101): Show |
intron_variant | MODIFIER | c.1297-3728C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54386063 | |||||||
chr6:54386095 | C | T | 2 | a0001c0010t0001g0244 a0001c0010t0001g0309 |
2 | HG02647.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1297-3696C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54386095 | |||||||
chr6:54386103 | C | G | 2 | a0001c0001t0001g0038 a0001c0001t0001g0097 |
2 | HG03831.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1297-3688C>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54386103 | |||||||
chr6:54386187 | G | A | 1 | a0001c0001t0001g0288 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1297-3604G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54386187 | |||||||
chr6:54386264 | T | C | 1 | a0001c0001t0001g0207 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1297-3527T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54386264 | |||||||
chr6:54386358 | A | C | 113 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(110): Show |
116 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.1297-3433A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54386358 | |||||||
chr6:54386360 | G | C | 3 | a0003c0003t0001g0070 a0003c0003t0001g0071 a0005c0005t0001g0278 |
3 | HG02895.hp1 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1297-3431G>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54386360 | |||||||
chr6:54386526 | C | T | 10 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0093 others(7): Show |
12 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.1297-3265C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54386526 | |||||||
chr6:54386557 | A | T | 2 | a0001c0001t0001g0038 a0001c0001t0001g0097 |
2 | HG03831.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1297-3234A>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54386557 | |||||||
chr6:54386699 | G | A | 1 | a0002c0002t0001g0333 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1297-3092G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54386699 | |||||||
chr6:54386719 | C | T | 1 | a0001c0001t0001g0256 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1297-3072C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54386719 | |||||||
chr6:54386744 | A | C | 99 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0093 others(96): Show |
103 | HG00642.hp2 HG01123.hp2 HG01884.hp1 others(100): Show |
intron_variant | MODIFIER | c.1297-3047A>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54386744 | |||||||
chr6:54386748 | C | A | 1 | a0004c0021t0004g0201 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1297-3043C>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54386748 | |||||||
chr6:54386893 | T | C | 10 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0093 others(7): Show |
12 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.1297-2898T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54386893 | |||||||
chr6:54387272 | G | T | 1 | a0001c0001t0001g0281 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1297-2519G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54387272 | |||||||
chr6:54387323 | G | C | 2 | a0001c0001t0001g0177 a0001c0001t0001g0281 |
2 | HG02897.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1297-2468G>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54387323 | |||||||
chr6:54387426 | G | T | 2 | a0012c0009t0001g0208 a0012c0009t0001g0209 |
2 | HG02109.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1297-2365G>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54387426 | |||||||
chr6:54387464 | TA | T | 94 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0093 others(91): Show |
98 | HG00642.hp2 HG01123.hp2 HG01884.hp1 others(95): Show |
intron_variant | MODIFIER | c.1297-2319delA | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr6 | 54387464 | ||||||
chr6:54387494 | A | G | 82 | a0001c0001t0001g0285 a0001c0001t0001g0286 a0001c0001t0001g0308 others(79): Show |
84 | HG00642.hp2 HG01123.hp2 HG01884.hp1 others(81): Show |
intron_variant | MODIFIER | c.1297-2297A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54387494 | |||||||
chr6:54387531 | C | G | 4 | a0014c0014t0003g0276 a0014c0014t0003g0277 a0015c0015t0001g0279 others(1): Show |
4 | HG02970.hp1 HG03130.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1297-2260C>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54387531 | |||||||
chr6:54387653 | T | A | 77 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0038 others(74): Show |
79 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.1297-2138T>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54387653 | |||||||
chr6:54387762 | C | T | 1 | a0017c0018t0001g0087 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1297-2029C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54387762 | |||||||
chr6:54387800 | A | G | 1 | a0004c0021t0004g0201 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1297-1991A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54387800 | |||||||
chr6:54387918 | T | G | 2 | a0001c0010t0001g0244 a0001c0010t0001g0309 |
2 | HG02647.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1297-1873T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54387918 | |||||||
chr6:54387975 | G | A | 2 | a0001c0001t0001g0102 a0001c0001t0001g0103 |
2 | HG00741.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.1297-1816G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54387975 | |||||||
chr6:54388241 | A | G | 1 | a0003c0003t0001g0163 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1297-1550A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54388241 | |||||||
chr6:54388283 | C | T | 79 | a0001c0001t0001g0285 a0001c0001t0001g0286 a0001c0001t0001g0308 others(76): Show |
81 | HG00642.hp2 HG01123.hp2 HG01884.hp1 others(78): Show |
intron_variant | MODIFIER | c.1297-1508C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54388283 | |||||||
chr6:54388359 | G | A | 2 | a0001c0001t0001g0308 a0001c0001t0001g0310 |
2 | HG03225.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1297-1432G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54388359 | |||||||
chr6:54388398 | C | G | 131 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0093 others(128): Show |
137 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.1297-1393C>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54388398 | |||||||
chr6:54388580 | C | T | 6 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0175 others(3): Show |
6 | HG02451.hp1 HG02630.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1297-1211C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54388580 | |||||||
chr6:54388581 | G | A | 9 | a0003c0003t0001g0043 a0003c0003t0001g0046 a0003c0003t0001g0047 others(6): Show |
9 | HG00099.hp1 HG01261.hp1 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.1297-1210G>A | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54388581 | |||||||
chr6:54388731 | C | T | 2 | a0001c0001t0001g0245 a0017c0018t0001g0087 |
2 | HG02258.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1297-1060C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54388731 | |||||||
chr6:54388821 | A | G | 1 | a0001c0001t0001g0207 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1297-970A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54388821 | |||||||
chr6:54389132 | A | G | 37 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0250 others(34): Show |
39 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.1297-659A>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54389132 | |||||||
chr6:54389175 | T | C | 7 | a0001c0001t0001g0011 a0001c0001t0001g0210 a0001c0001t0001g0212 others(4): Show |
8 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(5): Show |
intron_variant | MODIFIER | c.1297-616T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54389175 | |||||||
chr6:54389227 | C | T | 1 | a0003c0003t0001g0047 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1297-564C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54389227 | |||||||
chr6:54389301 | T | C | 38 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0250 others(35): Show |
40 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.1297-490T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54389301 | |||||||
chr6:54389325 | C | T | 10 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0093 others(7): Show |
12 | HG02027.hp1 HG02071.hp2 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.1297-466C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54389325 | |||||||
chr6:54389537 | C | T | 1 | a0017c0018t0001g0242 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1297-254C>T | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54389537 | |||||||
chr6:54389776 | T | C | 1 | a0001c0001t0001g0143 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1297-15T>C | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54389776 | |||||||
chr6:54389782 | T | G | 67 | a0002c0002t0001g0008 a0002c0002t0001g0013 a0002c0002t0001g0074 others(64): Show |
69 | HG00642.hp2 HG01123.hp2 HG02056.hp2 others(66): Show |
intron_variant | MODIFIER | c.1297-9T>G | TINAG | ENSG00000137251.16 | transcript | ENST00000259782.9 | protein_coding | 10/10 | chr6 | 54389782 |