Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 923 |
| ensemblid | ENSG00000013725.14 |
| hgncid | 1691 |
| symbol | CD6 |
| name | CD6 molecule |
| refseq_nuc | NM_006725.5 |
| refseq_prot | NP_006716.3 |
| ensembl_nuc | ENST00000313421.11 |
| ensembl_prot | ENSP00000323280.7 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 60971680 |
| end | 61020377 |
| strand | + |
| ver | v1.2 |
| region | chr11:60971680-61020377 |
| region5000 | chr11:60966680-61025377 |
| regionname0 | CD6_chr11_60971680_61020377 |
| regionname5000 | CD6_chr11_60966680_61025377 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 668 | 112 | 30 | 17 | 48 | 6 | 10 | 32 | CD6_chr11_60966680_61025377 | CD6 | MWLFF others(663): Show |
chr11 | 60966680 | 61025377 |
| a0002 | 0/0 | 668 | 90 | 46 | 18 | 17 | 1 | 8 | 11 | CD6_chr11_60966680_61025377 | CD6 | MWLFF others(663): Show |
chr11 | 60966680 | 61025377 |
| a0003 | 0/0 | 668 | 31 | 6 | 1 | 17 | 0 | 7 | 11 | CD6_chr11_60966680_61025377 | CD6 | MWLFF others(663): Show |
chr11 | 60966680 | 61025377 |
| a0004 | 0/1 | 668 | 27 | 4 | 14 | 0 | 3 | 5 | 0 | CD6_chr11_60966680_61025377 | CD6 | MWLFF others(663): Show |
chr11 | 60966680 | 61025377 |
| a0005 | 0/0 | 668 | 21 | 1 | 12 | 3 | 1 | 4 | 1 | CD6_chr11_60966680_61025377 | CD6 | MWLFF others(663): Show |
chr11 | 60966680 | 61025377 |
| a0006 | 0/0 | 668 | 8 | 0 | 0 | 6 | 0 | 2 | 4 | CD6_chr11_60966680_61025377 | CD6 | MWLFF others(663): Show |
chr11 | 60966680 | 61025377 |
| a0007 | 0/0 | 668 | 5 | 1 | 2 | 0 | 0 | 2 | 0 | CD6_chr11_60966680_61025377 | CD6 | MWLFF others(663): Show |
chr11 | 60966680 | 61025377 |
| a0008 | 0/0 | 668 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | CD6_chr11_60966680_61025377 | CD6 | MWLFF others(663): Show |
chr11 | 60966680 | 61025377 |
| a0009 | 0/0 | 668 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | MWLFF others(663): Show |
chr11 | 60966680 | 61025377 |
| a0010 | 0/0 | 668 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CD6_chr11_60966680_61025377 | CD6 | MWLFF others(663): Show |
chr11 | 60966680 | 61025377 |
| a0011 | 0/0 | 668 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | MWLFF others(663): Show |
chr11 | 60966680 | 61025377 |
| a0012 | 0/0 | 668 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CD6_chr11_60966680_61025377 | CD6 | MWLFF others(663): Show |
chr11 | 60966680 | 61025377 |
| a0013 | 0/0 | 668 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | MWLFF others(663): Show |
chr11 | 60966680 | 61025377 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 2004 | 84 | 6 | 15 | 47 | 6 | 9 | CD6_chr11_60966680_61025377 | CD6 | ATGTG others(1999): Show |
chr11 | 60966680 | 61025377 | ||
| a0001c0007 | 0/0 | 2004 | 20 | 20 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | ATGTG others(1999): Show |
chr11 | 60966680 | 61025377 | ||
| a0001c0010 | 0/0 | 2004 | 5 | 4 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | ATGTG others(1999): Show |
chr11 | 60966680 | 61025377 | ||
| a0001c0014 | 0/0 | 2004 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | ATGTG others(1999): Show |
chr11 | 60966680 | 61025377 | ||
| a0001c0018 | 0/0 | 2004 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | ATGTG others(1999): Show |
chr11 | 60966680 | 61025377 | ||
| a0001c0019 | 0/0 | 2004 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | ATGTG others(1999): Show |
chr11 | 60966680 | 61025377 | ||
| a0002c0002 | 0/0 | 2004 | 43 | 24 | 4 | 14 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | ATGTG others(1999): Show |
chr11 | 60966680 | 61025377 | ||
| a0002c0003 | 0/0 | 2004 | 41 | 17 | 14 | 3 | 1 | 6 | CD6_chr11_60966680_61025377 | CD6 | ATGTG others(1999): Show |
chr11 | 60966680 | 61025377 | ||
| a0002c0009 | 0/0 | 2004 | 5 | 5 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | ATGTG others(1999): Show |
chr11 | 60966680 | 61025377 | ||
| a0002c0016 | 0/0 | 2004 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | ATGTG others(1999): Show |
chr11 | 60966680 | 61025377 | ||
| a0003c0005 | 0/0 | 2004 | 26 | 1 | 1 | 17 | 0 | 7 | CD6_chr11_60966680_61025377 | CD6 | ATGTG others(1999): Show |
chr11 | 60966680 | 61025377 | ||
| a0003c0011 | 0/0 | 2004 | 5 | 5 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | ATGTG others(1999): Show |
chr11 | 60966680 | 61025377 | ||
| a0004c0004 | 0/1 | 2004 | 27 | 4 | 14 | 0 | 3 | 5 | CD6_chr11_60966680_61025377 | CD6 | ATGTG others(1999): Show |
chr11 | 60966680 | 61025377 | ||
| a0005c0006 | 0/0 | 2004 | 21 | 1 | 12 | 3 | 1 | 4 | CD6_chr11_60966680_61025377 | CD6 | ATGTG others(1999): Show |
chr11 | 60966680 | 61025377 | ||
| a0006c0008 | 0/0 | 2004 | 8 | 0 | 0 | 6 | 0 | 2 | CD6_chr11_60966680_61025377 | CD6 | ATGTG others(1999): Show |
chr11 | 60966680 | 61025377 | ||
| a0007c0012 | 0/0 | 2004 | 5 | 1 | 2 | 0 | 0 | 2 | CD6_chr11_60966680_61025377 | CD6 | ATGTG others(1999): Show |
chr11 | 60966680 | 61025377 | ||
| a0008c0013 | 0/0 | 2004 | 3 | 0 | 0 | 3 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | ATGTG others(1999): Show |
chr11 | 60966680 | 61025377 | ||
| a0009c0021 | 0/0 | 2004 | 1 | 0 | 0 | 0 | 1 | 0 | CD6_chr11_60966680_61025377 | CD6 | ATGTG others(1999): Show |
chr11 | 60966680 | 61025377 | ||
| a0010c0020 | 0/0 | 2004 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | ATGTG others(1999): Show |
chr11 | 60966680 | 61025377 | ||
| a0011c0015 | 0/0 | 2004 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | ATGTG others(1999): Show |
chr11 | 60966680 | 61025377 | ||
| a0012c0022 | 0/0 | 2004 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | ATGTG others(1999): Show |
chr11 | 60966680 | 61025377 | ||
| a0013c0017 | 0/0 | 2004 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | ATGTG others(1999): Show |
chr11 | 60966680 | 61025377 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3252 | 79 | 3 | 14 | 46 | 6 | 9 | CD6_chr11_60966680_61025377 | CD6 | ACTCA others(3247): Show |
chr11 | 60966680 | 61025377 |
| a0001c0001t0007 | 0/0 | 3252 | 2 | 2 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | ACTCA others(3247): Show |
chr11 | 60966680 | 61025377 |
| a0001c0001t0008 | 0/0 | 3252 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | ACTCA others(3247): Show |
chr11 | 60966680 | 61025377 |
| a0001c0001t0009 | 0/0 | 3252 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | ACTCA others(3247): Show |
chr11 | 60966680 | 61025377 |
| a0001c0001t0011 | 0/0 | 3252 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | ACTCA others(3247): Show |
chr11 | 60966680 | 61025377 |
| a0001c0007t0001 | 0/0 | 3252 | 15 | 15 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | ACTCA others(3247): Show |
chr11 | 60966680 | 61025377 |
| a0001c0007t0002 | 0/0 | 3252 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | ACTCA others(3247): Show |
chr11 | 60966680 | 61025377 |
| a0001c0007t0005 | 0/0 | 3252 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | ACTCA others(3247): Show |
chr11 | 60966680 | 61025377 |
| a0001c0007t0006 | 0/0 | 3252 | 2 | 2 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | ACTCA others(3247): Show |
chr11 | 60966680 | 61025377 |
| a0001c0007t0012 | 0/0 | 3252 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | ACTCA others(3247): Show |
chr11 | 60966680 | 61025377 |
| a0001c0010t0002 | 0/0 | 3252 | 5 | 4 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | ACTCA others(3247): Show |
chr11 | 60966680 | 61025377 |
| a0001c0014t0001 | 0/0 | 3252 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | ACTCA others(3247): Show |
chr11 | 60966680 | 61025377 |
| a0001c0018t0001 | 0/0 | 3252 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | ACTCA others(3247): Show |
chr11 | 60966680 | 61025377 |
| a0001c0019t0013 | 0/0 | 3252 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | ACTCA others(3247): Show |
chr11 | 60966680 | 61025377 |
| a0002c0002t0001 | 0/0 | 3252 | 42 | 23 | 4 | 14 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | ACTCA others(3247): Show |
chr11 | 60966680 | 61025377 |
| a0002c0002t0014 | 0/0 | 3252 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | ACTCA others(3247): Show |
chr11 | 60966680 | 61025377 |
| a0002c0003t0001 | 0/0 | 3252 | 41 | 17 | 14 | 3 | 1 | 6 | CD6_chr11_60966680_61025377 | CD6 | ACTCA others(3247): Show |
chr11 | 60966680 | 61025377 |
| a0002c0009t0001 | 0/0 | 3252 | 5 | 5 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | ACTCA others(3247): Show |
chr11 | 60966680 | 61025377 |
| a0002c0016t0001 | 0/0 | 3252 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | ACTCA others(3247): Show |
chr11 | 60966680 | 61025377 |
| a0003c0005t0001 | 0/0 | 3252 | 26 | 1 | 1 | 17 | 0 | 7 | CD6_chr11_60966680_61025377 | CD6 | ACTCA others(3247): Show |
chr11 | 60966680 | 61025377 |
| a0003c0011t0001 | 0/0 | 3252 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | ACTCA others(3247): Show |
chr11 | 60966680 | 61025377 |
| a0003c0011t0004 | 0/0 | 3252 | 3 | 3 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | ACTCA others(3247): Show |
chr11 | 60966680 | 61025377 |
| a0003c0011t0005 | 0/0 | 3252 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | ACTCA others(3247): Show |
chr11 | 60966680 | 61025377 |
| a0004c0004t0001 | 0/1 | 3252 | 27 | 4 | 14 | 0 | 3 | 5 | CD6_chr11_60966680_61025377 | CD6 | ACTCA others(3247): Show |
chr11 | 60966680 | 61025377 |
| a0005c0006t0001 | 0/0 | 3252 | 21 | 1 | 12 | 3 | 1 | 4 | CD6_chr11_60966680_61025377 | CD6 | ACTCA others(3247): Show |
chr11 | 60966680 | 61025377 |
| a0006c0008t0001 | 0/0 | 3252 | 8 | 0 | 0 | 6 | 0 | 2 | CD6_chr11_60966680_61025377 | CD6 | ACTCA others(3247): Show |
chr11 | 60966680 | 61025377 |
| a0007c0012t0001 | 0/0 | 3252 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | ACTCA others(3247): Show |
chr11 | 60966680 | 61025377 |
| a0007c0012t0003 | 0/0 | 3252 | 3 | 1 | 1 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | ACTCA others(3247): Show |
chr11 | 60966680 | 61025377 |
| a0007c0012t0010 | 0/0 | 3252 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | ACTCA others(3247): Show |
chr11 | 60966680 | 61025377 |
| a0008c0013t0001 | 0/0 | 3252 | 3 | 0 | 0 | 3 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | ACTCA others(3247): Show |
chr11 | 60966680 | 61025377 |
| a0009c0021t0001 | 0/0 | 3252 | 1 | 0 | 0 | 0 | 1 | 0 | CD6_chr11_60966680_61025377 | CD6 | ACTCA others(3247): Show |
chr11 | 60966680 | 61025377 |
| a0010c0020t0001 | 0/0 | 3252 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | ACTCA others(3247): Show |
chr11 | 60966680 | 61025377 |
| a0011c0015t0001 | 0/0 | 3252 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | ACTCA others(3247): Show |
chr11 | 60966680 | 61025377 |
| a0012c0022t0001 | 0/0 | 3252 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | ACTCA others(3247): Show |
chr11 | 60966680 | 61025377 |
| a0013c0017t0001 | 0/0 | 3252 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | ACTCA others(3247): Show |
chr11 | 60966680 | 61025377 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0007g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0007g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0008g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0009g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0001t0011g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0007t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0007t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0007t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0007t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0007t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0007t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0007t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0007t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0007t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0007t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0007t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0007t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0007t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0007t0002g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0007t0005g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0007t0006g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0007t0006g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0007t0012g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0010t0002g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0010t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0010t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0010t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0014t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0018t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0001c0019t0013g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0002t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0002t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0002t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0002t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0002t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0002t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0002t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0002t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0002t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0002t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0002t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0002t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0002t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0002t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0002t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0002t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0002t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0002t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0002t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0002t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0002t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0002t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0002t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0002t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0002t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0002t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0002t0014g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0003t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0003t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0003t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0003t0001g0012 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0003t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0003t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0003t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0003t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0003t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0003t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0003t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0003t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0003t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0003t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0003t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0003t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0003t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0003t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0003t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0003t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0003t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0003t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0003t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0003t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0003t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0003t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0003t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0003t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0003t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0003t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0003t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0003t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0003t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0003t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0003t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0003t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0003t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0009t0001g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0009t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0009t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0002c0016t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0003c0005t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0003c0005t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0003c0005t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0003c0005t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0003c0005t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0003c0005t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0003c0005t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0003c0005t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0003c0005t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0003c0005t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0003c0005t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0003c0005t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0003c0005t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0003c0005t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0003c0005t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0003c0005t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0003c0005t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0003c0005t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0003c0005t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0003c0005t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0003c0005t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0003c0005t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0003c0005t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0003c0005t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0003c0005t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0003c0011t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0003c0011t0004g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0003c0011t0004g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0003c0011t0004g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0003c0011t0005g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0004c0004t0001g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0004c0004t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0004c0004t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0004c0004t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0004c0004t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0004c0004t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0004c0004t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0004c0004t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0004c0004t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0004c0004t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0004c0004t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0004c0004t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0004c0004t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0004c0004t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0004c0004t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0004c0004t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0004c0004t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0004c0004t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0004c0004t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0004c0004t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0004c0004t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0004c0004t0001g0272 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0004c0004t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0004c0004t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0005c0006t0001g0009 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0005c0006t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0005c0006t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0005c0006t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0005c0006t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0005c0006t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0005c0006t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0005c0006t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0005c0006t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0005c0006t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0005c0006t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0005c0006t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0005c0006t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0005c0006t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0005c0006t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0005c0006t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0005c0006t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0005c0006t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0005c0006t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0006c0008t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0006c0008t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0006c0008t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0006c0008t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0006c0008t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0006c0008t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0006c0008t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0006c0008t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0007c0012t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0007c0012t0003g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0007c0012t0003g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0007c0012t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0007c0012t0010g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0008c0013t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0008c0013t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0008c0013t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0009c0021t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0010c0020t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0011c0015t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0012c0022t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| a0013c0017t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0063 | EUR | GBR | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG00099 | hp2 | a0002 | c0003 | t0001 | g0012 | EUR | GBR | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0062 | EUR | GBR | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG00140 | hp2 | a0005 | c0006 | t0001 | g0123 | EUR | GBR | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG00323 | hp1 | a0004 | c0004 | t0001 | g0166 | EUR | FIN | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG00323 | hp2 | a0009 | c0021 | t0001 | g0130 | EUR | FIN | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG00408 | hp1 | a0003 | c0005 | t0001 | g0086 | EAS | CHS | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | CHS | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | CHS | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG00423 | hp2 | a0003 | c0005 | t0001 | g0101 | EAS | CHS | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG00438 | hp1 | a0002 | c0002 | t0001 | g0180 | EAS | CHS | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG00438 | hp2 | a0002 | c0003 | t0001 | g0060 | EAS | CHS | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | CHS | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | CHS | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | CHS | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | CHS | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | CHS | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | CHS | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG00639 | hp1 | a0005 | c0006 | t0001 | g0033 | AMR | PUR | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG00639 | hp2 | a0004 | c0004 | t0001 | g0273 | AMR | PUR | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG00673 | hp1 | a0006 | c0008 | t0001 | g0075 | EAS | CHS | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | CHS | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG00735 | hp1 | a0002 | c0002 | t0001 | g0204 | AMR | PUR | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG00735 | hp2 | a0002 | c0002 | t0001 | g0106 | AMR | PUR | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG00741 | hp2 | a0002 | c0003 | t0001 | g0241 | AMR | PUR | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01069 | hp1 | a0002 | c0003 | t0001 | g0004 | AMR | PUR | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01069 | hp2 | a0004 | c0004 | t0001 | g0016 | AMR | PUR | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01070 | hp1 | a0002 | c0003 | t0001 | g0012 | AMR | PUR | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01070 | hp2 | a0004 | c0004 | t0001 | g0016 | AMR | PUR | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01071 | hp1 | a0002 | c0003 | t0001 | g0203 | AMR | PUR | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01071 | hp2 | a0002 | c0003 | t0001 | g0004 | AMR | PUR | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01081 | hp1 | a0007 | c0012 | t0003 | g0034 | AMR | PUR | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01099 | hp1 | a0002 | c0003 | t0001 | g0242 | AMR | PUR | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01099 | hp2 | a0005 | c0006 | t0001 | g0199 | AMR | PUR | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01106 | hp2 | a0005 | c0006 | t0001 | g0124 | AMR | PUR | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01109 | hp1 | a0002 | c0002 | t0001 | g0072 | AMR | PUR | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01109 | hp2 | a0001 | c0010 | t0002 | g0134 | AMR | PUR | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01167 | hp2 | a0002 | c0003 | t0001 | g0245 | AMR | PUR | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01168 | hp1 | a0005 | c0006 | t0001 | g0275 | AMR | PUR | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01168 | hp2 | a0004 | c0004 | t0001 | g0191 | AMR | PUR | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01169 | hp1 | a0005 | c0006 | t0001 | g0276 | AMR | PUR | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01175 | hp1 | a0004 | c0004 | t0001 | g0077 | AMR | PUR | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01192 | hp1 | a0003 | c0005 | t0001 | g0088 | AMR | PUR | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01192 | hp2 | a0004 | c0004 | t0001 | g0236 | AMR | PUR | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01243 | hp1 | a0002 | c0003 | t0001 | g0022 | AMR | PUR | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01243 | hp2 | a0002 | c0002 | t0001 | g0083 | AMR | PUR | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01255 | hp1 | a0002 | c0003 | t0001 | g0008 | AMR | CLM | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01255 | hp2 | a0005 | c0006 | t0001 | g0192 | AMR | CLM | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01256 | hp1 | a0005 | c0006 | t0001 | g0243 | AMR | CLM | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01256 | hp2 | a0002 | c0003 | t0001 | g0008 | AMR | CLM | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01257 | hp2 | a0002 | c0003 | t0001 | g0217 | AMR | CLM | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01258 | hp2 | a0005 | c0006 | t0001 | g0244 | AMR | CLM | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01261 | hp1 | a0002 | c0003 | t0001 | g0040 | AMR | CLM | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01261 | hp2 | a0005 | c0006 | t0001 | g0013 | AMR | CLM | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01346 | hp1 | a0002 | c0003 | t0001 | g0218 | AMR | CLM | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01346 | hp2 | a0004 | c0004 | t0001 | g0019 | AMR | CLM | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01358 | hp1 | a0001 | c0018 | t0001 | g0148 | AMR | CLM | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01358 | hp2 | a0004 | c0004 | t0001 | g0019 | AMR | CLM | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01361 | hp1 | a0007 | c0012 | t0001 | g0036 | AMR | CLM | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | CLM | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01433 | hp1 | a0005 | c0006 | t0001 | g0090 | AMR | CLM | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01496 | hp1 | a0002 | c0003 | t0001 | g0221 | AMR | CLM | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01496 | hp2 | a0004 | c0004 | t0001 | g0078 | AMR | CLM | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0208 | EUR | IBS | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01515 | hp2 | a0004 | c0004 | t0001 | g0271 | EUR | IBS | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0020 | EUR | IBS | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0152 | EUR | IBS | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0020 | EUR | IBS | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01517 | hp2 | a0004 | c0004 | t0001 | g0269 | EUR | IBS | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01884 | hp1 | a0001 | c0001 | t0011 | g0277 | AFR | ACB | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | ACB | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01891 | hp1 | a0002 | c0003 | t0001 | g0216 | AFR | ACB | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01891 | hp2 | a0002 | c0002 | t0001 | g0085 | AFR | ACB | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01943 | hp1 | a0004 | c0004 | t0001 | g0167 | AMR | PEL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PEL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01952 | hp2 | a0001 | c0001 | t0008 | g0268 | AMR | PEL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02004 | hp1 | a0004 | c0004 | t0001 | g0205 | AMR | PEL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02004 | hp2 | a0005 | c0006 | t0001 | g0009 | AMR | PEL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02055 | hp1 | a0004 | c0004 | t0001 | g0112 | AFR | ACB | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02055 | hp2 | a0004 | c0004 | t0001 | g0280 | AFR | ACB | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02056 | hp1 | a0003 | c0005 | t0001 | g0100 | EAS | KHV | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02071 | hp2 | a0002 | c0002 | t0001 | g0250 | EAS | KHV | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | KHV | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02074 | hp2 | a0005 | c0006 | t0001 | g0117 | EAS | KHV | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02080 | hp2 | a0006 | c0008 | t0001 | g0248 | EAS | KHV | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02083 | hp1 | a0002 | c0002 | t0001 | g0255 | EAS | KHV | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02083 | hp2 | a0003 | c0005 | t0001 | g0010 | EAS | KHV | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02129 | hp1 | a0002 | c0003 | t0001 | g0108 | EAS | KHV | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | KHV | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | KHV | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02132 | hp2 | a0002 | c0002 | t0001 | g0262 | EAS | KHV | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02145 | hp1 | a0002 | c0002 | t0001 | g0240 | AFR | ACB | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02145 | hp2 | a0003 | c0011 | t0004 | g0046 | AFR | ACB | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02165 | hp1 | a0005 | c0006 | t0001 | g0009 | EAS | CDX | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02165 | hp2 | a0003 | c0005 | t0001 | g0163 | EAS | CDX | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02257 | hp1 | a0001 | c0007 | t0001 | g0256 | AFR | ACB | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02257 | hp2 | a0002 | c0003 | t0001 | g0135 | AFR | ACB | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02258 | hp1 | a0002 | c0003 | t0001 | g0264 | AFR | ACB | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02258 | hp2 | a0003 | c0011 | t0001 | g0226 | AFR | ACB | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02280 | hp1 | a0002 | c0003 | t0001 | g0230 | AFR | ACB | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02280 | hp2 | a0002 | c0002 | t0001 | g0011 | AFR | ACB | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02293 | hp2 | a0004 | c0004 | t0001 | g0160 | AMR | PEL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02300 | hp1 | a0004 | c0004 | t0001 | g0270 | AMR | PEL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PEL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02572 | hp1 | a0001 | c0007 | t0001 | g0247 | AFR | GWD | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02602 | hp1 | a0004 | c0004 | t0001 | g0200 | SAS | PJL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02602 | hp2 | a0005 | c0006 | t0001 | g0118 | SAS | PJL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02615 | hp1 | a0002 | c0009 | t0001 | g0025 | AFR | GWD | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02615 | hp2 | a0005 | c0006 | t0001 | g0246 | AFR | GWD | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02622 | hp1 | a0004 | c0004 | t0001 | g0209 | AFR | GWD | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02622 | hp2 | a0002 | c0009 | t0001 | g0024 | AFR | GWD | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02630 | hp1 | a0001 | c0001 | t0007 | g0041 | AFR | GWD | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02630 | hp2 | a0002 | c0002 | t0014 | g0237 | AFR | GWD | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02647 | hp1 | a0002 | c0002 | t0001 | g0222 | AFR | GWD | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02647 | hp2 | a0002 | c0003 | t0001 | g0023 | AFR | GWD | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02683 | hp1 | a0006 | c0008 | t0001 | g0064 | SAS | PJL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02698 | hp1 | a0003 | c0005 | t0001 | g0206 | SAS | PJL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02698 | hp2 | a0002 | c0003 | t0001 | g0215 | SAS | PJL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02717 | hp1 | a0001 | c0010 | t0002 | g0015 | AFR | GWD | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02717 | hp2 | a0002 | c0003 | t0001 | g0002 | AFR | GWD | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02723 | hp2 | a0002 | c0002 | t0001 | g0238 | AFR | GWD | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02738 | hp2 | a0005 | c0006 | t0001 | g0029 | SAS | PJL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02809 | hp1 | a0002 | c0002 | t0001 | g0056 | AFR | GWD | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02809 | hp2 | a0002 | c0003 | t0001 | g0239 | AFR | GWD | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02818 | hp1 | a0001 | c0007 | t0001 | g0021 | AFR | GWD | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02818 | hp2 | a0002 | c0002 | t0001 | g0026 | AFR | GWD | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02886 | hp1 | a0001 | c0007 | t0001 | g0018 | AFR | GWD | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02886 | hp2 | a0002 | c0002 | t0001 | g0071 | AFR | GWD | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02895 | hp1 | a0001 | c0010 | t0002 | g0234 | AFR | GWD | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02895 | hp2 | a0001 | c0007 | t0006 | g0131 | AFR | GWD | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02896 | hp1 | a0002 | c0002 | t0001 | g0225 | AFR | GWD | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02896 | hp2 | a0002 | c0003 | t0001 | g0082 | AFR | GWD | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02897 | hp1 | a0001 | c0007 | t0006 | g0132 | AFR | GWD | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02897 | hp2 | a0002 | c0002 | t0001 | g0228 | AFR | GWD | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02965 | hp1 | a0002 | c0009 | t0001 | g0001 | AFR | ESN | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02965 | hp2 | a0002 | c0003 | t0001 | g0232 | AFR | ESN | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02970 | hp1 | a0002 | c0002 | t0001 | g0211 | AFR | ESN | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02970 | hp2 | a0002 | c0009 | t0001 | g0001 | AFR | ESN | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02976 | hp1 | a0001 | c0007 | t0001 | g0018 | AFR | ESN | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02976 | hp2 | a0002 | c0002 | t0001 | g0196 | AFR | ESN | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03017 | hp1 | a0010 | c0020 | t0001 | g0043 | SAS | PJL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03017 | hp2 | a0006 | c0008 | t0001 | g0139 | SAS | PJL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03041 | hp1 | a0001 | c0007 | t0001 | g0251 | AFR | GWD | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03041 | hp2 | a0002 | c0003 | t0001 | g0042 | AFR | GWD | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03098 | hp1 | a0001 | c0007 | t0001 | g0219 | AFR | MSL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03098 | hp2 | a0002 | c0003 | t0001 | g0267 | AFR | MSL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03130 | hp1 | a0001 | c0010 | t0002 | g0233 | AFR | ESN | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03130 | hp2 | a0002 | c0002 | t0001 | g0039 | AFR | ESN | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03195 | hp1 | a0002 | c0002 | t0001 | g0103 | AFR | ESN | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03195 | hp2 | a0001 | c0007 | t0005 | g0274 | AFR | ESN | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03209 | hp1 | a0002 | c0002 | t0001 | g0092 | AFR | MSL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03209 | hp2 | a0011 | c0015 | t0001 | g0279 | AFR | MSL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03225 | hp1 | a0003 | c0011 | t0004 | g0278 | AFR | MSL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03225 | hp2 | a0001 | c0007 | t0001 | g0227 | AFR | MSL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03453 | hp1 | a0002 | c0003 | t0001 | g0037 | AFR | MSL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03453 | hp2 | a0003 | c0011 | t0004 | g0045 | AFR | MSL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03486 | hp1 | a0002 | c0003 | t0001 | g0235 | AFR | MSL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03486 | hp2 | a0001 | c0007 | t0012 | g0017 | AFR | MSL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03491 | hp2 | a0004 | c0004 | t0001 | g0069 | SAS | PJL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03492 | hp1 | a0004 | c0004 | t0001 | g0005 | SAS | PJL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03492 | hp2 | a0002 | c0003 | t0001 | g0067 | SAS | PJL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03516 | hp1 | a0001 | c0007 | t0001 | g0266 | AFR | ESN | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03516 | hp2 | a0002 | c0002 | t0001 | g0133 | AFR | ESN | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03540 | hp1 | a0002 | c0002 | t0001 | g0197 | AFR | GWD | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03540 | hp2 | a0001 | c0007 | t0001 | g0259 | AFR | GWD | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03579 | hp1 | a0001 | c0007 | t0001 | g0265 | AFR | MSL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03579 | hp2 | a0001 | c0001 | t0007 | g0258 | AFR | MSL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03654 | hp2 | a0004 | c0004 | t0001 | g0005 | SAS | PJL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03669 | hp1 | a0003 | c0005 | t0001 | g0044 | SAS | PJL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03669 | hp2 | a0003 | c0005 | t0001 | g0093 | SAS | PJL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03688 | hp1 | a0002 | c0002 | t0001 | g0263 | SAS | STU | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03688 | hp2 | a0002 | c0003 | t0001 | g0125 | SAS | STU | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03704 | hp2 | a0012 | c0022 | t0001 | g0212 | SAS | PJL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0201 | SAS | BEB | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03831 | hp2 | a0005 | c0006 | t0001 | g0087 | SAS | BEB | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03834 | hp1 | a0005 | c0006 | t0001 | g0115 | SAS | BEB | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03834 | hp2 | a0002 | c0003 | t0001 | g0027 | SAS | BEB | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03927 | hp1 | a0002 | c0016 | t0001 | g0116 | SAS | BEB | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03927 | hp2 | a0003 | c0005 | t0001 | g0028 | SAS | BEB | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03942 | hp1 | a0007 | c0012 | t0010 | g0030 | SAS | BEB | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03942 | hp2 | a0004 | c0004 | t0001 | g0068 | SAS | BEB | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0210 | SAS | BEB | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG04184 | hp2 | a0003 | c0005 | t0001 | g0161 | SAS | BEB | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG04199 | hp1 | a0002 | c0003 | t0001 | g0182 | SAS | STU | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | STU | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG04204 | hp1 | a0003 | c0005 | t0001 | g0127 | SAS | STU | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG04204 | hp2 | a0002 | c0003 | t0001 | g0031 | SAS | STU | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG04228 | hp1 | a0003 | c0005 | t0001 | g0079 | SAS | STU | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0105 | SAS | STU | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18522 | hp1 | a0002 | c0003 | t0001 | g0002 | AFR | YRI | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18522 | hp2 | a0001 | c0007 | t0001 | g0047 | AFR | YRI | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | CHB | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18747 | hp2 | a0003 | c0005 | t0001 | g0184 | EAS | CHB | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18940 | hp1 | a0008 | c0013 | t0001 | g0113 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18946 | hp1 | a0003 | c0005 | t0001 | g0010 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18947 | hp1 | a0002 | c0003 | t0001 | g0168 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18947 | hp2 | a0002 | c0002 | t0001 | g0138 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18949 | hp1 | a0002 | c0002 | t0001 | g0051 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18949 | hp2 | a0003 | c0005 | t0001 | g0057 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18951 | hp1 | a0005 | c0006 | t0001 | g0158 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18952 | hp1 | a0006 | c0008 | t0001 | g0183 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18952 | hp2 | a0001 | c0014 | t0001 | g0154 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18960 | hp2 | a0003 | c0005 | t0001 | g0164 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18970 | hp1 | a0002 | c0002 | t0001 | g0155 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18971 | hp2 | a0002 | c0002 | t0001 | g0254 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18975 | hp1 | a0003 | c0005 | t0001 | g0249 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18977 | hp1 | a0002 | c0002 | t0001 | g0054 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18977 | hp2 | a0006 | c0008 | t0001 | g0119 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18982 | hp2 | a0003 | c0005 | t0001 | g0120 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18990 | hp1 | a0003 | c0005 | t0001 | g0159 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18990 | hp2 | a0001 | c0001 | t0009 | g0175 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18994 | hp1 | a0003 | c0005 | t0001 | g0107 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18994 | hp2 | a0002 | c0002 | t0001 | g0052 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA19005 | hp2 | a0003 | c0005 | t0001 | g0162 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA19007 | hp1 | a0008 | c0013 | t0001 | g0144 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA19009 | hp2 | a0002 | c0002 | t0001 | g0111 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA19030 | hp1 | a0002 | c0003 | t0001 | g0220 | AFR | LWK | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA19030 | hp2 | a0001 | c0007 | t0001 | g0017 | AFR | LWK | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA19043 | hp1 | a0001 | c0007 | t0001 | g0223 | AFR | LWK | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA19043 | hp2 | a0001 | c0010 | t0002 | g0015 | AFR | LWK | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA19057 | hp2 | a0003 | c0005 | t0001 | g0252 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA19063 | hp1 | a0002 | c0002 | t0001 | g0055 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA19063 | hp2 | a0003 | c0005 | t0001 | g0186 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA19068 | hp1 | a0006 | c0008 | t0001 | g0076 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA19081 | hp1 | a0006 | c0008 | t0001 | g0165 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA19085 | hp1 | a0003 | c0005 | t0001 | g0171 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA19088 | hp1 | a0008 | c0013 | t0001 | g0143 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA19088 | hp2 | a0002 | c0002 | t0001 | g0261 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA19091 | hp1 | a0002 | c0002 | t0001 | g0053 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA19240 | hp1 | a0002 | c0002 | t0001 | g0073 | AFR | YRI | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA19240 | hp2 | a0001 | c0007 | t0002 | g0257 | AFR | YRI | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA20129 | hp1 | a0003 | c0011 | t0005 | g0048 | AFR | ASW | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA20129 | hp2 | a0004 | c0004 | t0001 | g0050 | AFR | ASW | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA20905 | hp1 | a0001 | c0019 | t0013 | g0137 | SAS | GIH | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA20905 | hp2 | a0007 | c0012 | t0003 | g0032 | SAS | GIH | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01123 | hp1 | a0005 | c0006 | t0001 | g0013 | AMR | CLM | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG01123 | hp2 | a0004 | c0004 | t0001 | g0121 | AMR | CLM | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02109 | hp1 | a0007 | c0012 | t0003 | g0035 | AFR | ACB | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02109 | hp2 | a0002 | c0002 | t0001 | g0224 | AFR | ACB | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02486 | hp1 | a0003 | c0005 | t0001 | g0229 | AFR | ACB | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG02486 | hp2 | a0002 | c0003 | t0001 | g0213 | AFR | ACB | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03471 | hp1 | a0002 | c0002 | t0001 | g0011 | AFR | MSL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG03471 | hp2 | a0001 | c0007 | t0001 | g0021 | AFR | MSL | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG06807 | hp1 | a0002 | c0002 | t0001 | g0070 | AFR | USA | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| HG06807 | hp2 | a0002 | c0009 | t0001 | g0001 | AFR | USA | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA20300 | hp1 | a0002 | c0002 | t0001 | g0038 | AFR | USA | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA20300 | hp2 | a0002 | c0003 | t0001 | g0231 | AFR | USA | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA21309 | hp1 | a0013 | c0017 | t0001 | g0214 | AFR | LWK | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| NA21309 | hp2 | a0002 | c0002 | t0001 | g0193 | AFR | LWK | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| homoSapiens | chm13v2 | a0004 | c0004 | t0001 | g0272 | REF | REF | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0003 | REF | REF | CD6_chr11_60966680_61025377 | CD6 | chr11 | 60966680 | 61025377 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:61007755 | C | T | 2 | a0007 a0012 |
6 | HG01081.hp1 HG01361.hp1 HG02109.hp1 others(3): Show |
missense_variant | MODERATE | c.314C>T | p.Pro105Leu | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 3/13 | 500/3252 | 314/2007 | 105/668 | chr11 | 61007755 | |||
| chr11:61007889 | C | T | 1 | a0009 | 1 | HG00323.hp2 | missense_variant | MODERATE | c.448C>T | p.Arg150Trp | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 3/13 | 634/3252 | 448/2007 | 150/668 | chr11 | 61007889 | |||
| chr11:61008714 | C | T | 2 | a0005 a0010 |
22 | HG00140.hp2 HG00639.hp1 HG01099.hp2 others(19): Show |
missense_variant | MODERATE | c.650C>T | p.Thr217Met | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 4/13 | 836/3252 | 650/2007 | 217/668 | chr11 | 61008714 | |||
| chr11:61008737 | C | T | 4 | a0002 a0004 a0011 others(1): Show |
118 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(115): Show |
missense_variant | MODERATE | c.673C>T | p.Arg225Trp | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 4/13 | 859/3252 | 673/2007 | 225/668 | chr11 | 61008737 | |||
| chr11:61008834 | C | T | 8 | a0002 a0003 a0004 others(5): Show |
179 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(176): Show |
missense_variant | MODERATE | c.770C>T | p.Ala257Val | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 4/13 | 956/3252 | 770/2007 | 257/668 | chr11 | 61008834 | |||
| chr11:61009601 | G | A | 1 | a0004 | 26 | HG00323.hp1 HG00639.hp2 HG01069.hp2 others(23): Show |
missense_variant | MODERATE | c.811G>A | p.Ala271Thr | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 5/13 | 997/3252 | 811/2007 | 271/668 | chr11 | 61009601 | |||
| chr11:61015767 | G | A | 1 | a0011 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.1442G>A | p.Gly481Asp | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 9/13 | 1628/3252 | 1442/2007 | 481/668 | chr11 | 61015767 | |||
| chr11:61017791 | A | G | 1 | a0007 | 5 | HG01081.hp1 HG01361.hp1 HG02109.hp1 others(2): Show |
missense_variant | MODERATE | c.1615A>G | p.Thr539Ala | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 11/13 | 1801/3252 | 1615/2007 | 539/668 | chr11 | 61017791 | |||
| chr11:61017992 | G | A | 4 | a0005 a0006 a0008 others(1): Show |
33 | HG00140.hp2 HG00639.hp1 HG00673.hp1 others(30): Show |
missense_variant | MODERATE | c.1816G>A | p.Gly606Ser | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 11/13 | 2002/3252 | 1816/2007 | 606/668 | chr11 | 61017992 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:61007774 | G | A | 1 | a0001c0014 | 1 | NA18952.hp2 | synonymous_variant | LOW | c.333G>A | p.Gly111Gly | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 3/13 | 519/3252 | 333/2007 | 111/668 | chr11 | 61007774 | |||
| chr11:61008631 | T | C | 5 | a0002c0003 a0002c0009 a0002c0016 others(2): Show |
49 | HG00099.hp2 HG00438.hp2 HG00741.hp2 others(46): Show |
synonymous_variant | LOW | c.567T>C | p.Thr189Thr | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 4/13 | 753/3252 | 567/2007 | 189/668 | chr11 | 61008631 | |||
| chr11:61008718 | C | T | 1 | a0001c0019 | 1 | NA20905.hp1 | synonymous_variant | LOW | c.654C>T | p.Pro218Pro | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 4/13 | 840/3252 | 654/2007 | 218/668 | chr11 | 61008718 | |||
| chr11:61008835 | G | C | 5 | a0002c0003 a0002c0009 a0002c0016 others(2): Show |
49 | HG00099.hp2 HG00438.hp2 HG00741.hp2 others(46): Show |
synonymous_variant | LOW | c.771G>C | p.Ala257Ala | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 4/13 | 957/3252 | 771/2007 | 257/668 | chr11 | 61008835 | |||
| chr11:61009573 | G | A | 1 | a0001c0010 | 5 | HG01109.hp2 HG02717.hp1 HG02895.hp1 others(2): Show |
splice_region_variant&synonymous_variant | LOW | c.783G>A | p.Glu261Glu | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 5/13 | 969/3252 | 783/2007 | 261/668 | chr11 | 61009573 | |||
| chr11:61017841 | G | A | 1 | a0001c0018 | 1 | HG01358.hp1 | synonymous_variant | LOW | c.1665G>A | p.Gln555Gln | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 11/13 | 1851/3252 | 1665/2007 | 555/668 | chr11 | 61017841 | |||
| chr11:61017880 | A | G | 13 | a0001c0007 a0001c0010 a0002c0003 others(10): Show |
142 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(139): Show |
synonymous_variant | LOW | c.1704A>G | p.Ser568Ser | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 11/13 | 1890/3252 | 1704/2007 | 568/668 | chr11 | 61017880 | |||
| chr11:61017991 | C | T | 2 | a0002c0009 a0004c0004 |
31 | HG00323.hp1 HG00639.hp2 HG01069.hp2 others(28): Show |
synonymous_variant | LOW | c.1815C>T | p.Ala605Ala | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 11/13 | 2001/3252 | 1815/2007 | 605/668 | chr11 | 61017991 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:61019432 | C | T | 1 | a0002c0002t0014 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*114C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 13/13 | 114 | chr11 | 61019432 | ||||||
| chr11:61019465 | T | C | 1 | a0001c0001t0008 | 1 | HG01952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*147T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 13/13 | 147 | chr11 | 61019465 | ||||||
| chr11:61019685 | G | A | 1 | a0001c0001t0009 | 1 | NA18990.hp2 | 3_prime_UTR_variant | MODIFIER | c.*367G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 13/13 | 367 | chr11 | 61019685 | ||||||
| chr11:61019737 | G | A | 2 | a0007c0012t0003 a0007c0012t0010 |
4 | HG01081.hp1 HG02109.hp1 HG03942.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*419G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 13/13 | 419 | chr11 | 61019737 | ||||||
| chr11:61019823 | C | T | 1 | a0001c0019t0013 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*505C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 13/13 | 505 | chr11 | 61019823 | ||||||
| chr11:61019832 | G | C | 2 | a0001c0007t0005 a0003c0011t0005 |
2 | HG03195.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*514G>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 13/13 | 514 | chr11 | 61019832 | ||||||
| chr11:61019854 | C | T | 2 | a0001c0007t0012 a0003c0011t0004 |
4 | HG02145.hp2 HG03225.hp1 HG03453.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*536C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 13/13 | 536 | chr11 | 61019854 | ||||||
| chr11:61019873 | G | A | 2 | a0001c0007t0002 a0001c0010t0002 |
6 | HG01109.hp2 HG02717.hp1 HG02895.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*555G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 13/13 | 555 | chr11 | 61019873 | ||||||
| chr11:61020031 | A | G | 1 | a0007c0012t0010 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*713A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 13/13 | 713 | chr11 | 61020031 | ||||||
| chr11:61020180 | G | A | 1 | a0001c0007t0012 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*862G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 13/13 | 862 | chr11 | 61020180 | ||||||
| chr11:61020204 | T | G | 1 | a0001c0007t0006 | 2 | HG02895.hp2 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*886T>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 13/13 | 886 | chr11 | 61020204 | ||||||
| chr11:61020268 | G | A | 1 | a0001c0001t0011 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*950G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 13/13 | 950 | chr11 | 61020268 | ||||||
| chr11:61020280 | G | A | 1 | a0001c0001t0007 | 2 | HG02630.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*962G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 13/13 | 962 | chr11 | 61020280 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:60971922 | C | T | 1 | a0004c0004t0001g0280 | 1 | HG02055.hp2 | splice_region_variant&intron_variant | LOW | c.49+8C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60971922 | |||||||
| chr11:60971969 | C | T | 3 | a0001c0001t0011g0277 a0003c0011t0004g0278 a0011c0015t0001g0279 |
3 | HG01884.hp1 HG03209.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.49+55C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60971969 | |||||||
| chr11:60972084 | A | T | 1 | a0001c0007t0001g0021 | 2 | HG02818.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.49+170A>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60972084 | |||||||
| chr11:60972215 | G | C | 3 | a0002c0003t0001g0002 a0002c0003t0001g0022 a0002c0003t0001g0023 |
4 | HG01243.hp1 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.49+301G>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60972215 | |||||||
| chr11:60972279 | A | G | 259 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(256): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.49+365A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60972279 | |||||||
| chr11:60972291 | G | A | 4 | a0002c0002t0001g0026 a0002c0009t0001g0001 a0002c0009t0001g0024 others(1): Show |
6 | HG02615.hp1 HG02622.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.49+377G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60972291 | |||||||
| chr11:60972360 | T | G | 273 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(270): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.49+446T>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60972360 | |||||||
| chr11:60972476 | G | A | 1 | a0002c0003t0001g0027 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.49+562G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60972476 | |||||||
| chr11:60972584 | C | G | 1 | a0001c0001t0001g0020 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.49+670C>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60972584 | |||||||
| chr11:60972787 | G | C | 9 | a0002c0003t0001g0031 a0003c0005t0001g0028 a0005c0006t0001g0029 others(6): Show |
9 | HG00639.hp1 HG01081.hp1 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.49+873G>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60972787 | |||||||
| chr11:60972795 | G | A | 1 | a0010c0020t0001g0043 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.49+881G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60972795 | |||||||
| chr11:60972827 | A | T | 8 | a0001c0007t0005g0274 a0004c0004t0001g0019 a0004c0004t0001g0269 others(5): Show |
9 | HG00639.hp2 HG01168.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.49+913A>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60972827 | |||||||
| chr11:60972832 | G | A | 1 | a0003c0005t0001g0044 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.49+918G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60972832 | |||||||
| chr11:60972863 | C | T | 1 | a0001c0001t0008g0268 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.49+949C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60972863 | |||||||
| chr11:60973063 | G | A | 1 | a0003c0005t0001g0044 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.49+1149G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60973063 | |||||||
| chr11:60973143 | A | G | 34 | a0001c0001t0001g0253 a0001c0001t0001g0260 a0001c0001t0007g0258 others(31): Show |
36 | HG00741.hp2 HG01099.hp1 HG01167.hp2 others(33): Show |
intron_variant | MODIFIER | c.49+1229A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60973143 | |||||||
| chr11:60973181 | C | A | 194 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0020 others(191): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.49+1267C>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60973181 | |||||||
| chr11:60973294 | G | C | 5 | a0001c0007t0001g0021 a0001c0007t0001g0047 a0003c0011t0004g0045 others(2): Show |
6 | HG02145.hp2 HG02818.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.49+1380G>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60973294 | |||||||
| chr11:60973305 | A | G | 1 | a0002c0003t0001g0023 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.49+1391A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60973305 | |||||||
| chr11:60973385 | C | T | 1 | a0002c0003t0001g0267 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.49+1471C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60973385 | |||||||
| chr11:60973539 | T | C | 1 | a0001c0001t0001g0049 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.49+1625T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60973539 | |||||||
| chr11:60973572 | CAT | C | 9 | a0001c0007t0005g0274 a0004c0004t0001g0019 a0004c0004t0001g0050 others(6): Show |
10 | HG00639.hp2 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.49+1660_49+1661del others(2): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60973572 | ||||||
| chr11:60973584 | T | C | 1 | a0004c0004t0001g0280 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.49+1670T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60973584 | |||||||
| chr11:60973779 | G | A | 1 | a0003c0011t0004g0045 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.49+1865G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60973779 | |||||||
| chr11:60974020 | A | G | 1 | a0002c0002t0001g0211 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.49+2106A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60974020 | |||||||
| chr11:60974234 | G | A | 4 | a0001c0007t0001g0021 a0001c0007t0001g0047 a0003c0011t0004g0045 others(1): Show |
5 | HG02145.hp2 HG02818.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.49+2320G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60974234 | |||||||
| chr11:60974314 | C | G | 1 | a0001c0007t0001g0021 | 2 | HG02818.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.49+2400C>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60974314 | |||||||
| chr11:60974355 | G | A | 7 | a0002c0002t0001g0051 a0002c0002t0001g0052 a0002c0002t0001g0053 others(4): Show |
7 | HG03704.hp2 HG03834.hp2 NA18949.hp1 others(4): Show |
intron_variant | MODIFIER | c.49+2441G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60974355 | |||||||
| chr11:60974383 | A | G | 4 | a0002c0002t0001g0026 a0002c0009t0001g0001 a0002c0009t0001g0024 others(1): Show |
6 | HG02615.hp1 HG02622.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.49+2469A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60974383 | |||||||
| chr11:60974443 | C | T | 4 | a0002c0002t0001g0026 a0002c0009t0001g0001 a0002c0009t0001g0024 others(1): Show |
6 | HG02615.hp1 HG02622.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.49+2529C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60974443 | |||||||
| chr11:60974449 | G | A | 1 | a0002c0003t0001g0004 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.49+2535G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60974449 | |||||||
| chr11:60974530 | C | G | 2 | a0002c0003t0001g0027 a0012c0022t0001g0212 |
2 | HG03704.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.49+2616C>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60974530 | |||||||
| chr11:60974566 | T | C | 2 | a0002c0003t0001g0027 a0012c0022t0001g0212 |
2 | HG03704.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.49+2652T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60974566 | |||||||
| chr11:60974809 | G | T | 1 | a0001c0001t0001g0210 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.49+2895G>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60974809 | |||||||
| chr11:60974812 | T | C | 1 | a0002c0002t0001g0056 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.49+2898T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60974812 | |||||||
| chr11:60974827 | C | T | 1 | a0007c0012t0001g0036 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.49+2913C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60974827 | |||||||
| chr11:60975124 | ATATTT | A | 234 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(231): Show |
248 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.49+3219_49+3223del others(5): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60975124 | ||||||
| chr11:60975133 | TTTA | T | 4 | a0001c0007t0001g0021 a0001c0007t0001g0047 a0003c0011t0004g0045 others(1): Show |
5 | HG02145.hp2 HG02818.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.49+3221_49+3223del others(3): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60975133 | ||||||
| chr11:60975166 | C | T | 1 | a0001c0001t0007g0041 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.49+3252C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60975166 | |||||||
| chr11:60975316 | A | G | 238 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(235): Show |
253 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.49+3402A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60975316 | |||||||
| chr11:60975424 | G | A | 9 | a0001c0007t0005g0274 a0004c0004t0001g0019 a0004c0004t0001g0050 others(6): Show |
10 | HG00639.hp2 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.49+3510G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60975424 | |||||||
| chr11:60975627 | C | G | 4 | a0001c0007t0001g0021 a0001c0007t0001g0047 a0003c0011t0004g0045 others(1): Show |
5 | HG02145.hp2 HG02818.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.49+3713C>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60975627 | |||||||
| chr11:60975767 | T | G | 278 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(275): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.49+3853T>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60975767 | |||||||
| chr11:60975777 | C | T | 1 | a0001c0001t0001g0190 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.49+3863C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60975777 | |||||||
| chr11:60975836 | A | G | 1 | a0004c0004t0001g0280 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.49+3922A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60975836 | |||||||
| chr11:60976081 | C | T | 3 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0189 |
3 | HG00558.hp2 HG02129.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.49+4167C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60976081 | |||||||
| chr11:60976103 | A | G | 278 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(275): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.49+4189A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60976103 | |||||||
| chr11:60976124 | T | C | 28 | a0001c0001t0001g0014 a0001c0001t0011g0277 a0001c0007t0001g0219 others(25): Show |
30 | HG01167.hp1 HG01169.hp2 HG01257.hp2 others(27): Show |
intron_variant | MODIFIER | c.49+4210T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60976124 | |||||||
| chr11:60976142 | A | G | 1 | a0003c0005t0001g0186 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.49+4228A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60976142 | |||||||
| chr11:60976172 | C | T | 1 | a0004c0004t0001g0209 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.49+4258C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60976172 | |||||||
| chr11:60976198 | A | C | 1 | a0001c0001t0001g0185 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.49+4284A>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60976198 | |||||||
| chr11:60976318 | A | C | 11 | a0002c0003t0001g0027 a0002c0003t0001g0031 a0003c0005t0001g0028 others(8): Show |
11 | HG00639.hp1 HG01081.hp1 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.49+4404A>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60976318 | |||||||
| chr11:60976323 | T | C | 2 | a0004c0004t0001g0191 a0005c0006t0001g0192 |
2 | HG01168.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.49+4409T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60976323 | |||||||
| chr11:60976381 | T | G | 238 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(235): Show |
253 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.49+4467T>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60976381 | |||||||
| chr11:60976467 | G | A | 1 | a0003c0005t0001g0057 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.49+4553G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60976467 | |||||||
| chr11:60976485 | C | T | 1 | a0007c0012t0003g0035 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.49+4571C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60976485 | |||||||
| chr11:60976517 | T | C | 1 | a0002c0003t0001g0213 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.49+4603T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60976517 | |||||||
| chr11:60976586 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.49+4672G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60976586 | |||||||
| chr11:60976646 | T | C | 1 | a0001c0001t0001g0059 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.49+4732T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60976646 | |||||||
| chr11:60976752 | G | A | 5 | a0002c0003t0001g0241 a0002c0003t0001g0242 a0002c0003t0001g0245 others(2): Show |
5 | HG00741.hp2 HG01099.hp1 HG01167.hp2 others(2): Show |
intron_variant | MODIFIER | c.49+4838G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60976752 | |||||||
| chr11:60976771 | G | C | 8 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(5): Show |
8 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(5): Show |
intron_variant | MODIFIER | c.49+4857G>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60976771 | |||||||
| chr11:60976796 | C | T | 13 | a0002c0002t0001g0026 a0002c0003t0001g0031 a0002c0009t0001g0001 others(10): Show |
15 | HG00639.hp1 HG01081.hp1 HG01361.hp1 others(12): Show |
intron_variant | MODIFIER | c.49+4882C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60976796 | |||||||
| chr11:60977321 | G | A | 9 | a0002c0003t0001g0031 a0003c0005t0001g0028 a0005c0006t0001g0029 others(6): Show |
9 | HG00639.hp1 HG01081.hp1 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.49+5407G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60977321 | |||||||
| chr11:60977414 | T | C | 1 | a0004c0004t0001g0280 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.49+5500T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60977414 | |||||||
| chr11:60977544 | C | T | 1 | a0001c0001t0007g0041 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.49+5630C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60977544 | |||||||
| chr11:60977596 | C | G | 159 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0020 others(156): Show |
166 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.49+5682C>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60977596 | |||||||
| chr11:60977675 | G | A | 1 | a0001c0001t0001g0006 | 2 | NA18948.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.49+5761G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60977675 | |||||||
| chr11:60977775 | G | A | 6 | a0004c0004t0001g0019 a0004c0004t0001g0050 a0004c0004t0001g0269 others(3): Show |
7 | HG00639.hp2 HG01346.hp2 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.49+5861G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60977775 | |||||||
| chr11:60978034 | T | C | 4 | a0002c0002t0001g0070 a0002c0002t0001g0071 a0002c0002t0001g0072 others(1): Show |
4 | HG01109.hp1 HG02886.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.49+6120T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60978034 | |||||||
| chr11:60978086 | A | G | 1 | a0003c0005t0001g0184 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.49+6172A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60978086 | |||||||
| chr11:60978256 | G | A | 1 | a0005c0006t0001g0246 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.49+6342G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60978256 | |||||||
| chr11:60978261 | C | T | 1 | a0010c0020t0001g0043 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.49+6347C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60978261 | |||||||
| chr11:60978269 | G | A | 6 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(3): Show |
6 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(3): Show |
intron_variant | MODIFIER | c.49+6355G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60978269 | |||||||
| chr11:60978295 | C | T | 4 | a0002c0002t0001g0238 a0002c0002t0014g0237 a0002c0003t0001g0239 others(1): Show |
4 | HG02630.hp2 HG02723.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.49+6381C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60978295 | |||||||
| chr11:60978299 | T | C | 7 | a0001c0007t0005g0274 a0004c0004t0001g0019 a0004c0004t0001g0050 others(4): Show |
8 | HG00639.hp2 HG01346.hp2 HG01358.hp2 others(5): Show |
intron_variant | MODIFIER | c.49+6385T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60978299 | |||||||
| chr11:60978540 | C | T | 2 | a0001c0007t0001g0265 a0001c0007t0001g0266 |
2 | HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.49+6626C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60978540 | |||||||
| chr11:60978874 | A | G | 1 | a0006c0008t0001g0183 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.49+6960A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60978874 | |||||||
| chr11:60978875 | T | C | 4 | a0002c0002t0001g0026 a0002c0009t0001g0001 a0002c0009t0001g0024 others(1): Show |
6 | HG02615.hp1 HG02622.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.49+6961T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60978875 | |||||||
| chr11:60978932 | C | T | 3 | a0001c0007t0001g0047 a0003c0011t0004g0045 a0003c0011t0004g0046 |
3 | HG02145.hp2 HG03453.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.49+7018C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60978932 | |||||||
| chr11:60978986 | C | T | 4 | a0002c0002t0001g0026 a0002c0009t0001g0001 a0002c0009t0001g0024 others(1): Show |
6 | HG02615.hp1 HG02622.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.49+7072C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60978986 | |||||||
| chr11:60979338 | C | T | 7 | a0001c0007t0005g0274 a0004c0004t0001g0019 a0004c0004t0001g0050 others(4): Show |
8 | HG00639.hp2 HG01346.hp2 HG01358.hp2 others(5): Show |
intron_variant | MODIFIER | c.49+7424C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60979338 | |||||||
| chr11:60979420 | G | A | 13 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(10): Show |
14 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(11): Show |
intron_variant | MODIFIER | c.49+7506G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60979420 | |||||||
| chr11:60979460 | T | G | 1 | a0013c0017t0001g0214 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.49+7546T>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60979460 | |||||||
| chr11:60979464 | C | CT | 8 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0007t0001g0021 others(5): Show |
9 | HG01884.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.49+7564dupT | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60979464 | ||||||
| chr11:60979464 | CT | C | 9 | a0001c0001t0001g0014 a0002c0002t0001g0026 a0002c0003t0001g0215 others(6): Show |
12 | HG01167.hp1 HG01169.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.49+7564delT | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60979464 | ||||||
| chr11:60979549 | C | A | 1 | a0001c0001t0001g0074 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.49+7635C>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60979549 | |||||||
| chr11:60979592 | G | A | 2 | a0002c0003t0001g0027 a0012c0022t0001g0212 |
2 | HG03704.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.49+7678G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60979592 | |||||||
| chr11:60979657 | G | A | 4 | a0002c0002t0001g0026 a0002c0009t0001g0001 a0002c0009t0001g0024 others(1): Show |
6 | HG02615.hp1 HG02622.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.49+7743G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60979657 | |||||||
| chr11:60979695 | T | C | 1 | a0001c0001t0001g0185 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.49+7781T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60979695 | |||||||
| chr11:60979764 | G | A | 163 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0020 others(160): Show |
172 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.49+7850G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60979764 | |||||||
| chr11:60979771 | C | T | 6 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(3): Show |
6 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(3): Show |
intron_variant | MODIFIER | c.49+7857C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60979771 | |||||||
| chr11:60979871 | G | A | 1 | a0004c0004t0001g0209 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.49+7957G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60979871 | |||||||
| chr11:60979901 | C | T | 1 | a0001c0001t0001g0181 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.49+7987C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60979901 | |||||||
| chr11:60979938 | C | T | 1 | a0002c0002t0001g0180 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.49+8024C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60979938 | |||||||
| chr11:60980041 | G | A | 2 | a0006c0008t0001g0075 a0006c0008t0001g0183 |
2 | HG00673.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.49+8127G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60980041 | |||||||
| chr11:60980047 | G | T | 1 | a0001c0001t0001g0179 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.49+8133G>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60980047 | |||||||
| chr11:60980253 | A | G | 277 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(274): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.49+8339A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60980253 | |||||||
| chr11:60980274 | C | T | 2 | a0002c0003t0001g0027 a0012c0022t0001g0212 |
2 | HG03704.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.49+8360C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60980274 | |||||||
| chr11:60980305 | G | C | 252 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(249): Show |
268 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.49+8391G>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60980305 | |||||||
| chr11:60980327 | A | AC | 157 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0020 others(154): Show |
164 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.49+8418dupC | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60980327 | ||||||
| chr11:60980327 | A | ACC | 5 | a0001c0001t0001g0178 a0002c0002t0001g0026 a0002c0009t0001g0001 others(2): Show |
7 | HG00423.hp1 HG02615.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.49+8417_49+8418dup others(2): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60980327 | ||||||
| chr11:60980327 | A | C | 1 | a0002c0002t0001g0055 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.49+8413A>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60980327 | |||||||
| chr11:60980507 | A | G | 1 | a0002c0002t0001g0055 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.49+8593A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60980507 | |||||||
| chr11:60980508 | G | A | 1 | a0002c0002t0001g0055 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.49+8594G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60980508 | |||||||
| chr11:60980508 | GA | G | 65 | a0001c0001t0001g0014 a0001c0001t0001g0253 a0001c0001t0001g0260 others(62): Show |
70 | HG00741.hp2 HG01069.hp2 HG01070.hp2 others(67): Show |
intron_variant | MODIFIER | c.49+8604delA | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60980508 | ||||||
| chr11:60980513 | A | T | 1 | a0010c0020t0001g0043 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.49+8599A>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60980513 | |||||||
| chr11:60980550 | C | A | 6 | a0004c0004t0001g0019 a0004c0004t0001g0050 a0004c0004t0001g0269 others(3): Show |
7 | HG00639.hp2 HG01346.hp2 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.49+8636C>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60980550 | |||||||
| chr11:60980553 | G | T | 1 | a0002c0002t0001g0055 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.49+8639G>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60980553 | |||||||
| chr11:60980766 | G | C | 4 | a0002c0002t0001g0026 a0002c0009t0001g0001 a0002c0009t0001g0024 others(1): Show |
6 | HG02615.hp1 HG02622.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.49+8852G>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60980766 | |||||||
| chr11:60980797 | ACCACTGC others(5): Show |
A | 11 | a0002c0003t0001g0027 a0002c0003t0001g0031 a0003c0005t0001g0028 others(8): Show |
11 | HG00639.hp1 HG01081.hp1 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.49+8884_49+8895del others(12): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60980797 | |||||||
| chr11:60980835 | G | A | 1 | a0002c0003t0001g0060 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.49+8921G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60980835 | |||||||
| chr11:60980876 | C | T | 1 | a0001c0007t0005g0274 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.49+8962C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60980876 | |||||||
| chr11:60981186 | C | T | 1 | a0001c0001t0001g0177 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.49+9272C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60981186 | |||||||
| chr11:60981358 | C | T | 4 | a0001c0010t0002g0015 a0001c0010t0002g0233 a0001c0010t0002g0234 others(1): Show |
5 | HG02717.hp1 HG02895.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.49+9444C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60981358 | |||||||
| chr11:60981467 | C | T | 172 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0020 others(169): Show |
182 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.49+9553C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60981467 | |||||||
| chr11:60981539 | G | T | 3 | a0001c0001t0001g0174 a0001c0001t0001g0176 a0001c0001t0009g0175 |
3 | HG00558.hp1 HG02132.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.49+9625G>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60981539 | |||||||
| chr11:60981625 | C | T | 1 | a0001c0001t0001g0173 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.49+9711C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60981625 | |||||||
| chr11:60981629 | A | G | 5 | a0001c0001t0007g0041 a0001c0010t0002g0015 a0001c0010t0002g0233 others(2): Show |
6 | HG02630.hp1 HG02717.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.49+9715A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60981629 | |||||||
| chr11:60981704 | C | G | 234 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(231): Show |
248 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.49+9790C>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60981704 | |||||||
| chr11:60981774 | T | C | 34 | a0001c0001t0001g0253 a0001c0001t0001g0260 a0001c0001t0007g0258 others(31): Show |
37 | HG00741.hp2 HG01069.hp2 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.49+9860T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60981774 | |||||||
| chr11:60981784 | G | A | 58 | a0001c0001t0001g0014 a0001c0001t0001g0253 a0001c0001t0001g0260 others(55): Show |
62 | HG00741.hp2 HG01069.hp2 HG01070.hp2 others(59): Show |
intron_variant | MODIFIER | c.49+9870G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60981784 | |||||||
| chr11:60981986 | A | T | 8 | a0001c0001t0001g0014 a0002c0003t0001g0215 a0002c0003t0001g0216 others(5): Show |
9 | HG01167.hp1 HG01169.hp2 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.49+10072A>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60981986 | |||||||
| chr11:60982002 | C | G | 1 | a0002c0002t0001g0263 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.49+10088C>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60982002 | |||||||
| chr11:60982042 | G | A | 1 | a0001c0001t0001g0084 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.49+10128G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60982042 | |||||||
| chr11:60982068 | CG | C | 210 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0020 others(207): Show |
225 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.49+10165delG | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60982068 | ||||||
| chr11:60982088 | A | G | 10 | a0002c0003t0001g0027 a0002c0003t0001g0031 a0003c0005t0001g0028 others(7): Show |
10 | HG00639.hp1 HG01081.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.49+10174A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60982088 | |||||||
| chr11:60982097 | G | A | 5 | a0001c0001t0007g0041 a0001c0007t0001g0047 a0003c0011t0004g0045 others(2): Show |
5 | HG02055.hp2 HG02145.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.49+10183G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60982097 | |||||||
| chr11:60982112 | C | G | 1 | a0002c0002t0001g0055 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.49+10198C>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60982112 | |||||||
| chr11:60982113 | G | C | 1 | a0002c0002t0001g0055 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.49+10199G>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60982113 | |||||||
| chr11:60982123 | C | CGGTCTGT others(44): Show |
1 | a0002c0002t0001g0055 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.49+10232_49+10233i others(53): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60982123 | ||||||
| chr11:60982123 | C | CGGTCTGT others(44): Show |
1 | a0001c0001t0001g0187 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.49+10232_49+10233i others(53): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60982123 | ||||||
| chr11:60982123 | C | CGGTCTGT others(44): Show |
123 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0020 others(120): Show |
135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.49+10232_49+10233i others(53): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60982123 | ||||||
| chr11:60982123 | C | CGGTCTGT others(45): Show |
86 | a0001c0001t0001g0014 a0001c0001t0001g0058 a0001c0001t0001g0061 others(83): Show |
91 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.49+10232_49+10233i others(54): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60982123 | ||||||
| chr11:60982123 | C | CGGTCTGT others(46): Show |
42 | a0001c0001t0001g0084 a0001c0001t0001g0253 a0001c0001t0011g0277 others(39): Show |
43 | HG00423.hp2 HG00639.hp2 HG01081.hp1 others(40): Show |
intron_variant | MODIFIER | c.49+10232_49+10233i others(55): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60982123 | ||||||
| chr11:60982123 | C | CGGTCTGT others(47): Show |
16 | a0001c0001t0001g0066 a0001c0010t0002g0233 a0001c0010t0002g0234 others(13): Show |
17 | HG00639.hp1 HG01346.hp2 HG01358.hp2 others(14): Show |
intron_variant | MODIFIER | c.49+10232_49+10233i others(56): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60982123 | ||||||
| chr11:60982123 | C | CGGTCTGT others(48): Show |
2 | a0001c0001t0001g0065 a0001c0007t0005g0274 |
2 | HG02572.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.49+10232_49+10233i others(57): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60982123 | ||||||
| chr11:60982123 | C | CGGTCTGT others(46): Show |
1 | a0001c0007t0001g0021 | 2 | HG02818.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.49+10232_49+10233i others(55): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60982123 | ||||||
| chr11:60982123 | C | CGGTCTGT others(43): Show |
1 | a0002c0002t0001g0054 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.49+10232_49+10233i others(52): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60982123 | ||||||
| chr11:60982125 | G | GTCTGTGC others(45): Show |
5 | a0002c0003t0001g0241 a0002c0003t0001g0242 a0002c0003t0001g0245 others(2): Show |
5 | HG00741.hp2 HG01099.hp1 HG01167.hp2 others(2): Show |
intron_variant | MODIFIER | c.49+10232_49+10233i others(54): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60982125 | ||||||
| chr11:60982219 | T | C | 1 | a0003c0011t0001g0226 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.49+10305T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60982219 | |||||||
| chr11:60982519 | G | A | 3 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0006c0008t0001g0064 |
3 | HG00099.hp1 HG00140.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.49+10605G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60982519 | |||||||
| chr11:60982562 | C | T | 1 | a0002c0003t0001g0239 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.49+10648C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60982562 | |||||||
| chr11:60982576 | T | C | 243 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(240): Show |
258 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(255): Show |
intron_variant | MODIFIER | c.49+10662T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60982576 | |||||||
| chr11:60982653 | C | T | 1 | a0002c0003t0001g0060 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.49+10739C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60982653 | |||||||
| chr11:60982715 | G | C | 4 | a0001c0010t0002g0015 a0001c0010t0002g0233 a0001c0010t0002g0234 others(1): Show |
5 | HG02717.hp1 HG02895.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.49+10801G>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60982715 | |||||||
| chr11:60982719 | A | T | 1 | a0002c0003t0001g0218 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.49+10805A>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60982719 | |||||||
| chr11:60982743 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.49+10829C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60982743 | |||||||
| chr11:60982768 | G | A | 238 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(235): Show |
252 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(249): Show |
intron_variant | MODIFIER | c.49+10854G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60982768 | |||||||
| chr11:60982775 | G | A | 24 | a0001c0001t0001g0014 a0001c0001t0011g0277 a0001c0007t0001g0227 others(21): Show |
25 | HG01167.hp1 HG01169.hp2 HG01257.hp2 others(22): Show |
intron_variant | MODIFIER | c.49+10861G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60982775 | |||||||
| chr11:60982776 | A | G | 1 | a0002c0002t0001g0055 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.49+10862A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60982776 | |||||||
| chr11:60982826 | GTCTGCAG others(4): Show |
G | 243 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(240): Show |
258 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(255): Show |
intron_variant | MODIFIER | c.49+10916_49+10926d others(13): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60982826 | ||||||
| chr11:60982964 | G | T | 1 | a0001c0007t0001g0021 | 2 | HG02818.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.49+11050G>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60982964 | |||||||
| chr11:60983101 | T | C | 1 | a0001c0001t0007g0041 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.49+11187T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60983101 | |||||||
| chr11:60983202 | G | T | 253 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(250): Show |
270 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.49+11288G>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60983202 | |||||||
| chr11:60983247 | C | A | 5 | a0002c0002t0001g0051 a0002c0002t0001g0052 a0002c0002t0001g0053 others(2): Show |
5 | NA18949.hp1 NA18977.hp1 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.49+11333C>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60983247 | |||||||
| chr11:60983302 | G | C | 2 | a0003c0005t0001g0044 a0003c0005t0001g0127 |
2 | HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.49+11388G>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60983302 | |||||||
| chr11:60983394 | T | C | 5 | a0001c0001t0007g0041 a0001c0010t0002g0015 a0001c0010t0002g0233 others(2): Show |
6 | HG02630.hp1 HG02717.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.49+11480T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60983394 | |||||||
| chr11:60983453 | C | G | 7 | a0001c0007t0005g0274 a0004c0004t0001g0019 a0004c0004t0001g0050 others(4): Show |
8 | HG00639.hp2 HG01346.hp2 HG01358.hp2 others(5): Show |
intron_variant | MODIFIER | c.49+11539C>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60983453 | |||||||
| chr11:60983474 | G | A | 1 | a0002c0003t0001g0221 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.49+11560G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60983474 | |||||||
| chr11:60983505 | A | G | 1 | a0002c0003t0001g0060 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.49+11591A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60983505 | |||||||
| chr11:60983522 | T | C | 11 | a0002c0003t0001g0031 a0003c0005t0001g0028 a0005c0006t0001g0029 others(8): Show |
11 | HG00639.hp1 HG01081.hp1 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.49+11608T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60983522 | |||||||
| chr11:60983636 | T | G | 3 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0006c0008t0001g0064 |
3 | HG00099.hp1 HG00140.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.49+11722T>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60983636 | |||||||
| chr11:60983805 | G | A | 143 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0020 others(140): Show |
150 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.49+11891G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60983805 | |||||||
| chr11:60984087 | T | G | 5 | a0001c0001t0007g0041 a0001c0010t0002g0015 a0001c0010t0002g0233 others(2): Show |
6 | HG02630.hp1 HG02717.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.49+12173T>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60984087 | |||||||
| chr11:60984097 | C | A | 92 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0020 others(89): Show |
95 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.49+12183C>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60984097 | |||||||
| chr11:60984170 | A | G | 69 | a0001c0001t0001g0014 a0001c0001t0001g0253 a0001c0001t0001g0260 others(66): Show |
74 | HG00741.hp2 HG01069.hp2 HG01070.hp2 others(71): Show |
intron_variant | MODIFIER | c.49+12256A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60984170 | |||||||
| chr11:60984282 | A | G | 1 | a0004c0004t0001g0273 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.49+12368A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60984282 | |||||||
| chr11:60984330 | G | A | 1 | a0003c0011t0001g0226 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.49+12416G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60984330 | |||||||
| chr11:60984451 | C | T | 250 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(247): Show |
267 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.49+12537C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60984451 | |||||||
| chr11:60984500 | G | A | 279 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(276): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.49+12586G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60984500 | |||||||
| chr11:60984534 | G | A | 11 | a0001c0007t0005g0274 a0002c0002t0001g0026 a0002c0009t0001g0001 others(8): Show |
14 | HG00639.hp2 HG01346.hp2 HG01358.hp2 others(11): Show |
intron_variant | MODIFIER | c.49+12620G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60984534 | |||||||
| chr11:60984710 | T | C | 3 | a0001c0010t0002g0015 a0001c0010t0002g0233 a0001c0010t0002g0234 |
4 | HG02717.hp1 HG02895.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.49+12796T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60984710 | |||||||
| chr11:60984717 | G | A | 4 | a0002c0003t0001g0060 a0002c0003t0001g0067 a0002c0003t0001g0125 others(1): Show |
4 | HG00438.hp2 HG03492.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.49+12803G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60984717 | |||||||
| chr11:60984750 | A | G | 2 | a0001c0014t0001g0154 a0002c0002t0001g0155 |
2 | NA18952.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.49+12836A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60984750 | |||||||
| chr11:60984799 | T | A | 1 | a0001c0001t0001g0128 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.49+12885T>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60984799 | |||||||
| chr11:60984807 | G | C | 13 | a0002c0003t0001g0027 a0002c0003t0001g0031 a0003c0005t0001g0028 others(10): Show |
13 | HG00639.hp1 HG01081.hp1 HG01256.hp1 others(10): Show |
intron_variant | MODIFIER | c.49+12893G>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60984807 | |||||||
| chr11:60985074 | G | A | 2 | a0001c0001t0001g0065 a0001c0001t0001g0066 |
2 | HG01884.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.49+13160G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60985074 | |||||||
| chr11:60985142 | C | T | 3 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0006c0008t0001g0064 |
3 | HG00099.hp1 HG00140.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.49+13228C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60985142 | |||||||
| chr11:60985174 | C | CT | 33 | a0001c0001t0001g0065 a0001c0001t0001g0081 a0001c0001t0001g0198 others(30): Show |
38 | HG00099.hp2 HG00735.hp1 HG01070.hp1 others(35): Show |
intron_variant | MODIFIER | c.49+13286dupT | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60985174 | ||||||
| chr11:60985174 | C | CTT | 7 | a0001c0001t0001g0194 a0001c0001t0001g0201 a0002c0003t0001g0235 others(4): Show |
7 | HG01175.hp1 HG01496.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.49+13285_49+13286d others(4): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60985174 | ||||||
| chr11:60985174 | CT | C | 143 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0020 others(140): Show |
152 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.49+13286delT | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60985174 | ||||||
| chr11:60985174 | CTT | C | 10 | a0001c0001t0001g0091 a0001c0001t0001g0129 a0001c0001t0001g0156 others(7): Show |
11 | HG00639.hp2 HG01346.hp2 HG01358.hp2 others(8): Show |
intron_variant | MODIFIER | c.49+13285_49+13286d others(4): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60985174 | ||||||
| chr11:60985223 | G | A | 4 | a0001c0010t0002g0015 a0001c0010t0002g0233 a0001c0010t0002g0234 others(1): Show |
5 | HG02717.hp1 HG02895.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.49+13309G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60985223 | |||||||
| chr11:60985357 | G | T | 4 | a0002c0002t0001g0026 a0002c0009t0001g0001 a0002c0009t0001g0024 others(1): Show |
6 | HG02615.hp1 HG02622.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.49+13443G>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60985357 | |||||||
| chr11:60985400 | G | A | 1 | a0003c0005t0001g0127 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.49+13486G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60985400 | |||||||
| chr11:60985504 | T | C | 4 | a0001c0010t0002g0015 a0001c0010t0002g0233 a0001c0010t0002g0234 others(1): Show |
5 | HG02717.hp1 HG02895.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.49+13590T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60985504 | |||||||
| chr11:60985573 | A | AAT | 142 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0020 others(139): Show |
149 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.49+13671_49+13672d others(4): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60985573 | ||||||
| chr11:60985643 | A | C | 4 | a0001c0010t0002g0015 a0001c0010t0002g0233 a0001c0010t0002g0234 others(1): Show |
5 | HG02717.hp1 HG02895.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.49+13729A>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60985643 | |||||||
| chr11:60985681 | G | A | 2 | a0001c0001t0001g0065 a0001c0001t0001g0066 |
2 | HG01884.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.49+13767G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60985681 | |||||||
| chr11:60986018 | C | T | 1 | a0013c0017t0001g0214 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.49+14104C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60986018 | |||||||
| chr11:60986051 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.49+14137C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60986051 | |||||||
| chr11:60986244 | C | T | 1 | a0002c0003t0001g0231 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.49+14330C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60986244 | |||||||
| chr11:60986296 | T | C | 3 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0006c0008t0001g0064 |
3 | HG00099.hp1 HG00140.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.49+14382T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60986296 | |||||||
| chr11:60986468 | A | G | 5 | a0001c0001t0001g0014 a0002c0003t0001g0215 a0002c0003t0001g0216 others(2): Show |
6 | HG01167.hp1 HG01169.hp2 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.49+14554A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60986468 | |||||||
| chr11:60986488 | C | T | 3 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0006c0008t0001g0064 |
3 | HG00099.hp1 HG00140.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.49+14574C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60986488 | |||||||
| chr11:60986525 | C | G | 5 | a0001c0001t0007g0041 a0001c0010t0002g0015 a0001c0010t0002g0233 others(2): Show |
6 | HG02630.hp1 HG02717.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.49+14611C>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60986525 | |||||||
| chr11:60986614 | T | C | 1 | a0001c0007t0001g0047 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.49+14700T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60986614 | |||||||
| chr11:60986750 | C | T | 4 | a0002c0003t0001g0060 a0002c0003t0001g0067 a0002c0003t0001g0125 others(1): Show |
4 | HG00438.hp2 HG03492.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.49+14836C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60986750 | |||||||
| chr11:60986781 | T | C | 3 | a0001c0010t0002g0015 a0001c0010t0002g0233 a0001c0010t0002g0234 |
4 | HG02717.hp1 HG02895.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.49+14867T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60986781 | |||||||
| chr11:60986836 | G | A | 2 | a0001c0001t0001g0102 a0001c0001t0001g0190 |
2 | NA18946.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.49+14922G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60986836 | |||||||
| chr11:60987001 | G | A | 2 | a0002c0003t0001g0027 a0012c0022t0001g0212 |
2 | HG03704.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.49+15087G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60987001 | |||||||
| chr11:60987013 | G | A | 1 | a0002c0003t0001g0040 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.49+15099G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60987013 | |||||||
| chr11:60987043 | G | A | 4 | a0001c0010t0002g0015 a0001c0010t0002g0233 a0001c0010t0002g0234 others(1): Show |
5 | HG02717.hp1 HG02895.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.49+15129G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60987043 | |||||||
| chr11:60987081 | T | A | 2 | a0002c0003t0001g0022 a0002c0003t0001g0042 |
2 | HG01243.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.49+15167T>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60987081 | |||||||
| chr11:60987094 | C | T | 3 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0007t0001g0021 |
4 | HG01884.hp2 HG02572.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.49+15180C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60987094 | |||||||
| chr11:60987272 | T | C | 4 | a0002c0003t0001g0060 a0002c0003t0001g0067 a0002c0003t0001g0125 others(1): Show |
4 | HG00438.hp2 HG03492.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.49+15358T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60987272 | |||||||
| chr11:60987312 | G | A | 2 | a0004c0004t0001g0269 a0004c0004t0001g0271 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.49+15398G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60987312 | |||||||
| chr11:60987524 | T | A | 1 | a0005c0006t0001g0123 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.49+15610T>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60987524 | |||||||
| chr11:60987544 | G | GGT | 7 | a0001c0007t0005g0274 a0004c0004t0001g0019 a0004c0004t0001g0050 others(4): Show |
8 | HG00639.hp2 HG01346.hp2 HG01358.hp2 others(5): Show |
intron_variant | MODIFIER | c.49+15641_49+15642d others(4): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60987544 | ||||||
| chr11:60987545 | G | GTGTGTGT others(11): Show |
4 | a0005c0006t0001g0029 a0005c0006t0001g0033 a0005c0006t0001g0243 others(1): Show |
4 | HG00639.hp1 HG01256.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.49+15635_49+15652d others(20): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60987545 | ||||||
| chr11:60987723 | A | AGAGAG | 142 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0020 others(139): Show |
149 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.49+15809_49+15810i others(7): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60987723 | |||||||
| chr11:60987724 | T | G | 142 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0020 others(139): Show |
149 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.49+15810T>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60987724 | |||||||
| chr11:60987725 | C | A | 142 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0020 others(139): Show |
149 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.49+15811C>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60987725 | |||||||
| chr11:60987728 | T | G | 142 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0020 others(139): Show |
149 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.49+15814T>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60987728 | |||||||
| chr11:60987729 | T | G | 142 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0020 others(139): Show |
149 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.49+15815T>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60987729 | |||||||
| chr11:60987730 | T | A | 142 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0020 others(139): Show |
149 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.49+15816T>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60987730 | |||||||
| chr11:60987731 | C | G | 142 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0020 others(139): Show |
149 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.49+15817C>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60987731 | |||||||
| chr11:60987763 | A | T | 3 | a0002c0002t0001g0224 a0002c0002t0001g0225 a0002c0002t0001g0228 |
3 | HG02109.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.49+15849A>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60987763 | |||||||
| chr11:60987779 | C | T | 238 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(235): Show |
252 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(249): Show |
intron_variant | MODIFIER | c.49+15865C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60987779 | |||||||
| chr11:60987862 | A | G | 11 | a0002c0003t0001g0031 a0003c0005t0001g0028 a0005c0006t0001g0029 others(8): Show |
11 | HG00639.hp1 HG01081.hp1 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.49+15948A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60987862 | |||||||
| chr11:60987868 | G | T | 3 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0006c0008t0001g0064 |
3 | HG00099.hp1 HG00140.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.49+15954G>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60987868 | |||||||
| chr11:60987889 | C | T | 4 | a0002c0002t0001g0026 a0002c0009t0001g0001 a0002c0009t0001g0024 others(1): Show |
6 | HG02615.hp1 HG02622.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.49+15975C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60987889 | |||||||
| chr11:60987916 | G | T | 3 | a0002c0002t0001g0224 a0002c0002t0001g0225 a0002c0002t0001g0228 |
3 | HG02109.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.49+16002G>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60987916 | |||||||
| chr11:60987947 | A | T | 4 | a0001c0001t0001g0099 a0001c0001t0001g0172 a0001c0001t0001g0181 others(1): Show |
4 | HG02055.hp1 NA18747.hp1 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.49+16033A>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60987947 | |||||||
| chr11:60988012 | G | A | 11 | a0001c0007t0005g0274 a0002c0002t0001g0026 a0002c0009t0001g0001 others(8): Show |
14 | HG00639.hp2 HG01346.hp2 HG01358.hp2 others(11): Show |
intron_variant | MODIFIER | c.49+16098G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60988012 | |||||||
| chr11:60988045 | A | G | 21 | a0001c0001t0001g0081 a0001c0001t0001g0194 a0001c0001t0001g0198 others(18): Show |
24 | HG00099.hp2 HG00735.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.49+16131A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60988045 | |||||||
| chr11:60988478 | AGAG | A | 4 | a0001c0010t0002g0015 a0001c0010t0002g0233 a0001c0010t0002g0234 others(1): Show |
5 | HG02717.hp1 HG02895.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.49+16569_49+16571d others(5): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60988478 | ||||||
| chr11:60988619 | C | T | 4 | a0001c0010t0002g0015 a0001c0010t0002g0233 a0001c0010t0002g0234 others(1): Show |
5 | HG02717.hp1 HG02895.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.49+16705C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60988619 | |||||||
| chr11:60988703 | G | A | 140 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0049 others(137): Show |
146 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.49+16789G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60988703 | |||||||
| chr11:60988884 | G | T | 69 | a0001c0001t0001g0014 a0001c0001t0001g0253 a0001c0001t0001g0260 others(66): Show |
74 | HG00741.hp2 HG01069.hp2 HG01070.hp2 others(71): Show |
intron_variant | MODIFIER | c.49+16970G>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60988884 | |||||||
| chr11:60989116 | C | T | 171 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0020 others(168): Show |
180 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(177): Show |
intron_variant | MODIFIER | c.49+17202C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60989116 | |||||||
| chr11:60989287 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.50-17287C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60989287 | |||||||
| chr11:60989370 | C | T | 1 | a0001c0001t0007g0041 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.50-17204C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60989370 | |||||||
| chr11:60989677 | T | C | 1 | a0001c0001t0011g0277 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.50-16897T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60989677 | |||||||
| chr11:60989822 | G | A | 11 | a0002c0003t0001g0031 a0003c0005t0001g0028 a0005c0006t0001g0029 others(8): Show |
11 | HG00639.hp1 HG01081.hp1 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.50-16752G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60989822 | |||||||
| chr11:60989953 | A | T | 3 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0006c0008t0001g0064 |
3 | HG00099.hp1 HG00140.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.50-16621A>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60989953 | |||||||
| chr11:60989959 | C | G | 3 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0006c0008t0001g0064 |
3 | HG00099.hp1 HG00140.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.50-16615C>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60989959 | |||||||
| chr11:60990005 | T | A | 1 | a0009c0021t0001g0130 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.50-16569T>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60990005 | |||||||
| chr11:60990070 | A | T | 81 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0020 others(78): Show |
84 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.50-16504A>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60990070 | |||||||
| chr11:60990160 | C | T | 4 | a0001c0007t0001g0219 a0001c0007t0001g0223 a0002c0002t0001g0222 others(1): Show |
4 | HG01496.hp1 HG02647.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.50-16414C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60990160 | |||||||
| chr11:60990161 | C | T | 69 | a0001c0001t0001g0014 a0001c0001t0001g0253 a0001c0001t0001g0260 others(66): Show |
74 | HG00741.hp2 HG01069.hp2 HG01070.hp2 others(71): Show |
intron_variant | MODIFIER | c.50-16413C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60990161 | |||||||
| chr11:60990255 | C | T | 4 | a0002c0002t0001g0026 a0002c0009t0001g0001 a0002c0009t0001g0024 others(1): Show |
6 | HG02615.hp1 HG02622.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.50-16319C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60990255 | |||||||
| chr11:60990293 | C | T | 2 | a0001c0001t0001g0084 a0002c0002t0001g0254 |
2 | NA18971.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.50-16281C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60990293 | |||||||
| chr11:60990385 | C | T | 142 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0020 others(139): Show |
149 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.50-16189C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60990385 | |||||||
| chr11:60990504 | G | A | 2 | a0002c0003t0001g0027 a0012c0022t0001g0212 |
2 | HG03704.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.50-16070G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60990504 | |||||||
| chr11:60990544 | C | G | 1 | a0002c0003t0001g0267 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.50-16030C>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60990544 | |||||||
| chr11:60990651 | C | T | 3 | a0002c0003t0001g0216 a0002c0003t0001g0217 a0002c0003t0001g0218 |
3 | HG01257.hp2 HG01346.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.50-15923C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60990651 | |||||||
| chr11:60990732 | A | G | 2 | a0001c0001t0001g0089 a0001c0001t0001g0178 |
2 | HG00423.hp1 HG00597.hp2 |
intron_variant | MODIFIER | c.50-15842A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60990732 | |||||||
| chr11:60990752 | CAATG | C | 3 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0006c0008t0001g0064 |
3 | HG00099.hp1 HG00140.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.50-15821_50-15818d others(6): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60990752 | |||||||
| chr11:60990756 | G | T | 1 | a0003c0005t0001g0044 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.50-15818G>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60990756 | |||||||
| chr11:60990806 | A | AGGCTGAG others(111): Show |
2 | a0002c0003t0001g0027 a0012c0022t0001g0212 |
2 | HG03704.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.50-15768_50-15767i others(120): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60990806 | |||||||
| chr11:60990806 | A | AGGCTGAG others(111): Show |
15 | a0002c0003t0001g0031 a0002c0003t0001g0060 a0002c0003t0001g0067 others(12): Show |
15 | HG00438.hp2 HG00639.hp1 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.50-15768_50-15767i others(120): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60990806 | |||||||
| chr11:60990806 | A | AGGCTGAG others(113): Show |
143 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0020 others(140): Show |
150 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.50-15768_50-15767i others(122): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60990806 | |||||||
| chr11:60990808 | A | C | 160 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0020 others(157): Show |
167 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.50-15766A>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60990808 | |||||||
| chr11:60990949 | G | C | 1 | a0004c0004t0001g0273 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.50-15625G>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60990949 | |||||||
| chr11:60990989 | G | A | 1 | a0001c0001t0001g0102 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.50-15585G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60990989 | |||||||
| chr11:60991139 | C | T | 4 | a0002c0002t0001g0026 a0002c0009t0001g0001 a0002c0009t0001g0024 others(1): Show |
6 | HG02615.hp1 HG02622.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.50-15435C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60991139 | |||||||
| chr11:60991141 | T | C | 5 | a0001c0007t0001g0256 a0002c0002t0001g0026 a0002c0009t0001g0001 others(2): Show |
7 | HG02257.hp1 HG02615.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.50-15433T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60991141 | |||||||
| chr11:60991148 | TC | T | 4 | a0002c0002t0001g0026 a0002c0009t0001g0001 a0002c0009t0001g0024 others(1): Show |
6 | HG02615.hp1 HG02622.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.50-15425delC | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60991148 | |||||||
| chr11:60991149 | C | CT | 207 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0020 others(204): Show |
218 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(215): Show |
intron_variant | MODIFIER | c.50-15407dupT | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60991149 | ||||||
| chr11:60991149 | C | CTT | 12 | a0001c0001t0001g0014 a0002c0002t0001g0070 a0002c0002t0001g0180 others(9): Show |
13 | HG00323.hp2 HG00438.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.50-15408_50-15407d others(4): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60991149 | ||||||
| chr11:60991149 | CT | C | 18 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0202 others(15): Show |
19 | HG00639.hp1 HG01081.hp1 HG01256.hp1 others(16): Show |
intron_variant | MODIFIER | c.50-15407delT | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60991149 | ||||||
| chr11:60991152 | T | TC | 4 | a0002c0003t0001g0002 a0002c0003t0001g0022 a0002c0003t0001g0023 others(1): Show |
5 | HG01243.hp1 HG02647.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.50-15422_50-15421i others(3): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60991152 | |||||||
| chr11:60991228 | G | A | 4 | a0001c0007t0001g0251 a0001c0007t0001g0265 a0001c0007t0001g0266 others(1): Show |
4 | HG03041.hp1 HG03098.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.50-15346G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60991228 | |||||||
| chr11:60991297 | T | G | 4 | a0001c0010t0002g0015 a0001c0010t0002g0233 a0001c0010t0002g0234 others(1): Show |
5 | HG02717.hp1 HG02895.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.50-15277T>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60991297 | |||||||
| chr11:60991371 | T | C | 2 | a0002c0002t0001g0238 a0003c0011t0005g0048 |
2 | HG02723.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.50-15203T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60991371 | |||||||
| chr11:60991377 | TC | T | 2 | a0001c0007t0001g0021 a0003c0011t0004g0045 |
3 | HG02818.hp1 HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.50-15194delC | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60991377 | ||||||
| chr11:60991535 | C | T | 1 | a0002c0003t0001g0239 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.50-15039C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60991535 | |||||||
| chr11:60991555 | A | G | 10 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0007t0005g0274 others(7): Show |
11 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(8): Show |
intron_variant | MODIFIER | c.50-15019A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60991555 | |||||||
| chr11:60991571 | T | C | 9 | a0001c0001t0007g0258 a0001c0007t0001g0017 a0001c0007t0001g0018 others(6): Show |
10 | HG02257.hp1 HG02572.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.50-15003T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60991571 | |||||||
| chr11:60991648 | C | CT | 7 | a0001c0001t0007g0041 a0001c0010t0002g0015 a0001c0010t0002g0233 others(4): Show |
8 | HG02055.hp2 HG02145.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.50-14923dupT | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60991648 | ||||||
| chr11:60991856 | CTATATAT others(5): Show |
C | 11 | a0002c0003t0001g0031 a0003c0005t0001g0028 a0005c0006t0001g0029 others(8): Show |
11 | HG00639.hp1 HG01081.hp1 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.50-14698_50-14687d others(14): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60991856 | ||||||
| chr11:60991873 | T | G | 6 | a0002c0003t0001g0060 a0002c0003t0001g0067 a0002c0003t0001g0082 others(3): Show |
6 | HG00438.hp2 HG02896.hp2 HG03492.hp2 others(3): Show |
intron_variant | MODIFIER | c.50-14701T>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60991873 | |||||||
| chr11:60991898 | A | G | 2 | a0001c0007t0001g0021 a0003c0011t0004g0045 |
3 | HG02818.hp1 HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.50-14676A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60991898 | |||||||
| chr11:60991922 | G | T | 1 | a0002c0003t0001g0231 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.50-14652G>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60991922 | |||||||
| chr11:60991989 | C | G | 1 | a0001c0001t0007g0041 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.50-14585C>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60991989 | |||||||
| chr11:60992182 | T | C | 19 | a0001c0001t0001g0062 a0001c0001t0001g0104 a0001c0001t0007g0258 others(16): Show |
21 | HG00140.hp1 HG01433.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.50-14392T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60992182 | |||||||
| chr11:60992267 | C | T | 7 | a0001c0010t0002g0134 a0002c0002t0001g0038 a0002c0002t0001g0039 others(4): Show |
7 | HG01109.hp2 HG01243.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.50-14307C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60992267 | |||||||
| chr11:60992332 | C | CT | 95 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0020 others(92): Show |
98 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.50-14231dupT | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60992332 | ||||||
| chr11:60992375 | G | A | 22 | a0001c0001t0001g0122 a0001c0001t0001g0140 a0001c0001t0001g0156 others(19): Show |
22 | HG00438.hp2 HG00558.hp1 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.50-14199G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60992375 | |||||||
| chr11:60992656 | G | A | 1 | a0001c0001t0009g0175 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.50-13918G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60992656 | |||||||
| chr11:60992705 | G | A | 2 | a0005c0006t0001g0275 a0005c0006t0001g0276 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.50-13869G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60992705 | |||||||
| chr11:60992823 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.50-13751G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60992823 | |||||||
| chr11:60992843 | A | G | 1 | a0002c0002t0001g0155 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.50-13731A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60992843 | |||||||
| chr11:60992887 | C | T | 1 | a0002c0003t0001g0264 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.50-13687C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60992887 | |||||||
| chr11:60992933 | G | A | 2 | a0001c0001t0001g0065 a0001c0001t0001g0066 |
2 | HG01884.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.50-13641G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60992933 | |||||||
| chr11:60993058 | C | T | 94 | a0001c0001t0001g0201 a0002c0002t0001g0011 a0002c0002t0001g0026 others(91): Show |
100 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.50-13516C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60993058 | |||||||
| chr11:60993103 | G | A | 7 | a0001c0001t0001g0094 a0001c0001t0001g0102 a0001c0001t0001g0136 others(4): Show |
7 | NA18946.hp2 NA18951.hp2 NA18975.hp2 others(4): Show |
intron_variant | MODIFIER | c.50-13471G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60993103 | |||||||
| chr11:60993140 | C | G | 20 | a0005c0006t0001g0009 a0005c0006t0001g0013 a0005c0006t0001g0029 others(17): Show |
22 | HG00140.hp2 HG00639.hp1 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.50-13434C>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60993140 | |||||||
| chr11:60993322 | G | GAGAGAAT others(19): Show |
20 | a0005c0006t0001g0009 a0005c0006t0001g0013 a0005c0006t0001g0029 others(17): Show |
22 | HG00140.hp2 HG00639.hp1 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.50-13251_50-13250i others(28): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60993322 | ||||||
| chr11:60993435 | C | T | 6 | a0004c0004t0001g0019 a0004c0004t0001g0121 a0004c0004t0001g0166 others(3): Show |
7 | HG00323.hp1 HG01123.hp2 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.50-13139C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60993435 | |||||||
| chr11:60993480 | C | A | 279 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(276): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.50-13094C>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60993480 | |||||||
| chr11:60993499 | G | A | 20 | a0005c0006t0001g0009 a0005c0006t0001g0013 a0005c0006t0001g0029 others(17): Show |
22 | HG00140.hp2 HG00639.hp1 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.50-13075G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60993499 | |||||||
| chr11:60993507 | C | A | 1 | a0001c0007t0001g0256 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.50-13067C>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60993507 | |||||||
| chr11:60993508 | G | A | 5 | a0003c0005t0001g0229 a0003c0011t0001g0226 a0003c0011t0004g0045 others(2): Show |
5 | HG02145.hp2 HG02258.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.50-13066G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60993508 | |||||||
| chr11:60993525 | C | T | 5 | a0003c0005t0001g0229 a0003c0011t0001g0226 a0003c0011t0004g0045 others(2): Show |
5 | HG02145.hp2 HG02258.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.50-13049C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60993525 | |||||||
| chr11:60993530 | G | GT | 53 | a0001c0001t0001g0201 a0002c0003t0001g0004 a0003c0005t0001g0010 others(50): Show |
58 | HG00323.hp1 HG00423.hp2 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.50-13043dupT | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60993530 | ||||||
| chr11:60993583 | T | C | 1 | a0002c0016t0001g0116 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.50-12991T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60993583 | |||||||
| chr11:60993606 | C | T | 2 | a0001c0001t0001g0065 a0001c0001t0001g0066 |
2 | HG01884.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.50-12968C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60993606 | |||||||
| chr11:60993645 | G | A | 6 | a0007c0012t0001g0036 a0007c0012t0003g0032 a0007c0012t0003g0034 others(3): Show |
6 | HG01081.hp1 HG01361.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.50-12929G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60993645 | |||||||
| chr11:60993656 | T | A | 1 | a0002c0003t0001g0082 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.50-12918T>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60993656 | |||||||
| chr11:60993708 | G | A | 1 | a0003c0005t0001g0159 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.50-12866G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60993708 | |||||||
| chr11:60993849 | T | C | 19 | a0001c0001t0007g0258 a0001c0007t0001g0017 a0001c0007t0001g0018 others(16): Show |
21 | HG02055.hp2 HG02257.hp1 HG02572.hp1 others(18): Show |
intron_variant | MODIFIER | c.50-12725T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60993849 | |||||||
| chr11:60993904 | G | A | 1 | a0001c0001t0001g0260 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.50-12670G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60993904 | |||||||
| chr11:60994033 | C | T | 1 | a0002c0003t0001g0168 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.50-12541C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60994033 | |||||||
| chr11:60994096 | A | G | 279 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(276): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.50-12478A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60994096 | |||||||
| chr11:60994127 | G | A | 1 | a0002c0003t0001g0082 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.50-12447G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60994127 | |||||||
| chr11:60994167 | G | A | 2 | a0002c0002t0001g0196 a0002c0002t0001g0197 |
2 | HG02976.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.50-12407G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60994167 | |||||||
| chr11:60994241 | G | A | 5 | a0003c0005t0001g0229 a0003c0011t0001g0226 a0003c0011t0004g0045 others(2): Show |
5 | HG02145.hp2 HG02258.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.50-12333G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60994241 | |||||||
| chr11:60994272 | C | T | 5 | a0003c0005t0001g0229 a0003c0011t0001g0226 a0003c0011t0004g0045 others(2): Show |
5 | HG02145.hp2 HG02258.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.50-12302C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60994272 | |||||||
| chr11:60994302 | G | A | 1 | a0002c0003t0001g0125 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.50-12272G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60994302 | |||||||
| chr11:60994302 | G | T | 1 | a0001c0001t0007g0041 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.50-12272G>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60994302 | |||||||
| chr11:60994457 | C | CAAAAAAA others(2): Show |
53 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(50): Show |
57 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.50-12111_50-12103d others(11): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60994457 | ||||||
| chr11:60994457 | C | CAAAAAAA others(3): Show |
20 | a0001c0001t0001g0061 a0001c0001t0001g0080 a0001c0001t0001g0084 others(17): Show |
20 | HG00423.hp1 HG01106.hp1 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.50-12112_50-12103d others(12): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60994457 | ||||||
| chr11:60994457 | C | CAAAAAAA others(4): Show |
46 | a0001c0001t0001g0136 a0001c0001t0007g0258 a0001c0007t0001g0018 others(43): Show |
52 | HG00741.hp2 HG01071.hp1 HG01099.hp1 others(49): Show |
intron_variant | MODIFIER | c.50-12113_50-12103d others(13): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60994457 | ||||||
| chr11:60994457 | C | CAAAAAAA others(5): Show |
31 | a0001c0001t0011g0277 a0001c0007t0001g0017 a0001c0007t0001g0021 others(28): Show |
33 | HG00099.hp2 HG00438.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.50-12114_50-12103d others(14): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60994457 | ||||||
| chr11:60994457 | C | CAAAAAAA others(6): Show |
5 | a0002c0002t0001g0228 a0002c0003t0001g0082 a0002c0009t0001g0024 others(2): Show |
5 | HG01081.hp1 HG02622.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.50-12115_50-12103d others(15): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60994457 | ||||||
| chr11:60994457 | C | CAAAAAAA others(7): Show |
42 | a0001c0001t0001g0063 a0001c0001t0001g0202 a0001c0001t0001g0207 others(39): Show |
44 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.50-12116_50-12103d others(16): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60994457 | ||||||
| chr11:60994457 | C | CAAAAAAA others(8): Show |
49 | a0001c0001t0001g0049 a0001c0001t0001g0198 a0001c0001t0001g0201 others(46): Show |
52 | HG00323.hp1 HG00639.hp2 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.50-12103_50-12102i others(17): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60994457 | ||||||
| chr11:60994457 | C | CAAAAAAA others(9): Show |
8 | a0001c0001t0001g0152 a0002c0002t0001g0070 a0002c0002t0001g0073 others(5): Show |
9 | HG01123.hp2 HG01175.hp1 HG01346.hp2 others(6): Show |
intron_variant | MODIFIER | c.50-12103_50-12102i others(18): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60994457 | ||||||
| chr11:60994457 | C | CAAAAAAA others(10): Show |
2 | a0002c0002t0001g0071 a0002c0002t0001g0072 |
2 | HG01109.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.50-12103_50-12102i others(19): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60994457 | ||||||
| chr11:60994465 | A | AAAAAAAA others(8): Show |
6 | a0005c0006t0001g0087 a0005c0006t0001g0090 a0005c0006t0001g0115 others(3): Show |
6 | HG01433.hp1 HG02074.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.50-12103_50-12102i others(17): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60994465 | ||||||
| chr11:60994465 | A | AAAAAAAA others(7): Show |
14 | a0005c0006t0001g0009 a0005c0006t0001g0013 a0005c0006t0001g0029 others(11): Show |
16 | HG00140.hp2 HG00639.hp1 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.50-12103_50-12102i others(16): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60994465 | ||||||
| chr11:60994509 | G | A | 2 | a0002c0002t0001g0238 a0003c0011t0005g0048 |
2 | HG02723.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.50-12065G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60994509 | |||||||
| chr11:60994511 | A | G | 279 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(276): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.50-12063A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60994511 | |||||||
| chr11:60994562 | T | C | 1 | a0001c0001t0001g0095 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.50-12012T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60994562 | |||||||
| chr11:60994584 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.50-11990C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60994584 | |||||||
| chr11:60994777 | C | A | 2 | a0002c0002t0001g0238 a0003c0011t0005g0048 |
2 | HG02723.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.50-11797C>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60994777 | |||||||
| chr11:60995026 | G | A | 1 | a0001c0001t0007g0041 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.50-11548G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60995026 | |||||||
| chr11:60995102 | C | T | 76 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(73): Show |
80 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.50-11472C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60995102 | |||||||
| chr11:60995125 | CT | C | 73 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0011g0277 others(70): Show |
81 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.50-11438delT | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60995125 | ||||||
| chr11:60995128 | T | C | 94 | a0001c0001t0001g0201 a0002c0002t0001g0011 a0002c0002t0001g0026 others(91): Show |
100 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.50-11446T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60995128 | |||||||
| chr11:60995156 | C | T | 277 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(274): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.50-11418C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60995156 | |||||||
| chr11:60995237 | C | G | 1 | a0001c0001t0007g0041 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.50-11337C>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60995237 | |||||||
| chr11:60995284 | A | G | 49 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0011g0277 others(46): Show |
55 | HG00099.hp2 HG00438.hp2 HG00741.hp2 others(52): Show |
intron_variant | MODIFIER | c.50-11290A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60995284 | |||||||
| chr11:60995378 | C | T | 74 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(71): Show |
78 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.50-11196C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60995378 | |||||||
| chr11:60995426 | T | A | 14 | a0001c0010t0002g0015 a0001c0010t0002g0134 a0001c0010t0002g0233 others(11): Show |
18 | HG01109.hp2 HG01243.hp1 HG02615.hp1 others(15): Show |
intron_variant | MODIFIER | c.50-11148T>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60995426 | |||||||
| chr11:60995662 | C | A | 62 | a0002c0002t0001g0011 a0002c0002t0001g0026 a0002c0002t0001g0038 others(59): Show |
66 | HG00323.hp1 HG00438.hp1 HG00639.hp2 others(63): Show |
intron_variant | MODIFIER | c.50-10912C>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60995662 | |||||||
| chr11:60995724 | A | ATCTTTTC others(19): Show |
1 | a0002c0003t0001g0108 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.50-10849_50-10824d others(28): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60995724 | ||||||
| chr11:60995769 | G | A | 1 | a0001c0001t0007g0041 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.50-10805G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60995769 | |||||||
| chr11:60996001 | A | G | 1 | a0005c0006t0001g0199 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.50-10573A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60996001 | |||||||
| chr11:60996134 | T | C | 1 | a0001c0007t0001g0047 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.50-10440T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60996134 | |||||||
| chr11:60996296 | G | A | 14 | a0001c0010t0002g0015 a0001c0010t0002g0134 a0001c0010t0002g0233 others(11): Show |
18 | HG01109.hp2 HG01243.hp1 HG02615.hp1 others(15): Show |
intron_variant | MODIFIER | c.50-10278G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60996296 | |||||||
| chr11:60996360 | G | A | 76 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(73): Show |
80 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.50-10214G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60996360 | |||||||
| chr11:60996549 | C | T | 7 | a0001c0001t0001g0062 a0001c0001t0001g0098 a0001c0001t0001g0104 others(4): Show |
7 | HG00140.hp1 HG00323.hp2 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.50-10025C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60996549 | |||||||
| chr11:60996556 | A | G | 20 | a0005c0006t0001g0009 a0005c0006t0001g0013 a0005c0006t0001g0029 others(17): Show |
22 | HG00140.hp2 HG00639.hp1 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.50-10018A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60996556 | |||||||
| chr11:60996589 | C | T | 1 | a0003c0005t0001g0206 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.50-9985C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60996589 | |||||||
| chr11:60997130 | C | G | 20 | a0005c0006t0001g0009 a0005c0006t0001g0013 a0005c0006t0001g0029 others(17): Show |
22 | HG00140.hp2 HG00639.hp1 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.50-9444C>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60997130 | |||||||
| chr11:60997163 | G | A | 1 | a0006c0008t0001g0139 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.50-9411G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60997163 | |||||||
| chr11:60997192 | G | A | 177 | a0001c0001t0001g0049 a0001c0001t0001g0065 a0001c0001t0001g0066 others(174): Show |
191 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.50-9382G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60997192 | |||||||
| chr11:60997245 | G | T | 1 | a0001c0001t0001g0084 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.50-9329G>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60997245 | |||||||
| chr11:60997378 | C | CA | 6 | a0001c0001t0001g0094 a0001c0001t0001g0142 a0001c0007t0001g0256 others(3): Show |
6 | HG02257.hp1 HG02723.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.50-9182dupA | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60997378 | ||||||
| chr11:60997388 | A | T | 34 | a0001c0001t0001g0201 a0002c0003t0001g0004 a0002c0003t0001g0031 others(31): Show |
36 | HG00408.hp1 HG00423.hp2 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.50-9186A>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60997388 | |||||||
| chr11:60997393 | T | A | 9 | a0001c0001t0001g0049 a0001c0001t0001g0198 a0001c0001t0001g0202 others(6): Show |
9 | HG02074.hp2 HG03098.hp2 HG03492.hp2 others(6): Show |
intron_variant | MODIFIER | c.50-9181T>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60997393 | |||||||
| chr11:60997523 | A | T | 32 | a0001c0001t0001g0201 a0002c0003t0001g0004 a0003c0005t0001g0010 others(29): Show |
34 | HG00408.hp1 HG00423.hp2 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.50-9051A>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60997523 | |||||||
| chr11:60997700 | G | T | 1 | a0001c0007t0001g0227 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.50-8874G>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60997700 | |||||||
| chr11:60997715 | C | A | 259 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(256): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.50-8859C>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60997715 | |||||||
| chr11:60997739 | G | C | 1 | a0002c0002t0001g0056 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.50-8835G>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60997739 | |||||||
| chr11:60997828 | GA | G | 89 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0201 others(86): Show |
97 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.50-8743delA | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60997828 | ||||||
| chr11:60997883 | G | A | 29 | a0002c0003t0001g0004 a0003c0005t0001g0010 a0003c0005t0001g0044 others(26): Show |
31 | HG00408.hp1 HG00423.hp2 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.50-8691G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60997883 | |||||||
| chr11:60998041 | G | A | 6 | a0004c0004t0001g0005 a0004c0004t0001g0068 a0004c0004t0001g0069 others(3): Show |
7 | HG01168.hp2 HG02004.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.50-8533G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60998041 | |||||||
| chr11:60998081 | C | T | 89 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0201 others(86): Show |
97 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.50-8493C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60998081 | |||||||
| chr11:60998201 | A | G | 1 | a0003c0005t0001g0252 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.50-8373A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60998201 | |||||||
| chr11:60998512 | A | G | 63 | a0002c0002t0001g0011 a0002c0002t0001g0026 a0002c0002t0001g0038 others(60): Show |
67 | HG00323.hp1 HG00438.hp1 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.50-8062A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60998512 | |||||||
| chr11:60998606 | G | C | 1 | a0006c0008t0001g0076 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.50-7968G>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60998606 | |||||||
| chr11:60998607 | C | G | 1 | a0006c0008t0001g0076 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.50-7967C>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60998607 | |||||||
| chr11:60998614 | A | G | 5 | a0001c0001t0001g0049 a0001c0001t0001g0198 a0001c0001t0001g0202 others(2): Show |
5 | NA18952.hp2 NA18970.hp2 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.50-7960A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60998614 | |||||||
| chr11:60998648 | C | T | 49 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0011g0277 others(46): Show |
55 | HG00099.hp2 HG00438.hp2 HG00741.hp2 others(52): Show |
intron_variant | MODIFIER | c.50-7926C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60998648 | |||||||
| chr11:60998680 | C | T | 1 | a0001c0001t0001g0179 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.50-7894C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60998680 | |||||||
| chr11:60998714 | T | C | 1 | a0001c0001t0001g0014 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.50-7860T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60998714 | |||||||
| chr11:60998801 | T | A | 1 | a0006c0008t0001g0076 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.50-7773T>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60998801 | |||||||
| chr11:60998849 | GA | G | 97 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(94): Show |
103 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.50-7706delA | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60998849 | ||||||
| chr11:60998849 | GAA | G | 108 | a0001c0001t0001g0049 a0001c0001t0001g0061 a0001c0001t0001g0149 others(105): Show |
118 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.50-7707_50-7706del others(2): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60998849 | ||||||
| chr11:60998849 | GAAA | G | 8 | a0002c0003t0001g0267 a0006c0008t0001g0076 a0007c0012t0001g0036 others(5): Show |
8 | HG01081.hp1 HG01361.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.50-7708_50-7706del others(3): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 60998849 | ||||||
| chr11:60998934 | G | A | 2 | a0003c0011t0004g0045 a0003c0011t0004g0278 |
2 | HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.50-7640G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60998934 | |||||||
| chr11:60998965 | C | A | 2 | a0001c0001t0001g0128 a0001c0001t0001g0169 |
2 | HG00408.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.50-7609C>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60998965 | |||||||
| chr11:60999083 | G | A | 96 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(93): Show |
102 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.50-7491G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60999083 | |||||||
| chr11:60999090 | G | A | 1 | a0001c0001t0007g0041 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.50-7484G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60999090 | |||||||
| chr11:60999273 | T | C | 1 | a0003c0011t0001g0226 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.50-7301T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60999273 | |||||||
| chr11:60999400 | A | G | 6 | a0004c0004t0001g0019 a0004c0004t0001g0121 a0004c0004t0001g0166 others(3): Show |
7 | HG00323.hp1 HG01123.hp2 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.50-7174A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60999400 | |||||||
| chr11:60999469 | C | A | 2 | a0002c0002t0001g0193 a0002c0002t0014g0237 |
2 | HG02630.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.50-7105C>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60999469 | |||||||
| chr11:60999863 | A | G | 34 | a0001c0001t0001g0201 a0002c0003t0001g0004 a0003c0005t0001g0010 others(31): Show |
36 | HG00408.hp1 HG00423.hp2 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.50-6711A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60999863 | |||||||
| chr11:60999948 | T | G | 20 | a0005c0006t0001g0009 a0005c0006t0001g0013 a0005c0006t0001g0029 others(17): Show |
22 | HG00140.hp2 HG00639.hp1 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.50-6626T>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60999948 | |||||||
| chr11:60999995 | T | C | 1 | a0001c0001t0001g0150 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.50-6579T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 60999995 | |||||||
| chr11:61000072 | A | T | 1 | a0011c0015t0001g0279 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.50-6502A>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61000072 | |||||||
| chr11:61000222 | A | G | 259 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(256): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.50-6352A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61000222 | |||||||
| chr11:61000326 | T | TA | 150 | a0001c0001t0001g0049 a0001c0001t0001g0065 a0001c0001t0001g0066 others(147): Show |
162 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.50-6246dupA | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 61000326 | ||||||
| chr11:61000351 | A | G | 63 | a0002c0002t0001g0011 a0002c0002t0001g0026 a0002c0002t0001g0038 others(60): Show |
67 | HG00323.hp1 HG00438.hp1 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.50-6223A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61000351 | |||||||
| chr11:61000492 | C | T | 29 | a0001c0001t0001g0049 a0001c0001t0001g0198 a0001c0001t0001g0202 others(26): Show |
32 | HG00140.hp2 HG00639.hp1 HG01099.hp2 others(29): Show |
intron_variant | MODIFIER | c.50-6082C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61000492 | |||||||
| chr11:61000546 | T | A | 29 | a0001c0001t0001g0049 a0001c0001t0001g0198 a0001c0001t0001g0202 others(26): Show |
32 | HG00140.hp2 HG00639.hp1 HG01099.hp2 others(29): Show |
intron_variant | MODIFIER | c.50-6028T>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61000546 | |||||||
| chr11:61000565 | C | G | 1 | a0003c0005t0001g0044 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.50-6009C>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61000565 | |||||||
| chr11:61000572 | G | A | 177 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(174): Show |
187 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.50-6002G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61000572 | |||||||
| chr11:61001031 | A | T | 11 | a0001c0001t0001g0049 a0001c0001t0001g0198 a0001c0001t0001g0202 others(8): Show |
11 | HG01081.hp1 HG01361.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.50-5543A>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61001031 | |||||||
| chr11:61001198 | C | CT | 105 | a0001c0001t0007g0258 a0001c0001t0011g0277 a0001c0007t0001g0017 others(102): Show |
116 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.50-5356dupT | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 61001198 | ||||||
| chr11:61001198 | CT | C | 77 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(74): Show |
81 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.50-5356delT | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 61001198 | ||||||
| chr11:61001240 | G | A | 1 | a0002c0002t0001g0083 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.50-5334G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61001240 | |||||||
| chr11:61001254 | G | A | 3 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0004c0004t0001g0209 |
3 | HG01884.hp2 HG02572.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.50-5320G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61001254 | |||||||
| chr11:61001264 | C | T | 6 | a0001c0001t0001g0006 a0001c0001t0001g0151 a0007c0012t0001g0036 others(3): Show |
7 | HG01081.hp1 HG01361.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.50-5310C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61001264 | |||||||
| chr11:61001373 | T | A | 6 | a0007c0012t0001g0036 a0007c0012t0003g0032 a0007c0012t0003g0034 others(3): Show |
6 | HG01081.hp1 HG01361.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.50-5201T>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61001373 | |||||||
| chr11:61001481 | G | A | 138 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(135): Show |
146 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.50-5093G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61001481 | |||||||
| chr11:61001597 | C | CT | 20 | a0005c0006t0001g0009 a0005c0006t0001g0013 a0005c0006t0001g0029 others(17): Show |
22 | HG00140.hp2 HG00639.hp1 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.50-4974dupT | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 61001597 | ||||||
| chr11:61002062 | T | C | 20 | a0005c0006t0001g0009 a0005c0006t0001g0013 a0005c0006t0001g0029 others(17): Show |
22 | HG00140.hp2 HG00639.hp1 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.50-4512T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61002062 | |||||||
| chr11:61002245 | A | T | 39 | a0001c0001t0001g0201 a0002c0003t0001g0004 a0003c0005t0001g0010 others(36): Show |
41 | HG00408.hp1 HG00423.hp2 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.50-4329A>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61002245 | |||||||
| chr11:61002347 | G | A | 43 | a0001c0001t0011g0277 a0002c0003t0001g0002 a0002c0003t0001g0008 others(40): Show |
48 | HG00099.hp2 HG00438.hp2 HG00741.hp2 others(45): Show |
intron_variant | MODIFIER | c.50-4227G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61002347 | |||||||
| chr11:61002540 | G | C | 2 | a0001c0001t0001g0065 a0001c0001t0001g0066 |
2 | HG01884.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.50-4034G>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61002540 | |||||||
| chr11:61002720 | T | C | 259 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(256): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.50-3854T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61002720 | |||||||
| chr11:61002954 | C | CTCTTT | 58 | a0001c0001t0007g0041 a0002c0002t0001g0011 a0002c0002t0001g0026 others(55): Show |
62 | HG00323.hp1 HG00438.hp1 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.50-3598_50-3594dup others(5): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 61002954 | ||||||
| chr11:61002954 | C | CTCTTTTC others(3): Show |
73 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0020 others(70): Show |
76 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.50-3603_50-3594dup others(10): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 61002954 | ||||||
| chr11:61002954 | C | CTCTTTTC others(8): Show |
6 | a0001c0001t0001g0007 a0001c0001t0001g0059 a0001c0001t0001g0096 others(3): Show |
7 | HG00323.hp2 HG01257.hp1 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.50-3608_50-3594dup others(15): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 61002954 | ||||||
| chr11:61002954 | CTCTTT | C | 44 | a0001c0001t0011g0277 a0002c0002t0001g0092 a0002c0003t0001g0002 others(41): Show |
49 | HG00099.hp2 HG00438.hp2 HG00741.hp2 others(46): Show |
intron_variant | MODIFIER | c.50-3598_50-3594del others(5): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 61002954 | ||||||
| chr11:61002977 | T | TTTTCTTT others(3): Show |
1 | a0008c0013t0001g0143 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.50-3594_50-3593ins others(10): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 61002977 | ||||||
| chr11:61003069 | A | C | 1 | a0001c0001t0001g0177 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.50-3505A>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61003069 | |||||||
| chr11:61003089 | G | A | 1 | a0002c0003t0001g0239 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.50-3485G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61003089 | |||||||
| chr11:61003129 | T | C | 185 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(182): Show |
198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.50-3445T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61003129 | |||||||
| chr11:61003194 | A | T | 1 | a0001c0001t0001g0149 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.50-3380A>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61003194 | |||||||
| chr11:61003211 | C | T | 182 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(179): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.50-3363C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61003211 | |||||||
| chr11:61003261 | A | G | 63 | a0002c0002t0001g0011 a0002c0002t0001g0026 a0002c0002t0001g0038 others(60): Show |
67 | HG00323.hp1 HG00438.hp1 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.50-3313A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61003261 | |||||||
| chr11:61003605 | G | A | 24 | a0001c0010t0002g0015 a0001c0010t0002g0134 a0001c0010t0002g0233 others(21): Show |
27 | HG00140.hp2 HG00639.hp1 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.50-2969G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61003605 | |||||||
| chr11:61003648 | C | T | 2 | a0001c0001t0001g0065 a0001c0001t0001g0066 |
2 | HG01884.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.50-2926C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61003648 | |||||||
| chr11:61003649 | G | A | 1 | a0003c0005t0001g0229 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.50-2925G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61003649 | |||||||
| chr11:61003683 | G | A | 2 | a0003c0005t0001g0162 a0003c0005t0001g0171 |
2 | NA19005.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.50-2891G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61003683 | |||||||
| chr11:61003713 | G | A | 3 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0004c0004t0001g0209 |
3 | HG01884.hp2 HG02572.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.50-2861G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61003713 | |||||||
| chr11:61003877 | G | T | 2 | a0002c0002t0001g0133 a0002c0002t0001g0240 |
2 | HG02145.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.50-2697G>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61003877 | |||||||
| chr11:61003898 | G | A | 21 | a0004c0004t0001g0005 a0004c0004t0001g0016 a0004c0004t0001g0019 others(18): Show |
24 | HG00323.hp1 HG00639.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.50-2676G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61003898 | |||||||
| chr11:61003919 | AAAAT | A | 38 | a0001c0001t0001g0201 a0003c0005t0001g0010 a0003c0005t0001g0028 others(35): Show |
39 | HG00408.hp1 HG00423.hp2 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.50-2651_50-2648del others(4): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 61003919 | ||||||
| chr11:61003951 | C | A | 4 | a0002c0003t0001g0230 a0002c0003t0001g0231 a0002c0003t0001g0232 others(1): Show |
4 | HG02258.hp1 HG02280.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.50-2623C>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61003951 | |||||||
| chr11:61003978 | G | GCTCA | 278 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(275): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.50-2595_50-2592dup others(4): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 61003978 | ||||||
| chr11:61004226 | A | G | 2 | a0001c0001t0001g0006 a0001c0001t0001g0151 |
3 | NA18948.hp2 NA18986.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.50-2348A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61004226 | |||||||
| chr11:61004278 | A | G | 5 | a0001c0001t0001g0049 a0001c0001t0001g0198 a0001c0001t0001g0202 others(2): Show |
5 | NA18952.hp2 NA18970.hp2 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.50-2296A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61004278 | |||||||
| chr11:61004455 | G | A | 29 | a0003c0005t0001g0010 a0003c0005t0001g0028 a0003c0005t0001g0044 others(26): Show |
30 | HG00408.hp1 HG00423.hp2 HG00673.hp1 others(27): Show |
intron_variant | MODIFIER | c.50-2119G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61004455 | |||||||
| chr11:61004473 | C | A | 259 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(256): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.50-2101C>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61004473 | |||||||
| chr11:61004508 | G | A | 21 | a0004c0004t0001g0005 a0004c0004t0001g0016 a0004c0004t0001g0019 others(18): Show |
24 | HG00323.hp1 HG00639.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.50-2066G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61004508 | |||||||
| chr11:61004525 | T | C | 2 | a0001c0001t0001g0065 a0001c0001t0001g0066 |
2 | HG01884.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.50-2049T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61004525 | |||||||
| chr11:61004618 | C | T | 188 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(185): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.50-1956C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61004618 | |||||||
| chr11:61004619 | G | A | 1 | a0003c0011t0001g0226 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.50-1955G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61004619 | |||||||
| chr11:61004735 | C | G | 4 | a0003c0011t0001g0226 a0003c0011t0004g0045 a0003c0011t0004g0046 others(1): Show |
4 | HG02145.hp2 HG02258.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.50-1839C>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61004735 | |||||||
| chr11:61004796 | C | G | 43 | a0002c0003t0001g0002 a0002c0003t0001g0004 a0002c0003t0001g0008 others(40): Show |
49 | HG00099.hp2 HG00438.hp2 HG00741.hp2 others(46): Show |
intron_variant | MODIFIER | c.50-1778C>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61004796 | |||||||
| chr11:61004849 | A | G | 1 | a0001c0007t0001g0259 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.50-1725A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61004849 | |||||||
| chr11:61004909 | G | A | 23 | a0004c0004t0001g0005 a0004c0004t0001g0016 a0004c0004t0001g0019 others(20): Show |
26 | HG00323.hp1 HG00639.hp2 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.50-1665G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61004909 | |||||||
| chr11:61005067 | C | T | 2 | a0001c0001t0001g0065 a0001c0001t0001g0066 |
2 | HG01884.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.50-1507C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61005067 | |||||||
| chr11:61005128 | C | A | 1 | a0001c0001t0009g0175 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.50-1446C>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61005128 | |||||||
| chr11:61005220 | A | G | 1 | a0005c0006t0001g0033 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.50-1354A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61005220 | |||||||
| chr11:61005267 | G | T | 4 | a0001c0010t0002g0015 a0001c0010t0002g0134 a0001c0010t0002g0233 others(1): Show |
5 | HG01109.hp2 HG02717.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.50-1307G>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61005267 | |||||||
| chr11:61005370 | C | T | 1 | a0002c0003t0001g0027 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.50-1204C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61005370 | |||||||
| chr11:61005388 | C | T | 21 | a0004c0004t0001g0005 a0004c0004t0001g0016 a0004c0004t0001g0019 others(18): Show |
24 | HG00323.hp1 HG00639.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.50-1186C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61005388 | |||||||
| chr11:61005394 | C | T | 6 | a0006c0008t0001g0075 a0006c0008t0001g0076 a0006c0008t0001g0119 others(3): Show |
6 | HG00673.hp1 HG02080.hp2 NA18952.hp1 others(3): Show |
intron_variant | MODIFIER | c.50-1180C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61005394 | |||||||
| chr11:61005449 | A | C | 34 | a0001c0001t0001g0201 a0003c0005t0001g0010 a0003c0005t0001g0028 others(31): Show |
35 | HG00408.hp1 HG00423.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.50-1125A>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61005449 | |||||||
| chr11:61005595 | G | A | 3 | a0002c0003t0001g0004 a0002c0003t0001g0108 a0002c0003t0001g0168 |
4 | HG01069.hp1 HG01071.hp2 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.50-979G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61005595 | |||||||
| chr11:61005653 | T | C | 246 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(243): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.50-921T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61005653 | |||||||
| chr11:61005659 | T | C | 261 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(258): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.50-915T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61005659 | |||||||
| chr11:61005729 | C | T | 1 | a0001c0018t0001g0148 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.50-845C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61005729 | |||||||
| chr11:61005792 | G | A | 1 | a0002c0003t0001g0267 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.50-782G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61005792 | |||||||
| chr11:61005855 | T | C | 246 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(243): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.50-719T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61005855 | |||||||
| chr11:61005867 | G | A | 2 | a0002c0002t0001g0011 a0002c0002t0001g0211 |
3 | HG02280.hp2 HG02970.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.50-707G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61005867 | |||||||
| chr11:61005880 | G | A | 63 | a0002c0003t0001g0002 a0002c0003t0001g0004 a0002c0003t0001g0008 others(60): Show |
71 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.50-694G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61005880 | |||||||
| chr11:61005931 | C | CA | 89 | a0001c0001t0007g0041 a0001c0001t0007g0258 a0002c0003t0001g0002 others(86): Show |
100 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.50-630dupA | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 61005931 | ||||||
| chr11:61005941 | A | AG | 34 | a0001c0001t0001g0201 a0003c0005t0001g0010 a0003c0005t0001g0028 others(31): Show |
35 | HG00408.hp1 HG00423.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.50-633_50-632insG | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61005941 | |||||||
| chr11:61005941 | A | G | 32 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0081 others(29): Show |
32 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.50-633A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61005941 | |||||||
| chr11:61006232 | A | T | 6 | a0007c0012t0001g0036 a0007c0012t0003g0032 a0007c0012t0003g0034 others(3): Show |
6 | HG01081.hp1 HG01361.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.50-342A>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61006232 | |||||||
| chr11:61006417 | G | A | 1 | a0006c0008t0001g0183 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.50-157G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61006417 | |||||||
| chr11:61006462 | G | T | 1 | a0001c0010t0002g0134 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.50-112G>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 1/12 | chr11 | 61006462 | |||||||
| chr11:61006838 | A | G | 1 | a0001c0001t0001g0074 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.118+196A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 2/12 | chr11 | 61006838 | |||||||
| chr11:61006904 | G | A | 8 | a0002c0003t0001g0004 a0002c0003t0001g0060 a0002c0003t0001g0067 others(5): Show |
9 | HG00438.hp2 HG01069.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.118+262G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 2/12 | chr11 | 61006904 | |||||||
| chr11:61006952 | C | T | 4 | a0001c0010t0002g0015 a0001c0010t0002g0134 a0001c0010t0002g0233 others(1): Show |
5 | HG01109.hp2 HG02717.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.118+310C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 2/12 | chr11 | 61006952 | |||||||
| chr11:61007106 | G | C | 59 | a0001c0001t0001g0201 a0003c0005t0001g0010 a0003c0005t0001g0028 others(56): Show |
62 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.119-454G>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 2/12 | chr11 | 61007106 | |||||||
| chr11:61007184 | A | G | 59 | a0001c0001t0001g0201 a0003c0005t0001g0010 a0003c0005t0001g0028 others(56): Show |
62 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.119-376A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 2/12 | chr11 | 61007184 | |||||||
| chr11:61007287 | T | C | 5 | a0003c0005t0001g0229 a0003c0011t0001g0226 a0003c0011t0004g0045 others(2): Show |
5 | HG02145.hp2 HG02258.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.119-273T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 2/12 | chr11 | 61007287 | |||||||
| chr11:61007381 | G | A | 5 | a0001c0001t0001g0049 a0001c0001t0001g0198 a0001c0001t0001g0202 others(2): Show |
5 | NA18952.hp2 NA18970.hp2 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.119-179G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 2/12 | chr11 | 61007381 | |||||||
| chr11:61007480 | C | T | 1 | a0001c0001t0001g0020 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.119-80C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 2/12 | chr11 | 61007480 | |||||||
| chr11:61007535 | C | T | 79 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(76): Show |
83 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.119-25C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 2/12 | chr11 | 61007535 | |||||||
| chr11:61007920 | C | T | 1 | a0001c0007t0005g0274 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.469+10C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 3/12 | chr11 | 61007920 | |||||||
| chr11:61007957 | G | A | 1 | a0007c0012t0010g0030 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.469+47G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 3/12 | chr11 | 61007957 | |||||||
| chr11:61008155 | G | T | 23 | a0004c0004t0001g0005 a0004c0004t0001g0016 a0004c0004t0001g0019 others(20): Show |
26 | HG00323.hp1 HG00639.hp2 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.469+245G>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 3/12 | chr11 | 61008155 | |||||||
| chr11:61008861 | C | T | 21 | a0004c0004t0001g0005 a0004c0004t0001g0016 a0004c0004t0001g0019 others(18): Show |
24 | HG00323.hp1 HG00639.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.781+16C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 4/12 | chr11 | 61008861 | |||||||
| chr11:61008862 | A | G | 279 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(276): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.781+17A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 4/12 | chr11 | 61008862 | |||||||
| chr11:61008993 | A | G | 20 | a0005c0006t0001g0009 a0005c0006t0001g0013 a0005c0006t0001g0029 others(17): Show |
22 | HG00140.hp2 HG00639.hp1 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.781+148A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 4/12 | chr11 | 61008993 | |||||||
| chr11:61009012 | T | C | 75 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(72): Show |
79 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.781+167T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 4/12 | chr11 | 61009012 | |||||||
| chr11:61009182 | G | A | 4 | a0002c0003t0001g0230 a0002c0003t0001g0231 a0002c0003t0001g0232 others(1): Show |
4 | HG02258.hp1 HG02280.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.781+337G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 4/12 | chr11 | 61009182 | |||||||
| chr11:61009239 | A | G | 20 | a0005c0006t0001g0009 a0005c0006t0001g0013 a0005c0006t0001g0029 others(17): Show |
22 | HG00140.hp2 HG00639.hp1 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.782-333A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 4/12 | chr11 | 61009239 | |||||||
| chr11:61009309 | T | C | 110 | a0001c0007t0001g0256 a0002c0002t0001g0011 a0002c0002t0001g0026 others(107): Show |
120 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.782-263T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 4/12 | chr11 | 61009309 | |||||||
| chr11:61009334 | G | A | 23 | a0004c0004t0001g0005 a0004c0004t0001g0016 a0004c0004t0001g0019 others(20): Show |
26 | HG00323.hp1 HG00639.hp2 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.782-238G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 4/12 | chr11 | 61009334 | |||||||
| chr11:61009361 | G | A | 2 | a0006c0008t0001g0064 a0006c0008t0001g0139 |
2 | HG02683.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.782-211G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 4/12 | chr11 | 61009361 | |||||||
| chr11:61009361 | G | C | 1 | a0001c0001t0001g0260 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.782-211G>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 4/12 | chr11 | 61009361 | |||||||
| chr11:61009977 | CA | C | 5 | a0001c0001t0001g0049 a0001c0001t0001g0198 a0001c0001t0001g0202 others(2): Show |
5 | NA18952.hp2 NA18970.hp2 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.1084+105delA | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr11 | 61009977 | ||||||
| chr11:61010084 | A | T | 34 | a0001c0001t0001g0201 a0003c0005t0001g0010 a0003c0005t0001g0028 others(31): Show |
35 | HG00408.hp1 HG00423.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.1084+210A>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 5/12 | chr11 | 61010084 | |||||||
| chr11:61010236 | AC | A | 5 | a0003c0005t0001g0229 a0003c0011t0001g0226 a0003c0011t0004g0045 others(2): Show |
5 | HG02145.hp2 HG02258.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1084+365delC | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr11 | 61010236 | ||||||
| chr11:61010307 | A | G | 1 | a0002c0009t0001g0024 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1084+433A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 5/12 | chr11 | 61010307 | |||||||
| chr11:61010442 | C | T | 2 | a0001c0001t0001g0063 a0001c0001t0001g0152 |
2 | HG00099.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.1084+568C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 5/12 | chr11 | 61010442 | |||||||
| chr11:61010502 | A | G | 4 | a0001c0010t0002g0015 a0001c0010t0002g0134 a0001c0010t0002g0233 others(1): Show |
5 | HG01109.hp2 HG02717.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1085-568A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 5/12 | chr11 | 61010502 | |||||||
| chr11:61010519 | A | C | 1 | a0002c0002t0001g0103 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1085-551A>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 5/12 | chr11 | 61010519 | |||||||
| chr11:61010565 | A | C | 1 | a0008c0013t0001g0143 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1085-505A>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 5/12 | chr11 | 61010565 | |||||||
| chr11:61010788 | C | T | 2 | a0002c0003t0001g0031 a0002c0003t0001g0215 |
2 | HG02698.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1085-282C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 5/12 | chr11 | 61010788 | |||||||
| chr11:61010793 | T | C | 6 | a0007c0012t0001g0036 a0007c0012t0003g0032 a0007c0012t0003g0034 others(3): Show |
6 | HG01081.hp1 HG01361.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.1085-277T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 5/12 | chr11 | 61010793 | |||||||
| chr11:61010856 | A | T | 1 | a0001c0001t0011g0277 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1085-214A>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 5/12 | chr11 | 61010856 | |||||||
| chr11:61010977 | C | T | 5 | a0001c0007t0001g0256 a0002c0003t0001g0040 a0002c0003t0001g0220 others(2): Show |
5 | HG01261.hp1 HG01496.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1085-93C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 5/12 | chr11 | 61010977 | |||||||
| chr11:61011041 | T | C | 20 | a0005c0006t0001g0009 a0005c0006t0001g0013 a0005c0006t0001g0029 others(17): Show |
22 | HG00140.hp2 HG00639.hp1 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.1085-29T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 5/12 | chr11 | 61011041 | |||||||
| chr11:61011055 | G | A | 1 | a0003c0011t0004g0045 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1085-15G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 5/12 | chr11 | 61011055 | |||||||
| chr11:61011158 | C | T | 2 | a0002c0003t0001g0241 a0002c0003t0001g0245 |
2 | HG00741.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.1150+23C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 6/12 | chr11 | 61011158 | |||||||
| chr11:61011178 | C | CGGTGTGT others(8): Show |
1 | a0001c0001t0001g0179 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1150+44_1150+45ins others(15): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr11 | 61011178 | ||||||
| chr11:61011178 | C | CGT | 17 | a0001c0007t0001g0017 a0001c0007t0001g0018 a0001c0007t0001g0021 others(14): Show |
19 | HG02818.hp1 HG02886.hp1 HG02895.hp1 others(16): Show |
intron_variant | MODIFIER | c.1150+68_1150+69dup others(2): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr11 | 61011178 | ||||||
| chr11:61011178 | C | CGTGT | 36 | a0001c0001t0001g0049 a0001c0001t0001g0065 a0001c0001t0001g0066 others(33): Show |
39 | HG00140.hp2 HG00639.hp1 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.1150+66_1150+69dup others(4): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr11 | 61011178 | ||||||
| chr11:61011178 | C | CGTGTGT | 3 | a0002c0003t0001g0241 a0002c0003t0001g0245 a0005c0006t0001g0246 |
3 | HG00741.hp2 HG01167.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.1150+64_1150+69dup others(6): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr11 | 61011178 | ||||||
| chr11:61011178 | C | CGTGTGTG others(1): Show |
11 | a0001c0007t0001g0256 a0002c0003t0001g0027 a0002c0003t0001g0040 others(8): Show |
11 | HG01261.hp1 HG01496.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1150+62_1150+69dup others(8): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr11 | 61011178 | ||||||
| chr11:61011178 | C | CGTGTGTG others(3): Show |
40 | a0001c0001t0001g0080 a0001c0001t0009g0175 a0002c0002t0001g0038 others(37): Show |
44 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.1150+60_1150+69dup others(10): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr11 | 61011178 | ||||||
| chr11:61011178 | C | CGTGTGTG others(5): Show |
9 | a0001c0001t0001g0153 a0001c0001t0001g0260 a0001c0001t0011g0277 others(6): Show |
12 | HG01884.hp1 HG02280.hp2 HG02293.hp1 others(9): Show |
intron_variant | MODIFIER | c.1150+58_1150+69dup others(12): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr11 | 61011178 | ||||||
| chr11:61011178 | C | CGTGTGTG others(7): Show |
88 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(85): Show |
93 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.1150+56_1150+69dup others(14): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr11 | 61011178 | ||||||
| chr11:61011178 | C | CGTGTGTG others(9): Show |
27 | a0001c0001t0001g0089 a0001c0001t0001g0104 a0001c0001t0001g0177 others(24): Show |
27 | HG00597.hp1 HG00597.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.1150+54_1150+69dup others(16): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr11 | 61011178 | ||||||
| chr11:61011178 | C | CGTGTGTG others(11): Show |
20 | a0001c0001t0001g0081 a0001c0001t0001g0122 a0001c0001t0001g0126 others(17): Show |
20 | HG00438.hp1 HG01516.hp2 HG02071.hp1 others(17): Show |
intron_variant | MODIFIER | c.1150+52_1150+69dup others(18): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr11 | 61011178 | ||||||
| chr11:61011178 | C | CGTGTGTG others(13): Show |
2 | a0002c0002t0001g0261 a0003c0005t0001g0086 |
2 | HG00408.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1150+50_1150+69dup others(20): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr11 | 61011178 | ||||||
| chr11:61011232 | G | C | 4 | a0001c0010t0002g0015 a0001c0010t0002g0134 a0001c0010t0002g0233 others(1): Show |
5 | HG01109.hp2 HG02717.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1150+97G>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 6/12 | chr11 | 61011232 | |||||||
| chr11:61011242 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1150+107G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 6/12 | chr11 | 61011242 | |||||||
| chr11:61011246 | T | C | 43 | a0002c0002t0001g0011 a0002c0002t0001g0026 a0002c0002t0001g0038 others(40): Show |
44 | HG00438.hp1 HG00735.hp1 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.1150+111T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 6/12 | chr11 | 61011246 | |||||||
| chr11:61011411 | CA | C | 21 | a0002c0003t0001g0004 a0002c0003t0001g0008 a0002c0003t0001g0012 others(18): Show |
24 | HG00099.hp2 HG00438.hp2 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.1150+277delA | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 6/12 | chr11 | 61011411 | |||||||
| chr11:61011438 | T | C | 1 | a0004c0004t0001g0209 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1150+303T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 6/12 | chr11 | 61011438 | |||||||
| chr11:61011438 | T | TA | 20 | a0005c0006t0001g0009 a0005c0006t0001g0013 a0005c0006t0001g0029 others(17): Show |
22 | HG00140.hp2 HG00639.hp1 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.1150+304dupA | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr11 | 61011438 | ||||||
| chr11:61011490 | G | C | 2 | a0001c0001t0001g0063 a0001c0001t0001g0152 |
2 | HG00099.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.1150+355G>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 6/12 | chr11 | 61011490 | |||||||
| chr11:61011514 | A | G | 163 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(160): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.1150+379A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 6/12 | chr11 | 61011514 | |||||||
| chr11:61011636 | C | CAAGAAAG others(359): Show |
1 | a0003c0005t0001g0164 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1150+514_1150+515i others(368): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr11 | 61011636 | ||||||
| chr11:61011886 | T | C | 25 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0004c0004t0001g0005 others(22): Show |
28 | HG00323.hp1 HG00639.hp2 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.1150+751T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 6/12 | chr11 | 61011886 | |||||||
| chr11:61011975 | T | A | 1 | a0003c0005t0001g0171 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1150+840T>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 6/12 | chr11 | 61011975 | |||||||
| chr11:61011977 | C | T | 2 | a0005c0006t0001g0118 a0005c0006t0001g0192 |
2 | HG01255.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.1150+842C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 6/12 | chr11 | 61011977 | |||||||
| chr11:61012268 | G | A | 36 | a0002c0002t0001g0011 a0002c0002t0001g0026 a0002c0002t0001g0038 others(33): Show |
37 | HG00438.hp1 HG00735.hp1 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.1150+1133G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 6/12 | chr11 | 61012268 | |||||||
| chr11:61012290 | T | A | 4 | a0003c0011t0001g0226 a0003c0011t0004g0045 a0003c0011t0004g0046 others(1): Show |
4 | HG02145.hp2 HG02258.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1151-1133T>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 6/12 | chr11 | 61012290 | |||||||
| chr11:61012330 | T | C | 42 | a0001c0007t0001g0256 a0002c0003t0001g0002 a0002c0003t0001g0004 others(39): Show |
48 | HG00099.hp2 HG00438.hp2 HG00741.hp2 others(45): Show |
intron_variant | MODIFIER | c.1151-1093T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 6/12 | chr11 | 61012330 | |||||||
| chr11:61012351 | G | A | 24 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0004c0004t0001g0005 others(21): Show |
27 | HG00323.hp1 HG00639.hp2 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.1151-1072G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 6/12 | chr11 | 61012351 | |||||||
| chr11:61012356 | C | A | 163 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(160): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.1151-1067C>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 6/12 | chr11 | 61012356 | |||||||
| chr11:61012535 | G | A | 20 | a0005c0006t0001g0009 a0005c0006t0001g0013 a0005c0006t0001g0029 others(17): Show |
22 | HG00140.hp2 HG00639.hp1 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.1151-888G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 6/12 | chr11 | 61012535 | |||||||
| chr11:61012565 | C | G | 3 | a0002c0003t0001g0040 a0002c0003t0001g0220 a0002c0003t0001g0221 |
3 | HG01261.hp1 HG01496.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1151-858C>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 6/12 | chr11 | 61012565 | |||||||
| chr11:61012829 | G | A | 27 | a0001c0001t0001g0201 a0001c0007t0005g0274 a0003c0005t0001g0010 others(24): Show |
28 | HG00408.hp1 HG00423.hp2 HG01192.hp1 others(25): Show |
intron_variant | MODIFIER | c.1151-594G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 6/12 | chr11 | 61012829 | |||||||
| chr11:61012830 | G | A | 1 | a0006c0008t0001g0139 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1151-593G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 6/12 | chr11 | 61012830 | |||||||
| chr11:61013385 | A | G | 5 | a0002c0002t0001g0038 a0002c0002t0001g0039 a0002c0002t0001g0083 others(2): Show |
5 | HG01243.hp2 HG01891.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1151-38A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 6/12 | chr11 | 61013385 | |||||||
| chr11:61013622 | C | T | 36 | a0001c0001t0001g0201 a0003c0005t0001g0010 a0003c0005t0001g0028 others(33): Show |
37 | HG00408.hp1 HG00423.hp2 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.1291+59C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 7/12 | chr11 | 61013622 | |||||||
| chr11:61013638 | G | A | 21 | a0001c0007t0001g0017 a0001c0007t0001g0018 a0001c0007t0001g0021 others(18): Show |
23 | HG02145.hp2 HG02258.hp2 HG02572.hp1 others(20): Show |
intron_variant | MODIFIER | c.1291+75G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 7/12 | chr11 | 61013638 | |||||||
| chr11:61013651 | G | A | 21 | a0001c0007t0001g0017 a0001c0007t0001g0018 a0001c0007t0001g0021 others(18): Show |
23 | HG02145.hp2 HG02258.hp2 HG02572.hp1 others(20): Show |
intron_variant | MODIFIER | c.1291+88G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 7/12 | chr11 | 61013651 | |||||||
| chr11:61013790 | G | A | 2 | a0001c0001t0001g0145 a0003c0011t0001g0226 |
2 | HG00673.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.1292-129G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 7/12 | chr11 | 61013790 | |||||||
| chr11:61013791 | C | T | 5 | a0001c0001t0001g0049 a0001c0001t0001g0198 a0001c0001t0001g0202 others(2): Show |
5 | NA18952.hp2 NA18970.hp2 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.1292-128C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 7/12 | chr11 | 61013791 | |||||||
| chr11:61013793 | C | T | 4 | a0001c0001t0007g0041 a0001c0001t0007g0258 a0002c0002t0001g0133 others(1): Show |
4 | HG02145.hp1 HG02630.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1292-126C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 7/12 | chr11 | 61013793 | |||||||
| chr11:61014734 | C | CA | 9 | a0001c0001t0001g0049 a0001c0001t0001g0065 a0001c0001t0001g0066 others(6): Show |
9 | HG01884.hp2 HG02572.hp2 HG04184.hp2 others(6): Show |
intron_variant | MODIFIER | c.1387+735dupA | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 61014734 | ||||||
| chr11:61014734 | CA | C | 16 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0096 others(13): Show |
16 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(13): Show |
intron_variant | MODIFIER | c.1387+735delA | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 61014734 | ||||||
| chr11:61014741 | A | AC | 4 | a0001c0010t0002g0015 a0001c0010t0002g0134 a0001c0010t0002g0233 others(1): Show |
5 | HG01109.hp2 HG02717.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1387+727_1387+728i others(3): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 8/12 | chr11 | 61014741 | |||||||
| chr11:61014757 | T | G | 279 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(276): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.1387+743T>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 8/12 | chr11 | 61014757 | |||||||
| chr11:61014857 | G | C | 42 | a0001c0007t0001g0256 a0002c0003t0001g0002 a0002c0003t0001g0004 others(39): Show |
48 | HG00099.hp2 HG00438.hp2 HG00741.hp2 others(45): Show |
intron_variant | MODIFIER | c.1387+843G>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 8/12 | chr11 | 61014857 | |||||||
| chr11:61015126 | G | A | 2 | a0004c0004t0001g0269 a0004c0004t0001g0271 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1388-587G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 8/12 | chr11 | 61015126 | |||||||
| chr11:61015130 | TA | T | 6 | a0007c0012t0001g0036 a0007c0012t0003g0032 a0007c0012t0003g0034 others(3): Show |
6 | HG01081.hp1 HG01361.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.1388-580delA | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 61015130 | ||||||
| chr11:61015162 | G | A | 21 | a0004c0004t0001g0005 a0004c0004t0001g0016 a0004c0004t0001g0019 others(18): Show |
24 | HG00323.hp1 HG00639.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.1388-551G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 8/12 | chr11 | 61015162 | |||||||
| chr11:61015194 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1388-519G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 8/12 | chr11 | 61015194 | |||||||
| chr11:61015213 | A | G | 1 | a0001c0007t0005g0274 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1388-500A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 8/12 | chr11 | 61015213 | |||||||
| chr11:61015315 | A | G | 4 | a0001c0010t0002g0015 a0001c0010t0002g0134 a0001c0010t0002g0233 others(1): Show |
5 | HG01109.hp2 HG02717.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1388-398A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 8/12 | chr11 | 61015315 | |||||||
| chr11:61015351 | G | A | 4 | a0001c0010t0002g0015 a0001c0010t0002g0134 a0001c0010t0002g0233 others(1): Show |
5 | HG01109.hp2 HG02717.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1388-362G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 8/12 | chr11 | 61015351 | |||||||
| chr11:61015373 | A | C | 279 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(276): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.1388-340A>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 8/12 | chr11 | 61015373 | |||||||
| chr11:61015401 | T | C | 1 | a0002c0003t0001g0004 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1388-312T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 8/12 | chr11 | 61015401 | |||||||
| chr11:61015464 | G | A | 1 | a0002c0003t0001g0067 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1388-249G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 8/12 | chr11 | 61015464 | |||||||
| chr11:61015590 | A | G | 4 | a0005c0006t0001g0013 a0005c0006t0001g0199 a0005c0006t0001g0243 others(1): Show |
5 | HG01099.hp2 HG01123.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.1388-123A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 8/12 | chr11 | 61015590 | |||||||
| chr11:61015596 | C | T | 1 | a0001c0001t0001g0141 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1388-117C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 8/12 | chr11 | 61015596 | |||||||
| chr11:61015636 | C | T | 172 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(169): Show |
181 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.1388-77C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 8/12 | chr11 | 61015636 | |||||||
| chr11:61015654 | C | T | 279 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(276): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.1388-59C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 8/12 | chr11 | 61015654 | |||||||
| chr11:61015663 | A | G | 279 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(276): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.1388-50A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 8/12 | chr11 | 61015663 | |||||||
| chr11:61016013 | G | A | 1 | a0003c0005t0001g0044 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1510+178G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 9/12 | chr11 | 61016013 | |||||||
| chr11:61016013 | G | T | 1 | a0001c0001t0011g0277 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1510+178G>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 9/12 | chr11 | 61016013 | |||||||
| chr11:61016147 | G | T | 1 | a0002c0002t0001g0092 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1510+312G>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 9/12 | chr11 | 61016147 | |||||||
| chr11:61016159 | G | A | 23 | a0001c0007t0001g0017 a0001c0007t0001g0018 a0001c0007t0001g0021 others(20): Show |
25 | HG02145.hp2 HG02572.hp1 HG02818.hp1 others(22): Show |
intron_variant | MODIFIER | c.1510+324G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 9/12 | chr11 | 61016159 | |||||||
| chr11:61016188 | C | T | 1 | a0003c0011t0005g0048 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1510+353C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 9/12 | chr11 | 61016188 | |||||||
| chr11:61016205 | C | T | 2 | a0005c0006t0001g0275 a0005c0006t0001g0276 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1510+370C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 9/12 | chr11 | 61016205 | |||||||
| chr11:61016206 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1510+371G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 9/12 | chr11 | 61016206 | |||||||
| chr11:61016261 | C | T | 5 | a0007c0012t0001g0036 a0007c0012t0003g0032 a0007c0012t0003g0034 others(2): Show |
5 | HG01081.hp1 HG01361.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1510+426C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 9/12 | chr11 | 61016261 | |||||||
| chr11:61016332 | C | T | 31 | a0005c0006t0001g0009 a0005c0006t0001g0013 a0005c0006t0001g0029 others(28): Show |
33 | HG00140.hp2 HG00639.hp1 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.1510+497C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 9/12 | chr11 | 61016332 | |||||||
| chr11:61016487 | A | G | 1 | a0001c0001t0001g0104 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1510+652A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 9/12 | chr11 | 61016487 | |||||||
| chr11:61016510 | T | C | 1 | a0003c0005t0001g0057 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1510+675T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 9/12 | chr11 | 61016510 | |||||||
| chr11:61016637 | C | T | 3 | a0003c0005t0001g0159 a0003c0005t0001g0163 a0003c0005t0001g0184 |
3 | HG02165.hp2 NA18747.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.1510+802C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 9/12 | chr11 | 61016637 | |||||||
| chr11:61016638 | G | A | 1 | a0003c0011t0005g0048 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1510+803G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 9/12 | chr11 | 61016638 | |||||||
| chr11:61016679 | C | T | 1 | a0002c0003t0001g0213 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1511-800C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 9/12 | chr11 | 61016679 | |||||||
| chr11:61016803 | G | A | 117 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(114): Show |
122 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.1511-676G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 9/12 | chr11 | 61016803 | |||||||
| chr11:61016814 | C | T | 21 | a0001c0007t0001g0017 a0001c0007t0001g0018 a0001c0007t0001g0021 others(18): Show |
23 | HG02145.hp2 HG02258.hp2 HG02572.hp1 others(20): Show |
intron_variant | MODIFIER | c.1511-665C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 9/12 | chr11 | 61016814 | |||||||
| chr11:61016848 | C | T | 1 | a0004c0004t0001g0273 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1511-631C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 9/12 | chr11 | 61016848 | |||||||
| chr11:61016854 | CT | C | 2 | a0004c0004t0001g0016 a0004c0004t0001g0236 |
3 | HG01069.hp2 HG01070.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.1511-624delT | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 9/12 | chr11 | 61016854 | |||||||
| chr11:61016906 | C | A | 1 | a0003c0005t0001g0163 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1511-573C>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 9/12 | chr11 | 61016906 | |||||||
| chr11:61016929 | T | A | 1 | a0001c0007t0005g0274 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1511-550T>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 9/12 | chr11 | 61016929 | |||||||
| chr11:61017151 | CCTT | C | 31 | a0002c0009t0001g0001 a0002c0009t0001g0024 a0002c0009t0001g0025 others(28): Show |
36 | HG00323.hp1 HG00639.hp2 HG01069.hp2 others(33): Show |
intron_variant | MODIFIER | c.1511-325_1511-323d others(5): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr11 | 61017151 | ||||||
| chr11:61017396 | C | T | 2 | a0001c0001t0007g0041 a0001c0001t0007g0258 |
2 | HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1511-83C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 9/12 | chr11 | 61017396 | |||||||
| chr11:61017462 | A | G | 128 | a0001c0007t0001g0017 a0001c0007t0001g0018 a0001c0007t0001g0021 others(125): Show |
142 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.1511-17A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 9/12 | chr11 | 61017462 | |||||||
| chr11:61017464 | C | T | 1 | a0003c0005t0001g0186 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1511-15C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 9/12 | chr11 | 61017464 | |||||||
| chr11:61017566 | A | G | 128 | a0001c0007t0001g0017 a0001c0007t0001g0018 a0001c0007t0001g0021 others(125): Show |
142 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.1582+16A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 10/12 | chr11 | 61017566 | |||||||
| chr11:61018143 | G | A | 1 | a0001c0007t0005g0274 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1837+130G>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 11/12 | chr11 | 61018143 | |||||||
| chr11:61018178 | A | G | 1 | a0002c0002t0001g0051 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1838-111A>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 11/12 | chr11 | 61018178 | |||||||
| chr11:61018251 | T | C | 60 | a0001c0007t0001g0017 a0001c0007t0001g0018 a0001c0007t0001g0021 others(57): Show |
66 | HG00099.hp2 HG00438.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.1838-38T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 11/12 | chr11 | 61018251 | |||||||
| chr11:61018480 | C | CAAGGGGA others(12): Show |
60 | a0001c0007t0001g0017 a0001c0007t0001g0018 a0001c0007t0001g0021 others(57): Show |
66 | HG00099.hp2 HG00438.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.1942+93_1942+111du others(20): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr11 | 61018480 | ||||||
| chr11:61018677 | C | T | 1 | a0005c0006t0001g0123 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1942+284C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 12/12 | chr11 | 61018677 | |||||||
| chr11:61018681 | G | GGTA | 97 | a0001c0007t0001g0017 a0001c0007t0001g0018 a0001c0007t0001g0021 others(94): Show |
109 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.1942+290_1942+292d others(5): Show |
CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr11 | 61018681 | ||||||
| chr11:61018740 | C | A | 5 | a0001c0007t0002g0257 a0001c0010t0002g0015 a0001c0010t0002g0134 others(2): Show |
6 | HG01109.hp2 HG02717.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1942+347C>A | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 12/12 | chr11 | 61018740 | |||||||
| chr11:61018771 | T | G | 9 | a0002c0003t0001g0004 a0002c0003t0001g0060 a0002c0003t0001g0067 others(6): Show |
10 | HG00438.hp2 HG01069.hp1 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.1942+378T>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 12/12 | chr11 | 61018771 | |||||||
| chr11:61018817 | C | T | 3 | a0001c0001t0001g0110 a0001c0001t0001g0150 a0001c0001t0001g0153 |
3 | HG01943.hp2 HG01952.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.1942+424C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 12/12 | chr11 | 61018817 | |||||||
| chr11:61019002 | T | C | 97 | a0001c0007t0001g0017 a0001c0007t0001g0018 a0001c0007t0001g0021 others(94): Show |
109 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.1943-252T>C | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 12/12 | chr11 | 61019002 | |||||||
| chr11:61019002 | T | G | 1 | a0002c0003t0001g0125 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1943-252T>G | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 12/12 | chr11 | 61019002 | |||||||
| chr11:61019072 | C | T | 1 | a0001c0018t0001g0148 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1943-182C>T | CD6 | ENSG00000013725.14 | transcript | ENST00000313421.11 | protein_coding | 12/12 | chr11 | 61019072 |