Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 56253 |
| ensemblid | ENSG00000109943.9 |
| hgncid | 24313 |
| symbol | CRTAM |
| name | cytotoxic and regulatory T cell molecule |
| refseq_nuc | NM_019604.4 |
| refseq_prot | NP_062550.2 |
| ensembl_nuc | ENST00000227348.9 |
| ensembl_prot | ENSP00000227348.4 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 122838500 |
| end | 122872643 |
| strand | + |
| ver | v1.2 |
| region | chr11:122838500-122872643 |
| region5000 | chr11:122833500-122877643 |
| regionname0 | CRTAM_chr11_122838500_122872643 |
| regionname5000 | CRTAM_chr11_122833500_122877643 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 393 | 199 | 25 | 49 | 85 | 11 | 28 | 70 | CRTAM_chr11_122833500_122877643 | CRTAM | MWWRV others(388): Show |
chr11 | 122833500 | 122877643 |
| a0002 | 1/0 | 393 | 128 | 43 | 17 | 49 | 5 | 13 | 38 | CRTAM_chr11_122833500_122877643 | CRTAM | MWWRV others(388): Show |
chr11 | 122833500 | 122877643 |
| a0003 | 0/0 | 393 | 64 | 0 | 4 | 54 | 0 | 6 | 39 | CRTAM_chr11_122833500_122877643 | CRTAM | MWWRV others(388): Show |
chr11 | 122833500 | 122877643 |
| a0004 | 0/0 | 393 | 9 | 8 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | MWWRV others(388): Show |
chr11 | 122833500 | 122877643 |
| a0005 | 0/0 | 393 | 9 | 9 | 0 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | MWWRV others(388): Show |
chr11 | 122833500 | 122877643 |
| a0006 | 0/0 | 393 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | MWWRV others(388): Show |
chr11 | 122833500 | 122877643 |
| a0007 | 0/0 | 393 | 5 | 0 | 0 | 4 | 0 | 1 | 3 | CRTAM_chr11_122833500_122877643 | CRTAM | MWWRV others(388): Show |
chr11 | 122833500 | 122877643 |
| a0008 | 0/0 | 393 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | MWWRV others(388): Show |
chr11 | 122833500 | 122877643 |
| a0009 | 0/0 | 393 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | MWWRV others(388): Show |
chr11 | 122833500 | 122877643 |
| a0010 | 0/0 | 393 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | MWWRV others(388): Show |
chr11 | 122833500 | 122877643 |
| a0011 | 0/0 | 393 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | MWWRV others(388): Show |
chr11 | 122833500 | 122877643 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1179 | 192 | 19 | 48 | 85 | 11 | 28 | CRTAM_chr11_122833500_122877643 | CRTAM | ATGTG others(1174): Show |
chr11 | 122833500 | 122877643 | ||
| a0001c0005 | 0/0 | 1179 | 6 | 5 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | ATGTG others(1174): Show |
chr11 | 122833500 | 122877643 | ||
| a0001c0018 | 0/0 | 1179 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | ATGTG others(1174): Show |
chr11 | 122833500 | 122877643 | ||
| a0002c0002 | 1/0 | 1179 | 72 | 36 | 11 | 17 | 2 | 5 | CRTAM_chr11_122833500_122877643 | CRTAM | ATGTG others(1174): Show |
chr11 | 122833500 | 122877643 | ||
| a0002c0004 | 0/0 | 1179 | 54 | 6 | 6 | 31 | 3 | 8 | CRTAM_chr11_122833500_122877643 | CRTAM | ATGTG others(1174): Show |
chr11 | 122833500 | 122877643 | ||
| a0002c0016 | 0/0 | 1179 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | ATGTG others(1174): Show |
chr11 | 122833500 | 122877643 | ||
| a0002c0017 | 0/0 | 1179 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | ATGTG others(1174): Show |
chr11 | 122833500 | 122877643 | ||
| a0003c0003 | 0/0 | 1179 | 63 | 0 | 3 | 54 | 0 | 6 | CRTAM_chr11_122833500_122877643 | CRTAM | ATGTG others(1174): Show |
chr11 | 122833500 | 122877643 | ||
| a0003c0014 | 0/0 | 1179 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | ATGTG others(1174): Show |
chr11 | 122833500 | 122877643 | ||
| a0004c0008 | 0/0 | 1179 | 5 | 4 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | ATGTG others(1174): Show |
chr11 | 122833500 | 122877643 | ||
| a0004c0010 | 0/0 | 1179 | 3 | 3 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | ATGTG others(1174): Show |
chr11 | 122833500 | 122877643 | ||
| a0004c0015 | 0/0 | 1179 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | ATGTG others(1174): Show |
chr11 | 122833500 | 122877643 | ||
| a0005c0006 | 0/0 | 1179 | 6 | 6 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | ATGTG others(1174): Show |
chr11 | 122833500 | 122877643 | ||
| a0005c0012 | 0/0 | 1179 | 3 | 3 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | ATGTG others(1174): Show |
chr11 | 122833500 | 122877643 | ||
| a0006c0007 | 0/0 | 1179 | 6 | 6 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | ATGTG others(1174): Show |
chr11 | 122833500 | 122877643 | ||
| a0007c0009 | 0/0 | 1179 | 5 | 0 | 0 | 4 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | ATGTG others(1174): Show |
chr11 | 122833500 | 122877643 | ||
| a0008c0011 | 0/0 | 1179 | 3 | 2 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | ATGTG others(1174): Show |
chr11 | 122833500 | 122877643 | ||
| a0009c0013 | 0/0 | 1179 | 3 | 3 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | ATGTG others(1174): Show |
chr11 | 122833500 | 122877643 | ||
| a0010c0020 | 0/0 | 1179 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | ATGTG others(1174): Show |
chr11 | 122833500 | 122877643 | ||
| a0011c0019 | 0/0 | 1179 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | ATGTG others(1174): Show |
chr11 | 122833500 | 122877643 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2473 | 88 | 10 | 13 | 56 | 1 | 8 | CRTAM_chr11_122833500_122877643 | CRTAM | AGAAT others(2468): Show |
chr11 | 122833500 | 122877643 |
| a0001c0001t0002 | 0/1 | 2473 | 87 | 8 | 25 | 26 | 9 | 18 | CRTAM_chr11_122833500_122877643 | CRTAM | AGAAT others(2468): Show |
chr11 | 122833500 | 122877643 |
| a0001c0001t0004 | 0/0 | 2473 | 2 | 0 | 0 | 2 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | AGAAT others(2468): Show |
chr11 | 122833500 | 122877643 |
| a0001c0001t0007 | 0/0 | 2473 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | AGAAT others(2468): Show |
chr11 | 122833500 | 122877643 |
| a0001c0001t0008 | 0/0 | 2473 | 9 | 0 | 8 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | AGAAT others(2468): Show |
chr11 | 122833500 | 122877643 |
| a0001c0001t0012 | 0/0 | 2473 | 3 | 0 | 2 | 0 | 1 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | AGAAT others(2468): Show |
chr11 | 122833500 | 122877643 |
| a0001c0001t0016 | 0/0 | 2473 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | AGAAT others(2468): Show |
chr11 | 122833500 | 122877643 |
| a0001c0001t0018 | 0/0 | 2473 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | AGAAT others(2468): Show |
chr11 | 122833500 | 122877643 |
| a0001c0005t0001 | 0/0 | 2473 | 6 | 5 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | AGAAT others(2468): Show |
chr11 | 122833500 | 122877643 |
| a0001c0018t0011 | 0/0 | 2473 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | AGAAT others(2468): Show |
chr11 | 122833500 | 122877643 |
| a0002c0002t0001 | 0/0 | 2473 | 6 | 6 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | AGAAT others(2468): Show |
chr11 | 122833500 | 122877643 |
| a0002c0002t0005 | 1/0 | 2473 | 25 | 6 | 2 | 13 | 2 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | AGAAT others(2468): Show |
chr11 | 122833500 | 122877643 |
| a0002c0002t0006 | 0/0 | 2473 | 22 | 6 | 8 | 4 | 0 | 4 | CRTAM_chr11_122833500_122877643 | CRTAM | AGAAT others(2468): Show |
chr11 | 122833500 | 122877643 |
| a0002c0002t0007 | 0/0 | 2473 | 7 | 7 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | AGAAT others(2468): Show |
chr11 | 122833500 | 122877643 |
| a0002c0002t0009 | 0/0 | 2473 | 7 | 6 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | AGAAT others(2468): Show |
chr11 | 122833500 | 122877643 |
| a0002c0002t0010 | 0/0 | 2473 | 5 | 5 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | AGAAT others(2468): Show |
chr11 | 122833500 | 122877643 |
| a0002c0004t0001 | 0/0 | 2473 | 2 | 2 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | AGAAT others(2468): Show |
chr11 | 122833500 | 122877643 |
| a0002c0004t0003 | 0/0 | 2473 | 3 | 1 | 0 | 2 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | AGAAT others(2468): Show |
chr11 | 122833500 | 122877643 |
| a0002c0004t0004 | 0/0 | 2473 | 49 | 3 | 6 | 29 | 3 | 8 | CRTAM_chr11_122833500_122877643 | CRTAM | AGAAT others(2468): Show |
chr11 | 122833500 | 122877643 |
| a0002c0016t0001 | 0/0 | 2473 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | AGAAT others(2468): Show |
chr11 | 122833500 | 122877643 |
| a0002c0017t0004 | 0/0 | 2473 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | AGAAT others(2468): Show |
chr11 | 122833500 | 122877643 |
| a0003c0003t0003 | 0/0 | 2473 | 62 | 0 | 3 | 54 | 0 | 5 | CRTAM_chr11_122833500_122877643 | CRTAM | AGAAT others(2468): Show |
chr11 | 122833500 | 122877643 |
| a0003c0003t0017 | 0/0 | 2473 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | AGAAT others(2468): Show |
chr11 | 122833500 | 122877643 |
| a0003c0014t0003 | 0/0 | 2473 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | AGAAT others(2468): Show |
chr11 | 122833500 | 122877643 |
| a0004c0008t0001 | 0/0 | 2473 | 4 | 3 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | AGAAT others(2468): Show |
chr11 | 122833500 | 122877643 |
| a0004c0008t0014 | 0/0 | 2473 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | AGAAT others(2468): Show |
chr11 | 122833500 | 122877643 |
| a0004c0010t0007 | 0/0 | 2473 | 2 | 2 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | AGAAT others(2468): Show |
chr11 | 122833500 | 122877643 |
| a0004c0010t0015 | 0/0 | 2473 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | AGAAT others(2468): Show |
chr11 | 122833500 | 122877643 |
| a0004c0015t0004 | 0/0 | 2473 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | AGAAT others(2468): Show |
chr11 | 122833500 | 122877643 |
| a0005c0006t0004 | 0/0 | 2473 | 6 | 6 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | AGAAT others(2468): Show |
chr11 | 122833500 | 122877643 |
| a0005c0012t0009 | 0/0 | 2473 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | AGAAT others(2468): Show |
chr11 | 122833500 | 122877643 |
| a0005c0012t0010 | 0/0 | 2473 | 2 | 2 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | AGAAT others(2468): Show |
chr11 | 122833500 | 122877643 |
| a0006c0007t0001 | 0/0 | 2473 | 6 | 6 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | AGAAT others(2468): Show |
chr11 | 122833500 | 122877643 |
| a0007c0009t0003 | 0/0 | 2473 | 3 | 0 | 0 | 3 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | AGAAT others(2468): Show |
chr11 | 122833500 | 122877643 |
| a0007c0009t0013 | 0/0 | 2473 | 2 | 0 | 0 | 1 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | AGAAT others(2468): Show |
chr11 | 122833500 | 122877643 |
| a0008c0011t0001 | 0/0 | 2473 | 3 | 2 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | AGAAT others(2468): Show |
chr11 | 122833500 | 122877643 |
| a0009c0013t0011 | 0/0 | 2473 | 3 | 3 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | AGAAT others(2468): Show |
chr11 | 122833500 | 122877643 |
| a0010c0020t0005 | 0/0 | 2473 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | AGAAT others(2468): Show |
chr11 | 122833500 | 122877643 |
| a0011c0019t0009 | 0/0 | 2473 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | AGAAT others(2468): Show |
chr11 | 122833500 | 122877643 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0001g0003 | 0/0 | 7 | 0 | 1 | 5 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0001g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0001g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0001g0011 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0002g0007 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0002g0016 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0002g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0002g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0002g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0002g0031 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0002g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0002g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0002g0038 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0002g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0002g0041 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0002g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0002g0045 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0002g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0002g0153 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0002g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0004g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0004g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0007g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0008g0001 | 0/0 | 7 | 0 | 6 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0008g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0008g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0012g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0012g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0012g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0016g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0001t0018g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0005t0001g0022 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0005t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0005t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0005t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0001c0018t0011g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0002t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0002t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0002t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0002t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0002t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0002t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0002t0005g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0002t0005g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0002t0005g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0002t0005g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0002t0005g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0002t0005g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0002t0005g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0002t0005g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0002t0005g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0002t0005g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0002t0005g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0002t0005g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0002t0005g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0002t0005g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0002t0005g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0002t0005g0203 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0002t0005g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0002t0005g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0002t0005g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0002t0005g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0002t0005g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0002t0005g0322 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0002t0006g0017 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0002t0006g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0002t0006g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0002t0006g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0002t0006g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0002t0006g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0002t0006g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0002t0006g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0002t0006g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0002t0006g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0002t0006g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0002t0006g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0002t0006g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0002t0006g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0002t0006g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0002t0006g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0002t0006g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0002t0006g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0002t0006g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0002t0006g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0002t0007g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0002t0007g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0002t0007g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0002t0007g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0002t0007g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0002t0007g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0002t0007g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0002t0009g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0002t0009g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0002t0009g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0002t0009g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0002t0009g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0002t0009g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0002t0009g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0002t0010g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0002t0010g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0002t0010g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0002t0010g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0004t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0004t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0004t0003g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0004t0003g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0004t0004g0002 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0004t0004g0005 | 0/0 | 6 | 0 | 1 | 3 | 0 | 2 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0004t0004g0006 | 0/0 | 5 | 0 | 3 | 0 | 0 | 2 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0004t0004g0014 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0004t0004g0050 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0004t0004g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0004t0004g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0004t0004g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0004t0004g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0004t0004g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0004t0004g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0004t0004g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0004t0004g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0004t0004g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0004t0004g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0004t0004g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0004t0004g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0004t0004g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0004t0004g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0004t0004g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0004t0004g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0004t0004g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0004t0004g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0004t0004g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0004t0004g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0004t0004g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0004t0004g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0004t0004g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0004t0004g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0004t0004g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0004t0004g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0016t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0002c0017t0004g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0003c0003t0003g0004 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0003c0003t0003g0008 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0003c0003t0003g0012 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0003c0003t0003g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0003c0003t0003g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0003c0003t0003g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0003c0003t0003g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0003c0003t0003g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0003c0003t0003g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0003c0003t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0003c0003t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0003c0003t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0003c0003t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0003c0003t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0003c0003t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0003c0003t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0003c0003t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0003c0003t0003g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0003c0003t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0003c0003t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0003c0003t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0003c0003t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0003c0003t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0003c0003t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0003c0003t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0003c0003t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0003c0003t0003g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0003c0003t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0003c0003t0003g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0003c0003t0003g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0003c0003t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0003c0003t0003g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0003c0003t0003g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0003c0003t0003g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0003c0003t0003g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0003c0003t0003g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0003c0003t0003g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0003c0003t0003g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0003c0003t0003g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0003c0003t0003g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0003c0003t0017g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0003c0014t0003g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0004c0008t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0004c0008t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0004c0008t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0004c0008t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0004c0008t0014g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0004c0010t0007g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0004c0010t0007g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0004c0010t0015g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0004c0015t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0005c0006t0004g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0005c0006t0004g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0005c0006t0004g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0005c0006t0004g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0005c0006t0004g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0005c0012t0009g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0005c0012t0010g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0005c0012t0010g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0006c0007t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0006c0007t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0006c0007t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0006c0007t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0006c0007t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0007c0009t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0007c0009t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0007c0009t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0007c0009t0013g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0007c0009t0013g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0008c0011t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0008c0011t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0008c0011t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0009c0013t0011g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0009c0013t0011g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0010c0020t0005g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| a0011c0019t0009g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0004 | t0004 | g0014 | EUR | GBR | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG00099 | hp2 | a0002 | c0004 | t0004 | g0259 | EUR | GBR | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0151 | EUR | GBR | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG00140 | hp2 | a0002 | c0004 | t0004 | g0014 | EUR | GBR | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0038 | EUR | FIN | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0031 | EUR | FIN | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | CHS | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG00408 | hp2 | a0007 | c0009 | t0003 | g0026 | EAS | CHS | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG00423 | hp1 | a0003 | c0003 | t0003 | g0092 | EAS | CHS | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | CHS | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG00438 | hp1 | a0003 | c0003 | t0003 | g0008 | EAS | CHS | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG00438 | hp2 | a0001 | c0001 | t0004 | g0132 | EAS | CHS | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG00544 | hp1 | a0003 | c0003 | t0003 | g0272 | EAS | CHS | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG00544 | hp2 | a0002 | c0002 | t0005 | g0182 | EAS | CHS | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG00558 | hp1 | a0003 | c0003 | t0003 | g0277 | EAS | CHS | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | CHS | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | CHS | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG00597 | hp2 | a0002 | c0004 | t0004 | g0005 | EAS | CHS | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG00609 | hp1 | a0002 | c0002 | t0005 | g0018 | EAS | CHS | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | CHS | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG00621 | hp1 | a0003 | c0003 | t0003 | g0008 | EAS | CHS | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG00621 | hp2 | a0002 | c0002 | t0006 | g0172 | EAS | CHS | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0280 | AMR | PUR | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG00639 | hp2 | a0001 | c0001 | t0012 | g0168 | AMR | PUR | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0155 | AMR | PUR | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG00642 | hp2 | a0004 | c0008 | t0001 | g0320 | AMR | PUR | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG00673 | hp1 | a0003 | c0003 | t0003 | g0134 | EAS | CHS | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | CHS | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG00735 | hp1 | a0003 | c0003 | t0003 | g0012 | AMR | PUR | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG00735 | hp2 | a0001 | c0001 | t0012 | g0190 | AMR | PUR | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG00738 | hp1 | a0001 | c0001 | t0008 | g0001 | AMR | PUR | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG00738 | hp2 | a0002 | c0002 | t0006 | g0170 | AMR | PUR | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG00741 | hp1 | a0002 | c0004 | t0004 | g0056 | AMR | PUR | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0234 | AMR | PUR | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0030 | AMR | PUR | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0039 | AMR | PUR | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG01070 | hp1 | a0002 | c0004 | t0004 | g0006 | AMR | PUR | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0025 | AMR | PUR | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG01071 | hp1 | a0002 | c0004 | t0004 | g0006 | AMR | PUR | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0030 | AMR | PUR | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG01081 | hp1 | a0001 | c0001 | t0008 | g0001 | AMR | PUR | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG01081 | hp2 | a0002 | c0002 | t0006 | g0323 | AMR | PUR | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG01099 | hp1 | a0002 | c0002 | t0005 | g0220 | AMR | PUR | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG01099 | hp2 | a0002 | c0002 | t0006 | g0017 | AMR | PUR | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0303 | AMR | PUR | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0231 | AMR | PUR | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG01109 | hp1 | a0008 | c0011 | t0001 | g0209 | AMR | PUR | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG01167 | hp1 | a0002 | c0002 | t0009 | g0136 | AMR | PUR | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG01167 | hp2 | a0002 | c0004 | t0004 | g0005 | AMR | PUR | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0233 | AMR | PUR | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0126 | AMR | PUR | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0156 | AMR | PUR | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0039 | AMR | PUR | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0147 | AMR | PUR | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0242 | AMR | PUR | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG01243 | hp1 | a0002 | c0002 | t0006 | g0176 | AMR | PUR | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0302 | AMR | PUR | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | CLM | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG01256 | hp2 | a0001 | c0001 | t0008 | g0001 | AMR | CLM | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG01257 | hp2 | a0002 | c0002 | t0006 | g0017 | AMR | CLM | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG01258 | hp1 | a0002 | c0002 | t0006 | g0017 | AMR | CLM | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG01258 | hp2 | a0001 | c0001 | t0008 | g0001 | AMR | CLM | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG01261 | hp1 | a0003 | c0003 | t0003 | g0008 | AMR | CLM | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0160 | AMR | CLM | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0152 | AMR | CLM | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0016 | AMR | CLM | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0202 | AMR | CLM | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG01361 | hp2 | a0002 | c0002 | t0006 | g0173 | AMR | CLM | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0125 | AMR | CLM | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG01433 | hp2 | a0001 | c0001 | t0008 | g0078 | AMR | CLM | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0299 | AMR | CLM | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG01496 | hp2 | a0001 | c0005 | t0001 | g0022 | AMR | CLM | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0232 | EUR | IBS | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG01515 | hp2 | a0002 | c0002 | t0005 | g0322 | EUR | IBS | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0041 | EUR | IBS | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0045 | EUR | IBS | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0041 | EUR | IBS | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG01517 | hp2 | a0002 | c0002 | t0005 | g0321 | EUR | IBS | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | ACB | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG01884 | hp2 | a0002 | c0002 | t0009 | g0074 | AFR | ACB | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG01891 | hp1 | a0005 | c0006 | t0004 | g0042 | AFR | ACB | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0083 | AMR | PEL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG01934 | hp2 | a0001 | c0001 | t0008 | g0001 | AMR | PEL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG01943 | hp1 | a0001 | c0001 | t0008 | g0001 | AMR | PEL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | PEL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG01952 | hp2 | a0002 | c0002 | t0005 | g0192 | AMR | PEL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0038 | AMR | PEL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG01981 | hp1 | a0003 | c0003 | t0003 | g0188 | AMR | PEL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0090 | AMR | PEL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG01993 | hp1 | a0002 | c0004 | t0004 | g0241 | AMR | PEL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG01993 | hp2 | a0002 | c0004 | t0004 | g0006 | AMR | PEL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02015 | hp1 | a0003 | c0003 | t0003 | g0129 | EAS | KHV | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02015 | hp2 | a0002 | c0004 | t0004 | g0245 | EAS | KHV | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02027 | hp1 | a0003 | c0003 | t0003 | g0285 | EAS | KHV | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02027 | hp2 | a0002 | c0004 | t0004 | g0314 | EAS | KHV | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02040 | hp1 | a0003 | c0003 | t0003 | g0282 | EAS | KHV | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02040 | hp2 | a0003 | c0003 | t0003 | g0079 | EAS | KHV | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02055 | hp1 | a0002 | c0002 | t0006 | g0288 | AFR | ACB | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02055 | hp2 | a0002 | c0002 | t0010 | g0300 | AFR | ACB | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02056 | hp1 | a0002 | c0002 | t0005 | g0183 | EAS | KHV | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | KHV | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | KHV | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | KHV | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02074 | hp1 | a0002 | c0004 | t0004 | g0002 | EAS | KHV | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02074 | hp2 | a0002 | c0004 | t0004 | g0276 | EAS | KHV | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02080 | hp1 | a0003 | c0003 | t0003 | g0013 | EAS | KHV | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02080 | hp2 | a0002 | c0004 | t0004 | g0283 | EAS | KHV | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02083 | hp1 | a0001 | c0001 | t0004 | g0120 | EAS | KHV | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02083 | hp2 | a0003 | c0003 | t0003 | g0013 | EAS | KHV | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02129 | hp1 | a0003 | c0003 | t0003 | g0020 | EAS | KHV | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02135 | hp2 | a0003 | c0003 | t0003 | g0256 | EAS | KHV | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02145 | hp1 | a0006 | c0007 | t0001 | g0312 | AFR | ACB | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02145 | hp2 | a0005 | c0012 | t0010 | g0194 | AFR | ACB | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0169 | AMR | PEL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02148 | hp2 | a0001 | c0001 | t0008 | g0096 | AMR | PEL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | CDX | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02165 | hp2 | a0002 | c0002 | t0006 | g0260 | EAS | CDX | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02257 | hp1 | a0002 | c0002 | t0009 | g0318 | AFR | ACB | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02257 | hp2 | a0002 | c0004 | t0004 | g0243 | AFR | ACB | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02258 | hp1 | a0005 | c0012 | t0010 | g0305 | AFR | ACB | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02258 | hp2 | a0002 | c0002 | t0010 | g0301 | AFR | ACB | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02273 | hp2 | a0003 | c0014 | t0003 | g0012 | AMR | PEL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02280 | hp1 | a0005 | c0006 | t0004 | g0062 | AFR | ACB | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | ACB | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02451 | hp1 | a0010 | c0020 | t0005 | g0210 | AFR | ACB | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0216 | AFR | ACB | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0036 | AFR | GWD | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02572 | hp2 | a0002 | c0002 | t0001 | g0253 | AFR | GWD | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0154 | SAS | PJL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02602 | hp2 | a0002 | c0002 | t0006 | g0174 | SAS | PJL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02615 | hp1 | a0002 | c0002 | t0005 | g0191 | AFR | GWD | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02615 | hp2 | a0002 | c0002 | t0005 | g0295 | AFR | GWD | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02622 | hp1 | a0002 | c0002 | t0009 | g0138 | AFR | GWD | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02622 | hp2 | a0006 | c0007 | t0001 | g0311 | AFR | GWD | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02630 | hp1 | a0004 | c0010 | t0007 | g0213 | AFR | GWD | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02630 | hp2 | a0002 | c0002 | t0001 | g0159 | AFR | GWD | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02647 | hp1 | a0002 | c0002 | t0007 | g0290 | AFR | GWD | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0058 | AFR | GWD | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02683 | hp1 | a0003 | c0003 | t0003 | g0267 | SAS | PJL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02683 | hp2 | a0002 | c0002 | t0006 | g0177 | SAS | PJL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02698 | hp1 | a0007 | c0009 | t0013 | g0007 | SAS | PJL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0037 | SAS | PJL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02717 | hp1 | a0002 | c0002 | t0009 | g0165 | AFR | GWD | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02717 | hp2 | a0002 | c0002 | t0006 | g0287 | AFR | GWD | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02723 | hp1 | a0002 | c0002 | t0005 | g0250 | AFR | GWD | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02723 | hp2 | a0001 | c0005 | t0001 | g0022 | AFR | GWD | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0226 | SAS | PJL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0161 | SAS | PJL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02809 | hp1 | a0005 | c0006 | t0004 | g0200 | AFR | GWD | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02809 | hp2 | a0009 | c0013 | t0011 | g0211 | AFR | GWD | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02818 | hp1 | a0006 | c0007 | t0001 | g0310 | AFR | GWD | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02886 | hp1 | a0002 | c0002 | t0001 | g0289 | AFR | GWD | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0036 | AFR | GWD | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02895 | hp1 | a0004 | c0015 | t0004 | g0054 | AFR | GWD | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02895 | hp2 | a0001 | c0005 | t0001 | g0022 | AFR | GWD | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0141 | AFR | GWD | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02896 | hp2 | a0002 | c0002 | t0010 | g0049 | AFR | GWD | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02897 | hp1 | a0002 | c0002 | t0010 | g0049 | AFR | GWD | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02897 | hp2 | a0001 | c0005 | t0001 | g0304 | AFR | GWD | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0296 | AFR | ESN | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02922 | hp2 | a0002 | c0002 | t0007 | g0068 | AFR | ESN | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02965 | hp1 | a0002 | c0002 | t0007 | g0317 | AFR | ESN | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02965 | hp2 | a0002 | c0002 | t0001 | g0057 | AFR | ESN | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02970 | hp1 | a0002 | c0002 | t0007 | g0291 | AFR | ESN | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02970 | hp2 | a0002 | c0016 | t0001 | g0065 | AFR | ESN | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02976 | hp1 | a0009 | c0013 | t0011 | g0043 | AFR | ESN | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02976 | hp2 | a0002 | c0002 | t0006 | g0198 | AFR | ESN | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0221 | SAS | PJL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0248 | SAS | PJL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG03041 | hp1 | a0002 | c0004 | t0001 | g0066 | AFR | GWD | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG03041 | hp2 | a0001 | c0001 | t0007 | g0149 | AFR | GWD | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG03098 | hp1 | a0002 | c0004 | t0003 | g0251 | AFR | MSL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG03098 | hp2 | a0002 | c0004 | t0001 | g0313 | AFR | MSL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | ESN | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG03130 | hp2 | a0002 | c0002 | t0009 | g0297 | AFR | ESN | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG03139 | hp1 | a0001 | c0005 | t0001 | g0051 | AFR | ESN | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG03139 | hp2 | a0002 | c0002 | t0006 | g0063 | AFR | ESN | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0150 | AFR | ESN | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG03195 | hp2 | a0002 | c0002 | t0007 | g0205 | AFR | ESN | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG03209 | hp1 | a0002 | c0002 | t0007 | g0286 | AFR | MSL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG03209 | hp2 | a0001 | c0018 | t0011 | g0306 | AFR | MSL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | MSL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG03225 | hp2 | a0002 | c0002 | t0001 | g0298 | AFR | MSL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0246 | SAS | PJL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG03486 | hp1 | a0009 | c0013 | t0011 | g0043 | AFR | MSL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG03486 | hp2 | a0002 | c0002 | t0001 | g0319 | AFR | MSL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0016 | SAS | PJL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0045 | SAS | PJL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG03491 | hp1 | a0002 | c0004 | t0004 | g0005 | SAS | PJL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG03491 | hp2 | a0002 | c0002 | t0006 | g0175 | SAS | PJL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0016 | SAS | PJL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG03492 | hp2 | a0002 | c0004 | t0004 | g0005 | SAS | PJL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0162 | AFR | ESN | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG03516 | hp2 | a0002 | c0002 | t0009 | g0137 | AFR | ESN | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG03540 | hp2 | a0004 | c0008 | t0001 | g0212 | AFR | GWD | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG03579 | hp1 | a0004 | c0008 | t0001 | g0158 | AFR | MSL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG03579 | hp2 | a0002 | c0002 | t0005 | g0139 | AFR | MSL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0249 | SAS | PJL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG03654 | hp2 | a0003 | c0003 | t0003 | g0012 | SAS | PJL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG03669 | hp1 | a0003 | c0003 | t0003 | g0292 | SAS | PJL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0085 | SAS | PJL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0255 | SAS | STU | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG03688 | hp2 | a0002 | c0004 | t0004 | g0050 | SAS | STU | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG03704 | hp1 | a0003 | c0003 | t0003 | g0265 | SAS | PJL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0227 | SAS | PJL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0193 | SAS | BEB | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0007 | SAS | BEB | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0230 | SAS | BEB | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0143 | SAS | BEB | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG03927 | hp1 | a0002 | c0004 | t0004 | g0050 | SAS | BEB | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG03927 | hp2 | a0002 | c0004 | t0004 | g0006 | SAS | BEB | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0031 | SAS | BEB | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0273 | SAS | BEB | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0144 | SAS | STU | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG04115 | hp2 | a0003 | c0003 | t0003 | g0004 | SAS | STU | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG04184 | hp1 | a0001 | c0001 | t0016 | g0037 | SAS | BEB | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG04184 | hp2 | a0003 | c0003 | t0017 | g0225 | SAS | BEB | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG04199 | hp1 | a0001 | c0001 | t0018 | g0163 | SAS | STU | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG04199 | hp2 | a0002 | c0002 | t0006 | g0171 | SAS | STU | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG04204 | hp1 | a0002 | c0004 | t0004 | g0201 | SAS | STU | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG04204 | hp2 | a0002 | c0004 | t0004 | g0006 | SAS | STU | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG04228 | hp2 | a0002 | c0002 | t0005 | g0185 | SAS | STU | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18522 | hp1 | a0002 | c0002 | t0007 | g0316 | AFR | YRI | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18522 | hp2 | a0005 | c0006 | t0004 | g0195 | AFR | YRI | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18612 | hp1 | a0003 | c0003 | t0003 | g0008 | EAS | CHB | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | CHB | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18906 | hp1 | a0004 | c0008 | t0014 | g0252 | AFR | YRI | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18906 | hp2 | a0005 | c0012 | t0009 | g0215 | AFR | YRI | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18942 | hp1 | a0003 | c0003 | t0003 | g0266 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18942 | hp2 | a0002 | c0004 | t0003 | g0046 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18946 | hp1 | a0003 | c0003 | t0003 | g0279 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18947 | hp1 | a0002 | c0004 | t0004 | g0002 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18947 | hp2 | a0003 | c0003 | t0003 | g0004 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18948 | hp1 | a0002 | c0002 | t0005 | g0018 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18948 | hp2 | a0002 | c0004 | t0004 | g0005 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18949 | hp1 | a0002 | c0004 | t0004 | g0217 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18950 | hp1 | a0003 | c0003 | t0003 | g0004 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18951 | hp2 | a0002 | c0002 | t0005 | g0167 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18952 | hp2 | a0002 | c0002 | t0005 | g0040 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18953 | hp1 | a0007 | c0009 | t0013 | g0142 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18956 | hp1 | a0001 | c0001 | t0008 | g0001 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18956 | hp2 | a0003 | c0003 | t0003 | g0261 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18957 | hp1 | a0003 | c0003 | t0003 | g0048 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18957 | hp2 | a0002 | c0004 | t0004 | g0084 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18959 | hp1 | a0002 | c0002 | t0005 | g0184 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18959 | hp2 | a0003 | c0003 | t0003 | g0004 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18961 | hp1 | a0003 | c0003 | t0003 | g0247 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18963 | hp1 | a0003 | c0003 | t0003 | g0284 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18966 | hp2 | a0002 | c0002 | t0005 | g0040 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18968 | hp2 | a0003 | c0003 | t0003 | g0274 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18969 | hp1 | a0003 | c0003 | t0003 | g0268 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18969 | hp2 | a0002 | c0002 | t0005 | g0072 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18970 | hp1 | a0003 | c0003 | t0003 | g0032 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18972 | hp2 | a0003 | c0003 | t0003 | g0013 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18973 | hp1 | a0003 | c0003 | t0003 | g0128 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18974 | hp1 | a0003 | c0003 | t0003 | g0263 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18977 | hp1 | a0002 | c0004 | t0004 | g0238 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18977 | hp2 | a0003 | c0003 | t0003 | g0254 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18980 | hp2 | a0003 | c0003 | t0003 | g0034 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18981 | hp2 | a0002 | c0004 | t0004 | g0224 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18982 | hp1 | a0002 | c0004 | t0004 | g0002 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18982 | hp2 | a0003 | c0003 | t0003 | g0004 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18984 | hp1 | a0002 | c0004 | t0004 | g0179 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18985 | hp1 | a0003 | c0003 | t0003 | g0278 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18985 | hp2 | a0002 | c0002 | t0005 | g0018 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18986 | hp1 | a0002 | c0002 | t0005 | g0117 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18987 | hp1 | a0002 | c0004 | t0004 | g0124 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18989 | hp1 | a0003 | c0003 | t0003 | g0048 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18989 | hp2 | a0002 | c0004 | t0004 | g0133 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18990 | hp1 | a0002 | c0004 | t0004 | g0240 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18992 | hp2 | a0003 | c0003 | t0003 | g0004 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18994 | hp2 | a0003 | c0003 | t0003 | g0021 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18998 | hp1 | a0002 | c0002 | t0006 | g0086 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18998 | hp2 | a0002 | c0004 | t0004 | g0178 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18999 | hp1 | a0002 | c0002 | t0005 | g0106 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA18999 | hp2 | a0003 | c0003 | t0003 | g0020 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA19001 | hp1 | a0002 | c0004 | t0004 | g0082 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA19001 | hp2 | a0002 | c0004 | t0004 | g0071 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA19006 | hp1 | a0002 | c0004 | t0004 | g0229 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA19010 | hp1 | a0002 | c0004 | t0004 | g0146 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA19011 | hp1 | a0003 | c0003 | t0003 | g0269 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA19011 | hp2 | a0003 | c0003 | t0003 | g0091 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA19012 | hp2 | a0002 | c0004 | t0003 | g0046 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | LWK | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA19030 | hp2 | a0004 | c0010 | t0007 | g0206 | AFR | LWK | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA19043 | hp1 | a0002 | c0004 | t0004 | g0061 | AFR | LWK | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA19043 | hp2 | a0002 | c0002 | t0005 | g0187 | AFR | LWK | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA19054 | hp2 | a0003 | c0003 | t0003 | g0020 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA19056 | hp2 | a0003 | c0003 | t0003 | g0034 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA19057 | hp1 | a0003 | c0003 | t0003 | g0257 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA19057 | hp2 | a0002 | c0004 | t0004 | g0002 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA19058 | hp1 | a0003 | c0003 | t0003 | g0021 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA19060 | hp2 | a0003 | c0003 | t0003 | g0012 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA19062 | hp2 | a0003 | c0003 | t0003 | g0004 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA19063 | hp1 | a0002 | c0002 | t0006 | g0281 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA19063 | hp2 | a0002 | c0004 | t0004 | g0002 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA19066 | hp1 | a0003 | c0003 | t0003 | g0107 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA19068 | hp2 | a0002 | c0004 | t0004 | g0002 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA19070 | hp2 | a0002 | c0017 | t0004 | g0002 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA19072 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA19072 | hp2 | a0003 | c0003 | t0003 | g0008 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA19074 | hp2 | a0003 | c0003 | t0003 | g0013 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA19075 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA19076 | hp1 | a0003 | c0003 | t0003 | g0262 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA19077 | hp1 | a0002 | c0004 | t0004 | g0236 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA19078 | hp2 | a0003 | c0003 | t0003 | g0135 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA19079 | hp1 | a0003 | c0003 | t0003 | g0021 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA19079 | hp2 | a0002 | c0004 | t0004 | g0237 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA19081 | hp1 | a0002 | c0004 | t0004 | g0005 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA19081 | hp2 | a0007 | c0009 | t0003 | g0067 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA19084 | hp1 | a0003 | c0003 | t0003 | g0032 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA19084 | hp2 | a0002 | c0004 | t0004 | g0002 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA19086 | hp1 | a0002 | c0002 | t0005 | g0180 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA19086 | hp2 | a0007 | c0009 | t0003 | g0239 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA19091 | hp1 | a0003 | c0003 | t0003 | g0258 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA19240 | hp1 | a0008 | c0011 | t0001 | g0214 | AFR | YRI | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA19240 | hp2 | a0002 | c0002 | t0006 | g0064 | AFR | YRI | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | ASW | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | ASW | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0099 | EUR | TSI | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0148 | EUR | TSI | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA20805 | hp1 | a0001 | c0001 | t0012 | g0055 | EUR | TSI | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0228 | EUR | TSI | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA20905 | hp1 | a0002 | c0004 | t0004 | g0014 | SAS | GIH | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0307 | SAS | GIH | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0025 | AMR | CLM | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG01123 | hp2 | a0002 | c0002 | t0006 | g0199 | AMR | CLM | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02109 | hp1 | a0005 | c0006 | t0004 | g0196 | AFR | ACB | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02109 | hp2 | a0006 | c0007 | t0001 | g0024 | AFR | ACB | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02486 | hp1 | a0002 | c0004 | t0004 | g0164 | AFR | ACB | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02486 | hp2 | a0006 | c0007 | t0001 | g0024 | AFR | ACB | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02559 | hp1 | a0001 | c0005 | t0001 | g0197 | AFR | ACB | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG02559 | hp2 | a0002 | c0002 | t0006 | g0059 | AFR | ACB | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG03471 | hp1 | a0004 | c0008 | t0001 | g0052 | AFR | MSL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG03471 | hp2 | a0002 | c0002 | t0010 | g0166 | AFR | MSL | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG06807 | hp1 | a0008 | c0011 | t0001 | g0208 | AFR | USA | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| HG06807 | hp2 | a0006 | c0007 | t0001 | g0315 | AFR | USA | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA20300 | hp1 | a0011 | c0019 | t0009 | g0157 | AFR | USA | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA20300 | hp2 | a0005 | c0006 | t0004 | g0042 | AFR | USA | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA21309 | hp1 | a0004 | c0010 | t0015 | g0207 | AFR | LWK | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| NA21309 | hp2 | a0002 | c0002 | t0005 | g0294 | AFR | LWK | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0153 | REF | REF | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0005 | g0203 | REF | REF | CRTAM_chr11_122833500_122877643 | CRTAM | chr11 | 122833500 | 122877643 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:122850068 | A | C | 2 | a0009 a0010 |
4 | HG02451.hp1 HG02809.hp2 HG02976.hp1 others(1): Show |
missense_variant&splice_region_variant | MODERATE | c.47A>C | p.Glu16Ala | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 2/10 | 94/2473 | 47/1182 | 16/393 | chr11 | 122850068 | |||
| chr11:122851732 | C | A | 4 | a0004 a0008 a0009 others(1): Show |
16 | HG00642.hp2 HG01109.hp1 HG02451.hp1 others(13): Show |
missense_variant | MODERATE | c.233C>A | p.Ala78Asp | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 3/10 | 280/2473 | 233/1182 | 78/393 | chr11 | 122851732 | |||
| chr11:122855722 | A | G | 1 | a0006 | 6 | HG02109.hp2 HG02145.hp1 HG02486.hp2 others(3): Show |
missense_variant | MODERATE | c.518A>G | p.Asp173Gly | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/10 | 565/2473 | 518/1182 | 173/393 | chr11 | 122855722 | |||
| chr11:122862479 | C | T | 1 | a0011 | 1 | NA20300.hp1 | missense_variant | MODERATE | c.668C>T | p.Thr223Ile | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/10 | 715/2473 | 668/1182 | 223/393 | chr11 | 122862479 | |||
| chr11:122864660 | C | T | 1 | a0005 | 9 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
missense_variant | MODERATE | c.758C>T | p.Thr253Ile | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 7/10 | 805/2473 | 758/1182 | 253/393 | chr11 | 122864660 | |||
| chr11:122867553 | A | G | 5 | a0001 a0006 a0007 others(2): Show |
215 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(212): Show |
missense_variant&splice_region_variant | MODERATE | c.962A>G | p.Lys321Arg | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 8/10 | 1009/2473 | 962/1182 | 321/393 | chr11 | 122867553 | |||
| chr11:122871320 | C | G | 2 | a0003 a0007 |
69 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(66): Show |
missense_variant | MODERATE | c.1103C>G | p.Ala368Gly | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 10/10 | 1150/2473 | 1103/1182 | 368/393 | chr11 | 122871320 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:122850099 | C | A | 1 | a0003c0014 | 1 | HG02273.hp2 | synonymous_variant | LOW | c.78C>A | p.Ile26Ile | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 2/10 | 125/2473 | 78/1182 | 26/393 | chr11 | 122850099 | |||
| chr11:122854037 | G | A | 1 | a0001c0005 | 6 | HG01496.hp2 HG02559.hp1 HG02723.hp2 others(3): Show |
synonymous_variant | LOW | c.441G>A | p.Lys147Lys | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/10 | 488/2473 | 441/1182 | 147/393 | chr11 | 122854037 | |||
| chr11:122855783 | G | A | 5 | a0002c0016 a0004c0008 a0004c0015 others(2): Show |
11 | HG00642.hp2 HG02451.hp1 HG02809.hp2 others(8): Show |
synonymous_variant | LOW | c.579G>A | p.Thr193Thr | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/10 | 626/2473 | 579/1182 | 193/393 | chr11 | 122855783 | |||
| chr11:122871276 | C | T | 1 | a0002c0017 | 1 | NA19070.hp2 | synonymous_variant | LOW | c.1059C>T | p.His353His | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 10/10 | 1106/2473 | 1059/1182 | 353/393 | chr11 | 122871276 | |||
| chr11:122871342 | T | C | 6 | a0001c0018 a0002c0004 a0002c0017 others(3): Show |
66 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(63): Show |
synonymous_variant | LOW | c.1125T>C | p.Asn375Asn | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 10/10 | 1172/2473 | 1125/1182 | 375/393 | chr11 | 122871342 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:122871446 | C | A | 3 | a0002c0002t0006 a0002c0002t0010 a0005c0012t0010 |
29 | HG00621.hp2 HG00738.hp2 HG01081.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*47C>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 10/10 | 47 | chr11 | 122871446 | ||||||
| chr11:122871616 | A | C | 1 | a0001c0001t0018 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*217A>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 10/10 | 217 | chr11 | 122871616 | ||||||
| chr11:122871720 | T | G | 10 | a0001c0001t0001 a0001c0001t0008 a0001c0005t0001 others(7): Show |
126 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(123): Show |
3_prime_UTR_variant | MODIFIER | c.*321T>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 10/10 | 321 | chr11 | 122871720 | ||||||
| chr11:122871752 | A | T | 25 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(22): Show |
348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
3_prime_UTR_variant | MODIFIER | c.*353A>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 10/10 | 353 | chr11 | 122871752 | ||||||
| chr11:122872035 | T | A | 5 | a0001c0018t0011 a0002c0002t0009 a0005c0012t0009 others(2): Show |
13 | HG01167.hp1 HG01884.hp2 HG02257.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*636T>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 10/10 | 636 | chr11 | 122872035 | ||||||
| chr11:122872099 | C | A | 4 | a0001c0001t0002 a0001c0001t0012 a0001c0001t0016 others(1): Show |
91 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*700C>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 10/10 | 700 | chr11 | 122872099 | ||||||
| chr11:122872113 | C | T | 1 | a0001c0001t0016 | 1 | HG04184.hp1 | 3_prime_UTR_variant | MODIFIER | c.*714C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 10/10 | 714 | chr11 | 122872113 | ||||||
| chr11:122872114 | A | G | 34 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(31): Show |
392 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(389): Show |
3_prime_UTR_variant | MODIFIER | c.*715A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 10/10 | 715 | chr11 | 122872114 | ||||||
| chr11:122872171 | G | C | 9 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0012 others(6): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
3_prime_UTR_variant | MODIFIER | c.*772G>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 10/10 | 772 | chr11 | 122872171 | ||||||
| chr11:122872208 | T | C | 1 | a0004c0008t0014 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*809T>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 10/10 | 809 | chr11 | 122872208 | ||||||
| chr11:122872242 | G | A | 5 | a0001c0018t0011 a0002c0002t0009 a0005c0012t0009 others(2): Show |
13 | HG01167.hp1 HG01884.hp2 HG02257.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*843G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 10/10 | 843 | chr11 | 122872242 | ||||||
| chr11:122872295 | A | T | 2 | a0002c0002t0010 a0005c0012t0010 |
7 | HG02055.hp2 HG02145.hp2 HG02258.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*896A>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 10/10 | 896 | chr11 | 122872295 | ||||||
| chr11:122872335 | T | C | 1 | a0004c0010t0015 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*936T>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 10/10 | 936 | chr11 | 122872335 | ||||||
| chr11:122872345 | A | G | 1 | a0001c0001t0008 | 9 | HG00738.hp1 HG01081.hp1 HG01256.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*946A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 10/10 | 946 | chr11 | 122872345 | ||||||
| chr11:122872446 | T | C | 1 | a0007c0009t0013 | 2 | HG02698.hp1 NA18953.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1047T>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 10/10 | 1047 | chr11 | 122872446 | ||||||
| chr11:122872496 | T | C | 4 | a0001c0001t0002 a0001c0001t0012 a0001c0001t0016 others(1): Show |
91 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*1097T>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 10/10 | 1097 | chr11 | 122872496 | ||||||
| chr11:122872515 | G | A | 1 | a0001c0001t0012 | 3 | HG00639.hp2 HG00735.hp2 NA20805.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1116G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 10/10 | 1116 | chr11 | 122872515 | ||||||
| chr11:122872632 | C | T | 1 | a0003c0003t0017 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1233C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 10/10 | 1233 | chr11 | 122872632 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:122838843 | C | T | 3 | a0002c0002t0005g0321 a0002c0002t0005g0322 a0002c0002t0006g0323 |
3 | HG01081.hp2 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.46+251C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122838843 | |||||||
| chr11:122838894 | T | G | 5 | a0001c0001t0001g0053 a0001c0005t0001g0051 a0004c0008t0001g0052 others(2): Show |
6 | HG02109.hp2 HG02486.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.46+302T>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122838894 | |||||||
| chr11:122838925 | T | TTTTA | 25 | a0001c0001t0001g0302 a0001c0001t0001g0303 a0001c0001t0001g0308 others(22): Show |
31 | HG00642.hp2 HG01106.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.46+351_46+354dupTT others(2): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | 122838925 | ||||||
| chr11:122839029 | C | T | 1 | a0004c0008t0001g0320 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.46+437C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122839029 | |||||||
| chr11:122839077 | C | T | 1 | a0001c0001t0002g0299 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.46+485C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122839077 | |||||||
| chr11:122839093 | G | C | 3 | a0001c0001t0012g0055 a0002c0004t0004g0014 a0002c0004t0004g0056 |
5 | HG00099.hp1 HG00140.hp2 HG00741.hp1 others(2): Show |
intron_variant | MODIFIER | c.46+501G>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122839093 | |||||||
| chr11:122839154 | A | G | 1 | a0002c0002t0001g0298 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.46+562A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122839154 | |||||||
| chr11:122839181 | C | T | 1 | a0002c0002t0009g0297 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.46+589C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122839181 | |||||||
| chr11:122839187 | C | A | 10 | a0001c0001t0001g0060 a0001c0001t0002g0058 a0002c0002t0001g0057 others(7): Show |
10 | HG02280.hp1 HG02559.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.46+595C>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122839187 | |||||||
| chr11:122839227 | C | A | 1 | a0001c0001t0002g0025 | 2 | HG01070.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.46+635C>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122839227 | |||||||
| chr11:122839477 | A | G | 2 | a0001c0001t0002g0296 a0002c0002t0005g0295 |
2 | HG02615.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.46+885A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122839477 | |||||||
| chr11:122839548 | A | G | 1 | a0002c0002t0005g0294 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.46+956A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122839548 | |||||||
| chr11:122839573 | G | A | 3 | a0001c0001t0001g0026 a0007c0009t0003g0026 a0007c0009t0003g0067 |
3 | HG00408.hp2 NA18961.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.46+981G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122839573 | |||||||
| chr11:122839673 | A | G | 1 | a0001c0001t0002g0293 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.46+1081A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122839673 | |||||||
| chr11:122839804 | C | A | 1 | a0002c0002t0007g0068 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.46+1212C>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122839804 | |||||||
| chr11:122839853 | T | G | 177 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(174): Show |
230 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.46+1261T>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122839853 | |||||||
| chr11:122839933 | A | G | 177 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(174): Show |
230 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.46+1341A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122839933 | |||||||
| chr11:122840024 | C | T | 1 | a0003c0003t0003g0292 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.46+1432C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122840024 | |||||||
| chr11:122840159 | A | G | 11 | a0001c0001t0001g0060 a0001c0001t0002g0058 a0002c0002t0001g0057 others(8): Show |
11 | HG02280.hp1 HG02559.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.46+1567A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122840159 | |||||||
| chr11:122840263 | T | C | 1 | a0002c0004t0004g0201 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.46+1671T>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122840263 | |||||||
| chr11:122840271 | G | A | 1 | a0001c0001t0002g0202 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.46+1679G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122840271 | |||||||
| chr11:122840307 | T | C | 1 | a0001c0001t0001g0069 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.46+1715T>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122840307 | |||||||
| chr11:122840420 | C | CGT | 14 | a0001c0001t0001g0069 a0001c0001t0002g0193 a0001c0005t0001g0197 others(11): Show |
15 | HG01123.hp2 HG01891.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.46+1847_46+1848dup others(2): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | 122840420 | ||||||
| chr11:122840544 | G | A | 1 | a0001c0001t0001g0070 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.46+1952G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122840544 | |||||||
| chr11:122840582 | A | T | 1 | a0002c0002t0001g0298 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.46+1990A>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122840582 | |||||||
| chr11:122840655 | C | T | 36 | a0001c0001t0001g0181 a0001c0001t0001g0186 a0001c0001t0001g0189 others(33): Show |
42 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.46+2063C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122840655 | |||||||
| chr11:122841007 | G | T | 42 | a0001c0001t0001g0140 a0001c0001t0002g0007 a0001c0001t0002g0016 others(39): Show |
52 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.46+2415G>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122841007 | |||||||
| chr11:122841111 | T | C | 4 | a0001c0001t0001g0302 a0002c0002t0010g0049 a0002c0002t0010g0300 others(1): Show |
5 | HG01243.hp2 HG02055.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.46+2519T>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122841111 | |||||||
| chr11:122841128 | G | A | 3 | a0002c0002t0001g0289 a0002c0002t0007g0290 a0002c0002t0007g0291 |
3 | HG02647.hp1 HG02886.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.46+2536G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122841128 | |||||||
| chr11:122841181 | A | G | 1 | a0002c0002t0006g0288 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.46+2589A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122841181 | |||||||
| chr11:122841247 | C | T | 7 | a0001c0001t0001g0053 a0001c0005t0001g0051 a0002c0002t0006g0287 others(4): Show |
8 | HG02109.hp2 HG02486.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.46+2655C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122841247 | |||||||
| chr11:122841281 | A | C | 44 | a0001c0001t0001g0255 a0001c0001t0001g0273 a0001c0001t0001g0275 others(41): Show |
65 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.46+2689A>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122841281 | |||||||
| chr11:122841404 | A | AT | 78 | a0001c0001t0001g0033 a0001c0001t0001g0069 a0001c0001t0001g0140 others(75): Show |
95 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.46+2826dupT | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | 122841404 | ||||||
| chr11:122841404 | A | ATT | 59 | a0001c0001t0001g0019 a0001c0001t0001g0221 a0001c0001t0001g0222 others(56): Show |
79 | HG00099.hp1 HG00140.hp2 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.46+2825_46+2826dup others(2): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | 122841404 | ||||||
| chr11:122841404 | ATT | A | 20 | a0001c0001t0001g0053 a0001c0001t0001g0060 a0001c0001t0002g0058 others(17): Show |
21 | HG02109.hp2 HG02280.hp1 HG02486.hp2 others(18): Show |
intron_variant | MODIFIER | c.46+2825_46+2826del others(2): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | 122841404 | ||||||
| chr11:122841436 | C | T | 11 | a0001c0001t0001g0060 a0001c0001t0002g0058 a0002c0002t0001g0057 others(8): Show |
11 | HG02280.hp1 HG02559.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.46+2844C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122841436 | |||||||
| chr11:122841475 | A | G | 1 | a0001c0001t0002g0299 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.46+2883A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122841475 | |||||||
| chr11:122841494 | G | T | 4 | a0001c0001t0001g0302 a0002c0002t0010g0049 a0002c0002t0010g0300 others(1): Show |
5 | HG01243.hp2 HG02055.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.46+2902G>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122841494 | |||||||
| chr11:122841642 | C | T | 1 | a0001c0001t0018g0163 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.46+3050C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122841642 | |||||||
| chr11:122841695 | C | T | 1 | a0002c0002t0005g0192 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.46+3103C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122841695 | |||||||
| chr11:122841752 | T | C | 1 | a0002c0004t0004g0217 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.46+3160T>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122841752 | |||||||
| chr11:122841829 | A | G | 1 | a0001c0001t0002g0216 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.46+3237A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122841829 | |||||||
| chr11:122841878 | A | C | 277 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(274): Show |
357 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(354): Show |
intron_variant | MODIFIER | c.46+3286A>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122841878 | |||||||
| chr11:122841880 | T | A | 1 | a0004c0008t0001g0320 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.46+3288T>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122841880 | |||||||
| chr11:122841948 | A | G | 1 | a0001c0001t0004g0132 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.46+3356A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122841948 | |||||||
| chr11:122842141 | C | T | 2 | a0005c0012t0009g0215 a0008c0011t0001g0214 |
2 | NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.46+3549C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122842141 | |||||||
| chr11:122842220 | G | A | 2 | a0002c0002t0005g0250 a0002c0004t0003g0251 |
2 | HG02723.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.46+3628G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122842220 | |||||||
| chr11:122842267 | A | ATGTT | 10 | a0002c0002t0001g0289 a0002c0002t0001g0298 a0002c0002t0006g0281 others(7): Show |
13 | HG02027.hp1 HG02040.hp1 HG02080.hp1 others(10): Show |
intron_variant | MODIFIER | c.46+3700_46+3703dup others(4): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | 122842267 | ||||||
| chr11:122842267 | ATGTT | A | 2 | a0001c0001t0002g0044 a0001c0001t0002g0218 |
3 | NA18952.hp1 NA18974.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.46+3700_46+3703del others(4): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | 122842267 | ||||||
| chr11:122842294 | T | C | 1 | a0002c0002t0007g0286 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.46+3702T>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122842294 | |||||||
| chr11:122842483 | C | T | 1 | a0001c0001t0001g0303 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.46+3891C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122842483 | |||||||
| chr11:122842517 | G | C | 1 | a0002c0002t0006g0288 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.46+3925G>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122842517 | |||||||
| chr11:122842526 | G | C | 2 | a0001c0018t0011g0306 a0005c0012t0010g0305 |
2 | HG02258.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.46+3934G>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122842526 | |||||||
| chr11:122842588 | A | G | 1 | a0001c0001t0002g0280 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.46+3996A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122842588 | |||||||
| chr11:122842627 | T | A | 44 | a0001c0001t0001g0255 a0001c0001t0001g0273 a0001c0001t0001g0275 others(41): Show |
65 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.46+4035T>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122842627 | |||||||
| chr11:122842711 | A | G | 1 | a0001c0001t0001g0131 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.46+4119A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122842711 | |||||||
| chr11:122842762 | G | A | 1 | a0002c0002t0007g0068 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.46+4170G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122842762 | |||||||
| chr11:122842762 | G | C | 1 | a0002c0004t0004g0071 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.46+4170G>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122842762 | |||||||
| chr11:122842794 | C | T | 5 | a0002c0002t0001g0319 a0002c0002t0007g0316 a0002c0002t0007g0317 others(2): Show |
5 | HG00642.hp2 HG02257.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.46+4202C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122842794 | |||||||
| chr11:122842850 | C | T | 256 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(253): Show |
331 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.46+4258C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122842850 | |||||||
| chr11:122842866 | A | G | 2 | a0005c0012t0009g0215 a0008c0011t0001g0214 |
2 | NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.46+4274A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122842866 | |||||||
| chr11:122842878 | T | G | 1 | a0001c0001t0002g0219 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.46+4286T>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122842878 | |||||||
| chr11:122842896 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.46+4304C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122842896 | |||||||
| chr11:122842903 | C | T | 2 | a0003c0003t0003g0278 a0003c0003t0003g0279 |
2 | NA18946.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.46+4311C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122842903 | |||||||
| chr11:122842936 | G | A | 1 | a0002c0002t0005g0072 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.46+4344G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122842936 | |||||||
| chr11:122843102 | A | G | 174 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(171): Show |
226 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.46+4510A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122843102 | |||||||
| chr11:122843109 | G | A | 1 | a0001c0001t0001g0073 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.46+4517G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122843109 | |||||||
| chr11:122843424 | G | A | 1 | a0002c0002t0005g0167 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.46+4832G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122843424 | |||||||
| chr11:122843501 | C | T | 7 | a0001c0001t0001g0033 a0001c0001t0001g0069 a0001c0005t0001g0197 others(4): Show |
9 | HG01891.hp1 HG01891.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.46+4909C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122843501 | |||||||
| chr11:122843665 | C | T | 1 | a0001c0001t0002g0162 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.46+5073C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122843665 | |||||||
| chr11:122843811 | A | G | 1 | a0006c0007t0001g0315 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.46+5219A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122843811 | |||||||
| chr11:122843856 | A | T | 1 | a0004c0010t0007g0213 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.46+5264A>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122843856 | |||||||
| chr11:122843888 | G | A | 1 | a0002c0002t0001g0319 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.46+5296G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122843888 | |||||||
| chr11:122844074 | A | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(152): Show |
198 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(195): Show |
intron_variant | MODIFIER | c.46+5482A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122844074 | |||||||
| chr11:122844117 | G | A | 3 | a0001c0001t0001g0009 a0001c0001t0001g0075 a0001c0001t0001g0076 |
6 | HG02056.hp2 HG02135.hp1 NA18978.hp1 others(3): Show |
intron_variant | MODIFIER | c.46+5525G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122844117 | |||||||
| chr11:122844760 | A | T | 1 | a0002c0004t0003g0251 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.47-5308A>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122844760 | |||||||
| chr11:122844907 | G | A | 10 | a0002c0002t0007g0205 a0004c0008t0014g0252 a0004c0010t0007g0206 others(7): Show |
11 | HG01109.hp1 HG02451.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.47-5161G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122844907 | |||||||
| chr11:122844938 | A | G | 10 | a0001c0001t0001g0060 a0001c0001t0002g0058 a0002c0002t0001g0057 others(7): Show |
10 | HG02280.hp1 HG02559.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.47-5130A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122844938 | |||||||
| chr11:122845018 | G | A | 16 | a0001c0001t0001g0060 a0001c0001t0002g0058 a0002c0002t0001g0057 others(13): Show |
16 | HG01167.hp1 HG01884.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.47-5050G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122845018 | |||||||
| chr11:122845088 | G | A | 1 | a0001c0001t0002g0077 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.47-4980G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122845088 | |||||||
| chr11:122845155 | G | A | 1 | a0002c0004t0004g0217 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.47-4913G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122845155 | |||||||
| chr11:122845195 | C | T | 1 | a0004c0008t0001g0212 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.47-4873C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122845195 | |||||||
| chr11:122845214 | G | A | 1 | a0001c0001t0008g0078 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.47-4854G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122845214 | |||||||
| chr11:122845235 | G | C | 3 | a0001c0005t0001g0022 a0001c0005t0001g0051 a0001c0005t0001g0304 |
5 | HG01496.hp2 HG02723.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.47-4833G>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122845235 | |||||||
| chr11:122845288 | A | G | 2 | a0001c0005t0001g0022 a0001c0005t0001g0304 |
4 | HG01496.hp2 HG02723.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.47-4780A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122845288 | |||||||
| chr11:122845330 | C | T | 38 | a0001c0001t0001g0181 a0001c0001t0001g0186 a0001c0001t0001g0189 others(35): Show |
44 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.47-4738C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122845330 | |||||||
| chr11:122845333 | G | A | 153 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(150): Show |
195 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(192): Show |
intron_variant | MODIFIER | c.47-4735G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122845333 | |||||||
| chr11:122845523 | G | A | 1 | a0004c0008t0001g0212 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.47-4545G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122845523 | |||||||
| chr11:122845610 | G | T | 1 | a0001c0001t0002g0248 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.47-4458G>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122845610 | |||||||
| chr11:122845662 | A | G | 49 | a0001c0001t0001g0076 a0001c0001t0001g0255 a0001c0001t0001g0273 others(46): Show |
71 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.47-4406A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122845662 | |||||||
| chr11:122845878 | C | T | 1 | a0002c0002t0007g0286 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.47-4190C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122845878 | |||||||
| chr11:122846004 | C | T | 326 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(323): Show |
425 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(422): Show |
intron_variant | MODIFIER | c.47-4064C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122846004 | |||||||
| chr11:122846020 | C | A | 1 | a0001c0001t0012g0168 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.47-4048C>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122846020 | |||||||
| chr11:122846073 | C | T | 1 | a0002c0004t0001g0066 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.47-3995C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122846073 | |||||||
| chr11:122846107 | T | C | 3 | a0002c0002t0001g0289 a0002c0002t0007g0290 a0002c0002t0007g0291 |
3 | HG02647.hp1 HG02886.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.47-3961T>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122846107 | |||||||
| chr11:122846135 | G | A | 3 | a0001c0005t0001g0022 a0001c0005t0001g0051 a0001c0005t0001g0304 |
5 | HG01496.hp2 HG02723.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.47-3933G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122846135 | |||||||
| chr11:122846394 | C | T | 1 | a0002c0004t0003g0251 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.47-3674C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122846394 | |||||||
| chr11:122846409 | A | AG | 230 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(227): Show |
300 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.47-3659_47-3658ins others(1): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122846409 | |||||||
| chr11:122846533 | C | T | 1 | a0003c0003t0003g0277 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.47-3535C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122846533 | |||||||
| chr11:122846554 | A | G | 8 | a0001c0001t0001g0033 a0001c0001t0001g0069 a0001c0005t0001g0197 others(5): Show |
10 | HG01891.hp1 HG01891.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.47-3514A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122846554 | |||||||
| chr11:122846620 | CTCTG | C | 30 | a0001c0001t0001g0060 a0001c0001t0002g0058 a0001c0001t0002g0169 others(27): Show |
32 | HG00621.hp2 HG00738.hp2 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.47-3428_47-3425del others(4): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | 122846620 | ||||||
| chr11:122846678 | C | T | 12 | a0001c0001t0001g0302 a0001c0005t0001g0022 a0001c0005t0001g0051 others(9): Show |
15 | HG01243.hp2 HG01496.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.47-3390C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122846678 | |||||||
| chr11:122846802 | T | A | 1 | a0002c0004t0003g0251 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.47-3266T>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122846802 | |||||||
| chr11:122846812 | T | G | 2 | a0003c0003t0003g0032 a0003c0003t0003g0254 |
3 | NA18970.hp1 NA18977.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.47-3256T>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122846812 | |||||||
| chr11:122846897 | A | C | 1 | a0002c0002t0007g0286 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.47-3171A>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122846897 | |||||||
| chr11:122846910 | A | G | 1 | a0001c0001t0002g0296 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.47-3158A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122846910 | |||||||
| chr11:122847073 | G | A | 1 | a0002c0002t0006g0281 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.47-2995G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122847073 | |||||||
| chr11:122847074 | A | G | 1 | a0002c0002t0006g0281 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.47-2994A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122847074 | |||||||
| chr11:122847234 | C | T | 2 | a0002c0002t0001g0298 a0002c0002t0007g0068 |
2 | HG02922.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.47-2834C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122847234 | |||||||
| chr11:122847357 | G | C | 49 | a0001c0001t0001g0221 a0001c0001t0001g0255 a0001c0001t0001g0273 others(46): Show |
71 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.47-2711G>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122847357 | |||||||
| chr11:122847387 | A | G | 1 | a0002c0002t0006g0281 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.47-2681A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122847387 | |||||||
| chr11:122847441 | T | C | 49 | a0001c0001t0001g0221 a0001c0001t0001g0255 a0001c0001t0001g0273 others(46): Show |
71 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.47-2627T>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122847441 | |||||||
| chr11:122847511 | G | A | 30 | a0001c0001t0001g0060 a0001c0001t0002g0058 a0001c0001t0002g0169 others(27): Show |
32 | HG00621.hp2 HG00738.hp2 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.47-2557G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122847511 | |||||||
| chr11:122847573 | C | T | 1 | a0001c0001t0002g0123 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.47-2495C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122847573 | |||||||
| chr11:122847620 | A | G | 1 | a0002c0004t0004g0201 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.47-2448A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122847620 | |||||||
| chr11:122847641 | G | T | 2 | a0001c0001t0001g0121 a0001c0001t0001g0122 |
2 | NA19060.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.47-2427G>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122847641 | |||||||
| chr11:122847982 | A | T | 49 | a0001c0001t0001g0221 a0001c0001t0001g0255 a0001c0001t0001g0273 others(46): Show |
71 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.47-2086A>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122847982 | |||||||
| chr11:122848012 | G | A | 1 | a0002c0004t0004g0124 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.47-2056G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122848012 | |||||||
| chr11:122848012 | G | C | 1 | a0002c0002t0006g0281 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.47-2056G>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122848012 | |||||||
| chr11:122848013 | C | G | 1 | a0002c0002t0006g0281 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.47-2055C>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122848013 | |||||||
| chr11:122848026 | G | A | 30 | a0001c0001t0001g0060 a0001c0001t0002g0058 a0001c0001t0002g0169 others(27): Show |
32 | HG00621.hp2 HG00738.hp2 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.47-2042G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122848026 | |||||||
| chr11:122848112 | G | T | 6 | a0002c0002t0001g0159 a0002c0002t0001g0253 a0002c0002t0009g0165 others(3): Show |
6 | HG02572.hp2 HG02630.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.47-1956G>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122848112 | |||||||
| chr11:122848138 | T | C | 3 | a0004c0008t0001g0052 a0004c0008t0001g0320 a0006c0007t0001g0024 |
4 | HG00642.hp2 HG02109.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.47-1930T>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122848138 | |||||||
| chr11:122848161 | A | G | 1 | a0002c0002t0006g0177 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.47-1907A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122848161 | |||||||
| chr11:122848310 | C | A | 1 | a0002c0002t0006g0288 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.47-1758C>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122848310 | |||||||
| chr11:122848421 | A | C | 1 | a0002c0002t0005g0250 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.47-1647A>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122848421 | |||||||
| chr11:122848538 | A | C | 1 | a0001c0001t0002g0162 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.47-1530A>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122848538 | |||||||
| chr11:122848721 | G | T | 9 | a0001c0001t0001g0302 a0001c0005t0001g0022 a0001c0005t0001g0051 others(6): Show |
12 | HG01243.hp2 HG01496.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.47-1347G>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122848721 | |||||||
| chr11:122848782 | T | A | 1 | a0003c0003t0003g0247 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.47-1286T>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122848782 | |||||||
| chr11:122848821 | A | T | 28 | a0001c0001t0001g0060 a0001c0001t0002g0058 a0002c0002t0001g0057 others(25): Show |
30 | HG00621.hp2 HG00738.hp2 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.47-1247A>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122848821 | |||||||
| chr11:122848878 | T | C | 2 | a0001c0001t0001g0131 a0001c0001t0001g0249 |
2 | HG01109.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.47-1190T>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122848878 | |||||||
| chr11:122849052 | G | A | 5 | a0001c0005t0001g0197 a0005c0006t0004g0042 a0005c0006t0004g0195 others(2): Show |
6 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.47-1016G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122849052 | |||||||
| chr11:122849154 | C | T | 2 | a0002c0002t0005g0139 a0002c0002t0005g0191 |
2 | HG02615.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.47-914C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122849154 | |||||||
| chr11:122849171 | C | A | 25 | a0001c0001t0001g0060 a0001c0001t0001g0255 a0001c0001t0002g0058 others(22): Show |
27 | HG00621.hp2 HG00738.hp2 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.47-897C>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122849171 | |||||||
| chr11:122849284 | A | G | 1 | a0001c0001t0004g0120 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.47-784A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122849284 | |||||||
| chr11:122849311 | G | T | 1 | a0001c0001t0001g0119 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.47-757G>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122849311 | |||||||
| chr11:122849447 | T | G | 5 | a0001c0005t0001g0197 a0005c0006t0004g0042 a0005c0006t0004g0195 others(2): Show |
6 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.47-621T>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122849447 | |||||||
| chr11:122849534 | C | T | 1 | a0001c0001t0001g0118 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.47-534C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122849534 | |||||||
| chr11:122849555 | C | G | 1 | a0002c0002t0001g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.47-513C>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122849555 | |||||||
| chr11:122849593 | G | C | 2 | a0002c0004t0004g0178 a0002c0004t0004g0179 |
2 | NA18984.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.47-475G>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122849593 | |||||||
| chr11:122849613 | T | C | 14 | a0001c0001t0001g0204 a0001c0001t0001g0308 a0001c0001t0001g0309 others(11): Show |
18 | HG01884.hp1 HG02027.hp2 HG02071.hp1 others(15): Show |
intron_variant | MODIFIER | c.47-455T>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122849613 | |||||||
| chr11:122849707 | A | T | 2 | a0002c0002t0007g0290 a0002c0002t0007g0291 |
2 | HG02647.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.47-361A>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122849707 | |||||||
| chr11:122849709 | T | C | 1 | a0003c0003t0003g0282 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.47-359T>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122849709 | |||||||
| chr11:122849821 | C | A | 1 | a0002c0002t0005g0180 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.47-247C>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122849821 | |||||||
| chr11:122849824 | C | T | 1 | a0001c0001t0002g0246 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.47-244C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122849824 | |||||||
| chr11:122850002 | C | T | 22 | a0001c0001t0001g0069 a0001c0001t0002g0016 a0001c0001t0002g0025 others(19): Show |
28 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.47-66C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 1/9 | chr11 | 122850002 | |||||||
| chr11:122850244 | A | G | 1 | a0001c0001t0001g0303 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.193+30A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 2/9 | chr11 | 122850244 | |||||||
| chr11:122850287 | G | A | 2 | a0002c0002t0005g0139 a0002c0002t0005g0191 |
2 | HG02615.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.193+73G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 2/9 | chr11 | 122850287 | |||||||
| chr11:122850640 | A | G | 18 | a0001c0001t0001g0186 a0001c0001t0001g0189 a0001c0001t0002g0041 others(15): Show |
22 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.193+426A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 2/9 | chr11 | 122850640 | |||||||
| chr11:122850893 | A | G | 4 | a0001c0005t0001g0022 a0001c0005t0001g0051 a0001c0005t0001g0197 others(1): Show |
6 | HG01496.hp2 HG02559.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.193+679A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 2/9 | chr11 | 122850893 | |||||||
| chr11:122850988 | G | A | 2 | a0002c0002t0001g0057 a0002c0004t0001g0066 |
2 | HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.194-705G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 2/9 | chr11 | 122850988 | |||||||
| chr11:122851266 | TA | T | 267 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(264): Show |
344 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(341): Show |
intron_variant | MODIFIER | c.194-410delA | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 122851266 | ||||||
| chr11:122851317 | T | C | 6 | a0001c0001t0001g0302 a0002c0002t0005g0139 a0002c0002t0005g0191 others(3): Show |
7 | HG01243.hp2 HG02055.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.194-376T>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 2/9 | chr11 | 122851317 | |||||||
| chr11:122851564 | A | G | 1 | a0002c0002t0001g0298 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.194-129A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 2/9 | chr11 | 122851564 | |||||||
| chr11:122851592 | A | T | 30 | a0001c0001t0001g0204 a0001c0001t0001g0308 a0001c0001t0001g0309 others(27): Show |
34 | HG00642.hp2 HG01109.hp1 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.194-101A>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 2/9 | chr11 | 122851592 | |||||||
| chr11:122851604 | C | T | 1 | a0002c0004t0004g0245 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.194-89C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 2/9 | chr11 | 122851604 | |||||||
| chr11:122851630 | G | A | 4 | a0001c0005t0001g0022 a0001c0005t0001g0051 a0001c0005t0001g0197 others(1): Show |
6 | HG01496.hp2 HG02559.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.194-63G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 2/9 | chr11 | 122851630 | |||||||
| chr11:122851960 | G | A | 1 | a0001c0001t0001g0033 | 2 | HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.346+115G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 3/9 | chr11 | 122851960 | |||||||
| chr11:122852076 | C | T | 2 | a0002c0002t0007g0290 a0002c0002t0007g0291 |
2 | HG02647.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.346+231C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 3/9 | chr11 | 122852076 | |||||||
| chr11:122852197 | G | C | 1 | a0002c0002t0001g0319 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.346+352G>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 3/9 | chr11 | 122852197 | |||||||
| chr11:122852285 | C | G | 1 | a0001c0001t0001g0249 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.346+440C>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 3/9 | chr11 | 122852285 | |||||||
| chr11:122852589 | T | C | 18 | a0001c0001t0001g0186 a0001c0001t0001g0189 a0001c0001t0002g0041 others(15): Show |
22 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.346+744T>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 3/9 | chr11 | 122852589 | |||||||
| chr11:122852734 | C | T | 6 | a0001c0001t0001g0302 a0002c0002t0005g0139 a0002c0002t0005g0191 others(3): Show |
7 | HG01243.hp2 HG02055.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.346+889C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 3/9 | chr11 | 122852734 | |||||||
| chr11:122852779 | A | G | 3 | a0009c0013t0011g0043 a0009c0013t0011g0211 a0010c0020t0005g0210 |
4 | HG02451.hp1 HG02809.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.346+934A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 3/9 | chr11 | 122852779 | |||||||
| chr11:122852879 | T | G | 3 | a0001c0001t0001g0308 a0001c0001t0001g0309 a0001c0001t0002g0023 |
5 | HG02071.hp1 NA18950.hp2 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.346+1034T>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 3/9 | chr11 | 122852879 | |||||||
| chr11:122852885 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.346+1040C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 3/9 | chr11 | 122852885 | |||||||
| chr11:122853015 | C | T | 1 | a0003c0003t0003g0135 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.347-928C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 3/9 | chr11 | 122853015 | |||||||
| chr11:122853043 | A | C | 97 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(94): Show |
134 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.347-900A>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 3/9 | chr11 | 122853043 | |||||||
| chr11:122853070 | C | CT | 71 | a0001c0001t0001g0116 a0001c0001t0001g0122 a0001c0001t0001g0186 others(68): Show |
98 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.347-860dupT | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 122853070 | ||||||
| chr11:122853070 | C | CTT | 7 | a0004c0008t0014g0252 a0005c0006t0004g0195 a0005c0006t0004g0196 others(4): Show |
8 | HG02109.hp1 HG02145.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.347-861_347-860dup others(2): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 122853070 | ||||||
| chr11:122853070 | C | CTTT | 6 | a0002c0016t0001g0065 a0004c0008t0001g0052 a0004c0008t0001g0158 others(3): Show |
6 | HG00642.hp2 HG02895.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.347-862_347-860dup others(3): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 122853070 | ||||||
| chr11:122853195 | G | A | 5 | a0002c0002t0009g0074 a0002c0002t0009g0136 a0002c0002t0009g0137 others(2): Show |
5 | HG01167.hp1 HG01884.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.347-748G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 3/9 | chr11 | 122853195 | |||||||
| chr11:122853207 | A | G | 1 | a0008c0011t0001g0214 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.347-736A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 3/9 | chr11 | 122853207 | |||||||
| chr11:122853294 | T | C | 1 | a0001c0001t0002g0162 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.347-649T>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 3/9 | chr11 | 122853294 | |||||||
| chr11:122853378 | C | T | 5 | a0005c0006t0004g0042 a0005c0006t0004g0195 a0005c0006t0004g0196 others(2): Show |
6 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.347-565C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 3/9 | chr11 | 122853378 | |||||||
| chr11:122853458 | C | T | 26 | a0001c0001t0001g0060 a0001c0001t0001g0255 a0001c0001t0002g0058 others(23): Show |
28 | HG00621.hp2 HG00738.hp2 HG01081.hp2 others(25): Show |
intron_variant | MODIFIER | c.347-485C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 3/9 | chr11 | 122853458 | |||||||
| chr11:122853546 | C | T | 5 | a0002c0002t0009g0074 a0002c0002t0009g0136 a0002c0002t0009g0137 others(2): Show |
5 | HG01167.hp1 HG01884.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.347-397C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 3/9 | chr11 | 122853546 | |||||||
| chr11:122853557 | A | G | 3 | a0001c0018t0011g0306 a0002c0002t0007g0286 a0005c0012t0010g0305 |
3 | HG02258.hp1 HG03209.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.347-386A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 3/9 | chr11 | 122853557 | |||||||
| chr11:122853884 | CT | C | 97 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(94): Show |
134 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.347-56delT | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 122853884 | ||||||
| chr11:122854218 | G | C | 26 | a0001c0001t0001g0060 a0001c0001t0001g0255 a0001c0001t0002g0058 others(23): Show |
28 | HG00621.hp2 HG00738.hp2 HG01081.hp2 others(25): Show |
intron_variant | MODIFIER | c.490+132G>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/9 | chr11 | 122854218 | |||||||
| chr11:122854393 | C | T | 2 | a0001c0001t0001g0115 a0001c0001t0001g0116 |
2 | NA19077.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.490+307C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/9 | chr11 | 122854393 | |||||||
| chr11:122854471 | G | A | 97 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(94): Show |
134 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.490+385G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/9 | chr11 | 122854471 | |||||||
| chr11:122854486 | A | G | 9 | a0001c0018t0011g0306 a0002c0002t0007g0286 a0002c0002t0009g0074 others(6): Show |
9 | HG01167.hp1 HG01884.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.490+400A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/9 | chr11 | 122854486 | |||||||
| chr11:122854516 | T | TAC | 106 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(103): Show |
143 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.490+431_490+432ins others(2): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr11 | 122854516 | ||||||
| chr11:122854661 | C | CA | 63 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0114 others(60): Show |
73 | HG00597.hp1 HG00609.hp1 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.490+589dupA | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr11 | 122854661 | ||||||
| chr11:122854661 | C | CAA | 102 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(99): Show |
136 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.490+588_490+589dup others(2): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr11 | 122854661 | ||||||
| chr11:122854856 | C | A | 31 | a0001c0001t0001g0060 a0001c0001t0001g0255 a0001c0001t0002g0058 others(28): Show |
34 | HG00621.hp2 HG00738.hp2 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.490+770C>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/9 | chr11 | 122854856 | |||||||
| chr11:122854865 | C | T | 1 | a0002c0002t0005g0250 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.490+779C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/9 | chr11 | 122854865 | |||||||
| chr11:122855046 | C | T | 4 | a0001c0001t0001g0302 a0002c0002t0010g0049 a0002c0002t0010g0300 others(1): Show |
5 | HG01243.hp2 HG02055.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.491-649C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/9 | chr11 | 122855046 | |||||||
| chr11:122855047 | G | A | 13 | a0001c0001t0001g0204 a0001c0001t0001g0308 a0001c0001t0001g0309 others(10): Show |
16 | HG01884.hp1 HG02027.hp2 HG02071.hp1 others(13): Show |
intron_variant | MODIFIER | c.491-648G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/9 | chr11 | 122855047 | |||||||
| chr11:122855163 | C | T | 97 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(94): Show |
134 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.491-532C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/9 | chr11 | 122855163 | |||||||
| chr11:122855235 | C | T | 5 | a0002c0002t0009g0074 a0002c0002t0009g0136 a0002c0002t0009g0137 others(2): Show |
5 | HG01167.hp1 HG01884.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.491-460C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/9 | chr11 | 122855235 | |||||||
| chr11:122855275 | C | T | 3 | a0001c0001t0002g0216 a0002c0004t0004g0164 a0002c0004t0004g0243 |
3 | HG02257.hp2 HG02451.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.491-420C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/9 | chr11 | 122855275 | |||||||
| chr11:122855407 | A | T | 1 | a0002c0002t0006g0281 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.491-288A>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/9 | chr11 | 122855407 | |||||||
| chr11:122855440 | A | T | 1 | a0002c0002t0006g0281 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.491-255A>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/9 | chr11 | 122855440 | |||||||
| chr11:122855458 | T | C | 75 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(72): Show |
106 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.491-237T>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/9 | chr11 | 122855458 | |||||||
| chr11:122855471 | A | T | 4 | a0001c0001t0001g0302 a0002c0002t0010g0049 a0002c0002t0010g0300 others(1): Show |
5 | HG01243.hp2 HG02055.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.491-224A>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/9 | chr11 | 122855471 | |||||||
| chr11:122855544 | C | G | 1 | a0002c0002t0006g0281 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.491-151C>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/9 | chr11 | 122855544 | |||||||
| chr11:122855545 | C | G | 1 | a0002c0002t0006g0281 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.491-150C>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/9 | chr11 | 122855545 | |||||||
| chr11:122855546 | A | G | 1 | a0002c0002t0006g0281 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.491-149A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/9 | chr11 | 122855546 | |||||||
| chr11:122855550 | C | G | 1 | a0002c0002t0006g0281 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.491-145C>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/9 | chr11 | 122855550 | |||||||
| chr11:122855551 | C | G | 1 | a0002c0002t0006g0281 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.491-144C>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/9 | chr11 | 122855551 | |||||||
| chr11:122855552 | A | G | 1 | a0002c0002t0006g0281 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.491-143A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/9 | chr11 | 122855552 | |||||||
| chr11:122855553 | A | G | 1 | a0002c0002t0006g0281 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.491-142A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/9 | chr11 | 122855553 | |||||||
| chr11:122855554 | G | A | 1 | a0002c0002t0001g0298 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.491-141G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/9 | chr11 | 122855554 | |||||||
| chr11:122855555 | C | G | 1 | a0002c0002t0006g0281 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.491-140C>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/9 | chr11 | 122855555 | |||||||
| chr11:122855556 | C | T | 1 | a0002c0002t0006g0281 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.491-139C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/9 | chr11 | 122855556 | |||||||
| chr11:122855557 | T | A | 1 | a0002c0002t0006g0281 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.491-138T>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/9 | chr11 | 122855557 | |||||||
| chr11:122855560 | A | T | 1 | a0002c0002t0006g0281 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.491-135A>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/9 | chr11 | 122855560 | |||||||
| chr11:122855561 | C | T | 1 | a0002c0002t0006g0281 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.491-134C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/9 | chr11 | 122855561 | |||||||
| chr11:122855564 | G | T | 1 | a0002c0002t0006g0281 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.491-131G>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/9 | chr11 | 122855564 | |||||||
| chr11:122855577 | G | A | 1 | a0001c0001t0001g0303 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.491-118G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/9 | chr11 | 122855577 | |||||||
| chr11:122855623 | C | T | 1 | a0002c0002t0006g0281 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.491-72C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/9 | chr11 | 122855623 | |||||||
| chr11:122855641 | C | A | 1 | a0001c0001t0002g0226 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.491-54C>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/9 | chr11 | 122855641 | |||||||
| chr11:122855642 | C | A | 1 | a0002c0002t0006g0281 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.491-53C>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/9 | chr11 | 122855642 | |||||||
| chr11:122855644 | A | T | 1 | a0002c0002t0006g0281 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.491-51A>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/9 | chr11 | 122855644 | |||||||
| chr11:122855645 | C | T | 5 | a0004c0010t0007g0206 a0004c0010t0007g0213 a0004c0010t0015g0207 others(2): Show |
5 | HG01109.hp1 HG02630.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.491-50C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/9 | chr11 | 122855645 | |||||||
| chr11:122855648 | C | T | 1 | a0002c0002t0006g0281 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.491-47C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/9 | chr11 | 122855648 | |||||||
| chr11:122855657 | G | T | 1 | a0002c0002t0006g0281 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.491-38G>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/9 | chr11 | 122855657 | |||||||
| chr11:122855675 | C | A | 1 | a0001c0001t0002g0148 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.491-20C>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/9 | chr11 | 122855675 | |||||||
| chr11:122855691 | A | G | 2 | a0002c0002t0007g0290 a0002c0002t0007g0291 |
2 | HG02647.hp1 HG02970.hp1 |
splice_region_variant&intron_variant | LOW | c.491-4A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 4/9 | chr11 | 122855691 | |||||||
| chr11:122855870 | A | T | 1 | a0002c0002t0006g0281 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.652+14A>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122855870 | |||||||
| chr11:122855877 | T | C | 2 | a0002c0002t0007g0068 a0002c0002t0007g0205 |
2 | HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.652+21T>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122855877 | |||||||
| chr11:122855955 | A | T | 1 | a0002c0002t0006g0281 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.652+99A>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122855955 | |||||||
| chr11:122855997 | C | T | 75 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(72): Show |
106 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.652+141C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122855997 | |||||||
| chr11:122856148 | G | A | 2 | a0002c0004t0004g0164 a0002c0004t0004g0243 |
2 | HG02257.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.652+292G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122856148 | |||||||
| chr11:122856228 | T | G | 4 | a0001c0001t0002g0036 a0001c0001t0002g0150 a0001c0001t0002g0162 others(1): Show |
5 | HG02572.hp1 HG02886.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.652+372T>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122856228 | |||||||
| chr11:122856361 | C | T | 40 | a0001c0001t0001g0060 a0001c0001t0001g0255 a0001c0001t0001g0302 others(37): Show |
44 | HG00621.hp2 HG00738.hp2 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.652+505C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122856361 | |||||||
| chr11:122856672 | C | T | 4 | a0001c0001t0002g0147 a0001c0001t0002g0154 a0001c0001t0002g0155 others(1): Show |
4 | HG00642.hp1 HG01175.hp1 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.652+816C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122856672 | |||||||
| chr11:122856869 | C | T | 83 | a0001c0001t0001g0060 a0001c0001t0001g0255 a0001c0001t0001g0273 others(80): Show |
109 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.652+1013C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122856869 | |||||||
| chr11:122856997 | C | G | 1 | a0002c0002t0006g0287 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.652+1141C>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122856997 | |||||||
| chr11:122857220 | G | A | 1 | a0001c0001t0002g0058 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.652+1364G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122857220 | |||||||
| chr11:122857232 | G | A | 13 | a0001c0001t0001g0204 a0001c0001t0001g0308 a0001c0001t0001g0309 others(10): Show |
16 | HG01884.hp1 HG02027.hp2 HG02071.hp1 others(13): Show |
intron_variant | MODIFIER | c.652+1376G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122857232 | |||||||
| chr11:122857244 | A | G | 266 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(263): Show |
343 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(340): Show |
intron_variant | MODIFIER | c.652+1388A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122857244 | |||||||
| chr11:122857394 | G | A | 31 | a0001c0001t0001g0060 a0001c0001t0001g0255 a0001c0001t0002g0058 others(28): Show |
34 | HG00621.hp2 HG00738.hp2 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.652+1538G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122857394 | |||||||
| chr11:122857456 | G | A | 99 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(96): Show |
136 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.652+1600G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122857456 | |||||||
| chr11:122857464 | G | A | 2 | a0001c0001t0002g0227 a0001c0001t0002g0228 |
2 | HG03710.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.652+1608G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122857464 | |||||||
| chr11:122857479 | GAAT | G | 4 | a0004c0010t0007g0213 a0004c0010t0015g0207 a0008c0011t0001g0208 others(1): Show |
4 | HG01109.hp1 HG02630.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.652+1628_652+1630d others(5): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122857479 | ||||||
| chr11:122857772 | G | A | 2 | a0003c0003t0003g0256 a0003c0003t0017g0225 |
2 | HG02135.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.652+1916G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122857772 | |||||||
| chr11:122857946 | T | C | 1 | a0002c0004t0003g0251 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.652+2090T>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122857946 | |||||||
| chr11:122858140 | T | A | 1 | a0003c0003t0003g0257 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.652+2284T>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122858140 | |||||||
| chr11:122858206 | C | T | 1 | a0002c0002t0006g0288 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.652+2350C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122858206 | |||||||
| chr11:122858350 | G | A | 1 | a0001c0001t0001g0087 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.652+2494G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122858350 | |||||||
| chr11:122858361 | G | C | 1 | a0002c0002t0001g0298 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.652+2505G>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122858361 | |||||||
| chr11:122858398 | A | G | 1 | a0002c0004t0004g0245 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.652+2542A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122858398 | |||||||
| chr11:122858399 | T | C | 95 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(92): Show |
130 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.652+2543T>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122858399 | |||||||
| chr11:122858440 | G | GGTCTTGA others(6): Show |
1 | a0001c0001t0002g0156 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.652+2586_652+2598d others(15): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122858440 | ||||||
| chr11:122858560 | CCTT | C | 10 | a0002c0016t0001g0065 a0004c0008t0001g0052 a0004c0008t0001g0158 others(7): Show |
11 | HG00642.hp2 HG02451.hp1 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.652+2707_652+2709d others(5): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122858560 | ||||||
| chr11:122858618 | C | G | 1 | a0004c0008t0014g0252 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.652+2762C>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122858618 | |||||||
| chr11:122858693 | T | C | 1 | a0001c0001t0001g0088 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.652+2837T>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122858693 | |||||||
| chr11:122858808 | G | T | 1 | a0003c0003t0003g0274 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.652+2952G>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122858808 | |||||||
| chr11:122858969 | C | A | 5 | a0002c0002t0009g0074 a0002c0002t0009g0136 a0002c0002t0009g0137 others(2): Show |
5 | HG01167.hp1 HG01884.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.652+3113C>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122858969 | |||||||
| chr11:122859057 | G | T | 1 | a0004c0008t0014g0252 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.652+3201G>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122859057 | |||||||
| chr11:122859382 | A | G | 7 | a0002c0002t0007g0286 a0002c0002t0009g0074 a0002c0002t0009g0136 others(4): Show |
7 | HG01167.hp1 HG01884.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.653-3082A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122859382 | |||||||
| chr11:122859404 | T | G | 5 | a0005c0006t0004g0042 a0005c0006t0004g0195 a0005c0006t0004g0196 others(2): Show |
6 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.653-3060T>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122859404 | |||||||
| chr11:122859431 | G | GA | 222 | a0001c0001t0001g0019 a0001c0001t0001g0060 a0001c0001t0001g0069 others(219): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.653-3024dupA | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122859431 | ||||||
| chr11:122859431 | G | GAA | 7 | a0001c0005t0001g0022 a0001c0005t0001g0051 a0001c0005t0001g0197 others(4): Show |
9 | HG01496.hp2 HG02559.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.653-3025_653-3024d others(4): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122859431 | ||||||
| chr11:122859435 | A | AC | 95 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(92): Show |
130 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.653-3029_653-3028i others(3): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122859435 | |||||||
| chr11:122859936 | T | TATCATC | 90 | a0001c0001t0001g0060 a0001c0001t0001g0255 a0001c0001t0001g0273 others(87): Show |
118 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(115): Show |
intron_variant | MODIFIER | c.653-2526_653-2521d others(8): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122859936 | ||||||
| chr11:122860011 | C | T | 1 | a0001c0001t0002g0307 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.653-2453C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122860011 | |||||||
| chr11:122860046 | A | C | 4 | a0001c0005t0001g0022 a0001c0005t0001g0051 a0001c0005t0001g0197 others(1): Show |
6 | HG01496.hp2 HG02559.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.653-2418A>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122860046 | |||||||
| chr11:122860092 | G | C | 2 | a0002c0002t0007g0068 a0002c0002t0007g0205 |
2 | HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.653-2372G>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122860092 | |||||||
| chr11:122860153 | T | C | 5 | a0006c0007t0001g0024 a0006c0007t0001g0310 a0006c0007t0001g0311 others(2): Show |
6 | HG02109.hp2 HG02145.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.653-2311T>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122860153 | |||||||
| chr11:122860160 | A | G | 218 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(215): Show |
285 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(282): Show |
intron_variant | MODIFIER | c.653-2304A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122860160 | |||||||
| chr11:122860273 | C | T | 2 | a0001c0001t0002g0155 a0001c0001t0002g0156 |
2 | HG00642.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.653-2191C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122860273 | |||||||
| chr11:122860278 | G | A | 1 | a0002c0002t0005g0040 | 2 | NA18952.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.653-2186G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122860278 | |||||||
| chr11:122860454 | TA | T | 10 | a0001c0001t0002g0007 a0001c0001t0002g0035 a0001c0001t0002g0143 others(7): Show |
14 | HG02698.hp1 HG02723.hp1 HG03831.hp2 others(11): Show |
intron_variant | MODIFIER | c.653-2009delA | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122860454 | |||||||
| chr11:122860633 | G | A | 39 | a0001c0001t0001g0069 a0001c0001t0002g0007 a0001c0001t0002g0016 others(36): Show |
49 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.653-1831G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122860633 | |||||||
| chr11:122860684 | A | G | 95 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(92): Show |
130 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.653-1780A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122860684 | |||||||
| chr11:122860719 | T | A | 1 | a0001c0001t0001g0089 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.653-1745T>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122860719 | |||||||
| chr11:122860757 | G | A | 93 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(90): Show |
128 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.653-1707G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122860757 | |||||||
| chr11:122860772 | C | A | 30 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(27): Show |
50 | HG00423.hp1 HG00423.hp2 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.653-1692C>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122860772 | |||||||
| chr11:122860789 | G | A | 1 | a0002c0004t0004g0245 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.653-1675G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122860789 | |||||||
| chr11:122860922 | C | T | 1 | a0001c0001t0001g0273 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.653-1542C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122860922 | |||||||
| chr11:122861023 | A | G | 1 | a0002c0004t0004g0084 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.653-1441A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122861023 | |||||||
| chr11:122861024 | G | A | 75 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(72): Show |
106 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.653-1440G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122861024 | |||||||
| chr11:122861120 | T | C | 1 | a0002c0004t0004g0229 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.653-1344T>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122861120 | |||||||
| chr11:122861165 | C | T | 2 | a0002c0002t0007g0290 a0002c0002t0007g0291 |
2 | HG02647.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.653-1299C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122861165 | |||||||
| chr11:122861228 | A | G | 25 | a0001c0001t0001g0204 a0001c0001t0001g0308 a0001c0001t0001g0309 others(22): Show |
30 | HG01167.hp1 HG01496.hp2 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.653-1236A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122861228 | |||||||
| chr11:122861348 | G | GTA | 11 | a0001c0001t0001g0099 a0001c0001t0001g0101 a0001c0001t0001g0102 others(8): Show |
11 | HG01192.hp2 HG01358.hp2 HG01952.hp1 others(8): Show |
intron_variant | MODIFIER | c.653-1103_653-1102d others(4): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861348 | ||||||
| chr11:122861348 | G | GTATA | 80 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(77): Show |
110 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.653-1105_653-1102d others(6): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861348 | ||||||
| chr11:122861348 | GTA | G | 147 | a0001c0001t0001g0060 a0001c0001t0001g0069 a0001c0001t0001g0186 others(144): Show |
185 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(182): Show |
intron_variant | MODIFIER | c.653-1103_653-1102d others(4): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861348 | ||||||
| chr11:122861361 | T | C | 4 | a0002c0002t0005g0183 a0002c0002t0005g0184 a0002c0004t0004g0259 others(1): Show |
4 | HG00099.hp2 HG02056.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.653-1103T>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122861361 | |||||||
| chr11:122861377 | T | C | 19 | a0001c0001t0001g0186 a0001c0001t0001g0189 a0001c0018t0011g0306 others(16): Show |
22 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.653-1087T>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122861377 | |||||||
| chr11:122861386 | GTATATA | G | 4 | a0002c0002t0005g0139 a0002c0002t0005g0191 a0002c0002t0007g0316 others(1): Show |
4 | HG02615.hp1 HG02965.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.653-1048_653-1043d others(8): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861386 | ||||||
| chr11:122861386 | GTATATAT others(3): Show |
G | 4 | a0001c0001t0001g0080 a0001c0001t0001g0112 a0002c0002t0007g0291 others(1): Show |
4 | HG02970.hp1 HG03540.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.653-1052_653-1043d others(12): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861386 | ||||||
| chr11:122861386 | GTATATAT others(5): Show |
G | 3 | a0001c0001t0001g0098 a0001c0001t0001g0204 a0001c0001t0002g0097 |
3 | HG00673.hp2 HG01884.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.653-1054_653-1043d others(14): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861386 | ||||||
| chr11:122861386 | GTATATAT others(7): Show |
G | 1 | a0004c0010t0007g0206 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.653-1056_653-1043d others(16): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861386 | ||||||
| chr11:122861386 | GTATATAT others(11): Show |
G | 9 | a0001c0001t0001g0189 a0002c0002t0005g0018 a0002c0002t0005g0040 others(6): Show |
12 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(9): Show |
intron_variant | MODIFIER | c.653-1060_653-1043d others(20): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861386 | ||||||
| chr11:122861386 | GTATATAT others(13): Show |
G | 1 | a0002c0004t0004g0241 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.653-1062_653-1043d others(22): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861386 | ||||||
| chr11:122861386 | GTATATAT others(15): Show |
G | 1 | a0002c0004t0004g0124 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.653-1064_653-1043d others(24): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861386 | ||||||
| chr11:122861400 | ATATATAT others(24): Show |
A | 5 | a0001c0001t0001g0060 a0001c0001t0002g0058 a0002c0002t0006g0059 others(2): Show |
5 | HG02280.hp1 HG02559.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.653-1062_653-1032d others(33): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861400 | ||||||
| chr11:122861400 | ATATATAT others(25): Show |
A | 19 | a0001c0001t0001g0255 a0002c0002t0001g0057 a0002c0002t0001g0319 others(16): Show |
21 | HG00621.hp2 HG00738.hp2 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.653-1062_653-1031d others(34): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861400 | ||||||
| chr11:122861400 | ATATATAT others(26): Show |
A | 1 | a0002c0002t0006g0198 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.653-1062_653-1030d others(35): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861400 | ||||||
| chr11:122861401 | TATATATA others(10): Show |
T | 1 | a0002c0002t0005g0183 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.653-1062_653-1046d others(19): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122861401 | |||||||
| chr11:122861401 | TATATATA others(12): Show |
T | 1 | a0002c0002t0005g0117 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.653-1062_653-1044d others(21): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122861401 | |||||||
| chr11:122861402 | ATATATAT others(12): Show |
A | 1 | a0002c0002t0007g0205 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.653-1060_653-1042d others(21): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861402 | ||||||
| chr11:122861402 | ATATATAT others(13): Show |
A | 1 | a0002c0002t0007g0068 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.653-1060_653-1041d others(22): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861402 | ||||||
| chr11:122861402 | ATATATAT others(16): Show |
A | 2 | a0004c0010t0015g0207 a0008c0011t0001g0208 |
2 | HG06807.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.653-1060_653-1038d others(25): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861402 | ||||||
| chr11:122861402 | ATATATAT others(17): Show |
A | 1 | a0004c0010t0007g0213 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.653-1060_653-1037d others(26): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861402 | ||||||
| chr11:122861402 | ATATATAT others(24): Show |
A | 1 | a0002c0002t0006g0063 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.653-1060_653-1030d others(33): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861402 | ||||||
| chr11:122861404 | ATATATAT others(12): Show |
A | 2 | a0003c0003t0003g0079 a0003c0003t0003g0256 |
2 | HG02040.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.653-1058_653-1040d others(21): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861404 | ||||||
| chr11:122861404 | ATATATAT others(14): Show |
A | 2 | a0001c0001t0002g0264 a0003c0003t0003g0284 |
2 | NA18953.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.653-1058_653-1038d others(23): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861404 | ||||||
| chr11:122861404 | ATATATAT others(15): Show |
A | 1 | a0003c0003t0003g0048 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.653-1058_653-1037d others(24): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861404 | ||||||
| chr11:122861405 | TATATATA others(6): Show |
T | 1 | a0002c0004t0004g0240 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.653-1058_653-1046d others(15): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122861405 | |||||||
| chr11:122861406 | ATATATAT others(11): Show |
A | 3 | a0002c0004t0003g0251 a0003c0003t0003g0004 a0003c0003t0003g0020 |
4 | HG03098.hp1 NA18992.hp2 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.653-1056_653-1039d others(20): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861406 | ||||||
| chr11:122861406 | ATATATAT others(12): Show |
A | 30 | a0001c0001t0002g0270 a0001c0001t0002g0271 a0001c0001t0002g0280 others(27): Show |
41 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.653-1056_653-1038d others(21): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861406 | ||||||
| chr11:122861406 | ATATATAT others(13): Show |
A | 8 | a0003c0003t0003g0008 a0003c0003t0003g0034 a0003c0003t0003g0048 others(5): Show |
8 | HG00544.hp1 HG02027.hp1 NA18612.hp1 others(5): Show |
intron_variant | MODIFIER | c.653-1056_653-1037d others(22): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861406 | ||||||
| chr11:122861407 | TATATATA others(6): Show |
T | 1 | a0001c0001t0001g0118 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.653-1056_653-1044d others(15): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122861407 | |||||||
| chr11:122861408 | ATATATAT others(6): Show |
A | 14 | a0001c0001t0001g0019 a0001c0001t0001g0070 a0001c0001t0001g0089 others(11): Show |
16 | HG00423.hp1 HG01109.hp2 HG01346.hp2 others(13): Show |
intron_variant | MODIFIER | c.653-1054_653-1042d others(15): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861408 | ||||||
| chr11:122861408 | ATATATAT others(7): Show |
A | 5 | a0001c0001t0001g0003 a0001c0001t0001g0102 a0001c0001t0002g0027 others(2): Show |
5 | HG00280.hp1 HG00609.hp2 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.653-1054_653-1041d others(16): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861408 | ||||||
| chr11:122861408 | ATATATAT others(8): Show |
A | 3 | a0001c0001t0002g0025 a0001c0001t0002g0148 a0001c0001t0002g0169 |
3 | HG01123.hp1 HG02148.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.653-1054_653-1040d others(17): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861408 | ||||||
| chr11:122861408 | ATATATAT others(9): Show |
A | 1 | a0001c0001t0002g0025 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.653-1054_653-1039d others(18): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861408 | ||||||
| chr11:122861408 | ATATATAT others(11): Show |
A | 6 | a0001c0001t0001g0273 a0003c0003t0003g0004 a0003c0003t0003g0008 others(3): Show |
7 | HG00735.hp1 HG01261.hp1 HG03654.hp2 others(4): Show |
intron_variant | MODIFIER | c.653-1054_653-1037d others(20): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861408 | ||||||
| chr11:122861408 | ATATATAT others(12): Show |
A | 5 | a0003c0003t0003g0004 a0003c0003t0003g0278 a0003c0003t0003g0279 others(2): Show |
5 | HG03669.hp1 NA18946.hp1 NA18985.hp1 others(2): Show |
intron_variant | MODIFIER | c.653-1054_653-1036d others(21): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861408 | ||||||
| chr11:122861408 | ATATATAT others(13): Show |
A | 1 | a0002c0002t0009g0165 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.653-1054_653-1035d others(22): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861408 | ||||||
| chr11:122861408 | ATATATAT others(14): Show |
A | 1 | a0002c0002t0001g0253 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.653-1054_653-1034d others(23): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861408 | ||||||
| chr11:122861409 | TATATATA others(4): Show |
T | 3 | a0004c0008t0001g0158 a0004c0008t0014g0252 a0004c0015t0004g0054 |
3 | HG02895.hp1 HG03579.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.653-1054_653-1044d others(13): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122861409 | |||||||
| chr11:122861410 | ATATATAT others(4): Show |
A | 4 | a0001c0001t0001g0010 a0001c0001t0001g0111 a0004c0008t0001g0052 others(1): Show |
6 | HG00408.hp1 HG03471.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.653-1052_653-1042d others(13): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861410 | ||||||
| chr11:122861410 | ATATATAT others(5): Show |
A | 12 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0015 others(9): Show |
14 | HG00423.hp2 HG01346.hp1 HG01943.hp1 others(11): Show |
intron_variant | MODIFIER | c.653-1052_653-1041d others(14): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861410 | ||||||
| chr11:122861410 | ATATATAT others(6): Show |
A | 33 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0028 others(30): Show |
39 | HG00438.hp2 HG00735.hp2 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.653-1052_653-1040d others(15): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861410 | ||||||
| chr11:122861410 | ATATATAT others(7): Show |
A | 24 | a0001c0001t0002g0007 a0001c0001t0002g0035 a0001c0001t0002g0036 others(21): Show |
28 | HG00639.hp2 HG00642.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.653-1052_653-1039d others(16): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861410 | ||||||
| chr11:122861410 | ATATATAT others(8): Show |
A | 7 | a0001c0001t0001g0001 a0001c0001t0001g0087 a0001c0001t0001g0109 others(4): Show |
7 | HG00140.hp1 HG01516.hp1 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.653-1052_653-1038d others(17): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861410 | ||||||
| chr11:122861410 | ATATATAT others(14): Show |
A | 2 | a0001c0001t0002g0143 a0001c0001t0002g0144 |
2 | HG03834.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.653-1052_653-1032d others(23): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861410 | ||||||
| chr11:122861412 | ATATATAT others(3): Show |
A | 2 | a0002c0016t0001g0065 a0004c0008t0001g0320 |
2 | HG00642.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.653-1050_653-1041d others(12): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861412 | ||||||
| chr11:122861412 | ATATATAT others(4): Show |
A | 2 | a0001c0001t0001g0003 a0010c0020t0005g0210 |
2 | HG02451.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.653-1050_653-1040d others(13): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861412 | ||||||
| chr11:122861412 | ATATATAT others(5): Show |
A | 2 | a0001c0001t0008g0001 a0001c0001t0008g0096 |
5 | HG00738.hp1 HG01258.hp2 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.653-1050_653-1039d others(14): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861412 | ||||||
| chr11:122861412 | ATATATAT others(6): Show |
A | 13 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0053 others(10): Show |
18 | HG01243.hp2 HG01256.hp2 HG02056.hp2 others(15): Show |
intron_variant | MODIFIER | c.653-1050_653-1038d others(15): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861412 | ||||||
| chr11:122861412 | ATATATAT others(7): Show |
A | 2 | a0001c0001t0001g0114 a0001c0001t0002g0037 |
2 | HG02698.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.653-1050_653-1037d others(16): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861412 | ||||||
| chr11:122861412 | ATATATAT others(8): Show |
A | 5 | a0001c0001t0002g0016 a0001c0005t0001g0022 a0001c0005t0001g0197 others(2): Show |
7 | HG01109.hp1 HG01358.hp1 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.653-1050_653-1036d others(17): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861412 | ||||||
| chr11:122861412 | ATATATAT others(9): Show |
A | 1 | a0001c0005t0001g0051 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.653-1050_653-1035d others(18): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861412 | ||||||
| chr11:122861412 | ATATATAT others(10): Show |
A | 1 | a0002c0002t0010g0166 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.653-1050_653-1034d others(19): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861412 | ||||||
| chr11:122861412 | ATATATAT others(13): Show |
A | 5 | a0002c0002t0009g0074 a0002c0002t0009g0136 a0002c0002t0009g0137 others(2): Show |
5 | HG01167.hp1 HG01884.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.653-1050_653-1031d others(22): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861412 | ||||||
| chr11:122861412 | ATATATAT others(15): Show |
A | 1 | a0009c0013t0011g0211 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.653-1050_653-1029d others(24): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861412 | ||||||
| chr11:122861414 | ATATATAT others(3): Show |
A | 1 | a0007c0009t0003g0067 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.653-1048_653-1039d others(12): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861414 | ||||||
| chr11:122861414 | ATATATAT others(11): Show |
A | 1 | a0002c0002t0009g0297 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.653-1048_653-1031d others(20): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861414 | ||||||
| chr11:122861416 | A | T | 3 | a0002c0002t0005g0139 a0002c0002t0005g0187 a0002c0002t0005g0191 |
3 | HG02615.hp1 HG03579.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.653-1048A>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122861416 | |||||||
| chr11:122861416 | ATATATTT others(4): Show |
A | 1 | a0002c0004t0001g0313 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.653-1046_653-1036d others(13): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861416 | ||||||
| chr11:122861418 | A | AT | 14 | a0001c0001t0001g0222 a0001c0001t0001g0275 a0001c0001t0002g0083 others(11): Show |
16 | HG01106.hp2 HG01261.hp2 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.653-1045dupT | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861418 | ||||||
| chr11:122861418 | A | ATTT | 3 | a0001c0001t0002g0226 a0001c0018t0011g0306 a0002c0004t0004g0236 |
3 | HG02738.hp1 HG03209.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.653-1045_653-1044i others(5): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861418 | ||||||
| chr11:122861418 | A | T | 13 | a0001c0001t0002g0047 a0001c0001t0002g0202 a0001c0001t0002g0242 others(10): Show |
13 | HG01192.hp2 HG01361.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.653-1046A>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122861418 | |||||||
| chr11:122861418 | ATATTTTT others(3): Show |
A | 2 | a0005c0006t0004g0042 a0005c0006t0004g0196 |
3 | HG01891.hp1 HG02109.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.653-1044_653-1035d others(12): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861418 | ||||||
| chr11:122861418 | ATATTTTT others(4): Show |
A | 1 | a0005c0012t0009g0215 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.653-1044_653-1034d others(13): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861418 | ||||||
| chr11:122861420 | A | ATATATAT others(6): Show |
1 | a0002c0004t0004g0005 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.653-1043_653-1042i others(15): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861420 | ||||||
| chr11:122861420 | A | ATATATAT others(4): Show |
1 | a0002c0002t0006g0287 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.653-1043_653-1042i others(13): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861420 | ||||||
| chr11:122861420 | A | ATT | 10 | a0001c0001t0001g0235 a0001c0001t0002g0031 a0001c0001t0002g0044 others(7): Show |
10 | HG01099.hp1 HG02074.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.653-1015_653-1014d others(4): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122861420 | ||||||
| chr11:122861420 | A | T | 47 | a0001c0001t0001g0189 a0001c0001t0001g0222 a0001c0001t0001g0275 others(44): Show |
58 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.653-1044A>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122861420 | |||||||
| chr11:122861422 | T | A | 2 | a0002c0004t0003g0046 a0002c0004t0004g0259 |
3 | HG00099.hp2 NA18942.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.653-1042T>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122861422 | |||||||
| chr11:122861422 | T | G | 1 | a0001c0001t0001g0204 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.653-1042T>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122861422 | |||||||
| chr11:122861423 | T | G | 3 | a0001c0001t0001g0070 a0001c0001t0001g0104 a0001c0001t0001g0105 |
3 | HG03130.hp1 HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.653-1041T>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122861423 | |||||||
| chr11:122861426 | T | A | 2 | a0001c0001t0002g0307 a0006c0007t0001g0310 |
2 | HG02818.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.653-1038T>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122861426 | |||||||
| chr11:122861451 | G | T | 1 | a0002c0002t0005g0187 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.653-1013G>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122861451 | |||||||
| chr11:122861470 | C | T | 2 | a0002c0002t0009g0165 a0002c0002t0010g0166 |
2 | HG02717.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.653-994C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122861470 | |||||||
| chr11:122861475 | G | A | 6 | a0002c0002t0009g0074 a0002c0002t0009g0136 a0002c0002t0009g0137 others(3): Show |
6 | HG01167.hp1 HG01884.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.653-989G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122861475 | |||||||
| chr11:122861538 | C | T | 20 | a0001c0001t0001g0255 a0002c0002t0001g0057 a0002c0002t0001g0319 others(17): Show |
22 | HG00621.hp2 HG00738.hp2 HG01081.hp2 others(19): Show |
intron_variant | MODIFIER | c.653-926C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122861538 | |||||||
| chr11:122861592 | A | G | 1 | a0002c0004t0004g0124 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.653-872A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122861592 | |||||||
| chr11:122861596 | C | T | 21 | a0001c0001t0001g0060 a0001c0001t0001g0186 a0001c0001t0001g0189 others(18): Show |
24 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(21): Show |
intron_variant | MODIFIER | c.653-868C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122861596 | |||||||
| chr11:122861600 | C | T | 1 | a0001c0001t0002g0202 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.653-864C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122861600 | |||||||
| chr11:122861895 | T | C | 1 | a0001c0001t0001g0130 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.653-569T>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122861895 | |||||||
| chr11:122861989 | G | T | 6 | a0002c0002t0009g0074 a0002c0002t0009g0136 a0002c0002t0009g0137 others(3): Show |
6 | HG01167.hp1 HG01884.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.653-475G>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122861989 | |||||||
| chr11:122862004 | A | G | 191 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(188): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(248): Show |
intron_variant | MODIFIER | c.653-460A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122862004 | |||||||
| chr11:122862019 | G | GA | 37 | a0001c0001t0002g0007 a0001c0001t0002g0016 a0001c0001t0002g0025 others(34): Show |
48 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.653-437dupA | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 122862019 | ||||||
| chr11:122862045 | T | G | 1 | a0001c0001t0001g0099 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.653-419T>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122862045 | |||||||
| chr11:122862087 | T | C | 2 | a0001c0018t0011g0306 a0005c0012t0010g0305 |
2 | HG02258.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.653-377T>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122862087 | |||||||
| chr11:122862164 | G | T | 42 | a0001c0001t0002g0007 a0001c0001t0002g0016 a0001c0001t0002g0025 others(39): Show |
53 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.653-300G>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122862164 | |||||||
| chr11:122862167 | A | T | 1 | a0002c0002t0006g0064 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.653-297A>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122862167 | |||||||
| chr11:122862191 | A | G | 2 | a0002c0002t0007g0316 a0002c0002t0007g0317 |
2 | HG02965.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.653-273A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122862191 | |||||||
| chr11:122862275 | A | C | 1 | a0002c0002t0005g0167 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.653-189A>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122862275 | |||||||
| chr11:122862372 | C | T | 1 | a0001c0001t0001g0204 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.653-92C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 5/9 | chr11 | 122862372 | |||||||
| chr11:122862721 | G | A | 5 | a0005c0006t0004g0042 a0005c0006t0004g0195 a0005c0006t0004g0196 others(2): Show |
6 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.733+177G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | chr11 | 122862721 | |||||||
| chr11:122862816 | C | A | 1 | a0002c0004t0004g0259 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.733+272C>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | chr11 | 122862816 | |||||||
| chr11:122862894 | TG | T | 47 | a0001c0001t0002g0007 a0001c0001t0002g0016 a0001c0001t0002g0025 others(44): Show |
59 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.733+351delG | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | chr11 | 122862894 | |||||||
| chr11:122862937 | G | T | 1 | a0004c0010t0007g0206 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.733+393G>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | chr11 | 122862937 | |||||||
| chr11:122862941 | C | T | 1 | a0002c0004t0004g0238 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.733+397C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | chr11 | 122862941 | |||||||
| chr11:122862950 | G | C | 5 | a0001c0001t0002g0023 a0001c0001t0002g0193 a0001c0001t0002g0270 others(2): Show |
7 | HG02071.hp1 HG03831.hp1 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.733+406G>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | chr11 | 122862950 | |||||||
| chr11:122863109 | A | G | 221 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(218): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(299): Show |
intron_variant | MODIFIER | c.733+565A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | chr11 | 122863109 | |||||||
| chr11:122863228 | C | CGAAA | 103 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(100): Show |
135 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.733+703_733+706dup others(4): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 122863228 | ||||||
| chr11:122863228 | C | CGAAAGAA others(5): Show |
2 | a0002c0002t0007g0291 a0002c0002t0007g0316 |
2 | HG02970.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.733+695_733+706dup others(12): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 122863228 | ||||||
| chr11:122863228 | C | CGAAAGAA others(9): Show |
1 | a0002c0002t0007g0290 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.733+691_733+706dup others(16): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 122863228 | ||||||
| chr11:122863247 | A | G | 3 | a0002c0002t0010g0049 a0002c0002t0010g0300 a0002c0002t0010g0301 |
4 | HG02055.hp2 HG02258.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.733+703A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | chr11 | 122863247 | |||||||
| chr11:122863251 | G | A | 4 | a0002c0002t0010g0049 a0002c0002t0010g0300 a0002c0002t0010g0301 others(1): Show |
5 | HG02055.hp2 HG02258.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.733+707G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | chr11 | 122863251 | |||||||
| chr11:122863255 | A | G | 2 | a0001c0001t0001g0019 a0001c0001t0001g0127 |
4 | NA18973.hp2 NA19000.hp1 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.733+711A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | chr11 | 122863255 | |||||||
| chr11:122863257 | G | A | 4 | a0002c0002t0010g0049 a0002c0002t0010g0300 a0002c0002t0010g0301 others(1): Show |
5 | HG02055.hp2 HG02258.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.733+713G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | chr11 | 122863257 | |||||||
| chr11:122863258 | A | G | 3 | a0002c0002t0010g0049 a0002c0002t0010g0300 a0002c0002t0010g0301 |
4 | HG02055.hp2 HG02258.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.733+714A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | chr11 | 122863258 | |||||||
| chr11:122863262 | GAAAGAAA others(3): Show |
G | 41 | a0001c0001t0002g0264 a0003c0003t0003g0004 a0003c0003t0003g0008 others(38): Show |
63 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.733+730_733+739del others(10): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 122863262 | ||||||
| chr11:122863264 | A | G | 1 | a0002c0004t0003g0251 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.733+720A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | chr11 | 122863264 | |||||||
| chr11:122863270 | G | A | 3 | a0002c0002t0010g0049 a0002c0002t0010g0300 a0002c0002t0010g0301 |
4 | HG02055.hp2 HG02258.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.733+726G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | chr11 | 122863270 | |||||||
| chr11:122863272 | A | AAAAG | 253 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(250): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.733+740_733+743dup others(4): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 122863272 | ||||||
| chr11:122863272 | A | G | 3 | a0002c0002t0010g0049 a0002c0002t0010g0300 a0002c0002t0010g0301 |
4 | HG02055.hp2 HG02258.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.733+728A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | chr11 | 122863272 | |||||||
| chr11:122863288 | A | G | 7 | a0001c0001t0002g0083 a0002c0002t0006g0177 a0002c0002t0006g0287 others(4): Show |
7 | HG01934.hp1 HG02630.hp1 HG02683.hp2 others(4): Show |
intron_variant | MODIFIER | c.733+744A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | chr11 | 122863288 | |||||||
| chr11:122863290 | G | A | 6 | a0001c0001t0002g0083 a0002c0002t0006g0177 a0002c0002t0006g0287 others(3): Show |
6 | HG01934.hp1 HG02630.hp1 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.733+746G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | chr11 | 122863290 | |||||||
| chr11:122863290 | G | T | 2 | a0003c0003t0003g0134 a0003c0003t0003g0269 |
2 | HG00673.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.733+746G>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | chr11 | 122863290 | |||||||
| chr11:122863300 | G | A | 6 | a0002c0002t0006g0287 a0002c0004t0003g0251 a0004c0010t0007g0206 others(3): Show |
6 | HG02630.hp1 HG02717.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.733+756G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | chr11 | 122863300 | |||||||
| chr11:122863304 | A | G | 4 | a0002c0002t0006g0287 a0004c0010t0007g0213 a0004c0010t0015g0207 others(1): Show |
4 | HG02630.hp1 HG02717.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.733+760A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | chr11 | 122863304 | |||||||
| chr11:122863306 | GAAAAGAA others(8): Show |
G | 1 | a0002c0004t0003g0251 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.733+766_733+780del others(15): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 122863306 | ||||||
| chr11:122863310 | A | G | 4 | a0002c0002t0006g0287 a0004c0010t0007g0213 a0004c0010t0015g0207 others(1): Show |
4 | HG02630.hp1 HG02717.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.733+766A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | chr11 | 122863310 | |||||||
| chr11:122863311 | G | A | 4 | a0002c0002t0006g0287 a0004c0010t0007g0213 a0004c0010t0015g0207 others(1): Show |
4 | HG02630.hp1 HG02717.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.733+767G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | chr11 | 122863311 | |||||||
| chr11:122863311 | GAAAGAAA others(3): Show |
G | 1 | a0001c0001t0002g0156 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.733+779_733+788del others(10): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 122863311 | ||||||
| chr11:122863313 | A | G | 1 | a0002c0002t0006g0177 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.733+769A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | chr11 | 122863313 | |||||||
| chr11:122863321 | A | AAAAG | 22 | a0001c0001t0001g0003 a0001c0001t0001g0119 a0001c0001t0001g0130 others(19): Show |
23 | HG00609.hp2 HG01106.hp1 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.733+805_733+808dup others(4): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 122863321 | ||||||
| chr11:122863321 | A | AAAAGAAA others(1): Show |
3 | a0001c0001t0002g0108 a0001c0001t0002g0299 a0001c0001t0008g0001 |
3 | HG01496.hp1 HG01943.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.733+801_733+808dup others(8): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 122863321 | ||||||
| chr11:122863321 | A | AAAAGAAA others(5): Show |
1 | a0001c0001t0002g0027 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.733+797_733+808dup others(12): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 122863321 | ||||||
| chr11:122863321 | AAAAG | A | 18 | a0001c0001t0001g0010 a0002c0002t0001g0289 a0002c0002t0001g0298 others(15): Show |
19 | HG00642.hp2 HG02615.hp1 HG02647.hp1 others(16): Show |
intron_variant | MODIFIER | c.733+805_733+808del others(4): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 122863321 | ||||||
| chr11:122863321 | AAAAGAAA others(1): Show |
A | 42 | a0001c0001t0002g0264 a0002c0002t0007g0291 a0003c0003t0003g0004 others(39): Show |
64 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.733+801_733+808del others(8): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 122863321 | ||||||
| chr11:122863322 | AAAGAAAG others(8): Show |
A | 3 | a0002c0002t0010g0049 a0002c0002t0010g0300 a0002c0002t0010g0301 |
4 | HG02055.hp2 HG02258.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.733+781_733+795del others(15): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 122863322 | ||||||
| chr11:122863325 | GAAAGAA | G | 3 | a0004c0010t0007g0213 a0004c0010t0015g0207 a0008c0011t0001g0208 |
3 | HG02630.hp1 HG06807.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.733+783_733+788del others(6): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 122863325 | ||||||
| chr11:122863329 | GAAAGAAA others(15): Show |
G | 1 | a0001c0001t0002g0085 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.733+805_733+826del others(22): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 122863329 | ||||||
| chr11:122863333 | GAAAGAAA others(11): Show |
G | 2 | a0001c0001t0002g0151 a0007c0009t0003g0239 |
2 | HG00140.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.733+826_733+843del others(18): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 122863333 | ||||||
| chr11:122863337 | GAAAGAAA others(7): Show |
G | 19 | a0001c0001t0002g0007 a0001c0001t0002g0035 a0001c0001t0002g0036 others(16): Show |
24 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.733+809_733+822del others(14): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 122863337 | ||||||
| chr11:122863341 | GAAAGAAA others(3): Show |
G | 11 | a0001c0001t0002g0016 a0001c0001t0002g0038 a0001c0001t0002g0041 others(8): Show |
14 | HG00639.hp2 HG01346.hp2 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.733+809_733+818del others(10): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 122863341 | ||||||
| chr11:122863343 | AAGAAAGA others(5): Show |
A | 1 | a0002c0004t0004g0229 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.733+801_733+812del others(12): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 122863343 | ||||||
| chr11:122863345 | GAAAGAA | G | 4 | a0001c0001t0002g0025 a0001c0001t0002g0037 a0001c0001t0002g0148 others(1): Show |
4 | HG01123.hp1 HG02698.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.733+809_733+814del others(6): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 122863345 | ||||||
| chr11:122863347 | AAGAAAAA others(1): Show |
A | 49 | a0001c0001t0001g0222 a0001c0001t0001g0235 a0001c0001t0002g0030 others(46): Show |
70 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(67): Show |
intron_variant | MODIFIER | c.733+805_733+812del others(8): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 122863347 | ||||||
| chr11:122863349 | G | A | 2 | a0002c0004t0003g0251 a0010c0020t0005g0210 |
2 | HG02451.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.733+805G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | chr11 | 122863349 | |||||||
| chr11:122863349 | GAA | G | 7 | a0001c0001t0002g0025 a0001c0001t0002g0156 a0001c0001t0007g0149 others(4): Show |
8 | HG01070.hp2 HG01175.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.733+809_733+810del others(2): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 122863349 | ||||||
| chr11:122863351 | A | AAG | 3 | a0001c0001t0002g0039 a0002c0002t0005g0250 a0002c0004t0004g0005 |
4 | HG01069.hp2 HG01175.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.733+808_733+809ins others(2): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 122863351 | ||||||
| chr11:122863351 | A | AAGAAAGA others(3): Show |
1 | a0002c0002t0001g0253 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.733+808_733+809ins others(10): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 122863351 | ||||||
| chr11:122863351 | A | AAGAAAGA others(19): Show |
1 | a0002c0002t0009g0165 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.733+808_733+809ins others(26): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 122863351 | ||||||
| chr11:122863351 | A | G | 3 | a0002c0004t0003g0251 a0004c0010t0007g0206 a0010c0020t0005g0210 |
3 | HG02451.hp1 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.733+807A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | chr11 | 122863351 | |||||||
| chr11:122863351 | AAAAG | A | 27 | a0001c0001t0001g0302 a0001c0001t0002g0083 a0001c0001t0002g0232 others(24): Show |
30 | HG00621.hp2 HG00738.hp2 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.733+823_733+826del others(4): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 122863351 | ||||||
| chr11:122863353 | A | G | 1 | a0002c0002t0006g0198 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.733+809A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | chr11 | 122863353 | |||||||
| chr11:122863355 | G | A | 1 | a0002c0002t0006g0198 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.733+811G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | chr11 | 122863355 | |||||||
| chr11:122863477 | A | G | 1 | a0008c0011t0001g0209 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.733+933A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | chr11 | 122863477 | |||||||
| chr11:122863603 | C | A | 1 | a0002c0002t0006g0170 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.734-1033C>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | chr11 | 122863603 | |||||||
| chr11:122863626 | GTACCA | G | 6 | a0002c0002t0001g0289 a0002c0002t0001g0298 a0002c0002t0005g0139 others(3): Show |
6 | HG02615.hp1 HG02886.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.734-1006_734-1002d others(7): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 122863626 | ||||||
| chr11:122863791 | A | G | 1 | a0002c0004t0004g0006 | 5 | HG01070.hp1 HG01071.hp1 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.734-845A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | chr11 | 122863791 | |||||||
| chr11:122864000 | C | A | 1 | a0007c0009t0013g0142 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.734-636C>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | chr11 | 122864000 | |||||||
| chr11:122864166 | C | T | 1 | a0004c0008t0014g0252 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.734-470C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 6/9 | chr11 | 122864166 | |||||||
| chr11:122864794 | G | A | 9 | a0002c0002t0001g0159 a0002c0002t0009g0074 a0002c0002t0009g0136 others(6): Show |
9 | HG01167.hp1 HG01884.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.817+75G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 7/9 | chr11 | 122864794 | |||||||
| chr11:122864850 | T | C | 12 | a0001c0001t0002g0007 a0001c0001t0002g0035 a0001c0001t0002g0044 others(9): Show |
17 | HG02698.hp1 HG03831.hp2 HG03834.hp2 others(14): Show |
intron_variant | MODIFIER | c.817+131T>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 7/9 | chr11 | 122864850 | |||||||
| chr11:122864925 | C | T | 1 | a0001c0018t0011g0306 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.817+206C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 7/9 | chr11 | 122864925 | |||||||
| chr11:122865031 | T | A | 1 | a0001c0001t0002g0307 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.817+312T>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 7/9 | chr11 | 122865031 | |||||||
| chr11:122865045 | T | A | 19 | a0002c0002t0001g0319 a0002c0002t0006g0017 a0002c0002t0006g0063 others(16): Show |
21 | HG00621.hp2 HG00738.hp2 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.817+326T>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 7/9 | chr11 | 122865045 | |||||||
| chr11:122865101 | A | G | 3 | a0002c0002t0006g0176 a0002c0002t0006g0177 a0002c0002t0006g0323 |
3 | HG01081.hp2 HG01243.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.817+382A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 7/9 | chr11 | 122865101 | |||||||
| chr11:122865188 | C | G | 3 | a0001c0001t0001g0026 a0007c0009t0003g0026 a0007c0009t0003g0067 |
3 | HG00408.hp2 NA18961.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.817+469C>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 7/9 | chr11 | 122865188 | |||||||
| chr11:122865241 | G | T | 8 | a0002c0002t0009g0074 a0002c0002t0009g0136 a0002c0002t0009g0137 others(5): Show |
8 | HG01167.hp1 HG01884.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.817+522G>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 7/9 | chr11 | 122865241 | |||||||
| chr11:122865325 | G | A | 1 | a0002c0002t0009g0136 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.817+606G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 7/9 | chr11 | 122865325 | |||||||
| chr11:122865408 | CT | C | 67 | a0001c0001t0002g0007 a0001c0001t0002g0016 a0001c0001t0002g0023 others(64): Show |
85 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.817+690delT | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 7/9 | chr11 | 122865408 | |||||||
| chr11:122865454 | T | C | 3 | a0003c0003t0003g0261 a0003c0003t0003g0262 a0003c0003t0003g0263 |
3 | NA18956.hp2 NA18974.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.817+735T>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 7/9 | chr11 | 122865454 | |||||||
| chr11:122865499 | G | A | 76 | a0001c0001t0002g0007 a0001c0001t0002g0016 a0001c0001t0002g0023 others(73): Show |
95 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.817+780G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 7/9 | chr11 | 122865499 | |||||||
| chr11:122865514 | A | T | 308 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(305): Show |
404 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(401): Show |
intron_variant | MODIFIER | c.817+795A>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 7/9 | chr11 | 122865514 | |||||||
| chr11:122865562 | A | G | 52 | a0002c0002t0001g0057 a0002c0002t0001g0159 a0002c0002t0001g0289 others(49): Show |
72 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(69): Show |
intron_variant | MODIFIER | c.817+843A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 7/9 | chr11 | 122865562 | |||||||
| chr11:122865569 | A | T | 1 | a0002c0004t0003g0251 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.817+850A>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 7/9 | chr11 | 122865569 | |||||||
| chr11:122865580 | C | T | 1 | a0002c0002t0005g0250 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.817+861C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 7/9 | chr11 | 122865580 | |||||||
| chr11:122865717 | C | G | 2 | a0002c0002t0005g0139 a0002c0002t0005g0191 |
2 | HG02615.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.817+998C>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 7/9 | chr11 | 122865717 | |||||||
| chr11:122865718 | A | G | 86 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(83): Show |
117 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.817+999A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 7/9 | chr11 | 122865718 | |||||||
| chr11:122865738 | C | T | 1 | a0001c0001t0002g0097 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.817+1019C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 7/9 | chr11 | 122865738 | |||||||
| chr11:122865849 | T | G | 4 | a0001c0001t0002g0226 a0001c0001t0002g0230 a0001c0001t0002g0231 others(1): Show |
4 | HG01106.hp2 HG02738.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.817+1130T>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 7/9 | chr11 | 122865849 | |||||||
| chr11:122865863 | C | T | 76 | a0001c0001t0002g0007 a0001c0001t0002g0016 a0001c0001t0002g0023 others(73): Show |
95 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.817+1144C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 7/9 | chr11 | 122865863 | |||||||
| chr11:122865892 | C | G | 6 | a0002c0002t0001g0319 a0002c0016t0001g0065 a0004c0008t0001g0052 others(3): Show |
6 | HG00642.hp2 HG02970.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.817+1173C>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 7/9 | chr11 | 122865892 | |||||||
| chr11:122866145 | A | C | 166 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(163): Show |
217 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.818-1264A>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 7/9 | chr11 | 122866145 | |||||||
| chr11:122866520 | CCTT | C | 4 | a0001c0001t0002g0023 a0001c0001t0002g0264 a0001c0001t0002g0270 others(1): Show |
6 | HG02071.hp1 NA18945.hp1 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.818-888_818-886del others(3): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 7/9 | chr11 | 122866520 | |||||||
| chr11:122866607 | CT | C | 74 | a0001c0001t0002g0007 a0001c0001t0002g0016 a0001c0001t0002g0023 others(71): Show |
93 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.818-787delT | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr11 | 122866607 | ||||||
| chr11:122866769 | A | G | 1 | a0002c0002t0006g0175 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.818-640A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 7/9 | chr11 | 122866769 | |||||||
| chr11:122866774 | T | A | 27 | a0001c0001t0002g0023 a0001c0001t0002g0030 a0001c0001t0002g0031 others(24): Show |
33 | HG00280.hp2 HG00639.hp1 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.818-635T>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 7/9 | chr11 | 122866774 | |||||||
| chr11:122866919 | T | C | 1 | a0002c0004t0003g0251 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.818-490T>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 7/9 | chr11 | 122866919 | |||||||
| chr11:122866997 | A | G | 41 | a0003c0003t0003g0004 a0003c0003t0003g0008 a0003c0003t0003g0012 others(38): Show |
63 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.818-412A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 7/9 | chr11 | 122866997 | |||||||
| chr11:122867025 | T | C | 1 | a0002c0002t0001g0253 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.818-384T>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 7/9 | chr11 | 122867025 | |||||||
| chr11:122867057 | T | C | 1 | a0001c0001t0002g0193 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.818-352T>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 7/9 | chr11 | 122867057 | |||||||
| chr11:122867102 | C | T | 216 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(213): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.818-307C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 7/9 | chr11 | 122867102 | |||||||
| chr11:122867225 | G | C | 2 | a0002c0002t0001g0159 a0002c0002t0001g0298 |
2 | HG02630.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.818-184G>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 7/9 | chr11 | 122867225 | |||||||
| chr11:122867324 | GT | G | 7 | a0002c0002t0005g0250 a0002c0002t0010g0049 a0002c0002t0010g0166 others(4): Show |
8 | HG02055.hp2 HG02145.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.818-84delT | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 7/9 | chr11 | 122867324 | |||||||
| chr11:122867354 | CA | C | 25 | a0001c0001t0001g0019 a0001c0001t0001g0028 a0001c0001t0001g0089 others(22): Show |
29 | HG00423.hp2 HG00741.hp1 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.818-39delA | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr11 | 122867354 | ||||||
| chr11:122867354 | CAA | C | 270 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(267): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.818-40_818-39delAA | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr11 | 122867354 | ||||||
| chr11:122867354 | CAAA | C | 15 | a0001c0001t0002g0234 a0002c0002t0001g0057 a0002c0002t0001g0159 others(12): Show |
17 | HG00642.hp2 HG00741.hp2 HG02129.hp1 others(14): Show |
intron_variant | MODIFIER | c.818-41_818-39delAA others(1): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr11 | 122867354 | ||||||
| chr11:122867592 | G | A | 6 | a0002c0002t0001g0319 a0002c0016t0001g0065 a0004c0008t0001g0052 others(3): Show |
6 | HG00642.hp2 HG02970.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.964+37G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 8/9 | chr11 | 122867592 | |||||||
| chr11:122867739 | C | T | 1 | a0001c0005t0001g0197 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.964+184C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 8/9 | chr11 | 122867739 | |||||||
| chr11:122868010 | T | C | 40 | a0002c0004t0003g0046 a0002c0004t0003g0251 a0002c0004t0004g0002 others(37): Show |
60 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(57): Show |
splice_region_variant&intron_variant | LOW | c.965-3T>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 8/9 | chr11 | 122868010 | |||||||
| chr11:122868188 | A | ATG | 27 | a0001c0001t0002g0045 a0001c0001t0002g0047 a0001c0001t0002g0108 others(24): Show |
29 | HG00621.hp2 HG00741.hp2 HG01433.hp1 others(26): Show |
intron_variant | MODIFIER | c.1051+137_1051+138d others(4): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 122868188 | ||||||
| chr11:122868188 | A | ATGTG | 20 | a0001c0001t0002g0023 a0001c0001t0002g0031 a0001c0001t0002g0155 others(17): Show |
25 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.1051+135_1051+138d others(6): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 122868188 | ||||||
| chr11:122868188 | A | ATGTGTG | 12 | a0001c0001t0002g0083 a0001c0001t0002g0126 a0001c0001t0002g0230 others(9): Show |
13 | HG01123.hp2 HG01167.hp1 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.1051+133_1051+138d others(8): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 122868188 | ||||||
| chr11:122868188 | A | ATGTGTGT others(1): Show |
6 | a0001c0001t0002g0227 a0002c0002t0001g0159 a0002c0002t0001g0298 others(3): Show |
6 | HG02630.hp2 HG02717.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1051+131_1051+138d others(10): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 122868188 | ||||||
| chr11:122868188 | A | ATGTGTGT others(3): Show |
7 | a0001c0001t0002g0228 a0001c0001t0002g0231 a0001c0001t0002g0233 others(4): Show |
7 | HG01106.hp2 HG01168.hp1 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.1051+129_1051+138d others(12): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 122868188 | ||||||
| chr11:122868188 | A | ATGTGTGT others(5): Show |
2 | a0001c0001t0002g0202 a0011c0019t0009g0157 |
2 | HG01361.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1051+127_1051+138d others(14): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 122868188 | ||||||
| chr11:122868188 | A | ATGTGTGT others(7): Show |
1 | a0001c0001t0002g0226 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1051+125_1051+138d others(16): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 122868188 | ||||||
| chr11:122868188 | A | G | 1 | a0001c0001t0002g0280 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1051+89A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | chr11 | 122868188 | |||||||
| chr11:122868188 | ATG | A | 37 | a0001c0001t0001g0130 a0001c0001t0001g0302 a0001c0001t0002g0016 others(34): Show |
49 | HG01192.hp1 HG01243.hp2 HG01358.hp1 others(46): Show |
intron_variant | MODIFIER | c.1051+137_1051+138d others(4): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 122868188 | ||||||
| chr11:122868188 | ATGTG | A | 61 | a0001c0001t0001g0015 a0001c0001t0001g0029 a0001c0001t0001g0103 others(58): Show |
88 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(85): Show |
intron_variant | MODIFIER | c.1051+135_1051+138d others(6): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 122868188 | ||||||
| chr11:122868188 | ATGTGTG | A | 29 | a0001c0001t0001g0010 a0001c0001t0001g0080 a0001c0001t0001g0081 others(26): Show |
43 | HG00558.hp2 HG01099.hp1 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.1051+133_1051+138d others(8): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 122868188 | ||||||
| chr11:122868188 | ATGTGTGT others(1): Show |
A | 55 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0019 others(52): Show |
72 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.1051+131_1051+138d others(10): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 122868188 | ||||||
| chr11:122868188 | ATGTGTGT others(3): Show |
A | 21 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0026 others(18): Show |
30 | HG00408.hp2 HG00438.hp2 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.1051+129_1051+138d others(12): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 122868188 | ||||||
| chr11:122868188 | ATGTGTGT others(5): Show |
A | 2 | a0001c0001t0001g0110 a0008c0011t0001g0214 |
2 | HG01257.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1051+127_1051+138d others(14): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 122868188 | ||||||
| chr11:122868188 | ATGTGTGT others(7): Show |
A | 1 | a0003c0003t0003g0284 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1051+125_1051+138d others(16): Show |
CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 122868188 | ||||||
| chr11:122868247 | G | A | 4 | a0002c0002t0001g0057 a0002c0002t0001g0159 a0002c0002t0001g0289 others(1): Show |
4 | HG02630.hp2 HG02886.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1051+148G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | chr11 | 122868247 | |||||||
| chr11:122868866 | G | A | 3 | a0002c0016t0001g0065 a0004c0008t0001g0052 a0004c0008t0001g0320 |
3 | HG00642.hp2 HG02970.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1051+767G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | chr11 | 122868866 | |||||||
| chr11:122868928 | G | A | 1 | a0001c0001t0002g0151 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1051+829G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | chr11 | 122868928 | |||||||
| chr11:122868933 | C | T | 1 | a0002c0002t0006g0063 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1051+834C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | chr11 | 122868933 | |||||||
| chr11:122868958 | G | A | 7 | a0002c0002t0007g0068 a0002c0002t0007g0205 a0002c0002t0007g0286 others(4): Show |
7 | HG02647.hp1 HG02922.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.1051+859G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | chr11 | 122868958 | |||||||
| chr11:122868967 | C | A | 1 | a0001c0001t0002g0025 | 2 | HG01070.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.1051+868C>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | chr11 | 122868967 | |||||||
| chr11:122869009 | A | G | 217 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(214): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.1051+910A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | chr11 | 122869009 | |||||||
| chr11:122869051 | C | A | 1 | a0002c0002t0005g0117 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1051+952C>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | chr11 | 122869051 | |||||||
| chr11:122869375 | A | C | 20 | a0002c0002t0006g0017 a0002c0002t0006g0059 a0002c0002t0006g0063 others(17): Show |
22 | HG00621.hp2 HG00738.hp2 HG01081.hp2 others(19): Show |
intron_variant | MODIFIER | c.1051+1276A>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | chr11 | 122869375 | |||||||
| chr11:122869387 | A | G | 42 | a0003c0003t0003g0004 a0003c0003t0003g0008 a0003c0003t0003g0012 others(39): Show |
64 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.1051+1288A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | chr11 | 122869387 | |||||||
| chr11:122869493 | G | A | 3 | a0002c0002t0006g0171 a0002c0002t0006g0174 a0002c0002t0006g0175 |
3 | HG02602.hp2 HG03491.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1051+1394G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | chr11 | 122869493 | |||||||
| chr11:122869552 | A | G | 1 | a0001c0001t0001g0140 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1051+1453A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | chr11 | 122869552 | |||||||
| chr11:122869704 | G | A | 2 | a0001c0001t0002g0143 a0001c0001t0002g0144 |
2 | HG03834.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1052-1565G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | chr11 | 122869704 | |||||||
| chr11:122869820 | T | C | 4 | a0003c0003t0003g0048 a0003c0003t0003g0091 a0003c0003t0003g0272 others(1): Show |
5 | HG00544.hp1 NA18957.hp1 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.1052-1449T>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | chr11 | 122869820 | |||||||
| chr11:122869838 | G | C | 12 | a0002c0002t0001g0057 a0002c0002t0001g0159 a0002c0002t0001g0253 others(9): Show |
12 | HG00642.hp2 HG02572.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1052-1431G>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | chr11 | 122869838 | |||||||
| chr11:122870005 | C | T | 1 | a0002c0016t0001g0065 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1052-1264C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | chr11 | 122870005 | |||||||
| chr11:122870149 | T | C | 2 | a0004c0010t0007g0213 a0004c0010t0015g0207 |
2 | HG02630.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1052-1120T>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | chr11 | 122870149 | |||||||
| chr11:122870152 | G | T | 12 | a0002c0002t0001g0057 a0002c0002t0001g0159 a0002c0002t0001g0253 others(9): Show |
12 | HG00642.hp2 HG02572.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1052-1117G>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | chr11 | 122870152 | |||||||
| chr11:122870173 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1052-1096C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | chr11 | 122870173 | |||||||
| chr11:122870174 | G | A | 1 | a0002c0004t0004g0071 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1052-1095G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | chr11 | 122870174 | |||||||
| chr11:122870187 | C | T | 5 | a0002c0002t0007g0068 a0002c0002t0007g0205 a0002c0002t0007g0286 others(2): Show |
5 | HG02922.hp2 HG02965.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1052-1082C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | chr11 | 122870187 | |||||||
| chr11:122870219 | T | C | 7 | a0002c0002t0007g0068 a0002c0002t0007g0205 a0002c0002t0007g0286 others(4): Show |
7 | HG02647.hp1 HG02922.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.1052-1050T>C | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | chr11 | 122870219 | |||||||
| chr11:122870229 | C | T | 1 | a0003c0003t0003g0266 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1052-1040C>T | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | chr11 | 122870229 | |||||||
| chr11:122870291 | G | A | 2 | a0001c0001t0002g0037 a0001c0001t0016g0037 |
2 | HG02698.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.1052-978G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | chr11 | 122870291 | |||||||
| chr11:122870307 | C | G | 1 | a0001c0001t0001g0122 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1052-962C>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | chr11 | 122870307 | |||||||
| chr11:122870515 | G | A | 1 | a0002c0002t0005g0250 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1052-754G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | chr11 | 122870515 | |||||||
| chr11:122870628 | C | A | 2 | a0002c0002t0001g0057 a0002c0002t0001g0289 |
2 | HG02886.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1052-641C>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | chr11 | 122870628 | |||||||
| chr11:122870672 | A | G | 1 | a0001c0001t0001g0093 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1052-597A>G | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | chr11 | 122870672 | |||||||
| chr11:122871057 | T | A | 1 | a0001c0001t0008g0096 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1052-212T>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | chr11 | 122871057 | |||||||
| chr11:122871092 | G | A | 31 | a0001c0001t0007g0149 a0002c0002t0006g0017 a0002c0002t0006g0059 others(28): Show |
33 | HG00621.hp2 HG00738.hp2 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.1052-177G>A | CRTAM | ENSG00000109943.9 | transcript | ENST00000227348.9 | protein_coding | 9/9 | chr11 | 122871092 |