Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 64127 |
| ensemblid | ENSG00000167207.15 |
| hgncid | 5331 |
| symbol | NOD2 |
| name | nucleotide binding oligomerization domain containing 2 |
| refseq_nuc | NM_001370466.1 |
| refseq_prot | NP_001357395.1 |
| ensembl_nuc | ENST00000647318.2 |
| ensembl_prot | ENSP00000495993.1 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 50693606 |
| end | 50733075 |
| strand | + |
| ver | v1.2 |
| region | chr16:50693606-50733075 |
| region5000 | chr16:50688606-50738075 |
| regionname0 | NOD2_chr16_50693606_50733075 |
| regionname5000 | NOD2_chr16_50688606_50738075 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1013 | 249 | 72 | 47 | 97 | 10 | 21 | 78 | NOD2_chr16_50688606_50738075 | NOD2 | MCSQE others(1008): Show |
chr16 | 50688606 | 50738075 |
| a0002 | 0/0 | 1013 | 18 | 2 | 10 | 1 | 1 | 4 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | MCSQE others(1008): Show |
chr16 | 50688606 | 50738075 |
| a0003 | 0/0 | 1013 | 10 | 0 | 6 | 0 | 4 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | MCSQE others(1008): Show |
chr16 | 50688606 | 50738075 |
| a0004 | 0/0 | 1013 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | MCSQE others(1008): Show |
chr16 | 50688606 | 50738075 |
| a0005 | 0/0 | 1013 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | MCSQE others(1008): Show |
chr16 | 50688606 | 50738075 |
| a0006 | 0/0 | 1013 | 3 | 0 | 2 | 0 | 0 | 1 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | MCSQE others(1008): Show |
chr16 | 50688606 | 50738075 |
| a0007 | 0/0 | 1013 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | MCSQE others(1008): Show |
chr16 | 50688606 | 50738075 |
| a0008 | 0/0 | 1013 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | MCSQE others(1008): Show |
chr16 | 50688606 | 50738075 |
| a0009 | 0/0 | 1013 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | MCSQE others(1008): Show |
chr16 | 50688606 | 50738075 |
| a0010 | 0/0 | 1013 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | MCSQE others(1008): Show |
chr16 | 50688606 | 50738075 |
| a0011 | 0/0 | 1013 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | MCSQE others(1008): Show |
chr16 | 50688606 | 50738075 |
| a0012 | 0/0 | 1013 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | MCSQE others(1008): Show |
chr16 | 50688606 | 50738075 |
| a0013 | 0/0 | 1013 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | MCSQE others(1008): Show |
chr16 | 50688606 | 50738075 |
| a0014 | 0/0 | 1013 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | MCSQE others(1008): Show |
chr16 | 50688606 | 50738075 |
| a0015 | 0/0 | 1013 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | MCSQE others(1008): Show |
chr16 | 50688606 | 50738075 |
| a0016 | 0/0 | 1013 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | MCSQE others(1008): Show |
chr16 | 50688606 | 50738075 |
| a0017 | 0/0 | 1013 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | MCSQE others(1008): Show |
chr16 | 50688606 | 50738075 |
| a0018 | 0/0 | 1013 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NOD2_chr16_50688606_50738075 | NOD2 | MCSQE others(1008): Show |
chr16 | 50688606 | 50738075 |
| a0019 | 0/0 | 1013 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NOD2_chr16_50688606_50738075 | NOD2 | MCSQE others(1008): Show |
chr16 | 50688606 | 50738075 |
| a0020 | 0/0 | 1013 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | MCSQE others(1008): Show |
chr16 | 50688606 | 50738075 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 3039 | 153 | 38 | 28 | 66 | 5 | 15 | NOD2_chr16_50688606_50738075 | NOD2 | ATGTG others(3034): Show |
chr16 | 50688606 | 50738075 | ||
| a0001c0002 | 0/0 | 3039 | 35 | 8 | 3 | 23 | 0 | 1 | NOD2_chr16_50688606_50738075 | NOD2 | ATGTG others(3034): Show |
chr16 | 50688606 | 50738075 | ||
| a0001c0003 | 0/0 | 3039 | 30 | 19 | 3 | 7 | 1 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | ATGTG others(3034): Show |
chr16 | 50688606 | 50738075 | ||
| a0001c0004 | 0/0 | 3039 | 27 | 5 | 13 | 0 | 4 | 5 | NOD2_chr16_50688606_50738075 | NOD2 | ATGTG others(3034): Show |
chr16 | 50688606 | 50738075 | ||
| a0001c0018 | 0/0 | 3039 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | ATGTG others(3034): Show |
chr16 | 50688606 | 50738075 | ||
| a0001c0019 | 0/0 | 3039 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | ATGTG others(3034): Show |
chr16 | 50688606 | 50738075 | ||
| a0001c0025 | 0/1 | 3039 | 1 | 0 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | ATGTG others(3034): Show |
chr16 | 50688606 | 50738075 | ||
| a0001c0027 | 0/0 | 3039 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | ATGTG others(3034): Show |
chr16 | 50688606 | 50738075 | ||
| a0002c0005 | 0/0 | 3039 | 18 | 2 | 10 | 1 | 1 | 4 | NOD2_chr16_50688606_50738075 | NOD2 | ATGTG others(3034): Show |
chr16 | 50688606 | 50738075 | ||
| a0003c0006 | 0/0 | 3039 | 10 | 0 | 6 | 0 | 4 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | ATGTG others(3034): Show |
chr16 | 50688606 | 50738075 | ||
| a0004c0007 | 0/0 | 3039 | 6 | 6 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | ATGTG others(3034): Show |
chr16 | 50688606 | 50738075 | ||
| a0005c0008 | 0/0 | 3039 | 4 | 4 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | ATGTG others(3034): Show |
chr16 | 50688606 | 50738075 | ||
| a0005c0026 | 0/0 | 3039 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | ATGTG others(3034): Show |
chr16 | 50688606 | 50738075 | ||
| a0006c0010 | 0/0 | 3039 | 3 | 0 | 2 | 0 | 0 | 1 | NOD2_chr16_50688606_50738075 | NOD2 | ATGTG others(3034): Show |
chr16 | 50688606 | 50738075 | ||
| a0007c0009 | 0/0 | 3039 | 3 | 3 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | ATGTG others(3034): Show |
chr16 | 50688606 | 50738075 | ||
| a0008c0011 | 0/0 | 3039 | 3 | 3 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | ATGTG others(3034): Show |
chr16 | 50688606 | 50738075 | ||
| a0009c0013 | 0/0 | 3039 | 2 | 0 | 2 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | ATGTG others(3034): Show |
chr16 | 50688606 | 50738075 | ||
| a0010c0014 | 0/0 | 3039 | 2 | 2 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | ATGTG others(3034): Show |
chr16 | 50688606 | 50738075 | ||
| a0011c0012 | 0/0 | 3039 | 2 | 2 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | ATGTG others(3034): Show |
chr16 | 50688606 | 50738075 | ||
| a0012c0023 | 0/0 | 3039 | 1 | 0 | 0 | 0 | 1 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | ATGTG others(3034): Show |
chr16 | 50688606 | 50738075 | ||
| a0013c0028 | 0/0 | 3039 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | ATGTG others(3034): Show |
chr16 | 50688606 | 50738075 | ||
| a0014c0022 | 0/0 | 3039 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | ATGTG others(3034): Show |
chr16 | 50688606 | 50738075 | ||
| a0015c0021 | 0/0 | 3039 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | ATGTG others(3034): Show |
chr16 | 50688606 | 50738075 | ||
| a0016c0024 | 0/0 | 3039 | 1 | 0 | 0 | 0 | 1 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | ATGTG others(3034): Show |
chr16 | 50688606 | 50738075 | ||
| a0017c0020 | 0/0 | 3039 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | ATGTG others(3034): Show |
chr16 | 50688606 | 50738075 | ||
| a0018c0015 | 0/0 | 3039 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | ATGTG others(3034): Show |
chr16 | 50688606 | 50738075 | ||
| a0019c0017 | 0/0 | 3039 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | ATGTG others(3034): Show |
chr16 | 50688606 | 50738075 | ||
| a0020c0016 | 0/0 | 3039 | 1 | 0 | 0 | 0 | 1 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | ATGTG others(3034): Show |
chr16 | 50688606 | 50738075 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 4363 | 126 | 21 | 27 | 58 | 5 | 14 | NOD2_chr16_50688606_50738075 | NOD2 | GGAGC others(4358): Show |
chr16 | 50688606 | 50738075 |
| a0001c0001t0002 | 0/0 | 4363 | 19 | 13 | 1 | 5 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | GGAGC others(4358): Show |
chr16 | 50688606 | 50738075 |
| a0001c0001t0004 | 0/0 | 4363 | 3 | 3 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | GGAGC others(4358): Show |
chr16 | 50688606 | 50738075 |
| a0001c0001t0005 | 0/0 | 4363 | 1 | 0 | 0 | 0 | 0 | 1 | NOD2_chr16_50688606_50738075 | NOD2 | GGAGC others(4358): Show |
chr16 | 50688606 | 50738075 |
| a0001c0001t0006 | 0/0 | 4363 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | GGAGC others(4358): Show |
chr16 | 50688606 | 50738075 |
| a0001c0001t0007 | 0/0 | 4341 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | GGAGC others(4336): Show |
chr16 | 50688606 | 50738075 |
| a0001c0001t0008 | 0/0 | 4363 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | GGAGC others(4358): Show |
chr16 | 50688606 | 50738075 |
| a0001c0001t0010 | 0/0 | 4363 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | GGAGC others(4358): Show |
chr16 | 50688606 | 50738075 |
| a0001c0002t0002 | 0/0 | 4363 | 35 | 8 | 3 | 23 | 0 | 1 | NOD2_chr16_50688606_50738075 | NOD2 | GGAGC others(4358): Show |
chr16 | 50688606 | 50738075 |
| a0001c0003t0001 | 0/0 | 4363 | 11 | 8 | 2 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | GGAGC others(4358): Show |
chr16 | 50688606 | 50738075 |
| a0001c0003t0002 | 0/0 | 4363 | 13 | 5 | 1 | 6 | 1 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | GGAGC others(4358): Show |
chr16 | 50688606 | 50738075 |
| a0001c0003t0003 | 0/0 | 4363 | 6 | 6 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | GGAGC others(4358): Show |
chr16 | 50688606 | 50738075 |
| a0001c0004t0002 | 0/0 | 4363 | 25 | 5 | 11 | 0 | 4 | 5 | NOD2_chr16_50688606_50738075 | NOD2 | GGAGC others(4358): Show |
chr16 | 50688606 | 50738075 |
| a0001c0004t0005 | 0/0 | 4363 | 2 | 0 | 2 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | GGAGC others(4358): Show |
chr16 | 50688606 | 50738075 |
| a0001c0018t0001 | 0/0 | 4363 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | GGAGC others(4358): Show |
chr16 | 50688606 | 50738075 |
| a0001c0019t0001 | 0/0 | 4363 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | GGAGC others(4358): Show |
chr16 | 50688606 | 50738075 |
| a0001c0025t0001 | 0/1 | 4363 | 1 | 0 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | GGAGC others(4358): Show |
chr16 | 50688606 | 50738075 |
| a0001c0027t0002 | 0/0 | 4363 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | GGAGC others(4358): Show |
chr16 | 50688606 | 50738075 |
| a0002c0005t0001 | 0/0 | 4363 | 17 | 2 | 10 | 1 | 1 | 3 | NOD2_chr16_50688606_50738075 | NOD2 | GGAGC others(4358): Show |
chr16 | 50688606 | 50738075 |
| a0002c0005t0009 | 0/0 | 4363 | 1 | 0 | 0 | 0 | 0 | 1 | NOD2_chr16_50688606_50738075 | NOD2 | GGAGC others(4358): Show |
chr16 | 50688606 | 50738075 |
| a0003c0006t0002 | 0/0 | 4363 | 10 | 0 | 6 | 0 | 4 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | GGAGC others(4358): Show |
chr16 | 50688606 | 50738075 |
| a0004c0007t0002 | 0/0 | 4363 | 6 | 6 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | GGAGC others(4358): Show |
chr16 | 50688606 | 50738075 |
| a0005c0008t0002 | 0/0 | 4363 | 4 | 4 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | GGAGC others(4358): Show |
chr16 | 50688606 | 50738075 |
| a0005c0026t0002 | 0/0 | 4363 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | GGAGC others(4358): Show |
chr16 | 50688606 | 50738075 |
| a0006c0010t0001 | 0/0 | 4363 | 3 | 0 | 2 | 0 | 0 | 1 | NOD2_chr16_50688606_50738075 | NOD2 | GGAGC others(4358): Show |
chr16 | 50688606 | 50738075 |
| a0007c0009t0002 | 0/0 | 4363 | 3 | 3 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | GGAGC others(4358): Show |
chr16 | 50688606 | 50738075 |
| a0008c0011t0002 | 0/0 | 4363 | 3 | 3 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | GGAGC others(4358): Show |
chr16 | 50688606 | 50738075 |
| a0009c0013t0001 | 0/0 | 4363 | 2 | 0 | 2 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | GGAGC others(4358): Show |
chr16 | 50688606 | 50738075 |
| a0010c0014t0002 | 0/0 | 4363 | 2 | 2 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | GGAGC others(4358): Show |
chr16 | 50688606 | 50738075 |
| a0011c0012t0002 | 0/0 | 4363 | 2 | 2 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | GGAGC others(4358): Show |
chr16 | 50688606 | 50738075 |
| a0012c0023t0002 | 0/0 | 4363 | 1 | 0 | 0 | 0 | 1 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | GGAGC others(4358): Show |
chr16 | 50688606 | 50738075 |
| a0013c0028t0001 | 0/0 | 4363 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | GGAGC others(4358): Show |
chr16 | 50688606 | 50738075 |
| a0014c0022t0001 | 0/0 | 4363 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | GGAGC others(4358): Show |
chr16 | 50688606 | 50738075 |
| a0015c0021t0001 | 0/0 | 4363 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | GGAGC others(4358): Show |
chr16 | 50688606 | 50738075 |
| a0016c0024t0002 | 0/0 | 4363 | 1 | 0 | 0 | 0 | 1 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | GGAGC others(4358): Show |
chr16 | 50688606 | 50738075 |
| a0017c0020t0002 | 0/0 | 4363 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | GGAGC others(4358): Show |
chr16 | 50688606 | 50738075 |
| a0018c0015t0001 | 0/0 | 4363 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | GGAGC others(4358): Show |
chr16 | 50688606 | 50738075 |
| a0019c0017t0001 | 0/0 | 4363 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | GGAGC others(4358): Show |
chr16 | 50688606 | 50738075 |
| a0020c0016t0001 | 0/0 | 4363 | 1 | 0 | 0 | 0 | 1 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | GGAGC others(4358): Show |
chr16 | 50688606 | 50738075 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 10 | 0 | 7 | 0 | 1 | 2 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0002 | 0/0 | 8 | 0 | 1 | 7 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0037 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0002g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0002g0013 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0002g0017 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0002g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0004g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0004g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0004g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0005g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0006g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0007g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0008g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0001t0010g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0002t0002g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0002t0002g0018 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0002t0002g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0002t0002g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0002t0002g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0002t0002g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0002t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0002t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0002t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0002t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0002t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0002t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0002t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0002t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0002t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0003t0001g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0003t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0003t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0003t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0003t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0003t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0003t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0003t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0003t0002g0005 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0003t0002g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0003t0002g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0003t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0003t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0003t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0003t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0003t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0003t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0003t0003g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0003t0003g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0003t0003g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0003t0003g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0003t0003g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0004t0002g0003 | 0/0 | 5 | 0 | 3 | 0 | 1 | 1 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0004t0002g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0004t0002g0026 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0004t0002g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0004t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0004t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0004t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0004t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0004t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0004t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0004t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0004t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0004t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0004t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0004t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0004t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0004t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0004t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0004t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0004t0005g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0018t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0019t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0025t0001g0202 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0001c0027t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0002c0005t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0002c0005t0001g0007 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0002c0005t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0002c0005t0001g0020 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0002c0005t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0002c0005t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0002c0005t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0002c0005t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0002c0005t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0002c0005t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0002c0005t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0002c0005t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0002c0005t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0002c0005t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0002c0005t0009g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0003c0006t0002g0003 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0003c0006t0002g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0003c0006t0002g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0003c0006t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0003c0006t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0003c0006t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0003c0006t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0003c0006t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0004c0007t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0004c0007t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0004c0007t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0004c0007t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0004c0007t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0004c0007t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0005c0008t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0005c0008t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0005c0008t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0005c0008t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0005c0026t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0006c0010t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0006c0010t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0006c0010t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0007c0009t0002g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0007c0009t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0008c0011t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0008c0011t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0008c0011t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0009c0013t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0009c0013t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0010c0014t0002g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0011c0012t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0011c0012t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0012c0023t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0013c0028t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0014c0022t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0015c0021t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0016c0024t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0017c0020t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0018c0015t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0019c0017t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| a0020c0016t0001g0004 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0012 | c0023 | t0002 | g0053 | EUR | GBR | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG00140 | hp1 | a0003 | c0006 | t0002 | g0025 | EUR | GBR | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG00140 | hp2 | a0001 | c0004 | t0002 | g0084 | EUR | GBR | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG00280 | hp1 | a0001 | c0003 | t0002 | g0005 | EUR | FIN | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG00280 | hp2 | a0001 | c0004 | t0002 | g0098 | EUR | FIN | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG00323 | hp1 | a0001 | c0004 | t0002 | g0003 | EUR | FIN | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0155 | EUR | FIN | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | CHS | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG00408 | hp2 | a0001 | c0018 | t0001 | g0002 | EAS | CHS | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG00423 | hp2 | a0001 | c0002 | t0002 | g0209 | EAS | CHS | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG00621 | hp1 | a0001 | c0002 | t0002 | g0219 | EAS | CHS | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | CHS | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0017 | AMR | PUR | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG00642 | hp1 | a0002 | c0005 | t0001 | g0004 | AMR | PUR | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG00733 | hp1 | a0002 | c0005 | t0001 | g0198 | AMR | PUR | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG00735 | hp1 | a0006 | c0010 | t0001 | g0021 | AMR | PUR | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG00735 | hp2 | a0001 | c0004 | t0002 | g0086 | AMR | PUR | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG00738 | hp1 | a0001 | c0004 | t0002 | g0085 | AMR | PUR | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG00738 | hp2 | a0006 | c0010 | t0001 | g0067 | AMR | PUR | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG01070 | hp1 | a0002 | c0005 | t0001 | g0204 | AMR | PUR | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG01071 | hp2 | a0002 | c0005 | t0001 | g0205 | AMR | PUR | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG01074 | hp1 | a0001 | c0004 | t0002 | g0089 | AMR | PUR | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG01074 | hp2 | a0002 | c0005 | t0001 | g0201 | AMR | PUR | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG01081 | hp1 | a0002 | c0005 | t0001 | g0019 | AMR | PUR | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG01081 | hp2 | a0003 | c0006 | t0002 | g0075 | AMR | PUR | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG01099 | hp2 | a0003 | c0006 | t0002 | g0101 | AMR | PUR | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG01106 | hp1 | a0001 | c0003 | t0001 | g0079 | AMR | PUR | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG01106 | hp2 | a0001 | c0004 | t0002 | g0026 | AMR | PUR | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG01109 | hp1 | a0001 | c0003 | t0002 | g0081 | AMR | PUR | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG01109 | hp2 | a0013 | c0028 | t0001 | g0200 | AMR | PUR | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG01168 | hp1 | a0001 | c0004 | t0005 | g0028 | AMR | PUR | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG01168 | hp2 | a0003 | c0006 | t0002 | g0090 | AMR | PUR | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG01169 | hp2 | a0001 | c0004 | t0005 | g0028 | AMR | PUR | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG01175 | hp1 | a0002 | c0005 | t0001 | g0007 | AMR | PUR | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG01175 | hp2 | a0001 | c0002 | t0002 | g0018 | AMR | PUR | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG01192 | hp2 | a0001 | c0004 | t0002 | g0003 | AMR | PUR | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG01243 | hp1 | a0015 | c0021 | t0001 | g0004 | AMR | PUR | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG01255 | hp1 | a0003 | c0006 | t0002 | g0043 | AMR | CLM | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG01255 | hp2 | a0009 | c0013 | t0001 | g0004 | AMR | CLM | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | CLM | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG01256 | hp2 | a0003 | c0006 | t0002 | g0043 | AMR | CLM | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | CLM | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG01261 | hp2 | a0001 | c0004 | t0002 | g0003 | AMR | CLM | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG01361 | hp2 | a0002 | c0005 | t0001 | g0020 | AMR | CLM | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG01433 | hp1 | a0009 | c0013 | t0001 | g0063 | AMR | CLM | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | CLM | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG01496 | hp2 | a0001 | c0004 | t0002 | g0087 | AMR | CLM | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG01515 | hp1 | a0003 | c0006 | t0002 | g0206 | EUR | IBS | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG01515 | hp2 | a0016 | c0024 | t0002 | g0088 | EUR | IBS | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG01516 | hp1 | a0002 | c0005 | t0001 | g0020 | EUR | IBS | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0031 | EUR | IBS | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0031 | EUR | IBS | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG01517 | hp2 | a0003 | c0006 | t0002 | g0207 | EUR | IBS | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG01884 | hp1 | a0001 | c0003 | t0002 | g0024 | AFR | ACB | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG01884 | hp2 | a0001 | c0003 | t0003 | g0030 | AFR | ACB | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG01891 | hp1 | a0001 | c0003 | t0003 | g0030 | AFR | ACB | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG01891 | hp2 | a0004 | c0007 | t0002 | g0071 | AFR | ACB | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG01928 | hp2 | a0001 | c0002 | t0002 | g0018 | AMR | PEL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PEL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PEL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG01943 | hp1 | a0001 | c0004 | t0002 | g0025 | AMR | PEL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG01952 | hp2 | a0001 | c0004 | t0002 | g0095 | AMR | PEL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG01981 | hp1 | a0002 | c0005 | t0001 | g0019 | AMR | PEL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG01993 | hp1 | a0001 | c0004 | t0002 | g0003 | AMR | PEL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PEL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG02004 | hp2 | a0001 | c0002 | t0002 | g0018 | AMR | PEL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG02040 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | KHV | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | ACB | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG02055 | hp2 | a0001 | c0001 | t0006 | g0050 | AFR | ACB | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG02056 | hp2 | a0002 | c0005 | t0001 | g0007 | EAS | KHV | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG02132 | hp2 | a0001 | c0002 | t0002 | g0223 | EAS | KHV | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG02135 | hp1 | a0001 | c0003 | t0001 | g0115 | EAS | KHV | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | ACB | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG02145 | hp2 | a0005 | c0008 | t0002 | g0216 | AFR | ACB | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG02257 | hp1 | a0010 | c0014 | t0002 | g0033 | AFR | ACB | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | ACB | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG02258 | hp1 | a0001 | c0004 | t0002 | g0105 | AFR | ACB | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG02258 | hp2 | a0001 | c0002 | t0002 | g0082 | AFR | ACB | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG02273 | hp1 | a0001 | c0003 | t0001 | g0094 | AMR | PEL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG02273 | hp2 | a0001 | c0004 | t0002 | g0102 | AMR | PEL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG02280 | hp1 | a0007 | c0009 | t0002 | g0022 | AFR | ACB | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG02280 | hp2 | a0001 | c0003 | t0001 | g0077 | AFR | ACB | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG02300 | hp2 | a0002 | c0005 | t0001 | g0208 | AMR | PEL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG02451 | hp1 | a0001 | c0003 | t0001 | g0008 | AFR | ACB | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG02451 | hp2 | a0001 | c0001 | t0004 | g0058 | AFR | ACB | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG02572 | hp1 | a0001 | c0002 | t0002 | g0116 | AFR | GWD | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | GWD | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG02602 | hp1 | a0002 | c0005 | t0001 | g0065 | SAS | PJL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG02602 | hp2 | a0006 | c0010 | t0001 | g0066 | SAS | PJL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG02615 | hp1 | a0001 | c0002 | t0002 | g0034 | AFR | GWD | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0114 | AFR | GWD | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG02622 | hp1 | a0001 | c0003 | t0002 | g0024 | AFR | GWD | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG02622 | hp2 | a0001 | c0002 | t0002 | g0032 | AFR | GWD | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG02630 | hp1 | a0011 | c0012 | t0002 | g0070 | AFR | GWD | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG02630 | hp2 | a0005 | c0026 | t0002 | g0044 | AFR | GWD | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG02647 | hp1 | a0001 | c0003 | t0003 | g0108 | AFR | GWD | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG02647 | hp2 | a0001 | c0003 | t0002 | g0211 | AFR | GWD | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0182 | AFR | GWD | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG02717 | hp2 | a0001 | c0003 | t0002 | g0210 | AFR | GWD | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG02723 | hp1 | a0011 | c0012 | t0002 | g0069 | AFR | GWD | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG02723 | hp2 | a0008 | c0011 | t0002 | g0093 | AFR | GWD | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG02738 | hp1 | a0001 | c0004 | t0002 | g0054 | SAS | PJL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG02809 | hp1 | a0001 | c0003 | t0001 | g0008 | AFR | GWD | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG02809 | hp2 | a0001 | c0001 | t0004 | g0059 | AFR | GWD | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG02818 | hp1 | a0001 | c0003 | t0003 | g0055 | AFR | GWD | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG02818 | hp2 | a0001 | c0027 | t0002 | g0096 | AFR | GWD | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG02886 | hp1 | a0008 | c0011 | t0002 | g0091 | AFR | GWD | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG02886 | hp2 | a0001 | c0003 | t0001 | g0076 | AFR | GWD | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG02895 | hp1 | a0001 | c0002 | t0002 | g0034 | AFR | GWD | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG02895 | hp2 | a0004 | c0007 | t0002 | g0111 | AFR | GWD | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | GWD | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG02896 | hp2 | a0001 | c0019 | t0001 | g0064 | AFR | GWD | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | GWD | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG02897 | hp2 | a0001 | c0002 | t0002 | g0117 | AFR | GWD | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | ESN | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG02922 | hp2 | a0001 | c0004 | t0002 | g0125 | AFR | ESN | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG02970 | hp1 | a0001 | c0003 | t0001 | g0023 | AFR | ESN | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG02970 | hp2 | a0005 | c0008 | t0002 | g0214 | AFR | ESN | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0060 | AFR | ESN | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | ESN | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG03017 | hp1 | a0001 | c0004 | t0002 | g0027 | SAS | PJL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG03041 | hp1 | a0001 | c0002 | t0002 | g0112 | AFR | GWD | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG03041 | hp2 | a0002 | c0005 | t0001 | g0197 | AFR | GWD | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG03098 | hp1 | a0007 | c0009 | t0002 | g0068 | AFR | MSL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | MSL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG03130 | hp1 | a0004 | c0007 | t0002 | g0073 | AFR | ESN | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG03130 | hp2 | a0001 | c0003 | t0001 | g0008 | AFR | ESN | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | ESN | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG03139 | hp2 | a0017 | c0020 | t0002 | g0169 | AFR | ESN | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG03195 | hp1 | a0001 | c0004 | t0002 | g0106 | AFR | ESN | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG03195 | hp2 | a0001 | c0003 | t0002 | g0080 | AFR | ESN | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | MSL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | MSL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0040 | AFR | MSL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | MSL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG03239 | hp1 | a0001 | c0004 | t0002 | g0097 | SAS | PJL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG03239 | hp2 | a0001 | c0002 | t0002 | g0100 | SAS | PJL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG03453 | hp1 | a0010 | c0014 | t0002 | g0033 | AFR | MSL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG03453 | hp2 | a0004 | c0007 | t0002 | g0072 | AFR | MSL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG03486 | hp1 | a0001 | c0003 | t0001 | g0078 | AFR | MSL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG03486 | hp2 | a0001 | c0002 | t0002 | g0032 | AFR | MSL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | ESN | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | ESN | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG03540 | hp2 | a0002 | c0005 | t0001 | g0199 | AFR | GWD | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | MSL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | MSL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG03654 | hp1 | a0002 | c0005 | t0009 | g0007 | SAS | PJL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0174 | SAS | PJL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG03669 | hp1 | a0001 | c0004 | t0002 | g0027 | SAS | PJL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | STU | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG03688 | hp2 | a0002 | c0005 | t0001 | g0192 | SAS | STU | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0173 | SAS | BEB | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | BEB | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG04115 | hp1 | a0001 | c0004 | t0002 | g0003 | SAS | STU | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | STU | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG04204 | hp1 | a0001 | c0001 | t0005 | g0104 | SAS | STU | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | STU | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | STU | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG04228 | hp2 | a0002 | c0005 | t0001 | g0021 | SAS | STU | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA18906 | hp1 | a0001 | c0003 | t0001 | g0023 | AFR | YRI | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA18906 | hp2 | a0005 | c0008 | t0002 | g0044 | AFR | YRI | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA18940 | hp2 | a0001 | c0002 | t0002 | g0225 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA18941 | hp2 | a0001 | c0002 | t0002 | g0224 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA18942 | hp1 | a0001 | c0002 | t0002 | g0221 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA18945 | hp2 | a0001 | c0002 | t0002 | g0045 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA18947 | hp2 | a0001 | c0003 | t0002 | g0029 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA18950 | hp1 | a0001 | c0001 | t0008 | g0126 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA18957 | hp2 | a0001 | c0002 | t0002 | g0218 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA18960 | hp2 | a0001 | c0002 | t0002 | g0162 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA18961 | hp2 | a0001 | c0002 | t0002 | g0220 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA18964 | hp1 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA18978 | hp1 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA18979 | hp1 | a0001 | c0001 | t0010 | g0156 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA18982 | hp1 | a0001 | c0002 | t0002 | g0222 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA18995 | hp1 | a0001 | c0003 | t0002 | g0029 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA18995 | hp2 | a0001 | c0002 | t0002 | g0163 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA18999 | hp1 | a0001 | c0002 | t0002 | g0226 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA19002 | hp1 | a0018 | c0015 | t0001 | g0035 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA19002 | hp2 | a0001 | c0003 | t0002 | g0083 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA19005 | hp1 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA19011 | hp1 | a0001 | c0002 | t0002 | g0046 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA19011 | hp2 | a0001 | c0001 | t0007 | g0140 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | LWK | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA19030 | hp2 | a0008 | c0011 | t0002 | g0092 | AFR | LWK | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA19043 | hp1 | a0001 | c0003 | t0003 | g0107 | AFR | LWK | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | LWK | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA19054 | hp1 | a0001 | c0002 | t0002 | g0045 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA19057 | hp1 | a0019 | c0017 | t0001 | g0014 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA19062 | hp1 | a0001 | c0003 | t0002 | g0074 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA19072 | hp2 | a0001 | c0002 | t0002 | g0212 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA19078 | hp2 | a0001 | c0002 | t0002 | g0213 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA19080 | hp1 | a0001 | c0003 | t0002 | g0005 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA19081 | hp1 | a0001 | c0002 | t0002 | g0217 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA19083 | hp1 | a0001 | c0003 | t0002 | g0005 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA19084 | hp1 | a0001 | c0002 | t0002 | g0046 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | YRI | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0040 | AFR | YRI | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | ASW | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | ASW | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA20752 | hp1 | a0020 | c0016 | t0001 | g0004 | EUR | TSI | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA20752 | hp2 | a0001 | c0004 | t0002 | g0099 | EUR | TSI | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA20805 | hp1 | a0003 | c0006 | t0002 | g0003 | EUR | TSI | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0118 | EUR | TSI | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG01123 | hp1 | a0003 | c0006 | t0002 | g0003 | AMR | CLM | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG01123 | hp2 | a0014 | c0022 | t0001 | g0004 | AMR | CLM | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0168 | AFR | ACB | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG02109 | hp2 | a0001 | c0004 | t0002 | g0026 | AFR | ACB | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG02486 | hp1 | a0007 | c0009 | t0002 | g0022 | AFR | ACB | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0227 | AFR | ACB | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | ACB | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG02559 | hp2 | a0005 | c0008 | t0002 | g0215 | AFR | ACB | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG03471 | hp1 | a0001 | c0003 | t0003 | g0005 | AFR | MSL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG03471 | hp2 | a0001 | c0004 | t0002 | g0103 | AFR | MSL | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG06807 | hp1 | a0004 | c0007 | t0002 | g0183 | AFR | USA | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | USA | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0166 | AFR | USA | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA20300 | hp2 | a0004 | c0007 | t0002 | g0110 | AFR | USA | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | LWK | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | LWK | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| homoSapiens | chm13v2 | a0001 | c0025 | t0001 | g0202 | REF | REF | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0037 | REF | REF | NOD2_chr16_50688606_50738075 | NOD2 | chr16 | 50688606 | 50738075 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:50699742 | G | A | 1 | a0018 | 1 | NA19002.hp1 | missense_variant | MODERATE | c.247G>A | p.Ala83Thr | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/12 | 312/4363 | 247/3042 | 83/1013 | chr16 | 50699742 | |||
| chr16:50699827 | G | A | 1 | a0020 | 1 | NA20752.hp1 | missense_variant | MODERATE | c.332G>A | p.Arg111Gln | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/12 | 397/4363 | 332/3042 | 111/1013 | chr16 | 50699827 | |||
| chr16:50699832 | G | A | 1 | a0011 | 2 | HG02630.hp1 HG02723.hp1 |
missense_variant | MODERATE | c.337G>A | p.Ala113Thr | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/12 | 402/4363 | 337/3042 | 113/1013 | chr16 | 50699832 | |||
| chr16:50707880 | C | T | 1 | a0010 | 2 | HG02257.hp1 HG03453.hp1 |
missense_variant | MODERATE | c.485C>T | p.Thr162Met | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 3/12 | 550/4363 | 485/3042 | 162/1013 | chr16 | 50707880 | |||
| chr16:50710713 | C | T | 7 | a0002 a0006 a0009 others(4): Show |
27 | HG00642.hp1 HG00733.hp1 HG00735.hp1 others(24): Show |
missense_variant | MODERATE | c.721C>T | p.Pro241Ser | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/12 | 786/4363 | 721/3042 | 241/1013 | chr16 | 50710713 | |||
| chr16:50710786 | C | T | 1 | a0017 | 1 | HG03139.hp2 | missense_variant | MODERATE | c.794C>T | p.Ala265Val | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/12 | 859/4363 | 794/3042 | 265/1013 | chr16 | 50710786 | |||
| chr16:50710966 | A | G | 1 | a0007 | 3 | HG02280.hp1 HG02486.hp1 HG03098.hp1 |
missense_variant | MODERATE | c.974A>G | p.His325Arg | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/12 | 1039/4363 | 974/3042 | 325/1013 | chr16 | 50710966 | |||
| chr16:50711196 | G | A | 1 | a0019 | 1 | NA19057.hp1 | missense_variant | MODERATE | c.1204G>A | p.Ala402Thr | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/12 | 1269/4363 | 1204/3042 | 402/1013 | chr16 | 50711196 | |||
| chr16:50711685 | G | A | 1 | a0013 | 1 | HG01109.hp2 | missense_variant | MODERATE | c.1693G>A | p.Val565Met | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/12 | 1758/4363 | 1693/3042 | 565/1013 | chr16 | 50711685 | |||
| chr16:50711845 | C | G | 1 | a0016 | 1 | HG01515.hp2 | missense_variant | MODERATE | c.1853C>G | p.Pro618Arg | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/12 | 1918/4363 | 1853/3042 | 618/1013 | chr16 | 50711845 | |||
| chr16:50711962 | G | A | 1 | a0008 | 3 | HG02723.hp2 HG02886.hp1 NA19030.hp2 |
missense_variant | MODERATE | c.1970G>A | p.Arg657Gln | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/12 | 2035/4363 | 1970/3042 | 657/1013 | chr16 | 50711962 | |||
| chr16:50712015 | C | T | 1 | a0009 | 2 | HG01255.hp2 HG01433.hp1 |
missense_variant | MODERATE | c.2023C>T | p.Arg675Trp | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/12 | 2088/4363 | 2023/3042 | 675/1013 | chr16 | 50712015 | |||
| chr16:50712018 | C | T | 1 | a0012 | 1 | HG00099.hp1 | missense_variant | MODERATE | c.2026C>T | p.Arg676Cys | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/12 | 2091/4363 | 2026/3042 | 676/1013 | chr16 | 50712018 | |||
| chr16:50712085 | C | G | 1 | a0005 | 5 | HG02145.hp2 HG02559.hp2 HG02630.hp2 others(2): Show |
missense_variant | MODERATE | c.2093C>G | p.Ala698Gly | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/12 | 2158/4363 | 2093/3042 | 698/1013 | chr16 | 50712085 | |||
| chr16:50712280 | G | A | 1 | a0004 | 6 | HG01891.hp2 HG02895.hp2 HG03130.hp1 others(3): Show |
missense_variant | MODERATE | c.2288G>A | p.Arg763Gln | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/12 | 2353/4363 | 2288/3042 | 763/1013 | chr16 | 50712280 | |||
| chr16:50716899 | A | G | 1 | a0014 | 1 | HG01123.hp2 | missense_variant | MODERATE | c.2474A>G | p.Asn825Ser | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 6/12 | 2539/4363 | 2474/3042 | 825/1013 | chr16 | 50716899 | |||
| chr16:50716931 | A | G | 1 | a0015 | 1 | HG01243.hp1 | missense_variant | MODERATE | c.2506A>G | p.Met836Val | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 6/12 | 2571/4363 | 2506/3042 | 836/1013 | chr16 | 50716931 | |||
| chr16:50722629 | G | C | 1 | a0006 | 3 | HG00735.hp1 HG00738.hp2 HG02602.hp2 |
missense_variant | MODERATE | c.2641G>C | p.Gly881Arg | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 8/12 | 2706/4363 | 2641/3042 | 881/1013 | chr16 | 50722629 | |||
| chr16:50723365 | G | A | 1 | a0003 | 10 | HG00140.hp1 HG01081.hp2 HG01099.hp2 others(7): Show |
missense_variant | MODERATE | c.2782G>A | p.Val928Ile | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 9/12 | 2847/4363 | 2782/3042 | 928/1013 | chr16 | 50723365 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:50699753 | C | T | 1 | a0013c0028 | 1 | HG01109.hp2 | synonymous_variant | LOW | c.258C>T | p.Asp86Asp | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/12 | 323/4363 | 258/3042 | 86/1013 | chr16 | 50699753 | |||
| chr16:50699948 | C | G | 8 | a0001c0003 a0001c0004 a0001c0027 others(5): Show |
74 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(71): Show |
synonymous_variant | LOW | c.453C>G | p.Ser151Ser | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/12 | 518/4363 | 453/3042 | 151/1013 | chr16 | 50699948 | |||
| chr16:50710727 | C | T | 1 | a0001c0027 | 1 | HG02818.hp2 | synonymous_variant | LOW | c.735C>T | p.Ser245Ser | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/12 | 800/4363 | 735/3042 | 245/1013 | chr16 | 50710727 | |||
| chr16:50711192 | G | A | 1 | a0010c0014 | 2 | HG02257.hp1 HG03453.hp1 |
synonymous_variant | LOW | c.1200G>A | p.Pro400Pro | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/12 | 1265/4363 | 1200/3042 | 400/1013 | chr16 | 50711192 | |||
| chr16:50711288 | C | T | 8 | a0001c0019 a0002c0005 a0006c0010 others(5): Show |
28 | HG00642.hp1 HG00733.hp1 HG00735.hp1 others(25): Show |
synonymous_variant | LOW | c.1296C>T | p.Arg432Arg | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/12 | 1361/4363 | 1296/3042 | 432/1013 | chr16 | 50711288 | |||
| chr16:50711364 | C | T | 1 | a0004c0007 | 6 | HG01891.hp2 HG02895.hp2 HG03130.hp1 others(3): Show |
synonymous_variant | LOW | c.1372C>T | p.Leu458Leu | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/12 | 1437/4363 | 1372/3042 | 458/1013 | chr16 | 50711364 | |||
| chr16:50711672 | T | G | 8 | a0001c0002 a0001c0004 a0001c0027 others(5): Show |
80 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(77): Show |
synonymous_variant | LOW | c.1680T>G | p.Arg560Arg | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/12 | 1745/4363 | 1680/3042 | 560/1013 | chr16 | 50711672 | |||
| chr16:50716915 | C | T | 1 | a0001c0018 | 1 | HG00408.hp2 | synonymous_variant | LOW | c.2490C>T | p.Asp830Asp | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 6/12 | 2555/4363 | 2490/3042 | 830/1013 | chr16 | 50716915 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:50693632 | G | C | 1 | a0001c0001t0006 | 1 | HG02055.hp2 | 5_prime_UTR_variant | MODIFIER | c.-39G>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/12 | 5864 | chr16 | 50693632 | ||||||
| chr16:50731961 | A | G | 1 | a0001c0001t0010 | 1 | NA18979.hp1 | 3_prime_UTR_variant | MODIFIER | c.*142A>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 12/12 | 142 | chr16 | 50731961 | ||||||
| chr16:50732216 | A | C | 20 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(17): Show |
139 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(136): Show |
3_prime_UTR_variant | MODIFIER | c.*397A>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 12/12 | 397 | chr16 | 50732216 | ||||||
| chr16:50732278 | T | C | 1 | a0001c0001t0007 | 1 | NA19011.hp2 | 3_prime_UTR_variant | MODIFIER | c.*459T>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 12/12 | 459 | chr16 | 50732278 | ||||||
| chr16:50732290 | C | A | 1 | a0001c0001t0007 | 1 | NA19011.hp2 | 3_prime_UTR_variant | MODIFIER | c.*471C>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 12/12 | 471 | chr16 | 50732290 | ||||||
| chr16:50732291 | A | T | 1 | a0001c0001t0007 | 1 | NA19011.hp2 | 3_prime_UTR_variant | MODIFIER | c.*472A>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 12/12 | 472 | chr16 | 50732291 | ||||||
| chr16:50732292 | T | A | 1 | a0001c0001t0007 | 1 | NA19011.hp2 | 3_prime_UTR_variant | MODIFIER | c.*473T>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 12/12 | 473 | chr16 | 50732292 | ||||||
| chr16:50732293 | C | G | 1 | a0001c0001t0007 | 1 | NA19011.hp2 | 3_prime_UTR_variant | MODIFIER | c.*474C>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 12/12 | 474 | chr16 | 50732293 | ||||||
| chr16:50732302 | T | A | 1 | a0001c0001t0007 | 1 | NA19011.hp2 | 3_prime_UTR_variant | MODIFIER | c.*483T>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 12/12 | 483 | chr16 | 50732302 | ||||||
| chr16:50732303 | C | G | 1 | a0001c0001t0007 | 1 | NA19011.hp2 | 3_prime_UTR_variant | MODIFIER | c.*484C>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 12/12 | 484 | chr16 | 50732303 | ||||||
| chr16:50732304 | C | A | 1 | a0001c0001t0007 | 1 | NA19011.hp2 | 3_prime_UTR_variant | MODIFIER | c.*485C>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 12/12 | 485 | chr16 | 50732304 | ||||||
| chr16:50732305 | C | T | 1 | a0001c0001t0007 | 1 | NA19011.hp2 | 3_prime_UTR_variant | MODIFIER | c.*486C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 12/12 | 486 | chr16 | 50732305 | ||||||
| chr16:50732306 | C | A | 1 | a0001c0001t0007 | 1 | NA19011.hp2 | 3_prime_UTR_variant | MODIFIER | c.*487C>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 12/12 | 487 | chr16 | 50732306 | ||||||
| chr16:50732308 | T | G | 1 | a0001c0001t0007 | 1 | NA19011.hp2 | 3_prime_UTR_variant | MODIFIER | c.*489T>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 12/12 | 489 | chr16 | 50732308 | ||||||
| chr16:50732309 | C | T | 1 | a0001c0001t0007 | 1 | NA19011.hp2 | 3_prime_UTR_variant | MODIFIER | c.*490C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 12/12 | 490 | chr16 | 50732309 | ||||||
| chr16:50732310 | T | A | 1 | a0001c0001t0007 | 1 | NA19011.hp2 | 3_prime_UTR_variant | MODIFIER | c.*491T>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 12/12 | 491 | chr16 | 50732310 | ||||||
| chr16:50732312 | T | A | 1 | a0001c0001t0007 | 1 | NA19011.hp2 | 3_prime_UTR_variant | MODIFIER | c.*493T>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 12/12 | 493 | chr16 | 50732312 | ||||||
| chr16:50732314 | G | A | 1 | a0001c0001t0007 | 1 | NA19011.hp2 | 3_prime_UTR_variant | MODIFIER | c.*495G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 12/12 | 495 | chr16 | 50732314 | ||||||
| chr16:50732315 | TTCCTCCC others(15): Show |
T | 1 | a0001c0001t0007 | 1 | NA19011.hp2 | 3_prime_UTR_variant | MODIFIER | c.*498_*519delCCTCCC others(16): Show |
NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 12/12 | 498 | INFO_REALIGN_3_PRIME | chr16 | 50732315 | |||||
| chr16:50732340 | C | T | 1 | a0001c0003t0003 | 6 | HG01884.hp2 HG01891.hp1 HG02647.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*521C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 12/12 | 521 | chr16 | 50732340 | ||||||
| chr16:50732343 | A | T | 1 | a0001c0001t0007 | 1 | NA19011.hp2 | 3_prime_UTR_variant | MODIFIER | c.*524A>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 12/12 | 524 | chr16 | 50732343 | ||||||
| chr16:50732367 | T | G | 1 | a0001c0001t0007 | 1 | NA19011.hp2 | 3_prime_UTR_variant | MODIFIER | c.*548T>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 12/12 | 548 | chr16 | 50732367 | ||||||
| chr16:50732371 | G | T | 1 | a0001c0001t0007 | 1 | NA19011.hp2 | 3_prime_UTR_variant | MODIFIER | c.*552G>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 12/12 | 552 | chr16 | 50732371 | ||||||
| chr16:50732383 | C | A | 1 | a0001c0001t0007 | 1 | NA19011.hp2 | 3_prime_UTR_variant | MODIFIER | c.*564C>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 12/12 | 564 | chr16 | 50732383 | ||||||
| chr16:50732389 | C | A | 1 | a0001c0001t0007 | 1 | NA19011.hp2 | 3_prime_UTR_variant | MODIFIER | c.*570C>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 12/12 | 570 | chr16 | 50732389 | ||||||
| chr16:50732394 | A | T | 1 | a0001c0001t0007 | 1 | NA19011.hp2 | 3_prime_UTR_variant | MODIFIER | c.*575A>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 12/12 | 575 | chr16 | 50732394 | ||||||
| chr16:50732395 | T | G | 1 | a0001c0001t0007 | 1 | NA19011.hp2 | 3_prime_UTR_variant | MODIFIER | c.*576T>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 12/12 | 576 | chr16 | 50732395 | ||||||
| chr16:50732439 | G | A | 1 | a0001c0001t0004 | 3 | HG02451.hp2 HG02809.hp2 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*620G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 12/12 | 620 | chr16 | 50732439 | ||||||
| chr16:50732506 | C | T | 1 | a0002c0005t0009 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*687C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 12/12 | 687 | chr16 | 50732506 | ||||||
| chr16:50732565 | A | C | 1 | a0001c0001t0008 | 1 | NA18950.hp1 | 3_prime_UTR_variant | MODIFIER | c.*746A>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 12/12 | 746 | chr16 | 50732565 | ||||||
| chr16:50732975 | G | A | 18 | a0001c0001t0002 a0001c0001t0004 a0001c0002t0002 others(15): Show |
136 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(133): Show |
3_prime_UTR_variant | MODIFIER | c.*1156G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 12/12 | 1156 | chr16 | 50732975 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:50693726 | C | T | 26 | a0001c0001t0002g0017 a0001c0001t0002g0227 a0001c0002t0002g0006 others(23): Show |
35 | HG00423.hp2 HG00621.hp1 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.-9+64C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50693726 | |||||||
| chr16:50693877 | T | A | 1 | a0001c0001t0001g0047 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-9+215T>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50693877 | |||||||
| chr16:50693941 | T | TG | 29 | a0001c0001t0001g0049 a0001c0001t0001g0051 a0001c0001t0002g0017 others(26): Show |
38 | HG00423.hp2 HG00621.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.-9+282dupG | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50693941 | ||||||
| chr16:50694107 | C | T | 1 | a0002c0005t0001g0208 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-9+445C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50694107 | |||||||
| chr16:50694212 | T | G | 1 | a0001c0001t0001g0052 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-9+550T>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50694212 | |||||||
| chr16:50694502 | C | T | 3 | a0003c0006t0002g0043 a0003c0006t0002g0206 a0003c0006t0002g0207 |
4 | HG01255.hp1 HG01256.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+840C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50694502 | |||||||
| chr16:50694587 | G | C | 2 | a0001c0004t0002g0054 a0012c0023t0002g0053 |
2 | HG00099.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.-9+925G>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50694587 | |||||||
| chr16:50694695 | T | G | 27 | a0001c0001t0002g0017 a0001c0001t0002g0048 a0001c0001t0002g0227 others(24): Show |
36 | HG00423.hp2 HG00621.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.-9+1033T>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50694695 | |||||||
| chr16:50694816 | G | C | 1 | a0001c0003t0003g0055 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-9+1154G>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50694816 | |||||||
| chr16:50694942 | T | G | 1 | a0001c0001t0001g0056 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-9+1280T>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50694942 | |||||||
| chr16:50695082 | G | A | 1 | a0001c0002t0002g0209 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-9+1420G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50695082 | |||||||
| chr16:50695313 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-9+1651G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50695313 | |||||||
| chr16:50695432 | A | C | 2 | a0002c0005t0001g0204 a0002c0005t0001g0205 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-9+1770A>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50695432 | |||||||
| chr16:50695565 | A | G | 3 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0203 |
6 | NA18942.hp2 NA18956.hp2 NA19010.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9+1903A>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50695565 | |||||||
| chr16:50696014 | T | C | 1 | a0001c0001t0001g0203 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-9+2352T>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50696014 | |||||||
| chr16:50696139 | G | C | 3 | a0001c0001t0004g0058 a0001c0001t0004g0059 a0001c0001t0004g0060 |
3 | HG02451.hp2 HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-9+2477G>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50696139 | |||||||
| chr16:50696177 | G | T | 5 | a0002c0005t0001g0197 a0002c0005t0001g0198 a0002c0005t0001g0199 others(2): Show |
5 | HG00733.hp1 HG01074.hp2 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9+2515G>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50696177 | |||||||
| chr16:50696318 | G | A | 26 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0019t0001g0064 others(23): Show |
29 | HG00642.hp1 HG00733.hp1 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.-9+2656G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50696318 | |||||||
| chr16:50696535 | G | A | 65 | a0001c0001t0004g0058 a0001c0001t0004g0059 a0001c0001t0004g0060 others(62): Show |
83 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(80): Show |
intron_variant | MODIFIER | c.-9+2873G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50696535 | |||||||
| chr16:50696628 | T | C | 1 | a0001c0001t0001g0109 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-8-2860T>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50696628 | |||||||
| chr16:50696838 | G | A | 1 | a0001c0003t0002g0210 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-8-2650G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50696838 | |||||||
| chr16:50696954 | T | C | 1 | a0001c0001t0001g0031 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.-8-2534T>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50696954 | |||||||
| chr16:50696970 | C | T | 3 | a0001c0001t0001g0041 a0001c0001t0001g0195 a0001c0001t0001g0196 |
4 | HG01167.hp2 HG02145.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-2518C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50696970 | |||||||
| chr16:50697047 | G | A | 2 | a0004c0007t0002g0110 a0004c0007t0002g0111 |
2 | HG02895.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-8-2441G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50697047 | |||||||
| chr16:50697111 | T | C | 6 | a0004c0007t0002g0110 a0004c0007t0002g0111 a0007c0009t0002g0022 others(3): Show |
7 | HG02280.hp1 HG02486.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.-8-2377T>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50697111 | |||||||
| chr16:50697185 | G | A | 31 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0113 others(28): Show |
36 | HG00642.hp1 HG00733.hp1 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.-8-2303G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50697185 | |||||||
| chr16:50697186 | T | C | 2 | a0001c0003t0002g0210 a0001c0003t0002g0211 |
2 | HG02647.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-8-2302T>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50697186 | |||||||
| chr16:50697230 | C | T | 1 | a0001c0001t0001g0194 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-8-2258C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50697230 | |||||||
| chr16:50697399 | G | T | 1 | a0006c0010t0001g0067 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-8-2089G>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50697399 | |||||||
| chr16:50697807 | G | A | 6 | a0001c0001t0004g0058 a0001c0001t0004g0059 a0001c0001t0004g0060 others(3): Show |
6 | HG01891.hp2 HG02451.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8-1681G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50697807 | |||||||
| chr16:50697917 | T | A | 2 | a0004c0007t0002g0110 a0004c0007t0002g0111 |
2 | HG02895.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-8-1571T>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50697917 | |||||||
| chr16:50697984 | G | C | 6 | a0001c0001t0004g0058 a0001c0001t0004g0059 a0001c0001t0004g0060 others(3): Show |
6 | HG01891.hp2 HG02451.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8-1504G>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50697984 | |||||||
| chr16:50697992 | C | T | 1 | a0001c0001t0001g0015 | 3 | HG02074.hp1 HG02083.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.-8-1496C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50697992 | |||||||
| chr16:50698115 | C | T | 4 | a0001c0003t0003g0030 a0001c0003t0003g0055 a0001c0003t0003g0107 others(1): Show |
5 | HG01884.hp2 HG01891.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8-1373C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50698115 | |||||||
| chr16:50698197 | T | C | 2 | a0001c0002t0002g0212 a0001c0002t0002g0213 |
2 | NA19072.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.-8-1291T>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50698197 | |||||||
| chr16:50698204 | C | T | 1 | a0001c0001t0001g0193 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-8-1284C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50698204 | |||||||
| chr16:50698205 | G | A | 4 | a0007c0009t0002g0022 a0007c0009t0002g0068 a0011c0012t0002g0069 others(1): Show |
5 | HG02280.hp1 HG02486.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8-1283G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50698205 | |||||||
| chr16:50698222 | G | A | 25 | a0001c0001t0002g0017 a0001c0002t0002g0006 a0001c0002t0002g0018 others(22): Show |
34 | HG00423.hp2 HG00621.hp1 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.-8-1266G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50698222 | |||||||
| chr16:50698346 | G | A | 1 | a0001c0003t0001g0115 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-8-1142G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50698346 | |||||||
| chr16:50698395 | T | C | 1 | a0001c0001t0002g0227 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-8-1093T>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50698395 | |||||||
| chr16:50698511 | C | T | 6 | a0001c0001t0004g0058 a0001c0001t0004g0059 a0001c0001t0004g0060 others(3): Show |
6 | HG01891.hp2 HG02451.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8-977C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50698511 | |||||||
| chr16:50698558 | C | T | 2 | a0004c0007t0002g0110 a0004c0007t0002g0111 |
2 | HG02895.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-8-930C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50698558 | |||||||
| chr16:50698596 | C | T | 17 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0049 others(14): Show |
20 | HG01433.hp2 HG02055.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.-8-892C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50698596 | |||||||
| chr16:50698615 | G | A | 5 | a0005c0008t0002g0044 a0005c0008t0002g0214 a0005c0008t0002g0215 others(2): Show |
5 | HG02145.hp2 HG02559.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-873G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50698615 | |||||||
| chr16:50698792 | G | C | 3 | a0001c0001t0004g0058 a0001c0001t0004g0059 a0001c0001t0004g0060 |
3 | HG02451.hp2 HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-8-696G>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50698792 | |||||||
| chr16:50698878 | G | A | 3 | a0001c0002t0002g0034 a0001c0002t0002g0116 a0001c0002t0002g0117 |
4 | HG02572.hp1 HG02615.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-610G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50698878 | |||||||
| chr16:50698909 | ATC | A | 6 | a0001c0001t0004g0058 a0001c0001t0004g0059 a0001c0001t0004g0060 others(3): Show |
6 | HG01891.hp2 HG02451.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8-563_-8-562delCT | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50698909 | ||||||
| chr16:50698929 | C | CT | 26 | a0001c0001t0001g0041 a0001c0001t0001g0047 a0001c0001t0001g0051 others(23): Show |
28 | HG00621.hp2 HG01167.hp2 HG01261.hp1 others(25): Show |
intron_variant | MODIFIER | c.-8-543dupT | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50698929 | ||||||
| chr16:50698929 | CT | C | 12 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0120 others(9): Show |
12 | HG00733.hp2 HG01081.hp2 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.-8-543delT | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50698929 | ||||||
| chr16:50699119 | C | T | 1 | a0001c0002t0002g0226 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-8-369C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50699119 | |||||||
| chr16:50699128 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-8-360G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50699128 | |||||||
| chr16:50699129 | T | C | 4 | a0001c0002t0002g0032 a0001c0002t0002g0112 a0001c0004t0002g0125 others(1): Show |
6 | HG02257.hp1 HG02622.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8-359T>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50699129 | |||||||
| chr16:50699204 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-8-284C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50699204 | |||||||
| chr16:50699242 | A | G | 12 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0170 others(9): Show |
15 | HG02074.hp1 HG02080.hp2 HG02083.hp1 others(12): Show |
intron_variant | MODIFIER | c.-8-246A>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50699242 | |||||||
| chr16:50699301 | G | GTGTTTCT | 5 | a0001c0001t0002g0114 a0001c0002t0002g0032 a0001c0002t0002g0112 others(2): Show |
7 | HG02257.hp1 HG02615.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.-8-184_-8-178dupTT others(5): Show |
NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr16 | 50699301 | ||||||
| chr16:50699406 | G | C | 1 | a0001c0001t0002g0114 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-8-82G>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50699406 | |||||||
| chr16:50699459 | T | G | 1 | a0002c0005t0001g0208 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-8-29T>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50699459 | |||||||
| chr16:50699463 | G | T | 26 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0019t0001g0064 others(23): Show |
29 | HG00642.hp1 HG00733.hp1 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.-8-25G>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 1/11 | chr16 | 50699463 | |||||||
| chr16:50700057 | C | T | 5 | a0005c0008t0002g0044 a0005c0008t0002g0214 a0005c0008t0002g0215 others(2): Show |
5 | HG02145.hp2 HG02559.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.459+103C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50700057 | |||||||
| chr16:50700058 | A | G | 149 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0061 others(146): Show |
188 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.459+104A>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50700058 | |||||||
| chr16:50700122 | G | A | 147 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0061 others(144): Show |
186 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.459+168G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50700122 | |||||||
| chr16:50700224 | G | A | 6 | a0001c0001t0001g0113 a0002c0005t0001g0197 a0007c0009t0002g0022 others(3): Show |
7 | HG02280.hp1 HG02486.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.459+270G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50700224 | |||||||
| chr16:50700289 | AT | A | 8 | a0001c0001t0001g0164 a0001c0003t0001g0008 a0001c0003t0001g0023 others(5): Show |
12 | HG01106.hp1 HG01884.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.459+347delT | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 50700289 | ||||||
| chr16:50700381 | C | G | 4 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(1): Show |
4 | HG02717.hp1 HG03225.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.459+427C>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50700381 | |||||||
| chr16:50700911 | G | A | 2 | a0001c0001t0001g0035 a0018c0015t0001g0035 |
2 | NA18950.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.459+957G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50700911 | |||||||
| chr16:50701544 | G | A | 2 | a0001c0003t0002g0080 a0001c0003t0002g0081 |
2 | HG01109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.459+1590G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50701544 | |||||||
| chr16:50701578 | G | A | 1 | a0012c0023t0002g0053 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.459+1624G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50701578 | |||||||
| chr16:50701720 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.459+1766G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50701720 | |||||||
| chr16:50701857 | G | A | 1 | a0001c0002t0002g0082 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.459+1903G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50701857 | |||||||
| chr16:50701878 | TA | T | 7 | a0001c0002t0002g0032 a0001c0002t0002g0034 a0001c0002t0002g0112 others(4): Show |
10 | HG02257.hp1 HG02572.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.459+1925delA | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50701878 | |||||||
| chr16:50702030 | C | T | 68 | a0001c0001t0004g0058 a0001c0001t0004g0059 a0001c0001t0004g0060 others(65): Show |
88 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.459+2076C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50702030 | |||||||
| chr16:50702050 | A | T | 1 | a0001c0001t0002g0227 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.459+2096A>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50702050 | |||||||
| chr16:50702255 | A | G | 1 | a0001c0001t0002g0012 | 3 | HG02257.hp2 HG02976.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.459+2301A>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50702255 | |||||||
| chr16:50702296 | A | G | 1 | a0001c0004t0002g0102 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.459+2342A>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50702296 | |||||||
| chr16:50702301 | T | C | 1 | a0002c0005t0001g0198 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.459+2347T>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50702301 | |||||||
| chr16:50702513 | T | C | 7 | a0001c0002t0002g0032 a0001c0002t0002g0034 a0001c0002t0002g0112 others(4): Show |
10 | HG02257.hp1 HG02572.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.459+2559T>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50702513 | |||||||
| chr16:50702745 | A | G | 101 | a0001c0001t0002g0013 a0001c0001t0002g0017 a0001c0001t0002g0040 others(98): Show |
129 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.459+2791A>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50702745 | |||||||
| chr16:50703366 | G | A | 1 | a0001c0002t0002g0162 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.459+3412G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50703366 | |||||||
| chr16:50703531 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.459+3577C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50703531 | |||||||
| chr16:50703563 | C | T | 8 | a0001c0001t0001g0035 a0001c0001t0001g0157 a0001c0001t0001g0158 others(5): Show |
8 | HG00408.hp1 HG02135.hp2 NA18950.hp2 others(5): Show |
intron_variant | MODIFIER | c.459+3609C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50703563 | |||||||
| chr16:50703587 | C | T | 27 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0002g0227 others(24): Show |
30 | HG00642.hp1 HG00733.hp1 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.459+3633C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50703587 | |||||||
| chr16:50703638 | C | T | 3 | a0001c0001t0004g0058 a0001c0001t0004g0059 a0001c0001t0004g0060 |
3 | HG02451.hp2 HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.459+3684C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50703638 | |||||||
| chr16:50703683 | C | CA | 14 | a0001c0001t0001g0056 a0001c0001t0001g0113 a0001c0001t0001g0129 others(11): Show |
15 | HG01891.hp2 HG02280.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.459+3749dupA | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 50703683 | ||||||
| chr16:50703683 | CA | C | 12 | a0001c0001t0001g0051 a0001c0001t0001g0155 a0001c0001t0001g0187 others(9): Show |
15 | HG00323.hp2 HG02257.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.459+3749delA | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 50703683 | ||||||
| chr16:50703838 | G | T | 3 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 |
3 | HG03225.hp2 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.459+3884G>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50703838 | |||||||
| chr16:50704069 | A | G | 143 | a0001c0001t0001g0041 a0001c0001t0001g0061 a0001c0001t0001g0062 others(140): Show |
177 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.460-3786A>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50704069 | |||||||
| chr16:50704098 | C | A | 3 | a0001c0001t0001g0049 a0001c0001t0001g0051 a0001c0001t0006g0050 |
3 | HG02055.hp2 HG02922.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.460-3757C>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50704098 | |||||||
| chr16:50704332 | G | A | 2 | a0001c0001t0001g0127 a0001c0001t0008g0126 |
2 | NA18950.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.460-3523G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50704332 | |||||||
| chr16:50704380 | C | T | 2 | a0004c0007t0002g0072 a0004c0007t0002g0073 |
2 | HG03130.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.460-3475C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50704380 | |||||||
| chr16:50704532 | C | CT | 89 | a0001c0001t0002g0013 a0001c0001t0002g0017 a0001c0001t0002g0040 others(86): Show |
114 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.460-3310dupT | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 50704532 | ||||||
| chr16:50704532 | CT | C | 8 | a0001c0001t0001g0049 a0001c0001t0001g0051 a0001c0001t0006g0050 others(5): Show |
10 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.460-3310delT | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 50704532 | ||||||
| chr16:50704537 | T | TA | 7 | a0001c0002t0002g0032 a0001c0002t0002g0034 a0001c0002t0002g0112 others(4): Show |
10 | HG02257.hp1 HG02572.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.460-3318_460-3317i others(3): Show |
NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50704537 | |||||||
| chr16:50704546 | C | T | 1 | a0001c0002t0002g0218 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.460-3309C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50704546 | |||||||
| chr16:50704547 | T | C | 1 | a0001c0002t0002g0218 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.460-3308T>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50704547 | |||||||
| chr16:50704636 | T | C | 132 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0002g0013 others(129): Show |
165 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.460-3219T>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50704636 | |||||||
| chr16:50704746 | G | T | 2 | a0005c0008t0002g0215 a0005c0008t0002g0216 |
2 | HG02145.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.460-3109G>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50704746 | |||||||
| chr16:50704883 | A | G | 1 | a0001c0003t0001g0115 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.460-2972A>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50704883 | |||||||
| chr16:50704919 | G | A | 26 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0019t0001g0064 others(23): Show |
29 | HG00642.hp1 HG00733.hp1 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.460-2936G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50704919 | |||||||
| chr16:50705053 | T | G | 7 | a0001c0001t0002g0182 a0004c0007t0002g0071 a0004c0007t0002g0072 others(4): Show |
7 | HG01891.hp2 HG02717.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.460-2802T>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50705053 | |||||||
| chr16:50705194 | G | A | 133 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0002g0013 others(130): Show |
166 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.460-2661G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50705194 | |||||||
| chr16:50705288 | CTTTG | C | 5 | a0001c0003t0002g0024 a0007c0009t0002g0022 a0007c0009t0002g0068 others(2): Show |
7 | HG01884.hp1 HG02280.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.460-2554_460-2551d others(6): Show |
NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 50705288 | ||||||
| chr16:50705350 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.460-2505C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50705350 | |||||||
| chr16:50705539 | G | A | 26 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0019t0001g0064 others(23): Show |
29 | HG00642.hp1 HG00733.hp1 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.460-2316G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50705539 | |||||||
| chr16:50705662 | C | T | 3 | a0001c0001t0004g0058 a0001c0001t0004g0059 a0001c0001t0004g0060 |
3 | HG02451.hp2 HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.460-2193C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50705662 | |||||||
| chr16:50705671 | C | G | 26 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0019t0001g0064 others(23): Show |
29 | HG00642.hp1 HG00733.hp1 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.460-2184C>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50705671 | |||||||
| chr16:50705924 | A | G | 1 | a0001c0003t0002g0081 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.460-1931A>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50705924 | |||||||
| chr16:50705950 | G | A | 4 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0154 others(1): Show |
4 | HG01167.hp1 HG01169.hp1 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.460-1905G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50705950 | |||||||
| chr16:50706056 | G | A | 1 | a0001c0003t0001g0076 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.460-1799G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50706056 | |||||||
| chr16:50706263 | G | C | 16 | a0001c0001t0002g0013 a0001c0001t0002g0017 a0001c0001t0002g0040 others(13): Show |
21 | HG00639.hp2 HG02109.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.460-1592G>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50706263 | |||||||
| chr16:50706353 | G | C | 1 | a0001c0001t0001g0130 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.460-1502G>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50706353 | |||||||
| chr16:50706531 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.460-1324G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50706531 | |||||||
| chr16:50706698 | C | CT | 19 | a0001c0001t0001g0160 a0001c0001t0002g0013 a0001c0001t0002g0017 others(16): Show |
24 | HG00639.hp2 HG00735.hp1 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.460-1141dupT | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 50706698 | ||||||
| chr16:50706698 | CT | C | 9 | a0001c0001t0004g0058 a0001c0001t0008g0126 a0001c0004t0002g0087 others(6): Show |
9 | HG01070.hp1 HG01074.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.460-1141delT | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 50706698 | ||||||
| chr16:50706701 | T | TC | 4 | a0005c0008t0002g0044 a0005c0008t0002g0215 a0005c0008t0002g0216 others(1): Show |
4 | HG02145.hp2 HG02559.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.460-1154_460-1153i others(3): Show |
NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50706701 | |||||||
| chr16:50706720 | C | T | 3 | a0003c0006t0002g0075 a0003c0006t0002g0090 a0003c0006t0002g0101 |
3 | HG01081.hp2 HG01099.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.460-1135C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50706720 | |||||||
| chr16:50706853 | C | G | 66 | a0001c0002t0002g0006 a0001c0002t0002g0018 a0001c0002t0002g0045 others(63): Show |
86 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(83): Show |
intron_variant | MODIFIER | c.460-1002C>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50706853 | |||||||
| chr16:50706944 | C | T | 1 | a0001c0002t0002g0100 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.460-911C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50706944 | |||||||
| chr16:50706980 | G | A | 6 | a0004c0007t0002g0071 a0004c0007t0002g0072 a0004c0007t0002g0073 others(3): Show |
6 | HG01891.hp2 HG02895.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.460-875G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50706980 | |||||||
| chr16:50706995 | G | A | 3 | a0008c0011t0002g0091 a0008c0011t0002g0092 a0008c0011t0002g0093 |
3 | HG02723.hp2 HG02886.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.460-860G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50706995 | |||||||
| chr16:50707022 | T | C | 7 | a0001c0002t0002g0032 a0001c0002t0002g0034 a0001c0002t0002g0112 others(4): Show |
10 | HG02257.hp1 HG02572.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.460-833T>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50707022 | |||||||
| chr16:50707078 | A | G | 1 | a0001c0002t0002g0223 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.460-777A>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50707078 | |||||||
| chr16:50707233 | G | C | 6 | a0004c0007t0002g0071 a0004c0007t0002g0072 a0004c0007t0002g0073 others(3): Show |
6 | HG01891.hp2 HG02895.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.460-622G>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50707233 | |||||||
| chr16:50707275 | C | A | 69 | a0001c0001t0004g0058 a0001c0001t0004g0059 a0001c0001t0004g0060 others(66): Show |
89 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(86): Show |
intron_variant | MODIFIER | c.460-580C>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50707275 | |||||||
| chr16:50707551 | A | C | 66 | a0001c0002t0002g0006 a0001c0002t0002g0018 a0001c0002t0002g0045 others(63): Show |
86 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(83): Show |
intron_variant | MODIFIER | c.460-304A>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50707551 | |||||||
| chr16:50707772 | A | G | 1 | a0001c0001t0001g0152 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.460-83A>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50707772 | |||||||
| chr16:50707852 | T | C | 4 | a0001c0002t0002g0034 a0001c0002t0002g0116 a0001c0002t0002g0117 others(1): Show |
5 | HG02572.hp1 HG02615.hp1 HG02895.hp1 others(2): Show |
splice_region_variant&intron_variant | LOW | c.460-3T>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 2/11 | chr16 | 50707852 | |||||||
| chr16:50708150 | C | T | 1 | a0005c0008t0002g0216 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.565+190C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 3/11 | chr16 | 50708150 | |||||||
| chr16:50708151 | G | A | 10 | a0001c0001t0002g0013 a0001c0001t0002g0017 a0001c0001t0002g0040 others(7): Show |
15 | HG00639.hp2 HG02109.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.565+191G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 3/11 | chr16 | 50708151 | |||||||
| chr16:50708461 | G | A | 1 | a0001c0001t0001g0131 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.565+501G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 3/11 | chr16 | 50708461 | |||||||
| chr16:50708579 | A | T | 3 | a0001c0004t0002g0105 a0001c0004t0002g0106 a0001c0004t0002g0125 |
3 | HG02258.hp1 HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.565+619A>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 3/11 | chr16 | 50708579 | |||||||
| chr16:50708770 | G | A | 32 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0002g0227 others(29): Show |
37 | HG00642.hp1 HG00733.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.565+810G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 3/11 | chr16 | 50708770 | |||||||
| chr16:50708804 | C | T | 1 | a0001c0003t0002g0029 | 2 | NA18947.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.565+844C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 3/11 | chr16 | 50708804 | |||||||
| chr16:50708860 | C | A | 1 | a0001c0002t0002g0116 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.565+900C>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 3/11 | chr16 | 50708860 | |||||||
| chr16:50709025 | G | A | 4 | a0001c0001t0001g0177 a0001c0001t0001g0179 a0001c0001t0001g0180 others(1): Show |
4 | HG03209.hp1 HG03225.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.565+1065G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 3/11 | chr16 | 50709025 | |||||||
| chr16:50709027 | G | A | 32 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0002g0227 others(29): Show |
37 | HG00642.hp1 HG00733.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.565+1067G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 3/11 | chr16 | 50709027 | |||||||
| chr16:50709419 | C | T | 1 | a0004c0007t0002g0111 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.566-1139C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 3/11 | chr16 | 50709419 | |||||||
| chr16:50709420 | G | A | 65 | a0001c0002t0002g0006 a0001c0002t0002g0018 a0001c0002t0002g0045 others(62): Show |
85 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(82): Show |
intron_variant | MODIFIER | c.566-1138G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 3/11 | chr16 | 50709420 | |||||||
| chr16:50709636 | G | C | 1 | a0001c0001t0001g0132 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.566-922G>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 3/11 | chr16 | 50709636 | |||||||
| chr16:50709665 | C | T | 6 | a0004c0007t0002g0071 a0004c0007t0002g0072 a0004c0007t0002g0073 others(3): Show |
6 | HG01891.hp2 HG02895.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.566-893C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 3/11 | chr16 | 50709665 | |||||||
| chr16:50710008 | C | T | 65 | a0001c0002t0002g0006 a0001c0002t0002g0018 a0001c0002t0002g0045 others(62): Show |
85 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(82): Show |
intron_variant | MODIFIER | c.566-550C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 3/11 | chr16 | 50710008 | |||||||
| chr16:50710123 | C | T | 2 | a0007c0009t0002g0022 a0007c0009t0002g0068 |
3 | HG02280.hp1 HG02486.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.566-435C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 3/11 | chr16 | 50710123 | |||||||
| chr16:50710163 | C | T | 19 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(16): Show |
25 | HG01433.hp2 HG02055.hp2 HG02074.hp1 others(22): Show |
intron_variant | MODIFIER | c.566-395C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 3/11 | chr16 | 50710163 | |||||||
| chr16:50710188 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.566-370G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 3/11 | chr16 | 50710188 | |||||||
| chr16:50710226 | G | T | 3 | a0001c0002t0002g0032 a0001c0002t0002g0112 a0010c0014t0002g0033 |
5 | HG02257.hp1 HG02622.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.566-332G>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 3/11 | chr16 | 50710226 | |||||||
| chr16:50710481 | C | T | 1 | a0001c0004t0002g0099 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.566-77C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 3/11 | chr16 | 50710481 | |||||||
| chr16:50712383 | A | C | 1 | a0001c0004t0002g0098 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2381+10A>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | chr16 | 50712383 | |||||||
| chr16:50712440 | C | T | 1 | a0004c0007t0002g0073 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2381+67C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | chr16 | 50712440 | |||||||
| chr16:50712635 | C | G | 129 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0017 others(126): Show |
164 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.2381+262C>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | chr16 | 50712635 | |||||||
| chr16:50712874 | A | G | 1 | a0001c0001t0001g0178 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2381+501A>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | chr16 | 50712874 | |||||||
| chr16:50712903 | C | T | 6 | a0001c0001t0001g0011 a0001c0001t0001g0130 a0001c0001t0001g0149 others(3): Show |
8 | HG01071.hp1 HG01928.hp1 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.2381+530C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | chr16 | 50712903 | |||||||
| chr16:50713190 | G | T | 1 | a0001c0001t0001g0148 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.2381+817G>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | chr16 | 50713190 | |||||||
| chr16:50713277 | C | T | 2 | a0001c0001t0001g0147 a0004c0007t0002g0071 |
2 | HG01891.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.2381+904C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | chr16 | 50713277 | |||||||
| chr16:50713280 | C | G | 5 | a0001c0003t0002g0024 a0007c0009t0002g0022 a0007c0009t0002g0068 others(2): Show |
7 | HG01884.hp1 HG02280.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.2381+907C>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | chr16 | 50713280 | |||||||
| chr16:50713504 | C | G | 5 | a0001c0003t0002g0024 a0007c0009t0002g0022 a0007c0009t0002g0068 others(2): Show |
7 | HG01884.hp1 HG02280.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.2381+1131C>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | chr16 | 50713504 | |||||||
| chr16:50713698 | G | A | 1 | a0001c0001t0010g0156 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.2381+1325G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | chr16 | 50713698 | |||||||
| chr16:50713793 | C | T | 31 | a0001c0001t0001g0010 a0001c0003t0002g0024 a0001c0019t0001g0064 others(28): Show |
38 | HG00642.hp1 HG00733.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.2381+1420C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | chr16 | 50713793 | |||||||
| chr16:50713828 | C | G | 26 | a0001c0001t0001g0010 a0001c0019t0001g0064 a0002c0005t0001g0004 others(23): Show |
31 | HG00642.hp1 HG00733.hp1 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.2381+1455C>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | chr16 | 50713828 | |||||||
| chr16:50713833 | C | T | 6 | a0004c0007t0002g0071 a0004c0007t0002g0072 a0004c0007t0002g0073 others(3): Show |
6 | HG01891.hp2 HG02895.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.2381+1460C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | chr16 | 50713833 | |||||||
| chr16:50713924 | C | T | 1 | a0001c0001t0001g0039 | 2 | HG03017.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.2381+1551C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | chr16 | 50713924 | |||||||
| chr16:50713963 | G | A | 16 | a0001c0001t0002g0013 a0001c0001t0002g0017 a0001c0001t0002g0040 others(13): Show |
21 | HG00639.hp2 HG02109.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.2381+1590G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | chr16 | 50713963 | |||||||
| chr16:50714242 | C | G | 1 | a0001c0003t0001g0115 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2381+1869C>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | chr16 | 50714242 | |||||||
| chr16:50714329 | C | T | 1 | a0004c0007t0002g0183 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2381+1956C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | chr16 | 50714329 | |||||||
| chr16:50714330 | G | A | 1 | a0001c0001t0002g0114 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2381+1957G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | chr16 | 50714330 | |||||||
| chr16:50714404 | A | G | 2 | a0001c0003t0001g0076 a0001c0003t0001g0079 |
2 | HG01106.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2381+2031A>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | chr16 | 50714404 | |||||||
| chr16:50714437 | A | G | 1 | a0001c0001t0001g0171 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2381+2064A>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | chr16 | 50714437 | |||||||
| chr16:50714515 | C | T | 1 | a0007c0009t0002g0068 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2382-2072C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | chr16 | 50714515 | |||||||
| chr16:50714593 | G | A | 1 | a0001c0001t0001g0185 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2382-1994G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | chr16 | 50714593 | |||||||
| chr16:50714602 | C | CTG | 38 | a0001c0001t0001g0014 a0001c0001t0001g0038 a0001c0001t0001g0123 others(35): Show |
48 | HG00140.hp2 HG01167.hp2 HG01168.hp1 others(45): Show |
intron_variant | MODIFIER | c.2382-1945_2382-194 others(6): Show |
NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr16 | 50714602 | ||||||
| chr16:50714602 | C | CTGTG | 19 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0113 others(16): Show |
27 | HG00280.hp2 HG01175.hp2 HG01928.hp2 others(24): Show |
intron_variant | MODIFIER | c.2382-1947_2382-194 others(8): Show |
NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr16 | 50714602 | ||||||
| chr16:50714602 | CTG | C | 38 | a0001c0001t0001g0036 a0001c0001t0001g0129 a0001c0001t0001g0135 others(35): Show |
41 | HG00099.hp1 HG00323.hp2 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.2382-1945_2382-194 others(6): Show |
NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr16 | 50714602 | ||||||
| chr16:50714602 | CTGTG | C | 22 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0049 others(19): Show |
29 | HG00140.hp1 HG01070.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.2382-1947_2382-194 others(8): Show |
NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr16 | 50714602 | ||||||
| chr16:50714602 | CTGTGTGT others(7): Show |
C | 1 | a0001c0001t0001g0133 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2382-1957_2382-194 others(18): Show |
NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr16 | 50714602 | ||||||
| chr16:50714602 | CTGTGTGT others(11): Show |
C | 1 | a0001c0001t0001g0057 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2382-1961_2382-194 others(22): Show |
NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr16 | 50714602 | ||||||
| chr16:50714647 | A | T | 1 | a0011c0012t0002g0070 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2382-1940A>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | chr16 | 50714647 | |||||||
| chr16:50714710 | C | T | 1 | a0001c0001t0001g0015 | 3 | HG02074.hp1 HG02083.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.2382-1877C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | chr16 | 50714710 | |||||||
| chr16:50714789 | A | G | 1 | a0002c0005t0001g0065 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2382-1798A>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | chr16 | 50714789 | |||||||
| chr16:50714892 | G | A | 1 | a0001c0001t0001g0172 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2382-1695G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | chr16 | 50714892 | |||||||
| chr16:50714944 | T | C | 1 | a0001c0001t0001g0137 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.2382-1643T>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | chr16 | 50714944 | |||||||
| chr16:50715156 | T | G | 1 | a0001c0001t0001g0138 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2382-1431T>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | chr16 | 50715156 | |||||||
| chr16:50715255 | AT | A | 5 | a0001c0003t0002g0024 a0007c0009t0002g0022 a0007c0009t0002g0068 others(2): Show |
7 | HG01884.hp1 HG02280.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.2382-1329delT | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr16 | 50715255 | ||||||
| chr16:50715420 | CT | C | 67 | a0001c0001t0002g0012 a0001c0001t0002g0114 a0001c0001t0002g0227 others(64): Show |
89 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(86): Show |
intron_variant | MODIFIER | c.2382-1154delT | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr16 | 50715420 | ||||||
| chr16:50715420 | CTT | C | 16 | a0001c0001t0002g0013 a0001c0001t0002g0017 a0001c0001t0002g0040 others(13): Show |
21 | HG00639.hp2 HG02109.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.2382-1155_2382-115 others(6): Show |
NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr16 | 50715420 | ||||||
| chr16:50715460 | G | C | 3 | a0001c0004t0002g0105 a0001c0004t0002g0106 a0001c0004t0002g0125 |
3 | HG02258.hp1 HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2382-1127G>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | chr16 | 50715460 | |||||||
| chr16:50715463 | A | T | 129 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0017 others(126): Show |
164 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.2382-1124A>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | chr16 | 50715463 | |||||||
| chr16:50715497 | G | T | 25 | a0001c0019t0001g0064 a0002c0005t0001g0004 a0002c0005t0001g0007 others(22): Show |
28 | HG00642.hp1 HG00733.hp1 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.2382-1090G>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | chr16 | 50715497 | |||||||
| chr16:50715598 | G | C | 5 | a0005c0008t0002g0044 a0005c0008t0002g0214 a0005c0008t0002g0215 others(2): Show |
5 | HG02145.hp2 HG02559.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.2382-989G>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | chr16 | 50715598 | |||||||
| chr16:50715763 | G | A | 1 | a0001c0004t0002g0087 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2382-824G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | chr16 | 50715763 | |||||||
| chr16:50715765 | T | C | 1 | a0001c0001t0002g0114 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2382-822T>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | chr16 | 50715765 | |||||||
| chr16:50716132 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2382-455G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | chr16 | 50716132 | |||||||
| chr16:50716191 | G | A | 3 | a0001c0001t0004g0058 a0001c0001t0004g0059 a0001c0001t0004g0060 |
3 | HG02451.hp2 HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.2382-396G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | chr16 | 50716191 | |||||||
| chr16:50716224 | G | A | 3 | a0001c0001t0004g0058 a0001c0001t0004g0059 a0001c0001t0004g0060 |
3 | HG02451.hp2 HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.2382-363G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | chr16 | 50716224 | |||||||
| chr16:50716258 | T | G | 1 | a0001c0003t0002g0074 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.2382-329T>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 4/11 | chr16 | 50716258 | |||||||
| chr16:50716784 | G | C | 1 | a0001c0004t0002g0095 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2466-107G>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 5/11 | chr16 | 50716784 | |||||||
| chr16:50716849 | T | C | 6 | a0004c0007t0002g0071 a0004c0007t0002g0072 a0004c0007t0002g0073 others(3): Show |
6 | HG01891.hp2 HG02895.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.2466-42T>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 5/11 | chr16 | 50716849 | |||||||
| chr16:50716880 | G | T | 1 | a0001c0001t0002g0114 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2466-11G>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 5/11 | chr16 | 50716880 | |||||||
| chr16:50717030 | C | G | 2 | a0001c0001t0001g0136 a0001c0001t0001g0143 |
2 | NA18943.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.2549+56C>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 6/11 | chr16 | 50717030 | |||||||
| chr16:50717076 | C | T | 2 | a0004c0007t0002g0072 a0004c0007t0002g0073 |
2 | HG03130.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2549+102C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 6/11 | chr16 | 50717076 | |||||||
| chr16:50717264 | T | G | 132 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0017 others(129): Show |
167 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.2549+290T>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 6/11 | chr16 | 50717264 | |||||||
| chr16:50717487 | A | G | 67 | a0001c0001t0002g0012 a0001c0001t0005g0104 a0001c0002t0002g0006 others(64): Show |
89 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(86): Show |
intron_variant | MODIFIER | c.2549+513A>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 6/11 | chr16 | 50717487 | |||||||
| chr16:50717650 | C | T | 1 | a0001c0001t0001g0041 | 2 | HG02145.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2549+676C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 6/11 | chr16 | 50717650 | |||||||
| chr16:50717651 | G | T | 1 | a0001c0003t0003g0108 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2549+677G>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 6/11 | chr16 | 50717651 | |||||||
| chr16:50717810 | C | T | 6 | a0004c0007t0002g0071 a0004c0007t0002g0072 a0004c0007t0002g0073 others(3): Show |
6 | HG01891.hp2 HG02895.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.2549+836C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 6/11 | chr16 | 50717810 | |||||||
| chr16:50717876 | G | A | 67 | a0001c0001t0002g0012 a0001c0001t0002g0227 a0001c0002t0002g0006 others(64): Show |
89 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(86): Show |
intron_variant | MODIFIER | c.2549+902G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 6/11 | chr16 | 50717876 | |||||||
| chr16:50718061 | G | A | 124 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0017 others(121): Show |
159 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.2549+1087G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 6/11 | chr16 | 50718061 | |||||||
| chr16:50718179 | G | A | 1 | a0001c0001t0001g0139 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2549+1205G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 6/11 | chr16 | 50718179 | |||||||
| chr16:50718198 | C | T | 1 | a0001c0001t0001g0031 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.2549+1224C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 6/11 | chr16 | 50718198 | |||||||
| chr16:50718253 | G | A | 20 | a0001c0019t0001g0064 a0002c0005t0001g0004 a0002c0005t0001g0007 others(17): Show |
23 | HG00642.hp1 HG00735.hp1 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.2549+1279G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 6/11 | chr16 | 50718253 | |||||||
| chr16:50718373 | G | A | 7 | a0001c0002t0002g0032 a0001c0002t0002g0034 a0001c0002t0002g0112 others(4): Show |
10 | HG02257.hp1 HG02572.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.2549+1399G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 6/11 | chr16 | 50718373 | |||||||
| chr16:50718533 | C | A | 15 | a0001c0001t0002g0013 a0001c0001t0002g0017 a0001c0001t0002g0040 others(12): Show |
20 | HG00639.hp2 HG02109.hp1 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.2550-1392C>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 6/11 | chr16 | 50718533 | |||||||
| chr16:50718636 | C | T | 6 | a0004c0007t0002g0071 a0004c0007t0002g0072 a0004c0007t0002g0073 others(3): Show |
6 | HG01891.hp2 HG02895.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.2550-1289C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 6/11 | chr16 | 50718636 | |||||||
| chr16:50718671 | C | T | 7 | a0001c0002t0002g0032 a0001c0002t0002g0034 a0001c0002t0002g0112 others(4): Show |
10 | HG02257.hp1 HG02572.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.2550-1254C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 6/11 | chr16 | 50718671 | |||||||
| chr16:50718794 | G | A | 1 | a0007c0009t0002g0022 | 2 | HG02280.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.2550-1131G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 6/11 | chr16 | 50718794 | |||||||
| chr16:50718904 | T | C | 55 | a0001c0001t0002g0012 a0001c0002t0002g0006 a0001c0002t0002g0018 others(52): Show |
73 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(70): Show |
intron_variant | MODIFIER | c.2550-1021T>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 6/11 | chr16 | 50718904 | |||||||
| chr16:50719116 | C | T | 1 | a0005c0008t0002g0216 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2550-809C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 6/11 | chr16 | 50719116 | |||||||
| chr16:50719224 | C | T | 1 | a0001c0019t0001g0064 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2550-701C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 6/11 | chr16 | 50719224 | |||||||
| chr16:50719513 | G | A | 67 | a0001c0001t0002g0012 a0001c0001t0002g0227 a0001c0002t0002g0006 others(64): Show |
89 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(86): Show |
intron_variant | MODIFIER | c.2550-412G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 6/11 | chr16 | 50719513 | |||||||
| chr16:50719514 | C | G | 7 | a0001c0002t0002g0032 a0001c0002t0002g0034 a0001c0002t0002g0112 others(4): Show |
10 | HG02257.hp1 HG02572.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.2550-411C>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 6/11 | chr16 | 50719514 | |||||||
| chr16:50719639 | C | T | 15 | a0001c0001t0002g0013 a0001c0001t0002g0017 a0001c0001t0002g0040 others(12): Show |
20 | HG00639.hp2 HG02109.hp1 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.2550-286C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 6/11 | chr16 | 50719639 | |||||||
| chr16:50719730 | C | G | 3 | a0001c0001t0004g0058 a0001c0001t0004g0059 a0001c0001t0004g0060 |
3 | HG02451.hp2 HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.2550-195C>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 6/11 | chr16 | 50719730 | |||||||
| chr16:50720114 | G | A | 3 | a0001c0001t0004g0058 a0001c0001t0004g0059 a0001c0001t0004g0060 |
3 | HG02451.hp2 HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.2633+106G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 7/11 | chr16 | 50720114 | |||||||
| chr16:50720242 | G | C | 5 | a0005c0008t0002g0044 a0005c0008t0002g0214 a0005c0008t0002g0215 others(2): Show |
5 | HG02145.hp2 HG02559.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.2633+234G>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 7/11 | chr16 | 50720242 | |||||||
| chr16:50720279 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2633+271G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 7/11 | chr16 | 50720279 | |||||||
| chr16:50720479 | A | G | 2 | a0001c0001t0001g0190 a0001c0001t0001g0191 |
2 | NA18947.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.2633+471A>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 7/11 | chr16 | 50720479 | |||||||
| chr16:50720996 | G | A | 3 | a0003c0006t0002g0075 a0003c0006t0002g0090 a0003c0006t0002g0101 |
3 | HG01081.hp2 HG01099.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.2633+988G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 7/11 | chr16 | 50720996 | |||||||
| chr16:50721014 | C | T | 1 | a0001c0002t0002g0116 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2633+1006C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 7/11 | chr16 | 50721014 | |||||||
| chr16:50721277 | ATATT | A | 7 | a0001c0002t0002g0032 a0001c0002t0002g0034 a0001c0002t0002g0112 others(4): Show |
10 | HG02257.hp1 HG02572.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.2633+1274_2633+127 others(8): Show |
NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr16 | 50721277 | ||||||
| chr16:50721307 | C | T | 4 | a0001c0002t0002g0034 a0001c0002t0002g0116 a0001c0002t0002g0117 others(1): Show |
5 | HG02572.hp1 HG02615.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.2633+1299C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 7/11 | chr16 | 50721307 | |||||||
| chr16:50721366 | GT | G | 105 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0017 others(102): Show |
137 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.2634-1245delT | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr16 | 50721366 | ||||||
| chr16:50721374 | T | G | 1 | a0001c0001t0008g0126 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.2634-1248T>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 7/11 | chr16 | 50721374 | |||||||
| chr16:50721377 | TG | T | 9 | a0001c0001t0001g0113 a0001c0001t0001g0154 a0001c0001t0001g0177 others(6): Show |
9 | HG01167.hp2 HG02055.hp1 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.2634-1244delG | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 7/11 | chr16 | 50721377 | |||||||
| chr16:50721378 | G | T | 10 | a0001c0001t0001g0049 a0001c0001t0001g0170 a0001c0001t0001g0171 others(7): Show |
10 | HG01433.hp2 HG02080.hp2 HG02132.hp1 others(7): Show |
intron_variant | MODIFIER | c.2634-1244G>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 7/11 | chr16 | 50721378 | |||||||
| chr16:50721626 | G | T | 1 | a0007c0009t0002g0022 | 2 | HG02280.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.2634-996G>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 7/11 | chr16 | 50721626 | |||||||
| chr16:50721643 | C | T | 1 | a0001c0001t0002g0182 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2634-979C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 7/11 | chr16 | 50721643 | |||||||
| chr16:50721798 | T | G | 66 | a0001c0001t0002g0012 a0001c0002t0002g0006 a0001c0002t0002g0018 others(63): Show |
88 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(85): Show |
intron_variant | MODIFIER | c.2634-824T>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 7/11 | chr16 | 50721798 | |||||||
| chr16:50721818 | G | A | 3 | a0001c0003t0002g0024 a0011c0012t0002g0069 a0011c0012t0002g0070 |
4 | HG01884.hp1 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.2634-804G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 7/11 | chr16 | 50721818 | |||||||
| chr16:50721837 | T | C | 4 | a0001c0002t0002g0034 a0001c0002t0002g0116 a0001c0002t0002g0117 others(1): Show |
5 | HG02572.hp1 HG02615.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.2634-785T>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 7/11 | chr16 | 50721837 | |||||||
| chr16:50721840 | C | T | 1 | a0001c0002t0002g0225 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2634-782C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 7/11 | chr16 | 50721840 | |||||||
| chr16:50721894 | G | A | 10 | a0001c0001t0002g0013 a0001c0001t0002g0017 a0001c0001t0002g0040 others(7): Show |
15 | HG00639.hp2 HG02109.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.2634-728G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 7/11 | chr16 | 50721894 | |||||||
| chr16:50722009 | G | A | 1 | a0001c0001t0001g0171 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2634-613G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 7/11 | chr16 | 50722009 | |||||||
| chr16:50722156 | C | T | 1 | a0001c0001t0004g0060 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2634-466C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 7/11 | chr16 | 50722156 | |||||||
| chr16:50722364 | G | T | 1 | a0001c0001t0001g0177 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2634-258G>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 7/11 | chr16 | 50722364 | |||||||
| chr16:50722387 | C | G | 17 | a0001c0001t0002g0013 a0001c0001t0002g0017 a0001c0001t0002g0040 others(14): Show |
22 | HG00639.hp2 HG02109.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.2634-235C>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 7/11 | chr16 | 50722387 | |||||||
| chr16:50722500 | T | G | 2 | a0001c0001t0004g0059 a0001c0001t0004g0060 |
2 | HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.2634-122T>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 7/11 | chr16 | 50722500 | |||||||
| chr16:50722805 | C | T | 1 | a0001c0001t0002g0167 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.2717+100C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 8/11 | chr16 | 50722805 | |||||||
| chr16:50722863 | C | T | 11 | a0001c0001t0001g0161 a0002c0005t0001g0004 a0002c0005t0001g0019 others(8): Show |
13 | HG00642.hp1 HG01070.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.2717+158C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 8/11 | chr16 | 50722863 | |||||||
| chr16:50722970 | A | G | 20 | a0001c0019t0001g0064 a0002c0005t0001g0004 a0002c0005t0001g0007 others(17): Show |
23 | HG00642.hp1 HG00735.hp1 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.2717+265A>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 8/11 | chr16 | 50722970 | |||||||
| chr16:50723085 | T | TA | 17 | a0001c0001t0002g0013 a0001c0001t0002g0017 a0001c0001t0002g0040 others(14): Show |
22 | HG00639.hp2 HG02109.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.2718-200dupA | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr16 | 50723085 | ||||||
| chr16:50723085 | TA | T | 164 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(161): Show |
214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.2718-200delA | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr16 | 50723085 | ||||||
| chr16:50723139 | G | GA | 78 | a0001c0001t0001g0009 a0001c0001t0001g0146 a0001c0001t0001g0150 others(75): Show |
107 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(104): Show |
intron_variant | MODIFIER | c.2718-147dupA | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr16 | 50723139 | ||||||
| chr16:50723139 | GA | G | 10 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0047 others(7): Show |
14 | HG00621.hp2 HG01071.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.2718-147delA | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr16 | 50723139 | ||||||
| chr16:50723139 | GAAAAAA | G | 6 | a0004c0007t0002g0071 a0004c0007t0002g0072 a0004c0007t0002g0073 others(3): Show |
6 | HG01891.hp2 HG02895.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.2718-152_2718-147d others(8): Show |
NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr16 | 50723139 | ||||||
| chr16:50723277 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2718-24C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 8/11 | chr16 | 50723277 | |||||||
| chr16:50723573 | C | T | 1 | a0001c0004t0002g0089 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2801+189C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 9/11 | chr16 | 50723573 | |||||||
| chr16:50723631 | G | A | 2 | a0001c0003t0001g0076 a0001c0003t0001g0079 |
2 | HG01106.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2801+247G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 9/11 | chr16 | 50723631 | |||||||
| chr16:50723692 | A | G | 1 | a0001c0003t0001g0115 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2801+308A>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 9/11 | chr16 | 50723692 | |||||||
| chr16:50723734 | G | A | 4 | a0001c0002t0002g0046 a0001c0002t0002g0221 a0001c0002t0002g0223 others(1): Show |
5 | HG02132.hp2 NA18940.hp2 NA18942.hp1 others(2): Show |
intron_variant | MODIFIER | c.2801+350G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 9/11 | chr16 | 50723734 | |||||||
| chr16:50723969 | T | C | 2 | a0001c0001t0002g0114 a0001c0001t0002g0227 |
2 | HG02486.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.2801+585T>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 9/11 | chr16 | 50723969 | |||||||
| chr16:50724241 | A | G | 1 | a0001c0001t0001g0120 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2801+857A>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 9/11 | chr16 | 50724241 | |||||||
| chr16:50724593 | T | C | 7 | a0001c0001t0002g0182 a0004c0007t0002g0071 a0004c0007t0002g0072 others(4): Show |
7 | HG01891.hp2 HG02717.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.2802-896T>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 9/11 | chr16 | 50724593 | |||||||
| chr16:50724758 | T | A | 3 | a0001c0001t0004g0058 a0001c0001t0004g0059 a0001c0001t0004g0060 |
3 | HG02451.hp2 HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.2802-731T>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 9/11 | chr16 | 50724758 | |||||||
| chr16:50724927 | T | C | 234 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(231): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.2802-562T>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 9/11 | chr16 | 50724927 | |||||||
| chr16:50724938 | G | A | 20 | a0001c0019t0001g0064 a0002c0005t0001g0004 a0002c0005t0001g0007 others(17): Show |
23 | HG00642.hp1 HG00735.hp1 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.2802-551G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 9/11 | chr16 | 50724938 | |||||||
| chr16:50725100 | T | C | 1 | a0001c0001t0001g0039 | 2 | HG03017.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.2802-389T>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 9/11 | chr16 | 50725100 | |||||||
| chr16:50725230 | A | G | 1 | a0001c0001t0001g0195 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2802-259A>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 9/11 | chr16 | 50725230 | |||||||
| chr16:50725356 | AC | A | 65 | a0001c0001t0002g0012 a0001c0002t0002g0006 a0001c0002t0002g0018 others(62): Show |
87 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(84): Show |
intron_variant | MODIFIER | c.2802-132delC | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 9/11 | chr16 | 50725356 | |||||||
| chr16:50725358 | T | A | 65 | a0001c0001t0002g0012 a0001c0002t0002g0006 a0001c0002t0002g0018 others(62): Show |
87 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(84): Show |
intron_variant | MODIFIER | c.2802-131T>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 9/11 | chr16 | 50725358 | |||||||
| chr16:50725636 | A | T | 85 | a0001c0001t0002g0012 a0001c0002t0002g0006 a0001c0002t0002g0018 others(82): Show |
110 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(107): Show |
intron_variant | MODIFIER | c.2885+64A>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 10/11 | chr16 | 50725636 | |||||||
| chr16:50725820 | T | A | 1 | a0009c0013t0001g0063 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2885+248T>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 10/11 | chr16 | 50725820 | |||||||
| chr16:50726069 | A | C | 126 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0017 others(123): Show |
161 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.2885+497A>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 10/11 | chr16 | 50726069 | |||||||
| chr16:50726100 | G | A | 2 | a0001c0001t0002g0114 a0001c0001t0002g0227 |
2 | HG02486.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.2885+528G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 10/11 | chr16 | 50726100 | |||||||
| chr16:50726127 | C | T | 3 | a0003c0006t0002g0075 a0003c0006t0002g0090 a0003c0006t0002g0101 |
3 | HG01081.hp2 HG01099.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.2885+555C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 10/11 | chr16 | 50726127 | |||||||
| chr16:50726208 | C | T | 2 | a0001c0001t0001g0119 a0001c0001t0001g0141 |
2 | HG02040.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.2885+636C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 10/11 | chr16 | 50726208 | |||||||
| chr16:50726217 | G | A | 1 | a0001c0001t0004g0058 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2885+645G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 10/11 | chr16 | 50726217 | |||||||
| chr16:50726245 | G | GCCAAAAT others(307): Show |
7 | a0001c0001t0002g0182 a0004c0007t0002g0071 a0004c0007t0002g0072 others(4): Show |
7 | HG01891.hp2 HG02717.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.2885+684_2885+685i others(316): Show |
NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr16 | 50726245 | ||||||
| chr16:50726352 | C | A | 7 | a0001c0001t0001g0154 a0001c0001t0001g0177 a0001c0001t0001g0179 others(4): Show |
7 | HG01167.hp2 HG02055.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.2885+780C>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 10/11 | chr16 | 50726352 | |||||||
| chr16:50726360 | G | A | 1 | a0001c0001t0001g0185 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2885+788G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 10/11 | chr16 | 50726360 | |||||||
| chr16:50726425 | C | T | 1 | a0001c0003t0002g0029 | 2 | NA18947.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.2885+853C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 10/11 | chr16 | 50726425 | |||||||
| chr16:50726453 | C | T | 3 | a0001c0003t0002g0024 a0011c0012t0002g0069 a0011c0012t0002g0070 |
4 | HG01884.hp1 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.2885+881C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 10/11 | chr16 | 50726453 | |||||||
| chr16:50726492 | A | T | 7 | a0001c0001t0001g0154 a0001c0001t0001g0177 a0001c0001t0001g0179 others(4): Show |
7 | HG01167.hp2 HG02055.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.2885+920A>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 10/11 | chr16 | 50726492 | |||||||
| chr16:50726534 | C | T | 1 | a0001c0001t0001g0122 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.2885+962C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 10/11 | chr16 | 50726534 | |||||||
| chr16:50726777 | T | C | 7 | a0001c0001t0002g0182 a0004c0007t0002g0071 a0004c0007t0002g0072 others(4): Show |
7 | HG01891.hp2 HG02717.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.2885+1205T>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 10/11 | chr16 | 50726777 | |||||||
| chr16:50726916 | G | A | 1 | a0001c0001t0001g0144 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.2885+1344G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 10/11 | chr16 | 50726916 | |||||||
| chr16:50726927 | A | G | 126 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0017 others(123): Show |
161 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.2885+1355A>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 10/11 | chr16 | 50726927 | |||||||
| chr16:50727138 | CA | C | 43 | a0001c0001t0001g0119 a0001c0001t0002g0013 a0001c0001t0002g0017 others(40): Show |
52 | HG00639.hp2 HG00642.hp1 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.2885+1583delA | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr16 | 50727138 | ||||||
| chr16:50727177 | A | T | 18 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(15): Show |
24 | HG01433.hp2 HG02055.hp2 HG02074.hp1 others(21): Show |
intron_variant | MODIFIER | c.2885+1605A>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 10/11 | chr16 | 50727177 | |||||||
| chr16:50727507 | A | G | 1 | a0001c0001t0001g0170 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2885+1935A>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 10/11 | chr16 | 50727507 | |||||||
| chr16:50727523 | C | T | 65 | a0001c0001t0002g0012 a0001c0002t0002g0006 a0001c0002t0002g0018 others(62): Show |
87 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(84): Show |
intron_variant | MODIFIER | c.2885+1951C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 10/11 | chr16 | 50727523 | |||||||
| chr16:50727532 | A | G | 1 | a0001c0001t0002g0168 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2885+1960A>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 10/11 | chr16 | 50727532 | |||||||
| chr16:50727659 | G | A | 15 | a0001c0001t0002g0013 a0001c0001t0002g0017 a0001c0001t0002g0040 others(12): Show |
20 | HG00639.hp2 HG02109.hp1 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.2885+2087G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 10/11 | chr16 | 50727659 | |||||||
| chr16:50727669 | A | ATAGTCCA others(14): Show |
1 | a0001c0001t0007g0140 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.2885+2099_2885+211 others(25): Show |
NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr16 | 50727669 | ||||||
| chr16:50727729 | G | A | 1 | a0001c0004t0002g0105 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2886-2089G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 10/11 | chr16 | 50727729 | |||||||
| chr16:50727729 | G | T | 2 | a0001c0001t0002g0114 a0001c0001t0002g0227 |
2 | HG02486.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.2886-2089G>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 10/11 | chr16 | 50727729 | |||||||
| chr16:50727799 | A | T | 3 | a0001c0001t0004g0058 a0001c0001t0004g0059 a0001c0001t0004g0060 |
3 | HG02451.hp2 HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.2886-2019A>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 10/11 | chr16 | 50727799 | |||||||
| chr16:50728058 | C | T | 4 | a0001c0001t0001g0014 a0001c0001t0001g0190 a0001c0001t0001g0191 others(1): Show |
5 | NA18947.hp1 NA18986.hp2 NA19057.hp1 others(2): Show |
intron_variant | MODIFIER | c.2886-1760C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 10/11 | chr16 | 50728058 | |||||||
| chr16:50728075 | T | A | 1 | a0001c0027t0002g0096 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2886-1743T>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 10/11 | chr16 | 50728075 | |||||||
| chr16:50728126 | C | T | 15 | a0001c0001t0002g0013 a0001c0001t0002g0017 a0001c0001t0002g0040 others(12): Show |
20 | HG00639.hp2 HG02109.hp1 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.2886-1692C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 10/11 | chr16 | 50728126 | |||||||
| chr16:50728214 | T | A | 5 | a0005c0008t0002g0044 a0005c0008t0002g0214 a0005c0008t0002g0215 others(2): Show |
5 | HG02145.hp2 HG02559.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.2886-1604T>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 10/11 | chr16 | 50728214 | |||||||
| chr16:50728222 | A | G | 7 | a0001c0002t0002g0032 a0001c0002t0002g0034 a0001c0002t0002g0112 others(4): Show |
10 | HG02257.hp1 HG02572.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.2886-1596A>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 10/11 | chr16 | 50728222 | |||||||
| chr16:50728623 | T | G | 1 | a0001c0002t0002g0219 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2886-1195T>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 10/11 | chr16 | 50728623 | |||||||
| chr16:50728647 | C | A | 1 | a0013c0028t0001g0200 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2886-1171C>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 10/11 | chr16 | 50728647 | |||||||
| chr16:50728673 | T | C | 1 | a0001c0001t0001g0151 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.2886-1145T>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 10/11 | chr16 | 50728673 | |||||||
| chr16:50728860 | T | C | 2 | a0001c0004t0002g0085 a0001c0004t0002g0098 |
2 | HG00280.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.2886-958T>C | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 10/11 | chr16 | 50728860 | |||||||
| chr16:50729165 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2886-653G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 10/11 | chr16 | 50729165 | |||||||
| chr16:50729285 | A | G | 5 | a0005c0008t0002g0044 a0005c0008t0002g0214 a0005c0008t0002g0215 others(2): Show |
5 | HG02145.hp2 HG02559.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.2886-533A>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 10/11 | chr16 | 50729285 | |||||||
| chr16:50729398 | C | G | 1 | a0007c0009t0002g0022 | 2 | HG02280.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.2886-420C>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 10/11 | chr16 | 50729398 | |||||||
| chr16:50730205 | G | A | 25 | a0001c0001t0001g0142 a0001c0001t0002g0013 a0001c0001t0002g0017 others(22): Show |
30 | HG00639.hp2 HG01891.hp2 HG02074.hp2 others(27): Show |
intron_variant | MODIFIER | c.2969+304G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 11/11 | chr16 | 50730205 | |||||||
| chr16:50730315 | A | G | 15 | a0001c0001t0002g0013 a0001c0001t0002g0017 a0001c0001t0002g0040 others(12): Show |
20 | HG00639.hp2 HG02109.hp1 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.2969+414A>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 11/11 | chr16 | 50730315 | |||||||
| chr16:50730488 | C | T | 24 | a0001c0001t0002g0013 a0001c0001t0002g0017 a0001c0001t0002g0040 others(21): Show |
29 | HG00639.hp2 HG01891.hp2 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.2969+587C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 11/11 | chr16 | 50730488 | |||||||
| chr16:50730876 | C | T | 1 | a0001c0004t0002g0097 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2970-871C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 11/11 | chr16 | 50730876 | |||||||
| chr16:50730923 | G | A | 2 | a0001c0001t0002g0114 a0001c0001t0002g0227 |
2 | HG02486.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.2970-824G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 11/11 | chr16 | 50730923 | |||||||
| chr16:50730925 | G | A | 64 | a0001c0001t0002g0012 a0001c0002t0002g0006 a0001c0002t0002g0018 others(61): Show |
85 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(82): Show |
intron_variant | MODIFIER | c.2970-822G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 11/11 | chr16 | 50730925 | |||||||
| chr16:50731042 | C | T | 4 | a0001c0002t0002g0034 a0001c0002t0002g0116 a0001c0002t0002g0117 others(1): Show |
5 | HG02572.hp1 HG02615.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.2970-705C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 11/11 | chr16 | 50731042 | |||||||
| chr16:50731077 | G | A | 18 | a0001c0002t0002g0006 a0001c0002t0002g0018 a0001c0002t0002g0045 others(15): Show |
25 | HG00423.hp2 HG00621.hp1 HG01175.hp2 others(22): Show |
intron_variant | MODIFIER | c.2970-670G>A | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 11/11 | chr16 | 50731077 | |||||||
| chr16:50731140 | C | T | 1 | a0001c0001t0001g0146 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2970-607C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 11/11 | chr16 | 50731140 | |||||||
| chr16:50731308 | A | G | 1 | a0001c0001t0001g0173 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2970-439A>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 11/11 | chr16 | 50731308 | |||||||
| chr16:50731465 | A | G | 39 | a0001c0001t0002g0013 a0001c0001t0002g0017 a0001c0001t0002g0040 others(36): Show |
49 | HG00639.hp2 HG01884.hp1 HG01891.hp2 others(46): Show |
intron_variant | MODIFIER | c.2970-282A>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 11/11 | chr16 | 50731465 | |||||||
| chr16:50731599 | C | T | 1 | a0001c0002t0002g0213 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.2970-148C>T | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 11/11 | chr16 | 50731599 | |||||||
| chr16:50731614 | T | G | 4 | a0001c0001t0001g0014 a0001c0001t0001g0190 a0001c0001t0001g0191 others(1): Show |
5 | NA18947.hp1 NA18986.hp2 NA19057.hp1 others(2): Show |
intron_variant | MODIFIER | c.2970-133T>G | NOD2 | ENSG00000167207.15 | transcript | ENST00000647318.2 | protein_coding | 11/11 | chr16 | 50731614 |