Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 3714 |
| ensemblid | ENSG00000184916.9 |
| hgncid | 6189 |
| symbol | JAG2 |
| name | jagged canonical Notch ligand 2 |
| refseq_nuc | NM_002226.5 |
| refseq_prot | NP_002217.3 |
| ensembl_nuc | ENST00000331782.8 |
| ensembl_prot | ENSP00000328169.3 |
| mane_status | MANE Select |
| chr | chr14 |
| start | 105140995 |
| end | 105168776 |
| strand | - |
| ver | v1.2 |
| region | chr14:105140995-105168776 |
| region5000 | chr14:105135995-105173776 |
| regionname0 | JAG2_chr14_105140995_105168776 |
| regionname5000 | JAG2_chr14_105135995_105173776 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 1238 | 162 | 66 | 30 | 50 | 5 | 11 | 37 | JAG2_chr14_105135995_105173776 | JAG2 | MRAQG others(1233): Show |
chr14 | 105135995 | 105173776 |
| a0002 | 1/0 | 1238 | 124 | 16 | 20 | 59 | 9 | 19 | 39 | JAG2_chr14_105135995_105173776 | JAG2 | MRAQG others(1233): Show |
chr14 | 105135995 | 105173776 |
| a0003 | 0/1 | 1238 | 46 | 0 | 13 | 26 | 0 | 6 | 18 | JAG2_chr14_105135995_105173776 | JAG2 | MRAQG others(1233): Show |
chr14 | 105135995 | 105173776 |
| a0004 | 0/0 | 1238 | 9 | 0 | 0 | 9 | 0 | 0 | 6 | JAG2_chr14_105135995_105173776 | JAG2 | MRAQG others(1233): Show |
chr14 | 105135995 | 105173776 |
| a0005 | 0/0 | 1238 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | MRAQG others(1233): Show |
chr14 | 105135995 | 105173776 |
| a0006 | 0/0 | 1238 | 7 | 0 | 6 | 1 | 0 | 0 | 1 | JAG2_chr14_105135995_105173776 | JAG2 | MRAQG others(1233): Show |
chr14 | 105135995 | 105173776 |
| a0007 | 0/0 | 1238 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | MRAQG others(1233): Show |
chr14 | 105135995 | 105173776 |
| a0008 | 0/0 | 1238 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | MRAQG others(1233): Show |
chr14 | 105135995 | 105173776 |
| a0009 | 0/0 | 1238 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | MRAQG others(1233): Show |
chr14 | 105135995 | 105173776 |
| a0010 | 0/0 | 1238 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | JAG2_chr14_105135995_105173776 | JAG2 | MRAQG others(1233): Show |
chr14 | 105135995 | 105173776 |
| a0011 | 0/0 | 1238 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | JAG2_chr14_105135995_105173776 | JAG2 | MRAQG others(1233): Show |
chr14 | 105135995 | 105173776 |
| a0012 | 0/0 | 1238 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | JAG2_chr14_105135995_105173776 | JAG2 | MRAQG others(1233): Show |
chr14 | 105135995 | 105173776 |
| a0013 | 0/0 | 1238 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | JAG2_chr14_105135995_105173776 | JAG2 | MRAQG others(1233): Show |
chr14 | 105135995 | 105173776 |
| a0014 | 0/0 | 1238 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | JAG2_chr14_105135995_105173776 | JAG2 | MRAQG others(1233): Show |
chr14 | 105135995 | 105173776 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 3714 | 125 | 37 | 27 | 46 | 5 | 10 | JAG2_chr14_105135995_105173776 | JAG2 | ATGCG others(3709): Show |
chr14 | 105135995 | 105173776 | ||
| a0001c0005 | 0/0 | 3714 | 9 | 9 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | ATGCG others(3709): Show |
chr14 | 105135995 | 105173776 | ||
| a0001c0009 | 0/0 | 3714 | 5 | 5 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | ATGCG others(3709): Show |
chr14 | 105135995 | 105173776 | ||
| a0001c0010 | 0/0 | 3714 | 4 | 0 | 0 | 4 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | ATGCG others(3709): Show |
chr14 | 105135995 | 105173776 | ||
| a0001c0011 | 0/0 | 3714 | 4 | 4 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | ATGCG others(3709): Show |
chr14 | 105135995 | 105173776 | ||
| a0001c0012 | 0/0 | 3714 | 4 | 4 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | ATGCG others(3709): Show |
chr14 | 105135995 | 105173776 | ||
| a0001c0014 | 0/0 | 3714 | 2 | 2 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | ATGCG others(3709): Show |
chr14 | 105135995 | 105173776 | ||
| a0001c0017 | 0/0 | 3714 | 2 | 2 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | ATGCG others(3709): Show |
chr14 | 105135995 | 105173776 | ||
| a0001c0022 | 0/0 | 3714 | 1 | 1 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | ATGCG others(3709): Show |
chr14 | 105135995 | 105173776 | ||
| a0001c0024 | 0/0 | 3714 | 1 | 0 | 1 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | ATGCG others(3709): Show |
chr14 | 105135995 | 105173776 | ||
| a0001c0025 | 0/0 | 3714 | 1 | 0 | 0 | 0 | 0 | 1 | JAG2_chr14_105135995_105173776 | JAG2 | ATGCG others(3709): Show |
chr14 | 105135995 | 105173776 | ||
| a0001c0032 | 0/0 | 3714 | 1 | 0 | 1 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | ATGCG others(3709): Show |
chr14 | 105135995 | 105173776 | ||
| a0001c0033 | 0/0 | 3714 | 1 | 0 | 1 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | ATGCG others(3709): Show |
chr14 | 105135995 | 105173776 | ||
| a0001c0035 | 0/0 | 3714 | 1 | 1 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | ATGCG others(3709): Show |
chr14 | 105135995 | 105173776 | ||
| a0001c0036 | 0/0 | 3714 | 1 | 1 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | ATGCG others(3709): Show |
chr14 | 105135995 | 105173776 | ||
| a0002c0002 | 1/0 | 3714 | 116 | 13 | 20 | 56 | 9 | 17 | JAG2_chr14_105135995_105173776 | JAG2 | ATGCG others(3709): Show |
chr14 | 105135995 | 105173776 | ||
| a0002c0013 | 0/0 | 3714 | 3 | 0 | 0 | 2 | 0 | 1 | JAG2_chr14_105135995_105173776 | JAG2 | ATGCG others(3709): Show |
chr14 | 105135995 | 105173776 | ||
| a0002c0015 | 0/0 | 3714 | 2 | 2 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | ATGCG others(3709): Show |
chr14 | 105135995 | 105173776 | ||
| a0002c0016 | 0/0 | 3714 | 2 | 0 | 0 | 1 | 0 | 1 | JAG2_chr14_105135995_105173776 | JAG2 | ATGCG others(3709): Show |
chr14 | 105135995 | 105173776 | ||
| a0002c0030 | 0/0 | 3714 | 1 | 1 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | ATGCG others(3709): Show |
chr14 | 105135995 | 105173776 | ||
| a0003c0003 | 0/1 | 3714 | 36 | 0 | 5 | 24 | 0 | 6 | JAG2_chr14_105135995_105173776 | JAG2 | ATGCG others(3709): Show |
chr14 | 105135995 | 105173776 | ||
| a0003c0006 | 0/0 | 3714 | 8 | 0 | 6 | 2 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | ATGCG others(3709): Show |
chr14 | 105135995 | 105173776 | ||
| a0003c0026 | 0/0 | 3714 | 1 | 0 | 1 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | ATGCG others(3709): Show |
chr14 | 105135995 | 105173776 | ||
| a0003c0027 | 0/0 | 3714 | 1 | 0 | 1 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | ATGCG others(3709): Show |
chr14 | 105135995 | 105173776 | ||
| a0004c0004 | 0/0 | 3714 | 9 | 0 | 0 | 9 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | ATGCG others(3709): Show |
chr14 | 105135995 | 105173776 | ||
| a0005c0007 | 0/0 | 3714 | 7 | 7 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | ATGCG others(3709): Show |
chr14 | 105135995 | 105173776 | ||
| a0005c0021 | 0/0 | 3714 | 1 | 1 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | ATGCG others(3709): Show |
chr14 | 105135995 | 105173776 | ||
| a0006c0008 | 0/0 | 3714 | 7 | 0 | 6 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | ATGCG others(3709): Show |
chr14 | 105135995 | 105173776 | ||
| a0007c0023 | 0/0 | 3714 | 1 | 0 | 1 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | ATGCG others(3709): Show |
chr14 | 105135995 | 105173776 | ||
| a0008c0029 | 0/0 | 3714 | 1 | 1 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | ATGCG others(3709): Show |
chr14 | 105135995 | 105173776 | ||
| a0009c0034 | 0/0 | 3714 | 1 | 1 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | ATGCG others(3709): Show |
chr14 | 105135995 | 105173776 | ||
| a0010c0031 | 0/0 | 3714 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | ATGCG others(3709): Show |
chr14 | 105135995 | 105173776 | ||
| a0011c0028 | 0/0 | 3714 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | ATGCG others(3709): Show |
chr14 | 105135995 | 105173776 | ||
| a0012c0018 | 0/0 | 3714 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | ATGCG others(3709): Show |
chr14 | 105135995 | 105173776 | ||
| a0013c0019 | 0/0 | 3714 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | ATGCG others(3709): Show |
chr14 | 105135995 | 105173776 | ||
| a0014c0020 | 0/0 | 3714 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | ATGCG others(3709): Show |
chr14 | 105135995 | 105173776 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5773 | 110 | 33 | 21 | 42 | 5 | 9 | JAG2_chr14_105135995_105173776 | JAG2 | AGTCT others(5768): Show |
chr14 | 105135995 | 105173776 |
| a0001c0001t0002 | 0/0 | 5774 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | AGTCT others(5769): Show |
chr14 | 105135995 | 105173776 |
| a0001c0001t0006 | 0/0 | 5773 | 5 | 1 | 4 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | AGTCT others(5768): Show |
chr14 | 105135995 | 105173776 |
| a0001c0001t0007 | 0/0 | 5774 | 1 | 0 | 1 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | AGTCT others(5769): Show |
chr14 | 105135995 | 105173776 |
| a0001c0001t0008 | 0/0 | 5773 | 1 | 1 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | AGTCT others(5768): Show |
chr14 | 105135995 | 105173776 |
| a0001c0001t0009 | 0/0 | 5773 | 2 | 2 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | AGTCT others(5768): Show |
chr14 | 105135995 | 105173776 |
| a0001c0001t0010 | 0/0 | 5773 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | AGTCT others(5768): Show |
chr14 | 105135995 | 105173776 |
| a0001c0001t0012 | 0/0 | 5773 | 1 | 0 | 0 | 0 | 0 | 1 | JAG2_chr14_105135995_105173776 | JAG2 | AGTCT others(5768): Show |
chr14 | 105135995 | 105173776 |
| a0001c0001t0013 | 0/0 | 5773 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | AGTCT others(5768): Show |
chr14 | 105135995 | 105173776 |
| a0001c0001t0016 | 0/0 | 5773 | 1 | 0 | 1 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | AGTCT others(5768): Show |
chr14 | 105135995 | 105173776 |
| a0001c0001t0021 | 0/0 | 5773 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | AGTCT others(5768): Show |
chr14 | 105135995 | 105173776 |
| a0001c0005t0003 | 0/0 | 5773 | 9 | 9 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | AGTCT others(5768): Show |
chr14 | 105135995 | 105173776 |
| a0001c0009t0002 | 0/0 | 5774 | 1 | 1 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | AGTCT others(5769): Show |
chr14 | 105135995 | 105173776 |
| a0001c0009t0005 | 0/0 | 5773 | 4 | 4 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | AGTCT others(5768): Show |
chr14 | 105135995 | 105173776 |
| a0001c0010t0001 | 0/0 | 5773 | 3 | 0 | 0 | 3 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | AGTCT others(5768): Show |
chr14 | 105135995 | 105173776 |
| a0001c0010t0007 | 0/0 | 5774 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | AGTCT others(5769): Show |
chr14 | 105135995 | 105173776 |
| a0001c0011t0001 | 0/0 | 5773 | 3 | 3 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | AGTCT others(5768): Show |
chr14 | 105135995 | 105173776 |
| a0001c0011t0020 | 0/0 | 5773 | 1 | 1 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | AGTCT others(5768): Show |
chr14 | 105135995 | 105173776 |
| a0001c0012t0001 | 0/0 | 5773 | 4 | 4 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | AGTCT others(5768): Show |
chr14 | 105135995 | 105173776 |
| a0001c0014t0001 | 0/0 | 5773 | 1 | 1 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | AGTCT others(5768): Show |
chr14 | 105135995 | 105173776 |
| a0001c0014t0018 | 0/0 | 5773 | 1 | 1 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | AGTCT others(5768): Show |
chr14 | 105135995 | 105173776 |
| a0001c0017t0003 | 0/0 | 5773 | 2 | 2 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | AGTCT others(5768): Show |
chr14 | 105135995 | 105173776 |
| a0001c0022t0008 | 0/0 | 5773 | 1 | 1 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | AGTCT others(5768): Show |
chr14 | 105135995 | 105173776 |
| a0001c0024t0003 | 0/0 | 5773 | 1 | 0 | 1 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | AGTCT others(5768): Show |
chr14 | 105135995 | 105173776 |
| a0001c0025t0001 | 0/0 | 5773 | 1 | 0 | 0 | 0 | 0 | 1 | JAG2_chr14_105135995_105173776 | JAG2 | AGTCT others(5768): Show |
chr14 | 105135995 | 105173776 |
| a0001c0032t0002 | 0/0 | 5774 | 1 | 0 | 1 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | AGTCT others(5769): Show |
chr14 | 105135995 | 105173776 |
| a0001c0033t0005 | 0/0 | 5773 | 1 | 0 | 1 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | AGTCT others(5768): Show |
chr14 | 105135995 | 105173776 |
| a0001c0035t0001 | 0/0 | 5773 | 1 | 1 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | AGTCT others(5768): Show |
chr14 | 105135995 | 105173776 |
| a0001c0036t0001 | 0/0 | 5773 | 1 | 1 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | AGTCT others(5768): Show |
chr14 | 105135995 | 105173776 |
| a0002c0002t0001 | 0/0 | 5773 | 98 | 11 | 14 | 55 | 6 | 12 | JAG2_chr14_105135995_105173776 | JAG2 | AGTCT others(5768): Show |
chr14 | 105135995 | 105173776 |
| a0002c0002t0004 | 1/0 | 5773 | 13 | 1 | 4 | 0 | 3 | 4 | JAG2_chr14_105135995_105173776 | JAG2 | AGTCT others(5768): Show |
chr14 | 105135995 | 105173776 |
| a0002c0002t0007 | 0/0 | 5774 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | AGTCT others(5769): Show |
chr14 | 105135995 | 105173776 |
| a0002c0002t0010 | 0/0 | 5773 | 1 | 1 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | AGTCT others(5768): Show |
chr14 | 105135995 | 105173776 |
| a0002c0002t0011 | 0/0 | 5773 | 1 | 0 | 1 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | AGTCT others(5768): Show |
chr14 | 105135995 | 105173776 |
| a0002c0002t0017 | 0/0 | 5773 | 1 | 0 | 0 | 0 | 0 | 1 | JAG2_chr14_105135995_105173776 | JAG2 | AGTCT others(5768): Show |
chr14 | 105135995 | 105173776 |
| a0002c0002t0022 | 0/0 | 5748 | 1 | 0 | 1 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | AGTCT others(5743): Show |
chr14 | 105135995 | 105173776 |
| a0002c0013t0001 | 0/0 | 5773 | 2 | 0 | 0 | 2 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | AGTCT others(5768): Show |
chr14 | 105135995 | 105173776 |
| a0002c0013t0002 | 0/0 | 5774 | 1 | 0 | 0 | 0 | 0 | 1 | JAG2_chr14_105135995_105173776 | JAG2 | AGTCT others(5769): Show |
chr14 | 105135995 | 105173776 |
| a0002c0015t0001 | 0/0 | 5773 | 2 | 2 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | AGTCT others(5768): Show |
chr14 | 105135995 | 105173776 |
| a0002c0016t0001 | 0/0 | 5773 | 2 | 0 | 0 | 1 | 0 | 1 | JAG2_chr14_105135995_105173776 | JAG2 | AGTCT others(5768): Show |
chr14 | 105135995 | 105173776 |
| a0002c0030t0003 | 0/0 | 5773 | 1 | 1 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | AGTCT others(5768): Show |
chr14 | 105135995 | 105173776 |
| a0003c0003t0002 | 0/0 | 5774 | 34 | 0 | 5 | 23 | 0 | 6 | JAG2_chr14_105135995_105173776 | JAG2 | AGTCT others(5769): Show |
chr14 | 105135995 | 105173776 |
| a0003c0003t0014 | 0/1 | 5774 | 1 | 0 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | AGTCT others(5769): Show |
chr14 | 105135995 | 105173776 |
| a0003c0003t0015 | 0/0 | 5773 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | AGTCT others(5768): Show |
chr14 | 105135995 | 105173776 |
| a0003c0006t0002 | 0/0 | 5774 | 7 | 0 | 6 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | AGTCT others(5769): Show |
chr14 | 105135995 | 105173776 |
| a0003c0006t0023 | 0/0 | 5774 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | AGTCT others(5769): Show |
chr14 | 105135995 | 105173776 |
| a0003c0026t0001 | 0/0 | 5773 | 1 | 0 | 1 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | AGTCT others(5768): Show |
chr14 | 105135995 | 105173776 |
| a0003c0027t0001 | 0/0 | 5773 | 1 | 0 | 1 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | AGTCT others(5768): Show |
chr14 | 105135995 | 105173776 |
| a0004c0004t0001 | 0/0 | 5773 | 9 | 0 | 0 | 9 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | AGTCT others(5768): Show |
chr14 | 105135995 | 105173776 |
| a0005c0007t0003 | 0/0 | 5773 | 7 | 7 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | AGTCT others(5768): Show |
chr14 | 105135995 | 105173776 |
| a0005c0021t0003 | 0/0 | 5773 | 1 | 1 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | AGTCT others(5768): Show |
chr14 | 105135995 | 105173776 |
| a0006c0008t0001 | 0/0 | 5773 | 7 | 0 | 6 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | AGTCT others(5768): Show |
chr14 | 105135995 | 105173776 |
| a0007c0023t0001 | 0/0 | 5773 | 1 | 0 | 1 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | AGTCT others(5768): Show |
chr14 | 105135995 | 105173776 |
| a0008c0029t0001 | 0/0 | 5773 | 1 | 1 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | AGTCT others(5768): Show |
chr14 | 105135995 | 105173776 |
| a0009c0034t0001 | 0/0 | 5773 | 1 | 1 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | AGTCT others(5768): Show |
chr14 | 105135995 | 105173776 |
| a0010c0031t0001 | 0/0 | 5773 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | AGTCT others(5768): Show |
chr14 | 105135995 | 105173776 |
| a0011c0028t0001 | 0/0 | 5773 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | AGTCT others(5768): Show |
chr14 | 105135995 | 105173776 |
| a0012c0018t0001 | 0/0 | 5773 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | AGTCT others(5768): Show |
chr14 | 105135995 | 105173776 |
| a0013c0019t0001 | 0/0 | 5773 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | AGTCT others(5768): Show |
chr14 | 105135995 | 105173776 |
| a0014c0020t0019 | 0/0 | 5773 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | AGTCT others(5768): Show |
chr14 | 105135995 | 105173776 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0007 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0019 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 1 | 2 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0006g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0006g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0006g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0006g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0007g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0008g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0009g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0009g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0010g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0012g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0013g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0016g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0001t0021g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0005t0003g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0005t0003g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0005t0003g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0005t0003g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0005t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0005t0003g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0009t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0009t0005g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0010t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0010t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0010t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0010t0007g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0011t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0011t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0011t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0011t0020g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0012t0001g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0012t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0014t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0014t0018g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0017t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0017t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0022t0008g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0024t0003g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0025t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0032t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0033t0005g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0035t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0001c0036t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0002c0002t0001g0001 | 0/0 | 23 | 0 | 2 | 17 | 1 | 3 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0002c0002t0001g0003 | 0/0 | 7 | 0 | 6 | 0 | 1 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0002c0002t0001g0005 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0002c0002t0001g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0002c0002t0001g0016 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0002c0002t0001g0017 | 0/0 | 3 | 1 | 0 | 0 | 1 | 1 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0002c0002t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0002c0002t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0002c0002t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0002c0002t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0002c0002t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0002c0002t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0002c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0002c0002t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0002c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0002c0002t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0002c0002t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0002c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0002c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0002c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0002c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0002c0002t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0002c0002t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0002c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0002c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0002c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0002c0002t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0002c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0002c0002t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0002c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0002c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0002c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0002c0002t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0002c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0002c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0002c0002t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0002c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0002c0002t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0002c0002t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0002c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0002c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0002c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0002c0002t0004g0002 | 1/0 | 9 | 1 | 3 | 0 | 1 | 3 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0002c0002t0004g0030 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0002c0002t0004g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0002c0002t0004g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0002c0002t0007g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0002c0002t0010g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0002c0002t0011g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0002c0002t0017g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0002c0002t0022g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0002c0013t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0002c0013t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0002c0013t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0002c0015t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0002c0015t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0002c0016t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0002c0016t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0002c0030t0003g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0003c0003t0002g0009 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0003c0003t0002g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0003c0003t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0003c0003t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0003c0003t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0003c0003t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0003c0003t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0003c0003t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0003c0003t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0003c0003t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0003c0003t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0003c0003t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0003c0003t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0003c0003t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0003c0003t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0003c0003t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0003c0003t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0003c0003t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0003c0003t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0003c0003t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0003c0003t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0003c0003t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0003c0003t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0003c0003t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0003c0003t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0003c0003t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0003c0003t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0003c0003t0014g0253 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0003c0003t0015g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0003c0006t0002g0010 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0003c0006t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0003c0006t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0003c0006t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0003c0006t0023g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0003c0026t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0003c0027t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0004c0004t0001g0004 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0004c0004t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0004c0004t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0004c0004t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0005c0007t0003g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0005c0007t0003g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0005c0007t0003g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0005c0007t0003g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0005c0007t0003g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0005c0007t0003g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0005c0021t0003g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0006c0008t0001g0018 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0006c0008t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0006c0008t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0006c0008t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0006c0008t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0007c0023t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0008c0029t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0009c0034t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0010c0031t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0011c0028t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0012c0018t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0013c0019t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| a0014c0020t0019g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0020 | EUR | GBR | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG00099 | hp2 | a0002 | c0002 | t0001 | g0108 | EUR | GBR | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG00140 | hp1 | a0002 | c0002 | t0004 | g0002 | EUR | GBR | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG00140 | hp2 | a0002 | c0002 | t0001 | g0003 | EUR | GBR | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0020 | EUR | FIN | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG00280 | hp2 | a0002 | c0002 | t0001 | g0138 | EUR | FIN | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG00408 | hp1 | a0003 | c0003 | t0002 | g0094 | EAS | CHS | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG00408 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | CHS | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG00438 | hp1 | a0002 | c0002 | t0001 | g0025 | EAS | CHS | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG00438 | hp2 | a0004 | c0004 | t0001 | g0004 | EAS | CHS | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG00544 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | CHS | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG00544 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | CHS | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG00558 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | CHS | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG00558 | hp2 | a0004 | c0004 | t0001 | g0004 | EAS | CHS | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG00597 | hp1 | a0001 | c0001 | t0021 | g0045 | EAS | CHS | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG00597 | hp2 | a0002 | c0002 | t0001 | g0103 | EAS | CHS | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG00609 | hp1 | a0003 | c0006 | t0002 | g0147 | EAS | CHS | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG00609 | hp2 | a0003 | c0003 | t0002 | g0012 | EAS | CHS | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG00621 | hp1 | a0003 | c0003 | t0002 | g0012 | EAS | CHS | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | CHS | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG00639 | hp1 | a0001 | c0033 | t0005 | g0057 | AMR | PUR | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG00639 | hp2 | a0002 | c0002 | t0001 | g0130 | AMR | PUR | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0003 | AMR | PUR | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG00673 | hp1 | a0002 | c0002 | t0001 | g0122 | EAS | CHS | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | CHS | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG00735 | hp1 | a0001 | c0032 | t0002 | g0056 | AMR | PUR | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG00735 | hp2 | a0003 | c0003 | t0002 | g0064 | AMR | PUR | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG00741 | hp1 | a0001 | c0001 | t0007 | g0190 | AMR | PUR | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG00741 | hp2 | a0002 | c0002 | t0001 | g0142 | AMR | PUR | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG01071 | hp2 | a0001 | c0001 | t0006 | g0194 | AMR | PUR | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG01074 | hp1 | a0003 | c0026 | t0001 | g0078 | AMR | PUR | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG01106 | hp1 | a0003 | c0003 | t0002 | g0065 | AMR | PUR | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG01106 | hp2 | a0007 | c0023 | t0001 | g0171 | AMR | PUR | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG01109 | hp1 | a0002 | c0002 | t0001 | g0115 | AMR | PUR | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG01109 | hp2 | a0002 | c0002 | t0004 | g0002 | AMR | PUR | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | PUR | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG01168 | hp2 | a0001 | c0001 | t0006 | g0036 | AMR | PUR | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG01169 | hp2 | a0001 | c0001 | t0006 | g0036 | AMR | PUR | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG01175 | hp1 | a0001 | c0024 | t0003 | g0093 | AMR | PUR | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG01243 | hp2 | a0002 | c0002 | t0004 | g0002 | AMR | PUR | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG01256 | hp1 | a0003 | c0006 | t0002 | g0010 | AMR | CLM | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG01258 | hp2 | a0001 | c0001 | t0006 | g0191 | AMR | CLM | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG01261 | hp2 | a0006 | c0008 | t0001 | g0162 | AMR | CLM | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG01346 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG01346 | hp2 | a0003 | c0027 | t0001 | g0112 | AMR | CLM | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG01358 | hp1 | a0003 | c0003 | t0002 | g0066 | AMR | CLM | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG01358 | hp2 | a0002 | c0002 | t0004 | g0002 | AMR | CLM | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG01361 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG01361 | hp2 | a0003 | c0003 | t0002 | g0009 | AMR | CLM | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | CLM | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | CLM | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG01496 | hp1 | a0006 | c0008 | t0001 | g0018 | AMR | CLM | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG01496 | hp2 | a0003 | c0003 | t0002 | g0077 | AMR | CLM | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0123 | EUR | IBS | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0032 | EUR | IBS | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0175 | EUR | IBS | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0172 | EUR | IBS | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG01884 | hp1 | a0001 | c0009 | t0005 | g0008 | AFR | ACB | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG01891 | hp2 | a0001 | c0036 | t0001 | g0257 | AFR | ACB | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | PEL | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG01928 | hp2 | a0003 | c0006 | t0002 | g0010 | AMR | PEL | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PEL | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG01934 | hp2 | a0003 | c0006 | t0002 | g0149 | AMR | PEL | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG01952 | hp1 | a0002 | c0002 | t0001 | g0003 | AMR | PEL | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG01952 | hp2 | a0003 | c0006 | t0002 | g0010 | AMR | PEL | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG01975 | hp1 | a0006 | c0008 | t0001 | g0152 | AMR | PEL | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG01975 | hp2 | a0002 | c0002 | t0001 | g0136 | AMR | PEL | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG01981 | hp1 | a0002 | c0002 | t0001 | g0003 | AMR | PEL | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PEL | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG01993 | hp1 | a0002 | c0002 | t0001 | g0118 | AMR | PEL | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG01993 | hp2 | a0002 | c0002 | t0001 | g0003 | AMR | PEL | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02004 | hp1 | a0003 | c0006 | t0002 | g0010 | AMR | PEL | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02004 | hp2 | a0006 | c0008 | t0001 | g0018 | AMR | PEL | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | KHV | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02015 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02027 | hp2 | a0001 | c0010 | t0001 | g0197 | EAS | KHV | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02040 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | KHV | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | ACB | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02055 | hp2 | a0002 | c0002 | t0001 | g0143 | AFR | ACB | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02056 | hp2 | a0002 | c0002 | t0007 | g0124 | EAS | KHV | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02074 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02074 | hp2 | a0002 | c0002 | t0001 | g0144 | EAS | KHV | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02080 | hp1 | a0002 | c0002 | t0001 | g0141 | EAS | KHV | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | KHV | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02083 | hp1 | a0002 | c0016 | t0001 | g0129 | EAS | KHV | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02083 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | KHV | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02129 | hp1 | a0003 | c0003 | t0002 | g0095 | EAS | KHV | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02129 | hp2 | a0003 | c0003 | t0002 | g0012 | EAS | KHV | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02132 | hp1 | a0001 | c0010 | t0001 | g0192 | EAS | KHV | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02132 | hp2 | a0002 | c0002 | t0001 | g0029 | EAS | KHV | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02135 | hp1 | a0001 | c0010 | t0001 | g0258 | EAS | KHV | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02135 | hp2 | a0002 | c0002 | t0001 | g0139 | EAS | KHV | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | ACB | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02145 | hp2 | a0002 | c0002 | t0010 | g0107 | AFR | ACB | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02148 | hp1 | a0002 | c0002 | t0001 | g0003 | AMR | PEL | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02148 | hp2 | a0003 | c0006 | t0002 | g0080 | AMR | PEL | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02155 | hp1 | a0003 | c0003 | t0002 | g0012 | EAS | CDX | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02155 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | CDX | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02257 | hp1 | a0002 | c0002 | t0001 | g0016 | AFR | ACB | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02257 | hp2 | a0002 | c0002 | t0001 | g0017 | AFR | ACB | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02273 | hp1 | a0002 | c0002 | t0001 | g0003 | AMR | PEL | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02273 | hp2 | a0006 | c0008 | t0001 | g0018 | AMR | PEL | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02280 | hp1 | a0001 | c0012 | t0001 | g0015 | AFR | ACB | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | ACB | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02293 | hp1 | a0001 | c0001 | t0016 | g0177 | AMR | PEL | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02293 | hp2 | a0002 | c0002 | t0011 | g0039 | AMR | PEL | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02300 | hp1 | a0006 | c0008 | t0001 | g0150 | AMR | PEL | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02300 | hp2 | a0002 | c0002 | t0001 | g0016 | AMR | PEL | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02451 | hp1 | a0002 | c0002 | t0001 | g0016 | AFR | ACB | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02523 | hp1 | a0001 | c0010 | t0007 | g0195 | EAS | KHV | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02523 | hp2 | a0003 | c0003 | t0002 | g0096 | EAS | KHV | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02572 | hp1 | a0002 | c0002 | t0001 | g0043 | AFR | GWD | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02572 | hp2 | a0001 | c0005 | t0003 | g0014 | AFR | GWD | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0236 | SAS | PJL | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02602 | hp2 | a0002 | c0016 | t0001 | g0116 | SAS | PJL | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02622 | hp1 | a0001 | c0017 | t0003 | g0090 | AFR | GWD | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02622 | hp2 | a0001 | c0005 | t0003 | g0023 | AFR | GWD | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02630 | hp1 | a0001 | c0005 | t0003 | g0014 | AFR | GWD | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02630 | hp2 | a0002 | c0002 | t0001 | g0052 | AFR | GWD | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02647 | hp1 | a0005 | c0007 | t0003 | g0256 | AFR | GWD | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02647 | hp2 | a0001 | c0001 | t0008 | g0048 | AFR | GWD | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02683 | hp1 | a0001 | c0001 | t0012 | g0040 | SAS | PJL | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02683 | hp2 | a0002 | c0002 | t0004 | g0134 | SAS | PJL | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02698 | hp1 | a0003 | c0003 | t0002 | g0083 | SAS | PJL | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02698 | hp2 | a0002 | c0002 | t0001 | g0133 | SAS | PJL | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02717 | hp1 | a0008 | c0029 | t0001 | g0119 | AFR | GWD | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02723 | hp1 | a0005 | c0007 | t0003 | g0254 | AFR | GWD | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02723 | hp2 | a0001 | c0005 | t0003 | g0087 | AFR | GWD | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02735 | hp2 | a0002 | c0002 | t0004 | g0002 | SAS | PJL | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02738 | hp1 | a0002 | c0002 | t0001 | g0100 | SAS | PJL | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0220 | SAS | PJL | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | GWD | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02818 | hp1 | a0001 | c0017 | t0003 | g0088 | AFR | GWD | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02818 | hp2 | a0005 | c0007 | t0003 | g0240 | AFR | GWD | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02886 | hp1 | a0001 | c0005 | t0003 | g0014 | AFR | GWD | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02886 | hp2 | a0001 | c0005 | t0003 | g0091 | AFR | GWD | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02895 | hp1 | a0005 | c0007 | t0003 | g0239 | AFR | GWD | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02896 | hp2 | a0005 | c0021 | t0003 | g0242 | AFR | GWD | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02897 | hp1 | a0005 | c0007 | t0003 | g0241 | AFR | GWD | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02922 | hp1 | a0001 | c0009 | t0005 | g0008 | AFR | ESN | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02922 | hp2 | a0002 | c0002 | t0001 | g0031 | AFR | ESN | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | ESN | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02965 | hp2 | a0001 | c0012 | t0001 | g0015 | AFR | ESN | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02970 | hp1 | a0001 | c0011 | t0001 | g0226 | AFR | ESN | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | ESN | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02976 | hp2 | a0001 | c0001 | t0009 | g0082 | AFR | ESN | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG03017 | hp1 | a0003 | c0003 | t0002 | g0063 | SAS | PJL | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0187 | SAS | PJL | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG03041 | hp1 | a0002 | c0002 | t0001 | g0106 | AFR | GWD | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG03041 | hp2 | a0005 | c0007 | t0003 | g0038 | AFR | GWD | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG03098 | hp1 | a0001 | c0009 | t0002 | g0055 | AFR | MSL | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG03098 | hp2 | a0001 | c0011 | t0001 | g0188 | AFR | MSL | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG03130 | hp1 | a0001 | c0005 | t0003 | g0092 | AFR | ESN | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG03130 | hp2 | a0002 | c0015 | t0001 | g0145 | AFR | ESN | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | ESN | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG03139 | hp2 | a0001 | c0009 | t0005 | g0008 | AFR | ESN | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG03195 | hp1 | a0001 | c0012 | t0001 | g0015 | AFR | ESN | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | ESN | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG03209 | hp1 | a0002 | c0002 | t0001 | g0031 | AFR | MSL | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG03209 | hp2 | a0001 | c0035 | t0001 | g0227 | AFR | MSL | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG03225 | hp1 | a0001 | c0011 | t0001 | g0193 | AFR | MSL | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG03239 | hp1 | a0002 | c0002 | t0004 | g0002 | SAS | PJL | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG03239 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG03486 | hp1 | a0001 | c0005 | t0003 | g0023 | AFR | MSL | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | MSL | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG03492 | hp1 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG03492 | hp2 | a0003 | c0003 | t0002 | g0076 | SAS | PJL | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | ESN | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | ESN | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | GWD | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG03579 | hp1 | a0002 | c0002 | t0001 | g0105 | AFR | MSL | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG03579 | hp2 | a0001 | c0005 | t0003 | g0089 | AFR | MSL | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG03688 | hp1 | a0002 | c0002 | t0004 | g0002 | SAS | STU | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG03688 | hp2 | a0003 | c0003 | t0002 | g0059 | SAS | STU | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG03704 | hp1 | a0002 | c0002 | t0001 | g0017 | SAS | PJL | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG03704 | hp2 | a0002 | c0002 | t0001 | g0114 | SAS | PJL | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | BEB | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | BEB | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0245 | SAS | BEB | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG03834 | hp2 | a0002 | c0002 | t0001 | g0005 | SAS | BEB | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0225 | SAS | BEB | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG03927 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | BEB | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG04115 | hp1 | a0002 | c0002 | t0017 | g0137 | SAS | STU | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG04115 | hp2 | a0002 | c0002 | t0001 | g0132 | SAS | STU | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG04184 | hp1 | a0002 | c0002 | t0001 | g0042 | SAS | BEB | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG04184 | hp2 | a0002 | c0002 | t0001 | g0121 | SAS | BEB | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG04199 | hp1 | a0001 | c0025 | t0001 | g0243 | SAS | STU | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG04199 | hp2 | a0002 | c0013 | t0002 | g0131 | SAS | STU | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG04204 | hp1 | a0002 | c0002 | t0001 | g0126 | SAS | STU | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG04204 | hp2 | a0003 | c0003 | t0002 | g0053 | SAS | STU | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | STU | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG04228 | hp2 | a0003 | c0003 | t0002 | g0062 | SAS | STU | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | YRI | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA18522 | hp2 | a0001 | c0012 | t0001 | g0098 | AFR | YRI | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA18612 | hp1 | a0004 | c0004 | t0001 | g0160 | EAS | CHB | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA18612 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | CHB | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | CHB | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA18747 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | CHB | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA18942 | hp1 | a0001 | c0001 | t0013 | g0215 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA18942 | hp2 | a0002 | c0002 | t0001 | g0026 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA18944 | hp1 | a0003 | c0003 | t0002 | g0157 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA18944 | hp2 | a0002 | c0002 | t0001 | g0140 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA18945 | hp1 | a0003 | c0003 | t0002 | g0009 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA18945 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA18947 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA18948 | hp2 | a0004 | c0004 | t0001 | g0161 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA18950 | hp1 | a0010 | c0031 | t0001 | g0044 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA18950 | hp2 | a0011 | c0028 | t0001 | g0153 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA18951 | hp1 | a0002 | c0002 | t0001 | g0101 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA18952 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA18953 | hp1 | a0003 | c0006 | t0023 | g0260 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA18954 | hp1 | a0003 | c0003 | t0002 | g0075 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA18956 | hp1 | a0004 | c0004 | t0001 | g0004 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA18956 | hp2 | a0003 | c0003 | t0002 | g0070 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA18959 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA18963 | hp1 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA18963 | hp2 | a0003 | c0003 | t0002 | g0009 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA18966 | hp1 | a0002 | c0002 | t0001 | g0155 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA18966 | hp2 | a0003 | c0003 | t0002 | g0060 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA18969 | hp1 | a0002 | c0013 | t0001 | g0205 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA18969 | hp2 | a0003 | c0003 | t0002 | g0022 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA18970 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA18971 | hp1 | a0002 | c0002 | t0001 | g0117 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA18971 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA18979 | hp1 | a0002 | c0002 | t0001 | g0025 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA18979 | hp2 | a0002 | c0002 | t0001 | g0109 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA18980 | hp1 | a0003 | c0003 | t0002 | g0022 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA18980 | hp2 | a0013 | c0019 | t0001 | g0151 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA18981 | hp2 | a0004 | c0004 | t0001 | g0159 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA18983 | hp1 | a0003 | c0003 | t0002 | g0073 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA18983 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA18985 | hp1 | a0003 | c0003 | t0015 | g0074 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA18990 | hp1 | a0006 | c0008 | t0001 | g0154 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA18990 | hp2 | a0003 | c0003 | t0002 | g0061 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA18997 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA18998 | hp1 | a0002 | c0002 | t0001 | g0113 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA18998 | hp2 | a0001 | c0001 | t0010 | g0212 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA19000 | hp2 | a0002 | c0002 | t0001 | g0028 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA19002 | hp1 | a0003 | c0003 | t0002 | g0085 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA19003 | hp1 | a0002 | c0002 | t0001 | g0104 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA19003 | hp2 | a0002 | c0002 | t0001 | g0158 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA19005 | hp1 | a0002 | c0002 | t0001 | g0125 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA19007 | hp1 | a0002 | c0002 | t0001 | g0028 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA19007 | hp2 | a0002 | c0002 | t0001 | g0111 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA19010 | hp1 | a0002 | c0002 | t0001 | g0110 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA19011 | hp1 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA19011 | hp2 | a0002 | c0013 | t0001 | g0209 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA19012 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA19030 | hp1 | a0002 | c0030 | t0003 | g0054 | AFR | LWK | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA19030 | hp2 | a0005 | c0007 | t0003 | g0038 | AFR | LWK | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | LWK | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA19043 | hp2 | a0001 | c0014 | t0001 | g0252 | AFR | LWK | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA19056 | hp1 | a0002 | c0002 | t0001 | g0029 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA19056 | hp2 | a0004 | c0004 | t0001 | g0004 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA19057 | hp1 | a0002 | c0002 | t0001 | g0027 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA19060 | hp2 | a0003 | c0003 | t0002 | g0079 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA19063 | hp2 | a0002 | c0002 | t0001 | g0050 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA19064 | hp1 | a0002 | c0002 | t0001 | g0027 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA19066 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA19066 | hp2 | a0002 | c0002 | t0001 | g0026 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA19068 | hp1 | a0002 | c0002 | t0001 | g0120 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA19068 | hp2 | a0003 | c0003 | t0002 | g0097 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA19070 | hp1 | a0003 | c0003 | t0002 | g0009 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA19074 | hp2 | a0004 | c0004 | t0001 | g0004 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA19080 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA19081 | hp1 | a0002 | c0002 | t0001 | g0102 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA19081 | hp2 | a0004 | c0004 | t0001 | g0004 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA19083 | hp1 | a0003 | c0003 | t0002 | g0071 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA19085 | hp1 | a0002 | c0002 | t0001 | g0127 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA19088 | hp1 | a0003 | c0003 | t0002 | g0072 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA19090 | hp2 | a0014 | c0020 | t0019 | g0156 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA19091 | hp1 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | YRI | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | YRI | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | ASW | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA20129 | hp2 | a0001 | c0011 | t0020 | g0211 | AFR | ASW | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA20752 | hp1 | a0002 | c0002 | t0004 | g0030 | EUR | TSI | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA20752 | hp2 | a0002 | c0002 | t0001 | g0017 | EUR | TSI | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA20805 | hp1 | a0002 | c0002 | t0004 | g0135 | EUR | TSI | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA20805 | hp2 | a0002 | c0002 | t0001 | g0001 | EUR | TSI | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG01123 | hp1 | a0002 | c0002 | t0004 | g0030 | AMR | CLM | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG01123 | hp2 | a0002 | c0002 | t0022 | g0259 | AMR | CLM | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | ACB | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02109 | hp2 | a0001 | c0022 | t0008 | g0084 | AFR | ACB | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02486 | hp1 | a0001 | c0014 | t0018 | g0086 | AFR | ACB | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | ACB | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02559 | hp1 | a0002 | c0002 | t0004 | g0002 | AFR | ACB | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG02559 | hp2 | a0002 | c0002 | t0001 | g0051 | AFR | ACB | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG03471 | hp1 | a0009 | c0034 | t0001 | g0058 | AFR | MSL | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | MSL | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG06807 | hp1 | a0002 | c0015 | t0001 | g0146 | AFR | USA | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| HG06807 | hp2 | a0001 | c0009 | t0005 | g0008 | AFR | USA | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA18955 | hp1 | a0012 | c0018 | t0001 | g0210 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA20300 | hp1 | a0001 | c0001 | t0009 | g0081 | AFR | USA | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | USA | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA21309 | hp1 | a0001 | c0001 | t0006 | g0189 | AFR | LWK | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | LWK | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| homoSapiens | chm13v2 | a0003 | c0003 | t0014 | g0253 | REF | REF | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0004 | g0002 | REF | REF | JAG2_chr14_105135995_105173776 | JAG2 | chr14 | 105135995 | 105173776 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:105143494 | C | T | 1 | a0007 | 1 | HG01106.hp2 | missense_variant | MODERATE | c.3229G>A | p.Gly1077Ser | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 25/26 | 3585/5773 | 3229/3717 | 1077/1238 | chr14 | 105143494 | |||
| chr14:105143499 | G | A | 2 | a0004 a0014 |
10 | HG00438.hp2 HG00558.hp2 NA18612.hp1 others(7): Show |
missense_variant | MODERATE | c.3224C>T | p.Thr1075Met | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 25/26 | 3580/5773 | 3224/3717 | 1075/1238 | chr14 | 105143499 | |||
| chr14:105145832 | C | T | 1 | a0005 | 8 | HG02647.hp1 HG02723.hp1 HG02818.hp2 others(5): Show |
missense_variant | MODERATE | c.2851G>A | p.Ala951Thr | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 23/26 | 3207/5773 | 2851/3717 | 951/1238 | chr14 | 105145832 | |||
| chr14:105145924 | A | T | 1 | a0011 | 1 | NA18950.hp2 | missense_variant | MODERATE | c.2759T>A | p.Leu920Gln | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 23/26 | 3115/5773 | 2759/3717 | 920/1238 | chr14 | 105145924 | |||
| chr14:105146622 | C | T | 1 | a0008 | 1 | HG02717.hp1 | missense_variant | MODERATE | c.2582G>A | p.Arg861Gln | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 21/26 | 2938/5773 | 2582/3717 | 861/1238 | chr14 | 105146622 | |||
| chr14:105148185 | A | C | 1 | a0010 | 1 | NA18950.hp1 | missense_variant | MODERATE | c.2179T>G | p.Cys727Gly | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 17/26 | 2535/5773 | 2179/3717 | 727/1238 | chr14 | 105148185 | |||
| chr14:105148397 | C | T | 5 | a0004 a0006 a0011 others(2): Show |
19 | HG00438.hp2 HG00558.hp2 HG01261.hp2 others(16): Show |
missense_variant | MODERATE | c.2063G>A | p.Arg688His | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 16/26 | 2419/5773 | 2063/3717 | 688/1238 | chr14 | 105148397 | |||
| chr14:105148413 | A | C | 1 | a0010 | 1 | NA18950.hp1 | missense_variant | MODERATE | c.2047T>G | p.Cys683Gly | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 16/26 | 2403/5773 | 2047/3717 | 683/1238 | chr14 | 105148413 | |||
| chr14:105149311 | C | T | 1 | a0003 | 45 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(42): Show |
missense_variant | MODERATE | c.1612G>A | p.Asp538Asn | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 13/26 | 1968/5773 | 1612/3717 | 538/1238 | chr14 | 105149311 | |||
| chr14:105150705 | C | T | 7 | a0001 a0005 a0007 others(4): Show |
175 | HG00099.hp1 HG00280.hp1 HG00597.hp1 others(172): Show |
missense_variant | MODERATE | c.1501G>A | p.Glu501Lys | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 12/26 | 1857/5773 | 1501/3717 | 501/1238 | chr14 | 105150705 | |||
| chr14:105152190 | G | A | 1 | a0009 | 1 | HG03471.hp1 | missense_variant | MODERATE | c.890C>T | p.Thr297Ile | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 6/26 | 1246/5773 | 890/3717 | 297/1238 | chr14 | 105152190 | |||
| chr14:105157757 | A | T | 1 | a0012 | 1 | NA18955.hp1 | missense_variant | MODERATE | c.424T>A | p.Phe142Ile | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 3/26 | 780/5773 | 424/3717 | 142/1238 | chr14 | 105157757 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:105142824 | G | A | 6 | a0001c0005 a0001c0017 a0001c0024 others(3): Show |
21 | HG01175.hp1 HG02572.hp2 HG02622.hp1 others(18): Show |
synonymous_variant | LOW | c.3588C>T | p.Phe1196Phe | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 26/26 | 3944/5773 | 3588/3717 | 1196/1238 | chr14 | 105142824 | |||
| chr14:105142998 | A | G | 31 | a0001c0001 a0001c0005 a0001c0009 others(28): Show |
243 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(240): Show |
synonymous_variant | LOW | c.3414T>C | p.Ile1138Ile | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 26/26 | 3770/5773 | 3414/3717 | 1138/1238 | chr14 | 105142998 | |||
| chr14:105143022 | C | T | 2 | a0001c0014 a0009c0034 |
3 | HG02486.hp1 HG03471.hp1 NA19043.hp2 |
synonymous_variant | LOW | c.3390G>A | p.Pro1130Pro | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 26/26 | 3746/5773 | 3390/3717 | 1130/1238 | chr14 | 105143022 | |||
| chr14:105143504 | A | C | 1 | a0001c0022 | 1 | HG02109.hp2 | synonymous_variant | LOW | c.3219T>G | p.Val1073Val | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 25/26 | 3575/5773 | 3219/3717 | 1073/1238 | chr14 | 105143504 | |||
| chr14:105143591 | G | A | 1 | a0001c0010 | 4 | HG02027.hp2 HG02132.hp1 HG02135.hp1 others(1): Show |
synonymous_variant | LOW | c.3132C>T | p.Gly1044Gly | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 25/26 | 3488/5773 | 3132/3717 | 1044/1238 | chr14 | 105143591 | |||
| chr14:105144945 | A | G | 29 | a0001c0001 a0001c0005 a0001c0009 others(26): Show |
232 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(229): Show |
synonymous_variant | LOW | c.3069T>C | p.Ala1023Ala | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 24/26 | 3425/5773 | 3069/3717 | 1023/1238 | chr14 | 105144945 | |||
| chr14:105146681 | C | T | 1 | a0001c0017 | 2 | HG02622.hp1 HG02818.hp1 |
synonymous_variant | LOW | c.2523G>A | p.Thr841Thr | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 21/26 | 2879/5773 | 2523/3717 | 841/1238 | chr14 | 105146681 | |||
| chr14:105146702 | C | T | 3 | a0002c0015 a0003c0006 a0003c0026 |
11 | HG00609.hp1 HG01074.hp1 HG01256.hp1 others(8): Show |
synonymous_variant | LOW | c.2502G>A | p.Ser834Ser | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 21/26 | 2858/5773 | 2502/3717 | 834/1238 | chr14 | 105146702 | |||
| chr14:105147339 | A | G | 1 | a0005c0021 | 1 | HG02896.hp2 | synonymous_variant | LOW | c.2466T>C | p.Pro822Pro | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 20/26 | 2822/5773 | 2466/3717 | 822/1238 | chr14 | 105147339 | |||
| chr14:105148360 | G | A | 2 | a0001c0011 a0001c0035 |
5 | HG02970.hp1 HG03098.hp2 HG03209.hp2 others(2): Show |
synonymous_variant | LOW | c.2100C>T | p.Cys700Cys | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 16/26 | 2456/5773 | 2100/3717 | 700/1238 | chr14 | 105148360 | |||
| chr14:105148414 | G | A | 1 | a0010c0031 | 1 | NA18950.hp1 | synonymous_variant | LOW | c.2046C>T | p.Pro682Pro | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 16/26 | 2402/5773 | 2046/3717 | 682/1238 | chr14 | 105148414 | |||
| chr14:105148815 | T | C | 1 | a0001c0025 | 1 | HG04199.hp1 | synonymous_variant | LOW | c.1950A>G | p.Thr650Thr | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 15/26 | 2306/5773 | 1950/3717 | 650/1238 | chr14 | 105148815 | |||
| chr14:105150661 | G | A | 4 | a0001c0009 a0001c0032 a0001c0033 others(1): Show |
8 | HG00639.hp1 HG00735.hp1 HG01884.hp1 others(5): Show |
synonymous_variant | LOW | c.1545C>T | p.Asp515Asp | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 12/26 | 1901/5773 | 1545/3717 | 515/1238 | chr14 | 105150661 | |||
| chr14:105151103 | G | A | 1 | a0001c0032 | 1 | HG00735.hp1 | splice_region_variant&synonymous_variant | LOW | c.1269C>T | p.Asp423Asp | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 10/26 | 1625/5773 | 1269/3717 | 423/1238 | chr14 | 105151103 | |||
| chr14:105151672 | G | A | 1 | a0001c0012 | 4 | HG02280.hp1 HG02965.hp2 HG03195.hp1 others(1): Show |
synonymous_variant | LOW | c.1107C>T | p.Phe369Phe | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 8/26 | 1463/5773 | 1107/3717 | 369/1238 | chr14 | 105151672 | |||
| chr14:105152180 | G | A | 1 | a0001c0033 | 1 | HG00639.hp1 | synonymous_variant | LOW | c.900C>T | p.Gly300Gly | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 6/26 | 1256/5773 | 900/3717 | 300/1238 | chr14 | 105152180 | |||
| chr14:105155787 | G | A | 1 | a0001c0035 | 1 | HG03209.hp2 | synonymous_variant | LOW | c.678C>T | p.Tyr226Tyr | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 4/26 | 1034/5773 | 678/3717 | 226/1238 | chr14 | 105155787 | |||
| chr14:105155820 | G | A | 2 | a0001c0005 a0001c0017 |
11 | HG02572.hp2 HG02622.hp1 HG02622.hp2 others(8): Show |
synonymous_variant | LOW | c.645C>T | p.Asn215Asn | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 4/26 | 1001/5773 | 645/3717 | 215/1238 | chr14 | 105155820 | |||
| chr14:105167868 | G | A | 1 | a0001c0036 | 1 | HG01891.hp2 | synonymous_variant | LOW | c.306C>T | p.Ser102Ser | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/26 | 662/5773 | 306/3717 | 102/1238 | chr14 | 105167868 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:105141471 | C | T | 1 | a0001c0014t0018 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1224G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 26/26 | 1224 | chr14 | 105141471 | ||||||
| chr14:105141550 | C | T | 1 | a0002c0002t0017 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1145G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 26/26 | 1145 | chr14 | 105141550 | ||||||
| chr14:105141642 | C | T | 53 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 others(50): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(265): Show |
3_prime_UTR_variant | MODIFIER | c.*1053G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 26/26 | 1053 | chr14 | 105141642 | ||||||
| chr14:105141671 | C | T | 2 | a0001c0001t0008 a0001c0022t0008 |
2 | HG02109.hp2 HG02647.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1024G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 26/26 | 1024 | chr14 | 105141671 | ||||||
| chr14:105141945 | G | A | 1 | a0014c0020t0019 | 1 | NA19090.hp2 | 3_prime_UTR_variant | MODIFIER | c.*750C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 26/26 | 750 | chr14 | 105141945 | ||||||
| chr14:105142031 | G | C | 1 | a0001c0011t0020 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*664C>G | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 26/26 | 664 | chr14 | 105142031 | ||||||
| chr14:105142050 | G | A | 1 | a0001c0001t0006 | 5 | HG01071.hp2 HG01168.hp2 HG01169.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*645C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 26/26 | 645 | chr14 | 105142050 | ||||||
| chr14:105142066 | A | G | 58 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 others(55): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(347): Show |
3_prime_UTR_variant | MODIFIER | c.*629T>C | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 26/26 | 629 | chr14 | 105142066 | ||||||
| chr14:105142210 | T | C | 1 | a0001c0001t0021 | 1 | HG00597.hp1 | 3_prime_UTR_variant | MODIFIER | c.*485A>G | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 26/26 | 485 | chr14 | 105142210 | ||||||
| chr14:105142220 | C | T | 1 | a0001c0001t0016 | 1 | HG02293.hp1 | 3_prime_UTR_variant | MODIFIER | c.*475G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 26/26 | 475 | chr14 | 105142220 | ||||||
| chr14:105142227 | C | T | 9 | a0001c0001t0002 a0001c0001t0013 a0001c0009t0002 others(6): Show |
48 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*468G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 26/26 | 468 | chr14 | 105142227 | ||||||
| chr14:105142231 | G | A | 1 | a0001c0001t0006 | 5 | HG01071.hp2 HG01168.hp2 HG01169.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*464C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 26/26 | 464 | chr14 | 105142231 | ||||||
| chr14:105142421 | C | A | 3 | a0001c0001t0009 a0001c0009t0005 a0001c0033t0005 |
7 | HG00639.hp1 HG01884.hp1 HG02922.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*274G>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 26/26 | 274 | chr14 | 105142421 | ||||||
| chr14:105142428 | C | T | 2 | a0001c0009t0005 a0001c0033t0005 |
5 | HG00639.hp1 HG01884.hp1 HG02922.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*267G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 26/26 | 267 | chr14 | 105142428 | ||||||
| chr14:105142447 | G | A | 2 | a0001c0001t0010 a0002c0002t0010 |
2 | HG02145.hp2 NA18998.hp2 |
3_prime_UTR_variant | MODIFIER | c.*248C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 26/26 | 248 | chr14 | 105142447 | ||||||
| chr14:105142584 | G | GT | 10 | a0001c0001t0002 a0001c0001t0007 a0001c0009t0002 others(7): Show |
49 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*110dupA | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 26/26 | 110 | chr14 | 105142584 | ||||||
| chr14:105142584 | G | T | 1 | a0001c0001t0013 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*111C>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 26/26 | 111 | chr14 | 105142584 | ||||||
| chr14:105142637 | G | A | 6 | a0001c0005t0003 a0001c0017t0003 a0001c0024t0003 others(3): Show |
21 | HG01175.hp1 HG02572.hp2 HG02622.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*58C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 26/26 | 58 | chr14 | 105142637 | ||||||
| chr14:105168436 | C | G | 1 | a0001c0001t0012 | 1 | HG02683.hp1 | 5_prime_UTR_variant | MODIFIER | c.-16G>C | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 1/26 | 16 | chr14 | 105168436 | ||||||
| chr14:105168437 | CCGCCCGG others(18): Show |
C | 1 | a0002c0002t0022 | 1 | HG01123.hp2 | 5_prime_UTR_variant | MODIFIER | c.-42_-18delCGGGCGGC others(17): Show |
JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 1/26 | 18 | chr14 | 105168437 | ||||||
| chr14:105168742 | C | T | 1 | a0002c0002t0011 | 1 | HG02293.hp2 | 5_prime_UTR_variant | MODIFIER | c.-322G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 1/26 | 322 | chr14 | 105168742 | ||||||
| chr14:105168750 | C | G | 1 | a0003c0006t0023 | 1 | NA18953.hp1 | 5_prime_UTR_variant | MODIFIER | c.-330G>C | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 1/26 | 330 | chr14 | 105168750 | ||||||
| chr14:105168751 | G | C | 1 | a0003c0006t0023 | 1 | NA18953.hp1 | 5_prime_UTR_variant | MODIFIER | c.-331C>G | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 1/26 | 331 | chr14 | 105168751 | ||||||
| chr14:105168752 | C | A | 1 | a0003c0006t0023 | 1 | NA18953.hp1 | 5_prime_UTR_variant | MODIFIER | c.-332G>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 1/26 | 332 | chr14 | 105168752 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:105143193 | G | A | 1 | a0001c0011t0001g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3242-23C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 25/25 | chr14 | 105143193 | |||||||
| chr14:105143316 | C | T | 1 | a0001c0001t0006g0189 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3242-146G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 25/25 | chr14 | 105143316 | |||||||
| chr14:105143355 | G | A | 3 | a0002c0002t0001g0121 a0002c0002t0001g0123 a0002c0002t0022g0259 |
3 | HG01123.hp2 HG01515.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.3241+127C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 25/25 | chr14 | 105143355 | |||||||
| chr14:105143756 | C | G | 1 | a0002c0030t0003g0054 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3085-118G>C | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 24/25 | chr14 | 105143756 | |||||||
| chr14:105143759 | G | C | 1 | a0001c0001t0013g0215 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.3085-121C>G | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 24/25 | chr14 | 105143759 | |||||||
| chr14:105143778 | T | C | 191 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(188): Show |
241 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(238): Show |
intron_variant | MODIFIER | c.3085-140A>G | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 24/25 | chr14 | 105143778 | |||||||
| chr14:105143808 | G | A | 5 | a0001c0001t0001g0166 a0001c0001t0001g0214 a0001c0001t0001g0218 others(2): Show |
5 | HG02976.hp1 NA18942.hp1 NA18952.hp2 others(2): Show |
intron_variant | MODIFIER | c.3085-170C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 24/25 | chr14 | 105143808 | |||||||
| chr14:105143897 | A | G | 7 | a0005c0007t0003g0038 a0005c0007t0003g0239 a0005c0007t0003g0240 others(4): Show |
8 | HG02647.hp1 HG02723.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.3085-259T>C | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 24/25 | chr14 | 105143897 | |||||||
| chr14:105144002 | G | T | 1 | a0003c0003t0002g0072 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.3085-364C>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 24/25 | chr14 | 105144002 | |||||||
| chr14:105144024 | G | A | 1 | a0003c0003t0002g0065 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.3085-386C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 24/25 | chr14 | 105144024 | |||||||
| chr14:105144064 | C | T | 1 | a0002c0002t0001g0133 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.3085-426G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 24/25 | chr14 | 105144064 | |||||||
| chr14:105144065 | G | A | 1 | a0001c0005t0003g0023 | 2 | HG02622.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.3085-427C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 24/25 | chr14 | 105144065 | |||||||
| chr14:105144094 | T | G | 191 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(188): Show |
241 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(238): Show |
intron_variant | MODIFIER | c.3085-456A>C | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 24/25 | chr14 | 105144094 | |||||||
| chr14:105144328 | C | T | 1 | a0002c0002t0001g0120 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.3084+602G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 24/25 | chr14 | 105144328 | |||||||
| chr14:105144437 | T | C | 1 | a0002c0002t0001g0126 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.3084+493A>G | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 24/25 | chr14 | 105144437 | |||||||
| chr14:105145251 | G | A | 1 | a0002c0002t0001g0138 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2953-190C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 23/25 | chr14 | 105145251 | |||||||
| chr14:105145322 | C | G | 1 | a0011c0028t0001g0153 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2953-261G>C | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 23/25 | chr14 | 105145322 | |||||||
| chr14:105145341 | T | C | 8 | a0001c0001t0008g0048 a0001c0001t0009g0081 a0001c0001t0009g0082 others(5): Show |
11 | HG00639.hp1 HG01884.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.2953-280A>G | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 23/25 | chr14 | 105145341 | |||||||
| chr14:105145405 | C | G | 255 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(252): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(347): Show |
intron_variant | MODIFIER | c.2952+326G>C | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 23/25 | chr14 | 105145405 | |||||||
| chr14:105145423 | A | C | 1 | a0002c0002t0001g0100 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2952+308T>G | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 23/25 | chr14 | 105145423 | |||||||
| chr14:105145438 | A | G | 255 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(252): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(347): Show |
intron_variant | MODIFIER | c.2952+293T>C | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 23/25 | chr14 | 105145438 | |||||||
| chr14:105145447 | G | C | 3 | a0001c0014t0001g0252 a0001c0014t0018g0086 a0009c0034t0001g0058 |
3 | HG02486.hp1 HG03471.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2952+284C>G | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 23/25 | chr14 | 105145447 | |||||||
| chr14:105145474 | G | A | 7 | a0002c0002t0001g0016 a0002c0002t0001g0031 a0002c0002t0001g0043 others(4): Show |
10 | HG02055.hp2 HG02257.hp1 HG02300.hp2 others(7): Show |
intron_variant | MODIFIER | c.2952+257C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 23/25 | chr14 | 105145474 | |||||||
| chr14:105145478 | G | T | 1 | a0011c0028t0001g0153 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2952+253C>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 23/25 | chr14 | 105145478 | |||||||
| chr14:105145595 | G | C | 1 | a0011c0028t0001g0153 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2952+136C>G | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 23/25 | chr14 | 105145595 | |||||||
| chr14:105145597 | C | A | 1 | a0011c0028t0001g0153 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2952+134G>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 23/25 | chr14 | 105145597 | |||||||
| chr14:105146084 | C | T | 1 | a0001c0014t0001g0252 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2710-111G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 22/25 | chr14 | 105146084 | |||||||
| chr14:105146218 | A | G | 3 | a0001c0005t0003g0089 a0001c0017t0003g0088 a0001c0017t0003g0090 |
3 | HG02622.hp1 HG02818.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2709+167T>C | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 22/25 | chr14 | 105146218 | |||||||
| chr14:105146218 | A | T | 2 | a0001c0009t0005g0008 a0001c0033t0005g0057 |
5 | HG00639.hp1 HG01884.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.2709+167T>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 22/25 | chr14 | 105146218 | |||||||
| chr14:105146304 | C | T | 1 | a0003c0003t0002g0076 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.2709+81G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 22/25 | chr14 | 105146304 | |||||||
| chr14:105146330 | G | A | 1 | a0001c0025t0001g0243 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2709+55C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 22/25 | chr14 | 105146330 | |||||||
| chr14:105146351 | G | A | 1 | a0001c0001t0001g0219 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.2709+34C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 22/25 | chr14 | 105146351 | |||||||
| chr14:105146355 | A | G | 1 | a0011c0028t0001g0153 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2709+30T>C | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 22/25 | chr14 | 105146355 | |||||||
| chr14:105146548 | G | A | 40 | a0001c0001t0002g0168 a0001c0009t0002g0055 a0001c0014t0001g0252 others(37): Show |
50 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.2594-48C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 21/25 | chr14 | 105146548 | |||||||
| chr14:105146561 | A | C | 1 | a0005c0021t0003g0242 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2593+50T>G | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 21/25 | chr14 | 105146561 | |||||||
| chr14:105146562 | C | A | 1 | a0005c0021t0003g0242 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2593+49G>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 21/25 | chr14 | 105146562 | |||||||
| chr14:105146565 | A | C | 1 | a0005c0021t0003g0242 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2593+46T>G | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 21/25 | chr14 | 105146565 | |||||||
| chr14:105146566 | T | A | 1 | a0011c0028t0001g0153 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2593+45A>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 21/25 | chr14 | 105146566 | |||||||
| chr14:105146798 | C | T | 2 | a0001c0012t0001g0015 a0001c0012t0001g0098 |
4 | HG02280.hp1 HG02965.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2480-74G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 20/25 | chr14 | 105146798 | |||||||
| chr14:105146872 | G | A | 1 | a0004c0004t0001g0161 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.2480-148C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 20/25 | chr14 | 105146872 | |||||||
| chr14:105146909 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2480-185C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 20/25 | chr14 | 105146909 | |||||||
| chr14:105146941 | A | C | 39 | a0001c0001t0001g0020 a0001c0001t0001g0033 a0001c0001t0001g0179 others(36): Show |
43 | HG00099.hp1 HG00280.hp1 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.2480-217T>G | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 20/25 | chr14 | 105146941 | |||||||
| chr14:105146983 | G | A | 2 | a0001c0005t0003g0014 a0001c0005t0003g0092 |
4 | HG02572.hp2 HG02630.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.2480-259C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 20/25 | chr14 | 105146983 | |||||||
| chr14:105147042 | C | T | 1 | a0001c0001t0009g0081 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2479+284G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 20/25 | chr14 | 105147042 | |||||||
| chr14:105147206 | A | C | 1 | a0002c0002t0001g0028 | 2 | NA19000.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.2479+120T>G | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 20/25 | chr14 | 105147206 | |||||||
| chr14:105147245 | C | G | 1 | a0003c0006t0002g0147 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2479+81G>C | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 20/25 | chr14 | 105147245 | |||||||
| chr14:105147274 | C | T | 1 | a0002c0002t0004g0134 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2479+52G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 20/25 | chr14 | 105147274 | |||||||
| chr14:105147307 | G | A | 1 | a0001c0001t0008g0048 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2479+19C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 20/25 | chr14 | 105147307 | |||||||
| chr14:105147446 | C | T | 1 | a0002c0002t0001g0117 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.2394-35G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 19/25 | chr14 | 105147446 | |||||||
| chr14:105147571 | C | T | 8 | a0001c0005t0003g0014 a0001c0005t0003g0023 a0001c0005t0003g0087 others(5): Show |
11 | HG02572.hp2 HG02622.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.2366-44G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 18/25 | chr14 | 105147571 | |||||||
| chr14:105147586 | C | T | 1 | a0001c0014t0018g0086 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2366-59G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 18/25 | chr14 | 105147586 | |||||||
| chr14:105147638 | A | T | 1 | a0010c0031t0001g0044 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.2366-111T>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 18/25 | chr14 | 105147638 | |||||||
| chr14:105147674 | G | T | 1 | a0011c0028t0001g0153 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2365+98C>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 18/25 | chr14 | 105147674 | |||||||
| chr14:105147695 | C | G | 176 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(173): Show |
219 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.2365+77G>C | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 18/25 | chr14 | 105147695 | |||||||
| chr14:105147766 | A | G | 10 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(7): Show |
13 | HG00639.hp1 HG01884.hp1 HG02055.hp1 others(10): Show |
splice_region_variant&intron_variant | LOW | c.2365+6T>C | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 18/25 | chr14 | 105147766 | |||||||
| chr14:105147986 | G | A | 1 | a0002c0002t0001g0106 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2249-98C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 17/25 | chr14 | 105147986 | |||||||
| chr14:105148002 | GGGCAGGT | G | 4 | a0003c0003t0002g0059 a0003c0003t0002g0076 a0003c0003t0002g0077 others(1): Show |
4 | HG01496.hp2 HG02698.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.2248+107_2248+113d others(9): Show |
JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 17/25 | chr14 | 105148002 | |||||||
| chr14:105148039 | C | T | 1 | a0005c0007t0003g0256 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2248+77G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 17/25 | chr14 | 105148039 | |||||||
| chr14:105148084 | C | G | 1 | a0010c0031t0001g0044 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.2248+32G>C | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 17/25 | chr14 | 105148084 | |||||||
| chr14:105148085 | G | A | 1 | a0002c0002t0001g0130 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2248+31C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 17/25 | chr14 | 105148085 | |||||||
| chr14:105148086 | G | C | 1 | a0010c0031t0001g0044 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.2248+30C>G | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 17/25 | chr14 | 105148086 | |||||||
| chr14:105148087 | C | G | 1 | a0010c0031t0001g0044 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.2248+29G>C | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 17/25 | chr14 | 105148087 | |||||||
| chr14:105148102 | C | T | 1 | a0002c0016t0001g0116 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2248+14G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 17/25 | chr14 | 105148102 | |||||||
| chr14:105148246 | C | T | 2 | a0001c0005t0003g0014 a0001c0005t0003g0091 |
4 | HG02572.hp2 HG02630.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.2135-17G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 16/25 | chr14 | 105148246 | |||||||
| chr14:105148467 | C | CG | 10 | a0001c0001t0001g0198 a0001c0001t0001g0213 a0001c0001t0001g0236 others(7): Show |
10 | HG00673.hp1 HG02300.hp1 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.2021-29dupC | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 15/25 | chr14 | 105148467 | |||||||
| chr14:105148467 | C | T | 1 | a0002c0002t0001g0115 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2021-28G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 15/25 | chr14 | 105148467 | |||||||
| chr14:105148471 | G | T | 1 | a0011c0028t0001g0153 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2021-32C>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 15/25 | chr14 | 105148471 | |||||||
| chr14:105148500 | G | C | 12 | a0004c0004t0001g0004 a0004c0004t0001g0159 a0004c0004t0001g0160 others(9): Show |
19 | HG00438.hp2 HG00558.hp2 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.2021-61C>G | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 15/25 | chr14 | 105148500 | |||||||
| chr14:105148564 | C | T | 1 | a0001c0014t0018g0086 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2021-125G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 15/25 | chr14 | 105148564 | |||||||
| chr14:105148580 | G | A | 12 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(9): Show |
15 | HG00639.hp1 HG00735.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.2021-141C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 15/25 | chr14 | 105148580 | |||||||
| chr14:105148637 | T | C | 180 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(177): Show |
223 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(220): Show |
intron_variant | MODIFIER | c.2020+108A>G | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 15/25 | chr14 | 105148637 | |||||||
| chr14:105148667 | C | T | 1 | a0001c0001t0001g0229 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2020+78G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 15/25 | chr14 | 105148667 | |||||||
| chr14:105148684 | G | A | 1 | a0003c0003t0002g0064 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2020+61C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 15/25 | chr14 | 105148684 | |||||||
| chr14:105148689 | A | G | 181 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(178): Show |
224 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(221): Show |
intron_variant | MODIFIER | c.2020+56T>C | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 15/25 | chr14 | 105148689 | |||||||
| chr14:105148734 | G | A | 1 | a0006c0008t0001g0154 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.2020+11C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 15/25 | chr14 | 105148734 | |||||||
| chr14:105148869 | G | A | 1 | a0002c0002t0001g0104 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1907-11C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 14/25 | chr14 | 105148869 | |||||||
| chr14:105148925 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1906+12C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 14/25 | chr14 | 105148925 | |||||||
| chr14:105149367 | C | A | 1 | a0004c0004t0001g0161 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1603-47G>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 12/25 | chr14 | 105149367 | |||||||
| chr14:105149486 | C | T | 1 | a0003c0003t0002g0075 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1603-166G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 12/25 | chr14 | 105149486 | |||||||
| chr14:105149824 | G | A | 1 | a0001c0001t0001g0201 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1603-504C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 12/25 | chr14 | 105149824 | |||||||
| chr14:105149844 | A | AG | 7 | a0001c0009t0002g0055 a0001c0033t0005g0057 a0002c0002t0001g0113 others(4): Show |
7 | HG00639.hp1 HG02080.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.1603-525dupC | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 12/25 | chr14 | 105149844 | |||||||
| chr14:105149868 | T | TGGGGAGG others(45): Show |
6 | a0001c0024t0003g0093 a0002c0002t0001g0017 a0002c0002t0001g0052 others(3): Show |
9 | HG00673.hp1 HG01123.hp1 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.1603-600_1603-549d others(54): Show |
JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 12/25 | chr14 | 105149868 | |||||||
| chr14:105149868 | T | TGGGGAGG others(97): Show |
1 | a0002c0002t0001g0111 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1602+632_1603-549d others(106): Show |
JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 12/25 | chr14 | 105149868 | |||||||
| chr14:105149868 | T | TGGGGAGG others(149): Show |
1 | a0003c0027t0001g0112 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1603-549_1603-548i others(158): Show |
JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 12/25 | chr14 | 105149868 | |||||||
| chr14:105149868 | TGGGGAGG others(45): Show |
T | 125 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(122): Show |
153 | HG00099.hp1 HG00280.hp1 HG00597.hp1 others(150): Show |
intron_variant | MODIFIER | c.1603-600_1603-549d others(54): Show |
JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 12/25 | chr14 | 105149868 | |||||||
| chr14:105149897 | A | G | 1 | a0001c0009t0002g0055 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1603-577T>C | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 12/25 | chr14 | 105149897 | |||||||
| chr14:105149898 | GGGGGTGG others(96): Show |
G | 1 | a0001c0001t0001g0169 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1602+603_1603-579d others(2): Show |
JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 12/25 | chr14 | 105149898 | |||||||
| chr14:105149903 | TGGTAGGG others(40): Show |
T | 1 | a0001c0009t0002g0055 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1603-630_1603-584d others(49): Show |
JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 12/25 | chr14 | 105149903 | |||||||
| chr14:105149905 | G | GTAGGGAG others(148): Show |
2 | a0002c0015t0001g0145 a0002c0015t0001g0146 |
2 | HG03130.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1603-586_1603-585i others(157): Show |
JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 12/25 | chr14 | 105149905 | |||||||
| chr14:105149914 | T | C | 1 | a0009c0034t0001g0058 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1603-594A>G | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 12/25 | chr14 | 105149914 | |||||||
| chr14:105149915 | G | A | 1 | a0009c0034t0001g0058 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1603-595C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 12/25 | chr14 | 105149915 | |||||||
| chr14:105149919 | G | A | 1 | a0009c0034t0001g0058 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1603-599C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 12/25 | chr14 | 105149919 | |||||||
| chr14:105149919 | G | GGGGGGAG others(96): Show |
1 | a0003c0003t0002g0085 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1603-600_1603-599i others(105): Show |
JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 12/25 | chr14 | 105149919 | |||||||
| chr14:105149920 | G | T | 1 | a0009c0034t0001g0058 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1603-600C>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 12/25 | chr14 | 105149920 | |||||||
| chr14:105149926 | G | A | 1 | a0002c0002t0001g0133 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1603-606C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 12/25 | chr14 | 105149926 | |||||||
| chr14:105149942 | GTGGGGAA others(36): Show |
G | 1 | a0001c0001t0001g0196 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1602+619_1603-623d others(45): Show |
JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 12/25 | chr14 | 105149942 | |||||||
| chr14:105149944 | G | A | 1 | a0001c0001t0001g0207 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1603-624C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 12/25 | chr14 | 105149944 | |||||||
| chr14:105149948 | A | G | 1 | a0001c0001t0001g0207 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1603-628T>C | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 12/25 | chr14 | 105149948 | |||||||
| chr14:105149948 | AAGGGGGT others(45): Show |
A | 1 | a0002c0002t0001g0001 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1602+604_1603-629d others(54): Show |
JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 12/25 | chr14 | 105149948 | |||||||
| chr14:105149949 | A | AGGGGGTG others(46): Show |
2 | a0002c0002t0001g0001 a0002c0002t0001g0142 |
2 | HG00741.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.1603-630_1603-629i others(55): Show |
JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 12/25 | chr14 | 105149949 | |||||||
| chr14:105149950 | GGGGGTGG others(44): Show |
G | 1 | a0002c0002t0001g0011 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1602+603_1603-631d others(53): Show |
JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 12/25 | chr14 | 105149950 | |||||||
| chr14:105149957 | G | A | 2 | a0001c0001t0001g0207 a0002c0002t0001g0138 |
2 | HG00280.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1603-637C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 12/25 | chr14 | 105149957 | |||||||
| chr14:105149961 | GGAGGTGG others(44): Show |
G | 5 | a0001c0001t0001g0207 a0002c0002t0010g0107 a0004c0004t0001g0160 others(2): Show |
5 | HG02145.hp2 HG03471.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1602+592_1602+642d others(53): Show |
JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 12/25 | chr14 | 105149961 | |||||||
| chr14:105149971 | G | C | 1 | a0003c0003t0015g0074 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1602+633C>G | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 12/25 | chr14 | 105149971 | |||||||
| chr14:105149976 | G | A | 1 | a0002c0030t0003g0054 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1602+628C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 12/25 | chr14 | 105149976 | |||||||
| chr14:105150012 | T | G | 193 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(190): Show |
243 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(240): Show |
intron_variant | MODIFIER | c.1602+592A>C | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 12/25 | chr14 | 105150012 | |||||||
| chr14:105150012 | T | TGAGGTGG others(246): Show |
1 | a0002c0002t0001g0127 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1602+591_1602+592i others(255): Show |
JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 12/25 | chr14 | 105150012 | |||||||
| chr14:105150027 | G | A | 1 | a0001c0001t0001g0207 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1602+577C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 12/25 | chr14 | 105150027 | |||||||
| chr14:105150118 | A | AG | 7 | a0001c0001t0001g0068 a0001c0001t0012g0040 a0001c0009t0002g0055 others(4): Show |
7 | HG02055.hp1 HG02523.hp1 HG02683.hp1 others(4): Show |
intron_variant | MODIFIER | c.1602+485dupC | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 12/25 | chr14 | 105150118 | |||||||
| chr14:105150152 | T | C | 1 | a0002c0002t0001g0027 | 2 | NA19057.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.1602+452A>G | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 12/25 | chr14 | 105150152 | |||||||
| chr14:105150185 | C | T | 2 | a0001c0001t0001g0032 a0001c0001t0001g0174 |
3 | HG01261.hp1 HG01515.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.1602+419G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 12/25 | chr14 | 105150185 | |||||||
| chr14:105150221 | C | T | 33 | a0001c0014t0018g0086 a0003c0003t0002g0009 a0003c0003t0002g0012 others(30): Show |
43 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.1602+383G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 12/25 | chr14 | 105150221 | |||||||
| chr14:105150533 | G | T | 3 | a0001c0001t0001g0037 a0001c0001t0001g0230 a0001c0001t0001g0237 |
4 | HG02896.hp1 HG02897.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1602+71C>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 12/25 | chr14 | 105150533 | |||||||
| chr14:105150806 | G | A | 7 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0148 others(4): Show |
7 | HG02055.hp1 HG02109.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1429-29C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 11/25 | chr14 | 105150806 | |||||||
| chr14:105150819 | C | T | 1 | a0001c0011t0001g0188 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1429-42G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 11/25 | chr14 | 105150819 | |||||||
| chr14:105151130 | G | A | 7 | a0001c0001t0001g0019 a0001c0001t0001g0032 a0001c0001t0001g0046 others(4): Show |
10 | HG01081.hp2 HG01106.hp2 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.1268-26C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 9/25 | chr14 | 105151130 | |||||||
| chr14:105151175 | A | G | 11 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(8): Show |
11 | HG02055.hp1 HG02109.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.1268-71T>C | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 9/25 | chr14 | 105151175 | |||||||
| chr14:105151178 | C | T | 1 | a0001c0001t0001g0163 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1268-74G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 9/25 | chr14 | 105151178 | |||||||
| chr14:105151195 | A | C | 4 | a0002c0030t0003g0054 a0006c0008t0001g0018 a0006c0008t0001g0150 others(1): Show |
6 | HG01261.hp2 HG01496.hp1 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.1267+88T>G | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 9/25 | chr14 | 105151195 | |||||||
| chr14:105151195 | AGCAGCCC others(11): Show |
A | 2 | a0001c0001t0001g0230 a0001c0001t0001g0237 |
2 | NA19043.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1267+70_1267+87del others(18): Show |
JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 9/25 | chr14 | 105151195 | |||||||
| chr14:105151204 | A | AGCAGCCC others(11): Show |
1 | a0003c0003t0015g0074 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1267+78_1267+79ins others(18): Show |
JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 9/25 | chr14 | 105151204 | |||||||
| chr14:105151204 | A | C | 6 | a0002c0030t0003g0054 a0003c0003t0002g0079 a0006c0008t0001g0018 others(3): Show |
8 | HG01261.hp2 HG01496.hp1 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.1267+79T>G | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 9/25 | chr14 | 105151204 | |||||||
| chr14:105151213 | C | A | 6 | a0001c0001t0001g0047 a0001c0001t0001g0167 a0001c0001t0001g0178 others(3): Show |
6 | HG01175.hp2 HG02280.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.1267+70G>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 9/25 | chr14 | 105151213 | |||||||
| chr14:105151213 | C | CGCAGCCC others(2): Show |
153 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(150): Show |
194 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.1267+61_1267+69dup others(9): Show |
JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 9/25 | chr14 | 105151213 | |||||||
| chr14:105151222 | A | AGCAGCCC others(2): Show |
6 | a0004c0004t0001g0004 a0004c0004t0001g0159 a0004c0004t0001g0160 others(3): Show |
11 | HG00438.hp2 HG00558.hp2 NA18612.hp1 others(8): Show |
intron_variant | MODIFIER | c.1267+52_1267+60dup others(9): Show |
JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 9/25 | chr14 | 105151222 | |||||||
| chr14:105151222 | AGCAGCCC others(2): Show |
A | 8 | a0001c0014t0001g0252 a0005c0007t0003g0038 a0005c0007t0003g0239 others(5): Show |
9 | HG02647.hp1 HG02723.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1267+52_1267+60del others(9): Show |
JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 9/25 | chr14 | 105151222 | |||||||
| chr14:105151226 | G | GCCCCAGC others(3): Show |
1 | a0001c0001t0001g0238 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1267+56_1267+57ins others(10): Show |
JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 9/25 | chr14 | 105151226 | |||||||
| chr14:105151554 | C | T | 34 | a0003c0003t0002g0009 a0003c0003t0002g0012 a0003c0003t0002g0022 others(31): Show |
44 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.1153+72G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 8/25 | chr14 | 105151554 | |||||||
| chr14:105151803 | T | G | 1 | a0001c0001t0006g0194 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1040-64A>C | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 7/25 | chr14 | 105151803 | |||||||
| chr14:105151866 | T | C | 1 | a0001c0001t0001g0223 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1039+72A>G | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 7/25 | chr14 | 105151866 | |||||||
| chr14:105151929 | C | A | 1 | a0003c0003t0002g0097 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1039+9G>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 7/25 | chr14 | 105151929 | |||||||
| chr14:105152092 | C | T | 4 | a0001c0001t0008g0048 a0001c0001t0009g0081 a0001c0001t0009g0082 others(1): Show |
4 | HG02109.hp2 HG02647.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.920-35G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 6/25 | chr14 | 105152092 | |||||||
| chr14:105152123 | G | T | 4 | a0003c0003t0002g0012 a0003c0003t0002g0072 a0003c0003t0002g0073 others(1): Show |
7 | HG00609.hp2 HG00621.hp1 HG02129.hp2 others(4): Show |
intron_variant | MODIFIER | c.919+38C>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 6/25 | chr14 | 105152123 | |||||||
| chr14:105152333 | T | C | 193 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(190): Show |
243 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(240): Show |
intron_variant | MODIFIER | c.789-42A>G | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 5/25 | chr14 | 105152333 | |||||||
| chr14:105152391 | C | T | 1 | a0002c0002t0001g0105 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.789-100G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 5/25 | chr14 | 105152391 | |||||||
| chr14:105152392 | G | A | 7 | a0002c0002t0001g0003 a0002c0002t0001g0108 a0002c0002t0001g0130 others(4): Show |
13 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(10): Show |
intron_variant | MODIFIER | c.789-101C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 5/25 | chr14 | 105152392 | |||||||
| chr14:105152451 | C | T | 2 | a0002c0013t0002g0131 a0011c0028t0001g0153 |
2 | HG04199.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.789-160G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 5/25 | chr14 | 105152451 | |||||||
| chr14:105152496 | C | T | 1 | a0001c0001t0001g0230 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.789-205G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 5/25 | chr14 | 105152496 | |||||||
| chr14:105152549 | C | G | 34 | a0003c0003t0002g0009 a0003c0003t0002g0012 a0003c0003t0002g0022 others(31): Show |
44 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.789-258G>C | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 5/25 | chr14 | 105152549 | |||||||
| chr14:105152563 | C | T | 1 | a0007c0023t0001g0171 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.789-272G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 5/25 | chr14 | 105152563 | |||||||
| chr14:105152589 | C | G | 8 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(5): Show |
8 | HG02055.hp1 HG02109.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.789-298G>C | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 5/25 | chr14 | 105152589 | |||||||
| chr14:105153027 | C | T | 1 | a0003c0003t0002g0065 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.789-736G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 5/25 | chr14 | 105153027 | |||||||
| chr14:105153036 | A | G | 1 | a0002c0002t0001g0103 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.789-745T>C | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 5/25 | chr14 | 105153036 | |||||||
| chr14:105153120 | C | T | 1 | a0001c0001t0001g0247 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.789-829G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 5/25 | chr14 | 105153120 | |||||||
| chr14:105153356 | T | C | 1 | a0002c0002t0001g0029 | 2 | HG02132.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.789-1065A>G | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 5/25 | chr14 | 105153356 | |||||||
| chr14:105153410 | G | A | 1 | a0002c0030t0003g0054 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.789-1119C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 5/25 | chr14 | 105153410 | |||||||
| chr14:105153422 | C | T | 14 | a0002c0002t0001g0155 a0002c0002t0001g0158 a0004c0004t0001g0004 others(11): Show |
21 | HG00438.hp2 HG00558.hp2 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.789-1131G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 5/25 | chr14 | 105153422 | |||||||
| chr14:105153446 | C | T | 1 | a0001c0001t0001g0221 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.789-1155G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 5/25 | chr14 | 105153446 | |||||||
| chr14:105153657 | C | CA | 7 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0247 others(4): Show |
13 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.789-1367dupT | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 5/25 | chr14 | 105153657 | |||||||
| chr14:105153674 | C | T | 20 | a0001c0001t0001g0013 a0001c0001t0001g0034 a0001c0001t0001g0035 others(17): Show |
28 | HG00621.hp2 HG02027.hp1 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.789-1383G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 5/25 | chr14 | 105153674 | |||||||
| chr14:105153693 | G | A | 1 | a0001c0036t0001g0257 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.789-1402C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 5/25 | chr14 | 105153693 | |||||||
| chr14:105153914 | C | T | 1 | a0013c0019t0001g0151 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.789-1623G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 5/25 | chr14 | 105153914 | |||||||
| chr14:105154022 | G | A | 3 | a0001c0001t0001g0164 a0001c0001t0001g0217 a0001c0001t0001g0219 |
3 | NA18986.hp2 NA19064.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.788+1540C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 5/25 | chr14 | 105154022 | |||||||
| chr14:105154068 | C | T | 2 | a0002c0002t0001g0043 a0002c0002t0001g0105 |
2 | HG02572.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.788+1494G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 5/25 | chr14 | 105154068 | |||||||
| chr14:105154196 | C | T | 1 | a0003c0003t0002g0095 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.788+1366G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 5/25 | chr14 | 105154196 | |||||||
| chr14:105154281 | G | A | 1 | a0001c0001t0001g0250 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.788+1281C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 5/25 | chr14 | 105154281 | |||||||
| chr14:105154293 | C | T | 10 | a0002c0002t0001g0005 a0002c0002t0001g0026 a0002c0002t0001g0027 others(7): Show |
16 | HG00558.hp1 HG01346.hp2 HG02074.hp2 others(13): Show |
intron_variant | MODIFIER | c.788+1269G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 5/25 | chr14 | 105154293 | |||||||
| chr14:105154335 | T | TGCTGTCT others(8): Show |
1 | a0002c0002t0001g0051 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.788+1212_788+1226d others(17): Show |
JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 5/25 | chr14 | 105154335 | |||||||
| chr14:105154351 | G | A | 62 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(59): Show |
76 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(73): Show |
intron_variant | MODIFIER | c.788+1211C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 5/25 | chr14 | 105154351 | |||||||
| chr14:105154407 | T | C | 1 | a0003c0003t0002g0066 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.788+1155A>G | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 5/25 | chr14 | 105154407 | |||||||
| chr14:105154540 | C | G | 8 | a0001c0014t0001g0252 a0005c0007t0003g0038 a0005c0007t0003g0239 others(5): Show |
9 | HG02647.hp1 HG02723.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.788+1022G>C | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 5/25 | chr14 | 105154540 | |||||||
| chr14:105154615 | G | A | 1 | a0001c0025t0001g0243 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.788+947C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 5/25 | chr14 | 105154615 | |||||||
| chr14:105154741 | G | C | 6 | a0003c0006t0002g0010 a0003c0006t0002g0080 a0003c0006t0002g0147 others(3): Show |
9 | HG00609.hp1 HG01074.hp1 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.788+821C>G | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 5/25 | chr14 | 105154741 | |||||||
| chr14:105154778 | G | A | 1 | a0001c0001t0001g0246 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.788+784C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 5/25 | chr14 | 105154778 | |||||||
| chr14:105154799 | C | A | 2 | a0001c0001t0009g0081 a0001c0001t0009g0082 |
2 | HG02976.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.788+763G>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 5/25 | chr14 | 105154799 | |||||||
| chr14:105154831 | C | T | 1 | a0001c0005t0003g0087 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.788+731G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 5/25 | chr14 | 105154831 | |||||||
| chr14:105154848 | GCTACTCA others(16): Show |
G | 1 | a0002c0013t0001g0205 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.788+691_788+713del others(23): Show |
JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 5/25 | chr14 | 105154848 | |||||||
| chr14:105155026 | C | A | 1 | a0001c0001t0001g0232 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.788+536G>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 5/25 | chr14 | 105155026 | |||||||
| chr14:105155043 | C | T | 1 | a0001c0001t0001g0230 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.788+519G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 5/25 | chr14 | 105155043 | |||||||
| chr14:105155222 | A | AC | 20 | a0001c0001t0001g0047 a0001c0001t0001g0067 a0001c0001t0001g0068 others(17): Show |
21 | HG00438.hp1 HG01074.hp2 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.788+339dupG | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 5/25 | chr14 | 105155222 | |||||||
| chr14:105155222 | A | C | 1 | a0003c0003t0002g0070 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.788+340T>G | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 5/25 | chr14 | 105155222 | |||||||
| chr14:105155358 | A | G | 2 | a0002c0015t0001g0145 a0002c0015t0001g0146 |
2 | HG03130.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.788+204T>C | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 5/25 | chr14 | 105155358 | |||||||
| chr14:105155388 | T | C | 1 | a0005c0007t0003g0239 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.788+174A>G | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 5/25 | chr14 | 105155388 | |||||||
| chr14:105155412 | G | A | 2 | a0002c0015t0001g0145 a0002c0015t0001g0146 |
2 | HG03130.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.788+150C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 5/25 | chr14 | 105155412 | |||||||
| chr14:105155510 | G | A | 3 | a0002c0002t0001g0132 a0002c0002t0001g0133 a0002c0013t0002g0131 |
3 | HG02698.hp2 HG04115.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.788+52C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 5/25 | chr14 | 105155510 | |||||||
| chr14:105155626 | C | T | 2 | a0001c0001t0001g0199 a0002c0002t0001g0050 |
2 | NA19063.hp1 NA19063.hp2 |
splice_region_variant&intron_variant | LOW | c.728-4G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 4/25 | chr14 | 105155626 | |||||||
| chr14:105155676 | C | T | 1 | a0001c0001t0001g0176 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.728-54G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 4/25 | chr14 | 105155676 | |||||||
| chr14:105155719 | A | G | 256 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(253): Show |
351 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(348): Show |
intron_variant | MODIFIER | c.727+19T>C | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 4/25 | chr14 | 105155719 | |||||||
| chr14:105156063 | C | T | 1 | a0001c0001t0001g0249 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.476-74G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 3/25 | chr14 | 105156063 | |||||||
| chr14:105156182 | C | G | 1 | a0003c0003t0002g0079 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.476-193G>C | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 3/25 | chr14 | 105156182 | |||||||
| chr14:105156183 | G | C | 1 | a0003c0003t0002g0079 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.476-194C>G | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 3/25 | chr14 | 105156183 | |||||||
| chr14:105156201 | C | CT | 143 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(140): Show |
179 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.476-213_476-212ins others(1): Show |
JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 3/25 | chr14 | 105156201 | |||||||
| chr14:105156202 | G | A | 8 | a0001c0014t0001g0252 a0005c0007t0003g0038 a0005c0007t0003g0239 others(5): Show |
9 | HG02647.hp1 HG02723.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.476-213C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 3/25 | chr14 | 105156202 | |||||||
| chr14:105156226 | C | G | 6 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(3): Show |
6 | HG02055.hp1 HG02809.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.476-237G>C | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 3/25 | chr14 | 105156226 | |||||||
| chr14:105156246 | T | C | 3 | a0002c0002t0001g0136 a0002c0002t0001g0142 a0002c0002t0004g0135 |
3 | HG00741.hp2 HG01975.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.476-257A>G | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 3/25 | chr14 | 105156246 | |||||||
| chr14:105156324 | C | T | 1 | a0002c0030t0003g0054 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.476-335G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 3/25 | chr14 | 105156324 | |||||||
| chr14:105156503 | C | A | 1 | a0003c0003t0002g0097 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.476-514G>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 3/25 | chr14 | 105156503 | |||||||
| chr14:105156583 | C | G | 1 | a0001c0001t0001g0167 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.476-594G>C | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 3/25 | chr14 | 105156583 | |||||||
| chr14:105156585 | A | C | 1 | a0001c0001t0001g0167 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.476-596T>G | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 3/25 | chr14 | 105156585 | |||||||
| chr14:105156586 | G | A | 1 | a0001c0001t0001g0167 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.476-597C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 3/25 | chr14 | 105156586 | |||||||
| chr14:105156623 | G | T | 33 | a0003c0003t0002g0009 a0003c0003t0002g0012 a0003c0003t0002g0022 others(30): Show |
43 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.476-634C>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 3/25 | chr14 | 105156623 | |||||||
| chr14:105156666 | A | G | 17 | a0001c0005t0003g0014 a0001c0005t0003g0023 a0001c0005t0003g0087 others(14): Show |
21 | HG01175.hp1 HG02572.hp2 HG02622.hp1 others(18): Show |
intron_variant | MODIFIER | c.476-677T>C | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 3/25 | chr14 | 105156666 | |||||||
| chr14:105156763 | C | G | 1 | a0003c0003t0002g0079 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.476-774G>C | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 3/25 | chr14 | 105156763 | |||||||
| chr14:105156767 | C | T | 1 | a0002c0002t0001g0108 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.476-778G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 3/25 | chr14 | 105156767 | |||||||
| chr14:105156845 | A | AC | 8 | a0001c0001t0001g0180 a0001c0001t0001g0198 a0001c0001t0001g0208 others(5): Show |
8 | HG00597.hp1 HG01928.hp1 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.476-857dupG | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 3/25 | chr14 | 105156845 | |||||||
| chr14:105156890 | A | G | 4 | a0004c0004t0001g0004 a0004c0004t0001g0159 a0004c0004t0001g0160 others(1): Show |
9 | HG00438.hp2 HG00558.hp2 NA18612.hp1 others(6): Show |
intron_variant | MODIFIER | c.475+816T>C | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 3/25 | chr14 | 105156890 | |||||||
| chr14:105156921 | G | A | 1 | a0001c0010t0007g0195 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.475+785C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 3/25 | chr14 | 105156921 | |||||||
| chr14:105156924 | G | A | 30 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0024 others(27): Show |
40 | HG00621.hp2 HG00673.hp2 HG01168.hp1 others(37): Show |
intron_variant | MODIFIER | c.475+782C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 3/25 | chr14 | 105156924 | |||||||
| chr14:105156981 | G | A | 1 | a0001c0025t0001g0243 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.475+725C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 3/25 | chr14 | 105156981 | |||||||
| chr14:105157021 | A | T | 1 | a0001c0001t0001g0041 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.475+685T>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 3/25 | chr14 | 105157021 | |||||||
| chr14:105157041 | C | A | 1 | a0003c0003t0002g0079 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.475+665G>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 3/25 | chr14 | 105157041 | |||||||
| chr14:105157110 | G | A | 1 | a0003c0003t0002g0063 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.475+596C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 3/25 | chr14 | 105157110 | |||||||
| chr14:105157161 | C | T | 168 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(165): Show |
208 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.475+545G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 3/25 | chr14 | 105157161 | |||||||
| chr14:105157175 | T | C | 151 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(148): Show |
187 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.475+531A>G | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 3/25 | chr14 | 105157175 | |||||||
| chr14:105157275 | T | C | 109 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(106): Show |
135 | HG00099.hp1 HG00280.hp1 HG00597.hp1 others(132): Show |
intron_variant | MODIFIER | c.475+431A>G | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 3/25 | chr14 | 105157275 | |||||||
| chr14:105157338 | CA | C | 15 | a0002c0002t0001g0155 a0002c0002t0001g0158 a0003c0003t0002g0157 others(12): Show |
22 | HG00438.hp2 HG00558.hp2 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.475+367delT | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 3/25 | chr14 | 105157338 | |||||||
| chr14:105157342 | G | A | 1 | a0001c0024t0003g0093 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.475+364C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 3/25 | chr14 | 105157342 | |||||||
| chr14:105157584 | A | C | 1 | a0001c0001t0001g0037 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.475+122T>G | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 3/25 | chr14 | 105157584 | |||||||
| chr14:105157781 | C | T | 3 | a0001c0001t0001g0034 a0001c0001t0001g0208 a0002c0013t0001g0209 |
4 | HG00621.hp2 HG02027.hp1 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.418-18G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105157781 | |||||||
| chr14:105157816 | G | A | 1 | a0002c0002t0017g0137 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.418-53C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105157816 | |||||||
| chr14:105157848 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.418-85C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105157848 | |||||||
| chr14:105157942 | A | T | 1 | a0003c0003t0002g0079 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.418-179T>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105157942 | |||||||
| chr14:105158037 | C | T | 2 | a0001c0001t0008g0048 a0001c0022t0008g0084 |
2 | HG02109.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.418-274G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105158037 | |||||||
| chr14:105158044 | C | G | 1 | a0001c0024t0003g0093 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.418-281G>C | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105158044 | |||||||
| chr14:105158273 | C | T | 17 | a0001c0005t0003g0014 a0001c0005t0003g0023 a0001c0005t0003g0087 others(14): Show |
21 | HG01175.hp1 HG02572.hp2 HG02622.hp1 others(18): Show |
intron_variant | MODIFIER | c.418-510G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105158273 | |||||||
| chr14:105158356 | T | C | 191 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(188): Show |
241 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(238): Show |
intron_variant | MODIFIER | c.418-593A>G | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105158356 | |||||||
| chr14:105158532 | A | G | 8 | a0002c0002t0001g0016 a0002c0002t0001g0031 a0002c0002t0001g0043 others(5): Show |
11 | HG02055.hp2 HG02257.hp1 HG02300.hp2 others(8): Show |
intron_variant | MODIFIER | c.418-769T>C | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105158532 | |||||||
| chr14:105158577 | G | A | 1 | a0002c0002t0001g0138 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.418-814C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105158577 | |||||||
| chr14:105158622 | G | A | 1 | a0014c0020t0019g0156 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.418-859C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105158622 | |||||||
| chr14:105158692 | C | T | 7 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0247 others(4): Show |
13 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.418-929G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105158692 | |||||||
| chr14:105158811 | G | A | 1 | a0001c0017t0003g0090 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.418-1048C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105158811 | |||||||
| chr14:105158815 | G | A | 1 | a0002c0002t0001g0139 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.418-1052C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105158815 | |||||||
| chr14:105158825 | T | C | 1 | a0003c0003t0002g0064 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.418-1062A>G | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105158825 | |||||||
| chr14:105158829 | G | C | 1 | a0006c0008t0001g0162 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.418-1066C>G | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105158829 | |||||||
| chr14:105158986 | G | A | 1 | a0003c0003t0002g0079 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.418-1223C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105158986 | |||||||
| chr14:105159087 | C | T | 32 | a0003c0003t0002g0009 a0003c0003t0002g0012 a0003c0003t0002g0022 others(29): Show |
42 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.418-1324G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105159087 | |||||||
| chr14:105159141 | C | A | 1 | a0002c0002t0001g0050 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.418-1378G>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105159141 | |||||||
| chr14:105159228 | C | G | 1 | a0005c0007t0003g0239 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.418-1465G>C | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105159228 | |||||||
| chr14:105159275 | G | A | 1 | a0002c0002t0001g0140 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.418-1512C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105159275 | |||||||
| chr14:105159406 | C | T | 7 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0247 others(4): Show |
13 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.418-1643G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105159406 | |||||||
| chr14:105159411 | T | TC | 4 | a0001c0036t0001g0257 a0002c0002t0001g0141 a0002c0002t0001g0142 others(1): Show |
4 | HG00741.hp2 HG01891.hp2 HG02080.hp1 others(1): Show |
intron_variant | MODIFIER | c.418-1649dupG | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105159411 | |||||||
| chr14:105159540 | A | G | 1 | a0001c0001t0001g0184 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.418-1777T>C | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105159540 | |||||||
| chr14:105159551 | G | A | 1 | a0001c0001t0001g0037 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.418-1788C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105159551 | |||||||
| chr14:105159650 | C | T | 3 | a0001c0005t0003g0014 a0001c0005t0003g0091 a0001c0005t0003g0092 |
5 | HG02572.hp2 HG02630.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.418-1887G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105159650 | |||||||
| chr14:105159728 | A | G | 4 | a0001c0009t0002g0055 a0001c0009t0005g0008 a0001c0032t0002g0056 others(1): Show |
7 | HG00639.hp1 HG00735.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.418-1965T>C | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105159728 | |||||||
| chr14:105159768 | C | A | 1 | a0001c0001t0001g0196 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.418-2005G>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105159768 | |||||||
| chr14:105159770 | A | C | 17 | a0001c0005t0003g0014 a0001c0005t0003g0023 a0001c0005t0003g0087 others(14): Show |
21 | HG01175.hp1 HG02572.hp2 HG02622.hp1 others(18): Show |
intron_variant | MODIFIER | c.418-2007T>G | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105159770 | |||||||
| chr14:105159814 | C | T | 1 | a0001c0001t0001g0207 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.418-2051G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105159814 | |||||||
| chr14:105159844 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.418-2081G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105159844 | |||||||
| chr14:105159854 | A | AC | 190 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(187): Show |
240 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.418-2092dupG | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105159854 | |||||||
| chr14:105159886 | CTCCATCC others(13): Show |
C | 1 | a0003c0006t0002g0080 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.418-2143_418-2124d others(22): Show |
JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105159886 | |||||||
| chr14:105159902 | C | CCA | 167 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(164): Show |
207 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.418-2140_418-2139i others(4): Show |
JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105159902 | |||||||
| chr14:105159961 | C | T | 2 | a0001c0001t0001g0024 a0001c0001t0001g0041 |
3 | NA18975.hp2 NA18997.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.418-2198G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105159961 | |||||||
| chr14:105159990 | C | T | 3 | a0001c0001t0001g0183 a0001c0001t0001g0204 a0001c0001t0001g0244 |
3 | HG01928.hp1 HG02015.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.418-2227G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105159990 | |||||||
| chr14:105159993 | C | G | 15 | a0002c0002t0001g0155 a0002c0002t0001g0158 a0003c0003t0002g0157 others(12): Show |
22 | HG00438.hp2 HG00558.hp2 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.418-2230G>C | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105159993 | |||||||
| chr14:105160011 | C | T | 15 | a0002c0002t0001g0155 a0002c0002t0001g0158 a0003c0003t0002g0157 others(12): Show |
22 | HG00438.hp2 HG00558.hp2 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.418-2248G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105160011 | |||||||
| chr14:105160013 | C | G | 6 | a0001c0001t0001g0047 a0001c0001t0001g0167 a0001c0001t0001g0178 others(3): Show |
6 | HG01175.hp2 HG02280.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.418-2250G>C | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105160013 | |||||||
| chr14:105160075 | C | T | 1 | a0001c0001t0001g0228 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.418-2312G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105160075 | |||||||
| chr14:105160170 | C | G | 1 | a0002c0002t0001g0104 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.418-2407G>C | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105160170 | |||||||
| chr14:105160257 | G | A | 174 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(171): Show |
217 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.418-2494C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105160257 | |||||||
| chr14:105160419 | C | G | 4 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(1): Show |
4 | HG02055.hp1 HG02809.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.418-2656G>C | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105160419 | |||||||
| chr14:105160537 | A | T | 2 | a0001c0001t0008g0048 a0001c0022t0008g0084 |
2 | HG02109.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.418-2774T>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105160537 | |||||||
| chr14:105160681 | G | A | 6 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(3): Show |
6 | HG02055.hp1 HG02809.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.418-2918C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105160681 | |||||||
| chr14:105160784 | A | G | 1 | a0001c0001t0001g0047 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.418-3021T>C | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105160784 | |||||||
| chr14:105160858 | C | T | 4 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(1): Show |
4 | HG02055.hp1 HG02809.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.418-3095G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105160858 | |||||||
| chr14:105160863 | C | CA | 32 | a0001c0001t0001g0180 a0001c0001t0001g0203 a0001c0001t0001g0218 others(29): Show |
36 | HG01175.hp1 HG01358.hp1 HG02027.hp2 others(33): Show |
intron_variant | MODIFIER | c.418-3101dupT | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105160863 | |||||||
| chr14:105160867 | A | AAAAAAAA others(22): Show |
1 | a0001c0001t0001g0181 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.418-3133_418-3105d others(31): Show |
JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105160867 | |||||||
| chr14:105160963 | C | G | 4 | a0001c0009t0002g0055 a0001c0009t0005g0008 a0001c0032t0002g0056 others(1): Show |
7 | HG00639.hp1 HG00735.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.418-3200G>C | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105160963 | |||||||
| chr14:105160975 | G | C | 8 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0200 others(5): Show |
8 | HG00597.hp1 HG00673.hp2 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.418-3212C>G | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105160975 | |||||||
| chr14:105160990 | T | C | 1 | a0001c0036t0001g0257 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.418-3227A>G | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105160990 | |||||||
| chr14:105161114 | C | CGAGTGAG others(15): Show |
2 | a0001c0001t0001g0232 a0001c0001t0001g0251 |
2 | HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.418-3373_418-3352d others(24): Show |
JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105161114 | |||||||
| chr14:105161118 | T | C | 2 | a0001c0001t0001g0185 a0001c0001t0001g0245 |
2 | HG01099.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.418-3355A>G | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105161118 | |||||||
| chr14:105161146 | CTGTTGGG others(18): Show |
C | 4 | a0001c0001t0001g0183 a0001c0001t0001g0204 a0001c0001t0001g0220 others(1): Show |
4 | HG01928.hp1 HG02015.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.418-3408_418-3384d others(27): Show |
JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105161146 | |||||||
| chr14:105161393 | C | T | 2 | a0001c0001t0001g0164 a0001c0001t0001g0231 |
2 | NA19074.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.418-3630G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105161393 | |||||||
| chr14:105161507 | C | G | 1 | a0002c0002t0001g0103 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.418-3744G>C | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105161507 | |||||||
| chr14:105161605 | AG | A | 3 | a0001c0005t0003g0014 a0001c0005t0003g0091 a0001c0005t0003g0092 |
5 | HG02572.hp2 HG02630.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.418-3843delC | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105161605 | |||||||
| chr14:105161607 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.418-3844C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105161607 | |||||||
| chr14:105161672 | T | C | 6 | a0001c0009t0002g0055 a0001c0009t0005g0008 a0001c0014t0018g0086 others(3): Show |
9 | HG00639.hp1 HG00735.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.418-3909A>G | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105161672 | |||||||
| chr14:105161736 | A | ACAAACCT others(95): Show |
1 | a0002c0013t0001g0205 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.418-3974_418-3973i others(104): Show |
JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105161736 | |||||||
| chr14:105161751 | C | CGTCCTTC others(95): Show |
3 | a0001c0001t0001g0175 a0001c0001t0001g0224 a0001c0001t0001g0225 |
3 | HG01168.hp1 HG01516.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.418-3989_418-3988i others(104): Show |
JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105161751 | |||||||
| chr14:105161751 | C | CGTCCTTC others(44): Show |
5 | a0003c0003t0002g0062 a0003c0003t0002g0063 a0003c0003t0002g0064 others(2): Show |
5 | HG00735.hp2 HG01106.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.418-3989_418-3988i others(53): Show |
JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105161751 | |||||||
| chr14:105161751 | C | T | 1 | a0002c0013t0001g0205 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.418-3988G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105161751 | |||||||
| chr14:105161798 | T | C | 9 | a0001c0001t0001g0175 a0001c0001t0001g0224 a0001c0001t0001g0225 others(6): Show |
9 | HG00735.hp2 HG01106.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.418-4035A>G | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105161798 | |||||||
| chr14:105161798 | T | TCCCTGTC others(44): Show |
70 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(67): Show |
94 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.418-4086_418-4036d others(53): Show |
JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105161798 | |||||||
| chr14:105161798 | T | TCCCTGTC others(95): Show |
111 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(108): Show |
137 | HG00099.hp1 HG00280.hp1 HG00597.hp1 others(134): Show |
intron_variant | MODIFIER | c.418-4137_418-4036d others(104): Show |
JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105161798 | |||||||
| chr14:105161798 | TCCCTGTC others(44): Show |
T | 1 | a0002c0002t0001g0102 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.418-4086_418-4036d others(53): Show |
JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105161798 | |||||||
| chr14:105161838 | G | A | 1 | a0002c0002t0001g0144 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.418-4075C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105161838 | |||||||
| chr14:105161941 | G | C | 1 | a0003c0003t0002g0083 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.418-4178C>G | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105161941 | |||||||
| chr14:105162274 | G | A | 15 | a0002c0002t0001g0155 a0002c0002t0001g0158 a0003c0003t0002g0157 others(12): Show |
22 | HG00438.hp2 HG00558.hp2 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.418-4511C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105162274 | |||||||
| chr14:105162301 | A | T | 2 | a0001c0001t0001g0230 a0001c0001t0001g0237 |
2 | NA19043.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.418-4538T>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105162301 | |||||||
| chr14:105162306 | C | T | 2 | a0003c0003t0002g0061 a0003c0003t0002g0085 |
2 | NA18990.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.418-4543G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105162306 | |||||||
| chr14:105162341 | T | C | 1 | a0003c0006t0023g0260 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.418-4578A>G | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105162341 | |||||||
| chr14:105162353 | C | T | 6 | a0001c0001t0001g0033 a0001c0001t0001g0182 a0001c0001t0001g0184 others(3): Show |
7 | HG00642.hp1 HG01074.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.418-4590G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105162353 | |||||||
| chr14:105162354 | G | A | 1 | a0001c0001t0001g0246 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.418-4591C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105162354 | |||||||
| chr14:105162423 | A | G | 116 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(113): Show |
142 | HG00099.hp1 HG00280.hp1 HG00597.hp1 others(139): Show |
intron_variant | MODIFIER | c.418-4660T>C | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105162423 | |||||||
| chr14:105162451 | T | C | 3 | a0001c0001t0001g0179 a0001c0001t0001g0228 a0002c0013t0001g0205 |
3 | NA18969.hp1 NA18986.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.418-4688A>G | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105162451 | |||||||
| chr14:105162474 | C | CAAAGCCC others(179): Show |
2 | a0002c0015t0001g0145 a0002c0015t0001g0146 |
2 | HG03130.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.418-4712_418-4711i others(188): Show |
JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105162474 | |||||||
| chr14:105162474 | C | CAAAGCCC others(179): Show |
2 | a0002c0002t0001g0155 a0002c0002t0001g0158 |
2 | NA18966.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.418-4897_418-4712d others(188): Show |
JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105162474 | |||||||
| chr14:105162474 | C | CAAAGCCC others(365): Show |
7 | a0001c0001t0001g0007 a0001c0001t0001g0236 a0001c0001t0001g0248 others(4): Show |
13 | HG01167.hp1 HG01169.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.418-4712_418-4711i others(374): Show |
JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105162474 | |||||||
| chr14:105162474 | C | CAAAGCCC others(551): Show |
3 | a0001c0001t0001g0021 a0001c0001t0001g0247 a0001c0012t0001g0098 |
5 | HG01884.hp2 HG02717.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.418-4712_418-4711i others(560): Show |
JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105162474 | |||||||
| chr14:105162474 | C | CAAAGCCC others(737): Show |
3 | a0001c0001t0001g0228 a0001c0011t0001g0226 a0001c0035t0001g0227 |
3 | HG02970.hp1 HG03209.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.418-4712_418-4711i others(746): Show |
JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105162474 | |||||||
| chr14:105162474 | C | CAAAGCCC others(1667): Show |
1 | a0001c0001t0006g0036 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.418-4712_418-4711i others(1676): Show |
JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105162474 | |||||||
| chr14:105162474 | C | CAAAGCCC others(923): Show |
6 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(3): Show |
6 | HG01168.hp1 HG02293.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.418-4712_418-4711i others(932): Show |
JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105162474 | |||||||
| chr14:105162474 | C | CAAAGCCC others(1109): Show |
1 | a0001c0001t0001g0229 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.418-4712_418-4711i others(1118): Show |
JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105162474 | |||||||
| chr14:105162474 | C | CAAAGCCC others(1109): Show |
35 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0024 others(32): Show |
45 | HG00621.hp2 HG01175.hp2 HG02027.hp1 others(42): Show |
intron_variant | MODIFIER | c.418-4712_418-4711i others(1118): Show |
JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105162474 | |||||||
| chr14:105162474 | C | CAAAGCCC others(1295): Show |
9 | a0001c0001t0001g0019 a0001c0001t0001g0032 a0001c0001t0001g0049 others(6): Show |
12 | HG01081.hp1 HG01106.hp2 HG01256.hp2 others(9): Show |
intron_variant | MODIFIER | c.418-4712_418-4711i others(1304): Show |
JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105162474 | |||||||
| chr14:105162474 | C | CAAAGCCC others(1667): Show |
31 | a0001c0001t0001g0020 a0001c0001t0001g0033 a0001c0001t0001g0179 others(28): Show |
34 | HG00099.hp1 HG00280.hp1 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.418-4712_418-4711i others(1676): Show |
JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105162474 | |||||||
| chr14:105162474 | C | CAAAGCCC others(1853): Show |
1 | a0001c0001t0001g0046 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.418-4712_418-4711i others(1862): Show |
JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105162474 | |||||||
| chr14:105162474 | C | CAAAGCCC others(2039): Show |
1 | a0001c0001t0001g0170 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.418-4712_418-4711i others(2048): Show |
JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105162474 | |||||||
| chr14:105162474 | C | CAAAGCCC others(2411): Show |
2 | a0001c0001t0001g0182 a0001c0001t0001g0183 |
2 | HG01074.hp2 HG02015.hp1 |
intron_variant | MODIFIER | c.418-4712_418-4711i others(2420): Show |
JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105162474 | |||||||
| chr14:105162474 | C | CAAAGCCC others(10763): Show |
1 | a0001c0001t0001g0181 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.418-4712_418-4711i others(10772): Show |
JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105162474 | |||||||
| chr14:105162474 | C | CAAAGCCC others(1111): Show |
1 | a0001c0001t0001g0180 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.418-4712_418-4711i others(1120): Show |
JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105162474 | |||||||
| chr14:105162474 | C | CAAGCCCA others(1294): Show |
1 | a0001c0001t0001g0169 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.418-4712_418-4711i others(1303): Show |
JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105162474 | |||||||
| chr14:105162486 | T | TACCCCAG others(179): Show |
1 | a0002c0002t0001g0031 | 2 | HG02922.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.418-4909_418-4724d others(188): Show |
JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105162486 | |||||||
| chr14:105162529 | C | CCCAGGGC others(1102): Show |
1 | a0001c0001t0001g0167 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.418-4767_418-4766i others(1111): Show |
JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105162529 | |||||||
| chr14:105162534 | G | GGCACTGC others(366): Show |
1 | a0001c0001t0001g0235 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.418-4772_418-4771i others(375): Show |
JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105162534 | |||||||
| chr14:105162540 | G | A | 1 | a0001c0024t0003g0093 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.418-4777C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105162540 | |||||||
| chr14:105162547 | C | A | 1 | a0003c0003t0002g0085 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.418-4784G>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105162547 | |||||||
| chr14:105162564 | CCAGGGCA others(227): Show |
C | 12 | a0001c0005t0003g0014 a0001c0005t0003g0023 a0001c0005t0003g0087 others(9): Show |
16 | HG01175.hp1 HG02572.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.417+4959_418-4802d others(2): Show |
JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105162564 | |||||||
| chr14:105162569 | G | GCACCCCA others(4085): Show |
1 | a0001c0001t0001g0233 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.418-4807_418-4806i others(4094): Show |
JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105162569 | |||||||
| chr14:105162619 | A | AGCACTGC others(838): Show |
1 | a0001c0001t0001g0250 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.418-4857_418-4856i others(847): Show |
JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105162619 | |||||||
| chr14:105162664 | G | GCCCAGGG others(1751): Show |
1 | a0001c0001t0001g0231 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.418-4902_418-4901i others(1760): Show |
JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105162664 | |||||||
| chr14:105162664 | G | GCCCAGGG others(2766): Show |
1 | a0001c0001t0001g0251 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.418-4902_418-4901i others(2775): Show |
JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105162664 | |||||||
| chr14:105162665 | C | CCCAGGGT others(3510): Show |
1 | a0001c0001t0001g0230 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.418-4903_418-4902i others(3519): Show |
JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105162665 | |||||||
| chr14:105162665 | C | CCCAGGGT others(3696): Show |
1 | a0001c0001t0001g0237 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.418-4903_418-4902i others(3705): Show |
JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105162665 | |||||||
| chr14:105162670 | G | GGT | 2 | a0001c0001t0001g0037 a0001c0001t0001g0232 |
3 | HG02896.hp1 HG02897.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.418-4908_418-4907i others(4): Show |
JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105162670 | |||||||
| chr14:105162671 | A | G | 5 | a0001c0001t0001g0165 a0001c0001t0001g0230 a0001c0001t0001g0231 others(2): Show |
5 | HG01099.hp2 HG03516.hp2 NA19043.hp1 others(2): Show |
intron_variant | MODIFIER | c.418-4908T>C | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105162671 | |||||||
| chr14:105162672 | C | CCCCAGGT others(2223): Show |
1 | a0001c0001t0001g0037 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.418-4910_418-4909i others(2232): Show |
JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105162672 | |||||||
| chr14:105162672 | C | CCCCAGGT others(1851): Show |
1 | a0001c0001t0001g0232 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.418-4910_418-4909i others(1860): Show |
JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105162672 | |||||||
| chr14:105162672 | C | T | 2 | a0001c0001t0001g0165 a0001c0001t0001g0234 |
2 | HG01099.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.418-4909G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105162672 | |||||||
| chr14:105162676 | T | C | 6 | a0001c0001t0001g0037 a0001c0001t0001g0165 a0001c0001t0001g0231 others(3): Show |
7 | HG01099.hp2 HG01243.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.418-4913A>G | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105162676 | |||||||
| chr14:105162680 | G | T | 1 | a0001c0001t0001g0235 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.418-4917C>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105162680 | |||||||
| chr14:105162685 | A | G | 8 | a0001c0001t0001g0037 a0001c0001t0001g0165 a0001c0001t0001g0207 others(5): Show |
9 | HG01099.hp2 HG01243.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.418-4922T>C | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105162685 | |||||||
| chr14:105162689 | A | ACCCCAAA others(1854): Show |
1 | a0001c0001t0001g0165 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.418-4927_418-4926i others(1863): Show |
JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105162689 | |||||||
| chr14:105162689 | A | ACCCCAAA others(12456): Show |
1 | a0001c0001t0001g0234 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.418-4927_418-4926i others(12465): Show |
JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105162689 | |||||||
| chr14:105162697 | T | C | 2 | a0001c0001t0001g0165 a0001c0001t0001g0233 |
2 | HG01099.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.418-4934A>G | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105162697 | |||||||
| chr14:105162698 | A | C | 2 | a0001c0001t0001g0165 a0001c0001t0001g0233 |
2 | HG01099.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.418-4935T>G | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105162698 | |||||||
| chr14:105162706 | C | T | 43 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0024 others(40): Show |
53 | HG00621.hp2 HG01099.hp2 HG01168.hp1 others(50): Show |
intron_variant | MODIFIER | c.418-4943G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105162706 | |||||||
| chr14:105162709 | T | C | 64 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0024 others(61): Show |
77 | HG00621.hp2 HG01099.hp2 HG01167.hp2 others(74): Show |
intron_variant | MODIFIER | c.418-4946A>G | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105162709 | |||||||
| chr14:105162710 | C | A | 43 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0024 others(40): Show |
53 | HG00621.hp2 HG01099.hp2 HG01168.hp1 others(50): Show |
intron_variant | MODIFIER | c.418-4947G>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105162710 | |||||||
| chr14:105162712 | T | A | 43 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0024 others(40): Show |
53 | HG00621.hp2 HG01099.hp2 HG01168.hp1 others(50): Show |
intron_variant | MODIFIER | c.418-4949A>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105162712 | |||||||
| chr14:105162769 | TGTACCCA others(9): Show |
T | 57 | a0001c0001t0001g0128 a0002c0002t0001g0001 a0002c0002t0001g0003 others(54): Show |
98 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.417+4972_417+4987d others(18): Show |
JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105162769 | |||||||
| chr14:105162771 | T | C | 8 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0200 others(5): Show |
8 | HG00597.hp1 HG00673.hp2 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.417+4986A>G | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105162771 | |||||||
| chr14:105162781 | C | A | 9 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0037 others(6): Show |
16 | HG01167.hp1 HG01169.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.417+4976G>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105162781 | |||||||
| chr14:105162830 | C | T | 4 | a0004c0004t0001g0004 a0004c0004t0001g0159 a0004c0004t0001g0160 others(1): Show |
9 | HG00438.hp2 HG00558.hp2 NA18612.hp1 others(6): Show |
intron_variant | MODIFIER | c.417+4927G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105162830 | |||||||
| chr14:105162899 | C | T | 1 | a0001c0001t0001g0179 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.417+4858G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105162899 | |||||||
| chr14:105162920 | A | AC | 192 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(189): Show |
242 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(239): Show |
intron_variant | MODIFIER | c.417+4836dupG | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105162920 | |||||||
| chr14:105162952 | ACCCAAGT others(58): Show |
A | 1 | a0003c0003t0002g0157 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.417+4740_417+4804d others(67): Show |
JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105162952 | |||||||
| chr14:105163021 | AGGTCCAG others(10): Show |
A | 2 | a0001c0001t0008g0048 a0001c0022t0008g0084 |
2 | HG02109.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.417+4719_417+4735d others(19): Show |
JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105163021 | |||||||
| chr14:105163127 | C | T | 1 | a0003c0003t0002g0060 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.417+4630G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105163127 | |||||||
| chr14:105163247 | C | G | 191 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(188): Show |
241 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(238): Show |
intron_variant | MODIFIER | c.417+4510G>C | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105163247 | |||||||
| chr14:105163386 | C | T | 1 | a0003c0003t0002g0085 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.417+4371G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105163386 | |||||||
| chr14:105163387 | T | G | 1 | a0003c0003t0002g0085 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.417+4370A>C | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105163387 | |||||||
| chr14:105163440 | G | A | 1 | a0001c0001t0001g0236 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.417+4317C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105163440 | |||||||
| chr14:105163574 | ACTCCGCT others(25): Show |
A | 13 | a0001c0001t0001g0047 a0001c0005t0003g0014 a0001c0005t0003g0023 others(10): Show |
17 | HG01175.hp1 HG01175.hp2 HG02572.hp2 others(14): Show |
intron_variant | MODIFIER | c.417+4151_417+4182d others(34): Show |
JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105163574 | |||||||
| chr14:105163606 | C | A | 1 | a0001c0014t0018g0086 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.417+4151G>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105163606 | |||||||
| chr14:105163610 | C | T | 157 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(154): Show |
194 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.417+4147G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105163610 | |||||||
| chr14:105163650 | G | A | 171 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(168): Show |
212 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.417+4107C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105163650 | |||||||
| chr14:105163664 | G | A | 171 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(168): Show |
212 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.417+4093C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105163664 | |||||||
| chr14:105163695 | G | A | 171 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(168): Show |
212 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.417+4062C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105163695 | |||||||
| chr14:105163725 | G | A | 3 | a0001c0001t0001g0024 a0001c0001t0001g0041 a0001c0001t0001g0099 |
4 | NA18951.hp2 NA18975.hp2 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.417+4032C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105163725 | |||||||
| chr14:105163730 | C | T | 2 | a0002c0015t0001g0145 a0002c0015t0001g0146 |
2 | HG03130.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.417+4027G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105163730 | |||||||
| chr14:105163748 | C | T | 1 | a0002c0002t0001g0158 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.417+4009G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105163748 | |||||||
| chr14:105163749 | T | G | 1 | a0002c0002t0001g0158 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.417+4008A>C | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105163749 | |||||||
| chr14:105163816 | G | T | 8 | a0003c0006t0002g0149 a0006c0008t0001g0018 a0006c0008t0001g0150 others(5): Show |
10 | HG01261.hp2 HG01496.hp1 HG01934.hp2 others(7): Show |
intron_variant | MODIFIER | c.417+3941C>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105163816 | |||||||
| chr14:105163864 | C | G | 4 | a0001c0001t0001g0167 a0001c0001t0001g0178 a0001c0001t0002g0168 others(1): Show |
4 | HG03831.hp1 NA18948.hp1 NA18959.hp2 others(1): Show |
intron_variant | MODIFIER | c.417+3893G>C | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105163864 | |||||||
| chr14:105163942 | C | T | 1 | a0003c0003t0002g0094 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.417+3815G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105163942 | |||||||
| chr14:105163968 | G | A | 16 | a0002c0002t0001g0155 a0002c0002t0001g0158 a0003c0003t0002g0157 others(13): Show |
23 | HG00438.hp2 HG00558.hp2 HG01261.hp2 others(20): Show |
intron_variant | MODIFIER | c.417+3789C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105163968 | |||||||
| chr14:105164128 | G | A | 188 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(185): Show |
236 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(233): Show |
intron_variant | MODIFIER | c.417+3629C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105164128 | |||||||
| chr14:105164134 | C | T | 13 | a0001c0001t0001g0019 a0001c0001t0001g0032 a0001c0001t0001g0046 others(10): Show |
16 | HG01071.hp1 HG01081.hp2 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.417+3623G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105164134 | |||||||
| chr14:105164135 | G | A | 4 | a0004c0004t0001g0004 a0004c0004t0001g0159 a0004c0004t0001g0160 others(1): Show |
9 | HG00438.hp2 HG00558.hp2 NA18612.hp1 others(6): Show |
intron_variant | MODIFIER | c.417+3622C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105164135 | |||||||
| chr14:105164152 | C | T | 112 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(109): Show |
136 | HG00099.hp1 HG00280.hp1 HG00597.hp1 others(133): Show |
intron_variant | MODIFIER | c.417+3605G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105164152 | |||||||
| chr14:105164320 | C | A | 1 | a0002c0002t0001g0011 | 4 | NA18963.hp1 NA18971.hp2 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.417+3437G>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105164320 | |||||||
| chr14:105164375 | G | A | 1 | a0001c0024t0003g0093 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.417+3382C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105164375 | |||||||
| chr14:105164463 | G | A | 1 | a0001c0001t0001g0238 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.417+3294C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105164463 | |||||||
| chr14:105164479 | AGTGTGCA others(22): Show |
A | 1 | a0001c0001t0001g0166 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.417+3249_417+3277d others(31): Show |
JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105164479 | |||||||
| chr14:105164639 | T | C | 61 | a0001c0001t0001g0047 a0001c0001t0001g0067 a0001c0001t0001g0068 others(58): Show |
78 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(75): Show |
intron_variant | MODIFIER | c.417+3118A>G | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105164639 | |||||||
| chr14:105164820 | T | C | 5 | a0003c0003t0002g0022 a0003c0003t0002g0094 a0003c0003t0002g0095 others(2): Show |
6 | HG00408.hp1 HG02129.hp1 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.417+2937A>G | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105164820 | |||||||
| chr14:105164864 | G | A | 5 | a0005c0007t0003g0239 a0005c0007t0003g0240 a0005c0007t0003g0241 others(2): Show |
5 | HG02723.hp1 HG02818.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.417+2893C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105164864 | |||||||
| chr14:105164996 | G | C | 1 | a0001c0025t0001g0243 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.417+2761C>G | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105164996 | |||||||
| chr14:105165016 | C | T | 1 | a0002c0002t0001g0100 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.417+2741G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105165016 | |||||||
| chr14:105165023 | G | A | 1 | a0001c0001t0001g0250 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.417+2734C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105165023 | |||||||
| chr14:105165026 | C | T | 188 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(185): Show |
235 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.417+2731G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105165026 | |||||||
| chr14:105165275 | C | T | 2 | a0001c0001t0001g0167 a0001c0001t0002g0168 |
2 | NA18948.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.417+2482G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105165275 | |||||||
| chr14:105165573 | C | G | 75 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(72): Show |
99 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.417+2184G>C | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105165573 | |||||||
| chr14:105165642 | G | T | 1 | a0001c0001t0001g0166 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.417+2115C>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105165642 | |||||||
| chr14:105165643 | T | C | 1 | a0001c0001t0001g0166 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.417+2114A>G | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105165643 | |||||||
| chr14:105165643 | T | TC | 2 | a0003c0003t0002g0012 a0003c0006t0002g0147 |
5 | HG00609.hp1 HG00609.hp2 HG00621.hp1 others(2): Show |
intron_variant | MODIFIER | c.417+2113dupG | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105165643 | |||||||
| chr14:105165701 | G | A | 1 | a0006c0008t0001g0162 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.417+2056C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105165701 | |||||||
| chr14:105165723 | C | T | 6 | a0001c0009t0002g0055 a0001c0009t0005g0008 a0001c0032t0002g0056 others(3): Show |
9 | HG00639.hp1 HG00735.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.417+2034G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105165723 | |||||||
| chr14:105165761 | C | G | 1 | a0001c0001t0001g0246 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.417+1996G>C | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105165761 | |||||||
| chr14:105165938 | A | C | 1 | a0001c0001t0001g0166 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.417+1819T>G | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105165938 | |||||||
| chr14:105165943 | C | T | 16 | a0002c0002t0001g0155 a0002c0002t0001g0158 a0003c0003t0002g0157 others(13): Show |
23 | HG00438.hp2 HG00558.hp2 HG01261.hp2 others(20): Show |
intron_variant | MODIFIER | c.417+1814G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105165943 | |||||||
| chr14:105165946 | C | T | 1 | a0001c0001t0008g0048 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.417+1811G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105165946 | |||||||
| chr14:105166106 | G | C | 1 | a0001c0001t0001g0244 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.417+1651C>G | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105166106 | |||||||
| chr14:105166238 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.417+1519C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105166238 | |||||||
| chr14:105166263 | A | G | 1 | a0001c0001t0001g0165 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.417+1494T>C | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105166263 | |||||||
| chr14:105166459 | T | A | 1 | a0001c0001t0001g0245 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.417+1298A>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105166459 | |||||||
| chr14:105166460 | G | A | 1 | a0001c0001t0001g0245 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.417+1297C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105166460 | |||||||
| chr14:105166479 | A | G | 1 | a0003c0003t0002g0053 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.417+1278T>C | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105166479 | |||||||
| chr14:105166502 | C | G | 1 | a0002c0002t0001g0052 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.417+1255G>C | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105166502 | |||||||
| chr14:105166532 | C | T | 1 | a0002c0002t0001g0051 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.417+1225G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105166532 | |||||||
| chr14:105166618 | G | C | 1 | a0002c0002t0001g0050 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.417+1139C>G | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105166618 | |||||||
| chr14:105166704 | G | A | 8 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0246 others(5): Show |
14 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.417+1053C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105166704 | |||||||
| chr14:105166727 | A | G | 1 | a0001c0001t0001g0164 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.417+1030T>C | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105166727 | |||||||
| chr14:105166767 | G | A | 1 | a0001c0001t0001g0251 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.417+990C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105166767 | |||||||
| chr14:105166854 | C | A | 16 | a0002c0002t0001g0155 a0002c0002t0001g0158 a0003c0003t0002g0157 others(13): Show |
23 | HG00438.hp2 HG00558.hp2 HG01261.hp2 others(20): Show |
intron_variant | MODIFIER | c.417+903G>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105166854 | |||||||
| chr14:105166871 | C | T | 1 | a0001c0001t0001g0163 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.417+886G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105166871 | |||||||
| chr14:105167162 | G | A | 110 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(107): Show |
133 | HG00099.hp1 HG00280.hp1 HG00597.hp1 others(130): Show |
intron_variant | MODIFIER | c.417+595C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105167162 | |||||||
| chr14:105167163 | G | T | 1 | a0002c0002t0001g0050 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.417+594C>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105167163 | |||||||
| chr14:105167178 | G | A | 3 | a0001c0014t0001g0252 a0005c0007t0003g0038 a0005c0007t0003g0256 |
4 | HG02647.hp1 HG03041.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.417+579C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105167178 | |||||||
| chr14:105167207 | T | C | 189 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(186): Show |
237 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(234): Show |
intron_variant | MODIFIER | c.417+550A>G | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105167207 | |||||||
| chr14:105167254 | C | T | 1 | a0001c0001t0001g0049 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.417+503G>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105167254 | |||||||
| chr14:105167274 | C | A | 1 | a0005c0007t0003g0254 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.417+483G>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105167274 | |||||||
| chr14:105167538 | CGCGACCC others(4): Show |
C | 1 | a0001c0001t0001g0255 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.417+208_417+218del others(11): Show |
JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105167538 | |||||||
| chr14:105167542 | A | AC | 5 | a0001c0001t0001g0208 a0002c0002t0001g0142 a0003c0003t0002g0071 others(2): Show |
5 | HG00741.hp2 HG01496.hp2 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.417+214dupG | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105167542 | |||||||
| chr14:105167575 | G | A | 1 | a0005c0007t0003g0256 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.417+182C>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105167575 | |||||||
| chr14:105167670 | C | G | 1 | a0001c0001t0008g0048 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.417+87G>C | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | 105167670 | |||||||
| chr14:105168150 | G | T | 2 | a0001c0001t0001g0046 a0001c0001t0001g0047 |
2 | HG01081.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.67-43C>A | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 1/25 | chr14 | 105168150 | |||||||
| chr14:105168279 | C | A | 1 | a0001c0010t0001g0258 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.66+76G>T | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 1/25 | chr14 | 105168279 | |||||||
| chr14:105168326 | A | AC | 5 | a0001c0001t0001g0041 a0001c0001t0021g0045 a0002c0002t0001g0042 others(2): Show |
5 | HG00597.hp1 HG02572.hp1 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.66+28dupG | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 1/25 | chr14 | 105168326 | |||||||
| chr14:105168335 | G | C | 1 | a0003c0006t0023g0260 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.66+20C>G | JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 1/25 | chr14 | 105168335 |