Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 7472 |
| ensemblid | ENSG00000105989.10 |
| hgncid | 12780 |
| symbol | WNT2 |
| name | Wnt family member 2 |
| refseq_nuc | NM_003391.3 |
| refseq_prot | NP_003382.1 |
| ensembl_nuc | ENST00000265441.8 |
| ensembl_prot | ENSP00000265441.3 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 117275451 |
| end | 117323058 |
| strand | - |
| ver | v1.2 |
| region | chr7:117275451-117323058 |
| region5000 | chr7:117270451-117328058 |
| regionname0 | WNT2_chr7_117275451_117323058 |
| regionname5000 | WNT2_chr7_117270451_117328058 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 360 | 313 | 76 | 58 | 127 | 12 | 38 | 97 | WNT2_chr7_117270451_117328058 | WNT2 | MNAPL others(355): Show |
chr7 | 117270451 | 117328058 |
| a0002 | 0/0 | 360 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | MNAPR others(355): Show |
chr7 | 117270451 | 117328058 |
| a0003 | 0/0 | 360 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | MNAPL others(355): Show |
chr7 | 117270451 | 117328058 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1080 | 307 | 74 | 56 | 126 | 11 | 38 | WNT2_chr7_117270451_117328058 | WNT2 | ATGAA others(1075): Show |
chr7 | 117270451 | 117328058 | ||
| a0001c0002 | 0/0 | 1080 | 3 | 2 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | ATGAA others(1075): Show |
chr7 | 117270451 | 117328058 | ||
| a0001c0005 | 0/0 | 1080 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | ATGAA others(1075): Show |
chr7 | 117270451 | 117328058 | ||
| a0001c0006 | 0/0 | 1080 | 1 | 0 | 0 | 0 | 1 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | ATGAA others(1075): Show |
chr7 | 117270451 | 117328058 | ||
| a0001c0007 | 0/0 | 1080 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | ATGAA others(1075): Show |
chr7 | 117270451 | 117328058 | ||
| a0002c0003 | 0/0 | 1080 | 2 | 2 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | ATGAA others(1075): Show |
chr7 | 117270451 | 117328058 | ||
| a0003c0004 | 0/0 | 1080 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | ATGAA others(1075): Show |
chr7 | 117270451 | 117328058 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3857 | 72 | 23 | 12 | 27 | 2 | 8 | WNT2_chr7_117270451_117328058 | WNT2 | GCTTC others(3852): Show |
chr7 | 117270451 | 117328058 |
| a0001c0001t0002 | 0/0 | 3856 | 67 | 2 | 12 | 42 | 1 | 10 | WNT2_chr7_117270451_117328058 | WNT2 | GCTTC others(3851): Show |
chr7 | 117270451 | 117328058 |
| a0001c0001t0003 | 0/0 | 3856 | 67 | 2 | 9 | 47 | 1 | 8 | WNT2_chr7_117270451_117328058 | WNT2 | GCTTC others(3851): Show |
chr7 | 117270451 | 117328058 |
| a0001c0001t0004 | 0/0 | 3856 | 21 | 7 | 10 | 1 | 1 | 2 | WNT2_chr7_117270451_117328058 | WNT2 | GCTTC others(3851): Show |
chr7 | 117270451 | 117328058 |
| a0001c0001t0005 | 1/0 | 3856 | 9 | 2 | 2 | 0 | 1 | 3 | WNT2_chr7_117270451_117328058 | WNT2 | GCTTC others(3851): Show |
chr7 | 117270451 | 117328058 |
| a0001c0001t0006 | 0/0 | 3857 | 9 | 9 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | GCTTC others(3852): Show |
chr7 | 117270451 | 117328058 |
| a0001c0001t0007 | 0/1 | 3857 | 6 | 0 | 4 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | GCTTC others(3852): Show |
chr7 | 117270451 | 117328058 |
| a0001c0001t0008 | 0/0 | 3856 | 4 | 3 | 0 | 0 | 1 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | GCTTC others(3851): Show |
chr7 | 117270451 | 117328058 |
| a0001c0001t0009 | 0/0 | 3857 | 4 | 4 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | GCTTC others(3852): Show |
chr7 | 117270451 | 117328058 |
| a0001c0001t0010 | 0/0 | 3857 | 4 | 0 | 0 | 4 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | GCTTC others(3852): Show |
chr7 | 117270451 | 117328058 |
| a0001c0001t0011 | 0/0 | 3857 | 4 | 1 | 1 | 0 | 0 | 2 | WNT2_chr7_117270451_117328058 | WNT2 | GCTTC others(3852): Show |
chr7 | 117270451 | 117328058 |
| a0001c0001t0012 | 0/0 | 3857 | 4 | 4 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | GCTTC others(3852): Show |
chr7 | 117270451 | 117328058 |
| a0001c0001t0013 | 0/0 | 3857 | 3 | 1 | 0 | 2 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | GCTTC others(3852): Show |
chr7 | 117270451 | 117328058 |
| a0001c0001t0014 | 0/0 | 3857 | 3 | 0 | 1 | 0 | 1 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | GCTTC others(3852): Show |
chr7 | 117270451 | 117328058 |
| a0001c0001t0015 | 0/0 | 3857 | 3 | 2 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | GCTTC others(3852): Show |
chr7 | 117270451 | 117328058 |
| a0001c0001t0016 | 0/0 | 3857 | 3 | 3 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | GCTTC others(3852): Show |
chr7 | 117270451 | 117328058 |
| a0001c0001t0017 | 0/0 | 3856 | 3 | 0 | 1 | 0 | 2 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | GCTTC others(3851): Show |
chr7 | 117270451 | 117328058 |
| a0001c0001t0018 | 0/0 | 3856 | 2 | 2 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | GCTTC others(3851): Show |
chr7 | 117270451 | 117328058 |
| a0001c0001t0019 | 0/0 | 3857 | 2 | 0 | 1 | 0 | 1 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | GCTTC others(3852): Show |
chr7 | 117270451 | 117328058 |
| a0001c0001t0020 | 0/0 | 3856 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | GCTTC others(3851): Show |
chr7 | 117270451 | 117328058 |
| a0001c0001t0021 | 0/0 | 3856 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | GCTTC others(3851): Show |
chr7 | 117270451 | 117328058 |
| a0001c0001t0022 | 0/0 | 3856 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | GCTTC others(3851): Show |
chr7 | 117270451 | 117328058 |
| a0001c0001t0024 | 0/0 | 3856 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | GCTTC others(3851): Show |
chr7 | 117270451 | 117328058 |
| a0001c0001t0025 | 0/0 | 3856 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | GCTTC others(3851): Show |
chr7 | 117270451 | 117328058 |
| a0001c0001t0026 | 0/0 | 3856 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | GCTTC others(3851): Show |
chr7 | 117270451 | 117328058 |
| a0001c0001t0027 | 0/0 | 3857 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | GCTTC others(3852): Show |
chr7 | 117270451 | 117328058 |
| a0001c0001t0028 | 0/0 | 3857 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | GCTTC others(3852): Show |
chr7 | 117270451 | 117328058 |
| a0001c0001t0029 | 0/0 | 3856 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | GCTTC others(3851): Show |
chr7 | 117270451 | 117328058 |
| a0001c0001t0030 | 0/0 | 3857 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | GCTTC others(3852): Show |
chr7 | 117270451 | 117328058 |
| a0001c0001t0032 | 0/0 | 3857 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | GCTTC others(3852): Show |
chr7 | 117270451 | 117328058 |
| a0001c0001t0033 | 0/0 | 3857 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | GCTTC others(3852): Show |
chr7 | 117270451 | 117328058 |
| a0001c0001t0034 | 0/0 | 3857 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | GCTTC others(3852): Show |
chr7 | 117270451 | 117328058 |
| a0001c0001t0035 | 0/0 | 3857 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | GCTTC others(3852): Show |
chr7 | 117270451 | 117328058 |
| a0001c0001t0036 | 0/0 | 3857 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | GCTTC others(3852): Show |
chr7 | 117270451 | 117328058 |
| a0001c0001t0037 | 0/0 | 3856 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | GCTTC others(3851): Show |
chr7 | 117270451 | 117328058 |
| a0001c0001t0038 | 0/0 | 3857 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | GCTTC others(3852): Show |
chr7 | 117270451 | 117328058 |
| a0001c0002t0005 | 0/0 | 3856 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | GCTTC others(3851): Show |
chr7 | 117270451 | 117328058 |
| a0001c0002t0023 | 0/0 | 3857 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | GCTTC others(3852): Show |
chr7 | 117270451 | 117328058 |
| a0001c0002t0031 | 0/0 | 3857 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | GCTTC others(3852): Show |
chr7 | 117270451 | 117328058 |
| a0001c0005t0002 | 0/0 | 3856 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | GCTTC others(3851): Show |
chr7 | 117270451 | 117328058 |
| a0001c0006t0004 | 0/0 | 3856 | 1 | 0 | 0 | 0 | 1 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | GCTTC others(3851): Show |
chr7 | 117270451 | 117328058 |
| a0001c0007t0001 | 0/0 | 3857 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | GCTTC others(3852): Show |
chr7 | 117270451 | 117328058 |
| a0002c0003t0001 | 0/0 | 3857 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | GCTTC others(3852): Show |
chr7 | 117270451 | 117328058 |
| a0002c0003t0002 | 0/0 | 3856 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | GCTTC others(3851): Show |
chr7 | 117270451 | 117328058 |
| a0003c0004t0002 | 0/0 | 3856 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | GCTTC others(3851): Show |
chr7 | 117270451 | 117328058 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0001g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0002g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0002g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0002g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0002g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0003g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0003g0006 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0003g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0003g0012 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0003g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0003g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0003g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0003g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0003g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0003g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0003g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0003g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0004g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0004g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0004g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0004g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0004g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0004g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0004g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0004g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0004g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0004g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0004g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0004g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0004g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0004g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0004g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0004g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0004g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0004g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0004g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0004g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0004g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0005g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0005g0039 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0005g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0005g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0005g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0005g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0005g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0005g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0006g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0006g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0006g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0006g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0006g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0006g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0006g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0007g0007 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0007g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0007g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0007g0258 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0008g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0008g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0008g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0008g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0009g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0009g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0009g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0010g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0010g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0010g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0010g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0011g0014 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0011g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0011g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0012g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0012g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0012g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0012g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0013g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0013g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0013g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0014g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0014g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0014g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0015g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0015g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0015g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0016g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0016g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0016g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0017g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0017g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0017g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0018g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0019g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0019g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0020g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0021g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0022g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0024g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0025g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0026g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0027g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0028g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0029g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0030g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0032g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0033g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0034g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0035g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0036g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0037g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0001t0038g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0002t0005g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0002t0023g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0002t0031g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0005t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0006t0004g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0001c0007t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0002c0003t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0002c0003t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| a0003c0004t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0038 | EUR | GBR | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG00099 | hp2 | a0001 | c0006 | t0004 | g0197 | EUR | GBR | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG00140 | hp1 | a0001 | c0001 | t0005 | g0205 | EUR | GBR | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG00140 | hp2 | a0001 | c0001 | t0004 | g0060 | EUR | GBR | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG00323 | hp1 | a0001 | c0001 | t0014 | g0233 | EUR | FIN | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0133 | EUR | FIN | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0149 | EAS | CHS | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | CHS | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG00558 | hp2 | a0001 | c0001 | t0027 | g0091 | EAS | CHS | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0182 | EAS | CHS | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG00609 | hp2 | a0001 | c0001 | t0003 | g0083 | EAS | CHS | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0006 | AMR | PUR | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0128 | AMR | PUR | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG00733 | hp2 | a0001 | c0001 | t0007 | g0247 | AMR | PUR | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0017 | AMR | PUR | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG00738 | hp2 | a0001 | c0001 | t0004 | g0042 | AMR | PUR | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG00741 | hp1 | a0001 | c0001 | t0035 | g0243 | AMR | PUR | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG00741 | hp2 | a0001 | c0001 | t0017 | g0055 | AMR | PUR | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG01069 | hp1 | a0001 | c0001 | t0004 | g0103 | AMR | PUR | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG01069 | hp2 | a0001 | c0001 | t0007 | g0007 | AMR | PUR | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0223 | AMR | PUR | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG01070 | hp2 | a0001 | c0001 | t0004 | g0102 | AMR | PUR | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG01071 | hp1 | a0001 | c0001 | t0007 | g0007 | AMR | PUR | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0222 | AMR | PUR | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG01074 | hp1 | a0001 | c0001 | t0007 | g0007 | AMR | PUR | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG01074 | hp2 | a0001 | c0001 | t0004 | g0226 | AMR | PUR | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG01106 | hp1 | a0001 | c0001 | t0004 | g0114 | AMR | PUR | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0017 | AMR | PUR | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG01109 | hp1 | a0001 | c0001 | t0014 | g0117 | AMR | PUR | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0018 | AMR | PUR | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0232 | AMR | PUR | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG01175 | hp2 | a0001 | c0001 | t0019 | g0106 | AMR | PUR | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG01192 | hp2 | a0001 | c0001 | t0004 | g0225 | AMR | PUR | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG01243 | hp1 | a0001 | c0001 | t0015 | g0094 | AMR | PUR | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG01243 | hp2 | a0001 | c0001 | t0024 | g0260 | AMR | PUR | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG01255 | hp1 | a0001 | c0002 | t0031 | g0058 | AMR | CLM | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | CLM | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG01256 | hp1 | a0001 | c0001 | t0005 | g0013 | AMR | CLM | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | CLM | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG01258 | hp1 | a0001 | c0001 | t0005 | g0013 | AMR | CLM | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG01258 | hp2 | a0001 | c0001 | t0004 | g0259 | AMR | CLM | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0012 | AMR | CLM | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0221 | AMR | CLM | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG01346 | hp2 | a0001 | c0001 | t0004 | g0077 | AMR | CLM | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0275 | AMR | CLM | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG01358 | hp2 | a0001 | c0007 | t0001 | g0154 | AMR | CLM | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0277 | AMR | CLM | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG01433 | hp2 | a0001 | c0001 | t0004 | g0252 | AMR | CLM | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | CLM | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | CLM | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG01517 | hp1 | a0001 | c0001 | t0017 | g0056 | EUR | IBS | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG01517 | hp2 | a0001 | c0001 | t0008 | g0255 | EUR | IBS | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG01891 | hp1 | a0001 | c0001 | t0006 | g0217 | AFR | ACB | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG01891 | hp2 | a0001 | c0001 | t0018 | g0009 | AFR | ACB | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG01943 | hp1 | a0001 | c0001 | t0011 | g0244 | AMR | PEL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG01943 | hp2 | a0001 | c0001 | t0003 | g0088 | AMR | PEL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0057 | AMR | PEL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0210 | AMR | PEL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0104 | AMR | PEL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG01978 | hp2 | a0001 | c0001 | t0003 | g0159 | AMR | PEL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG01993 | hp2 | a0001 | c0001 | t0004 | g0194 | AMR | PEL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0192 | AMR | PEL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | KHV | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0144 | EAS | KHV | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | KHV | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG02056 | hp2 | a0001 | c0001 | t0003 | g0213 | EAS | KHV | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | KHV | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | KHV | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | KHV | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | KHV | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0176 | EAS | KHV | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | KHV | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0044 | EAS | KHV | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0165 | EAS | KHV | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0158 | EAS | KHV | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0271 | AFR | ACB | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG02145 | hp2 | a0001 | c0001 | t0012 | g0219 | AFR | ACB | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0018 | AMR | PEL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG02148 | hp2 | a0001 | c0001 | t0003 | g0134 | AMR | PEL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0163 | EAS | CDX | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | CDX | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG02165 | hp1 | a0001 | c0001 | t0033 | g0075 | EAS | CDX | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG02165 | hp2 | a0001 | c0001 | t0010 | g0137 | EAS | CDX | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG02257 | hp1 | a0001 | c0001 | t0004 | g0095 | AFR | ACB | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0059 | AFR | ACB | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG02258 | hp2 | a0001 | c0001 | t0032 | g0262 | AFR | ACB | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG02280 | hp1 | a0001 | c0001 | t0012 | g0273 | AFR | ACB | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | ACB | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0179 | AMR | PEL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | ACB | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | KHV | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG02572 | hp1 | a0001 | c0001 | t0006 | g0254 | AFR | GWD | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG02572 | hp2 | a0001 | c0001 | t0006 | g0005 | AFR | GWD | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0025 | SAS | PJL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG02602 | hp2 | a0001 | c0001 | t0004 | g0054 | SAS | PJL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG02615 | hp2 | a0001 | c0001 | t0021 | g0235 | AFR | GWD | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG02630 | hp1 | a0001 | c0001 | t0008 | g0251 | AFR | GWD | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0282 | AFR | GWD | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG02647 | hp1 | a0001 | c0001 | t0006 | g0264 | AFR | GWD | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG02647 | hp2 | a0001 | c0001 | t0015 | g0047 | AFR | GWD | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG02698 | hp1 | a0001 | c0001 | t0005 | g0043 | SAS | PJL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG02698 | hp2 | a0001 | c0001 | t0007 | g0037 | SAS | PJL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0090 | AFR | GWD | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG02717 | hp2 | a0001 | c0001 | t0011 | g0250 | AFR | GWD | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG02723 | hp1 | a0001 | c0001 | t0004 | g0246 | AFR | GWD | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0242 | SAS | PJL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG02738 | hp2 | a0001 | c0001 | t0014 | g0120 | SAS | PJL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG02809 | hp1 | a0001 | c0001 | t0005 | g0092 | AFR | GWD | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG02809 | hp2 | a0001 | c0001 | t0005 | g0236 | AFR | GWD | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG02818 | hp1 | a0001 | c0001 | t0016 | g0216 | AFR | GWD | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0272 | AFR | GWD | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG02896 | hp1 | a0001 | c0001 | t0006 | g0265 | AFR | GWD | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG02922 | hp2 | a0001 | c0001 | t0009 | g0218 | AFR | ESN | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG02965 | hp1 | a0001 | c0001 | t0028 | g0204 | AFR | ESN | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG02965 | hp2 | a0001 | c0001 | t0009 | g0274 | AFR | ESN | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG02976 | hp1 | a0001 | c0001 | t0018 | g0009 | AFR | ESN | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG02976 | hp2 | a0001 | c0002 | t0005 | g0249 | AFR | ESN | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG03017 | hp1 | a0001 | c0001 | t0005 | g0046 | SAS | PJL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0171 | SAS | PJL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG03041 | hp1 | a0001 | c0001 | t0006 | g0220 | AFR | GWD | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG03041 | hp2 | a0001 | c0001 | t0006 | g0261 | AFR | GWD | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | MSL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG03098 | hp2 | a0001 | c0001 | t0008 | g0206 | AFR | MSL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG03130 | hp1 | a0001 | c0001 | t0022 | g0074 | AFR | ESN | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG03130 | hp2 | a0001 | c0001 | t0025 | g0224 | AFR | ESN | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | ESN | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | ESN | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG03195 | hp2 | a0001 | c0001 | t0013 | g0156 | AFR | ESN | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG03209 | hp1 | a0001 | c0001 | t0016 | g0227 | AFR | MSL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | MSL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG03225 | hp1 | a0002 | c0003 | t0001 | g0026 | AFR | MSL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG03225 | hp2 | a0001 | c0001 | t0006 | g0005 | AFR | MSL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0008 | SAS | PJL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | MSL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG03453 | hp2 | a0001 | c0001 | t0038 | g0028 | AFR | MSL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | MSL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | MSL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0123 | SAS | PJL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG03490 | hp2 | a0001 | c0001 | t0011 | g0014 | SAS | PJL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0024 | SAS | PJL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG03491 | hp2 | a0001 | c0001 | t0004 | g0196 | SAS | PJL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG03492 | hp1 | a0001 | c0001 | t0011 | g0014 | SAS | PJL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0024 | SAS | PJL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0279 | AFR | GWD | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0280 | AFR | GWD | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG03579 | hp1 | a0001 | c0001 | t0015 | g0229 | AFR | MSL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG03579 | hp2 | a0001 | c0002 | t0023 | g0248 | AFR | MSL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG03654 | hp2 | a0001 | c0001 | t0037 | g0076 | SAS | PJL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0135 | SAS | PJL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0131 | SAS | STU | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0041 | SAS | STU | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0025 | SAS | PJL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0267 | SAS | PJL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0126 | SAS | PJL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0127 | SAS | PJL | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0253 | SAS | BEB | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0008 | SAS | BEB | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0129 | SAS | BEB | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | BEB | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0140 | SAS | STU | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | STU | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG04184 | hp1 | a0001 | c0001 | t0029 | g0098 | SAS | BEB | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG04184 | hp2 | a0001 | c0001 | t0005 | g0231 | SAS | BEB | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | STU | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0030 | SAS | STU | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA18522 | hp1 | a0001 | c0001 | t0009 | g0023 | AFR | YRI | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA18522 | hp2 | a0001 | c0001 | t0004 | g0237 | AFR | YRI | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | CHB | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | CHB | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | CHB | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0160 | EAS | CHB | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA18906 | hp1 | a0001 | c0001 | t0012 | g0215 | AFR | YRI | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA18906 | hp2 | a0001 | c0001 | t0036 | g0214 | AFR | YRI | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA18940 | hp1 | a0001 | c0001 | t0003 | g0200 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA18943 | hp2 | a0001 | c0001 | t0003 | g0107 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA18948 | hp1 | a0001 | c0001 | t0004 | g0151 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA18948 | hp2 | a0001 | c0001 | t0003 | g0068 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA18951 | hp2 | a0001 | c0001 | t0013 | g0172 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0187 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA18963 | hp1 | a0003 | c0004 | t0002 | g0063 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA18963 | hp2 | a0001 | c0001 | t0003 | g0138 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA18972 | hp2 | a0001 | c0001 | t0003 | g0202 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA18975 | hp1 | a0001 | c0001 | t0003 | g0170 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA18975 | hp2 | a0001 | c0001 | t0003 | g0185 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA18977 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA18977 | hp2 | a0001 | c0001 | t0003 | g0201 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA18982 | hp1 | a0001 | c0001 | t0010 | g0033 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA18982 | hp2 | a0001 | c0001 | t0010 | g0065 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA18985 | hp2 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA18986 | hp1 | a0001 | c0001 | t0003 | g0178 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA18990 | hp1 | a0001 | c0001 | t0003 | g0147 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA18992 | hp1 | a0001 | c0001 | t0003 | g0175 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA18993 | hp1 | a0001 | c0001 | t0003 | g0035 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0136 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0142 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA19002 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA19002 | hp2 | a0001 | c0001 | t0026 | g0112 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA19006 | hp1 | a0001 | c0005 | t0002 | g0207 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA19006 | hp2 | a0001 | c0001 | t0003 | g0208 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA19007 | hp2 | a0001 | c0001 | t0013 | g0052 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA19011 | hp1 | a0001 | c0001 | t0003 | g0150 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA19043 | hp1 | a0001 | c0001 | t0006 | g0005 | AFR | LWK | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | LWK | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA19055 | hp2 | a0001 | c0001 | t0003 | g0066 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA19060 | hp2 | a0001 | c0001 | t0010 | g0034 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA19066 | hp2 | a0001 | c0001 | t0003 | g0070 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA19072 | hp1 | a0001 | c0001 | t0003 | g0100 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA19075 | hp1 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA19081 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA19082 | hp1 | a0001 | c0001 | t0003 | g0101 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA19082 | hp2 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA19084 | hp2 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA19087 | hp2 | a0001 | c0001 | t0003 | g0164 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA19089 | hp2 | a0001 | c0001 | t0003 | g0184 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA19090 | hp1 | a0001 | c0001 | t0003 | g0189 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA19240 | hp1 | a0001 | c0001 | t0012 | g0281 | AFR | YRI | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0270 | AFR | YRI | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA20129 | hp1 | a0001 | c0001 | t0004 | g0228 | AFR | ASW | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA20129 | hp2 | a0001 | c0001 | t0008 | g0239 | AFR | ASW | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0268 | EUR | TSI | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0256 | EUR | TSI | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA20805 | hp1 | a0001 | c0001 | t0019 | g0069 | EUR | TSI | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA20805 | hp2 | a0001 | c0001 | t0017 | g0257 | EUR | TSI | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0238 | SAS | GIH | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA20905 | hp2 | a0001 | c0001 | t0020 | g0115 | SAS | GIH | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG01123 | hp1 | a0001 | c0001 | t0003 | g0087 | AMR | CLM | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | CLM | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | ACB | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG02109 | hp2 | a0002 | c0003 | t0002 | g0027 | AFR | ACB | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG02486 | hp1 | a0001 | c0001 | t0034 | g0278 | AFR | ACB | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG02559 | hp1 | a0001 | c0001 | t0016 | g0263 | AFR | ACB | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG06807 | hp1 | a0001 | c0001 | t0030 | g0269 | AFR | USA | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| HG06807 | hp2 | a0001 | c0001 | t0009 | g0023 | AFR | USA | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA21309 | hp1 | a0001 | c0001 | t0004 | g0230 | AFR | LWK | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | LWK | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0007 | g0258 | REF | REF | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0005 | g0039 | REF | REF | WNT2_chr7_117270451_117328058 | WNT2 | chr7 | 117270451 | 117328058 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:117297789 | C | T | 1 | a0003 | 1 | NA18963.hp1 | missense_variant | MODERATE | c.676G>A | p.Asp226Asn | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/5 | 745/3856 | 676/1083 | 226/360 | chr7 | 117297789 | |||
| chr7:117322976 | A | C | 1 | a0002 | 2 | HG02109.hp2 HG03225.hp1 |
missense_variant | MODERATE | c.14T>G | p.Leu5Arg | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 1/5 | 83/3856 | 14/1083 | 5/360 | chr7 | 117322976 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:117278179 | G | A | 1 | a0001c0005 | 1 | NA19006.hp1 | synonymous_variant | LOW | c.1059C>T | p.Asn353Asn | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 5/5 | 1128/3856 | 1059/1083 | 353/360 | chr7 | 117278179 | |||
| chr7:117297661 | G | A | 1 | a0001c0006 | 1 | HG00099.hp2 | synonymous_variant | LOW | c.804C>T | p.Leu268Leu | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/5 | 873/3856 | 804/1083 | 268/360 | chr7 | 117297661 | |||
| chr7:117297673 | C | T | 1 | a0001c0002 | 3 | HG01255.hp1 HG02976.hp2 HG03579.hp2 |
synonymous_variant | LOW | c.792G>A | p.Thr264Thr | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/5 | 861/3856 | 792/1083 | 264/360 | chr7 | 117297673 | |||
| chr7:117297838 | G | A | 1 | a0001c0007 | 1 | HG01358.hp2 | synonymous_variant | LOW | c.627C>T | p.His209His | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/5 | 696/3856 | 627/1083 | 209/360 | chr7 | 117297838 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:117275630 | G | C | 20 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0009 others(17): Show |
111 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(108): Show |
3_prime_UTR_variant | MODIFIER | c.*2525C>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 5/5 | 2525 | chr7 | 117275630 | ||||||
| chr7:117275729 | T | C | 7 | a0001c0001t0009 a0001c0001t0011 a0001c0001t0012 others(4): Show |
18 | HG01943.hp1 HG02145.hp2 HG02280.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*2426A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 5/5 | 2426 | chr7 | 117275729 | ||||||
| chr7:117275827 | T | G | 1 | a0001c0001t0024 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2328A>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 5/5 | 2328 | chr7 | 117275827 | ||||||
| chr7:117275830 | G | A | 3 | a0001c0001t0014 a0001c0001t0019 a0001c0001t0030 |
6 | HG00323.hp1 HG01109.hp1 HG01175.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2325C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 5/5 | 2325 | chr7 | 117275830 | ||||||
| chr7:117275845 | C | A | 1 | a0001c0001t0016 | 3 | HG02559.hp1 HG02818.hp1 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2310G>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 5/5 | 2310 | chr7 | 117275845 | ||||||
| chr7:117275852 | A | G | 1 | a0001c0001t0032 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2303T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 5/5 | 2303 | chr7 | 117275852 | ||||||
| chr7:117275897 | C | T | 1 | a0001c0001t0014 | 3 | HG00323.hp1 HG01109.hp1 HG02738.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2258G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 5/5 | 2258 | chr7 | 117275897 | ||||||
| chr7:117275928 | C | T | 1 | a0001c0001t0037 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2227G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 5/5 | 2227 | chr7 | 117275928 | ||||||
| chr7:117275958 | A | C | 36 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(33): Show |
277 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(274): Show |
3_prime_UTR_variant | MODIFIER | c.*2197T>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 5/5 | 2197 | chr7 | 117275958 | ||||||
| chr7:117276060 | T | A | 1 | a0001c0001t0036 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2095A>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 5/5 | 2095 | chr7 | 117276060 | ||||||
| chr7:117276086 | G | A | 3 | a0001c0001t0034 a0001c0001t0038 a0001c0002t0023 |
3 | HG02486.hp1 HG03453.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2069C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 5/5 | 2069 | chr7 | 117276086 | ||||||
| chr7:117276174 | A | G | 23 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0007 others(20): Show |
124 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(121): Show |
3_prime_UTR_variant | MODIFIER | c.*1981T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 5/5 | 1981 | chr7 | 117276174 | ||||||
| chr7:117276206 | C | A | 1 | a0001c0001t0012 | 4 | HG02145.hp2 HG02280.hp1 NA18906.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1949G>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 5/5 | 1949 | chr7 | 117276206 | ||||||
| chr7:117276359 | T | C | 9 | a0001c0001t0006 a0001c0001t0009 a0001c0001t0011 others(6): Show |
32 | HG01243.hp1 HG01891.hp1 HG01943.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*1796A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 5/5 | 1796 | chr7 | 117276359 | ||||||
| chr7:117276423 | G | A | 1 | a0001c0001t0036 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1732C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 5/5 | 1732 | chr7 | 117276423 | ||||||
| chr7:117276606 | T | C | 1 | a0001c0002t0031 | 1 | HG01255.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1549A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 5/5 | 1549 | chr7 | 117276606 | ||||||
| chr7:117276877 | A | G | 1 | a0001c0001t0028 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1278T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 5/5 | 1278 | chr7 | 117276877 | ||||||
| chr7:117276959 | T | C | 1 | a0001c0001t0029 | 1 | HG04184.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1196A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 5/5 | 1196 | chr7 | 117276959 | ||||||
| chr7:117277064 | C | T | 9 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0014 others(6): Show |
87 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*1091G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 5/5 | 1091 | chr7 | 117277064 | ||||||
| chr7:117277089 | G | A | 1 | a0001c0001t0018 | 2 | HG01891.hp2 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1066C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 5/5 | 1066 | chr7 | 117277089 | ||||||
| chr7:117277186 | C | T | 1 | a0001c0001t0030 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*969G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 5/5 | 969 | chr7 | 117277186 | ||||||
| chr7:117277191 | C | CA | 25 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0007 others(22): Show |
129 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(126): Show |
3_prime_UTR_variant | MODIFIER | c.*963_*964insT | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 5/5 | 963 | chr7 | 117277191 | ||||||
| chr7:117277373 | G | A | 31 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0007 others(28): Show |
193 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(190): Show |
3_prime_UTR_variant | MODIFIER | c.*782C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 5/5 | 782 | chr7 | 117277373 | ||||||
| chr7:117277613 | A | C | 1 | a0001c0001t0026 | 1 | NA19002.hp2 | 3_prime_UTR_variant | MODIFIER | c.*542T>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 5/5 | 542 | chr7 | 117277613 | ||||||
| chr7:117278006 | G | A | 11 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0008 others(8): Show |
44 | HG00099.hp2 HG00140.hp2 HG00733.hp2 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*149C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 5/5 | 149 | chr7 | 117278006 | ||||||
| chr7:117278031 | C | T | 12 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 others(9): Show |
51 | HG00099.hp2 HG00140.hp2 HG00733.hp2 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*124G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 5/5 | 124 | chr7 | 117278031 | ||||||
| chr7:117278070 | C | T | 1 | a0001c0001t0020 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*85G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 5/5 | 85 | chr7 | 117278070 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:117278432 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.854-48G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117278432 | |||||||
| chr7:117278700 | C | T | 1 | a0001c0001t0008g0251 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.854-316G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117278700 | |||||||
| chr7:117278738 | A | C | 107 | a0001c0001t0001g0032 a0001c0001t0001g0062 a0001c0001t0001g0071 others(104): Show |
117 | HG00323.hp2 HG00438.hp1 HG00558.hp2 others(114): Show |
intron_variant | MODIFIER | c.854-354T>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117278738 | |||||||
| chr7:117278777 | C | T | 3 | a0001c0001t0002g0067 a0001c0001t0003g0083 a0001c0001t0026g0112 |
3 | HG00609.hp2 NA18968.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.854-393G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117278777 | |||||||
| chr7:117278857 | A | G | 87 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(84): Show |
102 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.854-473T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117278857 | |||||||
| chr7:117279046 | C | T | 1 | a0001c0001t0001g0277 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.854-662G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117279046 | |||||||
| chr7:117279235 | C | T | 1 | a0001c0001t0003g0131 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.854-851G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117279235 | |||||||
| chr7:117279459 | G | C | 1 | a0001c0001t0003g0035 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.854-1075C>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117279459 | |||||||
| chr7:117279474 | T | C | 2 | a0001c0001t0012g0273 a0001c0001t0012g0281 |
2 | HG02280.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.854-1090A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117279474 | |||||||
| chr7:117279540 | G | T | 2 | a0001c0001t0001g0276 a0001c0001t0032g0262 |
2 | HG02258.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.854-1156C>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117279540 | |||||||
| chr7:117279562 | A | T | 1 | a0001c0001t0020g0115 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.854-1178T>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117279562 | |||||||
| chr7:117279599 | A | C | 3 | a0001c0001t0002g0282 a0001c0001t0008g0251 a0002c0003t0002g0027 |
3 | HG02109.hp2 HG02630.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.854-1215T>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117279599 | |||||||
| chr7:117279676 | C | T | 1 | a0001c0001t0003g0279 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.854-1292G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117279676 | |||||||
| chr7:117279924 | G | A | 186 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(183): Show |
208 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.854-1540C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117279924 | |||||||
| chr7:117279931 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.854-1547G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117279931 | |||||||
| chr7:117280081 | G | A | 2 | a0001c0001t0004g0060 a0001c0001t0004g0114 |
2 | HG00140.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.854-1697C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117280081 | |||||||
| chr7:117280117 | G | C | 1 | a0001c0001t0004g0077 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.854-1733C>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117280117 | |||||||
| chr7:117280175 | T | C | 1 | a0001c0001t0001g0277 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.854-1791A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117280175 | |||||||
| chr7:117280193 | C | A | 1 | a0001c0001t0001g0078 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.854-1809G>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117280193 | |||||||
| chr7:117280295 | A | T | 2 | a0001c0001t0011g0014 a0001c0001t0035g0243 |
3 | HG00741.hp1 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.854-1911T>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117280295 | |||||||
| chr7:117280532 | A | G | 1 | a0001c0001t0008g0255 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.854-2148T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117280532 | |||||||
| chr7:117280554 | T | C | 23 | a0001c0001t0001g0266 a0001c0001t0001g0276 a0001c0001t0003g0279 others(20): Show |
24 | HG00741.hp2 HG01074.hp2 HG01192.hp2 others(21): Show |
intron_variant | MODIFIER | c.854-2170A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117280554 | |||||||
| chr7:117280591 | A | G | 1 | a0001c0001t0001g0277 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.854-2207T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117280591 | |||||||
| chr7:117280654 | T | G | 103 | a0001c0001t0001g0019 a0001c0001t0001g0032 a0001c0001t0001g0053 others(100): Show |
112 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.854-2270A>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117280654 | |||||||
| chr7:117280663 | T | C | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(96): Show |
113 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.854-2279A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117280663 | |||||||
| chr7:117280696 | A | C | 1 | a0001c0001t0012g0215 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.854-2312T>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117280696 | |||||||
| chr7:117280709 | C | T | 2 | a0001c0001t0011g0014 a0001c0001t0035g0243 |
3 | HG00741.hp1 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.854-2325G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117280709 | |||||||
| chr7:117280828 | C | T | 1 | a0001c0001t0001g0277 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.854-2444G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117280828 | |||||||
| chr7:117280910 | A | C | 194 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(191): Show |
217 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.854-2526T>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117280910 | |||||||
| chr7:117280916 | T | C | 194 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(191): Show |
217 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.854-2532A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117280916 | |||||||
| chr7:117280940 | A | G | 1 | a0001c0001t0005g0013 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.854-2556T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117280940 | |||||||
| chr7:117281176 | C | G | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(195): Show |
223 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.854-2792G>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117281176 | |||||||
| chr7:117281243 | GTTA | G | 3 | a0001c0001t0004g0246 a0001c0001t0004g0272 a0001c0001t0006g0261 |
3 | HG02723.hp1 HG02818.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.854-2862_854-2860d others(5): Show |
WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117281243 | |||||||
| chr7:117281282 | G | A | 11 | a0001c0001t0002g0022 a0001c0001t0002g0049 a0001c0001t0002g0085 others(8): Show |
14 | HG02004.hp1 HG02129.hp1 HG02132.hp1 others(11): Show |
intron_variant | MODIFIER | c.854-2898C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117281282 | |||||||
| chr7:117281342 | A | C | 1 | a0001c0001t0012g0281 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.854-2958T>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117281342 | |||||||
| chr7:117281520 | G | A | 3 | a0001c0001t0001g0093 a0001c0001t0001g0122 a0001c0001t0015g0094 |
3 | HG01243.hp1 HG02615.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.854-3136C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117281520 | |||||||
| chr7:117281701 | C | T | 1 | a0001c0001t0008g0251 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.854-3317G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117281701 | |||||||
| chr7:117281924 | G | A | 2 | a0001c0001t0001g0125 a0001c0001t0001g0141 |
2 | HG03654.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.854-3540C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117281924 | |||||||
| chr7:117281935 | G | A | 2 | a0001c0001t0017g0055 a0001c0001t0017g0056 |
2 | HG00741.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.854-3551C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117281935 | |||||||
| chr7:117282003 | G | A | 2 | a0001c0001t0001g0032 a0001c0001t0005g0043 |
2 | HG02698.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.854-3619C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117282003 | |||||||
| chr7:117282157 | T | C | 2 | a0001c0001t0002g0036 a0001c0001t0002g0116 |
2 | NA18989.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.854-3773A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117282157 | |||||||
| chr7:117282174 | A | G | 2 | a0001c0001t0002g0080 a0001c0001t0002g0081 |
2 | HG00438.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.854-3790T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117282174 | |||||||
| chr7:117282263 | A | T | 96 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(93): Show |
110 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.854-3879T>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117282263 | |||||||
| chr7:117282400 | GAGGAGGA others(8): Show |
G | 1 | a0001c0001t0013g0052 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.854-4031_854-4017d others(17): Show |
WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117282400 | |||||||
| chr7:117282415 | A | AAAG | 109 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(106): Show |
123 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.854-4032_854-4031i others(5): Show |
WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117282415 | |||||||
| chr7:117282448 | A | G | 1 | a0001c0001t0017g0055 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.854-4064T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117282448 | |||||||
| chr7:117282685 | C | A | 4 | a0001c0001t0008g0251 a0001c0001t0017g0055 a0001c0001t0017g0056 others(1): Show |
4 | HG00741.hp2 HG01517.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.854-4301G>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117282685 | |||||||
| chr7:117282888 | T | G | 1 | a0001c0001t0015g0229 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.854-4504A>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117282888 | |||||||
| chr7:117282997 | G | A | 1 | a0001c0001t0012g0281 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.854-4613C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117282997 | |||||||
| chr7:117283129 | A | G | 1 | a0001c0001t0001g0276 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.854-4745T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117283129 | |||||||
| chr7:117283420 | G | A | 2 | a0001c0001t0001g0266 a0001c0001t0002g0282 |
2 | HG01496.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.854-5036C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117283420 | |||||||
| chr7:117283508 | T | A | 1 | a0001c0001t0038g0028 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.854-5124A>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117283508 | |||||||
| chr7:117283952 | G | T | 1 | a0001c0001t0001g0072 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.854-5568C>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117283952 | |||||||
| chr7:117284023 | AG | A | 5 | a0001c0001t0004g0225 a0001c0001t0004g0226 a0001c0001t0006g0264 others(2): Show |
5 | HG01074.hp2 HG01192.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.854-5640delC | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117284023 | |||||||
| chr7:117284155 | C | T | 2 | a0001c0001t0003g0134 a0001c0001t0003g0210 |
2 | HG01975.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.854-5771G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117284155 | |||||||
| chr7:117284199 | G | C | 2 | a0001c0001t0002g0128 a0001c0001t0002g0140 |
2 | HG00642.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.854-5815C>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117284199 | |||||||
| chr7:117284619 | C | G | 2 | a0001c0001t0001g0266 a0001c0001t0002g0282 |
2 | HG01496.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.854-6235G>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117284619 | |||||||
| chr7:117284635 | T | C | 1 | a0001c0001t0028g0204 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.854-6251A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117284635 | |||||||
| chr7:117285059 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.854-6675G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117285059 | |||||||
| chr7:117285412 | C | T | 2 | a0001c0001t0002g0238 a0001c0001t0005g0231 |
2 | HG04184.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.854-7028G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117285412 | |||||||
| chr7:117285424 | A | C | 2 | a0001c0001t0001g0266 a0001c0001t0002g0282 |
2 | HG01496.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.854-7040T>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117285424 | |||||||
| chr7:117285462 | T | C | 1 | a0001c0001t0001g0110 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.854-7078A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117285462 | |||||||
| chr7:117285490 | C | G | 1 | a0001c0001t0009g0274 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.854-7106G>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117285490 | |||||||
| chr7:117285548 | A | T | 2 | a0001c0001t0013g0052 a0001c0001t0015g0047 |
2 | HG02647.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.854-7164T>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117285548 | |||||||
| chr7:117286093 | G | T | 2 | a0001c0001t0001g0041 a0001c0001t0002g0008 |
3 | HG03239.hp2 HG03688.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.854-7709C>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117286093 | |||||||
| chr7:117286098 | G | A | 2 | a0001c0001t0018g0009 a0002c0003t0001g0026 |
3 | HG01891.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.854-7714C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117286098 | |||||||
| chr7:117286359 | C | T | 1 | a0001c0001t0015g0047 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.854-7975G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117286359 | |||||||
| chr7:117286578 | C | G | 110 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(107): Show |
124 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(121): Show |
intron_variant | MODIFIER | c.854-8194G>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117286578 | |||||||
| chr7:117286770 | A | AAAGACAA others(13): Show |
94 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(91): Show |
108 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(105): Show |
intron_variant | MODIFIER | c.854-8406_854-8387d others(22): Show |
WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117286770 | |||||||
| chr7:117286817 | G | A | 2 | a0001c0001t0004g0059 a0001c0001t0005g0236 |
2 | HG02257.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.854-8433C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117286817 | |||||||
| chr7:117287119 | C | T | 2 | a0001c0001t0018g0009 a0002c0003t0001g0026 |
3 | HG01891.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.854-8735G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117287119 | |||||||
| chr7:117287138 | T | C | 110 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(107): Show |
124 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(121): Show |
intron_variant | MODIFIER | c.854-8754A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117287138 | |||||||
| chr7:117287192 | C | T | 1 | a0001c0001t0001g0277 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.854-8808G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117287192 | |||||||
| chr7:117287206 | G | A | 96 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(93): Show |
110 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.854-8822C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117287206 | |||||||
| chr7:117287306 | C | T | 94 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(91): Show |
108 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(105): Show |
intron_variant | MODIFIER | c.854-8922G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117287306 | |||||||
| chr7:117287458 | A | G | 1 | a0001c0001t0002g0181 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.854-9074T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117287458 | |||||||
| chr7:117287493 | C | G | 2 | a0001c0001t0008g0251 a0002c0003t0002g0027 |
2 | HG02109.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.854-9109G>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117287493 | |||||||
| chr7:117287506 | T | A | 2 | a0001c0001t0001g0266 a0001c0001t0002g0282 |
2 | HG01496.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.854-9122A>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117287506 | |||||||
| chr7:117287533 | A | G | 6 | a0001c0001t0002g0067 a0001c0001t0002g0082 a0001c0001t0002g0188 others(3): Show |
6 | HG00609.hp2 NA18968.hp1 NA18992.hp2 others(3): Show |
intron_variant | MODIFIER | c.854-9149T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117287533 | |||||||
| chr7:117287598 | GTCTTATG others(6): Show |
G | 6 | a0001c0001t0006g0220 a0001c0001t0015g0229 a0001c0001t0016g0216 others(3): Show |
6 | HG02258.hp2 HG02559.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.854-9227_854-9215d others(15): Show |
WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117287598 | |||||||
| chr7:117287903 | G | A | 2 | a0001c0001t0003g0024 a0001c0001t0003g0253 |
3 | HG03491.hp1 HG03492.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.854-9519C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117287903 | |||||||
| chr7:117287918 | G | A | 1 | a0001c0001t0002g0128 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.854-9534C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117287918 | |||||||
| chr7:117288143 | A | G | 1 | a0001c0001t0003g0213 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.853+9469T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117288143 | |||||||
| chr7:117288267 | T | A | 1 | a0001c0001t0003g0164 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.853+9345A>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117288267 | |||||||
| chr7:117288317 | T | G | 104 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(101): Show |
118 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(115): Show |
intron_variant | MODIFIER | c.853+9295A>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117288317 | |||||||
| chr7:117288360 | T | C | 1 | a0001c0001t0032g0262 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.853+9252A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117288360 | |||||||
| chr7:117288570 | A | G | 2 | a0001c0001t0002g0267 a0001c0001t0020g0115 |
2 | HG03704.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.853+9042T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117288570 | |||||||
| chr7:117289011 | G | A | 74 | a0001c0001t0001g0019 a0001c0001t0001g0032 a0001c0001t0001g0053 others(71): Show |
82 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.853+8601C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117289011 | |||||||
| chr7:117289051 | C | CT | 96 | a0001c0001t0001g0019 a0001c0001t0001g0032 a0001c0001t0001g0062 others(93): Show |
104 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.853+8560dupA | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117289051 | |||||||
| chr7:117289051 | C | CTT | 23 | a0001c0001t0002g0124 a0001c0001t0002g0140 a0001c0001t0002g0177 others(20): Show |
24 | HG00323.hp2 HG01123.hp1 HG02129.hp2 others(21): Show |
intron_variant | MODIFIER | c.853+8559_853+8560d others(4): Show |
WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117289051 | |||||||
| chr7:117289198 | C | T | 1 | a0001c0001t0004g0054 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.853+8414G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117289198 | |||||||
| chr7:117289279 | T | C | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(109): Show |
126 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(123): Show |
intron_variant | MODIFIER | c.853+8333A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117289279 | |||||||
| chr7:117289329 | A | G | 1 | a0001c0001t0003g0164 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.853+8283T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117289329 | |||||||
| chr7:117289415 | T | A | 2 | a0001c0001t0001g0266 a0001c0001t0002g0282 |
2 | HG01496.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.853+8197A>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117289415 | |||||||
| chr7:117289432 | C | A | 1 | a0001c0001t0036g0214 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.853+8180G>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117289432 | |||||||
| chr7:117289440 | T | C | 2 | a0001c0001t0001g0266 a0001c0001t0002g0282 |
2 | HG01496.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.853+8172A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117289440 | |||||||
| chr7:117289477 | G | A | 1 | a0001c0001t0002g0238 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.853+8135C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117289477 | |||||||
| chr7:117289487 | A | T | 2 | a0001c0001t0008g0251 a0002c0003t0002g0027 |
2 | HG02109.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.853+8125T>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117289487 | |||||||
| chr7:117289719 | C | A | 11 | a0001c0001t0002g0022 a0001c0001t0002g0049 a0001c0001t0002g0085 others(8): Show |
14 | HG02004.hp1 HG02129.hp1 HG02132.hp1 others(11): Show |
intron_variant | MODIFIER | c.853+7893G>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117289719 | |||||||
| chr7:117289720 | G | A | 2 | a0001c0001t0001g0266 a0001c0001t0002g0282 |
2 | HG01496.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.853+7892C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117289720 | |||||||
| chr7:117289788 | A | G | 2 | a0001c0001t0011g0014 a0001c0001t0035g0243 |
3 | HG00741.hp1 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.853+7824T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117289788 | |||||||
| chr7:117290075 | G | T | 1 | a0001c0001t0001g0277 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.853+7537C>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117290075 | |||||||
| chr7:117290188 | G | A | 11 | a0001c0001t0001g0277 a0001c0001t0003g0279 a0001c0001t0004g0095 others(8): Show |
11 | HG00741.hp2 HG01433.hp1 HG01517.hp1 others(8): Show |
intron_variant | MODIFIER | c.853+7424C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117290188 | |||||||
| chr7:117290335 | A | G | 8 | a0001c0001t0001g0266 a0001c0001t0002g0282 a0001c0001t0006g0220 others(5): Show |
8 | HG01496.hp2 HG02258.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.853+7277T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117290335 | |||||||
| chr7:117290606 | T | G | 2 | a0001c0001t0002g0086 a0001c0001t0002g0192 |
2 | HG02004.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.853+7006A>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117290606 | |||||||
| chr7:117290841 | T | C | 106 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(103): Show |
120 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.853+6771A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117290841 | |||||||
| chr7:117290878 | C | A | 2 | a0001c0001t0018g0009 a0002c0003t0001g0026 |
3 | HG01891.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.853+6734G>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117290878 | |||||||
| chr7:117290908 | A | G | 111 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(108): Show |
125 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(122): Show |
intron_variant | MODIFIER | c.853+6704T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117290908 | |||||||
| chr7:117291045 | T | C | 6 | a0001c0001t0003g0279 a0001c0001t0004g0095 a0001c0001t0004g0237 others(3): Show |
6 | HG02257.hp1 HG02615.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.853+6567A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117291045 | |||||||
| chr7:117291076 | G | C | 1 | a0001c0001t0004g0237 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.853+6536C>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117291076 | |||||||
| chr7:117291269 | G | A | 2 | a0001c0001t0007g0007 a0001c0001t0007g0247 |
4 | HG00733.hp2 HG01069.hp2 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.853+6343C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117291269 | |||||||
| chr7:117291516 | T | A | 1 | a0001c0001t0003g0129 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.853+6096A>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117291516 | |||||||
| chr7:117291654 | C | T | 1 | a0001c0001t0002g0267 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.853+5958G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117291654 | |||||||
| chr7:117291939 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.853+5673C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117291939 | |||||||
| chr7:117291953 | T | A | 1 | a0001c0001t0003g0020 | 2 | NA18970.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.853+5659A>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117291953 | |||||||
| chr7:117291975 | T | C | 199 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(196): Show |
222 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.853+5637A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117291975 | |||||||
| chr7:117292020 | G | A | 1 | a0001c0001t0001g0277 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.853+5592C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117292020 | |||||||
| chr7:117292029 | G | A | 1 | a0001c0001t0008g0251 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.853+5583C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117292029 | |||||||
| chr7:117292114 | G | A | 3 | a0001c0001t0001g0280 a0001c0001t0028g0204 a0001c0001t0034g0278 |
3 | HG02486.hp1 HG02965.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.853+5498C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117292114 | |||||||
| chr7:117292132 | G | C | 1 | a0001c0001t0003g0185 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.853+5480C>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117292132 | |||||||
| chr7:117292141 | T | C | 3 | a0001c0001t0006g0005 a0001c0001t0006g0217 a0001c0001t0013g0156 |
5 | HG01891.hp1 HG02572.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.853+5471A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117292141 | |||||||
| chr7:117292270 | A | G | 1 | a0001c0001t0001g0277 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.853+5342T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117292270 | |||||||
| chr7:117292293 | T | TCA | 11 | a0001c0001t0001g0268 a0001c0001t0001g0280 a0001c0001t0003g0150 others(8): Show |
11 | HG02258.hp2 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.853+5317_853+5318d others(4): Show |
WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117292293 | |||||||
| chr7:117292293 | T | TCACA | 6 | a0001c0001t0003g0279 a0001c0001t0004g0095 a0001c0001t0004g0237 others(3): Show |
6 | HG02257.hp1 HG02615.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.853+5315_853+5318d others(6): Show |
WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117292293 | |||||||
| chr7:117292480 | A | G | 73 | a0001c0001t0001g0019 a0001c0001t0001g0032 a0001c0001t0001g0053 others(70): Show |
81 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.853+5132T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117292480 | |||||||
| chr7:117292493 | C | A | 1 | a0001c0001t0036g0214 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.853+5119G>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117292493 | |||||||
| chr7:117292501 | C | T | 1 | a0001c0001t0003g0066 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.853+5111G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117292501 | |||||||
| chr7:117292503 | G | T | 1 | a0001c0001t0003g0066 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.853+5109C>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117292503 | |||||||
| chr7:117292731 | G | A | 1 | a0001c0001t0001g0277 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.853+4881C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117292731 | |||||||
| chr7:117292786 | G | A | 1 | a0002c0003t0002g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.853+4826C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117292786 | |||||||
| chr7:117292803 | A | T | 1 | a0001c0001t0005g0013 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.853+4809T>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117292803 | |||||||
| chr7:117292864 | T | C | 1 | a0001c0001t0001g0245 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.853+4748A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117292864 | |||||||
| chr7:117293078 | T | C | 1 | a0001c0001t0013g0052 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.853+4534A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117293078 | |||||||
| chr7:117293130 | A | T | 15 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0051 others(12): Show |
18 | HG01243.hp1 HG01433.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.853+4482T>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117293130 | |||||||
| chr7:117293210 | GA | G | 86 | a0001c0001t0001g0019 a0001c0001t0001g0032 a0001c0001t0001g0053 others(83): Show |
95 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.853+4401delT | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117293210 | |||||||
| chr7:117293519 | G | C | 1 | a0001c0001t0003g0149 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.853+4093C>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117293519 | |||||||
| chr7:117293596 | A | G | 3 | a0001c0001t0012g0215 a0001c0001t0012g0219 a0001c0001t0036g0214 |
3 | HG02145.hp2 NA18906.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.853+4016T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117293596 | |||||||
| chr7:117293674 | T | G | 1 | a0001c0001t0001g0277 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.853+3938A>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117293674 | |||||||
| chr7:117293752 | G | A | 4 | a0001c0001t0008g0251 a0001c0001t0017g0055 a0001c0001t0017g0056 others(1): Show |
4 | HG00741.hp2 HG01517.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.853+3860C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117293752 | |||||||
| chr7:117293759 | G | A | 1 | a0001c0001t0002g0232 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.853+3853C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117293759 | |||||||
| chr7:117293846 | T | C | 2 | a0001c0001t0003g0003 a0001c0001t0003g0100 |
4 | HG02129.hp1 HG02132.hp1 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.853+3766A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117293846 | |||||||
| chr7:117294110 | G | C | 1 | a0001c0001t0002g0180 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.853+3502C>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117294110 | |||||||
| chr7:117294112 | T | C | 2 | a0001c0001t0002g0211 a0001c0001t0002g0212 |
2 | NA18957.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.853+3500A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117294112 | |||||||
| chr7:117294146 | G | A | 86 | a0001c0001t0001g0019 a0001c0001t0001g0032 a0001c0001t0001g0053 others(83): Show |
95 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.853+3466C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117294146 | |||||||
| chr7:117294328 | A | G | 2 | a0001c0001t0006g0264 a0001c0001t0006g0265 |
2 | HG02647.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.853+3284T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117294328 | |||||||
| chr7:117294415 | A | G | 2 | a0001c0001t0001g0041 a0001c0001t0002g0008 |
3 | HG03239.hp2 HG03688.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.853+3197T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117294415 | |||||||
| chr7:117294593 | TA | T | 189 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(186): Show |
212 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.853+3018delT | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117294593 | |||||||
| chr7:117294593 | TAA | T | 11 | a0001c0001t0003g0064 a0001c0001t0003g0159 a0001c0001t0003g0160 others(8): Show |
11 | HG00741.hp2 HG01517.hp1 HG01978.hp2 others(8): Show |
intron_variant | MODIFIER | c.853+3017_853+3018d others(4): Show |
WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117294593 | |||||||
| chr7:117294667 | T | A | 2 | a0001c0001t0001g0139 a0001c0001t0003g0138 |
2 | NA18963.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.853+2945A>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117294667 | |||||||
| chr7:117294737 | C | T | 1 | a0001c0001t0001g0240 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.853+2875G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117294737 | |||||||
| chr7:117294758 | G | A | 7 | a0001c0001t0004g0225 a0001c0001t0004g0226 a0001c0001t0006g0264 others(4): Show |
8 | HG01074.hp2 HG01192.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.853+2854C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117294758 | |||||||
| chr7:117294783 | A | G | 3 | a0001c0001t0003g0187 a0001c0001t0003g0201 a0001c0001t0003g0202 |
3 | NA18954.hp1 NA18972.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.853+2829T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117294783 | |||||||
| chr7:117294945 | C | A | 2 | a0001c0001t0004g0230 a0001c0001t0004g0252 |
2 | HG01433.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.853+2667G>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117294945 | |||||||
| chr7:117295024 | G | T | 1 | a0001c0001t0025g0224 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.853+2588C>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117295024 | |||||||
| chr7:117295134 | T | C | 6 | a0001c0001t0003g0279 a0001c0001t0004g0095 a0001c0001t0004g0237 others(3): Show |
6 | HG02257.hp1 HG02615.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.853+2478A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117295134 | |||||||
| chr7:117295144 | C | T | 1 | a0001c0001t0003g0175 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.853+2468G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117295144 | |||||||
| chr7:117295149 | CAAGAT | C | 85 | a0001c0001t0001g0019 a0001c0001t0001g0032 a0001c0001t0001g0053 others(82): Show |
94 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.853+2458_853+2462d others(7): Show |
WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117295149 | |||||||
| chr7:117295150 | A | G | 1 | a0001c0001t0003g0175 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.853+2462T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117295150 | |||||||
| chr7:117295154 | T | C | 1 | a0001c0001t0003g0175 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.853+2458A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117295154 | |||||||
| chr7:117295198 | T | G | 5 | a0001c0001t0004g0095 a0001c0001t0004g0237 a0001c0001t0005g0236 others(2): Show |
5 | HG02257.hp1 HG02615.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.853+2414A>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117295198 | |||||||
| chr7:117295403 | A | G | 1 | a0001c0001t0003g0163 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.853+2209T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117295403 | |||||||
| chr7:117295424 | G | A | 86 | a0001c0001t0001g0019 a0001c0001t0001g0032 a0001c0001t0001g0053 others(83): Show |
95 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.853+2188C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117295424 | |||||||
| chr7:117295491 | TA | T | 86 | a0001c0001t0001g0019 a0001c0001t0001g0032 a0001c0001t0001g0053 others(83): Show |
95 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.853+2120delT | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117295491 | |||||||
| chr7:117295509 | A | G | 86 | a0001c0001t0001g0019 a0001c0001t0001g0032 a0001c0001t0001g0053 others(83): Show |
95 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.853+2103T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117295509 | |||||||
| chr7:117295746 | G | A | 1 | a0001c0001t0002g0275 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.853+1866C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117295746 | |||||||
| chr7:117296162 | A | C | 1 | a0001c0001t0002g0126 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.853+1450T>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117296162 | |||||||
| chr7:117296201 | G | A | 3 | a0001c0001t0003g0187 a0001c0001t0003g0201 a0001c0001t0003g0202 |
3 | NA18954.hp1 NA18972.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.853+1411C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117296201 | |||||||
| chr7:117296278 | G | A | 1 | a0001c0001t0012g0273 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.853+1334C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117296278 | |||||||
| chr7:117296610 | C | T | 1 | a0001c0001t0015g0229 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.853+1002G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117296610 | |||||||
| chr7:117296900 | G | A | 1 | a0001c0001t0001g0277 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.853+712C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117296900 | |||||||
| chr7:117297124 | C | T | 1 | a0001c0001t0028g0204 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.853+488G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117297124 | |||||||
| chr7:117297424 | C | T | 3 | a0001c0001t0001g0061 a0001c0001t0002g0017 a0001c0001t0002g0018 |
5 | HG00738.hp1 HG01106.hp2 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.853+188G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117297424 | |||||||
| chr7:117297461 | C | T | 1 | a0001c0001t0002g0090 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.853+151G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117297461 | |||||||
| chr7:117297466 | A | G | 102 | a0001c0001t0001g0019 a0001c0001t0001g0032 a0001c0001t0001g0053 others(99): Show |
111 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.853+146T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 4/4 | chr7 | 117297466 | |||||||
| chr7:117297966 | T | C | 104 | a0001c0001t0001g0019 a0001c0001t0001g0032 a0001c0001t0001g0053 others(101): Show |
113 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(110): Show |
intron_variant | MODIFIER | c.589-90A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117297966 | |||||||
| chr7:117298095 | G | A | 1 | a0001c0001t0002g0116 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.589-219C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117298095 | |||||||
| chr7:117298411 | G | A | 1 | a0001c0001t0019g0106 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.589-535C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117298411 | |||||||
| chr7:117298453 | G | C | 1 | a0001c0001t0005g0046 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.589-577C>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117298453 | |||||||
| chr7:117298986 | G | T | 3 | a0001c0001t0001g0266 a0001c0001t0002g0282 a0001c0001t0015g0047 |
3 | HG01496.hp2 HG02630.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.589-1110C>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117298986 | |||||||
| chr7:117299035 | AG | A | 3 | a0001c0001t0001g0266 a0001c0001t0002g0282 a0001c0001t0015g0047 |
3 | HG01496.hp2 HG02630.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.589-1160delC | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117299035 | |||||||
| chr7:117299233 | C | T | 1 | a0001c0001t0015g0047 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.589-1357G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117299233 | |||||||
| chr7:117299362 | T | A | 1 | a0001c0001t0002g0238 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.589-1486A>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117299362 | |||||||
| chr7:117299364 | A | G | 2 | a0001c0001t0001g0032 a0001c0001t0005g0043 |
2 | HG02698.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.589-1488T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117299364 | |||||||
| chr7:117299447 | T | G | 1 | a0001c0001t0001g0277 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.589-1571A>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117299447 | |||||||
| chr7:117299494 | CT | C | 93 | a0001c0001t0001g0019 a0001c0001t0001g0032 a0001c0001t0001g0053 others(90): Show |
102 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.589-1619delA | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117299494 | |||||||
| chr7:117299581 | C | G | 2 | a0001c0001t0002g0238 a0001c0001t0005g0231 |
2 | HG04184.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.589-1705G>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117299581 | |||||||
| chr7:117299707 | G | C | 1 | a0001c0001t0002g0181 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.589-1831C>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117299707 | |||||||
| chr7:117299736 | T | C | 1 | a0001c0001t0015g0094 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.589-1860A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117299736 | |||||||
| chr7:117299841 | A | G | 1 | a0001c0001t0005g0092 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.589-1965T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117299841 | |||||||
| chr7:117299847 | A | T | 1 | a0001c0001t0001g0276 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.589-1971T>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117299847 | |||||||
| chr7:117299874 | T | C | 1 | a0001c0001t0013g0052 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.589-1998A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117299874 | |||||||
| chr7:117299994 | A | G | 109 | a0001c0001t0001g0019 a0001c0001t0001g0032 a0001c0001t0001g0053 others(106): Show |
118 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.589-2118T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117299994 | |||||||
| chr7:117300155 | T | TA | 6 | a0001c0001t0003g0279 a0001c0001t0004g0095 a0001c0001t0004g0237 others(3): Show |
6 | HG02257.hp1 HG02615.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.589-2280dupT | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117300155 | |||||||
| chr7:117300326 | A | G | 1 | a0001c0001t0004g0259 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.589-2450T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117300326 | |||||||
| chr7:117300432 | G | A | 1 | a0001c0001t0029g0098 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.589-2556C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117300432 | |||||||
| chr7:117300482 | G | A | 10 | a0001c0001t0001g0266 a0001c0001t0002g0282 a0001c0001t0008g0251 others(7): Show |
10 | HG00741.hp2 HG01496.hp2 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.589-2606C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117300482 | |||||||
| chr7:117300614 | T | A | 101 | a0001c0001t0001g0019 a0001c0001t0001g0032 a0001c0001t0001g0053 others(98): Show |
109 | HG00140.hp1 HG00323.hp2 HG00609.hp1 others(106): Show |
intron_variant | MODIFIER | c.589-2738A>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117300614 | |||||||
| chr7:117301010 | G | A | 3 | a0001c0001t0012g0215 a0001c0001t0012g0219 a0001c0001t0036g0214 |
3 | HG02145.hp2 NA18906.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.589-3134C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117301010 | |||||||
| chr7:117301015 | A | G | 4 | a0001c0001t0002g0022 a0001c0001t0002g0190 a0001c0001t0003g0189 others(1): Show |
5 | NA18612.hp1 NA18954.hp2 NA19006.hp1 others(2): Show |
intron_variant | MODIFIER | c.589-3139T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117301015 | |||||||
| chr7:117301048 | C | CT | 126 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(123): Show |
145 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.589-3173dupA | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117301048 | |||||||
| chr7:117301097 | A | G | 1 | a0001c0001t0004g0114 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.589-3221T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117301097 | |||||||
| chr7:117301163 | G | A | 3 | a0001c0001t0006g0220 a0001c0001t0016g0216 a0001c0001t0016g0227 |
3 | HG02818.hp1 HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.589-3287C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117301163 | |||||||
| chr7:117301182 | C | G | 27 | a0001c0001t0001g0029 a0001c0001t0001g0168 a0001c0001t0001g0234 others(24): Show |
29 | HG00738.hp2 HG00741.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.589-3306G>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117301182 | |||||||
| chr7:117301202 | G | A | 2 | a0001c0001t0002g0238 a0001c0001t0005g0231 |
2 | HG04184.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.589-3326C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117301202 | |||||||
| chr7:117301223 | C | T | 5 | a0001c0001t0001g0266 a0001c0001t0012g0215 a0001c0001t0012g0219 others(2): Show |
5 | HG01496.hp2 HG02145.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.589-3347G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117301223 | |||||||
| chr7:117301246 | T | C | 3 | a0001c0002t0005g0249 a0001c0002t0023g0248 a0002c0003t0002g0027 |
3 | HG02109.hp2 HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.589-3370A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117301246 | |||||||
| chr7:117301289 | G | A | 6 | a0001c0001t0002g0050 a0001c0001t0002g0096 a0001c0001t0002g0097 others(3): Show |
6 | HG02040.hp1 HG02071.hp2 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.589-3413C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117301289 | |||||||
| chr7:117301293 | A | T | 1 | a0001c0001t0001g0277 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.589-3417T>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117301293 | |||||||
| chr7:117301401 | G | A | 1 | a0001c0001t0008g0239 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.589-3525C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117301401 | |||||||
| chr7:117301593 | C | T | 2 | a0001c0001t0002g0036 a0001c0001t0002g0116 |
2 | NA18989.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.589-3717G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117301593 | |||||||
| chr7:117301769 | G | A | 1 | a0001c0001t0003g0182 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.589-3893C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117301769 | |||||||
| chr7:117301802 | C | CT | 24 | a0001c0001t0001g0109 a0001c0001t0001g0157 a0001c0001t0001g0242 others(21): Show |
25 | HG01192.hp2 HG01433.hp2 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.589-3927dupA | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117301802 | |||||||
| chr7:117301802 | CT | C | 10 | a0001c0001t0001g0032 a0001c0001t0001g0145 a0001c0001t0001g0146 others(7): Show |
11 | HG01070.hp1 HG01261.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.589-3927delA | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117301802 | |||||||
| chr7:117301915 | C | T | 9 | a0001c0001t0003g0150 a0001c0001t0004g0151 a0001c0001t0005g0046 others(6): Show |
11 | HG02572.hp2 HG02630.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.589-4039G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117301915 | |||||||
| chr7:117301961 | C | T | 12 | a0001c0001t0004g0225 a0001c0001t0004g0226 a0001c0001t0004g0228 others(9): Show |
13 | HG01074.hp2 HG01192.hp2 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.589-4085G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117301961 | |||||||
| chr7:117302061 | G | A | 131 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(128): Show |
149 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(146): Show |
intron_variant | MODIFIER | c.589-4185C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117302061 | |||||||
| chr7:117302124 | T | C | 2 | a0001c0001t0001g0276 a0001c0001t0001g0277 |
2 | HG01433.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.589-4248A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117302124 | |||||||
| chr7:117302221 | T | C | 1 | a0001c0001t0003g0208 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.589-4345A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117302221 | |||||||
| chr7:117302265 | C | T | 1 | a0002c0003t0002g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.589-4389G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117302265 | |||||||
| chr7:117302303 | A | C | 1 | a0001c0001t0001g0040 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.589-4427T>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117302303 | |||||||
| chr7:117302379 | G | T | 121 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(118): Show |
139 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.589-4503C>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117302379 | |||||||
| chr7:117302451 | A | T | 6 | a0001c0001t0001g0146 a0001c0001t0001g0280 a0001c0001t0009g0274 others(3): Show |
6 | HG02486.hp1 HG02965.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.589-4575T>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117302451 | |||||||
| chr7:117302484 | C | T | 4 | a0001c0001t0006g0217 a0001c0001t0006g0220 a0001c0001t0016g0216 others(1): Show |
4 | HG01891.hp1 HG02818.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.589-4608G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117302484 | |||||||
| chr7:117302867 | G | A | 1 | a0001c0001t0001g0167 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.589-4991C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117302867 | |||||||
| chr7:117302960 | T | C | 1 | a0001c0001t0002g0090 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.589-5084A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117302960 | |||||||
| chr7:117303025 | C | T | 1 | a0001c0001t0004g0246 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.589-5149G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117303025 | |||||||
| chr7:117303081 | C | T | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(126): Show |
147 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.589-5205G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117303081 | |||||||
| chr7:117303274 | G | A | 1 | a0002c0003t0002g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.589-5398C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117303274 | |||||||
| chr7:117303283 | T | C | 2 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
2 | HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.589-5407A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117303283 | |||||||
| chr7:117303470 | A | G | 3 | a0001c0001t0002g0104 a0001c0001t0008g0255 a0001c0001t0019g0106 |
3 | HG01175.hp2 HG01517.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.589-5594T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117303470 | |||||||
| chr7:117303646 | G | A | 2 | a0001c0001t0002g0183 a0001c0001t0002g0198 |
2 | NA19063.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.589-5770C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117303646 | |||||||
| chr7:117303651 | C | T | 1 | a0001c0001t0013g0052 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.589-5775G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117303651 | |||||||
| chr7:117303683 | T | G | 2 | a0001c0001t0011g0014 a0001c0001t0035g0243 |
3 | HG00741.hp1 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.589-5807A>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117303683 | |||||||
| chr7:117303739 | A | T | 131 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(128): Show |
152 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(149): Show |
intron_variant | MODIFIER | c.589-5863T>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117303739 | |||||||
| chr7:117304092 | C | T | 1 | a0001c0001t0028g0204 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.589-6216G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117304092 | |||||||
| chr7:117304229 | T | A | 110 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(107): Show |
128 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.589-6353A>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117304229 | |||||||
| chr7:117304355 | G | C | 1 | a0001c0001t0001g0110 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.589-6479C>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117304355 | |||||||
| chr7:117304432 | AT | A | 68 | a0001c0001t0001g0015 a0001c0001t0001g0029 a0001c0001t0001g0053 others(65): Show |
75 | HG00323.hp1 HG00733.hp2 HG00738.hp1 others(72): Show |
intron_variant | MODIFIER | c.589-6557delA | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117304432 | |||||||
| chr7:117304432 | ATT | A | 16 | a0001c0001t0002g0096 a0001c0001t0004g0228 a0001c0001t0004g0252 others(13): Show |
17 | HG01433.hp2 HG02145.hp2 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.589-6558_589-6557d others(4): Show |
WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117304432 | |||||||
| chr7:117304432 | ATTT | A | 94 | a0001c0001t0001g0001 a0001c0001t0001g0038 a0001c0001t0001g0040 others(91): Show |
106 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.589-6559_589-6557d others(5): Show |
WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117304432 | |||||||
| chr7:117304432 | ATTTT | A | 17 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0016 others(14): Show |
23 | HG00558.hp2 HG01192.hp1 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.589-6560_589-6557d others(6): Show |
WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117304432 | |||||||
| chr7:117304624 | C | T | 9 | a0001c0001t0001g0029 a0001c0001t0004g0042 a0001c0001t0004g0054 others(6): Show |
10 | HG00738.hp2 HG00741.hp1 HG00741.hp2 others(7): Show |
intron_variant | MODIFIER | c.589-6748G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117304624 | |||||||
| chr7:117304636 | A | G | 2 | a0001c0001t0001g0276 a0001c0001t0001g0277 |
2 | HG01433.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.589-6760T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117304636 | |||||||
| chr7:117304786 | A | G | 3 | a0001c0001t0012g0215 a0001c0001t0012g0219 a0001c0001t0036g0214 |
3 | HG02145.hp2 NA18906.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.589-6910T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117304786 | |||||||
| chr7:117304897 | T | C | 3 | a0001c0001t0012g0215 a0001c0001t0012g0219 a0001c0001t0036g0214 |
3 | HG02145.hp2 NA18906.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.589-7021A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117304897 | |||||||
| chr7:117304963 | G | T | 3 | a0001c0001t0012g0273 a0001c0001t0016g0263 a0001c0001t0032g0262 |
3 | HG02258.hp2 HG02280.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.589-7087C>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117304963 | |||||||
| chr7:117304967 | G | C | 1 | a0002c0003t0002g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.589-7091C>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117304967 | |||||||
| chr7:117305128 | C | T | 3 | a0001c0001t0012g0273 a0001c0001t0016g0263 a0001c0001t0032g0262 |
3 | HG02258.hp2 HG02280.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.589-7252G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117305128 | |||||||
| chr7:117305281 | G | A | 1 | a0001c0001t0002g0282 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.589-7405C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117305281 | |||||||
| chr7:117305444 | T | C | 1 | a0001c0001t0038g0028 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.589-7568A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117305444 | |||||||
| chr7:117305529 | G | T | 13 | a0001c0001t0001g0029 a0001c0001t0001g0266 a0001c0001t0004g0042 others(10): Show |
14 | HG00738.hp2 HG00741.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.589-7653C>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117305529 | |||||||
| chr7:117305925 | G | A | 1 | a0001c0001t0001g0045 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.589-8049C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117305925 | |||||||
| chr7:117306321 | G | A | 6 | a0001c0001t0001g0146 a0001c0001t0001g0280 a0001c0001t0009g0274 others(3): Show |
6 | HG02486.hp1 HG02965.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.589-8445C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117306321 | |||||||
| chr7:117306336 | G | A | 1 | a0001c0001t0001g0032 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.589-8460C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117306336 | |||||||
| chr7:117306389 | T | G | 5 | a0001c0001t0001g0093 a0001c0001t0001g0122 a0001c0001t0004g0095 others(2): Show |
5 | HG01243.hp1 HG02257.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.589-8513A>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117306389 | |||||||
| chr7:117306616 | A | C | 3 | a0001c0001t0028g0204 a0001c0002t0005g0249 a0001c0002t0023g0248 |
3 | HG02965.hp1 HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.588+8455T>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117306616 | |||||||
| chr7:117306637 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.588+8434G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117306637 | |||||||
| chr7:117306759 | C | T | 1 | a0002c0003t0002g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.588+8312G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117306759 | |||||||
| chr7:117306939 | G | A | 1 | a0002c0003t0002g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.588+8132C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117306939 | |||||||
| chr7:117307142 | A | C | 14 | a0001c0001t0001g0168 a0001c0001t0001g0242 a0001c0001t0001g0245 others(11): Show |
14 | HG00323.hp1 HG01123.hp2 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.588+7929T>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117307142 | |||||||
| chr7:117307145 | G | C | 3 | a0001c0001t0028g0204 a0001c0002t0005g0249 a0001c0002t0023g0248 |
3 | HG02965.hp1 HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.588+7926C>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117307145 | |||||||
| chr7:117307257 | T | G | 2 | a0001c0001t0006g0005 a0001c0001t0013g0156 |
4 | HG02572.hp2 HG03195.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.588+7814A>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117307257 | |||||||
| chr7:117307409 | T | A | 1 | a0001c0001t0034g0278 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.588+7662A>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117307409 | |||||||
| chr7:117307728 | G | C | 1 | a0001c0001t0003g0184 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.588+7343C>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117307728 | |||||||
| chr7:117308117 | C | A | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(145): Show |
170 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(167): Show |
intron_variant | MODIFIER | c.588+6954G>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117308117 | |||||||
| chr7:117308353 | C | T | 5 | a0001c0001t0001g0038 a0001c0001t0004g0059 a0001c0001t0004g0060 others(2): Show |
5 | HG00099.hp1 HG00140.hp2 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.588+6718G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117308353 | |||||||
| chr7:117308807 | T | C | 6 | a0001c0001t0002g0050 a0001c0001t0002g0096 a0001c0001t0002g0097 others(3): Show |
6 | HG02040.hp1 HG02071.hp2 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.588+6264A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117308807 | |||||||
| chr7:117308859 | A | G | 1 | a0001c0001t0013g0172 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.588+6212T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117308859 | |||||||
| chr7:117309027 | T | TA | 8 | a0001c0001t0001g0099 a0001c0001t0001g0242 a0001c0001t0002g0188 others(5): Show |
8 | HG01243.hp2 HG02109.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.588+6043dupT | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117309027 | |||||||
| chr7:117309053 | C | A | 12 | a0001c0001t0001g0015 a0001c0001t0001g0105 a0001c0001t0001g0110 others(9): Show |
14 | HG00642.hp2 HG03017.hp2 HG03491.hp1 others(11): Show |
intron_variant | MODIFIER | c.588+6018G>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117309053 | |||||||
| chr7:117309144 | C | T | 1 | a0001c0001t0002g0022 | 2 | NA18954.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.588+5927G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117309144 | |||||||
| chr7:117309145 | G | A | 1 | a0001c0001t0001g0038 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.588+5926C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117309145 | |||||||
| chr7:117309184 | C | CA | 29 | a0001c0001t0001g0168 a0001c0001t0001g0234 a0001c0001t0001g0240 others(26): Show |
29 | HG00323.hp1 HG01123.hp2 HG01175.hp1 others(26): Show |
intron_variant | MODIFIER | c.588+5886dupT | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117309184 | |||||||
| chr7:117309196 | A | T | 1 | a0001c0001t0036g0214 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.588+5875T>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117309196 | |||||||
| chr7:117309197 | T | A | 1 | a0001c0001t0001g0053 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.588+5874A>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117309197 | |||||||
| chr7:117309232 | C | T | 114 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(111): Show |
134 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(131): Show |
intron_variant | MODIFIER | c.588+5839G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117309232 | |||||||
| chr7:117309429 | C | A | 1 | a0001c0001t0006g0217 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.588+5642G>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117309429 | |||||||
| chr7:117309858 | C | A | 8 | a0001c0001t0001g0268 a0001c0001t0002g0025 a0001c0001t0002g0256 others(5): Show |
11 | HG00733.hp2 HG01069.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.588+5213G>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117309858 | |||||||
| chr7:117309867 | T | G | 2 | a0001c0001t0001g0113 a0001c0001t0001g0121 |
2 | HG03453.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.588+5204A>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117309867 | |||||||
| chr7:117309937 | A | G | 14 | a0001c0001t0001g0125 a0001c0001t0001g0141 a0001c0001t0002g0126 others(11): Show |
14 | HG00642.hp2 HG03017.hp2 HG03654.hp1 others(11): Show |
intron_variant | MODIFIER | c.588+5134T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117309937 | |||||||
| chr7:117309950 | ATC | A | 5 | a0001c0001t0006g0217 a0001c0001t0006g0220 a0001c0001t0012g0273 others(2): Show |
5 | HG01891.hp1 HG02280.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.588+5119_588+5120d others(4): Show |
WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117309950 | |||||||
| chr7:117310276 | C | T | 5 | a0001c0001t0006g0217 a0001c0001t0006g0220 a0001c0001t0012g0273 others(2): Show |
5 | HG01891.hp1 HG02280.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.588+4795G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117310276 | |||||||
| chr7:117310386 | G | A | 1 | a0001c0001t0001g0053 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.588+4685C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117310386 | |||||||
| chr7:117310438 | T | C | 3 | a0001c0001t0001g0015 a0001c0001t0001g0105 a0001c0001t0001g0110 |
4 | NA18965.hp1 NA18971.hp1 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.588+4633A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117310438 | |||||||
| chr7:117310582 | C | CA | 67 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0045 others(64): Show |
71 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(68): Show |
intron_variant | MODIFIER | c.588+4488dupT | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117310582 | |||||||
| chr7:117310582 | C | CAA | 14 | a0001c0001t0001g0245 a0001c0001t0001g0277 a0001c0001t0002g0275 others(11): Show |
14 | HG00741.hp1 HG01123.hp2 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.588+4487_588+4488d others(4): Show |
WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117310582 | |||||||
| chr7:117310582 | CA | C | 8 | a0001c0001t0002g0123 a0001c0001t0002g0188 a0001c0001t0003g0057 others(5): Show |
8 | HG01975.hp1 HG01993.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.588+4488delT | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117310582 | |||||||
| chr7:117310702 | C | T | 6 | a0001c0001t0001g0266 a0001c0001t0006g0217 a0001c0001t0006g0220 others(3): Show |
6 | HG01496.hp2 HG01891.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.588+4369G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117310702 | |||||||
| chr7:117310749 | T | C | 8 | a0001c0001t0001g0146 a0001c0001t0001g0280 a0001c0001t0003g0024 others(5): Show |
9 | HG02486.hp1 HG02630.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.588+4322A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117310749 | |||||||
| chr7:117310777 | T | G | 1 | a0001c0001t0001g0266 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.588+4294A>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117310777 | |||||||
| chr7:117311165 | A | T | 2 | a0001c0001t0017g0055 a0001c0001t0017g0056 |
2 | HG00741.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.588+3906T>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117311165 | |||||||
| chr7:117311337 | T | C | 1 | a0001c0001t0004g0042 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.588+3734A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117311337 | |||||||
| chr7:117311395 | T | G | 3 | a0001c0001t0028g0204 a0001c0002t0005g0249 a0001c0002t0023g0248 |
3 | HG02965.hp1 HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.588+3676A>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117311395 | |||||||
| chr7:117311431 | A | G | 2 | a0001c0001t0001g0029 a0001c0001t0004g0054 |
2 | HG02559.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.588+3640T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117311431 | |||||||
| chr7:117311599 | G | A | 4 | a0001c0001t0006g0217 a0001c0001t0006g0220 a0001c0001t0016g0216 others(1): Show |
4 | HG01891.hp1 HG02818.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.588+3472C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117311599 | |||||||
| chr7:117311617 | G | A | 36 | a0001c0001t0001g0234 a0001c0001t0001g0240 a0001c0001t0001g0241 others(33): Show |
39 | HG00323.hp1 HG00733.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.588+3454C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117311617 | |||||||
| chr7:117312010 | C | T | 3 | a0001c0001t0012g0273 a0001c0001t0016g0263 a0001c0001t0032g0262 |
3 | HG02258.hp2 HG02280.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.588+3061G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117312010 | |||||||
| chr7:117312072 | C | T | 2 | a0001c0001t0006g0005 a0001c0001t0013g0156 |
4 | HG02572.hp2 HG03195.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.588+2999G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117312072 | |||||||
| chr7:117312250 | G | A | 48 | a0001c0001t0001g0234 a0001c0001t0001g0240 a0001c0001t0001g0241 others(45): Show |
52 | HG00323.hp1 HG00733.hp2 HG00741.hp1 others(49): Show |
intron_variant | MODIFIER | c.588+2821C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117312250 | |||||||
| chr7:117312300 | G | C | 4 | a0001c0001t0006g0217 a0001c0001t0006g0220 a0001c0001t0016g0216 others(1): Show |
4 | HG01891.hp1 HG02818.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.588+2771C>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117312300 | |||||||
| chr7:117312334 | G | A | 2 | a0001c0001t0002g0143 a0001c0001t0003g0144 |
2 | HG02040.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.588+2737C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117312334 | |||||||
| chr7:117312617 | T | C | 4 | a0001c0001t0006g0217 a0001c0001t0006g0220 a0001c0001t0016g0216 others(1): Show |
4 | HG01891.hp1 HG02818.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.588+2454A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117312617 | |||||||
| chr7:117312687 | A | C | 66 | a0001c0001t0001g0146 a0001c0001t0001g0234 a0001c0001t0001g0240 others(63): Show |
71 | HG00323.hp1 HG00733.hp2 HG00741.hp1 others(68): Show |
intron_variant | MODIFIER | c.588+2384T>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117312687 | |||||||
| chr7:117312701 | G | T | 2 | a0001c0001t0004g0151 a0001c0001t0005g0046 |
2 | HG03017.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.588+2370C>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117312701 | |||||||
| chr7:117312729 | T | G | 12 | a0001c0001t0004g0225 a0001c0001t0004g0226 a0001c0001t0004g0228 others(9): Show |
13 | HG01074.hp2 HG01192.hp2 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.588+2342A>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117312729 | |||||||
| chr7:117312878 | T | C | 1 | a0001c0001t0001g0145 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.588+2193A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117312878 | |||||||
| chr7:117313106 | C | T | 1 | a0001c0001t0001g0153 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.588+1965G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117313106 | |||||||
| chr7:117313247 | T | C | 1 | a0001c0001t0001g0111 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.588+1824A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117313247 | |||||||
| chr7:117313582 | A | G | 1 | a0001c0001t0002g0169 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.588+1489T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117313582 | |||||||
| chr7:117313848 | T | C | 1 | a0001c0001t0002g0282 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.588+1223A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117313848 | |||||||
| chr7:117314063 | T | G | 59 | a0001c0001t0001g0146 a0001c0001t0001g0234 a0001c0001t0001g0240 others(56): Show |
63 | HG00323.hp1 HG00733.hp2 HG00741.hp1 others(60): Show |
intron_variant | MODIFIER | c.588+1008A>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117314063 | |||||||
| chr7:117314497 | G | A | 1 | a0001c0001t0001g0266 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.588+574C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117314497 | |||||||
| chr7:117314691 | GTCTAA | G | 44 | a0001c0001t0001g0234 a0001c0001t0001g0240 a0001c0001t0001g0241 others(41): Show |
47 | HG00323.hp1 HG00733.hp2 HG00741.hp1 others(44): Show |
intron_variant | MODIFIER | c.588+375_588+379del others(5): Show |
WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117314691 | |||||||
| chr7:117314702 | A | T | 2 | a0002c0003t0001g0026 a0002c0003t0002g0027 |
2 | HG02109.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.588+369T>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117314702 | |||||||
| chr7:117314731 | A | C | 137 | a0001c0001t0001g0019 a0001c0001t0001g0032 a0001c0001t0001g0045 others(134): Show |
146 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.588+340T>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117314731 | |||||||
| chr7:117314926 | G | A | 2 | a0001c0001t0001g0276 a0001c0001t0001g0277 |
2 | HG01433.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.588+145C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 3/4 | chr7 | 117314926 | |||||||
| chr7:117315400 | T | G | 1 | a0001c0001t0001g0155 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.311-52A>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 2/4 | chr7 | 117315400 | |||||||
| chr7:117315585 | T | C | 1 | a0001c0001t0003g0208 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.311-237A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 2/4 | chr7 | 117315585 | |||||||
| chr7:117315604 | A | G | 1 | a0001c0001t0010g0033 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.311-256T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 2/4 | chr7 | 117315604 | |||||||
| chr7:117315645 | C | T | 65 | a0001c0001t0001g0019 a0001c0001t0001g0032 a0001c0001t0001g0045 others(62): Show |
70 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.311-297G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 2/4 | chr7 | 117315645 | |||||||
| chr7:117315739 | C | T | 7 | a0001c0001t0006g0217 a0001c0001t0006g0220 a0001c0001t0012g0215 others(4): Show |
7 | HG01891.hp1 HG02145.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.311-391G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 2/4 | chr7 | 117315739 | |||||||
| chr7:117316034 | T | G | 1 | a0001c0001t0001g0016 | 2 | HG02451.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.311-686A>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 2/4 | chr7 | 117316034 | |||||||
| chr7:117316210 | C | A | 5 | a0001c0001t0001g0004 a0001c0001t0001g0155 a0001c0001t0001g0167 others(2): Show |
7 | HG01192.hp1 HG01255.hp2 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.311-862G>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 2/4 | chr7 | 117316210 | |||||||
| chr7:117316516 | T | C | 1 | a0001c0001t0003g0213 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.311-1168A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 2/4 | chr7 | 117316516 | |||||||
| chr7:117316863 | A | G | 2 | a0001c0001t0006g0005 a0001c0001t0013g0156 |
4 | HG02572.hp2 HG03195.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.311-1515T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 2/4 | chr7 | 117316863 | |||||||
| chr7:117317509 | TA | T | 140 | a0001c0001t0001g0019 a0001c0001t0001g0032 a0001c0001t0001g0045 others(137): Show |
152 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.311-2162delT | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 2/4 | chr7 | 117317509 | |||||||
| chr7:117317714 | G | A | 1 | a0001c0001t0016g0227 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.311-2366C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 2/4 | chr7 | 117317714 | |||||||
| chr7:117317912 | G | T | 1 | a0001c0001t0001g0125 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.311-2564C>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 2/4 | chr7 | 117317912 | |||||||
| chr7:117317973 | G | A | 7 | a0001c0001t0006g0217 a0001c0001t0006g0220 a0001c0001t0012g0215 others(4): Show |
7 | HG01891.hp1 HG02145.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.310+2594C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 2/4 | chr7 | 117317973 | |||||||
| chr7:117318014 | C | A | 1 | a0001c0001t0036g0214 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.310+2553G>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 2/4 | chr7 | 117318014 | |||||||
| chr7:117318117 | A | G | 1 | a0001c0001t0002g0124 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.310+2450T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 2/4 | chr7 | 117318117 | |||||||
| chr7:117318363 | C | T | 4 | a0001c0001t0012g0273 a0001c0001t0016g0263 a0001c0001t0032g0262 others(1): Show |
4 | HG02258.hp2 HG02280.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.310+2204G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 2/4 | chr7 | 117318363 | |||||||
| chr7:117319062 | G | T | 3 | a0001c0001t0001g0002 a0001c0001t0001g0051 a0001c0001t0018g0009 |
6 | HG01891.hp2 HG02258.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.310+1505C>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 2/4 | chr7 | 117319062 | |||||||
| chr7:117319094 | T | C | 4 | a0001c0001t0004g0230 a0001c0001t0004g0252 a0001c0001t0006g0264 others(1): Show |
4 | HG01433.hp2 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.310+1473A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 2/4 | chr7 | 117319094 | |||||||
| chr7:117319158 | C | T | 2 | a0001c0001t0004g0151 a0001c0001t0005g0046 |
2 | HG03017.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.310+1409G>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 2/4 | chr7 | 117319158 | |||||||
| chr7:117319214 | G | A | 1 | a0001c0001t0001g0266 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.310+1353C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 2/4 | chr7 | 117319214 | |||||||
| chr7:117319398 | G | A | 1 | a0001c0001t0026g0112 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.310+1169C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 2/4 | chr7 | 117319398 | |||||||
| chr7:117319521 | T | G | 1 | a0001c0001t0001g0113 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.310+1046A>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 2/4 | chr7 | 117319521 | |||||||
| chr7:117319522 | T | TG | 22 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0121 others(19): Show |
25 | HG00738.hp1 HG00738.hp2 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.310+1044dupC | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 2/4 | chr7 | 117319522 | |||||||
| chr7:117319522 | TG | T | 56 | a0001c0001t0001g0004 a0001c0001t0001g0048 a0001c0001t0001g0152 others(53): Show |
62 | HG00323.hp1 HG00733.hp2 HG00741.hp1 others(59): Show |
intron_variant | MODIFIER | c.310+1044delC | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 2/4 | chr7 | 117319522 | |||||||
| chr7:117319524 | G | C | 1 | a0001c0001t0005g0231 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.310+1043C>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 2/4 | chr7 | 117319524 | |||||||
| chr7:117319525 | G | C | 25 | a0001c0001t0001g0234 a0001c0001t0001g0240 a0001c0001t0001g0241 others(22): Show |
25 | HG00323.hp1 HG00741.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.310+1042C>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 2/4 | chr7 | 117319525 | |||||||
| chr7:117319529 | G | C | 1 | a0001c0001t0002g0123 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.310+1038C>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 2/4 | chr7 | 117319529 | |||||||
| chr7:117319530 | G | C | 70 | a0001c0001t0001g0019 a0001c0001t0001g0032 a0001c0001t0001g0045 others(67): Show |
75 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.310+1037C>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 2/4 | chr7 | 117319530 | |||||||
| chr7:117319532 | G | C | 1 | a0001c0001t0006g0254 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.310+1035C>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 2/4 | chr7 | 117319532 | |||||||
| chr7:117319771 | G | A | 1 | a0001c0001t0003g0150 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.310+796C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 2/4 | chr7 | 117319771 | |||||||
| chr7:117319791 | G | A | 5 | a0001c0001t0004g0225 a0001c0001t0004g0226 a0001c0001t0009g0023 others(2): Show |
6 | HG01074.hp2 HG01192.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.310+776C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 2/4 | chr7 | 117319791 | |||||||
| chr7:117319791 | G | T | 14 | a0001c0001t0001g0268 a0001c0001t0001g0276 a0001c0001t0001g0277 others(11): Show |
17 | HG00733.hp2 HG01069.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.310+776C>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 2/4 | chr7 | 117319791 | |||||||
| chr7:117320050 | C | A | 45 | a0001c0001t0001g0234 a0001c0001t0001g0240 a0001c0001t0001g0241 others(42): Show |
49 | HG00323.hp1 HG00733.hp2 HG00741.hp1 others(46): Show |
intron_variant | MODIFIER | c.310+517G>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 2/4 | chr7 | 117320050 | |||||||
| chr7:117320141 | C | G | 2 | a0001c0001t0007g0007 a0001c0001t0007g0247 |
4 | HG00733.hp2 HG01069.hp2 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.310+426G>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 2/4 | chr7 | 117320141 | |||||||
| chr7:117320442 | G | A | 1 | a0001c0001t0008g0206 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.310+125C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 2/4 | chr7 | 117320442 | |||||||
| chr7:117320524 | A | T | 1 | a0001c0001t0001g0152 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.310+43T>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 2/4 | chr7 | 117320524 | |||||||
| chr7:117321354 | A | T | 3 | a0001c0001t0003g0035 a0001c0001t0010g0033 a0001c0001t0010g0034 |
3 | NA18982.hp1 NA18993.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.84-561T>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 1/4 | chr7 | 117321354 | |||||||
| chr7:117321694 | TTAAG | T | 3 | a0001c0001t0012g0215 a0001c0001t0012g0219 a0001c0001t0036g0214 |
3 | HG02145.hp2 NA18906.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.84-905_84-902delCT others(2): Show |
WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 1/4 | chr7 | 117321694 | |||||||
| chr7:117321737 | T | C | 2 | a0002c0003t0001g0026 a0002c0003t0002g0027 |
2 | HG02109.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.84-944A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 1/4 | chr7 | 117321737 | |||||||
| chr7:117321836 | G | A | 1 | a0001c0001t0004g0151 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.84-1043C>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 1/4 | chr7 | 117321836 | |||||||
| chr7:117321960 | T | C | 1 | a0001c0001t0016g0227 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.83+947A>G | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 1/4 | chr7 | 117321960 | |||||||
| chr7:117322409 | A | G | 3 | a0001c0001t0004g0246 a0001c0001t0004g0272 a0001c0001t0006g0261 |
3 | HG02723.hp1 HG02818.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.83+498T>C | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 1/4 | chr7 | 117322409 | |||||||
| chr7:117322419 | A | T | 3 | a0001c0001t0004g0246 a0001c0001t0004g0272 a0001c0001t0006g0261 |
3 | HG02723.hp1 HG02818.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.83+488T>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 1/4 | chr7 | 117322419 | |||||||
| chr7:117322536 | T | TAC | 127 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(124): Show |
147 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(144): Show |
intron_variant | MODIFIER | c.83+369_83+370dupGT | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 1/4 | chr7 | 117322536 | |||||||
| chr7:117322536 | T | TACAC | 52 | a0001c0001t0001g0004 a0001c0001t0001g0152 a0001c0001t0001g0153 others(49): Show |
60 | HG00609.hp1 HG00642.hp1 HG01070.hp1 others(57): Show |
intron_variant | MODIFIER | c.83+367_83+370dupGT others(2): Show |
WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 1/4 | chr7 | 117322536 | |||||||
| chr7:117322536 | T | TACACAC | 33 | a0001c0001t0001g0191 a0001c0001t0001g0234 a0001c0001t0001g0240 others(30): Show |
33 | HG00099.hp2 HG00323.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.83+365_83+370dupGT others(4): Show |
WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 1/4 | chr7 | 117322536 | |||||||
| chr7:117322536 | T | TACACACA others(1): Show |
19 | a0001c0001t0001g0203 a0001c0001t0002g0256 a0001c0001t0003g0253 others(16): Show |
21 | HG00140.hp1 HG00733.hp2 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.83+363_83+370dupGT others(6): Show |
WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 1/4 | chr7 | 117322536 | |||||||
| chr7:117322536 | T | TACACACA others(3): Show |
18 | a0001c0001t0001g0266 a0001c0001t0001g0268 a0001c0001t0001g0270 others(15): Show |
21 | HG01496.hp2 HG01975.hp2 HG02056.hp1 others(18): Show |
intron_variant | MODIFIER | c.83+361_83+370dupGT others(8): Show |
WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 1/4 | chr7 | 117322536 | |||||||
| chr7:117322536 | T | TACACACA others(5): Show |
6 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0002g0275 others(3): Show |
6 | HG01358.hp1 HG01433.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.83+359_83+370dupGT others(10): Show |
WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 1/4 | chr7 | 117322536 | |||||||
| chr7:117322536 | T | TACACACA others(7): Show |
4 | a0001c0001t0002g0211 a0001c0001t0002g0212 a0001c0001t0003g0279 others(1): Show |
4 | HG02486.hp1 HG03540.hp1 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.83+357_83+370dupGT others(12): Show |
WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 1/4 | chr7 | 117322536 | |||||||
| chr7:117322536 | T | TACACACA others(9): Show |
2 | a0001c0001t0001g0280 a0001c0001t0012g0281 |
2 | HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.83+355_83+370dupGT others(14): Show |
WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 1/4 | chr7 | 117322536 | |||||||
| chr7:117322536 | T | TACACACA others(11): Show |
1 | a0001c0001t0002g0282 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.83+353_83+370dupGT others(16): Show |
WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 1/4 | chr7 | 117322536 | |||||||
| chr7:117322536 | TAC | T | 4 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0002g0030 others(1): Show |
4 | HG02559.hp2 HG03239.hp1 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.83+369_83+370delGT | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 1/4 | chr7 | 117322536 | |||||||
| chr7:117322771 | G | T | 1 | a0001c0001t0038g0028 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.83+136C>A | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 1/4 | chr7 | 117322771 | |||||||
| chr7:117322817 | C | A | 1 | a0001c0001t0003g0213 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.83+90G>T | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 1/4 | chr7 | 117322817 | |||||||
| chr7:117322879 | T | TC | 72 | a0001c0001t0001g0234 a0001c0001t0001g0240 a0001c0001t0001g0241 others(69): Show |
77 | HG00323.hp1 HG00733.hp2 HG00741.hp1 others(74): Show |
intron_variant | MODIFIER | c.83+27dupG | WNT2 | ENSG00000105989.10 | transcript | ENST00000265441.8 | protein_coding | 1/4 | chr7 | 117322879 |