Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 59341 |
| ensemblid | ENSG00000111199.12 |
| hgncid | 18083 |
| symbol | TRPV4 |
| name | transient receptor potential cation channel subfamily V member 4 |
| refseq_nuc | NM_021625.5 |
| refseq_prot | NP_067638.3 |
| ensembl_nuc | ENST00000261740.7 |
| ensembl_prot | ENSP00000261740.2 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 109783089 |
| end | 109833398 |
| strand | - |
| ver | v1.2 |
| region | chr12:109783089-109833398 |
| region5000 | chr12:109778089-109838398 |
| regionname0 | TRPV4_chr12_109783089_109833398 |
| regionname5000 | TRPV4_chr12_109778089_109838398 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 871 | 306 | 81 | 61 | 106 | 16 | 40 | 78 | TRPV4_chr12_109778089_109838398 | TRPV4 | MADSS others(866): Show |
chr12 | 109778089 | 109838398 |
| a0002 | 0/0 | 871 | 20 | 3 | 0 | 14 | 0 | 3 | 10 | TRPV4_chr12_109778089_109838398 | TRPV4 | MADSS others(866): Show |
chr12 | 109778089 | 109838398 |
| a0003 | 0/0 | 871 | 7 | 0 | 7 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | MADSS others(866): Show |
chr12 | 109778089 | 109838398 |
| a0004 | 0/0 | 871 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | MADSS others(866): Show |
chr12 | 109778089 | 109838398 |
| a0005 | 0/0 | 871 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | MADSS others(866): Show |
chr12 | 109778089 | 109838398 |
| a0006 | 0/0 | 871 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | MADSS others(866): Show |
chr12 | 109778089 | 109838398 |
| a0007 | 0/0 | 871 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | MADSS others(866): Show |
chr12 | 109778089 | 109838398 |
| a0008 | 0/0 | 871 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | MADSS others(866): Show |
chr12 | 109778089 | 109838398 |
| a0009 | 0/0 | 871 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | MADSS others(866): Show |
chr12 | 109778089 | 109838398 |
| a0010 | 0/0 | 871 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | MADSS others(866): Show |
chr12 | 109778089 | 109838398 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2613 | 96 | 11 | 11 | 65 | 3 | 6 | TRPV4_chr12_109778089_109838398 | TRPV4 | ATGGC others(2608): Show |
chr12 | 109778089 | 109838398 | ||
| a0001c0002 | 0/0 | 2613 | 75 | 8 | 22 | 32 | 2 | 11 | TRPV4_chr12_109778089_109838398 | TRPV4 | ATGGC others(2608): Show |
chr12 | 109778089 | 109838398 | ||
| a0001c0003 | 1/1 | 2613 | 55 | 17 | 19 | 5 | 7 | 5 | TRPV4_chr12_109778089_109838398 | TRPV4 | ATGGC others(2608): Show |
chr12 | 109778089 | 109838398 | ||
| a0001c0004 | 0/0 | 2613 | 26 | 14 | 3 | 2 | 1 | 6 | TRPV4_chr12_109778089_109838398 | TRPV4 | ATGGC others(2608): Show |
chr12 | 109778089 | 109838398 | ||
| a0001c0005 | 0/0 | 2613 | 23 | 14 | 2 | 0 | 0 | 7 | TRPV4_chr12_109778089_109838398 | TRPV4 | ATGGC others(2608): Show |
chr12 | 109778089 | 109838398 | ||
| a0001c0008 | 0/0 | 2613 | 6 | 4 | 2 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | ATGGC others(2608): Show |
chr12 | 109778089 | 109838398 | ||
| a0001c0009 | 0/0 | 2613 | 4 | 4 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | ATGGC others(2608): Show |
chr12 | 109778089 | 109838398 | ||
| a0001c0011 | 0/0 | 2613 | 3 | 0 | 1 | 0 | 0 | 2 | TRPV4_chr12_109778089_109838398 | TRPV4 | ATGGC others(2608): Show |
chr12 | 109778089 | 109838398 | ||
| a0001c0012 | 0/0 | 2613 | 3 | 3 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | ATGGC others(2608): Show |
chr12 | 109778089 | 109838398 | ||
| a0001c0013 | 0/0 | 2613 | 2 | 0 | 1 | 0 | 1 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | ATGGC others(2608): Show |
chr12 | 109778089 | 109838398 | ||
| a0001c0015 | 0/0 | 2613 | 2 | 0 | 0 | 1 | 0 | 1 | TRPV4_chr12_109778089_109838398 | TRPV4 | ATGGC others(2608): Show |
chr12 | 109778089 | 109838398 | ||
| a0001c0016 | 0/0 | 2613 | 2 | 0 | 0 | 0 | 2 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | ATGGC others(2608): Show |
chr12 | 109778089 | 109838398 | ||
| a0001c0019 | 0/0 | 2613 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | ATGGC others(2608): Show |
chr12 | 109778089 | 109838398 | ||
| a0001c0020 | 0/0 | 2613 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | ATGGC others(2608): Show |
chr12 | 109778089 | 109838398 | ||
| a0001c0022 | 0/0 | 2613 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | ATGGC others(2608): Show |
chr12 | 109778089 | 109838398 | ||
| a0001c0023 | 0/0 | 2613 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | ATGGC others(2608): Show |
chr12 | 109778089 | 109838398 | ||
| a0001c0024 | 0/0 | 2613 | 1 | 0 | 0 | 0 | 0 | 1 | TRPV4_chr12_109778089_109838398 | TRPV4 | ATGGC others(2608): Show |
chr12 | 109778089 | 109838398 | ||
| a0001c0025 | 0/0 | 2613 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | ATGGC others(2608): Show |
chr12 | 109778089 | 109838398 | ||
| a0001c0026 | 0/0 | 2613 | 1 | 0 | 0 | 0 | 0 | 1 | TRPV4_chr12_109778089_109838398 | TRPV4 | ATGGC others(2608): Show |
chr12 | 109778089 | 109838398 | ||
| a0001c0027 | 0/0 | 2613 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | ATGGC others(2608): Show |
chr12 | 109778089 | 109838398 | ||
| a0001c0030 | 0/0 | 2613 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | ATGGC others(2608): Show |
chr12 | 109778089 | 109838398 | ||
| a0002c0006 | 0/0 | 2613 | 18 | 3 | 0 | 13 | 0 | 2 | TRPV4_chr12_109778089_109838398 | TRPV4 | ATGGC others(2608): Show |
chr12 | 109778089 | 109838398 | ||
| a0002c0032 | 0/0 | 2613 | 1 | 0 | 0 | 0 | 0 | 1 | TRPV4_chr12_109778089_109838398 | TRPV4 | ATGGC others(2608): Show |
chr12 | 109778089 | 109838398 | ||
| a0002c0033 | 0/0 | 2613 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | ATGGC others(2608): Show |
chr12 | 109778089 | 109838398 | ||
| a0003c0007 | 0/0 | 2613 | 7 | 0 | 7 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | ATGGC others(2608): Show |
chr12 | 109778089 | 109838398 | ||
| a0004c0010 | 0/0 | 2613 | 3 | 0 | 3 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | ATGGC others(2608): Show |
chr12 | 109778089 | 109838398 | ||
| a0005c0014 | 0/0 | 2613 | 2 | 0 | 2 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | ATGGC others(2608): Show |
chr12 | 109778089 | 109838398 | ||
| a0006c0017 | 0/0 | 2613 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | ATGGC others(2608): Show |
chr12 | 109778089 | 109838398 | ||
| a0006c0018 | 0/0 | 2613 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | ATGGC others(2608): Show |
chr12 | 109778089 | 109838398 | ||
| a0007c0028 | 0/0 | 2613 | 1 | 0 | 1 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | ATGGC others(2608): Show |
chr12 | 109778089 | 109838398 | ||
| a0008c0029 | 0/0 | 2613 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | ATGGC others(2608): Show |
chr12 | 109778089 | 109838398 | ||
| a0009c0031 | 0/0 | 2613 | 1 | 0 | 0 | 0 | 0 | 1 | TRPV4_chr12_109778089_109838398 | TRPV4 | ATGGC others(2608): Show |
chr12 | 109778089 | 109838398 | ||
| a0010c0021 | 0/0 | 2613 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | ATGGC others(2608): Show |
chr12 | 109778089 | 109838398 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3228 | 96 | 11 | 11 | 65 | 3 | 6 | TRPV4_chr12_109778089_109838398 | TRPV4 | ATTCA others(3223): Show |
chr12 | 109778089 | 109838398 |
| a0001c0002t0001 | 0/0 | 3228 | 75 | 8 | 22 | 32 | 2 | 11 | TRPV4_chr12_109778089_109838398 | TRPV4 | ATTCA others(3223): Show |
chr12 | 109778089 | 109838398 |
| a0001c0003t0001 | 1/1 | 3228 | 54 | 17 | 18 | 5 | 7 | 5 | TRPV4_chr12_109778089_109838398 | TRPV4 | ATTCA others(3223): Show |
chr12 | 109778089 | 109838398 |
| a0001c0003t0004 | 0/0 | 3228 | 1 | 0 | 1 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | ATTCA others(3223): Show |
chr12 | 109778089 | 109838398 |
| a0001c0004t0001 | 0/0 | 3228 | 26 | 14 | 3 | 2 | 1 | 6 | TRPV4_chr12_109778089_109838398 | TRPV4 | ATTCA others(3223): Show |
chr12 | 109778089 | 109838398 |
| a0001c0005t0001 | 0/0 | 3228 | 22 | 14 | 2 | 0 | 0 | 6 | TRPV4_chr12_109778089_109838398 | TRPV4 | ATTCA others(3223): Show |
chr12 | 109778089 | 109838398 |
| a0001c0005t0002 | 0/0 | 3228 | 1 | 0 | 0 | 0 | 0 | 1 | TRPV4_chr12_109778089_109838398 | TRPV4 | ATTCA others(3223): Show |
chr12 | 109778089 | 109838398 |
| a0001c0008t0001 | 0/0 | 3228 | 6 | 4 | 2 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | ATTCA others(3223): Show |
chr12 | 109778089 | 109838398 |
| a0001c0009t0001 | 0/0 | 3228 | 4 | 4 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | ATTCA others(3223): Show |
chr12 | 109778089 | 109838398 |
| a0001c0011t0001 | 0/0 | 3228 | 3 | 0 | 1 | 0 | 0 | 2 | TRPV4_chr12_109778089_109838398 | TRPV4 | ATTCA others(3223): Show |
chr12 | 109778089 | 109838398 |
| a0001c0012t0001 | 0/0 | 3228 | 3 | 3 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | ATTCA others(3223): Show |
chr12 | 109778089 | 109838398 |
| a0001c0013t0001 | 0/0 | 3228 | 2 | 0 | 1 | 0 | 1 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | ATTCA others(3223): Show |
chr12 | 109778089 | 109838398 |
| a0001c0015t0001 | 0/0 | 3228 | 2 | 0 | 0 | 1 | 0 | 1 | TRPV4_chr12_109778089_109838398 | TRPV4 | ATTCA others(3223): Show |
chr12 | 109778089 | 109838398 |
| a0001c0016t0001 | 0/0 | 3228 | 2 | 0 | 0 | 0 | 2 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | ATTCA others(3223): Show |
chr12 | 109778089 | 109838398 |
| a0001c0019t0001 | 0/0 | 3228 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | ATTCA others(3223): Show |
chr12 | 109778089 | 109838398 |
| a0001c0020t0001 | 0/0 | 3228 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | ATTCA others(3223): Show |
chr12 | 109778089 | 109838398 |
| a0001c0022t0003 | 0/0 | 3228 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | ATTCA others(3223): Show |
chr12 | 109778089 | 109838398 |
| a0001c0023t0001 | 0/0 | 3228 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | ATTCA others(3223): Show |
chr12 | 109778089 | 109838398 |
| a0001c0024t0001 | 0/0 | 3228 | 1 | 0 | 0 | 0 | 0 | 1 | TRPV4_chr12_109778089_109838398 | TRPV4 | ATTCA others(3223): Show |
chr12 | 109778089 | 109838398 |
| a0001c0025t0001 | 0/0 | 3228 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | ATTCA others(3223): Show |
chr12 | 109778089 | 109838398 |
| a0001c0026t0001 | 0/0 | 3228 | 1 | 0 | 0 | 0 | 0 | 1 | TRPV4_chr12_109778089_109838398 | TRPV4 | ATTCA others(3223): Show |
chr12 | 109778089 | 109838398 |
| a0001c0027t0001 | 0/0 | 3228 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | ATTCA others(3223): Show |
chr12 | 109778089 | 109838398 |
| a0001c0030t0001 | 0/0 | 3228 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | ATTCA others(3223): Show |
chr12 | 109778089 | 109838398 |
| a0002c0006t0001 | 0/0 | 3228 | 18 | 3 | 0 | 13 | 0 | 2 | TRPV4_chr12_109778089_109838398 | TRPV4 | ATTCA others(3223): Show |
chr12 | 109778089 | 109838398 |
| a0002c0032t0001 | 0/0 | 3228 | 1 | 0 | 0 | 0 | 0 | 1 | TRPV4_chr12_109778089_109838398 | TRPV4 | ATTCA others(3223): Show |
chr12 | 109778089 | 109838398 |
| a0002c0033t0001 | 0/0 | 3228 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | ATTCA others(3223): Show |
chr12 | 109778089 | 109838398 |
| a0003c0007t0001 | 0/0 | 3228 | 7 | 0 | 7 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | ATTCA others(3223): Show |
chr12 | 109778089 | 109838398 |
| a0004c0010t0001 | 0/0 | 3228 | 3 | 0 | 3 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | ATTCA others(3223): Show |
chr12 | 109778089 | 109838398 |
| a0005c0014t0001 | 0/0 | 3228 | 2 | 0 | 2 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | ATTCA others(3223): Show |
chr12 | 109778089 | 109838398 |
| a0006c0017t0001 | 0/0 | 3228 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | ATTCA others(3223): Show |
chr12 | 109778089 | 109838398 |
| a0006c0018t0001 | 0/0 | 3228 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | ATTCA others(3223): Show |
chr12 | 109778089 | 109838398 |
| a0007c0028t0001 | 0/0 | 3228 | 1 | 0 | 1 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | ATTCA others(3223): Show |
chr12 | 109778089 | 109838398 |
| a0008c0029t0001 | 0/0 | 3228 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | ATTCA others(3223): Show |
chr12 | 109778089 | 109838398 |
| a0009c0031t0001 | 0/0 | 3228 | 1 | 0 | 0 | 0 | 0 | 1 | TRPV4_chr12_109778089_109838398 | TRPV4 | ATTCA others(3223): Show |
chr12 | 109778089 | 109838398 |
| a0010c0021t0001 | 0/0 | 3228 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | ATTCA others(3223): Show |
chr12 | 109778089 | 109838398 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0002t0001g0001 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0002t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0002t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0002t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0002t0001g0014 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0002t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0002t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0002t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0002t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0002t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0002t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0002t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0002t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0002t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0002t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0002t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0002t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0002t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0002t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0002t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0002t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0002t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0002t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0002t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0002t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0002t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0002t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0003t0001g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0003t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0003t0001g0017 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0003t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0003t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0003t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0003t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0003t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0003t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0003t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0003t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0003t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0003t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0003t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0003t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0003t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0003t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0003t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0003t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0003t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0003t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0003t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0003t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0003t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0003t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0003t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0003t0001g0105 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0003t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0003t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0003t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0003t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0003t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0003t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0003t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0003t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0003t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0003t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0003t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0003t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0003t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0003t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0003t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0003t0001g0233 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0003t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0003t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0003t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0003t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0003t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0003t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0003t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0003t0004g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0004t0001g0003 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0004t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0004t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0004t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0004t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0004t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0004t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0004t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0004t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0004t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0004t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0004t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0004t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0004t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0004t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0004t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0004t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0004t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0004t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0004t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0004t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0004t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0004t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0005t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0005t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0005t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0005t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0005t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0005t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0005t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0005t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0005t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0005t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0005t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0005t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0005t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0005t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0005t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0005t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0005t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0005t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0005t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0005t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0005t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0005t0002g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0008t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0008t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0008t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0008t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0008t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0008t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0009t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0009t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0009t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0009t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0011t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0011t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0011t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0012t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0012t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0013t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0013t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0015t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0015t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0016t0001g0012 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0019t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0020t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0022t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0023t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0024t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0025t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0026t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0027t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0001c0030t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0002c0006t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0002c0006t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0002c0006t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0002c0006t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0002c0006t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0002c0006t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0002c0006t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0002c0006t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0002c0006t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0002c0006t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0002c0006t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0002c0006t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0002c0006t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0002c0006t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0002c0006t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0002c0032t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0002c0033t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0003c0007t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0003c0007t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0003c0007t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0003c0007t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0003c0007t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0003c0007t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0003c0007t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0004c0010t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0004c0010t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0004c0010t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0005c0014t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0006c0017t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0006c0018t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0007c0028t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0008c0029t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0009c0031t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| a0010c0021t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0155 | EUR | GBR | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG00099 | hp2 | a0001 | c0003 | t0001 | g0017 | EUR | GBR | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0021 | EUR | FIN | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG00280 | hp2 | a0001 | c0002 | t0001 | g0209 | EUR | FIN | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG00323 | hp1 | a0001 | c0013 | t0001 | g0294 | EUR | FIN | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG00323 | hp2 | a0001 | c0003 | t0001 | g0110 | EUR | FIN | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | CHS | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | CHS | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | CHS | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | CHS | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | CHS | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | CHS | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0136 | EAS | CHS | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | CHS | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | CHS | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | CHS | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG00597 | hp1 | a0002 | c0006 | t0001 | g0054 | EAS | CHS | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG00597 | hp2 | a0001 | c0002 | t0001 | g0258 | EAS | CHS | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG00609 | hp1 | a0001 | c0002 | t0001 | g0227 | EAS | CHS | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | CHS | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | CHS | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | CHS | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG00639 | hp1 | a0001 | c0003 | t0001 | g0305 | AMR | PUR | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG00639 | hp2 | a0001 | c0003 | t0001 | g0304 | AMR | PUR | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG00642 | hp1 | a0001 | c0005 | t0001 | g0221 | AMR | PUR | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG00642 | hp2 | a0001 | c0003 | t0001 | g0098 | AMR | PUR | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | CHS | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | CHS | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG00733 | hp2 | a0001 | c0003 | t0001 | g0095 | AMR | PUR | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0015 | AMR | PUR | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG00735 | hp2 | a0001 | c0002 | t0001 | g0299 | AMR | PUR | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0290 | AMR | PUR | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG00738 | hp2 | a0004 | c0010 | t0001 | g0223 | AMR | PUR | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG01069 | hp1 | a0004 | c0010 | t0001 | g0222 | AMR | PUR | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG01069 | hp2 | a0001 | c0003 | t0001 | g0303 | AMR | PUR | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG01070 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG01070 | hp2 | a0001 | c0013 | t0001 | g0113 | AMR | PUR | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG01071 | hp2 | a0001 | c0003 | t0001 | g0023 | AMR | PUR | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0310 | AMR | PUR | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0135 | AMR | PUR | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0015 | AMR | PUR | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG01099 | hp1 | a0001 | c0008 | t0001 | g0219 | AMR | PUR | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0026 | AMR | PUR | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG01106 | hp2 | a0001 | c0003 | t0001 | g0039 | AMR | PUR | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG01109 | hp1 | a0001 | c0004 | t0001 | g0140 | AMR | PUR | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG01167 | hp1 | a0001 | c0004 | t0001 | g0003 | AMR | PUR | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG01167 | hp2 | a0001 | c0003 | t0001 | g0226 | AMR | PUR | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG01168 | hp1 | a0001 | c0003 | t0001 | g0079 | AMR | PUR | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0297 | AMR | PUR | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG01175 | hp2 | a0001 | c0002 | t0001 | g0289 | AMR | PUR | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG01192 | hp1 | a0001 | c0003 | t0001 | g0017 | AMR | PUR | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG01192 | hp2 | a0003 | c0007 | t0001 | g0089 | AMR | PUR | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG01243 | hp1 | a0004 | c0010 | t0001 | g0220 | AMR | PUR | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG01243 | hp2 | a0001 | c0003 | t0001 | g0083 | AMR | PUR | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG01256 | hp1 | a0005 | c0014 | t0001 | g0020 | AMR | CLM | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG01256 | hp2 | a0001 | c0011 | t0001 | g0146 | AMR | CLM | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG01258 | hp1 | a0001 | c0002 | t0001 | g0184 | AMR | CLM | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG01258 | hp2 | a0005 | c0014 | t0001 | g0020 | AMR | CLM | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | CLM | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG01261 | hp2 | a0001 | c0003 | t0001 | g0097 | AMR | CLM | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0106 | AMR | CLM | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | CLM | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG01358 | hp1 | a0001 | c0002 | t0001 | g0114 | AMR | CLM | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | CLM | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG01361 | hp1 | a0001 | c0003 | t0001 | g0232 | AMR | CLM | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG01361 | hp2 | a0001 | c0003 | t0004 | g0205 | AMR | CLM | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | CLM | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG01433 | hp2 | a0001 | c0003 | t0001 | g0292 | AMR | CLM | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0153 | AMR | CLM | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG01496 | hp2 | a0003 | c0007 | t0001 | g0093 | AMR | CLM | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG01515 | hp1 | a0001 | c0003 | t0001 | g0150 | EUR | IBS | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG01515 | hp2 | a0001 | c0016 | t0001 | g0012 | EUR | IBS | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG01516 | hp1 | a0001 | c0003 | t0001 | g0104 | EUR | IBS | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG01516 | hp2 | a0001 | c0004 | t0001 | g0203 | EUR | IBS | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG01517 | hp1 | a0001 | c0003 | t0001 | g0103 | EUR | IBS | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG01517 | hp2 | a0001 | c0016 | t0001 | g0012 | EUR | IBS | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG01884 | hp1 | a0001 | c0002 | t0001 | g0066 | AFR | ACB | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | ACB | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG01891 | hp1 | a0001 | c0002 | t0001 | g0034 | AFR | ACB | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | ACB | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG01928 | hp1 | a0001 | c0004 | t0001 | g0147 | AMR | PEL | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG01928 | hp2 | a0001 | c0002 | t0001 | g0188 | AMR | PEL | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG01934 | hp1 | a0001 | c0002 | t0001 | g0185 | AMR | PEL | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG01934 | hp2 | a0001 | c0003 | t0001 | g0030 | AMR | PEL | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG01943 | hp1 | a0001 | c0003 | t0001 | g0023 | AMR | PEL | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG01943 | hp2 | a0001 | c0003 | t0001 | g0163 | AMR | PEL | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG01952 | hp1 | a0003 | c0007 | t0001 | g0102 | AMR | PEL | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG01952 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG01978 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG01978 | hp2 | a0001 | c0008 | t0001 | g0107 | AMR | PEL | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0187 | AMR | PEL | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG01981 | hp2 | a0003 | c0007 | t0001 | g0094 | AMR | PEL | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG01993 | hp1 | a0007 | c0028 | t0001 | g0116 | AMR | PEL | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG01993 | hp2 | a0003 | c0007 | t0001 | g0092 | AMR | PEL | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG02004 | hp1 | a0003 | c0007 | t0001 | g0154 | AMR | PEL | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG02004 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | KHV | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG02015 | hp2 | a0002 | c0006 | t0001 | g0285 | EAS | KHV | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | ACB | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG02055 | hp2 | a0001 | c0003 | t0001 | g0059 | AFR | ACB | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | KHV | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG02074 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | KHV | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG02129 | hp1 | a0001 | c0003 | t0001 | g0293 | EAS | KHV | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | KHV | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG02132 | hp1 | a0002 | c0006 | t0001 | g0286 | EAS | KHV | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG02145 | hp2 | a0008 | c0029 | t0001 | g0172 | AFR | ACB | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG02148 | hp1 | a0003 | c0007 | t0001 | g0091 | AMR | PEL | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG02148 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0011 | EAS | CDX | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | CDX | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG02165 | hp1 | a0002 | c0006 | t0001 | g0047 | EAS | CDX | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0057 | EAS | CDX | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | ACB | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG02257 | hp2 | a0001 | c0008 | t0001 | g0070 | AFR | ACB | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG02258 | hp1 | a0001 | c0005 | t0001 | g0036 | AFR | ACB | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG02258 | hp2 | a0002 | c0006 | t0001 | g0007 | AFR | ACB | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG02280 | hp1 | a0001 | c0004 | t0001 | g0043 | AFR | ACB | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG02280 | hp2 | a0001 | c0002 | t0001 | g0194 | AFR | ACB | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG02293 | hp1 | a0001 | c0003 | t0001 | g0307 | AMR | PEL | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG02293 | hp2 | a0001 | c0002 | t0001 | g0101 | AMR | PEL | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG02451 | hp1 | a0001 | c0002 | t0001 | g0144 | AFR | ACB | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG02451 | hp2 | a0001 | c0004 | t0001 | g0040 | AFR | ACB | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | KHV | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0236 | EAS | KHV | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG02572 | hp1 | a0001 | c0005 | t0001 | g0029 | AFR | GWD | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG02572 | hp2 | a0002 | c0006 | t0001 | g0064 | AFR | GWD | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG02615 | hp1 | a0001 | c0004 | t0001 | g0005 | AFR | GWD | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG02615 | hp2 | a0001 | c0005 | t0001 | g0085 | AFR | GWD | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG02622 | hp1 | a0001 | c0003 | t0001 | g0151 | AFR | GWD | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG02622 | hp2 | a0001 | c0004 | t0001 | g0042 | AFR | GWD | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG02630 | hp1 | a0001 | c0004 | t0001 | g0005 | AFR | GWD | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG02630 | hp2 | a0001 | c0004 | t0001 | g0118 | AFR | GWD | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG02647 | hp1 | a0001 | c0002 | t0001 | g0193 | AFR | GWD | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG02647 | hp2 | a0001 | c0009 | t0001 | g0049 | AFR | GWD | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0167 | SAS | PJL | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG02698 | hp2 | a0002 | c0006 | t0001 | g0073 | SAS | PJL | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG02717 | hp1 | a0001 | c0003 | t0001 | g0077 | AFR | GWD | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG02717 | hp2 | a0006 | c0017 | t0001 | g0308 | AFR | GWD | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG02735 | hp1 | a0001 | c0005 | t0002 | g0037 | SAS | PJL | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG02735 | hp2 | a0001 | c0002 | t0001 | g0134 | SAS | PJL | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG02738 | hp1 | a0001 | c0004 | t0001 | g0204 | SAS | PJL | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0273 | SAS | PJL | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG02809 | hp1 | a0001 | c0003 | t0001 | g0164 | AFR | GWD | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG02809 | hp2 | a0001 | c0003 | t0001 | g0060 | AFR | GWD | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG02818 | hp1 | a0001 | c0004 | t0001 | g0312 | AFR | GWD | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG02818 | hp2 | a0001 | c0004 | t0001 | g0003 | AFR | GWD | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG02886 | hp1 | a0001 | c0008 | t0001 | g0072 | AFR | GWD | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG02886 | hp2 | a0001 | c0003 | t0001 | g0075 | AFR | GWD | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG02922 | hp1 | a0001 | c0019 | t0001 | g0309 | AFR | ESN | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG02922 | hp2 | a0001 | c0012 | t0001 | g0032 | AFR | ESN | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | ESN | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG02965 | hp2 | a0001 | c0002 | t0001 | g0159 | AFR | ESN | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG02970 | hp1 | a0001 | c0009 | t0001 | g0046 | AFR | ESN | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG02970 | hp2 | a0001 | c0004 | t0001 | g0041 | AFR | ESN | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG02976 | hp1 | a0001 | c0004 | t0001 | g0068 | AFR | ESN | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG02976 | hp2 | a0001 | c0005 | t0001 | g0088 | AFR | ESN | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG03017 | hp1 | a0001 | c0026 | t0001 | g0210 | SAS | PJL | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG03017 | hp2 | a0009 | c0031 | t0001 | g0200 | SAS | PJL | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | GWD | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG03041 | hp2 | a0001 | c0003 | t0001 | g0196 | AFR | GWD | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG03098 | hp1 | a0001 | c0002 | t0001 | g0133 | AFR | MSL | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG03098 | hp2 | a0001 | c0008 | t0001 | g0069 | AFR | MSL | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG03130 | hp1 | a0001 | c0004 | t0001 | g0003 | AFR | ESN | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG03130 | hp2 | a0001 | c0003 | t0001 | g0195 | AFR | ESN | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | ESN | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG03139 | hp2 | a0001 | c0003 | t0001 | g0139 | AFR | ESN | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG03195 | hp1 | a0001 | c0022 | t0003 | g0038 | AFR | ESN | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG03195 | hp2 | a0001 | c0020 | t0001 | g0160 | AFR | ESN | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG03209 | hp1 | a0001 | c0002 | t0001 | g0124 | AFR | MSL | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | MSL | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG03225 | hp1 | a0001 | c0005 | t0001 | g0016 | AFR | MSL | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG03225 | hp2 | a0001 | c0004 | t0001 | g0117 | AFR | MSL | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG03239 | hp1 | a0001 | c0005 | t0001 | g0229 | SAS | PJL | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0263 | SAS | PJL | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG03453 | hp1 | a0001 | c0005 | t0001 | g0086 | AFR | MSL | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG03453 | hp2 | a0001 | c0003 | t0001 | g0078 | AFR | MSL | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG03486 | hp1 | a0001 | c0030 | t0001 | g0028 | AFR | MSL | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG03486 | hp2 | a0001 | c0003 | t0001 | g0080 | AFR | MSL | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG03490 | hp1 | a0001 | c0003 | t0001 | g0008 | SAS | PJL | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG03490 | hp2 | a0001 | c0005 | t0001 | g0230 | SAS | PJL | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG03491 | hp1 | a0001 | c0004 | t0001 | g0142 | SAS | PJL | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0014 | SAS | PJL | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0014 | SAS | PJL | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG03492 | hp2 | a0001 | c0003 | t0001 | g0008 | SAS | PJL | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG03540 | hp1 | a0010 | c0021 | t0001 | g0125 | AFR | GWD | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG03540 | hp2 | a0001 | c0003 | t0001 | g0061 | AFR | GWD | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG03579 | hp1 | a0001 | c0003 | t0001 | g0082 | AFR | MSL | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG03579 | hp2 | a0001 | c0023 | t0001 | g0033 | AFR | MSL | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG03654 | hp1 | a0001 | c0005 | t0001 | g0128 | SAS | PJL | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG03654 | hp2 | a0001 | c0004 | t0001 | g0199 | SAS | PJL | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0248 | SAS | PJL | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0208 | SAS | PJL | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG03688 | hp1 | a0001 | c0004 | t0001 | g0148 | SAS | STU | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG03688 | hp2 | a0001 | c0005 | t0001 | g0149 | SAS | STU | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0272 | SAS | PJL | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0171 | SAS | PJL | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0161 | SAS | PJL | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG03710 | hp2 | a0001 | c0024 | t0001 | g0218 | SAS | PJL | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG03831 | hp1 | a0001 | c0004 | t0001 | g0202 | SAS | BEB | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG03831 | hp2 | a0001 | c0011 | t0001 | g0127 | SAS | BEB | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0181 | SAS | BEB | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG03834 | hp2 | a0001 | c0005 | t0001 | g0126 | SAS | BEB | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG03927 | hp1 | a0001 | c0004 | t0001 | g0283 | SAS | BEB | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG03927 | hp2 | a0001 | c0003 | t0001 | g0099 | SAS | BEB | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG03942 | hp1 | a0001 | c0005 | t0001 | g0027 | SAS | BEB | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG03942 | hp2 | a0001 | c0015 | t0001 | g0201 | SAS | BEB | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG04115 | hp1 | a0001 | c0011 | t0001 | g0145 | SAS | STU | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG04115 | hp2 | a0002 | c0032 | t0001 | g0065 | SAS | STU | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG04184 | hp1 | a0002 | c0006 | t0001 | g0035 | SAS | BEB | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG04184 | hp2 | a0001 | c0003 | t0001 | g0112 | SAS | BEB | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0291 | SAS | STU | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0175 | SAS | STU | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG04204 | hp1 | a0001 | c0003 | t0001 | g0121 | SAS | STU | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0174 | SAS | STU | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0137 | SAS | STU | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0311 | SAS | STU | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA18522 | hp1 | a0002 | c0006 | t0001 | g0007 | AFR | YRI | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA18522 | hp2 | a0001 | c0005 | t0001 | g0157 | AFR | YRI | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA18906 | hp1 | a0001 | c0005 | t0001 | g0158 | AFR | YRI | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA18906 | hp2 | a0001 | c0004 | t0001 | g0044 | AFR | YRI | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA18941 | hp1 | a0001 | c0002 | t0001 | g0176 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA18943 | hp2 | a0001 | c0002 | t0001 | g0178 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA18945 | hp2 | a0001 | c0002 | t0001 | g0295 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA18946 | hp1 | a0002 | c0006 | t0001 | g0053 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA18948 | hp1 | a0002 | c0006 | t0001 | g0004 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA18948 | hp2 | a0001 | c0003 | t0001 | g0009 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA18952 | hp2 | a0002 | c0006 | t0001 | g0051 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA18953 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA18954 | hp1 | a0001 | c0015 | t0001 | g0119 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA18957 | hp1 | a0001 | c0002 | t0001 | g0189 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA18966 | hp1 | a0001 | c0002 | t0001 | g0302 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA18968 | hp2 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA18973 | hp2 | a0001 | c0002 | t0001 | g0115 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA18974 | hp2 | a0002 | c0006 | t0001 | g0058 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA18982 | hp1 | a0001 | c0003 | t0001 | g0009 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA18985 | hp1 | a0001 | c0002 | t0001 | g0228 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA18985 | hp2 | a0001 | c0002 | t0001 | g0182 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA18991 | hp1 | a0001 | c0003 | t0001 | g0168 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA18992 | hp2 | a0001 | c0002 | t0001 | g0156 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA18994 | hp2 | a0002 | c0006 | t0001 | g0052 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA18995 | hp2 | a0001 | c0002 | t0001 | g0123 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA18998 | hp1 | a0001 | c0002 | t0001 | g0122 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA19002 | hp1 | a0001 | c0002 | t0001 | g0152 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA19002 | hp2 | a0002 | c0006 | t0001 | g0004 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA19007 | hp2 | a0001 | c0002 | t0001 | g0241 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA19009 | hp1 | a0001 | c0004 | t0001 | g0190 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0260 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA19011 | hp2 | a0001 | c0002 | t0001 | g0183 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA19030 | hp1 | a0001 | c0003 | t0001 | g0062 | AFR | LWK | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA19030 | hp2 | a0001 | c0005 | t0001 | g0207 | AFR | LWK | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA19043 | hp1 | a0001 | c0009 | t0001 | g0048 | AFR | LWK | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA19043 | hp2 | a0006 | c0018 | t0001 | g0076 | AFR | LWK | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA19054 | hp1 | a0002 | c0006 | t0001 | g0050 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA19054 | hp2 | a0001 | c0002 | t0001 | g0170 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA19056 | hp2 | a0001 | c0003 | t0001 | g0109 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA19064 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA19074 | hp1 | a0001 | c0002 | t0001 | g0165 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA19077 | hp2 | a0002 | c0006 | t0001 | g0004 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA19079 | hp2 | a0001 | c0002 | t0001 | g0179 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA19081 | hp1 | a0002 | c0006 | t0001 | g0056 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA19084 | hp1 | a0001 | c0002 | t0001 | g0301 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA19084 | hp2 | a0001 | c0027 | t0001 | g0259 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA19085 | hp2 | a0001 | c0002 | t0001 | g0180 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA19088 | hp2 | a0001 | c0002 | t0001 | g0177 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA19090 | hp1 | a0002 | c0033 | t0001 | g0055 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA19090 | hp2 | a0001 | c0004 | t0001 | g0141 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA19240 | hp1 | a0001 | c0009 | t0001 | g0045 | AFR | YRI | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA19240 | hp2 | a0001 | c0005 | t0001 | g0192 | AFR | YRI | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA20129 | hp1 | a0001 | c0003 | t0001 | g0084 | AFR | ASW | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA20129 | hp2 | a0001 | c0025 | t0001 | g0067 | AFR | ASW | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA20752 | hp1 | a0001 | c0003 | t0001 | g0111 | EUR | TSI | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0276 | EUR | TSI | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA20805 | hp1 | a0001 | c0003 | t0001 | g0306 | EUR | TSI | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0173 | EUR | TSI | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0186 | AMR | CLM | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG01123 | hp2 | a0001 | c0005 | t0001 | g0231 | AMR | CLM | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG02109 | hp1 | a0001 | c0004 | t0001 | g0198 | AFR | ACB | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG02109 | hp2 | a0001 | c0003 | t0001 | g0081 | AFR | ACB | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG02486 | hp1 | a0001 | c0005 | t0001 | g0063 | AFR | ACB | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | ACB | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG02559 | hp1 | a0001 | c0012 | t0001 | g0006 | AFR | ACB | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG02559 | hp2 | a0001 | c0008 | t0001 | g0071 | AFR | ACB | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG03471 | hp1 | a0001 | c0005 | t0001 | g0087 | AFR | MSL | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG03471 | hp2 | a0001 | c0005 | t0001 | g0074 | AFR | MSL | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG06807 | hp1 | a0001 | c0005 | t0001 | g0016 | AFR | USA | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| HG06807 | hp2 | a0001 | c0012 | t0001 | g0006 | AFR | USA | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | USA | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| NA20300 | hp2 | a0001 | c0003 | t0001 | g0031 | AFR | USA | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| homoSapiens | chm13v2 | a0001 | c0003 | t0001 | g0105 | REF | REF | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| homoSapiens | grch38p0 | a0001 | c0003 | t0001 | g0233 | REF | REF | TRPV4_chr12_109778089_109838398 | TRPV4 | chr12 | 109778089 | 109838398 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:109783656 | G | A | 1 | a0009 | 1 | HG03017.hp2 | missense_variant | MODERATE | c.2581C>T | p.Pro861Ser | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 16/16 | 2661/3228 | 2581/2616 | 861/871 | chr12 | 109783656 | |||
| chr12:109792763 | G | C | 2 | a0003 a0007 |
8 | HG01192.hp2 HG01496.hp2 HG01952.hp1 others(5): Show |
missense_variant | MODERATE | c.1713C>G | p.Ile571Met | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 11/16 | 1793/3228 | 1713/2616 | 571/871 | chr12 | 109792763 | |||
| chr12:109792792 | C | T | 1 | a0004 | 3 | HG00738.hp2 HG01069.hp1 HG01243.hp1 |
missense_variant | MODERATE | c.1684G>A | p.Val562Ile | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 11/16 | 1764/3228 | 1684/2616 | 562/871 | chr12 | 109792792 | |||
| chr12:109794442 | G | A | 1 | a0008 | 1 | HG02145.hp2 | missense_variant | MODERATE | c.1378C>T | p.Arg460Trp | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 8/16 | 1458/3228 | 1378/2616 | 460/871 | chr12 | 109794442 | |||
| chr12:109794444 | A | C | 1 | a0005 | 2 | HG01256.hp1 HG01258.hp2 |
missense_variant | MODERATE | c.1376T>G | p.Leu459Arg | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 8/16 | 1456/3228 | 1376/2616 | 459/871 | chr12 | 109794444 | |||
| chr12:109798673 | C | T | 1 | a0010 | 1 | HG03540.hp1 | missense_variant | MODERATE | c.1093G>A | p.Val365Met | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 6/16 | 1173/3228 | 1093/2616 | 365/871 | chr12 | 109798673 | |||
| chr12:109803054 | C | A | 1 | a0003 | 7 | HG01192.hp2 HG01496.hp2 HG01952.hp1 others(4): Show |
missense_variant | MODERATE | c.649G>T | p.Ala217Ser | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 4/16 | 729/3228 | 649/2616 | 217/871 | chr12 | 109803054 | |||
| chr12:109814742 | G | A | 1 | a0002 | 20 | HG00597.hp1 HG02015.hp2 HG02132.hp1 others(17): Show |
missense_variant | MODERATE | c.55C>T | p.Pro19Ser | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 2/16 | 135/3228 | 55/2616 | 19/871 | chr12 | 109814742 | |||
| chr12:109814769 | C | G | 1 | a0006 | 2 | HG02717.hp2 NA19043.hp2 |
missense_variant | MODERATE | c.28G>C | p.Ala10Pro | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 2/16 | 108/3228 | 28/2616 | 10/871 | chr12 | 109814769 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:109783720 | G | A | 1 | a0001c0026 | 1 | HG03017.hp1 | synonymous_variant | LOW | c.2517C>T | p.Asp839Asp | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 16/16 | 2597/3228 | 2517/2616 | 839/871 | chr12 | 109783720 | |||
| chr12:109783738 | G | A | 1 | a0001c0027 | 1 | NA19084.hp2 | synonymous_variant | LOW | c.2499C>T | p.Asn833Asn | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 16/16 | 2579/3228 | 2499/2616 | 833/871 | chr12 | 109783738 | |||
| chr12:109783765 | C | T | 1 | a0001c0030 | 1 | HG03486.hp1 | synonymous_variant | LOW | c.2472G>A | p.Ser824Ser | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 16/16 | 2552/3228 | 2472/2616 | 824/871 | chr12 | 109783765 | |||
| chr12:109784341 | C | G | 1 | a0001c0011 | 3 | HG01256.hp2 HG03831.hp2 HG04115.hp1 |
synonymous_variant | LOW | c.2433G>C | p.Ser811Ser | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 15/16 | 2513/3228 | 2433/2616 | 811/871 | chr12 | 109784341 | |||
| chr12:109788574 | G | A | 8 | a0001c0002 a0001c0008 a0001c0013 others(5): Show |
89 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(86): Show |
synonymous_variant | LOW | c.2034C>T | p.Ile678Ile | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 13/16 | 2114/3228 | 2034/2616 | 678/871 | chr12 | 109788574 | |||
| chr12:109792732 | G | A | 2 | a0001c0012 a0001c0025 |
4 | HG02559.hp1 HG02922.hp2 HG06807.hp2 others(1): Show |
synonymous_variant | LOW | c.1744C>T | p.Leu582Leu | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 11/16 | 1824/3228 | 1744/2616 | 582/871 | chr12 | 109792732 | |||
| chr12:109794479 | G | A | 2 | a0001c0009 a0006c0018 |
5 | HG02647.hp2 HG02970.hp1 NA19043.hp1 others(2): Show |
synonymous_variant | LOW | c.1341C>T | p.His447His | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 8/16 | 1421/3228 | 1341/2616 | 447/871 | chr12 | 109794479 | |||
| chr12:109800661 | C | T | 1 | a0002c0032 | 1 | HG04115.hp2 | synonymous_variant | LOW | c.810G>A | p.Gly270Gly | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 5/16 | 890/3228 | 810/2616 | 270/871 | chr12 | 109800661 | |||
| chr12:109800676 | G | A | 6 | a0001c0004 a0001c0012 a0001c0015 others(3): Show |
34 | HG01109.hp1 HG01167.hp1 HG01516.hp2 others(31): Show |
synonymous_variant | LOW | c.795C>T | p.His265His | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 5/16 | 875/3228 | 795/2616 | 265/871 | chr12 | 109800676 | |||
| chr12:109800682 | A | G | 10 | a0001c0005 a0001c0008 a0001c0020 others(7): Show |
56 | HG00597.hp1 HG00642.hp1 HG00738.hp2 others(53): Show |
synonymous_variant | LOW | c.789T>C | p.Asp263Asp | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 5/16 | 869/3228 | 789/2616 | 263/871 | chr12 | 109800682 | |||
| chr12:109803033 | T | G | 31 | a0001c0001 a0001c0002 a0001c0004 others(28): Show |
287 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(284): Show |
synonymous_variant | LOW | c.670A>C | p.Arg224Arg | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 4/16 | 750/3228 | 670/2616 | 224/871 | chr12 | 109803033 | |||
| chr12:109808306 | C | T | 1 | a0001c0024 | 1 | HG03710.hp2 | synonymous_variant | LOW | c.549G>A | p.Glu183Glu | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/16 | 629/3228 | 549/2616 | 183/871 | chr12 | 109808306 | |||
| chr12:109808459 | C | T | 1 | a0001c0019 | 1 | HG02922.hp1 | synonymous_variant | LOW | c.396G>A | p.Pro132Pro | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/16 | 476/3228 | 396/2616 | 132/871 | chr12 | 109808459 | |||
| chr12:109814716 | A | G | 7 | a0001c0019 a0001c0020 a0001c0022 others(4): Show |
7 | HG02717.hp2 HG02922.hp1 HG03195.hp1 others(4): Show |
synonymous_variant | LOW | c.81T>C | p.Gly27Gly | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 2/16 | 161/3228 | 81/2616 | 27/871 | chr12 | 109814716 | |||
| chr12:109814740 | G | A | 2 | a0006c0017 a0006c0018 |
2 | HG02717.hp2 NA19043.hp2 |
synonymous_variant | LOW | c.57C>T | p.Pro19Pro | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 2/16 | 137/3228 | 57/2616 | 19/871 | chr12 | 109814740 | |||
| chr12:109814764 | C | A | 1 | a0001c0016 | 2 | HG01515.hp2 HG01517.hp2 |
synonymous_variant | LOW | c.33G>T | p.Gly11Gly | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 2/16 | 113/3228 | 33/2616 | 11/871 | chr12 | 109814764 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:109783303 | C | G | 1 | a0001c0003t0004 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*318G>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 16/16 | 318 | chr12 | 109783303 | ||||||
| chr12:109783391 | C | T | 1 | a0001c0022t0003 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*230G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 16/16 | 230 | chr12 | 109783391 | ||||||
| chr12:109783470 | A | G | 1 | a0001c0005t0002 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*151T>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 16/16 | 151 | chr12 | 109783470 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:109783787 | A | C | 12 | a0001c0004t0001g0312 a0001c0005t0001g0029 a0001c0005t0001g0074 others(9): Show |
12 | HG00738.hp2 HG01069.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.2459-9T>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 15/15 | chr12 | 109783787 | |||||||
| chr12:109783815 | TG | T | 3 | a0001c0001t0001g0162 a0001c0001t0001g0224 a0001c0001t0001g0225 |
3 | HG01891.hp2 HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.2459-38delC | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 15/15 | chr12 | 109783815 | |||||||
| chr12:109783826 | G | C | 178 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(175): Show |
197 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.2459-48C>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 15/15 | chr12 | 109783826 | |||||||
| chr12:109783830 | G | A | 12 | a0001c0004t0001g0312 a0001c0005t0001g0029 a0001c0005t0001g0074 others(9): Show |
12 | HG00738.hp2 HG01069.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.2459-52C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 15/15 | chr12 | 109783830 | |||||||
| chr12:109783834 | G | A | 4 | a0001c0001t0001g0251 a0001c0001t0001g0262 a0001c0001t0001g0275 others(1): Show |
4 | HG02074.hp1 NA18967.hp1 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.2459-56C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 15/15 | chr12 | 109783834 | |||||||
| chr12:109783969 | C | G | 3 | a0001c0003t0001g0075 a0001c0003t0001g0151 a0001c0003t0001g0163 |
3 | HG01943.hp2 HG02622.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2459-191G>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 15/15 | chr12 | 109783969 | |||||||
| chr12:109783973 | A | T | 1 | a0003c0007t0001g0092 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.2459-195T>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 15/15 | chr12 | 109783973 | |||||||
| chr12:109784023 | G | A | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG02145.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2459-245C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 15/15 | chr12 | 109784023 | |||||||
| chr12:109784192 | C | T | 9 | a0001c0004t0001g0312 a0001c0005t0001g0029 a0001c0005t0001g0074 others(6): Show |
9 | HG02572.hp1 HG02615.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.2458+124G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 15/15 | chr12 | 109784192 | |||||||
| chr12:109784556 | G | A | 10 | a0001c0004t0001g0312 a0001c0005t0001g0029 a0001c0005t0001g0074 others(7): Show |
10 | HG02572.hp1 HG02615.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.2337-119C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 14/15 | chr12 | 109784556 | |||||||
| chr12:109784595 | C | T | 1 | a0001c0002t0001g0174 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2337-158G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 14/15 | chr12 | 109784595 | |||||||
| chr12:109784683 | T | A | 6 | a0001c0001t0001g0212 a0001c0001t0001g0215 a0001c0001t0001g0217 others(3): Show |
6 | HG01361.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2337-246A>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 14/15 | chr12 | 109784683 | |||||||
| chr12:109784730 | G | A | 12 | a0001c0004t0001g0312 a0001c0005t0001g0029 a0001c0005t0001g0074 others(9): Show |
12 | HG00738.hp2 HG01069.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.2337-293C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 14/15 | chr12 | 109784730 | |||||||
| chr12:109784776 | A | G | 12 | a0001c0004t0001g0312 a0001c0005t0001g0029 a0001c0005t0001g0074 others(9): Show |
12 | HG00738.hp2 HG01069.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.2337-339T>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 14/15 | chr12 | 109784776 | |||||||
| chr12:109784820 | G | A | 78 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0096 others(75): Show |
83 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.2337-383C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 14/15 | chr12 | 109784820 | |||||||
| chr12:109784840 | C | CA | 253 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(250): Show |
282 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.2337-404dupT | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 14/15 | chr12 | 109784840 | |||||||
| chr12:109784840 | C | CAA | 18 | a0001c0001t0001g0225 a0001c0001t0001g0245 a0001c0002t0001g0176 others(15): Show |
18 | HG01981.hp1 HG02055.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.2337-405_2337-404d others(4): Show |
TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 14/15 | chr12 | 109784840 | |||||||
| chr12:109784860 | C | CGT | 115 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0162 others(112): Show |
129 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(126): Show |
intron_variant | MODIFIER | c.2337-425_2337-424d others(4): Show |
TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 14/15 | chr12 | 109784860 | |||||||
| chr12:109784860 | C | CGTGT | 10 | a0001c0002t0001g0144 a0001c0002t0001g0186 a0001c0002t0001g0227 others(7): Show |
10 | HG00609.hp1 HG00738.hp2 HG01069.hp1 others(7): Show |
intron_variant | MODIFIER | c.2337-427_2337-424d others(6): Show |
TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 14/15 | chr12 | 109784860 | |||||||
| chr12:109784860 | C | CGTGTGTG others(1): Show |
7 | a0001c0005t0001g0074 a0001c0005t0001g0085 a0001c0005t0001g0086 others(4): Show |
7 | HG02615.hp2 HG02976.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.2337-431_2337-424d others(10): Show |
TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 14/15 | chr12 | 109784860 | |||||||
| chr12:109784860 | C | CGTGTGTG others(3): Show |
1 | a0001c0005t0001g0029 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2337-433_2337-424d others(12): Show |
TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 14/15 | chr12 | 109784860 | |||||||
| chr12:109784860 | CGT | C | 100 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(97): Show |
111 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.2337-425_2337-424d others(4): Show |
TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 14/15 | chr12 | 109784860 | |||||||
| chr12:109784876 | T | TGTGTGTG others(3): Show |
1 | a0001c0022t0003g0038 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2337-440_2337-439i others(12): Show |
TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 14/15 | chr12 | 109784876 | |||||||
| chr12:109785209 | G | A | 1 | a0001c0002t0001g0181 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2337-772C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 14/15 | chr12 | 109785209 | |||||||
| chr12:109785383 | T | A | 7 | a0001c0001t0001g0120 a0001c0001t0001g0131 a0001c0001t0001g0235 others(4): Show |
7 | HG00408.hp2 HG00609.hp2 HG02155.hp2 others(4): Show |
intron_variant | MODIFIER | c.2337-946A>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 14/15 | chr12 | 109785383 | |||||||
| chr12:109785425 | T | A | 1 | a0001c0023t0001g0033 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2337-988A>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 14/15 | chr12 | 109785425 | |||||||
| chr12:109785566 | A | G | 12 | a0001c0004t0001g0312 a0001c0005t0001g0029 a0001c0005t0001g0074 others(9): Show |
12 | HG00738.hp2 HG01069.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.2337-1129T>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 14/15 | chr12 | 109785566 | |||||||
| chr12:109785662 | A | G | 1 | a0001c0002t0001g0013 | 2 | NA18953.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.2336+1048T>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 14/15 | chr12 | 109785662 | |||||||
| chr12:109785680 | A | C | 5 | a0001c0001t0001g0162 a0001c0001t0001g0224 a0001c0001t0001g0225 others(2): Show |
5 | HG01891.hp2 HG02055.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.2336+1030T>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 14/15 | chr12 | 109785680 | |||||||
| chr12:109785758 | T | C | 4 | a0001c0001t0001g0212 a0001c0001t0001g0215 a0001c0001t0001g0217 others(1): Show |
4 | HG01361.hp2 HG02257.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2336+952A>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 14/15 | chr12 | 109785758 | |||||||
| chr12:109785812 | C | T | 1 | a0010c0021t0001g0125 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2336+898G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 14/15 | chr12 | 109785812 | |||||||
| chr12:109785813 | G | A | 8 | a0001c0002t0001g0001 a0001c0002t0001g0026 a0001c0002t0001g0153 others(5): Show |
13 | HG01070.hp1 HG01071.hp1 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.2336+897C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 14/15 | chr12 | 109785813 | |||||||
| chr12:109785890 | C | T | 1 | a0001c0027t0001g0259 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2336+820G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 14/15 | chr12 | 109785890 | |||||||
| chr12:109785928 | G | A | 74 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0096 others(71): Show |
79 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.2336+782C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 14/15 | chr12 | 109785928 | |||||||
| chr12:109786206 | T | G | 13 | a0001c0001t0001g0162 a0001c0001t0001g0214 a0001c0001t0001g0224 others(10): Show |
15 | HG01167.hp1 HG01884.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.2336+504A>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 14/15 | chr12 | 109786206 | |||||||
| chr12:109786287 | C | T | 1 | a0001c0004t0001g0283 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2336+423G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 14/15 | chr12 | 109786287 | |||||||
| chr12:109786331 | T | C | 12 | a0001c0004t0001g0312 a0001c0005t0001g0029 a0001c0005t0001g0074 others(9): Show |
12 | HG00738.hp2 HG01069.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.2336+379A>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 14/15 | chr12 | 109786331 | |||||||
| chr12:109786342 | T | A | 1 | a0001c0023t0001g0033 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2336+368A>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 14/15 | chr12 | 109786342 | |||||||
| chr12:109786369 | A | G | 181 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0024 others(178): Show |
198 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.2336+341T>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 14/15 | chr12 | 109786369 | |||||||
| chr12:109786412 | G | A | 1 | a0001c0009t0001g0045 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2336+298C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 14/15 | chr12 | 109786412 | |||||||
| chr12:109786469 | C | T | 12 | a0001c0004t0001g0312 a0001c0005t0001g0029 a0001c0005t0001g0074 others(9): Show |
12 | HG00738.hp2 HG01069.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.2336+241G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 14/15 | chr12 | 109786469 | |||||||
| chr12:109786490 | C | G | 1 | a0001c0002t0001g0174 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2336+220G>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 14/15 | chr12 | 109786490 | |||||||
| chr12:109786490 | C | T | 1 | a0001c0001t0001g0234 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2336+220G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 14/15 | chr12 | 109786490 | |||||||
| chr12:109786493 | G | A | 1 | a0001c0001t0001g0271 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.2336+217C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 14/15 | chr12 | 109786493 | |||||||
| chr12:109786586 | G | A | 1 | a0001c0009t0001g0046 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2336+124C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 14/15 | chr12 | 109786586 | |||||||
| chr12:109786635 | G | A | 1 | a0001c0001t0001g0287 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2336+75C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 14/15 | chr12 | 109786635 | |||||||
| chr12:109786842 | G | A | 1 | a0001c0005t0001g0086 | 1 | HG03453.hp1 | splice_region_variant&intron_variant | LOW | c.2209-5C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 13/15 | chr12 | 109786842 | |||||||
| chr12:109786919 | G | A | 1 | a0001c0001t0001g0025 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2209-82C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 13/15 | chr12 | 109786919 | |||||||
| chr12:109787009 | A | C | 1 | a0001c0019t0001g0309 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2209-172T>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 13/15 | chr12 | 109787009 | |||||||
| chr12:109787053 | C | A | 9 | a0001c0004t0001g0312 a0001c0005t0001g0029 a0001c0005t0001g0074 others(6): Show |
9 | HG02572.hp1 HG02615.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.2209-216G>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 13/15 | chr12 | 109787053 | |||||||
| chr12:109787088 | T | C | 1 | a0001c0001t0001g0025 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2209-251A>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 13/15 | chr12 | 109787088 | |||||||
| chr12:109787111 | C | T | 28 | a0001c0001t0001g0090 a0001c0001t0001g0212 a0001c0001t0001g0215 others(25): Show |
30 | HG01361.hp2 HG01433.hp1 HG01928.hp1 others(27): Show |
intron_variant | MODIFIER | c.2209-274G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 13/15 | chr12 | 109787111 | |||||||
| chr12:109787117 | A | C | 167 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0096 others(164): Show |
183 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.2209-280T>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 13/15 | chr12 | 109787117 | |||||||
| chr12:109787193 | G | A | 8 | a0001c0001t0001g0214 a0001c0004t0001g0003 a0001c0004t0001g0040 others(5): Show |
10 | HG01167.hp1 HG01884.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.2209-356C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 13/15 | chr12 | 109787193 | |||||||
| chr12:109787211 | A | G | 3 | a0004c0010t0001g0220 a0004c0010t0001g0222 a0004c0010t0001g0223 |
3 | HG00738.hp2 HG01069.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.2209-374T>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 13/15 | chr12 | 109787211 | |||||||
| chr12:109787289 | T | C | 3 | a0001c0009t0001g0046 a0001c0009t0001g0048 a0001c0009t0001g0049 |
3 | HG02647.hp2 HG02970.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2209-452A>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 13/15 | chr12 | 109787289 | |||||||
| chr12:109787290 | G | T | 6 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0254 others(3): Show |
6 | HG01109.hp1 HG02109.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.2209-453C>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 13/15 | chr12 | 109787290 | |||||||
| chr12:109787367 | G | T | 2 | a0001c0015t0001g0201 a0009c0031t0001g0200 |
2 | HG03017.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.2209-530C>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 13/15 | chr12 | 109787367 | |||||||
| chr12:109787446 | A | T | 1 | a0001c0002t0001g0208 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2209-609T>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 13/15 | chr12 | 109787446 | |||||||
| chr12:109787460 | C | G | 1 | a0006c0018t0001g0076 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2209-623G>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 13/15 | chr12 | 109787460 | |||||||
| chr12:109787462 | G | A | 74 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0096 others(71): Show |
79 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.2209-625C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 13/15 | chr12 | 109787462 | |||||||
| chr12:109787838 | C | T | 1 | a0001c0004t0001g0190 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2208+562G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 13/15 | chr12 | 109787838 | |||||||
| chr12:109787920 | C | T | 1 | a0001c0004t0001g0190 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2208+480G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 13/15 | chr12 | 109787920 | |||||||
| chr12:109787923 | G | A | 1 | a0001c0003t0001g0081 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2208+477C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 13/15 | chr12 | 109787923 | |||||||
| chr12:109787969 | T | G | 1 | a0010c0021t0001g0125 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2208+431A>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 13/15 | chr12 | 109787969 | |||||||
| chr12:109788067 | C | A | 5 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0004t0001g0140 others(2): Show |
5 | HG01109.hp1 HG02109.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.2208+333G>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 13/15 | chr12 | 109788067 | |||||||
| chr12:109788118 | C | G | 124 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0090 others(121): Show |
134 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.2208+282G>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 13/15 | chr12 | 109788118 | |||||||
| chr12:109788162 | C | T | 1 | a0001c0009t0001g0046 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2208+238G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 13/15 | chr12 | 109788162 | |||||||
| chr12:109788181 | C | T | 2 | a0001c0004t0001g0117 a0001c0004t0001g0118 |
2 | HG02630.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2208+219G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 13/15 | chr12 | 109788181 | |||||||
| chr12:109788257 | C | A | 1 | a0002c0006t0001g0035 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2208+143G>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 13/15 | chr12 | 109788257 | |||||||
| chr12:109788867 | C | T | 2 | a0001c0005t0001g0036 a0001c0005t0002g0037 |
2 | HG02258.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.1892-151G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 12/15 | chr12 | 109788867 | |||||||
| chr12:109788991 | A | G | 124 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0090 others(121): Show |
134 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.1892-275T>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 12/15 | chr12 | 109788991 | |||||||
| chr12:109789148 | G | C | 2 | a0001c0003t0001g0009 a0001c0003t0001g0109 |
3 | NA18948.hp2 NA18982.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.1892-432C>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 12/15 | chr12 | 109789148 | |||||||
| chr12:109789225 | A | G | 12 | a0001c0001t0001g0162 a0001c0001t0001g0224 a0001c0001t0001g0225 others(9): Show |
12 | HG01891.hp2 HG02055.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.1892-509T>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 12/15 | chr12 | 109789225 | |||||||
| chr12:109789290 | C | A | 1 | a0001c0009t0001g0045 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1892-574G>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 12/15 | chr12 | 109789290 | |||||||
| chr12:109789392 | C | T | 1 | a0010c0021t0001g0125 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1892-676G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 12/15 | chr12 | 109789392 | |||||||
| chr12:109789513 | G | A | 3 | a0001c0012t0001g0006 a0001c0012t0001g0032 a0001c0025t0001g0067 |
4 | HG02559.hp1 HG02922.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1892-797C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 12/15 | chr12 | 109789513 | |||||||
| chr12:109789562 | G | C | 8 | a0003c0007t0001g0089 a0003c0007t0001g0091 a0003c0007t0001g0092 others(5): Show |
8 | HG01192.hp2 HG01496.hp2 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.1892-846C>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 12/15 | chr12 | 109789562 | |||||||
| chr12:109790160 | C | T | 168 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(165): Show |
184 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.1892-1444G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 12/15 | chr12 | 109790160 | |||||||
| chr12:109790250 | C | T | 32 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(29): Show |
38 | HG00408.hp2 HG00423.hp1 HG00609.hp2 others(35): Show |
intron_variant | MODIFIER | c.1892-1534G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 12/15 | chr12 | 109790250 | |||||||
| chr12:109790619 | G | A | 1 | a0001c0001t0001g0310 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1891+1744C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 12/15 | chr12 | 109790619 | |||||||
| chr12:109790621 | G | A | 5 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0004t0001g0140 others(2): Show |
5 | HG01109.hp1 HG02109.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.1891+1742C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 12/15 | chr12 | 109790621 | |||||||
| chr12:109790708 | C | T | 3 | a0004c0010t0001g0220 a0004c0010t0001g0222 a0004c0010t0001g0223 |
3 | HG00738.hp2 HG01069.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.1891+1655G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 12/15 | chr12 | 109790708 | |||||||
| chr12:109790719 | CA | C | 12 | a0001c0004t0001g0312 a0001c0005t0001g0029 a0001c0005t0001g0074 others(9): Show |
12 | HG00738.hp2 HG01069.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.1891+1643delT | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 12/15 | chr12 | 109790719 | |||||||
| chr12:109790878 | G | A | 77 | a0001c0001t0001g0311 a0001c0002t0001g0001 a0001c0002t0001g0010 others(74): Show |
87 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.1891+1485C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 12/15 | chr12 | 109790878 | |||||||
| chr12:109790891 | C | T | 1 | a0002c0006t0001g0285 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1891+1472G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 12/15 | chr12 | 109790891 | |||||||
| chr12:109791089 | C | T | 76 | a0001c0001t0001g0311 a0001c0002t0001g0001 a0001c0002t0001g0010 others(73): Show |
86 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.1891+1274G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 12/15 | chr12 | 109791089 | |||||||
| chr12:109791100 | T | C | 11 | a0001c0001t0001g0162 a0001c0001t0001g0214 a0001c0001t0001g0224 others(8): Show |
13 | HG01167.hp1 HG01884.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.1891+1263A>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 12/15 | chr12 | 109791100 | |||||||
| chr12:109791297 | C | T | 1 | a0001c0005t0001g0085 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1891+1066G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 12/15 | chr12 | 109791297 | |||||||
| chr12:109791351 | A | T | 2 | a0001c0004t0001g0140 a0001c0004t0001g0198 |
2 | HG01109.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.1891+1012T>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 12/15 | chr12 | 109791351 | |||||||
| chr12:109791382 | A | G | 1 | a0006c0017t0001g0308 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1891+981T>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 12/15 | chr12 | 109791382 | |||||||
| chr12:109791452 | T | G | 1 | a0001c0002t0001g0135 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1891+911A>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 12/15 | chr12 | 109791452 | |||||||
| chr12:109791453 | A | G | 15 | a0001c0001t0001g0162 a0001c0001t0001g0224 a0001c0001t0001g0225 others(12): Show |
15 | HG00738.hp2 HG01069.hp1 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.1891+910T>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 12/15 | chr12 | 109791453 | |||||||
| chr12:109791479 | C | CT | 20 | a0001c0001t0001g0265 a0001c0001t0001g0267 a0001c0001t0001g0280 others(17): Show |
20 | HG00438.hp1 HG00438.hp2 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.1891+883dupA | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 12/15 | chr12 | 109791479 | |||||||
| chr12:109791479 | CT | C | 14 | a0001c0001t0001g0266 a0001c0001t0001g0269 a0001c0002t0001g0189 others(11): Show |
14 | HG02572.hp1 HG02615.hp2 HG02717.hp2 others(11): Show |
intron_variant | MODIFIER | c.1891+883delA | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 12/15 | chr12 | 109791479 | |||||||
| chr12:109791519 | G | A | 1 | a0001c0003t0001g0304 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1891+844C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 12/15 | chr12 | 109791519 | |||||||
| chr12:109791574 | CT | C | 3 | a0004c0010t0001g0220 a0004c0010t0001g0222 a0004c0010t0001g0223 |
3 | HG00738.hp2 HG01069.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.1891+788delA | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 12/15 | chr12 | 109791574 | |||||||
| chr12:109791602 | C | T | 1 | a0001c0009t0001g0048 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1891+761G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 12/15 | chr12 | 109791602 | |||||||
| chr12:109791629 | C | A | 2 | a0001c0001t0001g0130 a0001c0001t0001g0155 |
2 | HG00099.hp1 HG00733.hp1 |
intron_variant | MODIFIER | c.1891+734G>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 12/15 | chr12 | 109791629 | |||||||
| chr12:109791630 | G | A | 1 | a0001c0005t0001g0192 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1891+733C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 12/15 | chr12 | 109791630 | |||||||
| chr12:109791909 | G | A | 1 | a0001c0001t0001g0291 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1891+454C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 12/15 | chr12 | 109791909 | |||||||
| chr12:109791991 | G | A | 3 | a0004c0010t0001g0220 a0004c0010t0001g0222 a0004c0010t0001g0223 |
3 | HG00738.hp2 HG01069.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.1891+372C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 12/15 | chr12 | 109791991 | |||||||
| chr12:109792038 | A | C | 89 | a0001c0001t0001g0311 a0001c0002t0001g0001 a0001c0002t0001g0010 others(86): Show |
99 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.1891+325T>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 12/15 | chr12 | 109792038 | |||||||
| chr12:109792076 | C | CA | 96 | a0001c0001t0001g0162 a0001c0001t0001g0214 a0001c0001t0001g0224 others(93): Show |
108 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.1891+286dupT | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 12/15 | chr12 | 109792076 | |||||||
| chr12:109792218 | G | A | 1 | a0001c0001t0001g0265 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1891+145C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 12/15 | chr12 | 109792218 | |||||||
| chr12:109792243 | C | CA | 20 | a0001c0001t0001g0090 a0001c0001t0001g0215 a0001c0001t0001g0225 others(17): Show |
20 | HG00438.hp1 HG00438.hp2 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.1891+119dupT | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 12/15 | chr12 | 109792243 | |||||||
| chr12:109792243 | CA | C | 9 | a0001c0001t0001g0234 a0001c0001t0001g0274 a0001c0002t0001g0173 others(6): Show |
10 | HG01256.hp2 HG01516.hp2 HG02129.hp2 others(7): Show |
intron_variant | MODIFIER | c.1891+119delT | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 12/15 | chr12 | 109792243 | |||||||
| chr12:109792315 | C | T | 10 | a0001c0003t0001g0059 a0001c0003t0001g0061 a0001c0003t0001g0077 others(7): Show |
10 | HG01168.hp1 HG01243.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.1891+48G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 12/15 | chr12 | 109792315 | |||||||
| chr12:109792443 | C | T | 1 | a0001c0002t0001g0193 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1825-14G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 11/15 | chr12 | 109792443 | |||||||
| chr12:109792546 | C | A | 1 | a0001c0001t0001g0263 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1824+106G>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 11/15 | chr12 | 109792546 | |||||||
| chr12:109792548 | C | T | 1 | a0001c0004t0001g0141 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1824+104G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 11/15 | chr12 | 109792548 | |||||||
| chr12:109792648 | G | A | 1 | a0001c0003t0001g0196 | 1 | HG03041.hp2 | splice_region_variant&intron_variant | LOW | c.1824+4C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 11/15 | chr12 | 109792648 | |||||||
| chr12:109792907 | G | A | 77 | a0001c0001t0001g0311 a0001c0002t0001g0001 a0001c0002t0001g0010 others(74): Show |
87 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.1659-90C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 10/15 | chr12 | 109792907 | |||||||
| chr12:109793043 | G | T | 1 | a0002c0006t0001g0058 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1659-226C>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 10/15 | chr12 | 109793043 | |||||||
| chr12:109793065 | G | A | 1 | a0001c0005t0001g0157 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1659-248C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 10/15 | chr12 | 109793065 | |||||||
| chr12:109793153 | C | A | 1 | a0001c0001t0001g0256 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1659-336G>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 10/15 | chr12 | 109793153 | |||||||
| chr12:109793383 | C | G | 3 | a0001c0008t0001g0069 a0001c0008t0001g0070 a0001c0008t0001g0072 |
3 | HG02257.hp2 HG02886.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1658+144G>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 10/15 | chr12 | 109793383 | |||||||
| chr12:109793467 | C | T | 1 | a0001c0001t0001g0265 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1658+60G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 10/15 | chr12 | 109793467 | |||||||
| chr12:109793468 | T | A | 1 | a0001c0001t0001g0265 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1658+59A>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 10/15 | chr12 | 109793468 | |||||||
| chr12:109793469 | A | G | 1 | a0001c0001t0001g0265 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1658+58T>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 10/15 | chr12 | 109793469 | |||||||
| chr12:109793509 | C | T | 1 | a0003c0007t0001g0154 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1658+18G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 10/15 | chr12 | 109793509 | |||||||
| chr12:109793718 | C | T | 1 | a0001c0001t0001g0100 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1585-118G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 9/15 | chr12 | 109793718 | |||||||
| chr12:109793912 | C | G | 38 | a0001c0001t0001g0100 a0001c0001t0001g0131 a0001c0001t0001g0132 others(35): Show |
41 | HG00323.hp2 HG00597.hp2 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.1584+18G>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 9/15 | chr12 | 109793912 | |||||||
| chr12:109794077 | C | T | 2 | a0004c0010t0001g0222 a0004c0010t0001g0223 |
2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.1492-55G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 8/15 | chr12 | 109794077 | |||||||
| chr12:109794227 | G | A | 26 | a0001c0003t0001g0059 a0001c0003t0001g0061 a0001c0003t0001g0077 others(23): Show |
26 | HG00639.hp1 HG00642.hp1 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.1491+102C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 8/15 | chr12 | 109794227 | |||||||
| chr12:109794229 | G | T | 26 | a0001c0003t0001g0059 a0001c0003t0001g0061 a0001c0003t0001g0077 others(23): Show |
26 | HG00639.hp1 HG00642.hp1 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.1491+100C>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 8/15 | chr12 | 109794229 | |||||||
| chr12:109794243 | G | C | 11 | a0001c0004t0001g0003 a0001c0004t0001g0005 a0001c0004t0001g0040 others(8): Show |
14 | HG01109.hp1 HG01167.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1491+86C>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 8/15 | chr12 | 109794243 | |||||||
| chr12:109794611 | T | C | 3 | a0001c0001t0001g0162 a0001c0001t0001g0224 a0001c0001t0001g0225 |
3 | HG01891.hp2 HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1333-124A>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 7/15 | chr12 | 109794611 | |||||||
| chr12:109794839 | G | A | 48 | a0001c0001t0001g0254 a0001c0005t0001g0027 a0001c0005t0001g0029 others(45): Show |
51 | HG00597.hp1 HG00642.hp1 HG01099.hp1 others(48): Show |
intron_variant | MODIFIER | c.1333-352C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 7/15 | chr12 | 109794839 | |||||||
| chr12:109794879 | G | A | 97 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(94): Show |
107 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.1333-392C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 7/15 | chr12 | 109794879 | |||||||
| chr12:109794882 | G | C | 1 | a0001c0002t0001g0236 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1333-395C>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 7/15 | chr12 | 109794882 | |||||||
| chr12:109794886 | T | C | 1 | a0001c0003t0001g0151 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1333-399A>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 7/15 | chr12 | 109794886 | |||||||
| chr12:109794918 | T | G | 154 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(151): Show |
167 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.1333-431A>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 7/15 | chr12 | 109794918 | |||||||
| chr12:109794972 | C | T | 1 | a0001c0004t0001g0141 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1333-485G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 7/15 | chr12 | 109794972 | |||||||
| chr12:109795063 | A | G | 1 | a0006c0017t0001g0308 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1333-576T>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 7/15 | chr12 | 109795063 | |||||||
| chr12:109795160 | G | A | 1 | a0001c0001t0001g0216 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1333-673C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 7/15 | chr12 | 109795160 | |||||||
| chr12:109795450 | A | C | 1 | a0001c0002t0001g0171 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1333-963T>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 7/15 | chr12 | 109795450 | |||||||
| chr12:109795486 | T | G | 52 | a0001c0005t0001g0016 a0001c0005t0001g0027 a0001c0005t0001g0029 others(49): Show |
56 | HG00597.hp1 HG00642.hp1 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.1333-999A>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 7/15 | chr12 | 109795486 | |||||||
| chr12:109795606 | G | A | 12 | a0001c0005t0001g0029 a0001c0005t0001g0074 a0001c0005t0001g0085 others(9): Show |
12 | HG02257.hp2 HG02559.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.1332+919C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 7/15 | chr12 | 109795606 | |||||||
| chr12:109795695 | C | T | 52 | a0001c0005t0001g0016 a0001c0005t0001g0027 a0001c0005t0001g0029 others(49): Show |
56 | HG00597.hp1 HG00642.hp1 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.1332+830G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 7/15 | chr12 | 109795695 | |||||||
| chr12:109795712 | T | C | 1 | a0001c0002t0001g0258 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1332+813A>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 7/15 | chr12 | 109795712 | |||||||
| chr12:109795721 | A | G | 144 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(141): Show |
158 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.1332+804T>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 7/15 | chr12 | 109795721 | |||||||
| chr12:109795735 | T | C | 44 | a0001c0005t0001g0016 a0001c0005t0001g0027 a0001c0005t0001g0029 others(41): Show |
48 | HG00597.hp1 HG00642.hp1 HG01099.hp1 others(45): Show |
intron_variant | MODIFIER | c.1332+790A>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 7/15 | chr12 | 109795735 | |||||||
| chr12:109795737 | TTTTG | T | 3 | a0004c0010t0001g0222 a0004c0010t0001g0223 a0010c0021t0001g0125 |
3 | HG00738.hp2 HG01069.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1332+784_1332+787d others(6): Show |
TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 7/15 | chr12 | 109795737 | |||||||
| chr12:109795901 | C | G | 2 | a0001c0002t0001g0152 a0001c0002t0001g0156 |
2 | NA18992.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.1332+624G>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 7/15 | chr12 | 109795901 | |||||||
| chr12:109795929 | A | AT | 239 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(236): Show |
267 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(264): Show |
intron_variant | MODIFIER | c.1332+595dupA | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 7/15 | chr12 | 109795929 | |||||||
| chr12:109795939 | G | T | 259 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(256): Show |
287 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(284): Show |
intron_variant | MODIFIER | c.1332+586C>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 7/15 | chr12 | 109795939 | |||||||
| chr12:109796017 | C | G | 3 | a0001c0020t0001g0160 a0004c0010t0001g0222 a0004c0010t0001g0223 |
3 | HG00738.hp2 HG01069.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1332+508G>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 7/15 | chr12 | 109796017 | |||||||
| chr12:109796056 | A | G | 52 | a0001c0005t0001g0016 a0001c0005t0001g0027 a0001c0005t0001g0029 others(49): Show |
56 | HG00597.hp1 HG00642.hp1 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.1332+469T>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 7/15 | chr12 | 109796056 | |||||||
| chr12:109796474 | C | A | 2 | a0002c0006t0001g0050 a0002c0006t0001g0051 |
2 | NA18952.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.1332+51G>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 7/15 | chr12 | 109796474 | |||||||
| chr12:109796508 | C | T | 1 | a0001c0002t0001g0152 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1332+17G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 7/15 | chr12 | 109796508 | |||||||
| chr12:109796853 | T | C | 101 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(98): Show |
111 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.1153-149A>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 6/15 | chr12 | 109796853 | |||||||
| chr12:109796893 | C | T | 49 | a0001c0005t0001g0016 a0001c0005t0001g0027 a0001c0005t0001g0029 others(46): Show |
53 | HG00597.hp1 HG00642.hp1 HG01099.hp1 others(50): Show |
intron_variant | MODIFIER | c.1153-189G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 6/15 | chr12 | 109796893 | |||||||
| chr12:109796902 | T | C | 2 | a0001c0005t0001g0036 a0001c0005t0002g0037 |
2 | HG02258.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.1153-198A>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 6/15 | chr12 | 109796902 | |||||||
| chr12:109796958 | A | G | 2 | a0001c0005t0001g0029 a0001c0005t0001g0074 |
2 | HG02572.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1153-254T>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 6/15 | chr12 | 109796958 | |||||||
| chr12:109797134 | G | A | 2 | a0004c0010t0001g0222 a0004c0010t0001g0223 |
2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.1153-430C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 6/15 | chr12 | 109797134 | |||||||
| chr12:109797137 | C | T | 20 | a0001c0005t0001g0126 a0001c0005t0001g0128 a0001c0005t0001g0149 others(17): Show |
23 | HG00597.hp1 HG02015.hp2 HG02132.hp1 others(20): Show |
intron_variant | MODIFIER | c.1153-433G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 6/15 | chr12 | 109797137 | |||||||
| chr12:109797365 | G | T | 5 | a0001c0005t0001g0126 a0001c0005t0001g0128 a0001c0005t0001g0149 others(2): Show |
5 | HG02698.hp2 HG03654.hp1 HG03688.hp2 others(2): Show |
intron_variant | MODIFIER | c.1153-661C>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 6/15 | chr12 | 109797365 | |||||||
| chr12:109797465 | G | T | 2 | a0004c0010t0001g0222 a0004c0010t0001g0223 |
2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.1153-761C>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 6/15 | chr12 | 109797465 | |||||||
| chr12:109797705 | T | A | 52 | a0001c0005t0001g0016 a0001c0005t0001g0027 a0001c0005t0001g0029 others(49): Show |
56 | HG00597.hp1 HG00642.hp1 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.1152+909A>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 6/15 | chr12 | 109797705 | |||||||
| chr12:109797716 | T | G | 1 | a0001c0001t0001g0276 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1152+898A>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 6/15 | chr12 | 109797716 | |||||||
| chr12:109797827 | A | G | 52 | a0001c0005t0001g0016 a0001c0005t0001g0027 a0001c0005t0001g0029 others(49): Show |
56 | HG00597.hp1 HG00642.hp1 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.1152+787T>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 6/15 | chr12 | 109797827 | |||||||
| chr12:109798039 | G | A | 1 | a0001c0002t0001g0178 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1152+575C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 6/15 | chr12 | 109798039 | |||||||
| chr12:109798300 | G | A | 1 | a0001c0001t0001g0266 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1152+314C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 6/15 | chr12 | 109798300 | |||||||
| chr12:109798301 | A | G | 1 | a0001c0001t0001g0266 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1152+313T>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 6/15 | chr12 | 109798301 | |||||||
| chr12:109798314 | C | T | 31 | a0001c0005t0001g0016 a0001c0005t0001g0027 a0001c0005t0001g0029 others(28): Show |
32 | HG00642.hp1 HG00738.hp2 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.1152+300G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 6/15 | chr12 | 109798314 | |||||||
| chr12:109798351 | T | C | 1 | a0001c0020t0001g0160 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1152+263A>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 6/15 | chr12 | 109798351 | |||||||
| chr12:109798403 | T | C | 1 | a0001c0002t0001g0194 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1152+211A>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 6/15 | chr12 | 109798403 | |||||||
| chr12:109798542 | A | G | 3 | a0001c0020t0001g0160 a0004c0010t0001g0222 a0004c0010t0001g0223 |
3 | HG00738.hp2 HG01069.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1152+72T>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 6/15 | chr12 | 109798542 | |||||||
| chr12:109798574 | C | T | 4 | a0001c0008t0001g0069 a0001c0008t0001g0070 a0001c0008t0001g0071 others(1): Show |
4 | HG02257.hp2 HG02559.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1152+40G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 6/15 | chr12 | 109798574 | |||||||
| chr12:109798917 | G | A | 4 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0214 others(1): Show |
4 | HG01884.hp2 HG02145.hp1 HG02922.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.854-5C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 5/15 | chr12 | 109798917 | |||||||
| chr12:109798996 | C | T | 2 | a0004c0010t0001g0222 a0004c0010t0001g0223 |
2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.854-84G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 5/15 | chr12 | 109798996 | |||||||
| chr12:109799142 | A | G | 2 | a0004c0010t0001g0222 a0004c0010t0001g0223 |
2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.854-230T>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 5/15 | chr12 | 109799142 | |||||||
| chr12:109799148 | G | A | 3 | a0001c0005t0001g0126 a0001c0005t0001g0128 a0001c0005t0001g0149 |
3 | HG03654.hp1 HG03688.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.854-236C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 5/15 | chr12 | 109799148 | |||||||
| chr12:109799211 | G | A | 1 | a0001c0001t0001g0214 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.854-299C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 5/15 | chr12 | 109799211 | |||||||
| chr12:109799222 | G | A | 2 | a0001c0004t0001g0140 a0001c0004t0001g0198 |
2 | HG01109.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.854-310C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 5/15 | chr12 | 109799222 | |||||||
| chr12:109799336 | G | A | 1 | a0001c0002t0001g0177 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.854-424C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 5/15 | chr12 | 109799336 | |||||||
| chr12:109799366 | C | T | 2 | a0001c0004t0001g0141 a0001c0015t0001g0119 |
2 | NA18954.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.854-454G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 5/15 | chr12 | 109799366 | |||||||
| chr12:109799927 | CTTAT | C | 248 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(245): Show |
275 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.853+687_853+690del others(4): Show |
TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 5/15 | chr12 | 109799927 | |||||||
| chr12:109799927 | CTTATTTA others(1): Show |
C | 52 | a0001c0005t0001g0016 a0001c0005t0001g0027 a0001c0005t0001g0029 others(49): Show |
56 | HG00597.hp1 HG00642.hp1 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.853+683_853+690del others(8): Show |
TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 5/15 | chr12 | 109799927 | |||||||
| chr12:109799966 | A | G | 158 | a0001c0001t0001g0100 a0001c0001t0001g0166 a0001c0001t0001g0169 others(155): Show |
176 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(173): Show |
intron_variant | MODIFIER | c.853+652T>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 5/15 | chr12 | 109799966 | |||||||
| chr12:109800224 | C | T | 3 | a0001c0020t0001g0160 a0004c0010t0001g0222 a0004c0010t0001g0223 |
3 | HG00738.hp2 HG01069.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.853+394G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 5/15 | chr12 | 109800224 | |||||||
| chr12:109800243 | C | G | 1 | a0001c0011t0001g0145 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.853+375G>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 5/15 | chr12 | 109800243 | |||||||
| chr12:109800272 | G | T | 8 | a0001c0002t0001g0101 a0001c0002t0001g0114 a0001c0002t0001g0171 others(5): Show |
8 | HG00735.hp2 HG00738.hp1 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.853+346C>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 5/15 | chr12 | 109800272 | |||||||
| chr12:109800279 | T | A | 10 | a0001c0004t0001g0003 a0001c0004t0001g0005 a0001c0004t0001g0040 others(7): Show |
13 | HG01167.hp1 HG02280.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.853+339A>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 5/15 | chr12 | 109800279 | |||||||
| chr12:109800410 | A | G | 254 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(251): Show |
282 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.853+208T>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 5/15 | chr12 | 109800410 | |||||||
| chr12:109800410 | A | T | 1 | a0001c0001t0001g0266 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.853+208T>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 5/15 | chr12 | 109800410 | |||||||
| chr12:109800411 | C | CCAAGTT | 254 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(251): Show |
282 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.853+206_853+207ins others(6): Show |
TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 5/15 | chr12 | 109800411 | |||||||
| chr12:109800412 | T | C | 255 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(252): Show |
283 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.853+206A>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 5/15 | chr12 | 109800412 | |||||||
| chr12:109800460 | A | G | 52 | a0001c0005t0001g0016 a0001c0005t0001g0027 a0001c0005t0001g0029 others(49): Show |
56 | HG00597.hp1 HG00642.hp1 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.853+158T>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 5/15 | chr12 | 109800460 | |||||||
| chr12:109800462 | C | T | 3 | a0001c0003t0001g0075 a0001c0003t0001g0151 a0001c0003t0001g0163 |
3 | HG01943.hp2 HG02622.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.853+156G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 5/15 | chr12 | 109800462 | |||||||
| chr12:109800497 | A | G | 44 | a0001c0005t0001g0016 a0001c0005t0001g0027 a0001c0005t0001g0029 others(41): Show |
48 | HG00597.hp1 HG00642.hp1 HG01099.hp1 others(45): Show |
intron_variant | MODIFIER | c.853+121T>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 5/15 | chr12 | 109800497 | |||||||
| chr12:109800791 | G | A | 10 | a0001c0001t0001g0022 a0001c0001t0001g0138 a0001c0001t0001g0197 others(7): Show |
11 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(8): Show |
intron_variant | MODIFIER | c.713-33C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 4/15 | chr12 | 109800791 | |||||||
| chr12:109800819 | G | C | 2 | a0001c0009t0001g0048 a0001c0009t0001g0049 |
2 | HG02647.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.713-61C>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 4/15 | chr12 | 109800819 | |||||||
| chr12:109800843 | G | A | 2 | a0002c0006t0001g0050 a0002c0006t0001g0051 |
2 | NA18952.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.713-85C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 4/15 | chr12 | 109800843 | |||||||
| chr12:109800854 | G | C | 1 | a0006c0018t0001g0076 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.713-96C>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 4/15 | chr12 | 109800854 | |||||||
| chr12:109801026 | C | A | 1 | a0001c0019t0001g0309 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.713-268G>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 4/15 | chr12 | 109801026 | |||||||
| chr12:109801106 | C | A | 3 | a0001c0001t0001g0162 a0001c0001t0001g0224 a0001c0001t0001g0225 |
3 | HG01891.hp2 HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.713-348G>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 4/15 | chr12 | 109801106 | |||||||
| chr12:109801206 | C | T | 1 | a0001c0020t0001g0160 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.713-448G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 4/15 | chr12 | 109801206 | |||||||
| chr12:109801336 | T | A | 1 | a0001c0002t0001g0178 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.713-578A>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 4/15 | chr12 | 109801336 | |||||||
| chr12:109801471 | T | C | 1 | a0001c0020t0001g0160 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.713-713A>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 4/15 | chr12 | 109801471 | |||||||
| chr12:109801632 | G | A | 50 | a0001c0005t0001g0016 a0001c0005t0001g0027 a0001c0005t0001g0029 others(47): Show |
54 | HG00597.hp1 HG00642.hp1 HG01099.hp1 others(51): Show |
intron_variant | MODIFIER | c.713-874C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 4/15 | chr12 | 109801632 | |||||||
| chr12:109801645 | C | T | 1 | a0002c0032t0001g0065 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.713-887G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 4/15 | chr12 | 109801645 | |||||||
| chr12:109802090 | T | C | 1 | a0001c0002t0001g0189 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.712+901A>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 4/15 | chr12 | 109802090 | |||||||
| chr12:109802130 | C | CT | 46 | a0001c0001t0001g0214 a0001c0001t0001g0216 a0001c0005t0001g0016 others(43): Show |
51 | HG00597.hp1 HG00738.hp2 HG01069.hp1 others(48): Show |
intron_variant | MODIFIER | c.712+860dupA | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 4/15 | chr12 | 109802130 | |||||||
| chr12:109802130 | CT | C | 100 | a0001c0001t0001g0100 a0001c0001t0001g0166 a0001c0001t0001g0169 others(97): Show |
113 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(110): Show |
intron_variant | MODIFIER | c.712+860delA | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 4/15 | chr12 | 109802130 | |||||||
| chr12:109802197 | A | G | 1 | a0001c0020t0001g0160 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.712+794T>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 4/15 | chr12 | 109802197 | |||||||
| chr12:109802305 | C | CT | 46 | a0001c0002t0001g0159 a0001c0005t0001g0016 a0001c0005t0001g0027 others(43): Show |
50 | HG00597.hp1 HG00642.hp1 HG01099.hp1 others(47): Show |
intron_variant | MODIFIER | c.712+685dupA | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 4/15 | chr12 | 109802305 | |||||||
| chr12:109802322 | G | A | 48 | a0001c0005t0001g0016 a0001c0005t0001g0027 a0001c0005t0001g0029 others(45): Show |
52 | HG00597.hp1 HG00642.hp1 HG01099.hp1 others(49): Show |
intron_variant | MODIFIER | c.712+669C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 4/15 | chr12 | 109802322 | |||||||
| chr12:109802344 | C | T | 1 | a0001c0003t0001g0168 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.712+647G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 4/15 | chr12 | 109802344 | |||||||
| chr12:109802363 | G | A | 1 | a0001c0001t0001g0129 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.712+628C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 4/15 | chr12 | 109802363 | |||||||
| chr12:109802367 | T | C | 1 | a0001c0002t0001g0179 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.712+624A>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 4/15 | chr12 | 109802367 | |||||||
| chr12:109802399 | T | C | 1 | a0001c0001t0001g0251 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.712+592A>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 4/15 | chr12 | 109802399 | |||||||
| chr12:109802521 | T | G | 94 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(91): Show |
104 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.712+470A>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 4/15 | chr12 | 109802521 | |||||||
| chr12:109802566 | T | A | 1 | a0001c0023t0001g0033 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.712+425A>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 4/15 | chr12 | 109802566 | |||||||
| chr12:109802604 | C | CTTTTA | 5 | a0001c0005t0001g0126 a0001c0005t0001g0128 a0001c0005t0001g0149 others(2): Show |
5 | HG02698.hp2 HG03654.hp1 HG03688.hp2 others(2): Show |
intron_variant | MODIFIER | c.712+382_712+386dup others(5): Show |
TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 4/15 | chr12 | 109802604 | |||||||
| chr12:109802614 | A | AT | 9 | a0001c0001t0001g0022 a0001c0001t0001g0138 a0001c0001t0001g0197 others(6): Show |
10 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(7): Show |
intron_variant | MODIFIER | c.712+376dupA | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 4/15 | chr12 | 109802614 | |||||||
| chr12:109802614 | A | ATT | 88 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(85): Show |
97 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.712+375_712+376dup others(2): Show |
TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 4/15 | chr12 | 109802614 | |||||||
| chr12:109802615 | T | TTTTA | 41 | a0001c0005t0001g0016 a0001c0005t0001g0027 a0001c0005t0001g0029 others(38): Show |
45 | HG00597.hp1 HG00642.hp1 HG01099.hp1 others(42): Show |
intron_variant | MODIFIER | c.712+375_712+376ins others(4): Show |
TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 4/15 | chr12 | 109802615 | |||||||
| chr12:109802617 | T | TTA | 95 | a0001c0001t0001g0100 a0001c0001t0001g0166 a0001c0001t0001g0169 others(92): Show |
106 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.712+373_712+374ins others(2): Show |
TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 4/15 | chr12 | 109802617 | |||||||
| chr12:109802618 | T | TA | 12 | a0001c0004t0001g0003 a0001c0004t0001g0005 a0001c0004t0001g0040 others(9): Show |
15 | HG01109.hp1 HG01167.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.712+372_712+373ins others(1): Show |
TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 4/15 | chr12 | 109802618 | |||||||
| chr12:109802749 | C | T | 1 | a0001c0001t0001g0311 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.712+242G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 4/15 | chr12 | 109802749 | |||||||
| chr12:109802821 | T | A | 1 | a0001c0003t0001g0232 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.712+170A>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 4/15 | chr12 | 109802821 | |||||||
| chr12:109802838 | G | GCATC | 50 | a0001c0005t0001g0016 a0001c0005t0001g0027 a0001c0005t0001g0029 others(47): Show |
54 | HG00597.hp1 HG00642.hp1 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.712+149_712+152dup others(4): Show |
TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 4/15 | chr12 | 109802838 | |||||||
| chr12:109802875 | A | G | 4 | a0001c0008t0001g0069 a0001c0008t0001g0070 a0001c0008t0001g0071 others(1): Show |
4 | HG02257.hp2 HG02559.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.712+116T>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 4/15 | chr12 | 109802875 | |||||||
| chr12:109802981 | G | A | 1 | a0006c0017t0001g0308 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.712+10C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 4/15 | chr12 | 109802981 | |||||||
| chr12:109803173 | G | A | 1 | a0001c0002t0001g0302 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.560-30C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/15 | chr12 | 109803173 | |||||||
| chr12:109803349 | G | A | 2 | a0001c0001t0001g0143 a0001c0001t0001g0213 |
2 | HG01081.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.560-206C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/15 | chr12 | 109803349 | |||||||
| chr12:109803354 | G | A | 1 | a0001c0009t0001g0046 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.560-211C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/15 | chr12 | 109803354 | |||||||
| chr12:109803471 | G | A | 1 | a0001c0004t0001g0204 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.560-328C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/15 | chr12 | 109803471 | |||||||
| chr12:109803640 | G | A | 103 | a0001c0001t0001g0100 a0001c0001t0001g0166 a0001c0001t0001g0169 others(100): Show |
117 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(114): Show |
intron_variant | MODIFIER | c.560-497C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/15 | chr12 | 109803640 | |||||||
| chr12:109803835 | T | C | 4 | a0001c0005t0001g0085 a0001c0005t0001g0086 a0001c0005t0001g0087 others(1): Show |
4 | HG02615.hp2 HG02976.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.560-692A>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/15 | chr12 | 109803835 | |||||||
| chr12:109803860 | C | G | 1 | a0001c0001t0001g0281 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.560-717G>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/15 | chr12 | 109803860 | |||||||
| chr12:109803878 | G | A | 93 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(90): Show |
103 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.560-735C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/15 | chr12 | 109803878 | |||||||
| chr12:109803927 | T | C | 2 | a0001c0012t0001g0006 a0001c0012t0001g0032 |
3 | HG02559.hp1 HG02922.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.560-784A>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/15 | chr12 | 109803927 | |||||||
| chr12:109803944 | CT | C | 22 | a0001c0005t0001g0016 a0001c0005t0001g0027 a0001c0005t0001g0029 others(19): Show |
23 | HG00642.hp1 HG01099.hp1 HG01123.hp2 others(20): Show |
intron_variant | MODIFIER | c.560-802delA | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/15 | chr12 | 109803944 | |||||||
| chr12:109804013 | T | G | 94 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(91): Show |
104 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.560-870A>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/15 | chr12 | 109804013 | |||||||
| chr12:109804020 | G | A | 11 | a0001c0005t0001g0016 a0001c0005t0001g0157 a0001c0005t0001g0158 others(8): Show |
12 | HG00642.hp1 HG01099.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.560-877C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/15 | chr12 | 109804020 | |||||||
| chr12:109804346 | G | A | 2 | a0001c0003t0001g0075 a0001c0003t0001g0307 |
2 | HG02293.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.560-1203C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/15 | chr12 | 109804346 | |||||||
| chr12:109804561 | A | G | 6 | a0001c0003t0001g0062 a0001c0003t0001g0139 a0001c0003t0001g0163 others(3): Show |
6 | HG01943.hp2 HG02809.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.560-1418T>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/15 | chr12 | 109804561 | |||||||
| chr12:109804572 | G | A | 95 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(92): Show |
105 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.560-1429C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/15 | chr12 | 109804572 | |||||||
| chr12:109804601 | G | A | 1 | a0001c0005t0001g0063 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.560-1458C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/15 | chr12 | 109804601 | |||||||
| chr12:109804637 | T | C | 1 | a0001c0020t0001g0160 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.560-1494A>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/15 | chr12 | 109804637 | |||||||
| chr12:109804742 | C | T | 1 | a0001c0013t0001g0294 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.560-1599G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/15 | chr12 | 109804742 | |||||||
| chr12:109804776 | A | G | 156 | a0001c0001t0001g0100 a0001c0001t0001g0166 a0001c0001t0001g0169 others(153): Show |
174 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(171): Show |
intron_variant | MODIFIER | c.560-1633T>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/15 | chr12 | 109804776 | |||||||
| chr12:109804797 | T | C | 24 | a0001c0005t0001g0063 a0001c0005t0001g0126 a0001c0005t0001g0128 others(21): Show |
27 | HG00597.hp1 HG02015.hp2 HG02132.hp1 others(24): Show |
intron_variant | MODIFIER | c.560-1654A>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/15 | chr12 | 109804797 | |||||||
| chr12:109804827 | C | A | 1 | a0001c0024t0001g0218 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.560-1684G>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/15 | chr12 | 109804827 | |||||||
| chr12:109804984 | A | G | 3 | a0001c0003t0001g0079 a0001c0003t0001g0080 a0001c0003t0001g0081 |
3 | HG01168.hp1 HG02109.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.560-1841T>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/15 | chr12 | 109804984 | |||||||
| chr12:109805128 | A | C | 254 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(251): Show |
282 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.560-1985T>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/15 | chr12 | 109805128 | |||||||
| chr12:109805146 | C | G | 1 | a0001c0002t0001g0106 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.560-2003G>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/15 | chr12 | 109805146 | |||||||
| chr12:109805177 | G | A | 2 | a0001c0005t0001g0063 a0001c0025t0001g0067 |
2 | HG02486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.560-2034C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/15 | chr12 | 109805177 | |||||||
| chr12:109805201 | C | G | 1 | a0010c0021t0001g0125 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.560-2058G>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/15 | chr12 | 109805201 | |||||||
| chr12:109805220 | G | A | 1 | a0001c0003t0001g0098 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.560-2077C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/15 | chr12 | 109805220 | |||||||
| chr12:109805275 | C | G | 210 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(207): Show |
234 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(231): Show |
intron_variant | MODIFIER | c.560-2132G>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/15 | chr12 | 109805275 | |||||||
| chr12:109805286 | C | A | 1 | a0001c0001t0001g0291 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.560-2143G>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/15 | chr12 | 109805286 | |||||||
| chr12:109805392 | T | C | 1 | a0001c0002t0001g0165 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.560-2249A>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/15 | chr12 | 109805392 | |||||||
| chr12:109805418 | T | C | 1 | a0001c0003t0001g0150 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.560-2275A>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/15 | chr12 | 109805418 | |||||||
| chr12:109805666 | C | G | 1 | a0001c0012t0001g0032 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.560-2523G>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/15 | chr12 | 109805666 | |||||||
| chr12:109805753 | C | A | 40 | a0001c0005t0001g0016 a0001c0005t0001g0027 a0001c0005t0001g0029 others(37): Show |
44 | HG00597.hp1 HG00642.hp1 HG01099.hp1 others(41): Show |
intron_variant | MODIFIER | c.559+2543G>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/15 | chr12 | 109805753 | |||||||
| chr12:109805887 | A | G | 41 | a0001c0005t0001g0016 a0001c0005t0001g0027 a0001c0005t0001g0029 others(38): Show |
45 | HG00597.hp1 HG00642.hp1 HG01099.hp1 others(42): Show |
intron_variant | MODIFIER | c.559+2409T>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/15 | chr12 | 109805887 | |||||||
| chr12:109805959 | G | A | 29 | a0001c0005t0001g0016 a0001c0005t0001g0157 a0001c0005t0001g0158 others(26): Show |
33 | HG00597.hp1 HG00642.hp1 HG01099.hp1 others(30): Show |
intron_variant | MODIFIER | c.559+2337C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/15 | chr12 | 109805959 | |||||||
| chr12:109805984 | T | C | 1 | a0001c0019t0001g0309 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.559+2312A>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/15 | chr12 | 109805984 | |||||||
| chr12:109806124 | G | C | 4 | a0001c0005t0001g0027 a0001c0005t0001g0036 a0001c0005t0002g0037 others(1): Show |
4 | HG01978.hp2 HG02258.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.559+2172C>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/15 | chr12 | 109806124 | |||||||
| chr12:109806143 | C | T | 2 | a0001c0005t0001g0063 a0001c0025t0001g0067 |
2 | HG02486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.559+2153G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/15 | chr12 | 109806143 | |||||||
| chr12:109806145 | T | A | 30 | a0001c0005t0001g0016 a0001c0005t0001g0157 a0001c0005t0001g0158 others(27): Show |
34 | HG00597.hp1 HG00642.hp1 HG01099.hp1 others(31): Show |
intron_variant | MODIFIER | c.559+2151A>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/15 | chr12 | 109806145 | |||||||
| chr12:109806337 | G | A | 2 | a0001c0005t0001g0063 a0001c0025t0001g0067 |
2 | HG02486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.559+1959C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/15 | chr12 | 109806337 | |||||||
| chr12:109806358 | C | CT | 120 | a0001c0001t0001g0166 a0001c0001t0001g0169 a0001c0001t0001g0191 others(117): Show |
132 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.559+1937dupA | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/15 | chr12 | 109806358 | |||||||
| chr12:109806358 | C | CTT | 21 | a0001c0001t0001g0100 a0001c0002t0001g0066 a0001c0002t0001g0114 others(18): Show |
24 | HG00544.hp1 HG01167.hp1 HG01358.hp1 others(21): Show |
intron_variant | MODIFIER | c.559+1936_559+1937d others(4): Show |
TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/15 | chr12 | 109806358 | |||||||
| chr12:109806369 | T | TA | 41 | a0001c0002t0001g0193 a0001c0005t0001g0016 a0001c0005t0001g0027 others(38): Show |
45 | HG00642.hp1 HG01099.hp1 HG01123.hp2 others(42): Show |
intron_variant | MODIFIER | c.559+1926_559+1927i others(3): Show |
TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/15 | chr12 | 109806369 | |||||||
| chr12:109806370 | T | C | 2 | a0002c0006t0001g0050 a0002c0006t0001g0051 |
2 | NA18952.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.559+1926A>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/15 | chr12 | 109806370 | |||||||
| chr12:109806478 | T | C | 48 | a0001c0001t0001g0129 a0001c0001t0001g0224 a0001c0001t0001g0225 others(45): Show |
51 | HG00423.hp1 HG00597.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.559+1818A>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/15 | chr12 | 109806478 | |||||||
| chr12:109806490 | C | T | 32 | a0001c0004t0001g0312 a0001c0005t0001g0016 a0001c0005t0001g0157 others(29): Show |
36 | HG00597.hp1 HG00642.hp1 HG01099.hp1 others(33): Show |
intron_variant | MODIFIER | c.559+1806G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/15 | chr12 | 109806490 | |||||||
| chr12:109806495 | G | A | 35 | a0001c0004t0001g0042 a0001c0004t0001g0312 a0001c0005t0001g0016 others(32): Show |
39 | HG00597.hp1 HG00642.hp1 HG01099.hp1 others(36): Show |
intron_variant | MODIFIER | c.559+1801C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/15 | chr12 | 109806495 | |||||||
| chr12:109806502 | G | T | 1 | a0002c0006t0001g0073 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.559+1794C>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/15 | chr12 | 109806502 | |||||||
| chr12:109806503 | C | T | 1 | a0002c0006t0001g0073 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.559+1793G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/15 | chr12 | 109806503 | |||||||
| chr12:109806523 | T | C | 1 | a0001c0002t0001g0194 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.559+1773A>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/15 | chr12 | 109806523 | |||||||
| chr12:109806583 | A | G | 4 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0214 others(1): Show |
4 | HG01884.hp2 HG02145.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.559+1713T>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/15 | chr12 | 109806583 | |||||||
| chr12:109806699 | GA | G | 272 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(269): Show |
300 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.559+1596delT | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/15 | chr12 | 109806699 | |||||||
| chr12:109806706 | A | G | 3 | a0001c0001t0001g0298 a0001c0002t0001g0227 a0001c0002t0001g0228 |
3 | HG00609.hp1 NA18985.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.559+1590T>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/15 | chr12 | 109806706 | |||||||
| chr12:109806726 | T | C | 2 | a0004c0010t0001g0222 a0004c0010t0001g0223 |
2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.559+1570A>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/15 | chr12 | 109806726 | |||||||
| chr12:109806752 | T | TC | 3 | a0001c0001t0001g0191 a0001c0002t0001g0122 a0001c0002t0001g0301 |
3 | NA18967.hp2 NA18998.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.559+1543dupG | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/15 | chr12 | 109806752 | |||||||
| chr12:109806866 | AAAAAAAG | A | 17 | a0001c0003t0001g0062 a0001c0003t0001g0139 a0001c0003t0001g0163 others(14): Show |
18 | HG00642.hp1 HG01099.hp1 HG01123.hp2 others(15): Show |
intron_variant | MODIFIER | c.559+1423_559+1429d others(9): Show |
TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/15 | chr12 | 109806866 | |||||||
| chr12:109806867 | AAAAAAG | A | 17 | a0001c0005t0001g0029 a0001c0020t0001g0160 a0002c0006t0001g0004 others(14): Show |
20 | HG02015.hp2 HG02132.hp1 HG02165.hp1 others(17): Show |
intron_variant | MODIFIER | c.559+1423_559+1428d others(8): Show |
TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/15 | chr12 | 109806867 | |||||||
| chr12:109806868 | AAAAAG | A | 10 | a0001c0005t0001g0027 a0001c0005t0001g0036 a0001c0005t0001g0074 others(7): Show |
10 | HG00597.hp1 HG01978.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.559+1423_559+1427d others(7): Show |
TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/15 | chr12 | 109806868 | |||||||
| chr12:109806873 | G | GA | 10 | a0001c0001t0001g0262 a0001c0001t0001g0273 a0001c0001t0001g0281 others(7): Show |
10 | HG01109.hp1 HG02055.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.559+1422dupT | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/15 | chr12 | 109806873 | |||||||
| chr12:109806873 | GA | G | 71 | a0001c0001t0001g0100 a0001c0001t0001g0166 a0001c0001t0001g0169 others(68): Show |
80 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.559+1422delT | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/15 | chr12 | 109806873 | |||||||
| chr12:109806873 | GAA | G | 16 | a0001c0002t0001g0153 a0001c0002t0001g0258 a0001c0004t0001g0117 others(13): Show |
16 | HG00597.hp2 HG01496.hp1 HG01516.hp2 others(13): Show |
intron_variant | MODIFIER | c.559+1421_559+1422d others(4): Show |
TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/15 | chr12 | 109806873 | |||||||
| chr12:109807040 | G | A | 1 | a0001c0025t0001g0067 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.559+1256C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/15 | chr12 | 109807040 | |||||||
| chr12:109807047 | C | G | 1 | a0001c0001t0001g0298 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.559+1249G>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/15 | chr12 | 109807047 | |||||||
| chr12:109807048 | G | C | 1 | a0001c0001t0001g0298 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.559+1248C>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/15 | chr12 | 109807048 | |||||||
| chr12:109807137 | G | A | 4 | a0001c0001t0001g0143 a0001c0001t0001g0206 a0001c0001t0001g0213 others(1): Show |
5 | HG01081.hp1 HG01175.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.559+1159C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/15 | chr12 | 109807137 | |||||||
| chr12:109807189 | T | C | 1 | a0001c0004t0001g0140 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.559+1107A>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/15 | chr12 | 109807189 | |||||||
| chr12:109807204 | A | G | 1 | a0001c0002t0001g0153 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.559+1092T>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/15 | chr12 | 109807204 | |||||||
| chr12:109807208 | G | A | 17 | a0002c0006t0001g0004 a0002c0006t0001g0007 a0002c0006t0001g0035 others(14): Show |
20 | HG00597.hp1 HG02015.hp2 HG02132.hp1 others(17): Show |
intron_variant | MODIFIER | c.559+1088C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/15 | chr12 | 109807208 | |||||||
| chr12:109807263 | T | C | 44 | a0001c0003t0001g0062 a0001c0003t0001g0139 a0001c0003t0001g0163 others(41): Show |
48 | HG00597.hp1 HG00642.hp1 HG01099.hp1 others(45): Show |
intron_variant | MODIFIER | c.559+1033A>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/15 | chr12 | 109807263 | |||||||
| chr12:109807276 | C | CA | 9 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0214 others(6): Show |
9 | HG00738.hp2 HG01884.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.559+1019dupT | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/15 | chr12 | 109807276 | |||||||
| chr12:109807276 | CA | C | 106 | a0001c0001t0001g0166 a0001c0001t0001g0169 a0001c0001t0001g0191 others(103): Show |
121 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(118): Show |
intron_variant | MODIFIER | c.559+1019delT | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/15 | chr12 | 109807276 | |||||||
| chr12:109807276 | CAA | C | 44 | a0001c0002t0001g0189 a0001c0003t0001g0062 a0001c0003t0001g0139 others(41): Show |
48 | HG00597.hp1 HG00642.hp1 HG01099.hp1 others(45): Show |
intron_variant | MODIFIER | c.559+1018_559+1019d others(4): Show |
TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/15 | chr12 | 109807276 | |||||||
| chr12:109807358 | A | G | 1 | a0001c0005t0001g0074 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.559+938T>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/15 | chr12 | 109807358 | |||||||
| chr12:109807393 | C | CT | 16 | a0001c0001t0001g0242 a0001c0001t0001g0244 a0001c0001t0001g0255 others(13): Show |
16 | HG00609.hp1 HG00621.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.559+902dupA | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/15 | chr12 | 109807393 | |||||||
| chr12:109807393 | C | CTT | 25 | a0001c0005t0001g0027 a0001c0005t0001g0029 a0001c0005t0001g0036 others(22): Show |
28 | HG00597.hp1 HG01978.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.559+901_559+902dup others(2): Show |
TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/15 | chr12 | 109807393 | |||||||
| chr12:109807393 | C | CTTT | 19 | a0001c0003t0001g0062 a0001c0003t0001g0139 a0001c0003t0001g0163 others(16): Show |
20 | HG00642.hp1 HG01099.hp1 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.559+900_559+902dup others(3): Show |
TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/15 | chr12 | 109807393 | |||||||
| chr12:109807394 | T | C | 9 | a0001c0004t0001g0003 a0001c0004t0001g0005 a0001c0004t0001g0040 others(6): Show |
12 | HG01167.hp1 HG02280.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.559+902A>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/15 | chr12 | 109807394 | |||||||
| chr12:109807409 | T | C | 1 | a0001c0002t0001g0180 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.559+887A>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/15 | chr12 | 109807409 | |||||||
| chr12:109807412 | T | C | 1 | a0001c0001t0001g0211 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.559+884A>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/15 | chr12 | 109807412 | |||||||
| chr12:109807591 | G | A | 42 | a0001c0003t0001g0062 a0001c0003t0001g0139 a0001c0003t0001g0163 others(39): Show |
46 | HG00597.hp1 HG00642.hp1 HG01099.hp1 others(43): Show |
intron_variant | MODIFIER | c.559+705C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/15 | chr12 | 109807591 | |||||||
| chr12:109807734 | T | C | 1 | a0001c0020t0001g0160 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.559+562A>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/15 | chr12 | 109807734 | |||||||
| chr12:109807783 | A | G | 253 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(250): Show |
281 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(278): Show |
intron_variant | MODIFIER | c.559+513T>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/15 | chr12 | 109807783 | |||||||
| chr12:109807828 | G | A | 2 | a0001c0004t0001g0140 a0001c0004t0001g0198 |
2 | HG01109.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.559+468C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/15 | chr12 | 109807828 | |||||||
| chr12:109807845 | T | C | 1 | a0010c0021t0001g0125 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.559+451A>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/15 | chr12 | 109807845 | |||||||
| chr12:109808173 | C | T | 1 | a0001c0020t0001g0160 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.559+123G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 3/15 | chr12 | 109808173 | |||||||
| chr12:109808472 | G | A | 1 | a0001c0020t0001g0160 | 1 | HG03195.hp2 | splice_region_variant&intron_variant | LOW | c.387-4C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 2/15 | chr12 | 109808472 | |||||||
| chr12:109808564 | A | G | 253 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(250): Show |
281 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(278): Show |
intron_variant | MODIFIER | c.387-96T>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 2/15 | chr12 | 109808564 | |||||||
| chr12:109808578 | T | C | 106 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(103): Show |
116 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.387-110A>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 2/15 | chr12 | 109808578 | |||||||
| chr12:109808624 | T | G | 2 | a0001c0020t0001g0160 a0010c0021t0001g0125 |
2 | HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.387-156A>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 2/15 | chr12 | 109808624 | |||||||
| chr12:109808652 | G | A | 1 | a0001c0020t0001g0160 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.387-184C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 2/15 | chr12 | 109808652 | |||||||
| chr12:109808664 | T | C | 2 | a0001c0005t0001g0029 a0001c0005t0001g0074 |
2 | HG02572.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.387-196A>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 2/15 | chr12 | 109808664 | |||||||
| chr12:109808758 | TCCATCCA others(221): Show |
T | 1 | a0001c0001t0001g0162 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.387-518_387-291del | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 2/15 | chr12 | 109808758 | |||||||
| chr12:109808762 | TCCATCCA others(52): Show |
T | 1 | a0001c0020t0001g0160 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.387-353_387-295del others(59): Show |
TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 2/15 | chr12 | 109808762 | |||||||
| chr12:109809037 | CCCAT | C | 74 | a0001c0001t0001g0100 a0001c0001t0001g0166 a0001c0001t0001g0169 others(71): Show |
84 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.387-573_387-570del others(4): Show |
TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 2/15 | chr12 | 109809037 | |||||||
| chr12:109809266 | TAACTACC others(17): Show |
T | 2 | a0001c0020t0001g0160 a0010c0021t0001g0125 |
2 | HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.387-822_387-799del others(24): Show |
TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 2/15 | chr12 | 109809266 | |||||||
| chr12:109809315 | A | G | 1 | a0010c0021t0001g0125 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.387-847T>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 2/15 | chr12 | 109809315 | |||||||
| chr12:109809330 | A | G | 1 | a0001c0002t0001g0170 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.387-862T>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 2/15 | chr12 | 109809330 | |||||||
| chr12:109809333 | C | T | 1 | a0001c0022t0003g0038 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.387-865G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 2/15 | chr12 | 109809333 | |||||||
| chr12:109809368 | C | A | 1 | a0001c0002t0001g0122 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.387-900G>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 2/15 | chr12 | 109809368 | |||||||
| chr12:109809425 | GATCC | G | 4 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0214 others(1): Show |
4 | HG01884.hp2 HG02145.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.387-961_387-958del others(4): Show |
TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 2/15 | chr12 | 109809425 | |||||||
| chr12:109809431 | T | C | 6 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0009t0001g0045 others(3): Show |
6 | HG02055.hp1 HG02486.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.387-963A>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 2/15 | chr12 | 109809431 | |||||||
| chr12:109809455 | T | C | 18 | a0001c0001t0001g0242 a0001c0003t0001g0062 a0001c0003t0001g0139 others(15): Show |
19 | HG00642.hp1 HG01099.hp1 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.387-987A>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 2/15 | chr12 | 109809455 | |||||||
| chr12:109809459 | T | C | 18 | a0001c0001t0001g0242 a0001c0003t0001g0062 a0001c0003t0001g0139 others(15): Show |
19 | HG00642.hp1 HG01099.hp1 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.387-991A>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 2/15 | chr12 | 109809459 | |||||||
| chr12:109809460 | C | T | 18 | a0001c0001t0001g0242 a0001c0003t0001g0062 a0001c0003t0001g0139 others(15): Show |
19 | HG00642.hp1 HG01099.hp1 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.387-992G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 2/15 | chr12 | 109809460 | |||||||
| chr12:109809522 | T | G | 3 | a0001c0008t0001g0069 a0001c0008t0001g0070 a0001c0008t0001g0072 |
3 | HG02257.hp2 HG02886.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.387-1054A>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 2/15 | chr12 | 109809522 | |||||||
| chr12:109809589 | C | CCCAT | 6 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0214 others(3): Show |
6 | HG01884.hp2 HG02145.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.387-1125_387-1122d others(6): Show |
TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 2/15 | chr12 | 109809589 | |||||||
| chr12:109809619 | G | A | 90 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(87): Show |
100 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.387-1151C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 2/15 | chr12 | 109809619 | |||||||
| chr12:109809637 | C | T | 1 | a0001c0001t0001g0166 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.387-1169G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 2/15 | chr12 | 109809637 | |||||||
| chr12:109809652 | C | CCCAT | 100 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(97): Show |
110 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.387-1188_387-1185d others(6): Show |
TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 2/15 | chr12 | 109809652 | |||||||
| chr12:109809652 | C | T | 1 | a0001c0001t0001g0271 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.387-1184G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 2/15 | chr12 | 109809652 | |||||||
| chr12:109809656 | T | C | 1 | a0001c0003t0001g0099 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.387-1188A>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 2/15 | chr12 | 109809656 | |||||||
| chr12:109809664 | T | C | 1 | a0001c0020t0001g0160 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.387-1196A>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 2/15 | chr12 | 109809664 | |||||||
| chr12:109809787 | G | T | 1 | a0001c0005t0001g0063 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.387-1319C>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 2/15 | chr12 | 109809787 | |||||||
| chr12:109810284 | A | G | 96 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(93): Show |
106 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.387-1816T>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 2/15 | chr12 | 109810284 | |||||||
| chr12:109810743 | G | A | 1 | a0010c0021t0001g0125 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.387-2275C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 2/15 | chr12 | 109810743 | |||||||
| chr12:109810752 | A | G | 3 | a0001c0004t0001g0141 a0001c0004t0001g0147 a0001c0015t0001g0119 |
3 | HG01928.hp1 NA18954.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.387-2284T>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 2/15 | chr12 | 109810752 | |||||||
| chr12:109811044 | T | G | 96 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(93): Show |
106 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.387-2576A>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 2/15 | chr12 | 109811044 | |||||||
| chr12:109811109 | TTCATGAC others(44): Show |
T | 1 | a0001c0002t0001g0106 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.387-2692_387-2642d others(53): Show |
TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 2/15 | chr12 | 109811109 | |||||||
| chr12:109811140 | A | G | 252 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(249): Show |
280 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(277): Show |
intron_variant | MODIFIER | c.387-2672T>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 2/15 | chr12 | 109811140 | |||||||
| chr12:109811163 | G | T | 1 | a0001c0002t0001g0106 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.387-2695C>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 2/15 | chr12 | 109811163 | |||||||
| chr12:109811220 | G | A | 1 | a0001c0020t0001g0160 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.387-2752C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 2/15 | chr12 | 109811220 | |||||||
| chr12:109811271 | C | T | 16 | a0002c0006t0001g0004 a0002c0006t0001g0007 a0002c0006t0001g0047 others(13): Show |
19 | HG00597.hp1 HG02015.hp2 HG02132.hp1 others(16): Show |
intron_variant | MODIFIER | c.387-2803G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 2/15 | chr12 | 109811271 | |||||||
| chr12:109811477 | G | A | 1 | a0001c0002t0001g0241 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.386+2934C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 2/15 | chr12 | 109811477 | |||||||
| chr12:109811672 | GAA | G | 15 | a0002c0006t0001g0004 a0002c0006t0001g0007 a0002c0006t0001g0047 others(12): Show |
18 | HG00597.hp1 HG02015.hp2 HG02132.hp1 others(15): Show |
intron_variant | MODIFIER | c.386+2737_386+2738d others(4): Show |
TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 2/15 | chr12 | 109811672 | |||||||
| chr12:109811674 | A | G | 1 | a0002c0006t0001g0052 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.386+2737T>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 2/15 | chr12 | 109811674 | |||||||
| chr12:109811683 | A | C | 1 | a0001c0025t0001g0067 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.386+2728T>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 2/15 | chr12 | 109811683 | |||||||
| chr12:109811704 | T | C | 1 | a0006c0018t0001g0076 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.386+2707A>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 2/15 | chr12 | 109811704 | |||||||
| chr12:109811710 | A | T | 1 | a0001c0001t0001g0255 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.386+2701T>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 2/15 | chr12 | 109811710 | |||||||
| chr12:109811792 | C | T | 1 | a0001c0004t0001g0040 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.386+2619G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 2/15 | chr12 | 109811792 | |||||||
| chr12:109811831 | C | T | 1 | a0001c0005t0001g0126 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.386+2580G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 2/15 | chr12 | 109811831 | |||||||
| chr12:109812084 | A | G | 1 | a0001c0001t0001g0247 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.386+2327T>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 2/15 | chr12 | 109812084 | |||||||
| chr12:109812146 | G | A | 2 | a0001c0002t0001g0182 a0001c0002t0001g0183 |
2 | NA18985.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.386+2265C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 2/15 | chr12 | 109812146 | |||||||
| chr12:109812293 | G | A | 2 | a0001c0001t0001g0246 a0001c0001t0001g0268 |
2 | NA18953.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.386+2118C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 2/15 | chr12 | 109812293 | |||||||
| chr12:109812363 | G | A | 1 | a0001c0022t0003g0038 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.386+2048C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 2/15 | chr12 | 109812363 | |||||||
| chr12:109812386 | G | T | 5 | a0001c0001t0001g0212 a0001c0001t0001g0215 a0001c0001t0001g0216 others(2): Show |
5 | HG02257.hp1 HG02965.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.386+2025C>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 2/15 | chr12 | 109812386 | |||||||
| chr12:109812396 | T | A | 1 | a0001c0023t0001g0033 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.386+2015A>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 2/15 | chr12 | 109812396 | |||||||
| chr12:109812435 | T | C | 1 | a0001c0003t0001g0293 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.386+1976A>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 2/15 | chr12 | 109812435 | |||||||
| chr12:109812782 | A | G | 24 | a0001c0001t0001g0169 a0001c0020t0001g0160 a0001c0022t0003g0038 others(21): Show |
27 | HG00597.hp1 HG02015.hp2 HG02132.hp1 others(24): Show |
intron_variant | MODIFIER | c.386+1629T>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 2/15 | chr12 | 109812782 | |||||||
| chr12:109812873 | G | T | 2 | a0001c0001t0001g0224 a0001c0001t0001g0225 |
2 | HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.386+1538C>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 2/15 | chr12 | 109812873 | |||||||
| chr12:109812922 | A | C | 1 | a0001c0005t0001g0158 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.386+1489T>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 2/15 | chr12 | 109812922 | |||||||
| chr12:109812999 | G | T | 1 | a0001c0001t0001g0270 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.386+1412C>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 2/15 | chr12 | 109812999 | |||||||
| chr12:109813024 | G | GATA | 24 | a0001c0019t0001g0309 a0001c0020t0001g0160 a0001c0022t0003g0038 others(21): Show |
27 | HG00597.hp1 HG02015.hp2 HG02132.hp1 others(24): Show |
intron_variant | MODIFIER | c.386+1384_386+1386d others(5): Show |
TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 2/15 | chr12 | 109813024 | |||||||
| chr12:109813040 | G | T | 1 | a0001c0012t0001g0032 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.386+1371C>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 2/15 | chr12 | 109813040 | |||||||
| chr12:109813075 | A | G | 1 | a0001c0005t0001g0087 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.386+1336T>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 2/15 | chr12 | 109813075 | |||||||
| chr12:109813204 | G | C | 1 | a0001c0004t0001g0118 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.386+1207C>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 2/15 | chr12 | 109813204 | |||||||
| chr12:109813297 | C | G | 1 | a0001c0012t0001g0032 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.386+1114G>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 2/15 | chr12 | 109813297 | |||||||
| chr12:109813369 | G | A | 1 | a0001c0001t0001g0132 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.386+1042C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 2/15 | chr12 | 109813369 | |||||||
| chr12:109813417 | G | GA | 24 | a0001c0019t0001g0309 a0001c0020t0001g0160 a0001c0022t0003g0038 others(21): Show |
27 | HG00597.hp1 HG02015.hp2 HG02132.hp1 others(24): Show |
intron_variant | MODIFIER | c.386+993dupT | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 2/15 | chr12 | 109813417 | |||||||
| chr12:109813477 | G | A | 1 | a0001c0012t0001g0032 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.386+934C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 2/15 | chr12 | 109813477 | |||||||
| chr12:109813542 | TTTGTATA others(22): Show |
T | 2 | a0001c0003t0001g0077 a0001c0020t0001g0160 |
2 | HG02717.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.386+840_386+868del others(29): Show |
TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 2/15 | chr12 | 109813542 | |||||||
| chr12:109813581 | T | C | 2 | a0006c0017t0001g0308 a0006c0018t0001g0076 |
2 | HG02717.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.386+830A>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 2/15 | chr12 | 109813581 | |||||||
| chr12:109813582 | G | A | 1 | a0006c0018t0001g0076 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.386+829C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 2/15 | chr12 | 109813582 | |||||||
| chr12:109813731 | G | A | 10 | a0001c0004t0001g0003 a0001c0004t0001g0005 a0001c0004t0001g0040 others(7): Show |
13 | HG01109.hp1 HG01167.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.386+680C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 2/15 | chr12 | 109813731 | |||||||
| chr12:109813995 | A | G | 7 | a0001c0019t0001g0309 a0001c0020t0001g0160 a0001c0022t0003g0038 others(4): Show |
7 | HG02717.hp2 HG02922.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.386+416T>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 2/15 | chr12 | 109813995 | |||||||
| chr12:109814043 | GTATGGAT others(8): Show |
G | 8 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0214 others(5): Show |
8 | HG00738.hp2 HG01069.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.386+353_386+367del others(15): Show |
TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 2/15 | chr12 | 109814043 | |||||||
| chr12:109814199 | C | T | 6 | a0001c0020t0001g0160 a0001c0022t0003g0038 a0001c0023t0001g0033 others(3): Show |
6 | HG02717.hp2 HG03195.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.386+212G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 2/15 | chr12 | 109814199 | |||||||
| chr12:109814231 | C | T | 1 | a0001c0012t0001g0032 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.386+180G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 2/15 | chr12 | 109814231 | |||||||
| chr12:109814232 | G | A | 1 | a0001c0008t0001g0071 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.386+179C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 2/15 | chr12 | 109814232 | |||||||
| chr12:109814240 | T | C | 1 | a0010c0021t0001g0125 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.386+171A>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 2/15 | chr12 | 109814240 | |||||||
| chr12:109814863 | G | A | 2 | a0006c0017t0001g0308 a0006c0018t0001g0076 |
2 | HG02717.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-31-36C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109814863 | |||||||
| chr12:109814876 | G | A | 1 | a0001c0025t0001g0067 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-31-49C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109814876 | |||||||
| chr12:109815014 | G | A | 1 | a0001c0003t0001g0293 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-31-187C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109815014 | |||||||
| chr12:109815241 | C | T | 16 | a0001c0001t0001g0120 a0001c0002t0001g0057 a0001c0002t0001g0159 others(13): Show |
16 | HG01928.hp1 HG02165.hp2 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.-31-414G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109815241 | |||||||
| chr12:109815368 | T | C | 1 | a0001c0005t0001g0063 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-31-541A>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109815368 | |||||||
| chr12:109815444 | T | C | 15 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0214 others(12): Show |
15 | HG00738.hp2 HG01069.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.-31-617A>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109815444 | |||||||
| chr12:109815452 | T | G | 1 | a0010c0021t0001g0125 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-31-625A>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109815452 | |||||||
| chr12:109815458 | C | CATTTTAC others(3): Show |
1 | a0001c0003t0001g0109 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.-31-641_-31-632dup others(10): Show |
TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109815458 | |||||||
| chr12:109815669 | G | C | 1 | a0001c0001t0001g0287 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-31-842C>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109815669 | |||||||
| chr12:109815698 | C | A | 2 | a0001c0003t0001g0306 a0001c0003t0001g0307 |
2 | HG02293.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-31-871G>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109815698 | |||||||
| chr12:109815698 | C | T | 2 | a0001c0005t0001g0029 a0001c0030t0001g0028 |
2 | HG02572.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-31-871G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109815698 | |||||||
| chr12:109815885 | G | T | 1 | a0001c0001t0001g0252 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-31-1058C>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109815885 | |||||||
| chr12:109815890 | C | G | 2 | a0001c0004t0001g0140 a0001c0004t0001g0198 |
2 | HG01109.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.-31-1063G>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109815890 | |||||||
| chr12:109815955 | T | C | 8 | a0001c0012t0001g0032 a0001c0019t0001g0309 a0001c0020t0001g0160 others(5): Show |
8 | HG02717.hp2 HG02922.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.-31-1128A>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109815955 | |||||||
| chr12:109815966 | C | G | 1 | a0001c0002t0001g0184 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.-31-1139G>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109815966 | |||||||
| chr12:109815976 | G | A | 17 | a0002c0006t0001g0004 a0002c0006t0001g0007 a0002c0006t0001g0035 others(14): Show |
20 | HG00597.hp1 HG02015.hp2 HG02132.hp1 others(17): Show |
intron_variant | MODIFIER | c.-31-1149C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109815976 | |||||||
| chr12:109815988 | C | A | 1 | a0001c0004t0001g0147 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-31-1161G>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109815988 | |||||||
| chr12:109815989 | A | G | 7 | a0001c0019t0001g0309 a0001c0020t0001g0160 a0001c0022t0003g0038 others(4): Show |
7 | HG02717.hp2 HG02922.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.-31-1162T>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109815989 | |||||||
| chr12:109816066 | T | C | 4 | a0001c0019t0001g0309 a0001c0022t0003g0038 a0001c0023t0001g0033 others(1): Show |
4 | HG02922.hp1 HG03195.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-31-1239A>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109816066 | |||||||
| chr12:109816099 | G | A | 3 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0002t0001g0236 |
3 | HG02129.hp2 HG02155.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.-31-1272C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109816099 | |||||||
| chr12:109816102 | C | T | 1 | a0001c0002t0001g0135 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-31-1275G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109816102 | |||||||
| chr12:109816535 | T | C | 4 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0278 others(1): Show |
4 | HG00621.hp1 NA18941.hp2 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.-31-1708A>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109816535 | |||||||
| chr12:109816548 | C | T | 2 | a0001c0001t0001g0224 a0001c0001t0001g0225 |
2 | HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.-31-1721G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109816548 | |||||||
| chr12:109816652 | A | C | 252 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(249): Show |
280 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(277): Show |
intron_variant | MODIFIER | c.-31-1825T>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109816652 | |||||||
| chr12:109816658 | G | T | 1 | a0001c0020t0001g0160 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-31-1831C>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109816658 | |||||||
| chr12:109816734 | C | T | 1 | a0001c0003t0001g0008 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-31-1907G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109816734 | |||||||
| chr12:109816740 | T | C | 1 | a0001c0025t0001g0067 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-31-1913A>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109816740 | |||||||
| chr12:109816807 | C | G | 1 | a0001c0002t0001g0161 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-31-1980G>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109816807 | |||||||
| chr12:109816810 | C | A | 1 | a0001c0002t0001g0161 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-31-1983G>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109816810 | |||||||
| chr12:109816811 | T | A | 1 | a0001c0002t0001g0161 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-31-1984A>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109816811 | |||||||
| chr12:109816956 | A | G | 3 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0214 |
3 | HG01884.hp2 HG02145.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-31-2129T>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109816956 | |||||||
| chr12:109817141 | T | C | 1 | a0001c0002t0001g0184 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.-31-2314A>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109817141 | |||||||
| chr12:109817165 | T | G | 91 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(88): Show |
101 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.-31-2338A>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109817165 | |||||||
| chr12:109817220 | G | A | 2 | a0006c0017t0001g0308 a0006c0018t0001g0076 |
2 | HG02717.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-31-2393C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109817220 | |||||||
| chr12:109817322 | C | G | 11 | a0001c0003t0001g0062 a0001c0003t0001g0139 a0001c0003t0001g0163 others(8): Show |
11 | HG00642.hp1 HG01099.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.-31-2495G>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109817322 | |||||||
| chr12:109817372 | CT | C | 5 | a0001c0005t0001g0063 a0001c0009t0001g0045 a0001c0009t0001g0046 others(2): Show |
5 | HG02486.hp1 HG02647.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-31-2546delA | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109817372 | |||||||
| chr12:109817627 | C | T | 2 | a0006c0017t0001g0308 a0006c0018t0001g0076 |
2 | HG02717.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-31-2800G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109817627 | |||||||
| chr12:109817743 | A | C | 1 | a0002c0006t0001g0064 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-31-2916T>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109817743 | |||||||
| chr12:109817956 | A | G | 1 | a0001c0001t0001g0244 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-31-3129T>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109817956 | |||||||
| chr12:109817961 | G | A | 2 | a0001c0001t0001g0257 a0001c0001t0001g0269 |
2 | HG02015.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.-31-3134C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109817961 | |||||||
| chr12:109817999 | C | A | 1 | a0001c0024t0001g0218 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-31-3172G>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109817999 | |||||||
| chr12:109818000 | G | C | 1 | a0001c0005t0001g0087 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-31-3173C>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109818000 | |||||||
| chr12:109818228 | C | A | 2 | a0004c0010t0001g0222 a0004c0010t0001g0223 |
2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.-31-3401G>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109818228 | |||||||
| chr12:109818233 | C | T | 2 | a0001c0001t0001g0224 a0001c0001t0001g0225 |
2 | HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.-31-3406G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109818233 | |||||||
| chr12:109818257 | C | T | 1 | a0001c0019t0001g0309 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-31-3430G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109818257 | |||||||
| chr12:109818297 | G | A | 4 | a0001c0005t0001g0027 a0001c0005t0001g0036 a0001c0005t0002g0037 others(1): Show |
4 | HG01978.hp2 HG02258.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.-31-3470C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109818297 | |||||||
| chr12:109818335 | C | T | 2 | a0006c0017t0001g0308 a0006c0018t0001g0076 |
2 | HG02717.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-31-3508G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109818335 | |||||||
| chr12:109818418 | T | C | 4 | a0001c0019t0001g0309 a0001c0022t0003g0038 a0001c0023t0001g0033 others(1): Show |
4 | HG02922.hp1 HG03195.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-31-3591A>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109818418 | |||||||
| chr12:109818462 | C | T | 1 | a0001c0004t0001g0147 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-31-3635G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109818462 | |||||||
| chr12:109818520 | G | T | 17 | a0002c0006t0001g0004 a0002c0006t0001g0007 a0002c0006t0001g0035 others(14): Show |
20 | HG00597.hp1 HG02015.hp2 HG02132.hp1 others(17): Show |
intron_variant | MODIFIER | c.-31-3693C>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109818520 | |||||||
| chr12:109818795 | C | T | 1 | a0001c0003t0001g0109 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.-31-3968G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109818795 | |||||||
| chr12:109818913 | C | T | 1 | a0001c0019t0001g0309 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-31-4086G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109818913 | |||||||
| chr12:109819103 | G | T | 2 | a0001c0002t0001g0013 a0001c0003t0001g0168 |
3 | NA18953.hp2 NA18991.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.-31-4276C>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109819103 | |||||||
| chr12:109819149 | C | CTCTGTGG others(11): Show |
1 | a0001c0001t0001g0197 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-31-4340_-31-4323d others(20): Show |
TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109819149 | |||||||
| chr12:109819154 | T | C | 8 | a0001c0012t0001g0032 a0001c0019t0001g0309 a0001c0020t0001g0160 others(5): Show |
8 | HG02717.hp2 HG02922.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.-31-4327A>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109819154 | |||||||
| chr12:109819426 | C | T | 2 | a0001c0002t0001g0134 a0001c0002t0001g0167 |
2 | HG02698.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.-31-4599G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109819426 | |||||||
| chr12:109819436 | G | A | 2 | a0001c0005t0001g0029 a0001c0030t0001g0028 |
2 | HG02572.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-31-4609C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109819436 | |||||||
| chr12:109819484 | G | A | 1 | a0001c0005t0002g0037 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-31-4657C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109819484 | |||||||
| chr12:109819509 | G | A | 1 | a0001c0001t0001g0214 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-31-4682C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109819509 | |||||||
| chr12:109819549 | G | A | 2 | a0006c0017t0001g0308 a0006c0018t0001g0076 |
2 | HG02717.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-31-4722C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109819549 | |||||||
| chr12:109819550 | T | C | 9 | a0001c0002t0001g0001 a0001c0002t0001g0015 a0001c0002t0001g0026 others(6): Show |
15 | HG00735.hp1 HG01070.hp1 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.-31-4723A>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109819550 | |||||||
| chr12:109819699 | T | C | 99 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(96): Show |
109 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.-31-4872A>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109819699 | |||||||
| chr12:109819710 | T | C | 2 | a0004c0010t0001g0222 a0004c0010t0001g0223 |
2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.-31-4883A>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109819710 | |||||||
| chr12:109819711 | G | T | 1 | a0001c0003t0001g0109 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.-31-4884C>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109819711 | |||||||
| chr12:109819712 | C | G | 1 | a0001c0003t0001g0109 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.-31-4885G>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109819712 | |||||||
| chr12:109819724 | A | G | 107 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(104): Show |
117 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.-31-4897T>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109819724 | |||||||
| chr12:109819850 | C | T | 1 | a0001c0019t0001g0309 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-31-5023G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109819850 | |||||||
| chr12:109819870 | G | A | 4 | a0001c0001t0001g0100 a0001c0001t0001g0138 a0001c0001t0001g0288 others(1): Show |
5 | NA18968.hp2 NA18970.hp1 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.-31-5043C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109819870 | |||||||
| chr12:109820147 | G | T | 1 | a0001c0003t0001g0109 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.-31-5320C>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109820147 | |||||||
| chr12:109820248 | G | A | 1 | a0001c0004t0001g0068 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-31-5421C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109820248 | |||||||
| chr12:109820289 | G | A | 1 | a0001c0004t0001g0068 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-31-5462C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109820289 | |||||||
| chr12:109820304 | G | A | 102 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(99): Show |
112 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.-31-5477C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109820304 | |||||||
| chr12:109820402 | A | ACAGAGTG others(6): Show |
103 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(100): Show |
113 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.-31-5576_-31-5575i others(15): Show |
TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109820402 | |||||||
| chr12:109820513 | C | CTTTTTTT others(3): Show |
1 | a0001c0003t0004g0205 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-31-5687_-31-5686i others(12): Show |
TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109820513 | |||||||
| chr12:109820514 | C | CTTTTTTT others(1): Show |
23 | a0001c0001t0001g0021 a0001c0001t0001g0132 a0001c0001t0001g0211 others(20): Show |
24 | HG00280.hp1 HG00408.hp1 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.-31-5688_-31-5687i others(10): Show |
TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109820514 | |||||||
| chr12:109820514 | C | CTTTTTTT others(2): Show |
24 | a0001c0001t0001g0002 a0001c0001t0001g0022 a0001c0001t0001g0090 others(21): Show |
30 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(27): Show |
intron_variant | MODIFIER | c.-31-5688_-31-5687i others(11): Show |
TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109820514 | |||||||
| chr12:109820514 | C | CTTTTTTT others(3): Show |
17 | a0001c0001t0001g0019 a0001c0001t0001g0108 a0001c0001t0001g0129 others(14): Show |
18 | HG00408.hp2 HG00423.hp1 HG00609.hp2 others(15): Show |
intron_variant | MODIFIER | c.-31-5688_-31-5687i others(12): Show |
TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109820514 | |||||||
| chr12:109820514 | C | CTTTTTTT others(4): Show |
10 | a0001c0001t0001g0130 a0001c0001t0001g0234 a0001c0001t0001g0235 others(7): Show |
10 | HG00733.hp1 HG02074.hp1 HG02129.hp2 others(7): Show |
intron_variant | MODIFIER | c.-31-5688_-31-5687i others(13): Show |
TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109820514 | |||||||
| chr12:109820514 | C | CTTTTTTT others(5): Show |
3 | a0001c0001t0001g0018 a0001c0001t0001g0245 a0001c0001t0001g0246 |
4 | NA18973.hp1 NA18982.hp2 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.-31-5688_-31-5687i others(14): Show |
TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109820514 | |||||||
| chr12:109820514 | C | CTTTTTTT others(7): Show |
3 | a0001c0001t0001g0212 a0001c0001t0001g0216 a0001c0001t0001g0217 |
3 | HG02965.hp1 HG03041.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-31-5688_-31-5687i others(16): Show |
TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109820514 | |||||||
| chr12:109820514 | C | CTTTTTTT others(8): Show |
1 | a0001c0008t0001g0070 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-31-5688_-31-5687i others(17): Show |
TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109820514 | |||||||
| chr12:109820514 | C | CTTTTTTT others(9): Show |
2 | a0001c0001t0001g0215 a0001c0008t0001g0072 |
2 | HG02257.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-31-5688_-31-5687i others(18): Show |
TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109820514 | |||||||
| chr12:109820514 | C | CTTTTTTT others(10): Show |
1 | a0001c0008t0001g0069 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-31-5688_-31-5687i others(19): Show |
TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109820514 | |||||||
| chr12:109820514 | C | T | 5 | a0001c0001t0001g0143 a0001c0001t0001g0206 a0001c0001t0001g0213 others(2): Show |
6 | HG01081.hp1 HG01175.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.-31-5687G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109820514 | |||||||
| chr12:109820515 | TA | T | 4 | a0001c0009t0001g0045 a0001c0009t0001g0046 a0001c0009t0001g0048 others(1): Show |
4 | HG02647.hp2 HG02970.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.-31-5689delT | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109820515 | |||||||
| chr12:109820516 | A | AT | 37 | a0001c0001t0001g0197 a0001c0002t0001g0011 a0001c0002t0001g0106 others(34): Show |
41 | HG00544.hp1 HG00733.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.-31-5690dupA | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109820516 | |||||||
| chr12:109820516 | A | ATTTTTTT others(4): Show |
1 | a0001c0022t0003g0038 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-31-5700_-31-5690d others(13): Show |
TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109820516 | |||||||
| chr12:109820516 | A | ATTTTTTT others(5): Show |
1 | a0001c0023t0001g0033 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-31-5701_-31-5690d others(14): Show |
TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109820516 | |||||||
| chr12:109820516 | A | ATTTTTTT others(7): Show |
1 | a0001c0012t0001g0032 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-31-5703_-31-5690d others(16): Show |
TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109820516 | |||||||
| chr12:109820516 | A | ATTTTTTT others(8): Show |
1 | a0010c0021t0001g0125 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-31-5704_-31-5690d others(17): Show |
TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109820516 | |||||||
| chr12:109820516 | A | T | 94 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(91): Show |
104 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.-31-5689T>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109820516 | |||||||
| chr12:109820516 | AT | A | 40 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0214 others(37): Show |
44 | HG00323.hp2 HG00597.hp1 HG01884.hp2 others(41): Show |
intron_variant | MODIFIER | c.-31-5690delA | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109820516 | |||||||
| chr12:109820608 | C | G | 1 | a0001c0009t0001g0045 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-31-5781G>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109820608 | |||||||
| chr12:109820683 | G | A | 1 | a0001c0008t0001g0072 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-31-5856C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109820683 | |||||||
| chr12:109820697 | A | AT | 4 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0006c0017t0001g0308 others(1): Show |
4 | HG02055.hp1 HG02486.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-31-5871dupA | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109820697 | |||||||
| chr12:109820831 | C | T | 1 | a0001c0019t0001g0309 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-31-6004G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109820831 | |||||||
| chr12:109820857 | G | C | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG02145.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-31-6030C>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109820857 | |||||||
| chr12:109820861 | T | C | 8 | a0001c0001t0001g0191 a0001c0001t0001g0197 a0001c0002t0001g0011 others(5): Show |
9 | HG02074.hp2 HG02155.hp1 NA18957.hp1 others(6): Show |
intron_variant | MODIFIER | c.-31-6034A>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109820861 | |||||||
| chr12:109820987 | C | T | 1 | a0001c0005t0001g0229 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-31-6160G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109820987 | |||||||
| chr12:109821044 | G | A | 1 | a0001c0003t0001g0305 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-31-6217C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109821044 | |||||||
| chr12:109821371 | G | A | 1 | a0006c0018t0001g0076 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-31-6544C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109821371 | |||||||
| chr12:109821373 | C | T | 2 | a0006c0017t0001g0308 a0006c0018t0001g0076 |
2 | HG02717.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-31-6546G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109821373 | |||||||
| chr12:109821522 | A | G | 4 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0006c0017t0001g0308 others(1): Show |
4 | HG02055.hp1 HG02486.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-31-6695T>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109821522 | |||||||
| chr12:109821538 | AT | A | 101 | a0001c0001t0001g0100 a0001c0001t0001g0138 a0001c0001t0001g0162 others(98): Show |
113 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(110): Show |
intron_variant | MODIFIER | c.-31-6712delA | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109821538 | |||||||
| chr12:109821572 | C | T | 3 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0214 |
3 | HG01884.hp2 HG02145.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-31-6745G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109821572 | |||||||
| chr12:109821615 | C | T | 87 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(84): Show |
97 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.-31-6788G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109821615 | |||||||
| chr12:109821704 | G | A | 4 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0006c0017t0001g0308 others(1): Show |
4 | HG02055.hp1 HG02486.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-31-6877C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109821704 | |||||||
| chr12:109822046 | G | A | 16 | a0001c0003t0001g0062 a0001c0003t0001g0139 a0001c0003t0001g0163 others(13): Show |
17 | HG00642.hp1 HG01099.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.-31-7219C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109822046 | |||||||
| chr12:109822057 | G | C | 3 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0214 |
3 | HG01884.hp2 HG02145.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-31-7230C>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109822057 | |||||||
| chr12:109822089 | G | T | 1 | a0001c0001t0001g0244 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-31-7262C>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109822089 | |||||||
| chr12:109822121 | G | A | 2 | a0006c0017t0001g0308 a0006c0018t0001g0076 |
2 | HG02717.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-31-7294C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109822121 | |||||||
| chr12:109822337 | C | T | 2 | a0001c0005t0001g0029 a0001c0030t0001g0028 |
2 | HG02572.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-31-7510G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109822337 | |||||||
| chr12:109822376 | G | A | 4 | a0001c0008t0001g0069 a0001c0008t0001g0070 a0001c0008t0001g0071 others(1): Show |
4 | HG02257.hp2 HG02559.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-31-7549C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109822376 | |||||||
| chr12:109822692 | C | A | 1 | a0001c0001t0001g0279 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-31-7865G>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109822692 | |||||||
| chr12:109822699 | G | A | 4 | a0001c0005t0001g0063 a0001c0009t0001g0046 a0001c0009t0001g0048 others(1): Show |
4 | HG02486.hp1 HG02647.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-31-7872C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109822699 | |||||||
| chr12:109822897 | C | G | 141 | a0001c0001t0001g0100 a0001c0001t0001g0138 a0001c0001t0001g0162 others(138): Show |
159 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(156): Show |
intron_variant | MODIFIER | c.-31-8070G>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109822897 | |||||||
| chr12:109822932 | G | A | 2 | a0001c0001t0001g0096 a0001c0001t0001g0287 |
2 | HG00423.hp2 HG00621.hp2 |
intron_variant | MODIFIER | c.-31-8105C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109822932 | |||||||
| chr12:109822935 | G | A | 2 | a0001c0001t0001g0096 a0001c0001t0001g0287 |
2 | HG00423.hp2 HG00621.hp2 |
intron_variant | MODIFIER | c.-31-8108C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109822935 | |||||||
| chr12:109822958 | G | T | 2 | a0001c0001t0001g0096 a0001c0001t0001g0287 |
2 | HG00423.hp2 HG00621.hp2 |
intron_variant | MODIFIER | c.-31-8131C>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109822958 | |||||||
| chr12:109822969 | G | A | 2 | a0001c0003t0001g0075 a0001c0003t0001g0151 |
2 | HG02622.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-31-8142C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109822969 | |||||||
| chr12:109823110 | G | A | 1 | a0001c0005t0001g0029 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-31-8283C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109823110 | |||||||
| chr12:109823183 | C | T | 3 | a0001c0005t0001g0016 a0001c0005t0001g0192 a0001c0005t0001g0207 |
4 | HG03225.hp1 HG06807.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.-31-8356G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109823183 | |||||||
| chr12:109823220 | A | C | 3 | a0001c0005t0001g0029 a0001c0012t0001g0006 a0001c0030t0001g0028 |
4 | HG02559.hp1 HG02572.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-31-8393T>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109823220 | |||||||
| chr12:109823224 | C | T | 2 | a0001c0001t0001g0162 a0001c0002t0001g0133 |
2 | HG01891.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-31-8397G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109823224 | |||||||
| chr12:109823570 | G | A | 96 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(93): Show |
106 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.-31-8743C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109823570 | |||||||
| chr12:109823941 | T | TTG | 12 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0004t0001g0140 others(9): Show |
12 | HG01109.hp1 HG02055.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.-31-9116_-31-9115d others(4): Show |
TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109823941 | |||||||
| chr12:109823941 | T | TTGTG | 96 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(93): Show |
106 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.-31-9118_-31-9115d others(6): Show |
TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109823941 | |||||||
| chr12:109823962 | C | T | 60 | a0001c0001t0001g0100 a0001c0001t0001g0138 a0001c0001t0001g0166 others(57): Show |
70 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.-31-9135G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109823962 | |||||||
| chr12:109824044 | C | A | 1 | a0001c0002t0001g0106 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-31-9217G>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109824044 | |||||||
| chr12:109824216 | C | A | 4 | a0002c0006t0001g0007 a0002c0006t0001g0064 a0002c0006t0001g0073 others(1): Show |
5 | HG02258.hp2 HG02572.hp2 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.-32+9134G>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109824216 | |||||||
| chr12:109824245 | G | A | 1 | a0001c0003t0001g0084 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-32+9105C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109824245 | |||||||
| chr12:109824294 | C | T | 1 | a0001c0003t0001g0103 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.-32+9056G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109824294 | |||||||
| chr12:109824349 | T | A | 102 | a0001c0001t0001g0100 a0001c0001t0001g0138 a0001c0001t0001g0162 others(99): Show |
114 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.-32+9001A>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109824349 | |||||||
| chr12:109824493 | C | A | 3 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0214 |
3 | HG01884.hp2 HG02145.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-32+8857G>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109824493 | |||||||
| chr12:109824499 | T | C | 6 | a0001c0005t0001g0027 a0001c0005t0001g0036 a0001c0005t0001g0074 others(3): Show |
6 | HG01978.hp2 HG02258.hp1 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.-32+8851A>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109824499 | |||||||
| chr12:109824691 | G | A | 1 | a0001c0002t0001g0034 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-32+8659C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109824691 | |||||||
| chr12:109824756 | C | CAACAAAA others(3): Show |
105 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(102): Show |
115 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.-32+8584_-32+8593d others(12): Show |
TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109824756 | |||||||
| chr12:109824760 | A | AAAACAAA others(3): Show |
144 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0100 others(141): Show |
162 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(159): Show |
intron_variant | MODIFIER | c.-32+8580_-32+8589d others(12): Show |
TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109824760 | |||||||
| chr12:109824789 | T | G | 2 | a0004c0010t0001g0222 a0004c0010t0001g0223 |
2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.-32+8561A>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109824789 | |||||||
| chr12:109824827 | G | A | 1 | a0001c0005t0001g0027 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-32+8523C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109824827 | |||||||
| chr12:109824855 | G | C | 105 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(102): Show |
115 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.-32+8495C>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109824855 | |||||||
| chr12:109825003 | T | C | 106 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(103): Show |
116 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.-32+8347A>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109825003 | |||||||
| chr12:109825227 | A | G | 2 | a0001c0003t0001g0030 a0001c0003t0001g0031 |
2 | HG01934.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-32+8123T>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109825227 | |||||||
| chr12:109825510 | T | C | 3 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0214 |
3 | HG01884.hp2 HG02145.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-32+7840A>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109825510 | |||||||
| chr12:109825537 | C | T | 1 | a0001c0005t0001g0063 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-32+7813G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109825537 | |||||||
| chr12:109825726 | C | T | 1 | a0001c0002t0001g0241 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-32+7624G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109825726 | |||||||
| chr12:109825802 | G | A | 4 | a0001c0001t0001g0022 a0001c0001t0001g0280 a0001c0001t0001g0281 others(1): Show |
5 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(2): Show |
intron_variant | MODIFIER | c.-32+7548C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109825802 | |||||||
| chr12:109826053 | T | C | 2 | a0001c0001t0001g0224 a0001c0001t0001g0225 |
2 | HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.-32+7297A>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109826053 | |||||||
| chr12:109826084 | C | T | 3 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0214 |
3 | HG01884.hp2 HG02145.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-32+7266G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109826084 | |||||||
| chr12:109826100 | T | C | 1 | a0001c0002t0001g0144 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-32+7250A>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109826100 | |||||||
| chr12:109826232 | C | T | 1 | a0006c0017t0001g0308 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-32+7118G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109826232 | |||||||
| chr12:109826279 | C | T | 3 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0214 |
3 | HG01884.hp2 HG02145.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-32+7071G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109826279 | |||||||
| chr12:109826360 | C | G | 247 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(244): Show |
275 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.-32+6990G>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109826360 | |||||||
| chr12:109826487 | C | T | 1 | a0001c0001t0001g0166 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-32+6863G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109826487 | |||||||
| chr12:109826995 | T | C | 1 | a0001c0025t0001g0067 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-32+6355A>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109826995 | |||||||
| chr12:109826996 | AGCAGCTG others(8): Show |
A | 10 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0214 others(7): Show |
10 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.-32+6339_-32+6353d others(17): Show |
TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109826996 | |||||||
| chr12:109827098 | G | A | 99 | a0001c0001t0001g0100 a0001c0001t0001g0138 a0001c0001t0001g0162 others(96): Show |
111 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(108): Show |
intron_variant | MODIFIER | c.-32+6252C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109827098 | |||||||
| chr12:109827242 | C | A | 1 | a0002c0006t0001g0058 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-32+6108G>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109827242 | |||||||
| chr12:109827440 | C | T | 3 | a0001c0009t0001g0046 a0001c0009t0001g0048 a0001c0009t0001g0049 |
3 | HG02647.hp2 HG02970.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-32+5910G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109827440 | |||||||
| chr12:109827552 | A | AAC | 103 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(100): Show |
113 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.-32+5796_-32+5797d others(4): Show |
TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109827552 | |||||||
| chr12:109827552 | AAC | A | 52 | a0001c0002t0001g0057 a0001c0002t0001g0066 a0001c0004t0001g0003 others(49): Show |
58 | HG00597.hp1 HG01109.hp1 HG01167.hp1 others(55): Show |
intron_variant | MODIFIER | c.-32+5796_-32+5797d others(4): Show |
TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109827552 | |||||||
| chr12:109827572 | C | A | 6 | a0001c0002t0001g0159 a0001c0005t0001g0158 a0001c0019t0001g0309 others(3): Show |
6 | HG00738.hp2 HG01069.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.-32+5778G>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109827572 | |||||||
| chr12:109827650 | G | A | 110 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(107): Show |
120 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.-32+5700C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109827650 | |||||||
| chr12:109827665 | CAT | C | 4 | a0001c0005t0001g0085 a0001c0005t0001g0086 a0001c0005t0001g0087 others(1): Show |
4 | HG02615.hp2 HG02976.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-32+5683_-32+5684d others(4): Show |
TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109827665 | |||||||
| chr12:109827691 | CACAT | C | 9 | a0001c0004t0001g0003 a0001c0004t0001g0005 a0001c0004t0001g0040 others(6): Show |
12 | HG01167.hp1 HG02280.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.-32+5655_-32+5658d others(6): Show |
TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109827691 | |||||||
| chr12:109827745 | GACAT | G | 3 | a0001c0009t0001g0046 a0001c0009t0001g0048 a0001c0009t0001g0049 |
3 | HG02647.hp2 HG02970.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-32+5601_-32+5604d others(6): Show |
TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109827745 | |||||||
| chr12:109827781 | AACAT | A | 87 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(84): Show |
96 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.-32+5565_-32+5568d others(6): Show |
TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109827781 | |||||||
| chr12:109827791 | T | A | 1 | a0001c0001t0001g0284 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-32+5559A>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109827791 | |||||||
| chr12:109827795 | CAT | C | 3 | a0001c0002t0001g0156 a0002c0006t0001g0285 a0002c0006t0001g0286 |
3 | HG02015.hp2 HG02132.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.-32+5553_-32+5554d others(4): Show |
TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109827795 | |||||||
| chr12:109827845 | C | T | 1 | a0001c0002t0001g0165 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-32+5505G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109827845 | |||||||
| chr12:109827895 | T | G | 3 | a0001c0002t0001g0159 a0001c0005t0001g0158 a0001c0020t0001g0160 |
3 | HG02965.hp2 HG03195.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-32+5455A>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109827895 | |||||||
| chr12:109827898 | G | A | 268 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(265): Show |
297 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(294): Show |
intron_variant | MODIFIER | c.-32+5452C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109827898 | |||||||
| chr12:109828095 | C | A | 1 | a0001c0005t0001g0088 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-32+5255G>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109828095 | |||||||
| chr12:109828099 | T | C | 6 | a0001c0002t0001g0159 a0001c0004t0001g0043 a0001c0005t0001g0157 others(3): Show |
6 | HG02280.hp1 HG02965.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.-32+5251A>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109828099 | |||||||
| chr12:109828467 | G | A | 1 | a0001c0003t0001g0039 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-32+4883C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109828467 | |||||||
| chr12:109828468 | C | T | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG02145.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-32+4882G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109828468 | |||||||
| chr12:109828470 | G | A | 122 | a0001c0001t0001g0096 a0001c0001t0001g0100 a0001c0001t0001g0120 others(119): Show |
136 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.-32+4880C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109828470 | |||||||
| chr12:109828483 | A | AG | 4 | a0001c0005t0001g0229 a0001c0005t0001g0230 a0004c0010t0001g0222 others(1): Show |
4 | HG00738.hp2 HG01069.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.-32+4866dupC | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109828483 | |||||||
| chr12:109828625 | G | A | 1 | a0001c0003t0001g0292 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-32+4725C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109828625 | |||||||
| chr12:109828697 | G | A | 2 | a0001c0011t0001g0145 a0001c0011t0001g0146 |
2 | HG01256.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.-32+4653C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109828697 | |||||||
| chr12:109828703 | C | T | 1 | a0010c0021t0001g0125 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-32+4647G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109828703 | |||||||
| chr12:109828875 | C | T | 1 | a0001c0004t0001g0148 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-32+4475G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109828875 | |||||||
| chr12:109828876 | G | A | 2 | a0001c0002t0001g0208 a0001c0002t0001g0209 |
2 | HG00280.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.-32+4474C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109828876 | |||||||
| chr12:109829037 | T | A | 1 | a0003c0007t0001g0102 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-32+4313A>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109829037 | |||||||
| chr12:109829086 | C | T | 1 | a0001c0004t0001g0147 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-32+4264G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109829086 | |||||||
| chr12:109829090 | T | C | 2 | a0001c0001t0001g0120 a0001c0015t0001g0119 |
2 | NA18954.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.-32+4260A>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109829090 | |||||||
| chr12:109829461 | T | C | 1 | a0001c0002t0001g0124 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-32+3889A>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109829461 | |||||||
| chr12:109829587 | C | T | 1 | a0001c0005t0001g0074 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-32+3763G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109829587 | |||||||
| chr12:109829622 | C | T | 2 | a0002c0006t0001g0050 a0002c0006t0001g0051 |
2 | NA18952.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.-32+3728G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109829622 | |||||||
| chr12:109829662 | C | T | 2 | a0001c0005t0001g0027 a0010c0021t0001g0125 |
2 | HG03540.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-32+3688G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109829662 | |||||||
| chr12:109829682 | C | T | 1 | a0001c0002t0001g0124 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-32+3668G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109829682 | |||||||
| chr12:109829923 | C | T | 2 | a0001c0002t0001g0227 a0001c0002t0001g0228 |
2 | HG00609.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.-32+3427G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109829923 | |||||||
| chr12:109829976 | C | A | 1 | a0001c0003t0001g0293 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-32+3374G>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109829976 | |||||||
| chr12:109830050 | G | A | 129 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(126): Show |
144 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.-32+3300C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109830050 | |||||||
| chr12:109830116 | A | T | 1 | a0001c0002t0001g0010 | 2 | NA18968.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.-32+3234T>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109830116 | |||||||
| chr12:109830199 | G | GGCCA | 9 | a0001c0003t0001g0023 a0001c0003t0001g0303 a0001c0003t0001g0304 others(6): Show |
11 | HG00639.hp1 HG00639.hp2 HG01069.hp2 others(8): Show |
intron_variant | MODIFIER | c.-32+3147_-32+3150d others(6): Show |
TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109830199 | |||||||
| chr12:109830650 | T | G | 9 | a0001c0004t0001g0003 a0001c0004t0001g0005 a0001c0004t0001g0040 others(6): Show |
12 | HG01167.hp1 HG02280.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.-32+2700A>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109830650 | |||||||
| chr12:109830728 | T | A | 2 | a0001c0019t0001g0309 a0006c0017t0001g0308 |
2 | HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-32+2622A>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109830728 | |||||||
| chr12:109830848 | T | C | 1 | a0001c0001t0001g0310 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-32+2502A>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109830848 | |||||||
| chr12:109830940 | C | G | 1 | a0001c0002t0001g0123 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-32+2410G>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109830940 | |||||||
| chr12:109831068 | G | T | 1 | a0001c0001t0001g0212 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-32+2282C>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109831068 | |||||||
| chr12:109831135 | CGT | C | 141 | a0001c0001t0001g0090 a0001c0001t0001g0096 a0001c0001t0001g0100 others(138): Show |
155 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.-32+2213_-32+2214d others(4): Show |
TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109831135 | |||||||
| chr12:109831316 | G | A | 3 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0002t0001g0026 |
3 | HG01099.hp2 HG02145.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-32+2034C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109831316 | |||||||
| chr12:109831547 | C | T | 1 | a0001c0003t0001g0059 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-32+1803G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109831547 | |||||||
| chr12:109831598 | G | C | 1 | a0001c0003t0001g0121 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-32+1752C>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109831598 | |||||||
| chr12:109831639 | A | T | 14 | a0001c0002t0001g0057 a0001c0009t0001g0048 a0001c0009t0001g0049 others(11): Show |
17 | HG00597.hp1 HG02165.hp1 HG02165.hp2 others(14): Show |
intron_variant | MODIFIER | c.-32+1711T>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109831639 | |||||||
| chr12:109831711 | C | A | 37 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0002t0001g0057 others(34): Show |
41 | HG00597.hp1 HG00738.hp2 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.-32+1639G>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109831711 | |||||||
| chr12:109832091 | G | A | 1 | a0001c0026t0001g0210 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-32+1259C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109832091 | |||||||
| chr12:109832109 | C | T | 3 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0002t0001g0026 |
3 | HG01099.hp2 HG02145.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-32+1241G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109832109 | |||||||
| chr12:109832228 | G | A | 13 | a0001c0003t0001g0077 a0001c0003t0001g0078 a0001c0003t0001g0079 others(10): Show |
13 | HG01168.hp1 HG01243.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.-32+1122C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109832228 | |||||||
| chr12:109832274 | C | T | 2 | a0001c0001t0001g0224 a0001c0001t0001g0225 |
2 | HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.-32+1076G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109832274 | |||||||
| chr12:109832437 | T | G | 1 | a0001c0001t0001g0311 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-32+913A>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109832437 | |||||||
| chr12:109832644 | C | A | 34 | a0001c0001t0001g0090 a0001c0001t0001g0096 a0001c0001t0001g0100 others(31): Show |
36 | HG00323.hp2 HG00423.hp2 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.-32+706G>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109832644 | |||||||
| chr12:109832757 | G | A | 1 | a0001c0001t0001g0211 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-32+593C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109832757 | |||||||
| chr12:109832767 | G | A | 2 | a0004c0010t0001g0222 a0004c0010t0001g0223 |
2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.-32+583C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109832767 | |||||||
| chr12:109832773 | T | G | 6 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(3): Show |
6 | HG01884.hp2 HG02257.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-32+577A>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109832773 | |||||||
| chr12:109832784 | C | A | 1 | a0001c0024t0001g0218 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-32+566G>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109832784 | |||||||
| chr12:109832860 | G | A | 3 | a0001c0005t0001g0221 a0001c0008t0001g0219 a0004c0010t0001g0220 |
3 | HG00642.hp1 HG01099.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.-32+490C>T | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109832860 | |||||||
| chr12:109832916 | CAAG | C | 108 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(105): Show |
120 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.-32+431_-32+433del others(3): Show |
TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109832916 | |||||||
| chr12:109832962 | T | G | 2 | a0004c0010t0001g0222 a0004c0010t0001g0223 |
2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.-32+388A>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109832962 | |||||||
| chr12:109832969 | G | C | 2 | a0001c0001t0001g0224 a0001c0001t0001g0225 |
2 | HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.-32+381C>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109832969 | |||||||
| chr12:109833067 | C | T | 1 | a0001c0003t0001g0226 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-32+283G>A | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109833067 | |||||||
| chr12:109833148 | A | G | 217 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0090 others(214): Show |
238 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(235): Show |
intron_variant | MODIFIER | c.-32+202T>C | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109833148 | |||||||
| chr12:109833333 | G | C | 1 | a0001c0004t0001g0312 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-32+17C>G | TRPV4 | ENSG00000111199.12 | transcript | ENST00000261740.7 | protein_coding | 1/15 | chr12 | 109833333 |