Item | Value |
---|---|
geneid | 85397 |
ensemblid | ENSG00000135824.13 |
hgncid | 16810 |
symbol | RGS8 |
name | regulator of G protein signaling 8 |
refseq_nuc | NM_001102450.3 |
refseq_prot | NP_001095920.1 |
ensembl_nuc | ENST00000515211.2 |
ensembl_prot | ENSP00000511884.1 |
mane_status | MANE Select |
chr | chr1 |
start | 182641818 |
end | 182684587 |
strand | - |
ver | v1.2 |
region | chr1:182641818-182684587 |
region5000 | chr1:182636818-182689587 |
regionname0 | RGS8_chr1_182641818_182684587 |
regionname5000 | RGS8_chr1_182636818_182689587 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 180 | 295 | 91 | 50 | 120 | 8 | 26 | 90 | RGS8_chr1_182636818_182689587 | RGS8 | MAALL others(175): Show |
chr1 | 182636818 | 182689587 |
a0002 | 0/0 | 180 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | MAALL others(175): Show |
chr1 | 182636818 | 182689587 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 540 | 293 | 89 | 50 | 120 | 8 | 26 | RGS8_chr1_182636818_182689587 | RGS8 | ATGGC others(535): Show |
chr1 | 182636818 | 182689587 | ||
a0001c0003 | 0/0 | 540 | 2 | 2 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | ATGGC others(535): Show |
chr1 | 182636818 | 182689587 | ||
a0002c0002 | 0/0 | 540 | 3 | 3 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | ATGGC others(535): Show |
chr1 | 182636818 | 182689587 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5988 | 70 | 12 | 14 | 32 | 4 | 8 | RGS8_chr1_182636818_182689587 | RGS8 | ACTCG others(5983): Show |
chr1 | 182636818 | 182689587 |
a0001c0001t0002 | 0/0 | 5987 | 43 | 3 | 14 | 21 | 1 | 4 | RGS8_chr1_182636818_182689587 | RGS8 | ACTCG others(5982): Show |
chr1 | 182636818 | 182689587 |
a0001c0001t0003 | 0/0 | 5987 | 24 | 9 | 2 | 11 | 1 | 1 | RGS8_chr1_182636818_182689587 | RGS8 | ACTCG others(5982): Show |
chr1 | 182636818 | 182689587 |
a0001c0001t0004 | 0/0 | 5987 | 21 | 3 | 4 | 14 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | ACTCG others(5982): Show |
chr1 | 182636818 | 182689587 |
a0001c0001t0005 | 0/0 | 5989 | 13 | 0 | 1 | 6 | 0 | 6 | RGS8_chr1_182636818_182689587 | RGS8 | ACTCG others(5984): Show |
chr1 | 182636818 | 182689587 |
a0001c0001t0006 | 0/0 | 5987 | 7 | 3 | 0 | 2 | 0 | 2 | RGS8_chr1_182636818_182689587 | RGS8 | ACTCG others(5982): Show |
chr1 | 182636818 | 182689587 |
a0001c0001t0007 | 0/0 | 5989 | 8 | 7 | 1 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | ACTCG others(5984): Show |
chr1 | 182636818 | 182689587 |
a0001c0001t0008 | 0/0 | 5987 | 7 | 0 | 0 | 7 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | ACTCG others(5982): Show |
chr1 | 182636818 | 182689587 |
a0001c0001t0009 | 0/0 | 5986 | 7 | 2 | 0 | 5 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | ACTCG others(5981): Show |
chr1 | 182636818 | 182689587 |
a0001c0001t0010 | 0/0 | 5987 | 5 | 2 | 1 | 2 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | ACTCG others(5982): Show |
chr1 | 182636818 | 182689587 |
a0001c0001t0011 | 0/0 | 5989 | 5 | 3 | 2 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | ACTCG others(5984): Show |
chr1 | 182636818 | 182689587 |
a0001c0001t0012 | 0/0 | 5987 | 5 | 0 | 0 | 5 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | ACTCG others(5982): Show |
chr1 | 182636818 | 182689587 |
a0001c0001t0013 | 0/0 | 5987 | 4 | 4 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | ACTCG others(5982): Show |
chr1 | 182636818 | 182689587 |
a0001c0001t0014 | 0/0 | 5987 | 4 | 2 | 1 | 0 | 0 | 1 | RGS8_chr1_182636818_182689587 | RGS8 | ACTCG others(5982): Show |
chr1 | 182636818 | 182689587 |
a0001c0001t0015 | 0/0 | 5987 | 3 | 0 | 1 | 0 | 1 | 1 | RGS8_chr1_182636818_182689587 | RGS8 | ACTCG others(5982): Show |
chr1 | 182636818 | 182689587 |
a0001c0001t0016 | 0/0 | 5988 | 3 | 0 | 3 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | ACTCG others(5983): Show |
chr1 | 182636818 | 182689587 |
a0001c0001t0017 | 0/0 | 5988 | 3 | 3 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | ACTCG others(5983): Show |
chr1 | 182636818 | 182689587 |
a0001c0001t0018 | 0/0 | 5988 | 3 | 3 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | ACTCG others(5983): Show |
chr1 | 182636818 | 182689587 |
a0001c0001t0019 | 0/0 | 5987 | 2 | 2 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | ACTCG others(5982): Show |
chr1 | 182636818 | 182689587 |
a0001c0001t0020 | 0/0 | 5989 | 2 | 1 | 1 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | ACTCG others(5984): Show |
chr1 | 182636818 | 182689587 |
a0001c0001t0021 | 0/0 | 5987 | 2 | 2 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | ACTCG others(5982): Show |
chr1 | 182636818 | 182689587 |
a0001c0001t0023 | 0/0 | 5988 | 2 | 0 | 0 | 0 | 0 | 2 | RGS8_chr1_182636818_182689587 | RGS8 | ACTCG others(5983): Show |
chr1 | 182636818 | 182689587 |
a0001c0001t0024 | 0/0 | 5988 | 2 | 2 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | ACTCG others(5983): Show |
chr1 | 182636818 | 182689587 |
a0001c0001t0025 | 0/0 | 5987 | 2 | 1 | 1 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | ACTCG others(5982): Show |
chr1 | 182636818 | 182689587 |
a0001c0001t0026 | 0/0 | 5987 | 2 | 2 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | ACTCG others(5982): Show |
chr1 | 182636818 | 182689587 |
a0001c0001t0027 | 0/0 | 5988 | 2 | 0 | 0 | 2 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | ACTCG others(5983): Show |
chr1 | 182636818 | 182689587 |
a0001c0001t0028 | 0/0 | 5988 | 2 | 1 | 0 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | ACTCG others(5983): Show |
chr1 | 182636818 | 182689587 |
a0001c0001t0029 | 0/0 | 5988 | 2 | 0 | 1 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | ACTCG others(5983): Show |
chr1 | 182636818 | 182689587 |
a0001c0001t0030 | 0/0 | 5987 | 2 | 2 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | ACTCG others(5982): Show |
chr1 | 182636818 | 182689587 |
a0001c0001t0031 | 0/0 | 5988 | 1 | 0 | 0 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | ACTCG others(5983): Show |
chr1 | 182636818 | 182689587 |
a0001c0001t0032 | 0/0 | 5987 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | ACTCG others(5982): Show |
chr1 | 182636818 | 182689587 |
a0001c0001t0033 | 0/0 | 5988 | 1 | 0 | 0 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | ACTCG others(5983): Show |
chr1 | 182636818 | 182689587 |
a0001c0001t0034 | 0/0 | 5987 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | ACTCG others(5982): Show |
chr1 | 182636818 | 182689587 |
a0001c0001t0035 | 0/0 | 5988 | 1 | 0 | 0 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | ACTCG others(5983): Show |
chr1 | 182636818 | 182689587 |
a0001c0001t0036 | 0/0 | 5986 | 1 | 0 | 0 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | ACTCG others(5981): Show |
chr1 | 182636818 | 182689587 |
a0001c0001t0037 | 0/0 | 5988 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | ACTCG others(5983): Show |
chr1 | 182636818 | 182689587 |
a0001c0001t0038 | 0/0 | 5988 | 1 | 0 | 0 | 0 | 0 | 1 | RGS8_chr1_182636818_182689587 | RGS8 | ACTCG others(5983): Show |
chr1 | 182636818 | 182689587 |
a0001c0001t0039 | 0/0 | 5989 | 1 | 0 | 0 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | ACTCG others(5984): Show |
chr1 | 182636818 | 182689587 |
a0001c0001t0040 | 0/0 | 5989 | 1 | 0 | 1 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | ACTCG others(5984): Show |
chr1 | 182636818 | 182689587 |
a0001c0001t0041 | 0/0 | 5987 | 1 | 0 | 0 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | ACTCG others(5982): Show |
chr1 | 182636818 | 182689587 |
a0001c0001t0042 | 0/0 | 5987 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | ACTCG others(5982): Show |
chr1 | 182636818 | 182689587 |
a0001c0001t0043 | 0/0 | 5988 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | ACTCG others(5983): Show |
chr1 | 182636818 | 182689587 |
a0001c0001t0044 | 0/0 | 5987 | 1 | 0 | 0 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | ACTCG others(5982): Show |
chr1 | 182636818 | 182689587 |
a0001c0001t0045 | 0/0 | 5988 | 1 | 0 | 1 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | ACTCG others(5983): Show |
chr1 | 182636818 | 182689587 |
a0001c0001t0046 | 0/0 | 5987 | 1 | 0 | 0 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | ACTCG others(5982): Show |
chr1 | 182636818 | 182689587 |
a0001c0001t0047 | 0/0 | 5988 | 1 | 0 | 0 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | ACTCG others(5983): Show |
chr1 | 182636818 | 182689587 |
a0001c0001t0048 | 0/0 | 5987 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | ACTCG others(5982): Show |
chr1 | 182636818 | 182689587 |
a0001c0001t0049 | 0/0 | 5987 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | ACTCG others(5982): Show |
chr1 | 182636818 | 182689587 |
a0001c0001t0050 | 0/0 | 5989 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | ACTCG others(5984): Show |
chr1 | 182636818 | 182689587 |
a0001c0001t0051 | 0/0 | 5989 | 1 | 0 | 1 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | ACTCG others(5984): Show |
chr1 | 182636818 | 182689587 |
a0001c0001t0052 | 0/0 | 5987 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | ACTCG others(5982): Show |
chr1 | 182636818 | 182689587 |
a0001c0001t0053 | 0/0 | 5989 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | ACTCG others(5984): Show |
chr1 | 182636818 | 182689587 |
a0001c0001t0054 | 0/0 | 5987 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | ACTCG others(5982): Show |
chr1 | 182636818 | 182689587 |
a0001c0001t0055 | 0/0 | 5988 | 1 | 0 | 0 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | ACTCG others(5983): Show |
chr1 | 182636818 | 182689587 |
a0001c0001t0056 | 0/0 | 5987 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | ACTCG others(5982): Show |
chr1 | 182636818 | 182689587 |
a0001c0001t0057 | 0/0 | 5988 | 1 | 0 | 0 | 0 | 1 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | ACTCG others(5983): Show |
chr1 | 182636818 | 182689587 |
a0001c0001t0058 | 0/0 | 5987 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | ACTCG others(5982): Show |
chr1 | 182636818 | 182689587 |
a0001c0001t0059 | 0/0 | 5987 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | ACTCG others(5982): Show |
chr1 | 182636818 | 182689587 |
a0001c0001t0060 | 0/0 | 5989 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | ACTCG others(5984): Show |
chr1 | 182636818 | 182689587 |
a0001c0001t0061 | 0/0 | 5989 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | ACTCG others(5984): Show |
chr1 | 182636818 | 182689587 |
a0001c0001t0062 | 0/0 | 5987 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | ACTCG others(5982): Show |
chr1 | 182636818 | 182689587 |
a0001c0001t0063 | 0/0 | 5989 | 1 | 0 | 0 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | ACTCG others(5984): Show |
chr1 | 182636818 | 182689587 |
a0001c0001t0064 | 0/0 | 5987 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | ACTCG others(5982): Show |
chr1 | 182636818 | 182689587 |
a0001c0001t0065 | 0/0 | 5988 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | ACTCG others(5983): Show |
chr1 | 182636818 | 182689587 |
a0001c0001t0067 | 0/0 | 5987 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | ACTCG others(5982): Show |
chr1 | 182636818 | 182689587 |
a0001c0003t0022 | 0/0 | 5989 | 2 | 2 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | ACTCG others(5984): Show |
chr1 | 182636818 | 182689587 |
a0002c0002t0002 | 0/0 | 5987 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | ACTCG others(5982): Show |
chr1 | 182636818 | 182689587 |
a0002c0002t0006 | 0/0 | 5987 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | ACTCG others(5982): Show |
chr1 | 182636818 | 182689587 |
a0002c0002t0066 | 0/0 | 5987 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | ACTCG others(5982): Show |
chr1 | 182636818 | 182689587 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 5 | 0 | 3 | 2 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0001g0007 | 0/0 | 4 | 0 | 1 | 0 | 1 | 2 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0001g0011 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0002g0001 | 0/0 | 14 | 0 | 6 | 7 | 0 | 1 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0002g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0002g0010 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0002g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0003g0006 | 0/0 | 4 | 1 | 2 | 0 | 1 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0003g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0003g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0003g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0003g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0003g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0003g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0003g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0004g0002 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0004g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0004g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0004g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0004g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0004g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0004g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0004g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0004g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0004g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0004g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0004g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0004g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0004g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0005g0018 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0005g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0005g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0005g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0005g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0005g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0005g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0005g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0005g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0005g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0005g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0005g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0006g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0006g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0006g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0006g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0006g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0006g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0006g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0007g0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0007g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0007g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0007g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0007g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0008g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0008g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0008g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0009g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0009g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0009g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0009g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0009g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0009g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0009g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0010g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0010g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0010g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0010g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0011g0013 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0011g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0011g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0012g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0012g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0012g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0012g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0013g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0013g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0013g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0013g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0014g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0014g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0014g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0014g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0015g0009 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0016g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0016g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0016g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0017g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0017g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0018g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0018g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0018g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0019g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0019g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0020g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0020g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0021g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0021g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0023g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0023g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0024g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0024g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0025g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0025g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0026g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0026g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0027g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0028g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0028g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0029g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0029g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0030g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0030g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0031g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0032g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0033g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0034g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0035g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0036g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0037g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0038g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0039g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0040g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0041g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0042g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0043g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0044g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0045g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0046g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0047g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0048g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0049g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0050g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0051g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0052g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0053g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0054g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0055g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0056g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0057g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0058g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0059g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0060g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0061g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0062g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0063g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0064g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0065g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0001t0067g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0003t0022g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0001c0003t0022g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0002c0002t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0002c0002t0006g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
a0002c0002t0066g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0015 | g0009 | EUR | GBR | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG00099 | hp2 | a0001 | c0001 | t0003 | g0006 | EUR | GBR | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0121 | EUR | GBR | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | GBR | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG00423 | hp1 | a0001 | c0001 | t0008 | g0170 | EAS | CHS | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | CHS | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG00438 | hp1 | a0001 | c0001 | t0005 | g0151 | EAS | CHS | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | CHS | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | CHS | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG00558 | hp2 | a0001 | c0001 | t0003 | g0193 | EAS | CHS | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG00597 | hp1 | a0001 | c0001 | t0005 | g0077 | EAS | CHS | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG00597 | hp2 | a0001 | c0001 | t0027 | g0030 | EAS | CHS | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG00609 | hp2 | a0001 | c0001 | t0008 | g0004 | EAS | CHS | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG00621 | hp1 | a0001 | c0001 | t0003 | g0027 | EAS | CHS | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG00621 | hp2 | a0001 | c0001 | t0004 | g0214 | EAS | CHS | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG00639 | hp1 | a0001 | c0001 | t0003 | g0006 | AMR | PUR | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0111 | AMR | PUR | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG00642 | hp1 | a0001 | c0001 | t0014 | g0221 | AMR | PUR | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG00642 | hp2 | a0001 | c0001 | t0045 | g0231 | AMR | PUR | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | CHS | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG00741 | hp1 | a0001 | c0001 | t0005 | g0018 | AMR | PUR | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG00741 | hp2 | a0001 | c0001 | t0015 | g0009 | AMR | PUR | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG01069 | hp2 | a0001 | c0001 | t0025 | g0037 | AMR | PUR | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG01081 | hp1 | a0001 | c0001 | t0016 | g0228 | AMR | PUR | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG01099 | hp2 | a0001 | c0001 | t0020 | g0141 | AMR | PUR | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG01109 | hp1 | a0001 | c0001 | t0016 | g0031 | AMR | PUR | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG01109 | hp2 | a0001 | c0001 | t0011 | g0146 | AMR | PUR | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG01167 | hp1 | a0001 | c0001 | t0003 | g0006 | AMR | PUR | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0140 | AMR | PUR | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0162 | AMR | PUR | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG01192 | hp2 | a0001 | c0001 | t0051 | g0070 | AMR | PUR | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG01243 | hp1 | a0001 | c0001 | t0011 | g0013 | AMR | PUR | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG01255 | hp1 | a0001 | c0001 | t0029 | g0183 | AMR | CLM | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG01255 | hp2 | a0001 | c0001 | t0016 | g0105 | AMR | CLM | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG01256 | hp2 | a0001 | c0001 | t0004 | g0217 | AMR | CLM | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0109 | AMR | CLM | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | CLM | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0104 | AMR | CLM | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | CLM | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG01884 | hp1 | a0001 | c0001 | t0020 | g0035 | AFR | ACB | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG01884 | hp2 | a0001 | c0001 | t0030 | g0179 | AFR | ACB | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG01891 | hp1 | a0001 | c0001 | t0065 | g0033 | AFR | ACB | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG01891 | hp2 | a0001 | c0001 | t0004 | g0025 | AFR | ACB | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG01928 | hp1 | a0001 | c0001 | t0004 | g0222 | AMR | PEL | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG01928 | hp2 | a0001 | c0001 | t0004 | g0219 | AMR | PEL | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG01978 | hp1 | a0001 | c0001 | t0040 | g0136 | AMR | PEL | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG01978 | hp2 | a0001 | c0001 | t0004 | g0218 | AMR | PEL | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0017 | AMR | PEL | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG02055 | hp1 | a0001 | c0001 | t0048 | g0233 | AFR | ACB | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG02071 | hp1 | a0001 | c0001 | t0044 | g0076 | EAS | KHV | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG02071 | hp2 | a0001 | c0001 | t0003 | g0155 | EAS | KHV | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | KHV | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG02083 | hp1 | a0001 | c0001 | t0003 | g0139 | EAS | KHV | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | KHV | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG02129 | hp2 | a0001 | c0001 | t0003 | g0138 | EAS | KHV | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG02132 | hp2 | a0001 | c0001 | t0047 | g0117 | EAS | KHV | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG02145 | hp1 | a0001 | c0001 | t0003 | g0015 | AFR | ACB | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG02145 | hp2 | a0001 | c0001 | t0004 | g0025 | AFR | ACB | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG02258 | hp1 | a0001 | c0001 | t0007 | g0175 | AFR | ACB | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG02258 | hp2 | a0001 | c0001 | t0024 | g0206 | AFR | ACB | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG02280 | hp1 | a0001 | c0001 | t0024 | g0040 | AFR | ACB | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG02280 | hp2 | a0001 | c0001 | t0003 | g0045 | AFR | ACB | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PEL | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0017 | AMR | PEL | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG02300 | hp1 | a0001 | c0001 | t0010 | g0160 | AMR | PEL | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG02451 | hp1 | a0001 | c0001 | t0010 | g0021 | AFR | ACB | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG02451 | hp2 | a0001 | c0001 | t0042 | g0095 | AFR | ACB | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | KHV | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | KHV | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG02572 | hp1 | a0001 | c0001 | t0011 | g0149 | AFR | GWD | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG02572 | hp2 | a0001 | c0001 | t0026 | g0209 | AFR | GWD | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG02615 | hp1 | a0001 | c0001 | t0006 | g0054 | AFR | GWD | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG02615 | hp2 | a0001 | c0001 | t0013 | g0181 | AFR | GWD | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0132 | AFR | GWD | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG02622 | hp2 | a0001 | c0001 | t0064 | g0034 | AFR | GWD | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG02630 | hp1 | a0001 | c0001 | t0018 | g0172 | AFR | GWD | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG02647 | hp1 | a0001 | c0001 | t0021 | g0078 | AFR | GWD | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG02723 | hp2 | a0002 | c0002 | t0006 | g0038 | AFR | GWD | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG02818 | hp1 | a0001 | c0001 | t0058 | g0112 | AFR | GWD | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG02818 | hp2 | a0001 | c0001 | t0018 | g0042 | AFR | GWD | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG02886 | hp1 | a0001 | c0001 | t0062 | g0051 | AFR | GWD | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG02886 | hp2 | a0001 | c0001 | t0003 | g0234 | AFR | GWD | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG02895 | hp1 | a0001 | c0001 | t0013 | g0073 | AFR | GWD | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG02895 | hp2 | a0001 | c0001 | t0009 | g0135 | AFR | GWD | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG02896 | hp1 | a0001 | c0001 | t0007 | g0005 | AFR | GWD | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG02896 | hp2 | a0001 | c0001 | t0003 | g0015 | AFR | GWD | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG02897 | hp1 | a0001 | c0001 | t0007 | g0005 | AFR | GWD | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG02897 | hp2 | a0001 | c0001 | t0013 | g0074 | AFR | GWD | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG02922 | hp1 | a0001 | c0001 | t0004 | g0053 | AFR | ESN | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG02922 | hp2 | a0001 | c0001 | t0019 | g0046 | AFR | ESN | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG02965 | hp1 | a0001 | c0001 | t0032 | g0143 | AFR | ESN | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG02965 | hp2 | a0001 | c0001 | t0028 | g0052 | AFR | ESN | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG02970 | hp1 | a0001 | c0001 | t0011 | g0013 | AFR | ESN | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG02970 | hp2 | a0001 | c0001 | t0017 | g0032 | AFR | ESN | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG02976 | hp1 | a0001 | c0001 | t0021 | g0036 | AFR | ESN | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG02976 | hp2 | a0001 | c0001 | t0018 | g0197 | AFR | ESN | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG03017 | hp1 | a0001 | c0001 | t0006 | g0168 | SAS | PJL | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG03041 | hp1 | a0001 | c0001 | t0011 | g0013 | AFR | GWD | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG03041 | hp2 | a0001 | c0001 | t0013 | g0182 | AFR | GWD | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG03098 | hp1 | a0001 | c0001 | t0067 | g0044 | AFR | MSL | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG03098 | hp2 | a0001 | c0001 | t0007 | g0173 | AFR | MSL | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG03130 | hp2 | a0002 | c0002 | t0002 | g0066 | AFR | ESN | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG03139 | hp1 | a0001 | c0001 | t0025 | g0068 | AFR | ESN | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG03139 | hp2 | a0001 | c0001 | t0060 | g0055 | AFR | ESN | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG03195 | hp1 | a0001 | c0001 | t0007 | g0043 | AFR | ESN | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG03195 | hp2 | a0001 | c0001 | t0003 | g0133 | AFR | ESN | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG03209 | hp1 | a0001 | c0001 | t0014 | g0039 | AFR | MSL | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG03209 | hp2 | a0001 | c0001 | t0049 | g0225 | AFR | MSL | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG03225 | hp1 | a0001 | c0003 | t0022 | g0166 | AFR | MSL | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG03225 | hp2 | a0001 | c0001 | t0054 | g0067 | AFR | MSL | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0010 | SAS | PJL | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG03453 | hp1 | a0001 | c0001 | t0007 | g0005 | AFR | MSL | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG03453 | hp2 | a0001 | c0001 | t0026 | g0177 | AFR | MSL | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG03486 | hp1 | a0001 | c0001 | t0034 | g0131 | AFR | MSL | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | MSL | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | PJL | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG03490 | hp2 | a0001 | c0001 | t0038 | g0082 | SAS | PJL | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | ESN | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | ESN | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG03540 | hp1 | a0001 | c0001 | t0003 | g0064 | AFR | GWD | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG03540 | hp2 | a0001 | c0001 | t0052 | g0171 | AFR | GWD | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG03579 | hp1 | a0001 | c0001 | t0007 | g0005 | AFR | MSL | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | MSL | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG03669 | hp2 | a0001 | c0001 | t0006 | g0085 | SAS | PJL | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG03688 | hp1 | a0001 | c0001 | t0005 | g0083 | SAS | STU | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG03688 | hp2 | a0001 | c0001 | t0005 | g0087 | SAS | STU | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG03704 | hp2 | a0001 | c0001 | t0003 | g0186 | SAS | PJL | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0097 | SAS | BEB | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG03831 | hp2 | a0001 | c0001 | t0005 | g0018 | SAS | BEB | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG03834 | hp1 | a0001 | c0001 | t0015 | g0009 | SAS | BEB | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | BEB | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG03942 | hp1 | a0001 | c0001 | t0005 | g0204 | SAS | BEB | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG03942 | hp2 | a0001 | c0001 | t0005 | g0199 | SAS | BEB | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | STU | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0202 | SAS | STU | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG04184 | hp1 | a0001 | c0001 | t0005 | g0125 | SAS | BEB | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG04184 | hp2 | a0001 | c0001 | t0023 | g0130 | SAS | BEB | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | STU | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG04199 | hp2 | a0001 | c0001 | t0023 | g0169 | SAS | STU | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | YRI | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA18522 | hp2 | a0001 | c0001 | t0017 | g0014 | AFR | YRI | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | CHB | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHB | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHB | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CHB | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA18906 | hp1 | a0002 | c0002 | t0066 | g0174 | AFR | YRI | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA18906 | hp2 | a0001 | c0001 | t0019 | g0142 | AFR | YRI | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA18941 | hp2 | a0001 | c0001 | t0008 | g0004 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA18943 | hp1 | a0001 | c0001 | t0008 | g0004 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA18943 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA18950 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA18950 | hp2 | a0001 | c0001 | t0003 | g0189 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA18954 | hp1 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA18954 | hp2 | a0001 | c0001 | t0004 | g0216 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA18961 | hp2 | a0001 | c0001 | t0012 | g0029 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA18963 | hp1 | a0001 | c0001 | t0003 | g0075 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA18963 | hp2 | a0001 | c0001 | t0004 | g0226 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA18965 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA18966 | hp1 | a0001 | c0001 | t0005 | g0156 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA18966 | hp2 | a0001 | c0001 | t0063 | g0212 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA18968 | hp1 | a0001 | c0001 | t0008 | g0004 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA18973 | hp1 | a0001 | c0001 | t0029 | g0224 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA18974 | hp1 | a0001 | c0001 | t0009 | g0191 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA18974 | hp2 | a0001 | c0001 | t0004 | g0211 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA18977 | hp1 | a0001 | c0001 | t0035 | g0092 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA18977 | hp2 | a0001 | c0001 | t0041 | g0106 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA18978 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA18980 | hp1 | a0001 | c0001 | t0033 | g0161 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA18980 | hp2 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA18981 | hp2 | a0001 | c0001 | t0012 | g0210 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA18982 | hp2 | a0001 | c0001 | t0009 | g0190 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA18983 | hp1 | a0001 | c0001 | t0036 | g0048 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA18983 | hp2 | a0001 | c0001 | t0003 | g0185 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA18985 | hp1 | a0001 | c0001 | t0004 | g0207 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA18985 | hp2 | a0001 | c0001 | t0008 | g0084 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA18986 | hp1 | a0001 | c0001 | t0008 | g0004 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA18991 | hp1 | a0001 | c0001 | t0006 | g0059 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA18991 | hp2 | a0001 | c0001 | t0009 | g0115 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA18993 | hp1 | a0001 | c0001 | t0005 | g0195 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA18993 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA18995 | hp2 | a0001 | c0001 | t0028 | g0060 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA18997 | hp2 | a0001 | c0001 | t0012 | g0215 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA19000 | hp1 | a0001 | c0001 | t0055 | g0058 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA19000 | hp2 | a0001 | c0001 | t0005 | g0201 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA19001 | hp1 | a0001 | c0001 | t0010 | g0150 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA19001 | hp2 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA19002 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA19003 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA19004 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA19006 | hp1 | a0001 | c0001 | t0004 | g0227 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA19007 | hp2 | a0001 | c0001 | t0012 | g0029 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA19009 | hp1 | a0001 | c0001 | t0004 | g0129 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA19009 | hp2 | a0001 | c0001 | t0046 | g0108 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA19010 | hp1 | a0001 | c0001 | t0039 | g0123 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA19030 | hp1 | a0001 | c0001 | t0043 | g0099 | AFR | LWK | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA19030 | hp2 | a0001 | c0001 | t0014 | g0050 | AFR | LWK | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA19043 | hp1 | a0001 | c0001 | t0030 | g0178 | AFR | LWK | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA19043 | hp2 | a0001 | c0003 | t0022 | g0167 | AFR | LWK | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA19054 | hp1 | a0001 | c0001 | t0005 | g0122 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA19054 | hp2 | a0001 | c0001 | t0012 | g0213 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA19060 | hp2 | a0001 | c0001 | t0027 | g0030 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA19062 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA19065 | hp1 | a0001 | c0001 | t0010 | g0103 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA19065 | hp2 | a0001 | c0001 | t0006 | g0057 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA19074 | hp2 | a0001 | c0001 | t0031 | g0114 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA19091 | hp1 | a0001 | c0001 | t0009 | g0176 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA19091 | hp2 | a0001 | c0001 | t0009 | g0188 | EAS | JPT | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA19240 | hp1 | a0001 | c0001 | t0003 | g0100 | AFR | YRI | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA19240 | hp2 | a0001 | c0001 | t0017 | g0014 | AFR | YRI | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA20129 | hp1 | a0001 | c0001 | t0037 | g0148 | AFR | ASW | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | ASW | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0116 | EUR | TSI | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA20752 | hp2 | a0001 | c0001 | t0057 | g0220 | EUR | TSI | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0232 | EUR | TSI | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0198 | EUR | TSI | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | GIH | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA20905 | hp2 | a0001 | c0001 | t0014 | g0230 | SAS | GIH | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | CLM | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG01123 | hp2 | a0001 | c0001 | t0007 | g0041 | AMR | CLM | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG02109 | hp1 | a0001 | c0001 | t0053 | g0071 | AFR | ACB | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG02109 | hp2 | a0001 | c0001 | t0009 | g0062 | AFR | ACB | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG02486 | hp1 | a0001 | c0001 | t0059 | g0180 | AFR | ACB | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0119 | AFR | ACB | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG02559 | hp1 | a0001 | c0001 | t0010 | g0021 | AFR | ACB | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG02559 | hp2 | a0001 | c0001 | t0056 | g0128 | AFR | ACB | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG03471 | hp1 | a0001 | c0001 | t0050 | g0069 | AFR | MSL | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG03471 | hp2 | a0001 | c0001 | t0003 | g0165 | AFR | MSL | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG06807 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | USA | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
HG06807 | hp2 | a0001 | c0001 | t0006 | g0056 | AFR | USA | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0229 | AFR | USA | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | USA | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA21309 | hp1 | a0001 | c0001 | t0006 | g0127 | AFR | LWK | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
NA21309 | hp2 | a0001 | c0001 | t0061 | g0049 | AFR | LWK | RGS8_chr1_182636818_182689587 | RGS8 | chr1 | 182636818 | 182689587 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:182648213 | G | A | 1 | a0002 | 3 | HG02723.hp2 HG03130.hp2 NA18906.hp1 |
missense_variant | MODERATE | c.284C>T | p.Thr95Ile | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 7/8 | 811/5987 | 284/543 | 95/180 | chr1 | 182648213 | |||
chr1:182671729 | T | C | 2 | a0001 a0002 |
90 | HG00597.hp2 HG00621.hp2 HG00642.hp1 others(87): Show |
splice_region_variant | LOW | c.-176A>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 3/8 | chr1 | 182671729 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:182666880 | G | A | 1 | a0001c0003 | 2 | HG03225.hp1 NA19043.hp2 |
synonymous_variant | LOW | c.120C>T | p.Arg40Arg | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 5/8 | 647/5987 | 120/543 | 40/180 | chr1 | 182666880 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:182641883 | C | T | 7 | a0001c0001t0007 a0001c0001t0011 a0001c0001t0018 others(4): Show |
20 | HG01109.hp2 HG01123.hp2 HG01192.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*4852G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 8/8 | 4852 | chr1 | 182641883 | ||||||
chr1:182641974 | C | T | 1 | a0001c0001t0015 | 3 | HG00099.hp1 HG00741.hp2 HG03834.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4761G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 8/8 | 4761 | chr1 | 182641974 | ||||||
chr1:182642000 | G | A | 7 | a0001c0001t0007 a0001c0001t0011 a0001c0001t0018 others(4): Show |
20 | HG01109.hp2 HG01123.hp2 HG01192.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*4735C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 8/8 | 4735 | chr1 | 182642000 | ||||||
chr1:182642147 | C | G | 1 | a0001c0001t0065 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4588G>C | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 8/8 | 4588 | chr1 | 182642147 | ||||||
chr1:182642200 | G | A | 1 | a0001c0001t0064 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4535C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 8/8 | 4535 | chr1 | 182642200 | ||||||
chr1:182642295 | C | T | 6 | a0001c0001t0017 a0001c0001t0021 a0001c0001t0025 others(3): Show |
10 | HG01069.hp2 HG01891.hp1 HG02486.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*4440G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 8/8 | 4440 | chr1 | 182642295 | ||||||
chr1:182642339 | G | T | 5 | a0001c0001t0013 a0001c0001t0030 a0001c0001t0032 others(2): Show |
9 | HG01884.hp2 HG02055.hp1 HG02615.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*4396C>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 8/8 | 4396 | chr1 | 182642339 | ||||||
chr1:182642471 | G | A | 6 | a0001c0001t0017 a0001c0001t0021 a0001c0001t0025 others(3): Show |
10 | HG01069.hp2 HG01891.hp1 HG02486.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*4264C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 8/8 | 4264 | chr1 | 182642471 | ||||||
chr1:182642497 | T | G | 11 | a0001c0001t0007 a0001c0001t0011 a0001c0001t0018 others(8): Show |
26 | HG01099.hp2 HG01109.hp2 HG01123.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*4238A>C | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 8/8 | 4238 | chr1 | 182642497 | ||||||
chr1:182642570 | T | C | 6 | a0001c0001t0017 a0001c0001t0021 a0001c0001t0025 others(3): Show |
10 | HG01069.hp2 HG01891.hp1 HG02486.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*4165A>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 8/8 | 4165 | chr1 | 182642570 | ||||||
chr1:182642688 | C | T | 1 | a0001c0001t0056 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4047G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 8/8 | 4047 | chr1 | 182642688 | ||||||
chr1:182642747 | G | A | 2 | a0001c0001t0049 a0001c0001t0054 |
2 | HG03209.hp2 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3988C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 8/8 | 3988 | chr1 | 182642747 | ||||||
chr1:182642790 | G | C | 15 | a0001c0001t0007 a0001c0001t0011 a0001c0001t0017 others(12): Show |
32 | HG01069.hp2 HG01109.hp2 HG01123.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*3945C>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 8/8 | 3945 | chr1 | 182642790 | ||||||
chr1:182642913 | G | A | 1 | a0001c0001t0056 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3822C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 8/8 | 3822 | chr1 | 182642913 | ||||||
chr1:182643086 | G | A | 3 | a0001c0001t0042 a0001c0001t0043 a0001c0003t0022 |
4 | HG02451.hp2 HG03225.hp1 NA19030.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3649C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 8/8 | 3649 | chr1 | 182643086 | ||||||
chr1:182643143 | T | C | 1 | a0001c0001t0062 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3592A>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 8/8 | 3592 | chr1 | 182643143 | ||||||
chr1:182643192 | C | T | 6 | a0001c0001t0017 a0001c0001t0021 a0001c0001t0025 others(3): Show |
10 | HG01069.hp2 HG01891.hp1 HG02486.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3543G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 8/8 | 3543 | chr1 | 182643192 | ||||||
chr1:182643323 | G | C | 1 | a0001c0001t0041 | 1 | NA18977.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3412C>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 8/8 | 3412 | chr1 | 182643323 | ||||||
chr1:182643323 | G | GC | 16 | a0001c0001t0001 a0001c0001t0016 a0001c0001t0023 others(13): Show |
92 | HG00140.hp1 HG00140.hp2 HG00597.hp2 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*3411dupG | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 8/8 | 3411 | chr1 | 182643323 | ||||||
chr1:182643323 | G | GCC | 7 | a0001c0001t0005 a0001c0001t0020 a0001c0001t0039 others(4): Show |
21 | HG00438.hp1 HG00597.hp1 HG00741.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*3410_*3411dupGG | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 8/8 | 3411 | chr1 | 182643323 | ||||||
chr1:182643323 | G | GGC | 3 | a0001c0001t0017 a0001c0001t0050 a0001c0001t0065 |
5 | HG01891.hp1 HG02970.hp2 HG03471.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3411_*3412insGC | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 8/8 | 3411 | chr1 | 182643323 | ||||||
chr1:182643325 | C | A | 1 | a0001c0001t0036 | 1 | NA18983.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3410G>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 8/8 | 3410 | chr1 | 182643325 | ||||||
chr1:182643330 | CG | C | 2 | a0001c0001t0009 a0001c0001t0036 |
8 | HG02109.hp2 HG02895.hp2 NA18974.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3404delC | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 8/8 | 3404 | chr1 | 182643330 | ||||||
chr1:182643331 | G | C | 46 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(43): Show |
181 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(178): Show |
3_prime_UTR_variant | MODIFIER | c.*3404C>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 8/8 | 3404 | chr1 | 182643331 | ||||||
chr1:182643332 | C | G | 2 | a0001c0001t0017 a0001c0001t0065 |
4 | HG01891.hp1 HG02970.hp2 NA18522.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3403G>C | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 8/8 | 3403 | chr1 | 182643332 | ||||||
chr1:182643336 | C | CCG | 5 | a0001c0001t0007 a0001c0001t0011 a0001c0001t0051 others(2): Show |
16 | HG01109.hp2 HG01123.hp2 HG01192.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*3398_*3399insCG | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 8/8 | 3398 | chr1 | 182643336 | ||||||
chr1:182643336 | C | CG | 2 | a0001c0001t0018 a0001c0001t0037 |
4 | HG02630.hp1 HG02818.hp2 HG02976.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3398dupC | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 8/8 | 3398 | chr1 | 182643336 | ||||||
chr1:182643337 | G | A | 1 | a0001c0001t0036 | 1 | NA18983.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3398C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 8/8 | 3398 | chr1 | 182643337 | ||||||
chr1:182643403 | T | C | 1 | a0001c0001t0012 | 5 | NA18961.hp2 NA18981.hp2 NA18997.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3332A>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 8/8 | 3332 | chr1 | 182643403 | ||||||
chr1:182643465 | T | C | 6 | a0001c0001t0017 a0001c0001t0021 a0001c0001t0025 others(3): Show |
10 | HG01069.hp2 HG01891.hp1 HG02486.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3270A>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 8/8 | 3270 | chr1 | 182643465 | ||||||
chr1:182643574 | T | C | 21 | a0001c0001t0007 a0001c0001t0011 a0001c0001t0013 others(18): Show |
42 | HG01069.hp2 HG01109.hp2 HG01123.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*3161A>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 8/8 | 3161 | chr1 | 182643574 | ||||||
chr1:182643589 | A | G | 1 | a0001c0001t0040 | 1 | HG01978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3146T>C | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 8/8 | 3146 | chr1 | 182643589 | ||||||
chr1:182643604 | G | A | 1 | a0001c0001t0058 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3131C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 8/8 | 3131 | chr1 | 182643604 | ||||||
chr1:182643801 | G | A | 2 | a0001c0001t0008 a0001c0001t0033 |
8 | HG00423.hp1 HG00609.hp2 NA18941.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2934C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 8/8 | 2934 | chr1 | 182643801 | ||||||
chr1:182643850 | G | A | 1 | a0001c0001t0044 | 1 | HG02071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2885C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 8/8 | 2885 | chr1 | 182643850 | ||||||
chr1:182643911 | C | A | 1 | a0001c0001t0045 | 1 | HG00642.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2824G>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 8/8 | 2824 | chr1 | 182643911 | ||||||
chr1:182644308 | C | T | 1 | a0001c0001t0039 | 1 | NA19010.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2427G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 8/8 | 2427 | chr1 | 182644308 | ||||||
chr1:182644358 | G | C | 15 | a0001c0001t0004 a0001c0001t0008 a0001c0001t0010 others(12): Show |
56 | HG00423.hp1 HG00597.hp2 HG00609.hp2 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*2377C>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 8/8 | 2377 | chr1 | 182644358 | ||||||
chr1:182644394 | G | A | 2 | a0001c0001t0017 a0001c0001t0065 |
4 | HG01891.hp1 HG02970.hp2 NA18522.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2341C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 8/8 | 2341 | chr1 | 182644394 | ||||||
chr1:182644402 | A | G | 1 | a0001c0001t0021 | 2 | HG02647.hp1 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2333T>C | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 8/8 | 2333 | chr1 | 182644402 | ||||||
chr1:182644473 | C | T | 1 | a0001c0001t0026 | 2 | HG02572.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2262G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 8/8 | 2262 | chr1 | 182644473 | ||||||
chr1:182644503 | C | T | 13 | a0001c0001t0007 a0001c0001t0011 a0001c0001t0017 others(10): Show |
30 | HG01069.hp2 HG01109.hp2 HG01123.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*2232G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 8/8 | 2232 | chr1 | 182644503 | ||||||
chr1:182644504 | G | A | 2 | a0001c0001t0013 a0001c0001t0048 |
5 | HG02055.hp1 HG02615.hp2 HG02895.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2231C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 8/8 | 2231 | chr1 | 182644504 | ||||||
chr1:182644530 | C | T | 1 | a0001c0001t0038 | 1 | HG03490.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2205G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 8/8 | 2205 | chr1 | 182644530 | ||||||
chr1:182644531 | G | A | 15 | a0001c0001t0004 a0001c0001t0008 a0001c0001t0010 others(12): Show |
56 | HG00423.hp1 HG00597.hp2 HG00609.hp2 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*2204C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 8/8 | 2204 | chr1 | 182644531 | ||||||
chr1:182644633 | T | G | 21 | a0001c0001t0004 a0001c0001t0008 a0001c0001t0010 others(18): Show |
66 | HG00423.hp1 HG00597.hp2 HG00609.hp2 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*2102A>C | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 8/8 | 2102 | chr1 | 182644633 | ||||||
chr1:182644700 | G | A | 1 | a0001c0001t0023 | 2 | HG04184.hp2 HG04199.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2035C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 8/8 | 2035 | chr1 | 182644700 | ||||||
chr1:182644865 | C | G | 3 | a0001c0001t0011 a0001c0001t0037 a0001c0001t0060 |
7 | HG01109.hp2 HG01243.hp1 HG02572.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1870G>C | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 8/8 | 1870 | chr1 | 182644865 | ||||||
chr1:182644867 | C | T | 2 | a0001c0001t0017 a0001c0001t0065 |
4 | HG01891.hp1 HG02970.hp2 NA18522.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1868G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 8/8 | 1868 | chr1 | 182644867 | ||||||
chr1:182644914 | C | T | 1 | a0001c0001t0056 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1821G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 8/8 | 1821 | chr1 | 182644914 | ||||||
chr1:182644920 | C | T | 1 | a0001c0001t0036 | 1 | NA18983.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1815G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 8/8 | 1815 | chr1 | 182644920 | ||||||
chr1:182644968 | C | T | 6 | a0001c0001t0017 a0001c0001t0021 a0001c0001t0025 others(3): Show |
10 | HG01069.hp2 HG01891.hp1 HG02486.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1767G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 8/8 | 1767 | chr1 | 182644968 | ||||||
chr1:182644994 | T | C | 2 | a0001c0001t0049 a0001c0001t0054 |
2 | HG03209.hp2 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1741A>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 8/8 | 1741 | chr1 | 182644994 | ||||||
chr1:182645168 | A | G | 6 | a0001c0001t0017 a0001c0001t0021 a0001c0001t0025 others(3): Show |
10 | HG01069.hp2 HG01891.hp1 HG02486.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1567T>C | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 8/8 | 1567 | chr1 | 182645168 | ||||||
chr1:182645431 | G | A | 1 | a0001c0001t0046 | 1 | NA19009.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1304C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 8/8 | 1304 | chr1 | 182645431 | ||||||
chr1:182645477 | G | T | 2 | a0001c0001t0049 a0001c0001t0054 |
2 | HG03209.hp2 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1258C>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 8/8 | 1258 | chr1 | 182645477 | ||||||
chr1:182645651 | A | C | 2 | a0001c0001t0019 a0001c0001t0020 |
4 | HG01099.hp2 HG01884.hp1 HG02922.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1084T>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 8/8 | 1084 | chr1 | 182645651 | ||||||
chr1:182645889 | C | T | 1 | a0001c0001t0035 | 1 | NA18977.hp1 | 3_prime_UTR_variant | MODIFIER | c.*846G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 8/8 | 846 | chr1 | 182645889 | ||||||
chr1:182645939 | T | C | 2 | a0001c0001t0049 a0001c0001t0054 |
2 | HG03209.hp2 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*796A>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 8/8 | 796 | chr1 | 182645939 | ||||||
chr1:182645979 | C | T | 1 | a0001c0001t0049 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*756G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 8/8 | 756 | chr1 | 182645979 | ||||||
chr1:182646147 | A | G | 1 | a0001c0001t0034 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*588T>C | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 8/8 | 588 | chr1 | 182646147 | ||||||
chr1:182646309 | C | T | 15 | a0001c0001t0004 a0001c0001t0008 a0001c0001t0010 others(12): Show |
56 | HG00423.hp1 HG00597.hp2 HG00609.hp2 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*426G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 8/8 | 426 | chr1 | 182646309 | ||||||
chr1:182646574 | C | A | 1 | a0001c0001t0047 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*161G>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 8/8 | 161 | chr1 | 182646574 | ||||||
chr1:182646584 | C | A | 1 | a0001c0001t0030 | 2 | HG01884.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*151G>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 8/8 | 151 | chr1 | 182646584 | ||||||
chr1:182646612 | AC | A | 2 | a0001c0001t0017 a0001c0001t0065 |
4 | HG01891.hp1 HG02970.hp2 NA18522.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*122delG | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 8/8 | 122 | chr1 | 182646612 | ||||||
chr1:182646630 | C | G | 1 | a0001c0001t0031 | 1 | NA19074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*105G>C | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 8/8 | 105 | chr1 | 182646630 | ||||||
chr1:182646637 | C | T | 1 | a0001c0001t0056 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*98G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 8/8 | 98 | chr1 | 182646637 | ||||||
chr1:182671666 | C | T | 1 | a0001c0001t0055 | 1 | NA19000.hp1 | 5_prime_UTR_variant | MODIFIER | c.-113G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 3/8 | 2017 | chr1 | 182671666 | ||||||
chr1:182671713 | G | A | 4 | a0001c0001t0007 a0001c0001t0018 a0001c0001t0067 others(1): Show |
13 | HG01123.hp2 HG02258.hp1 HG02630.hp1 others(10): Show |
5_prime_UTR_variant | MODIFIER | c.-160C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 3/8 | 2064 | chr1 | 182671713 | ||||||
chr1:182671716 | T | G | 27 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 others(24): Show |
79 | HG00597.hp2 HG00621.hp2 HG00642.hp1 others(76): Show |
5_prime_UTR_variant | MODIFIER | c.-163A>C | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 3/8 | 2067 | chr1 | 182671716 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:182647001 | G | T | 51 | a0001c0001t0004g0002 a0001c0001t0004g0025 a0001c0001t0004g0053 others(48): Show |
66 | HG00423.hp1 HG00597.hp2 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.361-84C>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 7/7 | chr1 | 182647001 | |||||||
chr1:182647106 | G | A | 1 | a0001c0001t0011g0149 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.361-189C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 7/7 | chr1 | 182647106 | |||||||
chr1:182647279 | C | T | 43 | a0001c0001t0004g0002 a0001c0001t0004g0025 a0001c0001t0004g0053 others(40): Show |
57 | HG00423.hp1 HG00597.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.361-362G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 7/7 | chr1 | 182647279 | |||||||
chr1:182647638 | T | C | 9 | a0001c0001t0017g0014 a0001c0001t0017g0032 a0001c0001t0021g0036 others(6): Show |
10 | HG01069.hp2 HG01891.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.360+499A>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 7/7 | chr1 | 182647638 | |||||||
chr1:182647648 | T | C | 1 | a0001c0001t0008g0084 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.360+489A>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 7/7 | chr1 | 182647648 | |||||||
chr1:182647690 | A | G | 52 | a0001c0001t0004g0002 a0001c0001t0004g0025 a0001c0001t0004g0053 others(49): Show |
67 | HG00423.hp1 HG00597.hp2 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.360+447T>C | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 7/7 | chr1 | 182647690 | |||||||
chr1:182647700 | C | CT | 31 | a0001c0001t0004g0002 a0001c0001t0004g0025 a0001c0001t0004g0053 others(28): Show |
45 | HG00423.hp1 HG00597.hp2 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.360+436dupA | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 7/7 | chr1 | 182647700 | |||||||
chr1:182647712 | G | A | 1 | a0001c0001t0023g0169 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.360+425C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 7/7 | chr1 | 182647712 | |||||||
chr1:182647782 | T | C | 6 | a0001c0001t0001g0047 a0001c0001t0001g0088 a0001c0001t0001g0157 others(3): Show |
6 | NA18612.hp1 NA18983.hp1 NA18992.hp2 others(3): Show |
intron_variant | MODIFIER | c.360+355A>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 7/7 | chr1 | 182647782 | |||||||
chr1:182647897 | T | C | 15 | a0001c0001t0007g0005 a0001c0001t0007g0041 a0001c0001t0007g0043 others(12): Show |
20 | HG01109.hp2 HG01123.hp2 HG01192.hp2 others(17): Show |
intron_variant | MODIFIER | c.360+240A>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 7/7 | chr1 | 182647897 | |||||||
chr1:182647911 | T | C | 1 | a0001c0001t0001g0121 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.360+226A>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 7/7 | chr1 | 182647911 | |||||||
chr1:182648357 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.194-54C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182648357 | |||||||
chr1:182648386 | GT | G | 9 | a0001c0001t0017g0014 a0001c0001t0017g0032 a0001c0001t0021g0036 others(6): Show |
10 | HG01069.hp2 HG01891.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.194-84delA | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182648386 | |||||||
chr1:182648392 | G | A | 6 | a0001c0001t0019g0046 a0001c0001t0019g0142 a0001c0001t0020g0035 others(3): Show |
6 | HG01099.hp2 HG01884.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.194-89C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182648392 | |||||||
chr1:182648599 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.194-296A>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182648599 | |||||||
chr1:182648660 | G | A | 52 | a0001c0001t0004g0002 a0001c0001t0004g0025 a0001c0001t0004g0053 others(49): Show |
67 | HG00423.hp1 HG00597.hp2 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.194-357C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182648660 | |||||||
chr1:182648729 | C | T | 9 | a0001c0001t0017g0014 a0001c0001t0017g0032 a0001c0001t0021g0036 others(6): Show |
10 | HG01069.hp2 HG01891.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.194-426G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182648729 | |||||||
chr1:182648922 | A | G | 52 | a0001c0001t0004g0002 a0001c0001t0004g0025 a0001c0001t0004g0053 others(49): Show |
67 | HG00423.hp1 HG00597.hp2 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.194-619T>C | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182648922 | |||||||
chr1:182648926 | C | T | 9 | a0001c0001t0017g0014 a0001c0001t0017g0032 a0001c0001t0021g0036 others(6): Show |
10 | HG01069.hp2 HG01891.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.194-623G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182648926 | |||||||
chr1:182648973 | G | A | 4 | a0001c0001t0019g0046 a0001c0001t0019g0142 a0001c0001t0020g0035 others(1): Show |
4 | HG01099.hp2 HG01884.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.194-670C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182648973 | |||||||
chr1:182649044 | G | A | 4 | a0001c0001t0025g0037 a0001c0001t0025g0068 a0001c0001t0050g0069 others(1): Show |
4 | HG01069.hp2 HG02486.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.194-741C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182649044 | |||||||
chr1:182649125 | A | G | 52 | a0001c0001t0004g0002 a0001c0001t0004g0025 a0001c0001t0004g0053 others(49): Show |
67 | HG00423.hp1 HG00597.hp2 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.194-822T>C | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182649125 | |||||||
chr1:182649132 | C | T | 6 | a0001c0001t0006g0054 a0001c0001t0006g0056 a0001c0001t0028g0052 others(3): Show |
6 | HG02615.hp1 HG02723.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.194-829G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182649132 | |||||||
chr1:182649186 | C | A | 4 | a0001c0001t0007g0005 a0001c0001t0007g0043 a0001c0001t0018g0042 others(1): Show |
7 | HG02818.hp2 HG02896.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.194-883G>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182649186 | |||||||
chr1:182649311 | A | C | 1 | a0001c0001t0005g0151 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.194-1008T>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182649311 | |||||||
chr1:182649424 | T | G | 41 | a0001c0001t0004g0002 a0001c0001t0004g0025 a0001c0001t0004g0053 others(38): Show |
55 | HG00423.hp1 HG00597.hp2 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.194-1121A>C | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182649424 | |||||||
chr1:182649502 | TTA | T | 30 | a0001c0001t0004g0002 a0001c0001t0004g0025 a0001c0001t0004g0053 others(27): Show |
44 | HG00423.hp1 HG00597.hp2 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.194-1201_194-1200d others(4): Show |
RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182649502 | |||||||
chr1:182649704 | TA | T | 31 | a0001c0001t0004g0002 a0001c0001t0004g0025 a0001c0001t0004g0053 others(28): Show |
45 | HG00423.hp1 HG00597.hp2 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.194-1402delT | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182649704 | |||||||
chr1:182649846 | C | T | 51 | a0001c0001t0004g0002 a0001c0001t0004g0025 a0001c0001t0004g0053 others(48): Show |
66 | HG00423.hp1 HG00597.hp2 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.194-1543G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182649846 | |||||||
chr1:182649849 | C | G | 1 | a0001c0001t0003g0100 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.194-1546G>C | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182649849 | |||||||
chr1:182649905 | C | CT | 10 | a0001c0001t0001g0023 a0001c0001t0001g0134 a0001c0001t0001g0196 others(7): Show |
12 | HG00597.hp1 HG01981.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.194-1603dupA | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182649905 | |||||||
chr1:182649905 | C | CTTT | 34 | a0001c0001t0004g0002 a0001c0001t0004g0053 a0001c0001t0004g0129 others(31): Show |
48 | HG00423.hp1 HG00597.hp2 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.194-1605_194-1603d others(5): Show |
RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182649905 | |||||||
chr1:182649905 | C | CTTTT | 10 | a0001c0001t0004g0217 a0001c0001t0004g0218 a0001c0001t0004g0219 others(7): Show |
10 | HG01256.hp2 HG01928.hp1 HG01928.hp2 others(7): Show |
intron_variant | MODIFIER | c.194-1606_194-1603d others(6): Show |
RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182649905 | |||||||
chr1:182649905 | CT | C | 6 | a0001c0001t0007g0005 a0001c0001t0007g0041 a0001c0001t0007g0043 others(3): Show |
9 | HG01123.hp2 HG02818.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.194-1603delA | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182649905 | |||||||
chr1:182649981 | G | A | 1 | a0001c0001t0029g0224 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.194-1678C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182649981 | |||||||
chr1:182649987 | C | T | 9 | a0001c0001t0013g0073 a0001c0001t0013g0074 a0001c0001t0013g0181 others(6): Show |
9 | HG01884.hp2 HG02055.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.194-1684G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182649987 | |||||||
chr1:182650005 | G | A | 1 | a0001c0001t0001g0158 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.194-1702C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182650005 | |||||||
chr1:182650031 | C | T | 31 | a0001c0001t0004g0002 a0001c0001t0004g0025 a0001c0001t0004g0053 others(28): Show |
45 | HG00423.hp1 HG00597.hp2 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.194-1728G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182650031 | |||||||
chr1:182650037 | A | G | 52 | a0001c0001t0004g0002 a0001c0001t0004g0025 a0001c0001t0004g0053 others(49): Show |
67 | HG00423.hp1 HG00597.hp2 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.194-1734T>C | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182650037 | |||||||
chr1:182650038 | A | G | 1 | a0001c0001t0043g0099 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.194-1735T>C | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182650038 | |||||||
chr1:182650041 | AGCTGGGA others(126): Show |
A | 5 | a0001c0001t0011g0013 a0001c0001t0011g0146 a0001c0001t0011g0149 others(2): Show |
7 | HG01109.hp2 HG01243.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.194-1871_194-1739d others(2): Show |
RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182650041 | |||||||
chr1:182650056 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.194-1753G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182650056 | |||||||
chr1:182650060 | C | T | 10 | a0001c0001t0007g0005 a0001c0001t0007g0041 a0001c0001t0007g0043 others(7): Show |
13 | HG01123.hp2 HG01192.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.194-1757G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182650060 | |||||||
chr1:182650061 | G | A | 1 | a0001c0001t0064g0034 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.194-1758C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182650061 | |||||||
chr1:182650074 | G | A | 2 | a0001c0001t0009g0115 a0001c0001t0009g0190 |
2 | NA18982.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.194-1771C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182650074 | |||||||
chr1:182650142 | C | T | 2 | a0001c0001t0024g0040 a0001c0001t0024g0206 |
2 | HG02258.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.194-1839G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182650142 | |||||||
chr1:182650201 | C | T | 1 | a0001c0001t0001g0022 | 2 | NA18944.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.194-1898G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182650201 | |||||||
chr1:182650235 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.194-1932C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182650235 | |||||||
chr1:182650254 | G | A | 1 | a0001c0001t0001g0196 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.194-1951C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182650254 | |||||||
chr1:182650264 | A | C | 1 | a0001c0001t0009g0188 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.194-1961T>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182650264 | |||||||
chr1:182650412 | A | G | 43 | a0001c0001t0004g0002 a0001c0001t0004g0025 a0001c0001t0004g0053 others(40): Show |
57 | HG00423.hp1 HG00597.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.194-2109T>C | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182650412 | |||||||
chr1:182650422 | G | T | 2 | a0001c0001t0049g0225 a0001c0001t0054g0067 |
2 | HG03209.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.194-2119C>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182650422 | |||||||
chr1:182650450 | C | G | 1 | a0001c0001t0045g0231 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.194-2147G>C | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182650450 | |||||||
chr1:182650540 | T | C | 1 | a0001c0001t0003g0027 | 2 | HG00621.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.194-2237A>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182650540 | |||||||
chr1:182650712 | T | A | 1 | a0001c0001t0052g0171 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.194-2409A>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182650712 | |||||||
chr1:182650789 | A | G | 2 | a0001c0001t0025g0037 a0001c0001t0059g0180 |
2 | HG01069.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.194-2486T>C | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182650789 | |||||||
chr1:182650923 | T | C | 1 | a0001c0001t0049g0225 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.194-2620A>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182650923 | |||||||
chr1:182650958 | G | C | 5 | a0001c0001t0011g0013 a0001c0001t0011g0146 a0001c0001t0011g0149 others(2): Show |
7 | HG01109.hp2 HG01243.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.194-2655C>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182650958 | |||||||
chr1:182650969 | G | A | 1 | a0001c0001t0009g0062 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.194-2666C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182650969 | |||||||
chr1:182651003 | T | G | 73 | a0001c0001t0004g0002 a0001c0001t0004g0025 a0001c0001t0004g0053 others(70): Show |
93 | HG00423.hp1 HG00597.hp2 HG00609.hp2 others(90): Show |
intron_variant | MODIFIER | c.194-2700A>C | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182651003 | |||||||
chr1:182651016 | A | C | 73 | a0001c0001t0004g0002 a0001c0001t0004g0025 a0001c0001t0004g0053 others(70): Show |
93 | HG00423.hp1 HG00597.hp2 HG00609.hp2 others(90): Show |
intron_variant | MODIFIER | c.194-2713T>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182651016 | |||||||
chr1:182651070 | T | C | 1 | a0001c0001t0056g0128 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.194-2767A>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182651070 | |||||||
chr1:182651142 | G | A | 5 | a0001c0001t0011g0013 a0001c0001t0011g0146 a0001c0001t0011g0149 others(2): Show |
7 | HG01109.hp2 HG01243.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.194-2839C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182651142 | |||||||
chr1:182651177 | C | T | 1 | a0001c0001t0056g0128 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.194-2874G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182651177 | |||||||
chr1:182651219 | C | A | 9 | a0001c0001t0013g0073 a0001c0001t0013g0074 a0001c0001t0013g0181 others(6): Show |
9 | HG01884.hp2 HG02055.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.194-2916G>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182651219 | |||||||
chr1:182651343 | G | A | 1 | a0001c0001t0003g0138 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.194-3040C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182651343 | |||||||
chr1:182651395 | A | G | 1 | a0001c0001t0064g0034 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.194-3092T>C | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182651395 | |||||||
chr1:182651657 | T | C | 1 | a0001c0001t0001g0047 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.194-3354A>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182651657 | |||||||
chr1:182651719 | C | T | 47 | a0001c0001t0004g0002 a0001c0001t0004g0025 a0001c0001t0004g0053 others(44): Show |
61 | HG00423.hp1 HG00597.hp2 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.194-3416G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182651719 | |||||||
chr1:182651763 | G | A | 116 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(113): Show |
141 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.194-3460C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182651763 | |||||||
chr1:182651806 | GGGAAAAA others(11): Show |
G | 2 | a0001c0001t0024g0040 a0001c0001t0024g0206 |
2 | HG02258.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.194-3521_194-3504d others(20): Show |
RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182651806 | |||||||
chr1:182651878 | C | T | 1 | a0001c0001t0001g0116 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.194-3575G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182651878 | |||||||
chr1:182651918 | G | T | 1 | a0001c0001t0014g0230 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.194-3615C>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182651918 | |||||||
chr1:182652028 | C | T | 1 | a0001c0001t0002g0200 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.194-3725G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182652028 | |||||||
chr1:182652060 | G | A | 1 | a0001c0001t0056g0128 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.194-3757C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182652060 | |||||||
chr1:182652102 | A | G | 3 | a0001c0001t0001g0126 a0001c0001t0001g0153 a0001c0001t0001g0192 |
3 | HG01361.hp2 HG02630.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.194-3799T>C | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182652102 | |||||||
chr1:182652161 | T | C | 164 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(161): Show |
203 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.194-3858A>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182652161 | |||||||
chr1:182652403 | G | T | 1 | a0001c0001t0001g0163 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.194-4100C>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182652403 | |||||||
chr1:182652537 | C | T | 2 | a0001c0001t0021g0036 a0001c0001t0021g0078 |
2 | HG02647.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.194-4234G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182652537 | |||||||
chr1:182652620 | G | T | 1 | a0001c0001t0006g0085 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.194-4317C>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182652620 | |||||||
chr1:182652671 | G | A | 2 | a0001c0001t0049g0225 a0001c0001t0054g0067 |
2 | HG03209.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.194-4368C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182652671 | |||||||
chr1:182653017 | A | T | 1 | a0001c0001t0002g0104 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.194-4714T>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182653017 | |||||||
chr1:182653091 | A | G | 1 | a0001c0001t0024g0206 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.194-4788T>C | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182653091 | |||||||
chr1:182653126 | G | A | 10 | a0001c0001t0013g0073 a0001c0001t0013g0074 a0001c0001t0013g0181 others(7): Show |
10 | HG01884.hp2 HG02055.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.194-4823C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182653126 | |||||||
chr1:182653251 | C | T | 164 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(161): Show |
203 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.194-4948G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182653251 | |||||||
chr1:182653381 | AT | A | 26 | a0001c0001t0001g0159 a0001c0001t0002g0140 a0001c0001t0003g0015 others(23): Show |
33 | HG01109.hp2 HG01123.hp2 HG01168.hp1 others(30): Show |
intron_variant | MODIFIER | c.194-5079delA | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182653381 | |||||||
chr1:182653397 | A | T | 1 | a0001c0001t0001g0047 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.194-5094T>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182653397 | |||||||
chr1:182653581 | T | C | 164 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(161): Show |
203 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.194-5278A>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182653581 | |||||||
chr1:182653595 | G | A | 1 | a0001c0003t0022g0167 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.194-5292C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182653595 | |||||||
chr1:182653632 | T | C | 164 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(161): Show |
203 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.194-5329A>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182653632 | |||||||
chr1:182653669 | G | A | 30 | a0001c0001t0004g0002 a0001c0001t0004g0025 a0001c0001t0004g0053 others(27): Show |
44 | HG00423.hp1 HG00597.hp2 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.194-5366C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182653669 | |||||||
chr1:182653690 | T | C | 1 | a0001c0001t0007g0041 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.194-5387A>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182653690 | |||||||
chr1:182653830 | G | A | 4 | a0001c0001t0025g0037 a0001c0001t0025g0068 a0001c0001t0050g0069 others(1): Show |
4 | HG01069.hp2 HG02486.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.194-5527C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182653830 | |||||||
chr1:182653856 | A | G | 9 | a0001c0001t0013g0073 a0001c0001t0013g0074 a0001c0001t0013g0181 others(6): Show |
9 | HG01884.hp2 HG02055.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.194-5553T>C | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182653856 | |||||||
chr1:182653858 | G | A | 1 | a0001c0001t0010g0160 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.194-5555C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182653858 | |||||||
chr1:182653876 | G | A | 121 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(118): Show |
146 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.194-5573C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182653876 | |||||||
chr1:182653989 | GC | G | 31 | a0001c0001t0004g0002 a0001c0001t0004g0025 a0001c0001t0004g0053 others(28): Show |
45 | HG00423.hp1 HG00597.hp2 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.194-5687delG | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182653989 | |||||||
chr1:182654144 | T | A | 115 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(112): Show |
140 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.194-5841A>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182654144 | |||||||
chr1:182654214 | G | T | 116 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(113): Show |
141 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.194-5911C>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182654214 | |||||||
chr1:182654374 | G | A | 164 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(161): Show |
203 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.194-6071C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182654374 | |||||||
chr1:182654406 | C | A | 2 | a0001c0001t0026g0177 a0001c0001t0026g0209 |
2 | HG02572.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.194-6103G>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182654406 | |||||||
chr1:182654497 | A | G | 1 | a0001c0001t0003g0155 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.194-6194T>C | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182654497 | |||||||
chr1:182654506 | C | T | 1 | a0001c0001t0014g0039 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.194-6203G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182654506 | |||||||
chr1:182654710 | TA | T | 7 | a0001c0001t0019g0046 a0001c0001t0019g0142 a0001c0001t0020g0035 others(4): Show |
7 | HG01099.hp2 HG01884.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.194-6408delT | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182654710 | |||||||
chr1:182654722 | C | A | 171 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(168): Show |
211 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.194-6419G>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182654722 | |||||||
chr1:182654790 | G | A | 42 | a0001c0001t0004g0002 a0001c0001t0004g0025 a0001c0001t0004g0053 others(39): Show |
56 | HG00423.hp1 HG00597.hp2 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.194-6487C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182654790 | |||||||
chr1:182654889 | C | T | 1 | a0001c0001t0049g0225 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.194-6586G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182654889 | |||||||
chr1:182654949 | A | G | 1 | a0001c0001t0005g0087 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.194-6646T>C | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182654949 | |||||||
chr1:182655085 | C | A | 1 | a0001c0001t0007g0175 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.194-6782G>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182655085 | |||||||
chr1:182655170 | A | C | 7 | a0001c0001t0003g0026 a0001c0001t0003g0027 a0001c0001t0003g0075 others(4): Show |
9 | HG00621.hp1 HG02071.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.194-6867T>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182655170 | |||||||
chr1:182655233 | G | A | 122 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(119): Show |
147 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.194-6930C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182655233 | |||||||
chr1:182655280 | A | G | 164 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(161): Show |
203 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.194-6977T>C | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182655280 | |||||||
chr1:182655290 | T | C | 43 | a0001c0001t0004g0002 a0001c0001t0004g0025 a0001c0001t0004g0053 others(40): Show |
57 | HG00423.hp1 HG00597.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.194-6987A>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182655290 | |||||||
chr1:182655333 | G | A | 4 | a0001c0001t0008g0004 a0001c0001t0008g0084 a0001c0001t0008g0170 others(1): Show |
8 | HG00423.hp1 HG00609.hp2 NA18941.hp2 others(5): Show |
intron_variant | MODIFIER | c.194-7030C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182655333 | |||||||
chr1:182655548 | C | A | 111 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(108): Show |
135 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.194-7245G>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182655548 | |||||||
chr1:182655817 | TCTC | T | 123 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(120): Show |
148 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.194-7517_194-7515d others(5): Show |
RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182655817 | |||||||
chr1:182655999 | G | T | 2 | a0001c0001t0021g0036 a0001c0001t0021g0078 |
2 | HG02647.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.194-7696C>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182655999 | |||||||
chr1:182656065 | C | T | 1 | a0001c0001t0014g0039 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.194-7762G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182656065 | |||||||
chr1:182656123 | T | C | 41 | a0001c0001t0004g0002 a0001c0001t0004g0025 a0001c0001t0004g0053 others(38): Show |
55 | HG00423.hp1 HG00597.hp2 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.194-7820A>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182656123 | |||||||
chr1:182656279 | C | T | 163 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(160): Show |
202 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.194-7976G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182656279 | |||||||
chr1:182656281 | G | A | 1 | a0001c0001t0005g0204 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.194-7978C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182656281 | |||||||
chr1:182656442 | C | A | 116 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(113): Show |
141 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.194-8139G>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182656442 | |||||||
chr1:182656473 | T | C | 1 | a0001c0001t0045g0231 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.194-8170A>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182656473 | |||||||
chr1:182656557 | T | C | 45 | a0001c0001t0004g0002 a0001c0001t0004g0025 a0001c0001t0004g0053 others(42): Show |
59 | HG00423.hp1 HG00597.hp2 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.194-8254A>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182656557 | |||||||
chr1:182656568 | A | C | 2 | a0001c0001t0024g0040 a0001c0001t0024g0206 |
2 | HG02258.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.194-8265T>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182656568 | |||||||
chr1:182656697 | C | T | 1 | a0001c0001t0004g0219 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.194-8394G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182656697 | |||||||
chr1:182656802 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.194-8499G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182656802 | |||||||
chr1:182656870 | C | A | 44 | a0001c0001t0004g0002 a0001c0001t0004g0025 a0001c0001t0004g0053 others(41): Show |
58 | HG00423.hp1 HG00597.hp2 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.194-8567G>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182656870 | |||||||
chr1:182656896 | G | T | 119 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(116): Show |
144 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.194-8593C>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182656896 | |||||||
chr1:182657043 | G | A | 6 | a0001c0001t0007g0005 a0001c0001t0007g0041 a0001c0001t0007g0043 others(3): Show |
9 | HG01123.hp2 HG02818.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.194-8740C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182657043 | |||||||
chr1:182657082 | T | C | 4 | a0001c0001t0019g0046 a0001c0001t0019g0142 a0001c0001t0020g0035 others(1): Show |
4 | HG01099.hp2 HG01884.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.194-8779A>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182657082 | |||||||
chr1:182657088 | C | G | 1 | a0001c0001t0059g0180 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.194-8785G>C | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182657088 | |||||||
chr1:182657138 | T | C | 1 | a0001c0001t0005g0199 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.193+8831A>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182657138 | |||||||
chr1:182657177 | AATAGAGC others(13): Show |
A | 1 | a0001c0001t0007g0175 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.193+8772_193+8791d others(22): Show |
RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182657177 | |||||||
chr1:182657215 | A | G | 164 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(161): Show |
203 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.193+8754T>C | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182657215 | |||||||
chr1:182657332 | C | G | 1 | a0001c0001t0051g0070 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.193+8637G>C | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182657332 | |||||||
chr1:182657382 | T | G | 1 | a0001c0001t0001g0198 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.193+8587A>C | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182657382 | |||||||
chr1:182657485 | G | A | 1 | a0001c0001t0001g0205 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.193+8484C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182657485 | |||||||
chr1:182657603 | C | A | 123 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(120): Show |
148 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.193+8366G>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182657603 | |||||||
chr1:182657675 | C | T | 28 | a0001c0001t0004g0002 a0001c0001t0004g0025 a0001c0001t0004g0053 others(25): Show |
42 | HG00423.hp1 HG00597.hp2 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.193+8294G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182657675 | |||||||
chr1:182657720 | C | T | 124 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(121): Show |
149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.193+8249G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182657720 | |||||||
chr1:182657752 | T | C | 1 | a0001c0001t0063g0212 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.193+8217A>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182657752 | |||||||
chr1:182657967 | T | G | 1 | a0001c0001t0007g0043 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.193+8002A>C | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182657967 | |||||||
chr1:182657978 | C | A | 2 | a0001c0001t0024g0040 a0001c0001t0024g0206 |
2 | HG02258.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.193+7991G>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182657978 | |||||||
chr1:182658115 | A | G | 10 | a0001c0001t0013g0073 a0001c0001t0013g0074 a0001c0001t0013g0181 others(7): Show |
10 | HG01884.hp2 HG02055.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.193+7854T>C | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182658115 | |||||||
chr1:182658331 | G | A | 1 | a0001c0001t0024g0040 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.193+7638C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182658331 | |||||||
chr1:182658695 | A | C | 2 | a0001c0001t0021g0036 a0001c0001t0021g0078 |
2 | HG02647.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.193+7274T>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182658695 | |||||||
chr1:182658718 | G | A | 5 | a0001c0001t0011g0013 a0001c0001t0011g0146 a0001c0001t0011g0149 others(2): Show |
7 | HG01109.hp2 HG01243.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.193+7251C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182658718 | |||||||
chr1:182658766 | G | C | 122 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(119): Show |
147 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.193+7203C>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182658766 | |||||||
chr1:182658833 | C | A | 1 | a0001c0001t0024g0206 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.193+7136G>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182658833 | |||||||
chr1:182658880 | T | G | 9 | a0001c0001t0013g0073 a0001c0001t0013g0074 a0001c0001t0013g0181 others(6): Show |
9 | HG01884.hp2 HG02055.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.193+7089A>C | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182658880 | |||||||
chr1:182659365 | G | T | 1 | a0001c0001t0014g0039 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.193+6604C>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182659365 | |||||||
chr1:182659378 | G | A | 117 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(114): Show |
142 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.193+6591C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182659378 | |||||||
chr1:182659482 | C | T | 4 | a0001c0001t0001g0012 a0001c0001t0001g0154 a0001c0001t0001g0223 others(1): Show |
6 | NA18747.hp2 NA18973.hp1 NA18995.hp1 others(3): Show |
intron_variant | MODIFIER | c.193+6487G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182659482 | |||||||
chr1:182659527 | T | C | 233 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(230): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.193+6442A>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182659527 | |||||||
chr1:182659535 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.193+6434G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182659535 | |||||||
chr1:182659552 | A | C | 1 | a0001c0001t0052g0171 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.193+6417T>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182659552 | |||||||
chr1:182659572 | G | A | 10 | a0001c0001t0003g0133 a0001c0001t0004g0002 a0001c0001t0004g0129 others(7): Show |
17 | HG00597.hp2 HG03195.hp2 HG03486.hp1 others(14): Show |
intron_variant | MODIFIER | c.193+6397C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182659572 | |||||||
chr1:182659582 | C | T | 115 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(112): Show |
140 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.193+6387G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182659582 | |||||||
chr1:182659635 | G | T | 1 | a0001c0001t0049g0225 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.193+6334C>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182659635 | |||||||
chr1:182659657 | C | A | 9 | a0001c0001t0013g0073 a0001c0001t0013g0074 a0001c0001t0013g0181 others(6): Show |
9 | HG01884.hp2 HG02055.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.193+6312G>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182659657 | |||||||
chr1:182659817 | CA | C | 116 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(113): Show |
141 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.193+6151delT | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182659817 | |||||||
chr1:182660119 | A | C | 1 | a0001c0001t0014g0039 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.193+5850T>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182660119 | |||||||
chr1:182660124 | T | C | 4 | a0001c0001t0025g0068 a0001c0001t0049g0225 a0001c0001t0050g0069 others(1): Show |
4 | HG03139.hp1 HG03209.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.193+5845A>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182660124 | |||||||
chr1:182660131 | T | C | 1 | a0001c0001t0001g0107 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.193+5838A>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182660131 | |||||||
chr1:182660256 | A | C | 1 | a0001c0001t0004g0211 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.193+5713T>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182660256 | |||||||
chr1:182660315 | C | T | 1 | a0001c0001t0002g0098 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.193+5654G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182660315 | |||||||
chr1:182660327 | T | A | 18 | a0001c0001t0006g0054 a0001c0001t0006g0056 a0001c0001t0006g0057 others(15): Show |
18 | HG01069.hp2 HG02615.hp1 HG02723.hp2 others(15): Show |
intron_variant | MODIFIER | c.193+5642A>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182660327 | |||||||
chr1:182660465 | C | T | 11 | a0001c0001t0006g0127 a0001c0001t0013g0073 a0001c0001t0013g0074 others(8): Show |
11 | HG01884.hp2 HG02486.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.193+5504G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182660465 | |||||||
chr1:182660627 | G | A | 1 | a0001c0001t0014g0039 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.193+5342C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182660627 | |||||||
chr1:182660682 | T | C | 1 | a0001c0001t0049g0225 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.193+5287A>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182660682 | |||||||
chr1:182660784 | C | A | 1 | a0001c0001t0004g0214 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.193+5185G>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182660784 | |||||||
chr1:182660994 | C | T | 15 | a0001c0001t0004g0053 a0001c0001t0006g0054 a0001c0001t0006g0056 others(12): Show |
15 | HG01069.hp2 HG02615.hp1 HG02886.hp1 others(12): Show |
intron_variant | MODIFIER | c.193+4975G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182660994 | |||||||
chr1:182661031 | A | G | 1 | a0001c0001t0049g0225 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.193+4938T>C | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182661031 | |||||||
chr1:182661093 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.193+4876C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182661093 | |||||||
chr1:182661150 | T | A | 31 | a0001c0001t0004g0053 a0001c0001t0006g0054 a0001c0001t0006g0056 others(28): Show |
35 | HG01069.hp2 HG01123.hp2 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.193+4819A>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182661150 | |||||||
chr1:182661205 | G | A | 16 | a0001c0001t0007g0005 a0001c0001t0007g0041 a0001c0001t0007g0043 others(13): Show |
20 | HG01123.hp2 HG01891.hp1 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.193+4764C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182661205 | |||||||
chr1:182661308 | A | C | 2 | a0001c0001t0051g0070 a0001c0001t0052g0171 |
2 | HG01192.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.193+4661T>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182661308 | |||||||
chr1:182661808 | T | TCA | 41 | a0001c0001t0001g0065 a0001c0001t0001g0120 a0001c0001t0001g0163 others(38): Show |
54 | HG00558.hp1 HG00597.hp2 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.193+4159_193+4160d others(4): Show |
RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182661808 | |||||||
chr1:182661808 | T | TCACA | 6 | a0001c0001t0009g0191 a0001c0001t0019g0142 a0001c0001t0020g0035 others(3): Show |
6 | HG01099.hp2 HG01884.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.193+4157_193+4160d others(6): Show |
RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182661808 | |||||||
chr1:182661808 | T | TCACACAC others(5): Show |
1 | a0001c0001t0052g0171 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.193+4149_193+4160d others(14): Show |
RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182661808 | |||||||
chr1:182661808 | T | TCACACAC others(7): Show |
1 | a0001c0001t0051g0070 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.193+4147_193+4160d others(16): Show |
RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182661808 | |||||||
chr1:182661808 | TCA | T | 24 | a0001c0001t0001g0091 a0001c0001t0001g0145 a0001c0001t0001g0152 others(21): Show |
29 | HG01081.hp1 HG01123.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.193+4159_193+4160d others(4): Show |
RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182661808 | |||||||
chr1:182661808 | TCACA | T | 15 | a0001c0001t0001g0023 a0001c0001t0002g0096 a0001c0001t0003g0138 others(12): Show |
17 | HG00438.hp1 HG01891.hp1 HG02074.hp2 others(14): Show |
intron_variant | MODIFIER | c.193+4157_193+4160d others(6): Show |
RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182661808 | |||||||
chr1:182661808 | TCACACAC others(1): Show |
T | 6 | a0001c0001t0002g0132 a0001c0001t0003g0015 a0001c0001t0021g0078 others(3): Show |
7 | HG02145.hp1 HG02559.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.193+4153_193+4160d others(10): Show |
RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182661808 | |||||||
chr1:182661808 | TCACACAC others(3): Show |
T | 2 | a0001c0001t0003g0094 a0001c0001t0003g0133 |
2 | HG03195.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.193+4151_193+4160d others(12): Show |
RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182661808 | |||||||
chr1:182661927 | A | G | 1 | a0001c0001t0001g0016 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.193+4042T>C | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182661927 | |||||||
chr1:182662032 | G | A | 16 | a0001c0001t0007g0005 a0001c0001t0007g0041 a0001c0001t0007g0043 others(13): Show |
20 | HG01123.hp2 HG01891.hp1 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.193+3937C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182662032 | |||||||
chr1:182662287 | A | G | 3 | a0001c0001t0007g0005 a0001c0001t0007g0043 a0001c0001t0018g0042 |
6 | HG02818.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.193+3682T>C | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182662287 | |||||||
chr1:182662558 | G | A | 16 | a0001c0001t0007g0005 a0001c0001t0007g0041 a0001c0001t0007g0043 others(13): Show |
20 | HG01123.hp2 HG01891.hp1 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.193+3411C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182662558 | |||||||
chr1:182662569 | T | C | 94 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0022 others(91): Show |
108 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.193+3400A>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182662569 | |||||||
chr1:182662794 | T | C | 1 | a0001c0001t0014g0039 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.193+3175A>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182662794 | |||||||
chr1:182662952 | GGGA | G | 37 | a0001c0001t0006g0057 a0001c0001t0006g0059 a0001c0001t0006g0085 others(34): Show |
41 | HG01123.hp2 HG01255.hp1 HG01884.hp2 others(38): Show |
intron_variant | MODIFIER | c.193+3014_193+3016d others(5): Show |
RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182662952 | |||||||
chr1:182662963 | A | G | 42 | a0001c0001t0004g0053 a0001c0001t0006g0054 a0001c0001t0006g0056 others(39): Show |
46 | HG01123.hp2 HG01255.hp1 HG01884.hp2 others(43): Show |
intron_variant | MODIFIER | c.193+3006T>C | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182662963 | |||||||
chr1:182663015 | A | C | 1 | a0001c0001t0049g0225 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.193+2954T>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182663015 | |||||||
chr1:182663019 | G | A | 1 | a0001c0001t0049g0225 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.193+2950C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182663019 | |||||||
chr1:182663052 | C | A | 49 | a0001c0001t0004g0053 a0001c0001t0006g0054 a0001c0001t0006g0056 others(46): Show |
53 | HG01069.hp2 HG01123.hp2 HG01255.hp1 others(50): Show |
intron_variant | MODIFIER | c.193+2917G>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182663052 | |||||||
chr1:182663065 | T | C | 28 | a0001c0001t0006g0127 a0001c0001t0007g0005 a0001c0001t0007g0041 others(25): Show |
32 | HG01123.hp2 HG01255.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.193+2904A>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182663065 | |||||||
chr1:182663099 | T | C | 43 | a0001c0001t0004g0053 a0001c0001t0006g0054 a0001c0001t0006g0056 others(40): Show |
47 | HG01123.hp2 HG01255.hp1 HG01884.hp2 others(44): Show |
intron_variant | MODIFIER | c.193+2870A>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182663099 | |||||||
chr1:182663100 | G | A | 42 | a0001c0001t0004g0053 a0001c0001t0006g0054 a0001c0001t0006g0056 others(39): Show |
46 | HG01123.hp2 HG01255.hp1 HG01884.hp2 others(43): Show |
intron_variant | MODIFIER | c.193+2869C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182663100 | |||||||
chr1:182663173 | C | G | 1 | a0002c0002t0066g0174 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.193+2796G>C | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182663173 | |||||||
chr1:182663289 | T | G | 1 | a0001c0001t0014g0039 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.193+2680A>C | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182663289 | |||||||
chr1:182663320 | G | A | 42 | a0001c0001t0004g0053 a0001c0001t0006g0054 a0001c0001t0006g0056 others(39): Show |
46 | HG01123.hp2 HG01255.hp1 HG01884.hp2 others(43): Show |
intron_variant | MODIFIER | c.193+2649C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182663320 | |||||||
chr1:182663374 | T | C | 43 | a0001c0001t0004g0053 a0001c0001t0006g0054 a0001c0001t0006g0056 others(40): Show |
47 | HG01123.hp2 HG01255.hp1 HG01884.hp2 others(44): Show |
intron_variant | MODIFIER | c.193+2595A>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182663374 | |||||||
chr1:182663382 | C | T | 11 | a0001c0001t0006g0127 a0001c0001t0013g0073 a0001c0001t0013g0074 others(8): Show |
11 | HG01255.hp1 HG01884.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.193+2587G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182663382 | |||||||
chr1:182663452 | G | A | 45 | a0001c0001t0004g0053 a0001c0001t0006g0054 a0001c0001t0006g0056 others(42): Show |
49 | HG01123.hp2 HG01192.hp2 HG01255.hp1 others(46): Show |
intron_variant | MODIFIER | c.193+2517C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182663452 | |||||||
chr1:182663583 | T | C | 2 | a0001c0001t0025g0068 a0001c0001t0050g0069 |
2 | HG03139.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.193+2386A>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182663583 | |||||||
chr1:182663613 | C | T | 2 | a0001c0001t0051g0070 a0001c0001t0052g0171 |
2 | HG01192.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.193+2356G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182663613 | |||||||
chr1:182663656 | G | A | 1 | a0001c0001t0024g0206 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.193+2313C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182663656 | |||||||
chr1:182663795 | C | T | 13 | a0001c0001t0007g0005 a0001c0001t0007g0041 a0001c0001t0007g0043 others(10): Show |
17 | HG01123.hp2 HG01891.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.193+2174G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182663795 | |||||||
chr1:182663865 | C | G | 1 | a0001c0001t0003g0015 | 2 | HG02145.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.193+2104G>C | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182663865 | |||||||
chr1:182663947 | C | T | 5 | a0001c0001t0006g0127 a0001c0001t0026g0177 a0001c0001t0030g0178 others(2): Show |
5 | HG01884.hp2 HG02109.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.193+2022G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182663947 | |||||||
chr1:182664178 | C | T | 10 | a0001c0001t0007g0005 a0001c0001t0007g0041 a0001c0001t0007g0043 others(7): Show |
13 | HG01123.hp2 HG02258.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.193+1791G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182664178 | |||||||
chr1:182664264 | T | C | 1 | a0001c0001t0012g0215 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.193+1705A>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182664264 | |||||||
chr1:182664270 | A | G | 15 | a0001c0001t0006g0127 a0001c0001t0013g0073 a0001c0001t0013g0074 others(12): Show |
15 | HG01255.hp1 HG01884.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.193+1699T>C | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182664270 | |||||||
chr1:182664281 | A | AT | 29 | a0001c0001t0006g0127 a0001c0001t0007g0005 a0001c0001t0007g0041 others(26): Show |
33 | HG01123.hp2 HG01192.hp2 HG01255.hp1 others(30): Show |
intron_variant | MODIFIER | c.193+1687dupA | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182664281 | |||||||
chr1:182664284 | T | TA | 17 | a0001c0001t0002g0109 a0001c0001t0004g0053 a0001c0001t0006g0054 others(14): Show |
17 | HG01261.hp1 HG02615.hp1 HG02886.hp1 others(14): Show |
intron_variant | MODIFIER | c.193+1684dupT | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182664284 | |||||||
chr1:182664295 | C | A | 1 | a0002c0002t0006g0038 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.193+1674G>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182664295 | |||||||
chr1:182664397 | C | T | 1 | a0001c0001t0005g0204 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.193+1572G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182664397 | |||||||
chr1:182664465 | T | A | 5 | a0001c0001t0002g0132 a0001c0001t0003g0015 a0001c0001t0003g0133 others(2): Show |
6 | HG02145.hp1 HG02622.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.193+1504A>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182664465 | |||||||
chr1:182664666 | C | T | 5 | a0001c0001t0002g0132 a0001c0001t0003g0015 a0001c0001t0003g0133 others(2): Show |
6 | HG02145.hp1 HG02622.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.193+1303G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182664666 | |||||||
chr1:182664899 | C | T | 1 | a0001c0001t0002g0110 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.193+1070G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182664899 | |||||||
chr1:182664983 | C | T | 29 | a0001c0001t0004g0053 a0001c0001t0006g0054 a0001c0001t0006g0056 others(26): Show |
33 | HG01123.hp2 HG01891.hp1 HG02258.hp1 others(30): Show |
intron_variant | MODIFIER | c.193+986G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182664983 | |||||||
chr1:182665219 | T | C | 1 | a0001c0001t0001g0072 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.193+750A>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182665219 | |||||||
chr1:182665243 | A | G | 1 | a0001c0001t0061g0049 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.193+726T>C | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182665243 | |||||||
chr1:182665256 | C | T | 1 | a0002c0002t0006g0038 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.193+713G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182665256 | |||||||
chr1:182665324 | C | T | 5 | a0001c0001t0004g0217 a0001c0001t0004g0218 a0001c0001t0004g0219 others(2): Show |
5 | HG01256.hp2 HG01928.hp1 HG01928.hp2 others(2): Show |
intron_variant | MODIFIER | c.193+645G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182665324 | |||||||
chr1:182665455 | A | T | 43 | a0001c0001t0004g0053 a0001c0001t0006g0054 a0001c0001t0006g0056 others(40): Show |
47 | HG01123.hp2 HG01255.hp1 HG01884.hp2 others(44): Show |
intron_variant | MODIFIER | c.193+514T>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182665455 | |||||||
chr1:182665491 | C | A | 2 | a0001c0001t0001g0003 a0001c0001t0001g0124 |
6 | HG01952.hp2 HG01981.hp1 HG01993.hp2 others(3): Show |
intron_variant | MODIFIER | c.193+478G>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182665491 | |||||||
chr1:182665500 | C | G | 1 | a0001c0001t0011g0146 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.193+469G>C | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182665500 | |||||||
chr1:182665648 | A | G | 14 | a0001c0001t0006g0127 a0001c0001t0013g0073 a0001c0001t0013g0074 others(11): Show |
14 | HG01255.hp1 HG01884.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.193+321T>C | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 6/7 | chr1 | 182665648 | |||||||
chr1:182666230 | C | G | 2 | a0001c0001t0007g0173 a0001c0001t0018g0172 |
2 | HG02630.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.129-197G>C | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 5/7 | chr1 | 182666230 | |||||||
chr1:182666290 | G | A | 1 | a0001c0001t0039g0123 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.129-257C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 5/7 | chr1 | 182666290 | |||||||
chr1:182666490 | A | G | 6 | a0001c0001t0001g0019 a0001c0001t0005g0122 a0001c0001t0005g0201 others(3): Show |
7 | NA18960.hp2 NA18991.hp2 NA19000.hp2 others(4): Show |
intron_variant | MODIFIER | c.128+382T>C | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 5/7 | chr1 | 182666490 | |||||||
chr1:182666556 | A | G | 1 | a0001c0001t0061g0049 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.128+316T>C | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 5/7 | chr1 | 182666556 | |||||||
chr1:182666612 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.128+260G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 5/7 | chr1 | 182666612 | |||||||
chr1:182666655 | G | GA | 26 | a0001c0001t0002g0110 a0001c0001t0004g0053 a0001c0001t0006g0054 others(23): Show |
27 | HG01891.hp1 HG02129.hp1 HG02258.hp1 others(24): Show |
intron_variant | MODIFIER | c.128+216dupT | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 5/7 | chr1 | 182666655 | |||||||
chr1:182666801 | A | T | 42 | a0001c0001t0004g0053 a0001c0001t0006g0054 a0001c0001t0006g0056 others(39): Show |
46 | HG01123.hp2 HG01255.hp1 HG01884.hp2 others(43): Show |
intron_variant | MODIFIER | c.128+71T>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 5/7 | chr1 | 182666801 | |||||||
chr1:182667057 | C | T | 2 | a0001c0001t0007g0041 a0001c0001t0018g0197 |
2 | HG01123.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.27-84G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 4/7 | chr1 | 182667057 | |||||||
chr1:182667060 | C | T | 1 | a0002c0002t0006g0038 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.27-87G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 4/7 | chr1 | 182667060 | |||||||
chr1:182667112 | G | T | 1 | a0001c0001t0017g0032 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.27-139C>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 4/7 | chr1 | 182667112 | |||||||
chr1:182667158 | A | G | 2 | a0001c0001t0051g0070 a0001c0001t0052g0171 |
2 | HG01192.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.27-185T>C | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 4/7 | chr1 | 182667158 | |||||||
chr1:182667226 | G | A | 1 | a0001c0001t0004g0227 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.27-253C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 4/7 | chr1 | 182667226 | |||||||
chr1:182667571 | A | G | 1 | a0001c0001t0014g0039 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.27-598T>C | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 4/7 | chr1 | 182667571 | |||||||
chr1:182667701 | T | C | 1 | a0001c0001t0002g0111 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.27-728A>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 4/7 | chr1 | 182667701 | |||||||
chr1:182668035 | CCTGT | C | 13 | a0001c0001t0007g0005 a0001c0001t0007g0041 a0001c0001t0007g0043 others(10): Show |
17 | HG01123.hp2 HG01891.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.27-1066_27-1063del others(4): Show |
RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 4/7 | chr1 | 182668035 | |||||||
chr1:182668161 | C | A | 2 | a0001c0001t0001g0091 a0001c0001t0035g0092 |
2 | NA18948.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.27-1188G>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 4/7 | chr1 | 182668161 | |||||||
chr1:182668261 | A | G | 43 | a0001c0001t0004g0053 a0001c0001t0006g0054 a0001c0001t0006g0056 others(40): Show |
47 | HG01123.hp2 HG01255.hp1 HG01884.hp2 others(44): Show |
intron_variant | MODIFIER | c.27-1288T>C | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 4/7 | chr1 | 182668261 | |||||||
chr1:182668591 | G | A | 1 | a0002c0002t0006g0038 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.26+1033C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 4/7 | chr1 | 182668591 | |||||||
chr1:182668609 | A | G | 1 | a0001c0001t0001g0113 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.26+1015T>C | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 4/7 | chr1 | 182668609 | |||||||
chr1:182668787 | C | T | 11 | a0001c0001t0006g0127 a0001c0001t0013g0073 a0001c0001t0013g0074 others(8): Show |
11 | HG01255.hp1 HG01884.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.26+837G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 4/7 | chr1 | 182668787 | |||||||
chr1:182668799 | G | A | 1 | a0001c0001t0002g0144 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.26+825C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 4/7 | chr1 | 182668799 | |||||||
chr1:182668801 | A | T | 1 | a0001c0001t0042g0095 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.26+823T>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 4/7 | chr1 | 182668801 | |||||||
chr1:182668846 | C | T | 2 | a0001c0001t0001g0065 a0001c0001t0003g0064 |
2 | HG03516.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.26+778G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 4/7 | chr1 | 182668846 | |||||||
chr1:182668859 | T | A | 58 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0022 others(55): Show |
71 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.26+765A>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 4/7 | chr1 | 182668859 | |||||||
chr1:182668937 | T | C | 1 | a0001c0001t0049g0225 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.26+687A>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 4/7 | chr1 | 182668937 | |||||||
chr1:182668988 | G | C | 1 | a0002c0002t0006g0038 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.26+636C>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 4/7 | chr1 | 182668988 | |||||||
chr1:182669044 | T | C | 1 | a0001c0001t0004g0216 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.26+580A>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 4/7 | chr1 | 182669044 | |||||||
chr1:182669095 | C | T | 2 | a0001c0001t0002g0132 a0001c0001t0034g0131 |
2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.26+529G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 4/7 | chr1 | 182669095 | |||||||
chr1:182669261 | C | T | 1 | a0001c0001t0014g0039 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.26+363G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 4/7 | chr1 | 182669261 | |||||||
chr1:182669498 | G | A | 6 | a0001c0001t0007g0005 a0001c0001t0007g0041 a0001c0001t0007g0043 others(3): Show |
9 | HG01123.hp2 HG02818.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.26+126C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 4/7 | chr1 | 182669498 | |||||||
chr1:182669517 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.26+107G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 4/7 | chr1 | 182669517 | |||||||
chr1:182669524 | G | A | 13 | a0001c0001t0007g0005 a0001c0001t0007g0041 a0001c0001t0007g0043 others(10): Show |
17 | HG01123.hp2 HG01891.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.26+100C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 4/7 | chr1 | 182669524 | |||||||
chr1:182669823 | CG | C | 3 | a0001c0001t0017g0014 a0001c0001t0017g0032 a0001c0001t0065g0033 |
4 | HG01891.hp1 HG02970.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-103-72delC | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 3/7 | chr1 | 182669823 | |||||||
chr1:182669899 | C | T | 27 | a0001c0001t0004g0002 a0001c0001t0004g0025 a0001c0001t0004g0129 others(24): Show |
36 | HG00597.hp2 HG00621.hp2 HG01069.hp2 others(33): Show |
intron_variant | MODIFIER | c.-103-147G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 3/7 | chr1 | 182669899 | |||||||
chr1:182670207 | G | A | 1 | a0001c0001t0029g0183 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-103-455C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 3/7 | chr1 | 182670207 | |||||||
chr1:182670266 | T | C | 1 | a0001c0001t0014g0039 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-103-514A>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 3/7 | chr1 | 182670266 | |||||||
chr1:182670397 | G | A | 19 | a0001c0001t0004g0053 a0001c0001t0006g0054 a0001c0001t0006g0056 others(16): Show |
23 | HG01123.hp2 HG01891.hp1 HG02258.hp1 others(20): Show |
intron_variant | MODIFIER | c.-103-645C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 3/7 | chr1 | 182670397 | |||||||
chr1:182670426 | G | C | 15 | a0001c0001t0004g0053 a0001c0001t0006g0054 a0001c0001t0006g0056 others(12): Show |
15 | HG02615.hp1 HG02886.hp1 HG02922.hp1 others(12): Show |
intron_variant | MODIFIER | c.-103-674C>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 3/7 | chr1 | 182670426 | |||||||
chr1:182670684 | G | A | 1 | a0001c0001t0038g0082 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-103-932C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 3/7 | chr1 | 182670684 | |||||||
chr1:182670752 | T | C | 1 | a0001c0001t0056g0128 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-104+905A>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 3/7 | chr1 | 182670752 | |||||||
chr1:182670829 | G | A | 10 | a0001c0001t0007g0005 a0001c0001t0007g0041 a0001c0001t0007g0043 others(7): Show |
13 | HG01123.hp2 HG02258.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.-104+828C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 3/7 | chr1 | 182670829 | |||||||
chr1:182670916 | G | A | 1 | a0001c0001t0054g0067 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-104+741C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 3/7 | chr1 | 182670916 | |||||||
chr1:182670975 | G | A | 2 | a0001c0001t0021g0036 a0002c0002t0002g0066 |
2 | HG02976.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-104+682C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 3/7 | chr1 | 182670975 | |||||||
chr1:182671032 | C | T | 4 | a0001c0001t0006g0127 a0001c0001t0026g0177 a0001c0001t0030g0178 others(1): Show |
4 | HG01884.hp2 HG03453.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.-104+625G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 3/7 | chr1 | 182671032 | |||||||
chr1:182671115 | T | C | 2 | a0001c0001t0001g0023 a0001c0001t0003g0165 |
3 | HG02647.hp2 HG03130.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-104+542A>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 3/7 | chr1 | 182671115 | |||||||
chr1:182671220 | T | C | 66 | a0001c0001t0004g0002 a0001c0001t0004g0025 a0001c0001t0004g0053 others(63): Show |
79 | HG00597.hp2 HG00621.hp2 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.-104+437A>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 3/7 | chr1 | 182671220 | |||||||
chr1:182671316 | A | T | 1 | a0001c0001t0040g0136 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-104+341T>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 3/7 | chr1 | 182671316 | |||||||
chr1:182671415 | C | T | 1 | a0001c0001t0003g0185 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-104+242G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 3/7 | chr1 | 182671415 | |||||||
chr1:182671503 | A | G | 66 | a0001c0001t0004g0002 a0001c0001t0004g0025 a0001c0001t0004g0053 others(63): Show |
79 | HG00597.hp2 HG00621.hp2 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.-104+154T>C | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 3/7 | chr1 | 182671503 | |||||||
chr1:182671542 | C | T | 5 | a0001c0001t0025g0037 a0001c0001t0025g0068 a0001c0001t0048g0233 others(2): Show |
5 | HG01069.hp2 HG02055.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-104+115G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 3/7 | chr1 | 182671542 | |||||||
chr1:182671812 | A | G | 1 | a0001c0001t0014g0039 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-177-82T>C | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 2/7 | chr1 | 182671812 | |||||||
chr1:182671859 | T | C | 66 | a0001c0001t0004g0002 a0001c0001t0004g0025 a0001c0001t0004g0053 others(63): Show |
79 | HG00597.hp2 HG00621.hp2 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.-177-129A>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 2/7 | chr1 | 182671859 | |||||||
chr1:182671883 | A | G | 77 | a0001c0001t0004g0002 a0001c0001t0004g0025 a0001c0001t0004g0053 others(74): Show |
90 | HG00597.hp2 HG00621.hp2 HG00642.hp1 others(87): Show |
intron_variant | MODIFIER | c.-177-153T>C | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 2/7 | chr1 | 182671883 | |||||||
chr1:182671948 | G | A | 66 | a0001c0001t0004g0002 a0001c0001t0004g0025 a0001c0001t0004g0053 others(63): Show |
79 | HG00597.hp2 HG00621.hp2 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.-177-218C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 2/7 | chr1 | 182671948 | |||||||
chr1:182671951 | G | A | 1 | a0001c0001t0001g0012 | 3 | NA18747.hp2 NA18997.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.-177-221C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 2/7 | chr1 | 182671951 | |||||||
chr1:182671964 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-177-234C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 2/7 | chr1 | 182671964 | |||||||
chr1:182672232 | C | T | 4 | a0001c0001t0006g0127 a0001c0001t0026g0177 a0001c0001t0030g0178 others(1): Show |
4 | HG01884.hp2 HG03453.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.-177-502G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 2/7 | chr1 | 182672232 | |||||||
chr1:182672319 | A | G | 14 | a0001c0001t0004g0053 a0001c0001t0006g0054 a0001c0001t0006g0056 others(11): Show |
14 | HG02615.hp1 HG02886.hp1 HG02922.hp1 others(11): Show |
intron_variant | MODIFIER | c.-178+500T>C | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 2/7 | chr1 | 182672319 | |||||||
chr1:182672328 | G | C | 4 | a0001c0001t0007g0173 a0001c0001t0007g0175 a0001c0001t0018g0172 others(1): Show |
4 | HG02258.hp1 HG02630.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-178+491C>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 2/7 | chr1 | 182672328 | |||||||
chr1:182672535 | A | T | 1 | a0001c0001t0056g0128 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-178+284T>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 2/7 | chr1 | 182672535 | |||||||
chr1:182672946 | G | A | 1 | a0001c0001t0011g0013 | 3 | HG01243.hp1 HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-291-14C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182672946 | |||||||
chr1:182673051 | C | T | 1 | a0001c0001t0004g0217 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-291-119G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182673051 | |||||||
chr1:182673161 | C | T | 1 | a0001c0001t0002g0202 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-291-229G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182673161 | |||||||
chr1:182673213 | A | G | 1 | a0002c0002t0006g0038 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-291-281T>C | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182673213 | |||||||
chr1:182673233 | G | A | 1 | a0001c0001t0064g0034 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-291-301C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182673233 | |||||||
chr1:182673263 | C | T | 1 | a0001c0001t0056g0128 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-291-331G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182673263 | |||||||
chr1:182673425 | T | C | 1 | a0001c0001t0004g0222 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-291-493A>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182673425 | |||||||
chr1:182673548 | G | C | 1 | a0001c0001t0049g0225 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-291-616C>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182673548 | |||||||
chr1:182673578 | T | C | 4 | a0001c0001t0001g0019 a0001c0001t0005g0122 a0001c0001t0005g0201 others(1): Show |
5 | NA18960.hp2 NA19000.hp2 NA19010.hp1 others(2): Show |
intron_variant | MODIFIER | c.-291-646A>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182673578 | |||||||
chr1:182673675 | A | G | 1 | a0001c0001t0005g0125 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-291-743T>C | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182673675 | |||||||
chr1:182673722 | T | C | 29 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0016 others(26): Show |
43 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(40): Show |
intron_variant | MODIFIER | c.-291-790A>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182673722 | |||||||
chr1:182673844 | C | T | 1 | a0001c0001t0024g0206 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-291-912G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182673844 | |||||||
chr1:182673893 | T | A | 36 | a0001c0001t0004g0002 a0001c0001t0004g0025 a0001c0001t0004g0129 others(33): Show |
45 | HG00597.hp2 HG00621.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.-291-961A>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182673893 | |||||||
chr1:182673916 | C | T | 2 | a0001c0001t0051g0070 a0001c0001t0052g0171 |
2 | HG01192.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-291-984G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182673916 | |||||||
chr1:182674024 | G | T | 5 | a0001c0001t0001g0020 a0001c0001t0001g0134 a0001c0001t0003g0045 others(2): Show |
6 | HG02055.hp2 HG02280.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-291-1092C>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182674024 | |||||||
chr1:182674151 | G | A | 1 | a0001c0001t0002g0232 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-291-1219C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182674151 | |||||||
chr1:182674248 | C | A | 1 | a0001c0001t0001g0124 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-291-1316G>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182674248 | |||||||
chr1:182674491 | C | T | 1 | a0001c0001t0003g0094 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-291-1559G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182674491 | |||||||
chr1:182674543 | A | G | 1 | a0001c0001t0001g0088 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-291-1611T>C | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182674543 | |||||||
chr1:182674562 | A | T | 1 | a0001c0001t0054g0067 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-291-1630T>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182674562 | |||||||
chr1:182674600 | T | G | 3 | a0001c0001t0006g0059 a0001c0001t0028g0060 a0001c0001t0055g0058 |
3 | NA18991.hp1 NA18995.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.-291-1668A>C | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182674600 | |||||||
chr1:182674667 | A | G | 1 | a0001c0001t0001g0080 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-291-1735T>C | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182674667 | |||||||
chr1:182674868 | A | G | 10 | a0001c0001t0006g0127 a0001c0001t0013g0073 a0001c0001t0013g0074 others(7): Show |
10 | HG01255.hp1 HG01884.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.-291-1936T>C | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182674868 | |||||||
chr1:182674912 | G | C | 68 | a0001c0001t0004g0002 a0001c0001t0004g0025 a0001c0001t0004g0053 others(65): Show |
81 | HG00597.hp2 HG00621.hp2 HG00642.hp1 others(78): Show |
intron_variant | MODIFIER | c.-291-1980C>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182674912 | |||||||
chr1:182674913 | C | T | 65 | a0001c0001t0004g0002 a0001c0001t0004g0025 a0001c0001t0004g0053 others(62): Show |
78 | HG00597.hp2 HG00621.hp2 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.-291-1981G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182674913 | |||||||
chr1:182675025 | C | T | 5 | a0001c0001t0002g0132 a0001c0001t0003g0015 a0001c0001t0003g0133 others(2): Show |
6 | HG02145.hp1 HG02622.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.-291-2093G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182675025 | |||||||
chr1:182675026 | G | A | 15 | a0001c0001t0004g0053 a0001c0001t0006g0054 a0001c0001t0006g0056 others(12): Show |
15 | HG02615.hp1 HG02886.hp1 HG02922.hp1 others(12): Show |
intron_variant | MODIFIER | c.-291-2094C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182675026 | |||||||
chr1:182675133 | C | A | 5 | a0001c0001t0006g0057 a0001c0001t0006g0059 a0001c0001t0006g0085 others(2): Show |
5 | HG03669.hp2 NA18991.hp1 NA18995.hp2 others(2): Show |
intron_variant | MODIFIER | c.-291-2201G>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182675133 | |||||||
chr1:182675246 | G | T | 65 | a0001c0001t0004g0002 a0001c0001t0004g0025 a0001c0001t0004g0053 others(62): Show |
78 | HG00597.hp2 HG00621.hp2 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.-291-2314C>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182675246 | |||||||
chr1:182675537 | A | G | 1 | a0001c0001t0026g0177 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-291-2605T>C | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182675537 | |||||||
chr1:182675634 | G | A | 6 | a0001c0001t0004g0217 a0001c0001t0004g0218 a0001c0001t0004g0219 others(3): Show |
6 | HG00642.hp1 HG01256.hp2 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.-291-2702C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182675634 | |||||||
chr1:182675754 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-291-2822G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182675754 | |||||||
chr1:182676116 | C | G | 1 | a0001c0001t0001g0184 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-291-3184G>C | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182676116 | |||||||
chr1:182676129 | T | C | 1 | a0001c0001t0049g0225 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-291-3197A>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182676129 | |||||||
chr1:182676221 | T | C | 1 | a0001c0001t0002g0202 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-291-3289A>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182676221 | |||||||
chr1:182676401 | G | A | 2 | a0001c0001t0051g0070 a0001c0001t0052g0171 |
2 | HG01192.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-291-3469C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182676401 | |||||||
chr1:182676430 | G | A | 6 | a0001c0001t0013g0073 a0001c0001t0013g0074 a0001c0001t0013g0181 others(3): Show |
6 | HG01255.hp1 HG02486.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-291-3498C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182676430 | |||||||
chr1:182676522 | G | A | 1 | a0002c0002t0006g0038 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-291-3590C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182676522 | |||||||
chr1:182676616 | A | G | 2 | a0001c0001t0001g0091 a0001c0001t0035g0092 |
2 | NA18948.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.-291-3684T>C | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182676616 | |||||||
chr1:182676651 | C | A | 2 | a0001c0003t0022g0166 a0001c0003t0022g0167 |
2 | HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-291-3719G>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182676651 | |||||||
chr1:182676670 | G | T | 3 | a0001c0001t0005g0083 a0001c0001t0023g0130 a0001c0001t0023g0169 |
3 | HG03688.hp1 HG04184.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.-291-3738C>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182676670 | |||||||
chr1:182676702 | A | G | 2 | a0001c0001t0051g0070 a0001c0001t0052g0171 |
2 | HG01192.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-291-3770T>C | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182676702 | |||||||
chr1:182676774 | C | G | 2 | a0001c0001t0001g0065 a0001c0001t0003g0064 |
2 | HG03516.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-291-3842G>C | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182676774 | |||||||
chr1:182676783 | C | T | 1 | a0001c0001t0002g0090 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-291-3851G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182676783 | |||||||
chr1:182676808 | T | G | 1 | a0001c0001t0005g0125 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-291-3876A>C | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182676808 | |||||||
chr1:182676928 | C | T | 3 | a0001c0001t0049g0225 a0001c0001t0051g0070 a0001c0001t0052g0171 |
3 | HG01192.hp2 HG03209.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-291-3996G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182676928 | |||||||
chr1:182676949 | G | A | 1 | a0002c0002t0006g0038 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-291-4017C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182676949 | |||||||
chr1:182677013 | A | G | 65 | a0001c0001t0004g0002 a0001c0001t0004g0025 a0001c0001t0004g0053 others(62): Show |
78 | HG00597.hp2 HG00621.hp2 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.-291-4081T>C | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182677013 | |||||||
chr1:182677271 | T | C | 1 | a0001c0001t0061g0049 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-291-4339A>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182677271 | |||||||
chr1:182677278 | G | A | 14 | a0001c0001t0004g0053 a0001c0001t0006g0054 a0001c0001t0006g0056 others(11): Show |
14 | HG02615.hp1 HG02886.hp1 HG02922.hp1 others(11): Show |
intron_variant | MODIFIER | c.-291-4346C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182677278 | |||||||
chr1:182677375 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-291-4443G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182677375 | |||||||
chr1:182677552 | C | T | 1 | a0001c0001t0001g0072 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-291-4620G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182677552 | |||||||
chr1:182677629 | G | A | 1 | a0001c0001t0029g0224 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-291-4697C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182677629 | |||||||
chr1:182677665 | C | G | 1 | a0001c0001t0009g0176 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-291-4733G>C | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182677665 | |||||||
chr1:182677964 | G | C | 1 | a0001c0001t0051g0070 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-291-5032C>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182677964 | |||||||
chr1:182678154 | T | G | 1 | a0001c0001t0049g0225 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-291-5222A>C | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182678154 | |||||||
chr1:182678229 | G | T | 14 | a0001c0001t0004g0053 a0001c0001t0006g0054 a0001c0001t0006g0056 others(11): Show |
14 | HG02615.hp1 HG02886.hp1 HG02922.hp1 others(11): Show |
intron_variant | MODIFIER | c.-291-5297C>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182678229 | |||||||
chr1:182678234 | G | T | 14 | a0001c0001t0004g0053 a0001c0001t0006g0054 a0001c0001t0006g0056 others(11): Show |
14 | HG02615.hp1 HG02886.hp1 HG02922.hp1 others(11): Show |
intron_variant | MODIFIER | c.-291-5302C>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182678234 | |||||||
chr1:182678380 | A | G | 2 | a0001c0001t0001g0088 a0001c0001t0001g0089 |
2 | NA18612.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.-291-5448T>C | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182678380 | |||||||
chr1:182678388 | C | G | 1 | a0001c0001t0014g0039 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-291-5456G>C | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182678388 | |||||||
chr1:182678513 | G | T | 2 | a0001c0001t0051g0070 a0001c0001t0052g0171 |
2 | HG01192.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-291-5581C>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182678513 | |||||||
chr1:182678656 | C | T | 2 | a0001c0001t0001g0063 a0001c0001t0009g0062 |
2 | HG02109.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-292+5696G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182678656 | |||||||
chr1:182678679 | A | G | 1 | a0001c0001t0001g0016 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-292+5673T>C | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182678679 | |||||||
chr1:182679034 | C | T | 2 | a0001c0001t0051g0070 a0001c0001t0052g0171 |
2 | HG01192.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-292+5318G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182679034 | |||||||
chr1:182679052 | C | T | 1 | a0001c0001t0006g0085 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-292+5300G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182679052 | |||||||
chr1:182679294 | G | A | 2 | a0001c0001t0051g0070 a0001c0001t0052g0171 |
2 | HG01192.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-292+5058C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182679294 | |||||||
chr1:182679466 | C | G | 1 | a0001c0001t0005g0087 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-292+4886G>C | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182679466 | |||||||
chr1:182679917 | C | T | 13 | a0001c0001t0001g0061 a0001c0001t0004g0053 a0001c0001t0006g0054 others(10): Show |
13 | HG01261.hp2 HG02615.hp1 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.-292+4435G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182679917 | |||||||
chr1:182680044 | C | T | 1 | a0001c0001t0026g0209 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-292+4308G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182680044 | |||||||
chr1:182680242 | G | T | 1 | a0001c0001t0002g0086 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-292+4110C>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182680242 | |||||||
chr1:182680622 | G | GTTCATTC others(1): Show |
176 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0020 others(173): Show |
211 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(208): Show |
intron_variant | MODIFIER | c.-292+3722_-292+372 others(12): Show |
RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182680622 | |||||||
chr1:182680622 | G | GTTCATTC others(5): Show |
1 | a0001c0001t0024g0206 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-292+3718_-292+372 others(16): Show |
RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182680622 | |||||||
chr1:182680704 | A | T | 19 | a0001c0001t0001g0061 a0001c0001t0001g0063 a0001c0001t0001g0065 others(16): Show |
19 | HG01261.hp2 HG02109.hp2 HG02615.hp1 others(16): Show |
intron_variant | MODIFIER | c.-292+3648T>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182680704 | |||||||
chr1:182680718 | T | C | 4 | a0001c0001t0007g0173 a0001c0001t0007g0175 a0001c0001t0018g0172 others(1): Show |
4 | HG02258.hp1 HG02630.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-292+3634A>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182680718 | |||||||
chr1:182680734 | C | T | 42 | a0001c0001t0001g0061 a0001c0001t0001g0063 a0001c0001t0001g0065 others(39): Show |
46 | HG00642.hp2 HG01069.hp2 HG01123.hp2 others(43): Show |
intron_variant | MODIFIER | c.-292+3618G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182680734 | |||||||
chr1:182681020 | C | T | 1 | a0002c0002t0006g0038 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-292+3332G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182681020 | |||||||
chr1:182681101 | G | A | 12 | a0001c0001t0007g0005 a0001c0001t0007g0041 a0001c0001t0007g0043 others(9): Show |
15 | HG01069.hp2 HG01123.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.-292+3251C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182681101 | |||||||
chr1:182681113 | G | T | 2 | a0001c0001t0006g0168 a0001c0001t0014g0230 |
2 | HG03017.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-292+3239C>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182681113 | |||||||
chr1:182681236 | G | T | 7 | a0001c0001t0007g0005 a0001c0001t0007g0041 a0001c0001t0007g0043 others(4): Show |
10 | HG01123.hp2 HG01884.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.-292+3116C>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182681236 | |||||||
chr1:182681291 | C | T | 3 | a0001c0001t0017g0014 a0001c0001t0017g0032 a0001c0001t0065g0033 |
4 | HG01891.hp1 HG02970.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-292+3061G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182681291 | |||||||
chr1:182681327 | C | G | 1 | a0001c0001t0008g0084 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-292+3025G>C | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182681327 | |||||||
chr1:182681505 | A | C | 12 | a0001c0001t0007g0005 a0001c0001t0007g0041 a0001c0001t0007g0043 others(9): Show |
15 | HG01069.hp2 HG01123.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.-292+2847T>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182681505 | |||||||
chr1:182681506 | G | C | 12 | a0001c0001t0007g0005 a0001c0001t0007g0041 a0001c0001t0007g0043 others(9): Show |
15 | HG01069.hp2 HG01123.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.-292+2846C>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182681506 | |||||||
chr1:182681522 | C | A | 4 | a0001c0001t0017g0014 a0001c0001t0017g0032 a0001c0001t0064g0034 others(1): Show |
5 | HG01891.hp1 HG02622.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-292+2830G>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182681522 | |||||||
chr1:182681684 | C | T | 1 | a0001c0001t0001g0208 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-292+2668G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182681684 | |||||||
chr1:182681776 | G | A | 1 | a0001c0001t0004g0025 | 2 | HG01891.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.-292+2576C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182681776 | |||||||
chr1:182681854 | G | A | 4 | a0001c0001t0002g0232 a0001c0001t0006g0168 a0001c0001t0014g0230 others(1): Show |
4 | HG00642.hp2 HG03017.hp1 NA20805.hp1 others(1): Show |
intron_variant | MODIFIER | c.-292+2498C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182681854 | |||||||
chr1:182681883 | C | T | 1 | a0001c0001t0005g0083 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-292+2469G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182681883 | |||||||
chr1:182681991 | T | C | 1 | a0001c0001t0023g0169 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-292+2361A>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182681991 | |||||||
chr1:182682134 | C | T | 5 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(2): Show |
5 | HG01081.hp2 HG02293.hp1 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.-292+2218G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182682134 | |||||||
chr1:182682179 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-292+2173G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182682179 | |||||||
chr1:182682287 | C | T | 1 | a0001c0001t0004g0207 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-292+2065G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182682287 | |||||||
chr1:182682432 | C | A | 3 | a0001c0001t0002g0232 a0001c0001t0014g0230 a0001c0001t0045g0231 |
3 | HG00642.hp2 NA20805.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-292+1920G>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182682432 | |||||||
chr1:182682554 | A | G | 8 | a0001c0001t0003g0015 a0001c0001t0007g0173 a0001c0001t0007g0175 others(5): Show |
9 | HG01192.hp2 HG02145.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.-292+1798T>C | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182682554 | |||||||
chr1:182682877 | A | G | 30 | a0001c0001t0001g0061 a0001c0001t0001g0063 a0001c0001t0001g0065 others(27): Show |
31 | HG00642.hp2 HG01069.hp2 HG01261.hp2 others(28): Show |
intron_variant | MODIFIER | c.-292+1475T>C | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182682877 | |||||||
chr1:182682898 | CT | C | 31 | a0001c0001t0001g0028 a0001c0001t0001g0072 a0001c0001t0001g0184 others(28): Show |
34 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(31): Show |
intron_variant | MODIFIER | c.-292+1453delA | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182682898 | |||||||
chr1:182682903 | G | A | 1 | a0001c0001t0008g0170 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-292+1449C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182682903 | |||||||
chr1:182683429 | A | G | 77 | a0001c0001t0001g0028 a0001c0001t0001g0061 a0001c0001t0001g0063 others(74): Show |
84 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.-292+923T>C | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182683429 | |||||||
chr1:182683481 | T | C | 6 | a0001c0001t0007g0173 a0001c0001t0007g0175 a0001c0001t0018g0172 others(3): Show |
6 | HG01192.hp2 HG02258.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-292+871A>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182683481 | |||||||
chr1:182683528 | C | A | 30 | a0001c0001t0001g0061 a0001c0001t0001g0063 a0001c0001t0001g0065 others(27): Show |
31 | HG00642.hp2 HG01069.hp2 HG01261.hp2 others(28): Show |
intron_variant | MODIFIER | c.-292+824G>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182683528 | |||||||
chr1:182683528 | C | T | 6 | a0001c0001t0007g0173 a0001c0001t0007g0175 a0001c0001t0018g0172 others(3): Show |
6 | HG01192.hp2 HG02258.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-292+824G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182683528 | |||||||
chr1:182683627 | C | CA | 38 | a0001c0001t0001g0028 a0001c0001t0001g0184 a0001c0001t0001g0192 others(35): Show |
41 | HG00558.hp2 HG00621.hp1 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.-292+724dupT | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182683627 | |||||||
chr1:182683627 | CA | C | 56 | a0001c0001t0001g0047 a0001c0001t0001g0061 a0001c0001t0001g0063 others(53): Show |
67 | HG00597.hp2 HG00621.hp2 HG00642.hp1 others(64): Show |
intron_variant | MODIFIER | c.-292+724delT | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182683627 | |||||||
chr1:182683627 | CAA | C | 11 | a0001c0001t0002g0232 a0001c0001t0014g0230 a0001c0001t0017g0014 others(8): Show |
12 | HG00642.hp2 HG01069.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.-292+723_-292+724d others(4): Show |
RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182683627 | |||||||
chr1:182683698 | G | A | 7 | a0001c0001t0002g0232 a0001c0001t0014g0230 a0001c0001t0017g0014 others(4): Show |
8 | HG00642.hp2 HG01891.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-292+654C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182683698 | |||||||
chr1:182683726 | C | T | 7 | a0001c0001t0002g0232 a0001c0001t0014g0230 a0001c0001t0017g0014 others(4): Show |
8 | HG00642.hp2 HG01891.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-292+626G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182683726 | |||||||
chr1:182683730 | C | T | 1 | a0001c0001t0016g0031 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-292+622G>A | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182683730 | |||||||
chr1:182683759 | C | A | 25 | a0001c0001t0001g0208 a0001c0001t0001g0223 a0001c0001t0004g0002 others(22): Show |
33 | HG00597.hp2 HG00621.hp2 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.-292+593G>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182683759 | |||||||
chr1:182683832 | G | A | 2 | a0001c0001t0002g0229 a0001c0001t0016g0228 |
2 | HG01081.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-292+520C>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182683832 | |||||||
chr1:182683980 | G | C | 3 | a0001c0001t0002g0232 a0001c0001t0014g0230 a0001c0001t0045g0231 |
3 | HG00642.hp2 NA20805.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-292+372C>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182683980 | |||||||
chr1:182684154 | T | C | 1 | a0001c0001t0048g0233 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-292+198A>G | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182684154 | |||||||
chr1:182684199 | T | A | 1 | a0001c0001t0003g0234 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-292+153A>T | RGS8 | ENSG00000135824.13 | transcript | ENST00000515211.2 | protein_coding | 1/7 | chr1 | 182684199 |