Item | Value |
---|---|
geneid | 28984 |
ensemblid | ENSG00000102760.13 |
hgncid | 20369 |
symbol | RGCC |
name | regulator of cell cycle |
refseq_nuc | NM_014059.3 |
refseq_prot | NP_054778.2 |
ensembl_nuc | ENST00000379359.4 |
ensembl_prot | ENSP00000368664.3 |
mane_status | MANE Select |
chr | chr13 |
start | 41457550 |
end | 41470871 |
strand | + |
ver | v1.2 |
region | chr13:41457550-41470871 |
region5000 | chr13:41452550-41475871 |
regionname0 | RGCC_chr13_41457550_41470871 |
regionname5000 | RGCC_chr13_41452550_41475871 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 411 | 282 | 69 | 41 | 149 | 7 | 16 | RGCC_chr13_41452550_41475871 | RGCC | ATGAA others(406): Show |
chr13 | 41452550 | 41475871 | ||
a0001c0002 | 1/1 | 411 | 166 | 23 | 43 | 63 | 9 | 26 | RGCC_chr13_41452550_41475871 | RGCC | ATGAA others(406): Show |
chr13 | 41452550 | 41475871 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 958 | 280 | 68 | 41 | 149 | 7 | 15 | RGCC_chr13_41452550_41475871 | RGCC | AGGGC others(953): Show |
chr13 | 41452550 | 41475871 |
a0001c0001t0003 | 0/0 | 958 | 1 | 1 | 0 | 0 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | AGGGC others(953): Show |
chr13 | 41452550 | 41475871 |
a0001c0001t0004 | 0/0 | 958 | 1 | 0 | 0 | 0 | 0 | 1 | RGCC_chr13_41452550_41475871 | RGCC | AGGGC others(953): Show |
chr13 | 41452550 | 41475871 |
a0001c0002t0001 | 1/1 | 958 | 165 | 22 | 43 | 63 | 9 | 26 | RGCC_chr13_41452550_41475871 | RGCC | AGGGC others(953): Show |
chr13 | 41452550 | 41475871 |
a0001c0002t0002 | 0/0 | 958 | 1 | 1 | 0 | 0 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | AGGGC others(953): Show |
chr13 | 41452550 | 41475871 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0002 | 0/0 | 33 | 0 | 5 | 28 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0003 | 0/0 | 16 | 1 | 7 | 8 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0004 | 0/0 | 13 | 3 | 0 | 9 | 0 | 1 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0005 | 0/0 | 12 | 0 | 2 | 7 | 1 | 2 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0006 | 0/0 | 10 | 6 | 2 | 2 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0008 | 0/0 | 8 | 0 | 2 | 4 | 1 | 1 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0009 | 0/0 | 8 | 0 | 4 | 4 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0010 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0011 | 0/0 | 5 | 0 | 2 | 1 | 0 | 2 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0012 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0014 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0015 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0016 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0017 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0018 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0021 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0022 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0026 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0027 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0028 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0031 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0035 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0036 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0001t0004g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0002t0001g0001 | 0/0 | 74 | 2 | 12 | 42 | 4 | 14 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0002t0001g0007 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0002t0001g0013 | 0/0 | 4 | 0 | 0 | 3 | 1 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0002t0001g0019 | 0/0 | 5 | 0 | 3 | 0 | 0 | 2 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0002t0001g0020 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0002t0001g0023 | 0/0 | 4 | 1 | 1 | 1 | 0 | 1 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0002t0001g0024 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0002t0001g0025 | 1/0 | 4 | 3 | 0 | 0 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0002t0001g0029 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0002t0001g0032 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0002t0001g0033 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0002t0001g0034 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0002t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0002t0001g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0002t0001g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0002t0001g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0002t0001g0044 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0002t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0002t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0002t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0002t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0002t0001g0107 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0002t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0002t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0002t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0002t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0002t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0002t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0002t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0002t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0002t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0002t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0002t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0002t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0002t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0002t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0002t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0002t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0002t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0002t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
a0001c0002t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0076 | EUR | GBR | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG00099 | hp2 | a0001 | c0002 | t0001 | g0001 | EUR | GBR | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG00140 | hp1 | a0001 | c0002 | t0001 | g0032 | EUR | GBR | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | GBR | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0094 | EUR | FIN | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG00280 | hp2 | a0001 | c0002 | t0001 | g0020 | EUR | FIN | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | FIN | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG00323 | hp2 | a0001 | c0002 | t0001 | g0001 | EUR | FIN | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | CHS | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG00423 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG00438 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | CHS | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG00438 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG00544 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG00544 | hp2 | a0001 | c0002 | t0001 | g0090 | EAS | CHS | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | CHS | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG00597 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG00621 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG00621 | hp2 | a0001 | c0002 | t0001 | g0118 | EAS | CHS | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG00639 | hp1 | a0001 | c0002 | t0001 | g0020 | AMR | PUR | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG00642 | hp1 | a0001 | c0002 | t0001 | g0029 | AMR | PUR | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG00642 | hp2 | a0001 | c0002 | t0001 | g0134 | AMR | PUR | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | CHS | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | CHS | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG00738 | hp2 | a0001 | c0002 | t0001 | g0033 | AMR | PUR | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG01069 | hp1 | a0001 | c0002 | t0001 | g0042 | AMR | PUR | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG01069 | hp2 | a0001 | c0002 | t0001 | g0020 | AMR | PUR | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG01070 | hp1 | a0001 | c0002 | t0001 | g0019 | AMR | PUR | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG01070 | hp2 | a0001 | c0002 | t0001 | g0040 | AMR | PUR | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG01071 | hp1 | a0001 | c0002 | t0001 | g0042 | AMR | PUR | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG01071 | hp2 | a0001 | c0002 | t0001 | g0040 | AMR | PUR | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG01074 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG01081 | hp1 | a0001 | c0002 | t0001 | g0168 | AMR | PUR | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG01099 | hp1 | a0001 | c0002 | t0001 | g0020 | AMR | PUR | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG01099 | hp2 | a0001 | c0002 | t0001 | g0032 | AMR | PUR | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG01168 | hp1 | a0001 | c0002 | t0001 | g0041 | AMR | PUR | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG01168 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG01169 | hp2 | a0001 | c0002 | t0001 | g0041 | AMR | PUR | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG01175 | hp1 | a0001 | c0002 | t0001 | g0024 | AMR | PUR | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG01175 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG01243 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG01243 | hp2 | a0001 | c0002 | t0001 | g0044 | AMR | PUR | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG01255 | hp1 | a0001 | c0002 | t0001 | g0019 | AMR | CLM | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG01255 | hp2 | a0001 | c0002 | t0001 | g0029 | AMR | CLM | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG01256 | hp2 | a0001 | c0002 | t0001 | g0024 | AMR | CLM | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | CLM | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG01258 | hp1 | a0001 | c0002 | t0001 | g0024 | AMR | CLM | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG01261 | hp1 | a0001 | c0002 | t0001 | g0106 | AMR | CLM | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG01261 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG01358 | hp2 | a0001 | c0002 | t0001 | g0019 | AMR | CLM | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG01361 | hp1 | a0001 | c0002 | t0001 | g0029 | AMR | CLM | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG01361 | hp2 | a0001 | c0002 | t0001 | g0113 | AMR | CLM | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG01433 | hp2 | a0001 | c0002 | t0001 | g0126 | AMR | CLM | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG01515 | hp1 | a0001 | c0002 | t0001 | g0001 | EUR | IBS | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0031 | EUR | IBS | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG01517 | hp1 | a0001 | c0002 | t0001 | g0001 | EUR | IBS | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0031 | EUR | IBS | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG01884 | hp2 | a0001 | c0002 | t0001 | g0001 | AFR | ACB | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ACB | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG01934 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG01952 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PEL | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PEL | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG01978 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG01978 | hp2 | a0001 | c0002 | t0001 | g0023 | AMR | PEL | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG01993 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02004 | hp1 | a0001 | c0002 | t0001 | g0169 | AMR | PEL | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02015 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02027 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02027 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02040 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02056 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | KHV | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | KHV | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02083 | hp1 | a0001 | c0002 | t0001 | g0024 | EAS | KHV | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02083 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | KHV | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | KHV | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | KHV | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | KHV | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02148 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02148 | hp2 | a0001 | c0002 | t0001 | g0167 | AMR | PEL | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02155 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | CDX | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02155 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | CDX | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | CDX | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02165 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | CDX | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02273 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | ACB | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02280 | hp2 | a0001 | c0002 | t0001 | g0121 | AFR | ACB | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02293 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02300 | hp2 | a0001 | c0002 | t0001 | g0124 | AMR | PEL | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | ACB | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02451 | hp2 | a0001 | c0002 | t0001 | g0025 | AFR | ACB | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02572 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | GWD | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02602 | hp2 | a0001 | c0002 | t0001 | g0061 | SAS | PJL | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02647 | hp1 | a0001 | c0002 | t0001 | g0137 | AFR | GWD | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | GWD | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02683 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02698 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02738 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02738 | hp2 | a0001 | c0002 | t0001 | g0109 | SAS | PJL | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02809 | hp1 | a0001 | c0002 | t0001 | g0025 | AFR | GWD | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02809 | hp2 | a0001 | c0002 | t0001 | g0166 | AFR | GWD | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02818 | hp1 | a0001 | c0002 | t0001 | g0129 | AFR | GWD | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02895 | hp2 | a0001 | c0002 | t0001 | g0135 | AFR | GWD | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02896 | hp2 | a0001 | c0002 | t0001 | g0039 | AFR | GWD | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02897 | hp2 | a0001 | c0002 | t0001 | g0039 | AFR | GWD | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | ESN | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02965 | hp1 | a0001 | c0002 | t0001 | g0044 | AFR | ESN | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | ESN | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | ESN | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | ESN | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG03017 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG03017 | hp2 | a0001 | c0001 | t0004 | g0011 | SAS | PJL | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | MSL | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | MSL | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | ESN | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | ESN | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | ESN | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG03225 | hp1 | a0001 | c0002 | t0001 | g0100 | AFR | MSL | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | MSL | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG03453 | hp1 | a0001 | c0001 | t0003 | g0058 | AFR | MSL | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | MSL | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG03486 | hp2 | a0001 | c0002 | t0001 | g0136 | AFR | MSL | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG03490 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG03491 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG03492 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG03492 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | ESN | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | GWD | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG03579 | hp2 | a0001 | c0002 | t0001 | g0120 | AFR | MSL | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG03669 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG03669 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG03688 | hp1 | a0001 | c0002 | t0001 | g0111 | SAS | STU | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | STU | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG03704 | hp1 | a0001 | c0002 | t0001 | g0034 | SAS | PJL | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG03704 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG03710 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG03710 | hp2 | a0001 | c0002 | t0001 | g0117 | SAS | PJL | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | BEB | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | BEB | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG03834 | hp2 | a0001 | c0002 | t0001 | g0108 | SAS | BEB | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG03942 | hp1 | a0001 | c0002 | t0001 | g0019 | SAS | BEB | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | BEB | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG04184 | hp1 | a0001 | c0002 | t0001 | g0023 | SAS | BEB | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG04184 | hp2 | a0001 | c0002 | t0001 | g0116 | SAS | BEB | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | STU | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG04199 | hp2 | a0001 | c0002 | t0001 | g0019 | SAS | STU | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG04204 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | STU | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG04204 | hp2 | a0001 | c0002 | t0001 | g0034 | SAS | STU | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG04228 | hp1 | a0001 | c0002 | t0001 | g0034 | SAS | STU | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG04228 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | STU | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | YRI | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18522 | hp2 | a0001 | c0002 | t0001 | g0127 | AFR | YRI | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | CHB | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18612 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | CHB | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CHB | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | YRI | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | YRI | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18940 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18941 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18942 | hp2 | a0001 | c0002 | t0001 | g0115 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18943 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18944 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18947 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18950 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18950 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18951 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18953 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18956 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18959 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18961 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18962 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18963 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18964 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18964 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18965 | hp2 | a0001 | c0002 | t0001 | g0119 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18970 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18972 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18973 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18973 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18983 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18987 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18991 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18997 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA19001 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA19005 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA19007 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA19010 | hp1 | a0001 | c0002 | t0001 | g0114 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA19011 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | LWK | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | LWK | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA19058 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA19064 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA19065 | hp2 | a0001 | c0002 | t0001 | g0087 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA19066 | hp1 | a0001 | c0002 | t0001 | g0030 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA19067 | hp2 | a0001 | c0002 | t0001 | g0023 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA19083 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA19084 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA19085 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA19088 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA19088 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA19089 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA19091 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | YRI | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | YRI | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA20129 | hp1 | a0001 | c0002 | t0001 | g0112 | AFR | ASW | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ASW | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA20752 | hp1 | a0001 | c0002 | t0001 | g0033 | EUR | TSI | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA20752 | hp2 | a0001 | c0002 | t0001 | g0013 | EUR | TSI | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0104 | EUR | TSI | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA20805 | hp2 | a0001 | c0002 | t0001 | g0032 | EUR | TSI | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG01123 | hp1 | a0001 | c0002 | t0001 | g0110 | AMR | CLM | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02109 | hp1 | a0001 | c0002 | t0001 | g0025 | AFR | ACB | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | ACB | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02486 | hp2 | a0001 | c0002 | t0001 | g0050 | AFR | ACB | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02559 | hp1 | a0001 | c0002 | t0001 | g0052 | AFR | ACB | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | ACB | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | MSL | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | MSL | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | USA | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
HG06807 | hp2 | a0001 | c0002 | t0001 | g0023 | AFR | USA | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18955 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | USA | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA20300 | hp2 | a0001 | c0002 | t0001 | g0128 | AFR | USA | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | LWK | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
NA21309 | hp2 | a0001 | c0002 | t0002 | g0130 | AFR | LWK | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0107 | REF | REF | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0025 | REF | REF | RGCC_chr13_41452550_41475871 | RGCC | chr13 | 41452550 | 41475871 |
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:41458436 | T | C | 1 | a0001c0001 | 282 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(279): Show |
synonymous_variant | LOW | c.201T>C | p.Ser67Ser | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/5 | 359/958 | 201/414 | 67/137 | chr13 | 41458436 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:41457572 | G | A | 1 | a0001c0002t0002 | 1 | NA21309.hp2 | 5_prime_UTR_variant | MODIFIER | c.-136G>A | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 1/5 | 136 | chr13 | 41457572 | ||||||
chr13:41457576 | C | G | 1 | a0001c0001t0004 | 1 | HG03017.hp2 | 5_prime_UTR_variant | MODIFIER | c.-132C>G | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 1/5 | 132 | chr13 | 41457576 | ||||||
chr13:41470689 | C | T | 1 | a0001c0001t0003 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*204C>T | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 5/5 | 204 | chr13 | 41470689 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:41457790 | C | A | 1 | a0001c0002t0001g0050 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.49+34C>A | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 1/4 | chr13 | 41457790 | |||||||
chr13:41457979 | T | C | 1 | a0001c0001t0001g0051 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.49+223T>C | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 1/4 | chr13 | 41457979 | |||||||
chr13:41458037 | C | G | 2 | a0001c0001t0001g0170 a0001c0001t0001g0171 |
2 | HG02622.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.50-248C>G | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 1/4 | chr13 | 41458037 | |||||||
chr13:41458157 | G | A | 1 | a0001c0002t0001g0052 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.50-128G>A | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 1/4 | chr13 | 41458157 | |||||||
chr13:41458254 | C | T | 2 | a0001c0002t0001g0168 a0001c0002t0001g0169 |
2 | HG01081.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.50-31C>T | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 1/4 | chr13 | 41458254 | |||||||
chr13:41458256 | G | C | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | NA18988.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.50-29G>C | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 1/4 | chr13 | 41458256 | |||||||
chr13:41458590 | C | T | 1 | a0001c0002t0001g0167 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.235+120C>T | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41458590 | |||||||
chr13:41458765 | T | G | 5 | a0001c0001t0001g0015 a0001c0001t0001g0055 a0001c0001t0001g0056 others(2): Show |
9 | HG01884.hp1 HG02145.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.235+295T>G | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41458765 | |||||||
chr13:41458931 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.235+461G>A | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41458931 | |||||||
chr13:41459088 | G | A | 1 | a0001c0001t0001g0060 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.235+618G>A | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41459088 | |||||||
chr13:41459357 | C | T | 1 | a0001c0002t0001g0166 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.235+887C>T | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41459357 | |||||||
chr13:41459449 | G | C | 1 | a0001c0002t0001g0061 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.235+979G>C | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41459449 | |||||||
chr13:41459503 | G | A | 2 | a0001c0001t0001g0170 a0001c0001t0001g0171 |
2 | HG02622.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.235+1033G>A | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41459503 | |||||||
chr13:41459562 | G | C | 40 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0011 others(37): Show |
87 | HG00099.hp1 HG00735.hp1 HG00735.hp2 others(84): Show |
intron_variant | MODIFIER | c.235+1092G>C | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41459562 | |||||||
chr13:41459589 | T | A | 2 | a0001c0002t0001g0007 a0001c0002t0001g0087 |
10 | HG00438.hp1 HG02155.hp1 NA18953.hp2 others(7): Show |
intron_variant | MODIFIER | c.235+1119T>A | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41459589 | |||||||
chr13:41459640 | C | T | 3 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0165 |
3 | HG02451.hp1 HG02559.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.235+1170C>T | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41459640 | |||||||
chr13:41459657 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.235+1187G>A | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41459657 | |||||||
chr13:41459962 | A | C | 2 | a0001c0001t0001g0170 a0001c0001t0001g0171 |
2 | HG02622.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.235+1492A>C | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41459962 | |||||||
chr13:41460122 | A | C | 1 | a0001c0001t0001g0171 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.235+1652A>C | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41460122 | |||||||
chr13:41460124 | C | T | 38 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(35): Show |
103 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.235+1654C>T | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41460124 | |||||||
chr13:41460184 | A | G | 3 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0165 |
3 | HG02451.hp1 HG02559.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.235+1714A>G | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41460184 | |||||||
chr13:41460214 | T | C | 1 | a0001c0002t0001g0029 | 3 | HG00642.hp1 HG01255.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.235+1744T>C | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41460214 | |||||||
chr13:41460438 | G | A | 2 | a0001c0001t0001g0088 a0001c0001t0001g0089 |
2 | HG01891.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.235+1968G>A | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41460438 | |||||||
chr13:41460461 | A | G | 17 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0035 others(14): Show |
41 | HG00558.hp1 HG00673.hp1 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.235+1991A>G | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41460461 | |||||||
chr13:41460643 | T | C | 1 | a0001c0002t0001g0090 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.235+2173T>C | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41460643 | |||||||
chr13:41460691 | G | A | 13 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0012 others(10): Show |
40 | HG00280.hp1 HG00323.hp1 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.235+2221G>A | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41460691 | |||||||
chr13:41460813 | G | T | 1 | a0001c0001t0001g0154 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.235+2343G>T | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41460813 | |||||||
chr13:41460823 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.235+2353C>T | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41460823 | |||||||
chr13:41460917 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.235+2447C>T | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41460917 | |||||||
chr13:41461022 | G | A | 2 | a0001c0001t0001g0018 a0001c0001t0001g0031 |
8 | HG01515.hp2 HG01517.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.235+2552G>A | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41461022 | |||||||
chr13:41461181 | A | G | 1 | a0001c0001t0001g0089 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.235+2711A>G | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41461181 | |||||||
chr13:41461215 | C | A | 3 | a0001c0001t0001g0018 a0001c0001t0001g0031 a0001c0002t0001g0039 |
10 | HG01515.hp2 HG01517.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.235+2745C>A | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41461215 | |||||||
chr13:41461220 | G | C | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(132): Show |
369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.235+2750G>C | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41461220 | |||||||
chr13:41461457 | G | A | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(166): Show |
436 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(433): Show |
intron_variant | MODIFIER | c.235+2987G>A | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41461457 | |||||||
chr13:41461618 | C | T | 1 | a0001c0002t0001g0127 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.235+3148C>T | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41461618 | |||||||
chr13:41461930 | A | G | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(164): Show |
430 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(427): Show |
intron_variant | MODIFIER | c.235+3460A>G | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41461930 | |||||||
chr13:41462011 | A | C | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(146): Show |
400 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(397): Show |
intron_variant | MODIFIER | c.235+3541A>C | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41462011 | |||||||
chr13:41462186 | G | C | 4 | a0001c0001t0001g0021 a0001c0001t0001g0082 a0001c0001t0001g0083 others(1): Show |
7 | HG01496.hp2 HG02257.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.235+3716G>C | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41462186 | |||||||
chr13:41462263 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.235+3793C>T | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41462263 | |||||||
chr13:41462568 | C | G | 7 | a0001c0001t0001g0008 a0001c0001t0001g0022 a0001c0001t0001g0102 others(4): Show |
17 | HG00140.hp2 HG00738.hp1 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.235+4098C>G | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41462568 | |||||||
chr13:41462637 | C | T | 1 | a0001c0002t0001g0126 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.235+4167C>T | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41462637 | |||||||
chr13:41462745 | A | G | 2 | a0001c0001t0001g0018 a0001c0002t0001g0039 |
7 | HG01891.hp1 HG02109.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.236-4078A>G | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41462745 | |||||||
chr13:41462819 | T | C | 1 | a0001c0001t0001g0139 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.236-4004T>C | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41462819 | |||||||
chr13:41462828 | A | G | 6 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0098 others(3): Show |
6 | HG01891.hp2 HG01975.hp1 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.236-3995A>G | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41462828 | |||||||
chr13:41463186 | C | T | 1 | a0001c0001t0001g0081 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.236-3637C>T | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41463186 | |||||||
chr13:41463199 | G | C | 1 | a0001c0001t0001g0066 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.236-3624G>C | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41463199 | |||||||
chr13:41463271 | C | T | 1 | a0001c0001t0001g0038 | 2 | HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.236-3552C>T | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41463271 | |||||||
chr13:41463297 | C | T | 2 | a0001c0001t0001g0088 a0001c0001t0001g0089 |
2 | HG01891.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.236-3526C>T | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41463297 | |||||||
chr13:41463412 | C | T | 3 | a0001c0001t0001g0086 a0001c0001t0001g0125 a0001c0001t0003g0058 |
3 | HG02723.hp1 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.236-3411C>T | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41463412 | |||||||
chr13:41463442 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.236-3381C>T | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41463442 | |||||||
chr13:41463469 | CTGTGTGT others(1): Show |
C | 25 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0036 others(22): Show |
43 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.236-3327_236-3320d others(10): Show |
RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 41463469 | ||||||
chr13:41463469 | CTGTGTGT others(3): Show |
C | 13 | a0001c0001t0001g0043 a0001c0001t0001g0055 a0001c0001t0001g0056 others(10): Show |
14 | HG02280.hp2 HG02451.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.236-3329_236-3320d others(12): Show |
RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 41463469 | ||||||
chr13:41463469 | CTGTGTGT others(5): Show |
C | 105 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(102): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.236-3331_236-3320d others(14): Show |
RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 41463469 | ||||||
chr13:41463469 | CTGTGTGT others(7): Show |
C | 25 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0018 others(22): Show |
50 | HG00140.hp2 HG00738.hp1 HG01070.hp1 others(47): Show |
intron_variant | MODIFIER | c.236-3333_236-3320d others(16): Show |
RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 41463469 | ||||||
chr13:41463538 | T | C | 4 | a0001c0001t0001g0018 a0001c0001t0001g0031 a0001c0002t0001g0032 others(1): Show |
12 | HG00140.hp1 HG01099.hp2 HG01515.hp2 others(9): Show |
intron_variant | MODIFIER | c.236-3285T>C | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41463538 | |||||||
chr13:41463551 | C | T | 1 | a0001c0002t0001g0127 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.236-3272C>T | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41463551 | |||||||
chr13:41463659 | T | G | 2 | a0001c0001t0001g0091 a0001c0001t0001g0092 |
2 | HG02135.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.236-3164T>G | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41463659 | |||||||
chr13:41463755 | C | T | 1 | a0001c0001t0001g0028 | 3 | HG00741.hp1 HG01934.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.236-3068C>T | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41463755 | |||||||
chr13:41463784 | T | C | 15 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0060 others(12): Show |
31 | HG00280.hp2 HG00558.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.236-3039T>C | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41463784 | |||||||
chr13:41463799 | C | T | 87 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(84): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.236-3024C>T | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41463799 | |||||||
chr13:41463825 | T | C | 1 | a0001c0001t0001g0164 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.236-2998T>C | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41463825 | |||||||
chr13:41463947 | C | T | 2 | a0001c0001t0001g0171 a0001c0002t0001g0129 |
2 | HG02622.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.236-2876C>T | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41463947 | |||||||
chr13:41463950 | C | A | 66 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(63): Show |
166 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.236-2873C>A | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41463950 | |||||||
chr13:41463986 | G | C | 2 | a0001c0001t0001g0043 a0001c0001t0001g0132 |
3 | HG03225.hp2 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.236-2837G>C | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41463986 | |||||||
chr13:41464063 | T | A | 1 | a0001c0001t0001g0038 | 2 | HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.236-2760T>A | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41464063 | |||||||
chr13:41464113 | C | T | 2 | a0001c0001t0001g0088 a0001c0001t0001g0089 |
2 | HG01891.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.236-2710C>T | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41464113 | |||||||
chr13:41464337 | C | T | 2 | a0001c0001t0001g0043 a0001c0001t0001g0132 |
3 | HG03225.hp2 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.236-2486C>T | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41464337 | |||||||
chr13:41464472 | C | T | 2 | a0001c0001t0001g0086 a0001c0001t0003g0058 |
2 | HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.236-2351C>T | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41464472 | |||||||
chr13:41464479 | G | A | 1 | a0001c0001t0001g0158 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.236-2344G>A | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41464479 | |||||||
chr13:41464502 | A | G | 92 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(89): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.236-2321A>G | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41464502 | |||||||
chr13:41464538 | T | C | 1 | a0001c0001t0001g0069 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.236-2285T>C | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41464538 | |||||||
chr13:41464568 | C | T | 4 | a0001c0001t0001g0018 a0001c0001t0001g0031 a0001c0002t0001g0032 others(1): Show |
12 | HG00140.hp1 HG01099.hp2 HG01515.hp2 others(9): Show |
intron_variant | MODIFIER | c.236-2255C>T | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41464568 | |||||||
chr13:41464569 | G | A | 1 | a0001c0002t0001g0111 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.236-2254G>A | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41464569 | |||||||
chr13:41464612 | G | A | 1 | a0001c0001t0001g0104 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.236-2211G>A | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41464612 | |||||||
chr13:41464649 | T | C | 14 | a0001c0001t0001g0008 a0001c0001t0001g0022 a0001c0001t0001g0043 others(11): Show |
25 | HG00140.hp2 HG00738.hp1 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.236-2174T>C | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41464649 | |||||||
chr13:41464925 | G | C | 1 | a0001c0002t0001g0129 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.236-1898G>C | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41464925 | |||||||
chr13:41464962 | G | C | 2 | a0001c0001t0001g0141 a0001c0002t0001g0040 |
3 | HG01070.hp2 HG01071.hp2 NA18939.hp2 |
intron_variant | MODIFIER | c.236-1861G>C | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41464962 | |||||||
chr13:41465152 | C | A | 36 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0014 others(33): Show |
157 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(154): Show |
intron_variant | MODIFIER | c.236-1671C>A | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41465152 | |||||||
chr13:41465233 | C | G | 2 | a0001c0001t0001g0099 a0001c0002t0001g0100 |
2 | HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.236-1590C>G | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41465233 | |||||||
chr13:41465433 | G | T | 1 | a0001c0002t0001g0118 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.236-1390G>T | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41465433 | |||||||
chr13:41465512 | C | T | 2 | a0001c0001t0001g0088 a0001c0001t0001g0089 |
2 | HG01891.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.236-1311C>T | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41465512 | |||||||
chr13:41465553 | G | GCC | 87 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(84): Show |
248 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.236-1270_236-1269i others(4): Show |
RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41465553 | |||||||
chr13:41465554 | T | G | 87 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(84): Show |
248 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.236-1269T>G | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41465554 | |||||||
chr13:41465555 | A | T | 87 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(84): Show |
248 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.236-1268A>T | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41465555 | |||||||
chr13:41465601 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.236-1222C>T | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41465601 | |||||||
chr13:41466014 | C | G | 5 | a0001c0001t0001g0018 a0001c0001t0001g0031 a0001c0001t0001g0082 others(2): Show |
13 | HG00140.hp1 HG01099.hp2 HG01515.hp2 others(10): Show |
intron_variant | MODIFIER | c.236-809C>G | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41466014 | |||||||
chr13:41466024 | T | C | 1 | a0001c0001t0001g0171 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.236-799T>C | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41466024 | |||||||
chr13:41466068 | C | G | 4 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0076 others(1): Show |
4 | HG00099.hp1 HG00735.hp2 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.236-755C>G | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41466068 | |||||||
chr13:41466069 | A | ACACACAC others(7): Show |
2 | a0001c0001t0001g0088 a0001c0001t0001g0089 |
2 | HG01891.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.236-753_236-752ins others(14): Show |
RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 41466069 | ||||||
chr13:41466106 | G | A | 87 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(84): Show |
248 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.236-717G>A | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41466106 | |||||||
chr13:41466147 | ACT | A | 2 | a0001c0001t0001g0038 a0001c0001t0001g0142 |
3 | HG02055.hp1 HG03098.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.236-674_236-673del others(2): Show |
RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 41466147 | ||||||
chr13:41466155 | ACGCACAC others(29): Show |
A | 2 | a0001c0001t0001g0088 a0001c0001t0001g0089 |
2 | HG01891.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.236-666_236-631del others(36): Show |
RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 41466155 | ||||||
chr13:41466163 | ACT | A | 10 | a0001c0001t0001g0016 a0001c0001t0001g0064 a0001c0001t0001g0067 others(7): Show |
14 | HG01192.hp1 HG02258.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.236-656_236-655del others(2): Show |
RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 41466163 | ||||||
chr13:41466181 | ACACACAC others(3): Show |
A | 46 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0014 others(43): Show |
175 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.236-629_236-620del others(10): Show |
RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 41466181 | ||||||
chr13:41466195 | ACACACT | A | 3 | a0001c0001t0001g0020 a0001c0002t0001g0020 a0001c0002t0001g0134 |
6 | HG00280.hp2 HG00639.hp1 HG00639.hp2 others(3): Show |
intron_variant | MODIFIER | c.236-625_236-620del others(6): Show |
RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 41466195 | ||||||
chr13:41466197 | ACACT | A | 14 | a0001c0001t0001g0004 a0001c0001t0001g0038 a0001c0001t0001g0060 others(11): Show |
28 | HG00558.hp1 HG02055.hp1 HG02074.hp1 others(25): Show |
intron_variant | MODIFIER | c.236-623_236-620del others(4): Show |
RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 41466197 | ||||||
chr13:41466201 | T | A | 2 | a0001c0001t0001g0088 a0001c0001t0001g0089 |
2 | HG01891.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.236-622T>A | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41466201 | |||||||
chr13:41466202 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.236-621C>T | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41466202 | |||||||
chr13:41466203 | A | G | 1 | a0001c0001t0001g0038 | 2 | HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.236-620A>G | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41466203 | |||||||
chr13:41466204 | T | C | 2 | a0001c0001t0001g0088 a0001c0001t0001g0089 |
2 | HG01891.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.236-619T>C | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41466204 | |||||||
chr13:41466262 | C | A | 1 | a0001c0001t0001g0143 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.236-561C>A | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41466262 | |||||||
chr13:41466265 | G | GCA | 30 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0018 others(27): Show |
53 | HG00140.hp1 HG00140.hp2 HG00738.hp1 others(50): Show |
intron_variant | MODIFIER | c.236-546_236-545dup others(2): Show |
RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 41466265 | ||||||
chr13:41466285 | A | G | 2 | a0001c0001t0001g0088 a0001c0001t0001g0089 |
2 | HG01891.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.236-538A>G | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41466285 | |||||||
chr13:41466392 | C | G | 1 | a0001c0002t0001g0100 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.236-431C>G | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41466392 | |||||||
chr13:41466655 | C | T | 1 | a0001c0002t0001g0117 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.236-168C>T | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41466655 | |||||||
chr13:41466708 | G | T | 88 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(85): Show |
249 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(246): Show |
intron_variant | MODIFIER | c.236-115G>T | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 2/4 | chr13 | 41466708 | |||||||
chr13:41466973 | C | A | 2 | a0001c0001t0001g0144 a0001c0001t0001g0145 |
2 | NA18970.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.343+43C>A | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 3/4 | chr13 | 41466973 | |||||||
chr13:41466988 | A | G | 15 | a0001c0001t0001g0016 a0001c0001t0001g0043 a0001c0001t0001g0064 others(12): Show |
20 | HG01192.hp1 HG01891.hp2 HG01975.hp1 others(17): Show |
intron_variant | MODIFIER | c.343+58A>G | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 3/4 | chr13 | 41466988 | |||||||
chr13:41467057 | T | C | 2 | a0001c0002t0001g0112 a0001c0002t0001g0113 |
2 | HG01361.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.343+127T>C | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 3/4 | chr13 | 41467057 | |||||||
chr13:41467194 | C | CTCTCATG others(43): Show |
1 | a0001c0001t0001g0095 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.343+265_343+314dup others(50): Show |
RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr13 | 41467194 | ||||||
chr13:41467264 | T | C | 23 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0018 others(20): Show |
45 | HG00140.hp1 HG00140.hp2 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.343+334T>C | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 3/4 | chr13 | 41467264 | |||||||
chr13:41467359 | A | G | 23 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0018 others(20): Show |
45 | HG00140.hp1 HG00140.hp2 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.343+429A>G | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 3/4 | chr13 | 41467359 | |||||||
chr13:41467524 | A | G | 1 | a0001c0001t0001g0038 | 2 | HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.343+594A>G | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 3/4 | chr13 | 41467524 | |||||||
chr13:41467532 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.343+602G>A | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 3/4 | chr13 | 41467532 | |||||||
chr13:41467532 | G | T | 1 | a0001c0002t0001g0169 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.343+602G>T | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 3/4 | chr13 | 41467532 | |||||||
chr13:41467675 | A | G | 6 | a0001c0001t0001g0018 a0001c0001t0001g0031 a0001c0001t0001g0082 others(3): Show |
14 | HG00140.hp1 HG01099.hp2 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.343+745A>G | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 3/4 | chr13 | 41467675 | |||||||
chr13:41467689 | A | T | 3 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0002t0001g0100 |
3 | HG01981.hp2 HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.343+759A>T | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 3/4 | chr13 | 41467689 | |||||||
chr13:41467785 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.343+855C>T | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 3/4 | chr13 | 41467785 | |||||||
chr13:41467802 | C | T | 3 | a0001c0001t0001g0043 a0001c0001t0001g0132 a0001c0001t0001g0164 |
4 | HG03225.hp2 HG03453.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.343+872C>T | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 3/4 | chr13 | 41467802 | |||||||
chr13:41467803 | A | G | 94 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(91): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.343+873A>G | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 3/4 | chr13 | 41467803 | |||||||
chr13:41468137 | G | C | 2 | a0001c0001t0001g0171 a0001c0002t0002g0130 |
2 | HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.344-639G>C | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 3/4 | chr13 | 41468137 | |||||||
chr13:41468144 | G | A | 31 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0018 others(28): Show |
65 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.344-632G>A | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 3/4 | chr13 | 41468144 | |||||||
chr13:41468169 | C | T | 2 | a0001c0001t0001g0043 a0001c0001t0001g0132 |
3 | HG03225.hp2 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.344-607C>T | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 3/4 | chr13 | 41468169 | |||||||
chr13:41468246 | C | T | 25 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0020 others(22): Show |
51 | HG00140.hp2 HG00280.hp2 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.344-530C>T | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 3/4 | chr13 | 41468246 | |||||||
chr13:41468509 | A | G | 3 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0002t0001g0100 |
3 | HG01981.hp2 HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.344-267A>G | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 3/4 | chr13 | 41468509 | |||||||
chr13:41468520 | A | G | 1 | a0001c0001t0001g0038 | 2 | HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.344-256A>G | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 3/4 | chr13 | 41468520 | |||||||
chr13:41468650 | G | T | 1 | a0001c0001t0001g0038 | 2 | HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.344-126G>T | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 3/4 | chr13 | 41468650 | |||||||
chr13:41468664 | T | A | 1 | a0001c0001t0001g0070 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.344-112T>A | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 3/4 | chr13 | 41468664 | |||||||
chr13:41468666 | T | A | 1 | a0001c0001t0001g0070 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.344-110T>A | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 3/4 | chr13 | 41468666 | |||||||
chr13:41468688 | C | G | 2 | a0001c0001t0001g0099 a0001c0002t0001g0100 |
2 | HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.344-88C>G | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 3/4 | chr13 | 41468688 | |||||||
chr13:41468930 | G | GCAGAAAG others(1618): Show |
1 | a0001c0002t0001g0116 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.406+103_406+104ins others(1625): Show |
RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr13 | 41468930 | ||||||
chr13:41468950 | C | G | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(162): Show |
428 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(425): Show |
intron_variant | MODIFIER | c.406+112C>G | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 4/4 | chr13 | 41468950 | |||||||
chr13:41468982 | C | T | 1 | a0001c0002t0001g0137 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.406+144C>T | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 4/4 | chr13 | 41468982 | |||||||
chr13:41469129 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.406+291C>T | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 4/4 | chr13 | 41469129 | |||||||
chr13:41469130 | G | A | 25 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0020 others(22): Show |
51 | HG00140.hp2 HG00280.hp2 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.406+292G>A | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 4/4 | chr13 | 41469130 | |||||||
chr13:41469218 | G | A | 2 | a0001c0001t0001g0031 a0001c0002t0001g0032 |
6 | HG00140.hp1 HG01099.hp2 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.406+380G>A | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 4/4 | chr13 | 41469218 | |||||||
chr13:41469255 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.406+417G>A | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 4/4 | chr13 | 41469255 | |||||||
chr13:41469264 | G | GTAA | 3 | a0001c0001t0001g0078 a0001c0001t0001g0149 a0001c0002t0001g0136 |
3 | HG01192.hp2 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.406+457_406+459dup others(3): Show |
RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr13 | 41469264 | ||||||
chr13:41469264 | G | GTAATAAT others(2): Show |
4 | a0001c0001t0001g0016 a0001c0001t0001g0056 a0001c0001t0001g0079 others(1): Show |
8 | HG01192.hp1 HG02258.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.406+451_406+459dup others(9): Show |
RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr13 | 41469264 | ||||||
chr13:41469264 | G | GTAATAAT others(8): Show |
1 | a0001c0001t0001g0138 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.406+445_406+459dup others(15): Show |
RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr13 | 41469264 | ||||||
chr13:41469264 | G | GTAATGAT others(5): Show |
1 | a0001c0001t0001g0165 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.406+430_406+431ins others(12): Show |
RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr13 | 41469264 | ||||||
chr13:41469264 | GTAA | G | 17 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(14): Show |
43 | HG00673.hp2 HG01074.hp2 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.406+457_406+459del others(3): Show |
RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr13 | 41469264 | ||||||
chr13:41469264 | GTAATAA | G | 6 | a0001c0001t0001g0022 a0001c0001t0001g0063 a0001c0001t0001g0094 others(3): Show |
9 | HG00280.hp1 HG01081.hp2 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.406+454_406+459del others(6): Show |
RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr13 | 41469264 | ||||||
chr13:41469264 | GTAATAAT others(2): Show |
G | 3 | a0001c0001t0001g0070 a0001c0001t0001g0099 a0001c0001t0001g0146 |
3 | HG03041.hp1 HG03471.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.406+451_406+459del others(9): Show |
RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr13 | 41469264 | ||||||
chr13:41469264 | GTAATAAT others(5): Show |
G | 5 | a0001c0001t0001g0154 a0001c0001t0001g0156 a0001c0001t0001g0159 others(2): Show |
7 | HG02165.hp1 HG03704.hp1 HG04184.hp2 others(4): Show |
intron_variant | MODIFIER | c.406+448_406+459del others(12): Show |
RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr13 | 41469264 | ||||||
chr13:41469270 | A | G | 7 | a0001c0001t0001g0018 a0001c0001t0001g0031 a0001c0001t0001g0082 others(4): Show |
15 | HG00140.hp1 HG01099.hp2 HG01515.hp2 others(12): Show |
intron_variant | MODIFIER | c.406+432A>G | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 4/4 | chr13 | 41469270 | |||||||
chr13:41469283 | T | G | 2 | a0001c0001t0001g0045 a0001c0002t0002g0130 |
3 | NA18948.hp2 NA18962.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.406+445T>G | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 4/4 | chr13 | 41469283 | |||||||
chr13:41469283 | TAATAATA others(8): Show |
T | 4 | a0001c0002t0001g0024 a0001c0002t0001g0106 a0001c0002t0001g0112 others(1): Show |
7 | HG01175.hp1 HG01256.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.406+448_406+462del others(15): Show |
RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr13 | 41469283 | ||||||
chr13:41469286 | T | G | 3 | a0001c0001t0001g0002 a0001c0001t0001g0045 a0001c0002t0002g0130 |
4 | NA18948.hp2 NA18962.hp2 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.406+448T>G | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 4/4 | chr13 | 41469286 | |||||||
chr13:41469286 | T | TAAG | 3 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0152 |
3 | HG01496.hp2 NA18984.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.406+450_406+451ins others(3): Show |
RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr13 | 41469286 | ||||||
chr13:41469286 | TAATAATA others(5): Show |
T | 7 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0133 others(4): Show |
17 | HG00639.hp1 HG01952.hp1 HG02027.hp1 others(14): Show |
intron_variant | MODIFIER | c.406+451_406+462del others(12): Show |
RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr13 | 41469286 | ||||||
chr13:41469286 | TAATAATA others(8): Show |
T | 11 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0017 others(8): Show |
23 | HG00544.hp2 HG00597.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.406+451_406+465del others(15): Show |
RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr13 | 41469286 | ||||||
chr13:41469289 | T | G | 10 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0021 others(7): Show |
17 | HG01496.hp2 HG02040.hp2 HG02080.hp1 others(14): Show |
intron_variant | MODIFIER | c.406+451T>G | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 4/4 | chr13 | 41469289 | |||||||
chr13:41469289 | T | TAAGAAGA others(5): Show |
1 | a0001c0001t0001g0015 | 2 | HG02145.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.406+453_406+454ins others(12): Show |
RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr13 | 41469289 | ||||||
chr13:41469289 | TAATAATA others(5): Show |
T | 15 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0020 others(12): Show |
24 | HG00280.hp2 HG00639.hp2 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.406+454_406+465del others(12): Show |
RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr13 | 41469289 | ||||||
chr13:41469289 | TAATAATA others(8): Show |
T | 16 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0014 others(13): Show |
38 | HG00099.hp2 HG00323.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.406+454_406+468del others(15): Show |
RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr13 | 41469289 | ||||||
chr13:41469292 | T | G | 14 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(11): Show |
30 | HG00408.hp2 HG01496.hp2 HG02040.hp2 others(27): Show |
intron_variant | MODIFIER | c.406+454T>G | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 4/4 | chr13 | 41469292 | |||||||
chr13:41469292 | T | TAAGAAGA others(5): Show |
1 | a0001c0001t0001g0015 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.406+456_406+457ins others(12): Show |
RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr13 | 41469292 | ||||||
chr13:41469292 | TAATAAG | T | 5 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0026 others(2): Show |
14 | HG00140.hp2 HG00323.hp1 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.406+457_406+462del others(6): Show |
RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr13 | 41469292 | ||||||
chr13:41469292 | TAATAAGA others(2): Show |
T | 7 | a0001c0001t0001g0002 a0001c0001t0001g0031 a0001c0001t0001g0043 others(4): Show |
11 | HG01515.hp2 HG01517.hp2 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.406+457_406+465del others(9): Show |
RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr13 | 41469292 | ||||||
chr13:41469292 | TAATAAGA others(5): Show |
T | 11 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(8): Show |
32 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.406+457_406+468del others(12): Show |
RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr13 | 41469292 | ||||||
chr13:41469292 | TAATAAGA others(8): Show |
T | 7 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0017 others(4): Show |
31 | HG00423.hp1 HG00438.hp2 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.406+457_406+471del others(15): Show |
RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr13 | 41469292 | ||||||
chr13:41469292 | TAATAAGA others(14): Show |
T | 1 | a0001c0002t0001g0032 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.406+457_406+477del others(21): Show |
RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr13 | 41469292 | ||||||
chr13:41469295 | T | G | 29 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(26): Show |
61 | HG00408.hp2 HG00423.hp2 HG01109.hp1 others(58): Show |
intron_variant | MODIFIER | c.406+457T>G | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 4/4 | chr13 | 41469295 | |||||||
chr13:41469295 | T | TAATAAGA others(5): Show |
1 | a0001c0001t0001g0064 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.406+459_406+460ins others(12): Show |
RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr13 | 41469295 | ||||||
chr13:41469295 | T | TAATAAGA others(8): Show |
1 | a0001c0001t0001g0015 | 2 | HG01884.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.406+459_406+460ins others(15): Show |
RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr13 | 41469295 | ||||||
chr13:41469295 | T | TAATAATA others(5): Show |
1 | a0001c0001t0001g0067 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.406+459_406+460ins others(12): Show |
RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr13 | 41469295 | ||||||
chr13:41469295 | T | TAATAATA others(11): Show |
1 | a0001c0001t0001g0122 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.406+459_406+460ins others(18): Show |
RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr13 | 41469295 | ||||||
chr13:41469295 | TAAG | T | 35 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(32): Show |
59 | HG00099.hp1 HG00408.hp1 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.406+493_406+495del others(3): Show |
RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr13 | 41469295 | ||||||
chr13:41469295 | TAAGAAG | T | 7 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0132 others(4): Show |
8 | HG01069.hp1 HG01071.hp1 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.406+490_406+495del others(6): Show |
RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr13 | 41469295 | ||||||
chr13:41469295 | TAAGAAGA others(2): Show |
T | 6 | a0001c0001t0001g0002 a0001c0001t0001g0075 a0001c0001t0001g0142 others(3): Show |
11 | HG00558.hp2 HG01099.hp2 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.406+487_406+495del others(9): Show |
RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr13 | 41469295 | ||||||
chr13:41469295 | TAAGAAGA others(5): Show |
T | 6 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0003g0058 others(3): Show |
10 | HG01934.hp2 HG02155.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.406+484_406+495del others(12): Show |
RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr13 | 41469295 | ||||||
chr13:41469295 | TAAGAAGA others(8): Show |
T | 6 | a0001c0001t0001g0014 a0001c0001t0001g0051 a0001c0001t0001g0155 others(3): Show |
12 | HG00642.hp1 HG01255.hp2 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.406+481_406+495del others(15): Show |
RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr13 | 41469295 | ||||||
chr13:41469298 | G | T | 20 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(17): Show |
24 | HG01106.hp1 HG01192.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.406+460G>T | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 4/4 | chr13 | 41469298 | |||||||
chr13:41469301 | G | T | 26 | a0001c0001t0001g0010 a0001c0001t0001g0027 a0001c0001t0001g0030 others(23): Show |
42 | HG00735.hp2 HG00738.hp2 HG01123.hp1 others(39): Show |
intron_variant | MODIFIER | c.406+463G>T | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 4/4 | chr13 | 41469301 | |||||||
chr13:41469304 | G | T | 16 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0038 others(13): Show |
21 | HG01069.hp1 HG01071.hp1 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.406+466G>T | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 4/4 | chr13 | 41469304 | |||||||
chr13:41469307 | G | T | 8 | a0001c0001t0001g0057 a0001c0001t0001g0071 a0001c0001t0001g0075 others(5): Show |
9 | HG01069.hp1 HG01071.hp1 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.406+469G>T | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 4/4 | chr13 | 41469307 | |||||||
chr13:41469310 | G | T | 2 | a0001c0001t0003g0058 a0001c0002t0001g0120 |
2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.406+472G>T | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 4/4 | chr13 | 41469310 | |||||||
chr13:41469313 | G | T | 1 | a0001c0001t0003g0058 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.406+475G>T | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 4/4 | chr13 | 41469313 | |||||||
chr13:41469316 | G | T | 1 | a0001c0001t0003g0058 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.406+478G>T | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 4/4 | chr13 | 41469316 | |||||||
chr13:41469534 | G | A | 38 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0014 others(35): Show |
160 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.406+696G>A | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 4/4 | chr13 | 41469534 | |||||||
chr13:41469914 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.407-564G>A | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 4/4 | chr13 | 41469914 | |||||||
chr13:41469936 | C | T | 1 | a0001c0001t0001g0147 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.407-542C>T | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 4/4 | chr13 | 41469936 | |||||||
chr13:41470140 | CAGAT | C | 15 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0060 others(12): Show |
31 | HG00280.hp2 HG00558.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.407-334_407-331del others(4): Show |
RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr13 | 41470140 | ||||||
chr13:41470227 | A | G | 73 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(70): Show |
225 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.407-251A>G | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 4/4 | chr13 | 41470227 | |||||||
chr13:41470267 | C | T | 1 | a0001c0002t0001g0115 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.407-211C>T | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 4/4 | chr13 | 41470267 | |||||||
chr13:41470280 | A | G | 1 | a0001c0002t0001g0114 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.407-198A>G | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 4/4 | chr13 | 41470280 | |||||||
chr13:41470327 | G | T | 3 | a0001c0001t0001g0043 a0001c0001t0001g0132 a0001c0001t0001g0164 |
4 | HG03225.hp2 HG03453.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.407-151G>T | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 4/4 | chr13 | 41470327 | |||||||
chr13:41470328 | C | T | 2 | a0001c0001t0001g0055 a0001c0001t0001g0056 |
2 | HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.407-150C>T | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 4/4 | chr13 | 41470328 | |||||||
chr13:41470372 | A | G | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(163): Show |
429 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(426): Show |
intron_variant | MODIFIER | c.407-106A>G | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 4/4 | chr13 | 41470372 | |||||||
chr13:41470450 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.407-28G>A | RGCC | ENSG00000102760.13 | transcript | ENST00000379359.4 | protein_coding | 4/4 | chr13 | 41470450 |