Item | Value |
---|---|
geneid | 892 |
ensemblid | ENSG00000112237.13 |
hgncid | 1581 |
symbol | CCNC |
name | cyclin C |
refseq_nuc | NM_005190.4 |
refseq_prot | NP_005181.2 |
ensembl_nuc | ENST00000520429.6 |
ensembl_prot | ENSP00000428982.1 |
mane_status | MANE Select |
chr | chr6 |
start | 99542387 |
end | 99568660 |
strand | - |
ver | v1.2 |
region | chr6:99542387-99568660 |
region5000 | chr6:99537387-99573660 |
regionname0 | CCNC_chr6_99542387_99568660 |
regionname5000 | CCNC_chr6_99537387_99573660 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 849 | 408 | 84 | 78 | 182 | 14 | 48 | CCNC_chr6_99537387_99573660 | CCNC | ATGGC others(844): Show |
chr6 | 99537387 | 99573660 | ||
a0001c0002 | 0/0 | 849 | 2 | 0 | 0 | 2 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | ATGGC others(844): Show |
chr6 | 99537387 | 99573660 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 2153 | 329 | 76 | 61 | 148 | 11 | 31 | CCNC_chr6_99537387_99573660 | CCNC | GTCGC others(2148): Show |
chr6 | 99537387 | 99573660 |
a0001c0001t0002 | 0/0 | 2153 | 68 | 5 | 13 | 32 | 3 | 15 | CCNC_chr6_99537387_99573660 | CCNC | GTCGC others(2148): Show |
chr6 | 99537387 | 99573660 |
a0001c0001t0003 | 0/0 | 2153 | 4 | 0 | 3 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | GTCGC others(2148): Show |
chr6 | 99537387 | 99573660 |
a0001c0001t0004 | 0/0 | 2153 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | GTCGC others(2148): Show |
chr6 | 99537387 | 99573660 |
a0001c0001t0005 | 0/0 | 2153 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | GTCGC others(2148): Show |
chr6 | 99537387 | 99573660 |
a0001c0001t0006 | 0/0 | 2153 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | GTCGC others(2148): Show |
chr6 | 99537387 | 99573660 |
a0001c0001t0007 | 0/0 | 2153 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | GTCGC others(2148): Show |
chr6 | 99537387 | 99573660 |
a0001c0001t0008 | 0/0 | 2153 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | GTCGC others(2148): Show |
chr6 | 99537387 | 99573660 |
a0001c0001t0009 | 0/0 | 2153 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | GTCGC others(2148): Show |
chr6 | 99537387 | 99573660 |
a0001c0001t0010 | 0/0 | 2153 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | GTCGC others(2148): Show |
chr6 | 99537387 | 99573660 |
a0001c0002t0001 | 0/0 | 2153 | 2 | 0 | 0 | 2 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | GTCGC others(2148): Show |
chr6 | 99537387 | 99573660 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 40 | 0 | 2 | 35 | 0 | 3 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0002 | 1/0 | 14 | 1 | 12 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0003 | 0/0 | 13 | 2 | 1 | 10 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0004 | 0/0 | 12 | 0 | 1 | 11 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0006 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0008 | 0/0 | 7 | 0 | 6 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0010 | 0/0 | 6 | 3 | 2 | 0 | 1 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0011 | 0/0 | 6 | 4 | 1 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0012 | 0/0 | 6 | 1 | 0 | 5 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0013 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0014 | 0/0 | 5 | 0 | 1 | 0 | 1 | 3 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0015 | 0/0 | 5 | 0 | 3 | 0 | 1 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0017 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0018 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0019 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0020 | 0/0 | 4 | 0 | 0 | 1 | 0 | 3 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0024 | 0/0 | 3 | 1 | 0 | 0 | 2 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0025 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0026 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0028 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0029 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0033 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0036 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0044 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0148 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0002g0005 | 0/0 | 12 | 1 | 4 | 2 | 1 | 4 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0002g0007 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0002g0009 | 0/0 | 6 | 1 | 0 | 4 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0002g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0002g0021 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0002g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0002g0030 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0002g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0002g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0003g0022 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0003g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0004g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0005g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0006g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0007g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0008g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0009g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0001t0010g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0005 | EUR | GBR | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0024 | EUR | GBR | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0190 | EUR | GBR | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0024 | EUR | GBR | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0206 | EUR | FIN | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0014 | EUR | FIN | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0126 | EUR | FIN | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | FIN | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | CHS | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | CHS | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG00544 | hp2 | a0001 | c0001 | t0010 | g0188 | EAS | CHS | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | CHS | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | CHS | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG00642 | hp1 | a0001 | c0001 | t0003 | g0022 | AMR | PUR | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | CHS | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG00735 | hp1 | a0001 | c0001 | t0003 | g0022 | AMR | PUR | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0057 | AMR | PUR | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0021 | AMR | PUR | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01099 | hp2 | a0001 | c0001 | t0003 | g0046 | AMR | PUR | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01243 | hp2 | a0001 | c0001 | t0009 | g0103 | AMR | PUR | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | CLM | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | CLM | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0031 | AMR | CLM | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0031 | AMR | CLM | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | CLM | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0214 | AMR | CLM | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0054 | AMR | CLM | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | CLM | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | CLM | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0105 | EUR | IBS | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0128 | EUR | IBS | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0216 | AMR | PEL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PEL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0021 | AMR | PEL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PEL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PEL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | PEL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PEL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | KHV | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | KHV | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | KHV | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | KHV | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | ACB | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02145 | hp2 | a0001 | c0001 | t0002 | g0221 | AFR | ACB | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | CDX | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | ACB | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ACB | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | ACB | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02258 | hp2 | a0001 | c0001 | t0007 | g0154 | AFR | ACB | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0062 | SAS | PJL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | GWD | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02683 | hp1 | a0001 | c0001 | t0005 | g0137 | SAS | PJL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02717 | hp1 | a0001 | c0001 | t0004 | g0068 | AFR | GWD | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | GWD | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | GWD | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | GWD | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ESN | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | ESN | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ESN | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ESN | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | ESN | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | ESN | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ESN | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0052 | SAS | PJL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0217 | SAS | PJL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | MSL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | MSL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | ESN | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | ESN | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | ESN | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | MSL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03225 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | MSL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | MSL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | MSL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | MSL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | MSL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03486 | hp2 | a0001 | c0001 | t0002 | g0060 | AFR | MSL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0051 | SAS | PJL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0005 | SAS | PJL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0005 | SAS | PJL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | ESN | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0061 | AFR | ESN | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | MSL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | MSL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | STU | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0222 | SAS | STU | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0220 | SAS | PJL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0219 | SAS | PJL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0209 | SAS | PJL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0005 | SAS | PJL | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | BEB | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0053 | SAS | BEB | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | BEB | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0009 | SAS | BEB | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | BEB | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | STU | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | STU | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0218 | SAS | BEB | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | BEB | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | STU | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0005 | SAS | STU | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | STU | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | STU | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0063 | SAS | STU | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | STU | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | YRI | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | YRI | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | CHB | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | YRI | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | YRI | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18949 | hp1 | a0001 | c0002 | t0001 | g0168 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18949 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18967 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18970 | hp1 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18991 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18993 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19001 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19012 | hp1 | a0001 | c0002 | t0001 | g0169 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | LWK | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | LWK | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | LWK | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19043 | hp2 | a0001 | c0001 | t0008 | g0088 | AFR | LWK | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19055 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19067 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19086 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19089 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | YRI | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | YRI | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ASW | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | ASW | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0207 | EUR | TSI | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0030 | EUR | TSI | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0030 | EUR | TSI | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0010 | EUR | TSI | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA20905 | hp1 | a0001 | c0001 | t0006 | g0208 | SAS | GIH | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | GIH | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0049 | AMR | CLM | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | ACB | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | ACB | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | ACB | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | USA | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | USA | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | USA | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | USA | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | LWK | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | LWK | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0148 | REF | REF | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0002 | REF | REF | CCNC_chr6_99537387_99573660 | CCNC | chr6 | 99537387 | 99573660 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:99562882 | T | C | 1 | a0001c0002 | 2 | NA18949.hp1 NA19012.hp1 |
synonymous_variant | LOW | c.99A>G | p.Ser33Ser | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 2/12 | 232/2153 | 99/852 | 33/283 | chr6 | 99562882 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:99542488 | T | C | 1 | a0001c0001t0007 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1067A>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 12/12 | 1067 | chr6 | 99542488 | ||||||
chr6:99542576 | C | T | 1 | a0001c0001t0006 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*979G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 12/12 | 979 | chr6 | 99542576 | ||||||
chr6:99542809 | G | A | 1 | a0001c0001t0002 | 68 | HG00099.hp1 HG00621.hp1 HG01069.hp1 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*746C>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 12/12 | 746 | chr6 | 99542809 | ||||||
chr6:99542976 | T | C | 1 | a0001c0001t0008 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*579A>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 12/12 | 579 | chr6 | 99542976 | ||||||
chr6:99542980 | T | C | 1 | a0001c0001t0002 | 68 | HG00099.hp1 HG00621.hp1 HG01069.hp1 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*575A>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 12/12 | 575 | chr6 | 99542980 | ||||||
chr6:99543046 | C | T | 1 | a0001c0001t0005 | 1 | HG02683.hp1 | 3_prime_UTR_variant | MODIFIER | c.*509G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 12/12 | 509 | chr6 | 99543046 | ||||||
chr6:99543210 | A | G | 1 | a0001c0001t0004 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*345T>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 12/12 | 345 | chr6 | 99543210 | ||||||
chr6:99543317 | T | C | 1 | a0001c0001t0009 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*238A>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 12/12 | 238 | chr6 | 99543317 | ||||||
chr6:99543416 | T | C | 1 | a0001c0001t0010 | 1 | HG00544.hp2 | 3_prime_UTR_variant | MODIFIER | c.*139A>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 12/12 | 139 | chr6 | 99543416 | ||||||
chr6:99568541 | C | G | 1 | a0001c0001t0003 | 4 | HG00642.hp1 HG00735.hp1 HG01099.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-14G>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/12 | 14 | chr6 | 99568541 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:99543620 | G | A | 2 | a0001c0001t0001g0163 a0001c0001t0001g0171 |
2 | NA18957.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.798-11C>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 11/11 | chr6 | 99543620 | |||||||
chr6:99543702 | G | A | 6 | a0001c0001t0002g0030 a0001c0001t0002g0031 a0001c0001t0002g0051 others(3): Show |
8 | HG01069.hp1 HG01257.hp2 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.798-93C>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 11/11 | chr6 | 99543702 | |||||||
chr6:99543834 | T | G | 1 | a0001c0001t0001g0069 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.798-225A>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 11/11 | chr6 | 99543834 | |||||||
chr6:99544014 | CAA | C | 28 | a0001c0001t0001g0010 a0001c0001t0001g0024 a0001c0001t0001g0087 others(25): Show |
49 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(46): Show |
intron_variant | MODIFIER | c.798-407_798-406del others(2): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 11/11 | chr6 | 99544014 | |||||||
chr6:99544014 | CAAA | C | 181 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(178): Show |
334 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(331): Show |
intron_variant | MODIFIER | c.798-408_798-406del others(3): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 11/11 | chr6 | 99544014 | |||||||
chr6:99544089 | G | T | 1 | a0001c0001t0001g0089 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.798-480C>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 11/11 | chr6 | 99544089 | |||||||
chr6:99544116 | GAAAATGC others(15): Show |
G | 1 | a0001c0001t0001g0038 | 2 | HG02698.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.798-529_798-508del others(22): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 11/11 | chr6 | 99544116 | |||||||
chr6:99544630 | T | C | 1 | a0001c0001t0001g0072 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.797+482A>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 11/11 | chr6 | 99544630 | |||||||
chr6:99544729 | G | A | 1 | a0001c0001t0001g0015 | 5 | HG00323.hp2 HG00733.hp1 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.797+383C>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 11/11 | chr6 | 99544729 | |||||||
chr6:99544745 | G | GA | 25 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0026 others(22): Show |
44 | HG00639.hp1 HG00673.hp2 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.797+366dupT | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 11/11 | chr6 | 99544745 | |||||||
chr6:99544745 | G | GAA | 7 | a0001c0001t0001g0006 a0001c0001t0001g0064 a0001c0001t0001g0087 others(4): Show |
14 | HG00423.hp1 HG00544.hp1 HG02135.hp1 others(11): Show |
intron_variant | MODIFIER | c.797+365_797+366dup others(2): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 11/11 | chr6 | 99544745 | |||||||
chr6:99544745 | GA | G | 138 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(135): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.797+366delT | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 11/11 | chr6 | 99544745 | |||||||
chr6:99544751 | A | G | 1 | a0001c0001t0001g0132 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.797+361T>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 11/11 | chr6 | 99544751 | |||||||
chr6:99544854 | A | C | 1 | a0001c0001t0001g0115 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.797+258T>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 11/11 | chr6 | 99544854 | |||||||
chr6:99545312 | C | A | 83 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(80): Show |
165 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.679-82G>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 10/11 | chr6 | 99545312 | |||||||
chr6:99545350 | G | C | 6 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0038 others(3): Show |
14 | HG00673.hp1 HG02129.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.679-120C>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 10/11 | chr6 | 99545350 | |||||||
chr6:99545392 | G | A | 35 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0009 others(32): Show |
68 | HG00099.hp1 HG00621.hp1 HG01069.hp1 others(65): Show |
intron_variant | MODIFIER | c.679-162C>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 10/11 | chr6 | 99545392 | |||||||
chr6:99545665 | G | A | 1 | a0001c0001t0001g0119 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.679-435C>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 10/11 | chr6 | 99545665 | |||||||
chr6:99545779 | C | T | 1 | a0001c0001t0001g0194 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.679-549G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 10/11 | chr6 | 99545779 | |||||||
chr6:99545828 | AG | A | 2 | a0001c0001t0001g0027 a0001c0001t0001g0167 |
4 | NA18940.hp1 NA18955.hp1 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.678+566delC | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 10/11 | chr6 | 99545828 | |||||||
chr6:99545866 | G | T | 212 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(209): Show |
386 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(383): Show |
intron_variant | MODIFIER | c.678+529C>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 10/11 | chr6 | 99545866 | |||||||
chr6:99545992 | G | A | 1 | a0001c0001t0002g0053 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.678+403C>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 10/11 | chr6 | 99545992 | |||||||
chr6:99546032 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.678+363C>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 10/11 | chr6 | 99546032 | |||||||
chr6:99546113 | A | G | 1 | a0001c0001t0001g0089 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.678+282T>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 10/11 | chr6 | 99546113 | |||||||
chr6:99546172 | G | A | 1 | a0001c0001t0001g0114 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.678+223C>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 10/11 | chr6 | 99546172 | |||||||
chr6:99546186 | G | A | 35 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0009 others(32): Show |
68 | HG00099.hp1 HG00621.hp1 HG01069.hp1 others(65): Show |
intron_variant | MODIFIER | c.678+209C>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 10/11 | chr6 | 99546186 | |||||||
chr6:99546380 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.678+15G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 10/11 | chr6 | 99546380 | |||||||
chr6:99546630 | A | G | 1 | a0001c0001t0001g0184 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.599-156T>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 9/11 | chr6 | 99546630 | |||||||
chr6:99546722 | A | G | 3 | a0001c0001t0001g0028 a0001c0001t0001g0175 a0001c0001t0001g0176 |
5 | HG01891.hp2 HG02886.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.599-248T>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 9/11 | chr6 | 99546722 | |||||||
chr6:99546888 | G | A | 210 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(207): Show |
384 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(381): Show |
intron_variant | MODIFIER | c.599-414C>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 9/11 | chr6 | 99546888 | |||||||
chr6:99546953 | C | A | 1 | a0001c0001t0001g0119 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.599-479G>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 9/11 | chr6 | 99546953 | |||||||
chr6:99547060 | T | TACA | 68 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(65): Show |
125 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.599-587_599-586ins others(3): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 9/11 | chr6 | 99547060 | |||||||
chr6:99547088 | A | G | 1 | a0001c0001t0001g0199 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.599-614T>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 9/11 | chr6 | 99547088 | |||||||
chr6:99547177 | C | T | 210 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(207): Show |
384 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(381): Show |
intron_variant | MODIFIER | c.599-703G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 9/11 | chr6 | 99547177 | |||||||
chr6:99547444 | G | T | 69 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(66): Show |
126 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.599-970C>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 9/11 | chr6 | 99547444 | |||||||
chr6:99547468 | T | C | 8 | a0001c0001t0001g0024 a0001c0001t0001g0091 a0001c0001t0001g0102 others(5): Show |
10 | HG00099.hp2 HG00140.hp2 HG00733.hp2 others(7): Show |
intron_variant | MODIFIER | c.599-994A>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 9/11 | chr6 | 99547468 | |||||||
chr6:99547486 | C | CA | 42 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0013 others(39): Show |
95 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(92): Show |
intron_variant | MODIFIER | c.599-1013dupT | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 9/11 | chr6 | 99547486 | |||||||
chr6:99547600 | A | G | 1 | a0001c0001t0001g0077 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.599-1126T>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 9/11 | chr6 | 99547600 | |||||||
chr6:99547647 | T | G | 83 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(80): Show |
165 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.599-1173A>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 9/11 | chr6 | 99547647 | |||||||
chr6:99547650 | C | G | 22 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0065 others(19): Show |
24 | HG00735.hp2 HG01109.hp1 HG02145.hp1 others(21): Show |
intron_variant | MODIFIER | c.599-1176G>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 9/11 | chr6 | 99547650 | |||||||
chr6:99547753 | A | G | 68 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(65): Show |
125 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.599-1279T>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 9/11 | chr6 | 99547753 | |||||||
chr6:99548099 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.598+1409C>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 9/11 | chr6 | 99548099 | |||||||
chr6:99548101 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.598+1407C>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 9/11 | chr6 | 99548101 | |||||||
chr6:99548180 | C | T | 4 | a0001c0001t0002g0030 a0001c0001t0002g0031 a0001c0001t0002g0054 others(1): Show |
6 | HG01069.hp1 HG01257.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.598+1328G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 9/11 | chr6 | 99548180 | |||||||
chr6:99548486 | AAG | A | 22 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0029 others(19): Show |
40 | HG00140.hp1 HG00544.hp2 HG00609.hp2 others(37): Show |
intron_variant | MODIFIER | c.598+1020_598+1021d others(4): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 9/11 | chr6 | 99548486 | |||||||
chr6:99548540 | T | C | 212 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(209): Show |
386 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(383): Show |
intron_variant | MODIFIER | c.598+968A>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 9/11 | chr6 | 99548540 | |||||||
chr6:99548576 | AG | A | 83 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(80): Show |
165 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.598+931delC | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 9/11 | chr6 | 99548576 | |||||||
chr6:99548751 | C | T | 69 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(66): Show |
126 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.598+757G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 9/11 | chr6 | 99548751 | |||||||
chr6:99548772 | C | T | 83 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(80): Show |
165 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.598+736G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 9/11 | chr6 | 99548772 | |||||||
chr6:99548773 | A | AG | 3 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0147 |
11 | HG00280.hp2 HG00323.hp2 HG00733.hp1 others(8): Show |
intron_variant | MODIFIER | c.598+734dupC | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 9/11 | chr6 | 99548773 | |||||||
chr6:99548802 | CAA | C | 27 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0065 others(24): Show |
29 | HG00735.hp2 HG01109.hp1 HG02145.hp1 others(26): Show |
intron_variant | MODIFIER | c.598+704_598+705del others(2): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 9/11 | chr6 | 99548802 | |||||||
chr6:99548802 | CAAA | C | 125 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(122): Show |
237 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(234): Show |
intron_variant | MODIFIER | c.598+703_598+705del others(3): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 9/11 | chr6 | 99548802 | |||||||
chr6:99548802 | CAAAA | C | 55 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(52): Show |
115 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.598+702_598+705del others(4): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 9/11 | chr6 | 99548802 | |||||||
chr6:99548918 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.598+590G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 9/11 | chr6 | 99548918 | |||||||
chr6:99548949 | T | G | 1 | a0001c0001t0002g0054 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.598+559A>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 9/11 | chr6 | 99548949 | |||||||
chr6:99549076 | T | C | 1 | a0001c0001t0001g0193 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.598+432A>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 9/11 | chr6 | 99549076 | |||||||
chr6:99549081 | GTAC | G | 2 | a0001c0001t0001g0044 a0001c0001t0001g0202 |
3 | HG01099.hp1 HG02922.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.598+424_598+426del others(3): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 9/11 | chr6 | 99549081 | |||||||
chr6:99549172 | G | T | 1 | a0001c0001t0001g0074 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.598+336C>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 9/11 | chr6 | 99549172 | |||||||
chr6:99549288 | CA | C | 91 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(88): Show |
168 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.598+219delT | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 9/11 | chr6 | 99549288 | |||||||
chr6:99549288 | CAA | C | 53 | a0001c0001t0001g0025 a0001c0001t0001g0033 a0001c0001t0001g0034 others(50): Show |
89 | HG00099.hp1 HG00621.hp1 HG00735.hp2 others(86): Show |
intron_variant | MODIFIER | c.598+218_598+219del others(2): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 9/11 | chr6 | 99549288 | |||||||
chr6:99549289 | A | T | 3 | a0001c0001t0002g0031 a0001c0001t0002g0054 a0001c0001t0002g0057 |
4 | HG01069.hp1 HG01257.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.598+219T>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 9/11 | chr6 | 99549289 | |||||||
chr6:99549290 | A | C | 3 | a0001c0001t0002g0031 a0001c0001t0002g0054 a0001c0001t0002g0057 |
4 | HG01069.hp1 HG01257.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.598+218T>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 9/11 | chr6 | 99549290 | |||||||
chr6:99549445 | T | A | 1 | a0001c0001t0001g0078 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.598+63A>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 9/11 | chr6 | 99549445 | |||||||
chr6:99549951 | TCA | T | 68 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(65): Show |
125 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.530+265_530+266del others(2): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 8/11 | chr6 | 99549951 | |||||||
chr6:99549957 | T | A | 1 | a0001c0001t0001g0107 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.530+261A>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 8/11 | chr6 | 99549957 | |||||||
chr6:99549977 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.530+241G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 8/11 | chr6 | 99549977 | |||||||
chr6:99550166 | A | G | 1 | a0001c0001t0001g0173 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.530+52T>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 8/11 | chr6 | 99550166 | |||||||
chr6:99550641 | C | A | 1 | a0001c0001t0001g0107 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.439-332G>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 7/11 | chr6 | 99550641 | |||||||
chr6:99550642 | A | C | 1 | a0001c0001t0001g0107 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.439-333T>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 7/11 | chr6 | 99550642 | |||||||
chr6:99550659 | A | ATAATCTA others(319): Show |
1 | a0001c0001t0001g0069 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.438+333_438+334ins others(326): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 7/11 | chr6 | 99550659 | |||||||
chr6:99550659 | A | ATAATCTA others(321): Show |
1 | a0001c0001t0001g0034 | 2 | HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.438+333_438+334ins others(328): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 7/11 | chr6 | 99550659 | |||||||
chr6:99550659 | A | ATAATCTA others(327): Show |
2 | a0001c0001t0001g0076 a0001c0001t0001g0079 |
2 | HG03225.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.438+333_438+334ins others(334): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 7/11 | chr6 | 99550659 | |||||||
chr6:99550659 | A | ATAATCTA others(328): Show |
1 | a0001c0001t0001g0078 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.438+333_438+334ins others(335): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 7/11 | chr6 | 99550659 | |||||||
chr6:99550659 | A | ATAATCTA others(329): Show |
1 | a0001c0001t0001g0083 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.438+333_438+334ins others(336): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 7/11 | chr6 | 99550659 | |||||||
chr6:99550659 | A | ATAATCTA others(323): Show |
2 | a0001c0001t0001g0033 a0001c0001t0001g0085 |
3 | HG00735.hp2 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.438+333_438+334ins others(330): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 7/11 | chr6 | 99550659 | |||||||
chr6:99550659 | A | ATAATCTA others(324): Show |
3 | a0001c0001t0001g0066 a0001c0001t0001g0081 a0001c0001t0001g0082 |
3 | HG02886.hp2 HG03516.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.438+333_438+334ins others(331): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 7/11 | chr6 | 99550659 | |||||||
chr6:99550659 | A | ATAATCTA others(325): Show |
2 | a0001c0001t0001g0074 a0001c0001t0001g0075 |
2 | HG02258.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.438+333_438+334ins others(332): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 7/11 | chr6 | 99550659 | |||||||
chr6:99550659 | A | ATAATCTA others(326): Show |
3 | a0001c0001t0001g0073 a0001c0001t0001g0084 a0001c0001t0001g0203 |
3 | HG02723.hp2 HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.438+333_438+334ins others(333): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 7/11 | chr6 | 99550659 | |||||||
chr6:99550659 | A | ATAATCTA others(337): Show |
1 | a0001c0001t0001g0071 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.438+333_438+334ins others(344): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 7/11 | chr6 | 99550659 | |||||||
chr6:99550659 | A | ATAATCTA others(339): Show |
1 | a0001c0001t0004g0068 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.438+333_438+334ins others(346): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 7/11 | chr6 | 99550659 | |||||||
chr6:99550659 | A | ATAATCTA others(340): Show |
1 | a0001c0001t0001g0077 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.438+333_438+334ins others(347): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 7/11 | chr6 | 99550659 | |||||||
chr6:99550659 | A | ATAATCTA others(333): Show |
1 | a0001c0001t0001g0080 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.438+333_438+334ins others(340): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 7/11 | chr6 | 99550659 | |||||||
chr6:99550659 | A | ATAATCTA others(345): Show |
1 | a0001c0001t0001g0070 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.438+333_438+334ins others(352): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 7/11 | chr6 | 99550659 | |||||||
chr6:99550685 | C | T | 1 | a0001c0001t0001g0072 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.438+308G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 7/11 | chr6 | 99550685 | |||||||
chr6:99550771 | T | C | 1 | a0001c0001t0001g0034 | 2 | HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.438+222A>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 7/11 | chr6 | 99550771 | |||||||
chr6:99550876 | C | T | 1 | a0001c0001t0001g0161 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.438+117G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 7/11 | chr6 | 99550876 | |||||||
chr6:99550943 | C | T | 1 | a0001c0001t0001g0017 | 4 | HG02895.hp1 HG02897.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.438+50G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 7/11 | chr6 | 99550943 | |||||||
chr6:99550961 | T | G | 2 | a0001c0001t0001g0142 a0001c0001t0001g0146 |
2 | HG02622.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.438+32A>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 7/11 | chr6 | 99550961 | |||||||
chr6:99551143 | A | G | 35 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0009 others(32): Show |
68 | HG00099.hp1 HG00621.hp1 HG01069.hp1 others(65): Show |
intron_variant | MODIFIER | c.403-115T>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 6/11 | chr6 | 99551143 | |||||||
chr6:99551149 | T | G | 1 | a0001c0001t0001g0178 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.403-121A>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 6/11 | chr6 | 99551149 | |||||||
chr6:99551150 | T | A | 4 | a0001c0001t0002g0023 a0001c0001t0002g0032 a0001c0001t0002g0048 others(1): Show |
7 | HG00621.hp1 HG02132.hp2 NA18967.hp2 others(4): Show |
intron_variant | MODIFIER | c.403-122A>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 6/11 | chr6 | 99551150 | |||||||
chr6:99551439 | C | A | 1 | a0001c0001t0001g0121 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.402+401G>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 6/11 | chr6 | 99551439 | |||||||
chr6:99551679 | T | A | 1 | a0001c0001t0001g0156 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.402+161A>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 6/11 | chr6 | 99551679 | |||||||
chr6:99551717 | G | A | 1 | a0001c0001t0001g0034 | 2 | HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.402+123C>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 6/11 | chr6 | 99551717 | |||||||
chr6:99551735 | T | C | 1 | a0001c0001t0001g0160 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.402+105A>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 6/11 | chr6 | 99551735 | |||||||
chr6:99551906 | T | A | 1 | a0001c0001t0001g0107 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.347-11A>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99551906 | |||||||
chr6:99551907 | A | T | 1 | a0001c0001t0001g0107 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.347-12T>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99551907 | |||||||
chr6:99551917 | T | A | 1 | a0001c0001t0001g0107 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.347-22A>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99551917 | |||||||
chr6:99551966 | A | T | 3 | a0001c0001t0001g0207 a0001c0001t0001g0209 a0001c0001t0001g0211 |
3 | HG01070.hp2 HG03710.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.347-71T>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99551966 | |||||||
chr6:99552003 | T | C | 1 | a0001c0001t0001g0209 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.347-108A>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99552003 | |||||||
chr6:99552109 | A | G | 1 | a0001c0001t0001g0089 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.347-214T>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99552109 | |||||||
chr6:99552258 | A | G | 3 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0147 |
11 | HG00280.hp2 HG00323.hp2 HG00733.hp1 others(8): Show |
intron_variant | MODIFIER | c.347-363T>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99552258 | |||||||
chr6:99552609 | A | G | 212 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(209): Show |
386 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(383): Show |
intron_variant | MODIFIER | c.347-714T>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99552609 | |||||||
chr6:99552922 | G | C | 1 | a0001c0001t0001g0178 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.347-1027C>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99552922 | |||||||
chr6:99552966 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.347-1071G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99552966 | |||||||
chr6:99553014 | T | C | 212 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(209): Show |
386 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(383): Show |
intron_variant | MODIFIER | c.347-1119A>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99553014 | |||||||
chr6:99553039 | CA | C | 152 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(149): Show |
291 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(288): Show |
intron_variant | MODIFIER | c.347-1145delT | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99553039 | |||||||
chr6:99553235 | G | A | 1 | a0001c0001t0001g0043 | 2 | NA18940.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.347-1340C>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99553235 | |||||||
chr6:99553377 | C | G | 1 | a0001c0001t0001g0195 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.347-1482G>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99553377 | |||||||
chr6:99553430 | C | G | 1 | a0001c0001t0001g0089 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.347-1535G>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99553430 | |||||||
chr6:99553541 | C | A | 2 | a0001c0001t0001g0129 a0001c0001t0001g0197 |
2 | HG02602.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.347-1646G>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99553541 | |||||||
chr6:99553565 | A | G | 1 | a0001c0001t0002g0050 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.347-1670T>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99553565 | |||||||
chr6:99553662 | A | G | 1 | a0001c0001t0008g0088 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.347-1767T>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99553662 | |||||||
chr6:99554097 | T | A | 83 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(80): Show |
165 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.347-2202A>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99554097 | |||||||
chr6:99554210 | C | T | 2 | a0001c0001t0001g0067 a0001c0001t0001g0072 |
2 | HG04204.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.347-2315G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99554210 | |||||||
chr6:99554211 | G | A | 2 | a0001c0001t0001g0044 a0001c0001t0001g0202 |
3 | HG01099.hp1 HG02922.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.347-2316C>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99554211 | |||||||
chr6:99554510 | A | T | 1 | a0001c0001t0001g0089 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.347-2615T>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99554510 | |||||||
chr6:99554569 | A | C | 1 | a0001c0001t0001g0100 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.347-2674T>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99554569 | |||||||
chr6:99554617 | A | C | 83 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(80): Show |
165 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.347-2722T>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99554617 | |||||||
chr6:99554636 | T | C | 1 | a0001c0001t0001g0173 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.347-2741A>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99554636 | |||||||
chr6:99554742 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.347-2847G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99554742 | |||||||
chr6:99554960 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.347-3065C>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99554960 | |||||||
chr6:99554991 | A | G | 3 | a0001c0001t0001g0017 a0001c0001t0001g0097 a0001c0001t0008g0088 |
6 | HG02486.hp1 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.347-3096T>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99554991 | |||||||
chr6:99555027 | T | C | 212 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(209): Show |
386 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(383): Show |
intron_variant | MODIFIER | c.347-3132A>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99555027 | |||||||
chr6:99555069 | T | C | 1 | a0001c0001t0001g0176 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.347-3174A>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99555069 | |||||||
chr6:99555386 | T | C | 2 | a0001c0001t0001g0076 a0001c0001t0001g0083 |
2 | HG04199.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.346+3111A>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99555386 | |||||||
chr6:99555411 | A | G | 5 | a0001c0001t0001g0026 a0001c0001t0001g0149 a0001c0001t0001g0159 others(2): Show |
7 | HG00639.hp1 HG01346.hp1 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.346+3086T>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99555411 | |||||||
chr6:99555431 | G | C | 212 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(209): Show |
386 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(383): Show |
intron_variant | MODIFIER | c.346+3066C>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99555431 | |||||||
chr6:99555436 | CT | C | 210 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(207): Show |
384 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(381): Show |
intron_variant | MODIFIER | c.346+3060delA | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99555436 | |||||||
chr6:99555450 | T | C | 83 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(80): Show |
165 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.346+3047A>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99555450 | |||||||
chr6:99555463 | A | C | 1 | a0001c0001t0001g0203 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.346+3034T>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99555463 | |||||||
chr6:99555518 | G | A | 212 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(209): Show |
386 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(383): Show |
intron_variant | MODIFIER | c.346+2979C>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99555518 | |||||||
chr6:99555533 | GC | G | 3 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0147 |
11 | HG00280.hp2 HG00323.hp2 HG00733.hp1 others(8): Show |
intron_variant | MODIFIER | c.346+2963delG | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99555533 | |||||||
chr6:99555536 | T | G | 3 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0147 |
11 | HG00280.hp2 HG00323.hp2 HG00733.hp1 others(8): Show |
intron_variant | MODIFIER | c.346+2961A>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99555536 | |||||||
chr6:99555537 | A | T | 3 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0147 |
11 | HG00280.hp2 HG00323.hp2 HG00733.hp1 others(8): Show |
intron_variant | MODIFIER | c.346+2960T>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99555537 | |||||||
chr6:99555570 | C | G | 1 | a0001c0001t0001g0203 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.346+2927G>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99555570 | |||||||
chr6:99555602 | T | G | 1 | a0001c0001t0001g0122 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.346+2895A>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99555602 | |||||||
chr6:99555649 | C | T | 1 | a0001c0001t0002g0062 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.346+2848G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99555649 | |||||||
chr6:99555684 | C | T | 2 | a0001c0001t0001g0017 a0001c0001t0008g0088 |
5 | HG02895.hp1 HG02897.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.346+2813G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99555684 | |||||||
chr6:99555768 | T | A | 1 | a0001c0001t0001g0203 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.346+2729A>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99555768 | |||||||
chr6:99556004 | GTTC | G | 210 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(207): Show |
384 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(381): Show |
intron_variant | MODIFIER | c.346+2490_346+2492d others(5): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99556004 | |||||||
chr6:99556210 | C | T | 210 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(207): Show |
384 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(381): Show |
intron_variant | MODIFIER | c.346+2287G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99556210 | |||||||
chr6:99556296 | T | G | 1 | a0001c0001t0001g0065 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.346+2201A>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99556296 | |||||||
chr6:99556378 | T | C | 1 | a0001c0001t0001g0108 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.346+2119A>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99556378 | |||||||
chr6:99556554 | C | T | 1 | a0001c0001t0001g0158 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.346+1943G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99556554 | |||||||
chr6:99556675 | C | T | 69 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(66): Show |
126 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.346+1822G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99556675 | |||||||
chr6:99556685 | C | G | 1 | a0001c0001t0001g0065 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.346+1812G>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99556685 | |||||||
chr6:99556779 | G | A | 1 | a0001c0001t0002g0057 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.346+1718C>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99556779 | |||||||
chr6:99556812 | C | G | 2 | a0001c0001t0001g0067 a0001c0001t0001g0072 |
2 | HG04204.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.346+1685G>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99556812 | |||||||
chr6:99556812 | C | T | 35 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0009 others(32): Show |
68 | HG00099.hp1 HG00621.hp1 HG01069.hp1 others(65): Show |
intron_variant | MODIFIER | c.346+1685G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99556812 | |||||||
chr6:99556819 | G | A | 83 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(80): Show |
165 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.346+1678C>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99556819 | |||||||
chr6:99556819 | G | T | 2 | a0001c0001t0001g0067 a0001c0001t0001g0072 |
2 | HG04204.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.346+1678C>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99556819 | |||||||
chr6:99556910 | G | C | 1 | a0001c0001t0002g0057 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.346+1587C>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99556910 | |||||||
chr6:99556936 | A | T | 1 | a0001c0001t0001g0157 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.346+1561T>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99556936 | |||||||
chr6:99556956 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.346+1541C>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99556956 | |||||||
chr6:99557009 | A | G | 2 | a0001c0001t0002g0016 a0001c0001t0002g0059 |
5 | HG02080.hp1 NA18943.hp1 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.346+1488T>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99557009 | |||||||
chr6:99557049 | ATCTAAC | A | 35 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0009 others(32): Show |
68 | HG00099.hp1 HG00621.hp1 HG01069.hp1 others(65): Show |
intron_variant | MODIFIER | c.346+1442_346+1447d others(8): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99557049 | |||||||
chr6:99557077 | C | T | 1 | a0001c0001t0002g0049 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.346+1420G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99557077 | |||||||
chr6:99557112 | T | A | 2 | a0001c0001t0001g0124 a0001c0001t0001g0138 |
2 | NA18991.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.346+1385A>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99557112 | |||||||
chr6:99557121 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.346+1376G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99557121 | |||||||
chr6:99557284 | A | C | 1 | a0001c0001t0001g0111 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.346+1213T>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99557284 | |||||||
chr6:99557355 | T | C | 22 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0065 others(19): Show |
24 | HG00735.hp2 HG01109.hp1 HG02145.hp1 others(21): Show |
intron_variant | MODIFIER | c.346+1142A>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99557355 | |||||||
chr6:99557416 | T | C | 1 | a0001c0001t0005g0137 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.346+1081A>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99557416 | |||||||
chr6:99557421 | G | A | 35 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0009 others(32): Show |
68 | HG00099.hp1 HG00621.hp1 HG01069.hp1 others(65): Show |
intron_variant | MODIFIER | c.346+1076C>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99557421 | |||||||
chr6:99557438 | G | A | 31 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0019 others(28): Show |
58 | HG00423.hp1 HG00544.hp1 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.346+1059C>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99557438 | |||||||
chr6:99557503 | G | C | 64 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(61): Show |
128 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.346+994C>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99557503 | |||||||
chr6:99557503 | G | T | 2 | a0001c0001t0001g0110 a0001c0001t0001g0204 |
2 | HG01981.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.346+994C>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99557503 | |||||||
chr6:99557561 | C | T | 1 | a0001c0001t0001g0185 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.346+936G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99557561 | |||||||
chr6:99557776 | G | A | 34 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0009 others(31): Show |
67 | HG00099.hp1 HG00621.hp1 HG01069.hp1 others(64): Show |
intron_variant | MODIFIER | c.346+721C>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99557776 | |||||||
chr6:99557788 | CA | C | 37 | a0001c0001t0001g0065 a0001c0001t0001g0067 a0001c0001t0001g0072 others(34): Show |
69 | HG00099.hp1 HG00544.hp1 HG01069.hp1 others(66): Show |
intron_variant | MODIFIER | c.346+708delT | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99557788 | |||||||
chr6:99557788 | CAA | C | 6 | a0001c0001t0001g0089 a0001c0001t0001g0107 a0001c0001t0001g0108 others(3): Show |
6 | HG02257.hp2 HG02738.hp2 HG04115.hp2 others(3): Show |
intron_variant | MODIFIER | c.346+707_346+708del others(2): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99557788 | |||||||
chr6:99557801 | A | AG | 9 | a0001c0001t0001g0012 a0001c0001t0001g0018 a0001c0001t0001g0025 others(6): Show |
20 | HG00673.hp1 HG02129.hp1 HG02559.hp1 others(17): Show |
intron_variant | MODIFIER | c.346+695_346+696ins others(1): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99557801 | |||||||
chr6:99557803 | A | G | 1 | a0001c0001t0001g0153 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.346+694T>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99557803 | |||||||
chr6:99557805 | A | AAG | 12 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0043 others(9): Show |
27 | HG00140.hp1 HG00609.hp2 HG01123.hp2 others(24): Show |
intron_variant | MODIFIER | c.346+691_346+692ins others(2): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99557805 | |||||||
chr6:99557805 | A | AG | 69 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(66): Show |
141 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.346+691_346+692ins others(1): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99557805 | |||||||
chr6:99557805 | A | G | 10 | a0001c0001t0001g0012 a0001c0001t0001g0018 a0001c0001t0001g0025 others(7): Show |
21 | HG00673.hp1 HG02129.hp1 HG02559.hp1 others(18): Show |
intron_variant | MODIFIER | c.346+692T>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99557805 | |||||||
chr6:99557807 | A | G | 51 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0014 others(48): Show |
92 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.346+690T>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99557807 | |||||||
chr6:99557809 | G | A | 51 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0014 others(48): Show |
92 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.346+688C>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99557809 | |||||||
chr6:99557810 | A | G | 1 | a0001c0001t0001g0106 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.346+687T>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99557810 | |||||||
chr6:99557810 | AAAG | A | 77 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(74): Show |
159 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.346+684_346+686del others(3): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99557810 | |||||||
chr6:99557811 | A | G | 51 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0014 others(48): Show |
92 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.346+686T>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99557811 | |||||||
chr6:99557812 | AG | A | 16 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0042 others(13): Show |
31 | HG00140.hp1 HG00609.hp2 HG01123.hp2 others(28): Show |
intron_variant | MODIFIER | c.346+684delC | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99557812 | |||||||
chr6:99557813 | G | A | 51 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0014 others(48): Show |
92 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.346+684C>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99557813 | |||||||
chr6:99557813 | G | GA | 8 | a0001c0001t0001g0067 a0001c0001t0001g0072 a0001c0001t0001g0089 others(5): Show |
8 | HG02257.hp2 HG02738.hp2 HG04115.hp2 others(5): Show |
intron_variant | MODIFIER | c.346+683dupT | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99557813 | |||||||
chr6:99557868 | T | C | 1 | a0001c0001t0001g0097 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.346+629A>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99557868 | |||||||
chr6:99557899 | G | A | 83 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(80): Show |
165 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.346+598C>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99557899 | |||||||
chr6:99557944 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.346+553G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99557944 | |||||||
chr6:99557978 | A | C | 1 | a0001c0001t0001g0099 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.346+519T>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99557978 | |||||||
chr6:99557986 | C | T | 21 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0066 others(18): Show |
23 | HG00735.hp2 HG01109.hp1 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.346+511G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99557986 | |||||||
chr6:99558052 | C | T | 35 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0009 others(32): Show |
68 | HG00099.hp1 HG00621.hp1 HG01069.hp1 others(65): Show |
intron_variant | MODIFIER | c.346+445G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99558052 | |||||||
chr6:99558094 | G | A | 14 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0042 others(11): Show |
29 | HG00544.hp2 HG00609.hp2 HG01123.hp2 others(26): Show |
intron_variant | MODIFIER | c.346+403C>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99558094 | |||||||
chr6:99558108 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.346+389G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99558108 | |||||||
chr6:99558144 | A | G | 1 | a0001c0001t0001g0105 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.346+353T>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99558144 | |||||||
chr6:99558196 | T | C | 2 | a0001c0001t0002g0016 a0001c0001t0002g0059 |
5 | HG02080.hp1 NA18943.hp1 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.346+301A>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99558196 | |||||||
chr6:99558204 | G | A | 1 | a0001c0001t0002g0060 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.346+293C>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99558204 | |||||||
chr6:99558317 | A | T | 1 | a0001c0001t0001g0104 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.346+180T>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99558317 | |||||||
chr6:99558368 | T | G | 212 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(209): Show |
386 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(383): Show |
intron_variant | MODIFIER | c.346+129A>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 5/11 | chr6 | 99558368 | |||||||
chr6:99558620 | T | C | 1 | a0001c0001t0008g0088 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.295-72A>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 4/11 | chr6 | 99558620 | |||||||
chr6:99558815 | G | A | 2 | a0001c0001t0001g0181 a0001c0001t0001g0189 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.295-267C>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 4/11 | chr6 | 99558815 | |||||||
chr6:99558861 | T | G | 1 | a0001c0001t0001g0190 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.295-313A>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 4/11 | chr6 | 99558861 | |||||||
chr6:99559147 | T | C | 212 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(209): Show |
386 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(383): Show |
intron_variant | MODIFIER | c.295-599A>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 4/11 | chr6 | 99559147 | |||||||
chr6:99559191 | T | TA | 17 | a0001c0001t0001g0028 a0001c0001t0001g0036 a0001c0001t0001g0070 others(14): Show |
20 | HG00323.hp1 HG00423.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.295-644dupT | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 4/11 | chr6 | 99559191 | |||||||
chr6:99559197 | A | C | 1 | a0001c0001t0001g0084 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.295-649T>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 4/11 | chr6 | 99559197 | |||||||
chr6:99559362 | T | C | 9 | a0001c0001t0001g0012 a0001c0001t0001g0018 a0001c0001t0001g0025 others(6): Show |
20 | HG00673.hp1 HG02129.hp1 HG02559.hp1 others(17): Show |
intron_variant | MODIFIER | c.295-814A>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 4/11 | chr6 | 99559362 | |||||||
chr6:99559402 | T | TA | 3 | a0001c0001t0001g0037 a0001c0001t0001g0130 a0001c0001t0001g0131 |
4 | HG01175.hp2 HG01358.hp2 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.295-855dupT | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 4/11 | chr6 | 99559402 | |||||||
chr6:99559525 | T | A | 1 | a0001c0001t0001g0089 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.295-977A>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 4/11 | chr6 | 99559525 | |||||||
chr6:99559652 | TA | T | 91 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(88): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.295-1105delT | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 4/11 | chr6 | 99559652 | |||||||
chr6:99559662 | AT | A | 113 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(110): Show |
187 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(184): Show |
intron_variant | MODIFIER | c.295-1115delA | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 4/11 | chr6 | 99559662 | |||||||
chr6:99559663 | T | A | 7 | a0001c0001t0001g0011 a0001c0001t0001g0036 a0001c0001t0001g0037 others(4): Show |
14 | HG01175.hp2 HG01261.hp2 HG01358.hp2 others(11): Show |
intron_variant | MODIFIER | c.295-1115A>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 4/11 | chr6 | 99559663 | |||||||
chr6:99559720 | C | CT | 6 | a0001c0001t0001g0067 a0001c0001t0001g0072 a0001c0001t0001g0147 others(3): Show |
6 | HG02738.hp1 HG04204.hp1 NA18949.hp1 others(3): Show |
intron_variant | MODIFIER | c.295-1173dupA | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 4/11 | chr6 | 99559720 | |||||||
chr6:99559720 | CT | C | 76 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(73): Show |
152 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.295-1173delA | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 4/11 | chr6 | 99559720 | |||||||
chr6:99559843 | C | G | 3 | a0001c0001t0001g0028 a0001c0001t0001g0175 a0001c0001t0001g0176 |
5 | HG01891.hp2 HG02886.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.295-1295G>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 4/11 | chr6 | 99559843 | |||||||
chr6:99559880 | C | T | 1 | a0001c0001t0002g0063 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.295-1332G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 4/11 | chr6 | 99559880 | |||||||
chr6:99559908 | C | T | 1 | a0001c0001t0001g0098 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.295-1360G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 4/11 | chr6 | 99559908 | |||||||
chr6:99560025 | A | G | 1 | a0001c0001t0001g0097 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.294+1342T>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 4/11 | chr6 | 99560025 | |||||||
chr6:99560121 | A | G | 1 | a0001c0001t0001g0096 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.294+1246T>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 4/11 | chr6 | 99560121 | |||||||
chr6:99560213 | C | T | 212 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(209): Show |
386 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(383): Show |
intron_variant | MODIFIER | c.294+1154G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 4/11 | chr6 | 99560213 | |||||||
chr6:99560259 | T | C | 69 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(66): Show |
126 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.294+1108A>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 4/11 | chr6 | 99560259 | |||||||
chr6:99560368 | T | G | 1 | a0001c0001t0001g0089 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.294+999A>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 4/11 | chr6 | 99560368 | |||||||
chr6:99560395 | G | A | 1 | a0001c0001t0001g0133 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.294+972C>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 4/11 | chr6 | 99560395 | |||||||
chr6:99560411 | C | T | 212 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(209): Show |
386 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(383): Show |
intron_variant | MODIFIER | c.294+956G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 4/11 | chr6 | 99560411 | |||||||
chr6:99560530 | CAACTCTA others(7): Show |
C | 2 | a0001c0001t0001g0067 a0001c0001t0001g0072 |
2 | HG04204.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.294+823_294+836del others(14): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 4/11 | chr6 | 99560530 | |||||||
chr6:99560544 | G | C | 210 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(207): Show |
384 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(381): Show |
intron_variant | MODIFIER | c.294+823C>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 4/11 | chr6 | 99560544 | |||||||
chr6:99560716 | C | T | 21 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0029 others(18): Show |
39 | HG00140.hp1 HG00544.hp2 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.294+651G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 4/11 | chr6 | 99560716 | |||||||
chr6:99560759 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.294+608G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 4/11 | chr6 | 99560759 | |||||||
chr6:99560952 | T | C | 1 | a0001c0001t0001g0085 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.294+415A>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 4/11 | chr6 | 99560952 | |||||||
chr6:99561024 | C | T | 1 | a0001c0001t0001g0094 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.294+343G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 4/11 | chr6 | 99561024 | |||||||
chr6:99561754 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.140-73G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 2/11 | chr6 | 99561754 | |||||||
chr6:99561800 | A | T | 1 | a0001c0001t0001g0089 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.140-119T>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 2/11 | chr6 | 99561800 | |||||||
chr6:99561815 | A | C | 1 | a0001c0001t0002g0219 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.140-134T>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 2/11 | chr6 | 99561815 | |||||||
chr6:99561878 | TAAACAAC others(4): Show |
T | 2 | a0001c0001t0001g0206 a0001c0001t0002g0219 |
2 | HG00280.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.140-208_140-198del others(11): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 2/11 | chr6 | 99561878 | |||||||
chr6:99561974 | C | G | 1 | a0001c0001t0002g0215 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.140-293G>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 2/11 | chr6 | 99561974 | |||||||
chr6:99562041 | T | C | 1 | a0001c0001t0002g0061 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.140-360A>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 2/11 | chr6 | 99562041 | |||||||
chr6:99562290 | G | C | 210 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(207): Show |
384 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(381): Show |
intron_variant | MODIFIER | c.139+552C>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 2/11 | chr6 | 99562290 | |||||||
chr6:99562371 | C | T | 212 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(209): Show |
386 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(383): Show |
intron_variant | MODIFIER | c.139+471G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 2/11 | chr6 | 99562371 | |||||||
chr6:99562379 | C | CA | 20 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0029 others(17): Show |
38 | HG00140.hp1 HG00544.hp2 HG00609.hp2 others(35): Show |
intron_variant | MODIFIER | c.139+462dupT | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 2/11 | chr6 | 99562379 | |||||||
chr6:99562507 | C | T | 2 | a0001c0001t0001g0044 a0001c0001t0001g0202 |
3 | HG01099.hp1 HG02922.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.139+335G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 2/11 | chr6 | 99562507 | |||||||
chr6:99562727 | G | C | 35 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0009 others(32): Show |
68 | HG00099.hp1 HG00621.hp1 HG01069.hp1 others(65): Show |
intron_variant | MODIFIER | c.139+115C>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 2/11 | chr6 | 99562727 | |||||||
chr6:99562756 | A | C | 1 | a0001c0001t0002g0214 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.139+86T>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 2/11 | chr6 | 99562756 | |||||||
chr6:99562777 | AC | A | 68 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(65): Show |
125 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.139+64delG | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 2/11 | chr6 | 99562777 | |||||||
chr6:99563177 | T | C | 1 | a0001c0001t0001g0128 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.33-229A>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99563177 | |||||||
chr6:99563243 | C | T | 60 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(57): Show |
123 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.33-295G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99563243 | |||||||
chr6:99563636 | G | C | 83 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(80): Show |
165 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.33-688C>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99563636 | |||||||
chr6:99563657 | T | C | 1 | a0001c0001t0001g0170 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.33-709A>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99563657 | |||||||
chr6:99563658 | C | A | 1 | a0001c0001t0001g0170 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.33-710G>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99563658 | |||||||
chr6:99563904 | A | T | 1 | a0001c0001t0001g0142 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.33-956T>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99563904 | |||||||
chr6:99564051 | T | C | 1 | a0001c0001t0001g0192 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.33-1103A>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99564051 | |||||||
chr6:99564052 | G | C | 1 | a0001c0001t0002g0062 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.33-1104C>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99564052 | |||||||
chr6:99564147 | G | A | 2 | a0001c0001t0001g0211 a0001c0001t0002g0219 |
2 | HG01070.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.33-1199C>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99564147 | |||||||
chr6:99564153 | G | A | 3 | a0001c0001t0001g0018 a0001c0001t0001g0093 a0001c0001t0001g0140 |
6 | HG02723.hp1 HG02965.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.33-1205C>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99564153 | |||||||
chr6:99564221 | T | G | 35 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0009 others(32): Show |
68 | HG00099.hp1 HG00621.hp1 HG01069.hp1 others(65): Show |
intron_variant | MODIFIER | c.33-1273A>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99564221 | |||||||
chr6:99564237 | C | T | 9 | a0001c0001t0002g0005 a0001c0001t0002g0021 a0001c0001t0002g0214 others(6): Show |
23 | HG00099.hp1 HG01070.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.33-1289G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99564237 | |||||||
chr6:99564273 | A | C | 1 | a0001c0001t0001g0090 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.33-1325T>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99564273 | |||||||
chr6:99564422 | C | CA | 25 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0024 others(22): Show |
45 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(42): Show |
intron_variant | MODIFIER | c.33-1475dupT | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99564422 | |||||||
chr6:99564422 | CA | C | 86 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0019 others(83): Show |
142 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.33-1475delT | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99564422 | |||||||
chr6:99564422 | CAA | C | 12 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0073 others(9): Show |
29 | HG00280.hp2 HG00323.hp2 HG00733.hp1 others(26): Show |
intron_variant | MODIFIER | c.33-1476_33-1475del others(2): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99564422 | |||||||
chr6:99564450 | A | G | 2 | a0001c0001t0001g0067 a0001c0001t0001g0072 |
2 | HG04204.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.33-1502T>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99564450 | |||||||
chr6:99564517 | C | G | 1 | a0001c0001t0001g0090 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.33-1569G>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99564517 | |||||||
chr6:99564647 | G | C | 1 | a0001c0001t0001g0089 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.33-1699C>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99564647 | |||||||
chr6:99564723 | CAA | C | 3 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0147 |
11 | HG00280.hp2 HG00323.hp2 HG00733.hp1 others(8): Show |
intron_variant | MODIFIER | c.33-1777_33-1776del others(2): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99564723 | |||||||
chr6:99564809 | G | C | 1 | a0001c0001t0001g0141 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.33-1861C>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99564809 | |||||||
chr6:99565065 | G | A | 1 | a0001c0001t0001g0212 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.33-2117C>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99565065 | |||||||
chr6:99565079 | T | C | 210 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(207): Show |
384 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(381): Show |
intron_variant | MODIFIER | c.33-2131A>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99565079 | |||||||
chr6:99565316 | G | T | 1 | a0001c0001t0001g0065 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.33-2368C>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99565316 | |||||||
chr6:99565348 | A | G | 4 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0071 others(1): Show |
4 | HG02145.hp1 HG02717.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-2400T>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99565348 | |||||||
chr6:99565386 | G | C | 1 | a0001c0001t0001g0089 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.33-2438C>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99565386 | |||||||
chr6:99565388 | T | C | 1 | a0001c0001t0001g0089 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.33-2440A>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99565388 | |||||||
chr6:99565389 | A | T | 1 | a0001c0001t0001g0089 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.33-2441T>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99565389 | |||||||
chr6:99565390 | A | C | 1 | a0001c0001t0001g0089 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.33-2442T>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99565390 | |||||||
chr6:99565500 | T | A | 83 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(80): Show |
165 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.33-2552A>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99565500 | |||||||
chr6:99565529 | G | C | 1 | a0001c0001t0001g0065 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.33-2581C>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99565529 | |||||||
chr6:99565590 | A | G | 1 | a0001c0001t0001g0067 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.33-2642T>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99565590 | |||||||
chr6:99565817 | A | G | 68 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(65): Show |
125 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.32+2679T>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99565817 | |||||||
chr6:99566110 | T | C | 2 | a0001c0001t0001g0019 a0001c0001t0001g0174 |
5 | NA18941.hp2 NA18964.hp2 NA19001.hp2 others(2): Show |
intron_variant | MODIFIER | c.32+2386A>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99566110 | |||||||
chr6:99566130 | C | T | 1 | a0001c0001t0001g0066 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.32+2366G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99566130 | |||||||
chr6:99566268 | GTCTT | G | 153 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(150): Show |
292 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(289): Show |
intron_variant | MODIFIER | c.32+2224_32+2227del others(4): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99566268 | |||||||
chr6:99566277 | T | C | 1 | a0001c0001t0001g0025 | 3 | HG02559.hp1 HG02622.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.32+2219A>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99566277 | |||||||
chr6:99566444 | T | G | 35 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0009 others(32): Show |
68 | HG00099.hp1 HG00621.hp1 HG01069.hp1 others(65): Show |
intron_variant | MODIFIER | c.32+2052A>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99566444 | |||||||
chr6:99566586 | C | T | 35 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0009 others(32): Show |
68 | HG00099.hp1 HG00621.hp1 HG01069.hp1 others(65): Show |
intron_variant | MODIFIER | c.32+1910G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99566586 | |||||||
chr6:99566956 | C | T | 6 | a0001c0001t0001g0039 a0001c0001t0001g0142 a0001c0001t0001g0143 others(3): Show |
7 | HG01243.hp1 HG01884.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.32+1540G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99566956 | |||||||
chr6:99567022 | G | C | 1 | a0001c0001t0002g0063 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.32+1474C>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99567022 | |||||||
chr6:99567042 | T | C | 69 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(66): Show |
126 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.32+1454A>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99567042 | |||||||
chr6:99567194 | TA | T | 35 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0009 others(32): Show |
67 | HG00099.hp1 HG00621.hp1 HG01069.hp1 others(64): Show |
intron_variant | MODIFIER | c.32+1301delT | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99567194 | |||||||
chr6:99567244 | GCTT | G | 24 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0028 others(21): Show |
44 | HG00140.hp1 HG00544.hp2 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.32+1249_32+1251del others(3): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99567244 | |||||||
chr6:99567388 | CACACACA others(13): Show |
C | 2 | a0001c0001t0001g0017 a0001c0001t0008g0088 |
5 | HG02895.hp1 HG02897.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.32+1088_32+1107del others(20): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99567388 | |||||||
chr6:99567408 | T | TAC | 2 | a0001c0001t0001g0044 a0001c0001t0001g0202 |
3 | HG01099.hp1 HG02922.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.32+1086_32+1087dup others(2): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99567408 | |||||||
chr6:99567420 | C | T | 4 | a0001c0001t0001g0017 a0001c0001t0001g0086 a0001c0001t0001g0087 others(1): Show |
7 | HG02895.hp1 HG02897.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.32+1076G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99567420 | |||||||
chr6:99567428 | T | C | 8 | a0001c0001t0001g0017 a0001c0001t0001g0044 a0001c0001t0001g0086 others(5): Show |
12 | HG01099.hp1 HG02630.hp2 HG02895.hp1 others(9): Show |
intron_variant | MODIFIER | c.32+1068A>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99567428 | |||||||
chr6:99567428 | T | TAC | 142 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(139): Show |
277 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(274): Show |
intron_variant | MODIFIER | c.32+1066_32+1067dup others(2): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99567428 | |||||||
chr6:99567428 | T | TACAC | 3 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 |
3 | HG02602.hp1 NA18959.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.32+1064_32+1067dup others(4): Show |
CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99567428 | |||||||
chr6:99567540 | T | A | 6 | a0001c0001t0001g0044 a0001c0001t0001g0198 a0001c0001t0001g0199 others(3): Show |
7 | HG01099.hp1 HG02109.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.32+956A>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99567540 | |||||||
chr6:99567631 | G | T | 1 | a0001c0001t0001g0065 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.32+865C>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99567631 | |||||||
chr6:99567681 | A | G | 1 | a0001c0001t0001g0065 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.32+815T>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99567681 | |||||||
chr6:99567691 | T | G | 1 | a0001c0001t0001g0203 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.32+805A>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99567691 | |||||||
chr6:99567721 | A | G | 1 | a0001c0001t0001g0064 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.32+775T>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99567721 | |||||||
chr6:99568076 | G | C | 1 | a0001c0001t0001g0204 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.32+420C>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99568076 | |||||||
chr6:99568239 | C | T | 35 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0009 others(32): Show |
68 | HG00099.hp1 HG00621.hp1 HG01069.hp1 others(65): Show |
intron_variant | MODIFIER | c.32+257G>A | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99568239 | |||||||
chr6:99568319 | G | A | 1 | a0001c0001t0001g0213 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.32+177C>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99568319 | |||||||
chr6:99568364 | A | G | 212 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(209): Show |
386 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(383): Show |
intron_variant | MODIFIER | c.32+132T>C | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99568364 | |||||||
chr6:99568464 | G | C | 11 | a0001c0001t0002g0005 a0001c0001t0002g0021 a0001c0001t0002g0214 others(8): Show |
25 | HG00099.hp1 HG01070.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.32+32C>G | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99568464 | |||||||
chr6:99568486 | G | A | 2 | a0001c0001t0001g0045 a0001c0001t0001g0223 |
3 | NA19011.hp2 NA19081.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.32+10C>T | CCNC | ENSG00000112237.13 | transcript | ENST00000520429.6 | protein_coding | 1/11 | chr6 | 99568486 |