Item | Value |
---|---|
geneid | 905 |
ensemblid | ENSG00000082258.13 |
hgncid | 1600 |
symbol | CCNT2 |
name | cyclin T2 |
refseq_nuc | NM_058241.3 |
refseq_prot | NP_490595.1 |
ensembl_nuc | ENST00000264157.10 |
ensembl_prot | ENSP00000264157.5 |
mane_status | MANE Select |
chr | chr2 |
start | 134918822 |
end | 134959342 |
strand | + |
ver | v1.2 |
region | chr2:134918822-134959342 |
region5000 | chr2:134913822-134964342 |
regionname0 | CCNT2_chr2_134918822_134959342 |
regionname5000 | CCNT2_chr2_134913822_134964342 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 730 | 398 | 83 | 71 | 191 | 10 | 41 | 152 | CCNT2_chr2_134913822_134964342 | CCNT2 | MASGR others(725): Show |
chr2 | 134913822 | 134964342 |
a0002 | 0/0 | 730 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | CCNT2_chr2_134913822_134964342 | CCNT2 | MASGR others(725): Show |
chr2 | 134913822 | 134964342 |
a0003 | 0/0 | 730 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | MASGR others(725): Show |
chr2 | 134913822 | 134964342 |
a0004 | 0/0 | 730 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | MASGR others(725): Show |
chr2 | 134913822 | 134964342 |
a0005 | 0/0 | 730 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | MASGR others(725): Show |
chr2 | 134913822 | 134964342 |
a0006 | 0/0 | 730 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | MASGR others(725): Show |
chr2 | 134913822 | 134964342 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 2190 | 295 | 45 | 48 | 163 | 4 | 34 | CCNT2_chr2_134913822_134964342 | CCNT2 | ATGGC others(2185): Show |
chr2 | 134913822 | 134964342 | ||
a0001c0002 | 1/0 | 2190 | 83 | 18 | 23 | 28 | 6 | 7 | CCNT2_chr2_134913822_134964342 | CCNT2 | ATGGC others(2185): Show |
chr2 | 134913822 | 134964342 | ||
a0001c0003 | 0/0 | 2190 | 14 | 14 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | ATGGC others(2185): Show |
chr2 | 134913822 | 134964342 | ||
a0001c0004 | 0/0 | 2190 | 6 | 6 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | ATGGC others(2185): Show |
chr2 | 134913822 | 134964342 | ||
a0002c0005 | 0/0 | 2190 | 2 | 0 | 0 | 2 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | ATGGC others(2185): Show |
chr2 | 134913822 | 134964342 | ||
a0003c0007 | 0/0 | 2190 | 1 | 0 | 1 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | ATGGC others(2185): Show |
chr2 | 134913822 | 134964342 | ||
a0004c0006 | 0/0 | 2190 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | ATGGC others(2185): Show |
chr2 | 134913822 | 134964342 | ||
a0005c0008 | 0/0 | 2190 | 1 | 0 | 0 | 0 | 0 | 1 | CCNT2_chr2_134913822_134964342 | CCNT2 | ATGGC others(2185): Show |
chr2 | 134913822 | 134964342 | ||
a0006c0009 | 0/0 | 2190 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | ATGGC others(2185): Show |
chr2 | 134913822 | 134964342 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 6915 | 111 | 18 | 22 | 58 | 0 | 13 | CCNT2_chr2_134913822_134964342 | CCNT2 | GTGAA others(6910): Show |
chr2 | 134913822 | 134964342 |
a0001c0001t0003 | 0/0 | 6915 | 55 | 3 | 4 | 48 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | GTGAA others(6910): Show |
chr2 | 134913822 | 134964342 |
a0001c0001t0004 | 0/1 | 6911 | 53 | 7 | 15 | 20 | 1 | 9 | CCNT2_chr2_134913822_134964342 | CCNT2 | GTGAA others(6906): Show |
chr2 | 134913822 | 134964342 |
a0001c0001t0005 | 0/0 | 6915 | 36 | 3 | 0 | 24 | 0 | 9 | CCNT2_chr2_134913822_134964342 | CCNT2 | GTGAA others(6910): Show |
chr2 | 134913822 | 134964342 |
a0001c0001t0006 | 0/0 | 6915 | 13 | 0 | 3 | 10 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | GTGAA others(6910): Show |
chr2 | 134913822 | 134964342 |
a0001c0001t0007 | 0/0 | 6915 | 6 | 6 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | GTGAA others(6910): Show |
chr2 | 134913822 | 134964342 |
a0001c0001t0008 | 0/0 | 6915 | 5 | 0 | 2 | 0 | 2 | 1 | CCNT2_chr2_134913822_134964342 | CCNT2 | GTGAA others(6910): Show |
chr2 | 134913822 | 134964342 |
a0001c0001t0010 | 0/0 | 6915 | 3 | 3 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | GTGAA others(6910): Show |
chr2 | 134913822 | 134964342 |
a0001c0001t0011 | 0/0 | 6911 | 3 | 3 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | GTGAA others(6906): Show |
chr2 | 134913822 | 134964342 |
a0001c0001t0014 | 0/0 | 6911 | 1 | 0 | 0 | 0 | 0 | 1 | CCNT2_chr2_134913822_134964342 | CCNT2 | GTGAA others(6906): Show |
chr2 | 134913822 | 134964342 |
a0001c0001t0015 | 0/0 | 6915 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | GTGAA others(6910): Show |
chr2 | 134913822 | 134964342 |
a0001c0001t0016 | 0/0 | 6915 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | GTGAA others(6910): Show |
chr2 | 134913822 | 134964342 |
a0001c0001t0017 | 0/0 | 6915 | 1 | 0 | 1 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | GTGAA others(6910): Show |
chr2 | 134913822 | 134964342 |
a0001c0001t0018 | 0/0 | 6915 | 1 | 0 | 1 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | GTGAA others(6910): Show |
chr2 | 134913822 | 134964342 |
a0001c0001t0019 | 0/0 | 6915 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | GTGAA others(6910): Show |
chr2 | 134913822 | 134964342 |
a0001c0001t0020 | 0/0 | 6915 | 1 | 0 | 0 | 0 | 1 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | GTGAA others(6910): Show |
chr2 | 134913822 | 134964342 |
a0001c0001t0021 | 0/0 | 6915 | 1 | 0 | 0 | 0 | 0 | 1 | CCNT2_chr2_134913822_134964342 | CCNT2 | GTGAA others(6910): Show |
chr2 | 134913822 | 134964342 |
a0001c0001t0024 | 0/0 | 6915 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | GTGAA others(6910): Show |
chr2 | 134913822 | 134964342 |
a0001c0001t0025 | 0/0 | 6911 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | GTGAA others(6906): Show |
chr2 | 134913822 | 134964342 |
a0001c0002t0002 | 1/0 | 6920 | 78 | 14 | 23 | 27 | 6 | 7 | CCNT2_chr2_134913822_134964342 | CCNT2 | GTGAA others(6915): Show |
chr2 | 134913822 | 134964342 |
a0001c0002t0009 | 0/0 | 6920 | 3 | 3 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | GTGAA others(6915): Show |
chr2 | 134913822 | 134964342 |
a0001c0002t0013 | 0/0 | 6920 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | GTGAA others(6915): Show |
chr2 | 134913822 | 134964342 |
a0001c0002t0027 | 0/0 | 6920 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | GTGAA others(6915): Show |
chr2 | 134913822 | 134964342 |
a0001c0003t0002 | 0/0 | 6920 | 9 | 9 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | GTGAA others(6915): Show |
chr2 | 134913822 | 134964342 |
a0001c0003t0012 | 0/0 | 6920 | 2 | 2 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | GTGAA others(6915): Show |
chr2 | 134913822 | 134964342 |
a0001c0003t0022 | 0/0 | 6920 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | GTGAA others(6915): Show |
chr2 | 134913822 | 134964342 |
a0001c0003t0023 | 0/0 | 6920 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | GTGAA others(6915): Show |
chr2 | 134913822 | 134964342 |
a0001c0003t0026 | 0/0 | 6920 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | GTGAA others(6915): Show |
chr2 | 134913822 | 134964342 |
a0001c0004t0005 | 0/0 | 6915 | 6 | 6 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | GTGAA others(6910): Show |
chr2 | 134913822 | 134964342 |
a0002c0005t0005 | 0/0 | 6915 | 2 | 0 | 0 | 2 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | GTGAA others(6910): Show |
chr2 | 134913822 | 134964342 |
a0003c0007t0002 | 0/0 | 6920 | 1 | 0 | 1 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | GTGAA others(6915): Show |
chr2 | 134913822 | 134964342 |
a0004c0006t0002 | 0/0 | 6920 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | GTGAA others(6915): Show |
chr2 | 134913822 | 134964342 |
a0005c0008t0002 | 0/0 | 6920 | 1 | 0 | 0 | 0 | 0 | 1 | CCNT2_chr2_134913822_134964342 | CCNT2 | GTGAA others(6915): Show |
chr2 | 134913822 | 134964342 |
a0006c0009t0004 | 0/0 | 6911 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | GTGAA others(6906): Show |
chr2 | 134913822 | 134964342 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0007 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0008 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0015 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0003g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0003g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0003g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0003g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0003g0027 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0003g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0003g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0003g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0003g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0003g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0003g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0003g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0003g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0004g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0004g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0004g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0004g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0004g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0004g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0004g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0004g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0004g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0004g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0004g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0004g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0004g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0004g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0004g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0004g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0004g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0004g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0004g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0004g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0004g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0004g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0004g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0004g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0004g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0004g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0004g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0004g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0004g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0004g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0004g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0004g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0004g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0004g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0004g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0004g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0004g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0004g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0004g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0004g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0004g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0004g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0004g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0004g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0004g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0004g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0004g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0004g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0004g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0004g0276 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0004g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0005g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0005g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0005g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0005g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0005g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0005g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0005g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0005g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0005g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0005g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0005g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0005g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0005g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0005g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0005g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0005g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0005g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0005g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0005g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0005g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0005g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0005g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0005g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0005g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0005g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0005g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0005g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0005g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0005g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0005g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0005g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0005g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0005g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0005g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0005g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0005g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0006g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0006g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0006g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0006g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0006g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0006g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0006g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0006g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0006g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0006g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0006g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0006g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0006g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0007g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0007g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0007g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0007g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0007g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0007g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0008g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0008g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0008g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0008g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0008g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0010g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0010g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0010g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0011g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0011g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0011g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0014g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0015g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0016g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0017g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0018g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0019g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0020g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0021g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0024g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0001t0025g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0002t0002g0001 | 1/0 | 10 | 0 | 4 | 0 | 5 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0002t0002g0002 | 0/0 | 7 | 0 | 4 | 1 | 1 | 1 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0002t0002g0004 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0002t0002g0005 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0002t0002g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0002t0002g0009 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0002t0002g0010 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0002t0002g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0002t0002g0017 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0002t0002g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0002t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0002t0002g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0002t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0002t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0002t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0002t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0002t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0002t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0002t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0002t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0002t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0002t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0002t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0002t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0002t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0002t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0002t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0002t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0002t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0002t0002g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0002t0009g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0002t0009g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0002t0009g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0002t0013g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0002t0027g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0003t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0003t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0003t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0003t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0003t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0003t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0003t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0003t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0003t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0003t0012g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0003t0012g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0003t0022g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0003t0023g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0003t0026g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0004t0005g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0004t0005g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0004t0005g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0004t0005g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0004t0005g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0001c0004t0005g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0002c0005t0005g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0002c0005t0005g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0003c0007t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0004c0006t0002g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0005c0008t0002g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
a0006c0009t0004g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0002 | t0002 | g0001 | EUR | GBR | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG00140 | hp2 | a0001 | c0001 | t0004 | g0263 | EUR | GBR | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG00280 | hp1 | a0001 | c0002 | t0002 | g0001 | EUR | FIN | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG00280 | hp2 | a0001 | c0002 | t0002 | g0002 | EUR | FIN | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG00408 | hp1 | a0001 | c0001 | t0003 | g0027 | EAS | CHS | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG00408 | hp2 | a0001 | c0001 | t0006 | g0327 | EAS | CHS | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG00438 | hp1 | a0001 | c0002 | t0002 | g0006 | EAS | CHS | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG00438 | hp2 | a0001 | c0001 | t0003 | g0202 | EAS | CHS | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | CHS | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG00544 | hp2 | a0001 | c0001 | t0006 | g0289 | EAS | CHS | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG00558 | hp1 | a0001 | c0002 | t0002 | g0023 | EAS | CHS | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | CHS | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG00597 | hp1 | a0001 | c0001 | t0003 | g0220 | EAS | CHS | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | CHS | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG00609 | hp2 | a0001 | c0001 | t0006 | g0322 | EAS | CHS | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | CHS | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG00639 | hp2 | a0001 | c0001 | t0004 | g0253 | AMR | PUR | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG00642 | hp2 | a0001 | c0001 | t0004 | g0261 | AMR | PUR | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | CHS | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG00735 | hp1 | a0001 | c0001 | t0004 | g0268 | AMR | PUR | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG00738 | hp2 | a0001 | c0002 | t0002 | g0009 | AMR | PUR | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG00741 | hp1 | a0001 | c0001 | t0003 | g0186 | AMR | PUR | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG01069 | hp2 | a0001 | c0002 | t0002 | g0009 | AMR | PUR | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG01070 | hp1 | a0001 | c0002 | t0002 | g0046 | AMR | PUR | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG01070 | hp2 | a0001 | c0001 | t0004 | g0251 | AMR | PUR | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG01071 | hp1 | a0001 | c0002 | t0002 | g0067 | AMR | PUR | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG01074 | hp2 | a0001 | c0001 | t0004 | g0274 | AMR | PUR | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG01081 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | PUR | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG01081 | hp2 | a0001 | c0001 | t0004 | g0270 | AMR | PUR | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG01099 | hp1 | a0001 | c0002 | t0002 | g0009 | AMR | PUR | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG01099 | hp2 | a0001 | c0001 | t0008 | g0077 | AMR | PUR | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG01106 | hp1 | a0001 | c0002 | t0002 | g0053 | AMR | PUR | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG01106 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | PUR | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG01168 | hp1 | a0001 | c0001 | t0004 | g0235 | AMR | PUR | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG01169 | hp2 | a0001 | c0002 | t0002 | g0063 | AMR | PUR | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG01175 | hp2 | a0001 | c0002 | t0002 | g0058 | AMR | PUR | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG01192 | hp1 | a0001 | c0001 | t0004 | g0254 | AMR | PUR | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG01192 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PUR | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG01243 | hp1 | a0001 | c0001 | t0004 | g0252 | AMR | PUR | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG01243 | hp2 | a0001 | c0001 | t0018 | g0180 | AMR | PUR | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG01255 | hp1 | a0001 | c0001 | t0004 | g0255 | AMR | CLM | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG01255 | hp2 | a0001 | c0001 | t0003 | g0204 | AMR | CLM | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | CLM | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG01256 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | CLM | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG01257 | hp1 | a0001 | c0001 | t0004 | g0246 | AMR | CLM | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG01257 | hp2 | a0001 | c0002 | t0002 | g0010 | AMR | CLM | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG01261 | hp1 | a0001 | c0002 | t0002 | g0010 | AMR | CLM | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG01261 | hp2 | a0001 | c0001 | t0004 | g0258 | AMR | CLM | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG01346 | hp2 | a0001 | c0001 | t0003 | g0200 | AMR | CLM | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG01358 | hp1 | a0001 | c0001 | t0004 | g0239 | AMR | CLM | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG01358 | hp2 | a0001 | c0001 | t0017 | g0334 | AMR | CLM | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG01361 | hp1 | a0001 | c0001 | t0008 | g0099 | AMR | CLM | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | CLM | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | CLM | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG01515 | hp1 | a0001 | c0001 | t0020 | g0161 | EUR | IBS | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG01515 | hp2 | a0001 | c0002 | t0002 | g0001 | EUR | IBS | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG01516 | hp1 | a0001 | c0002 | t0002 | g0001 | EUR | IBS | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG01516 | hp2 | a0001 | c0001 | t0008 | g0079 | EUR | IBS | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG01517 | hp1 | a0001 | c0002 | t0002 | g0001 | EUR | IBS | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG01517 | hp2 | a0001 | c0001 | t0008 | g0078 | EUR | IBS | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PEL | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG01943 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PEL | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG01952 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | PEL | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG01952 | hp2 | a0001 | c0001 | t0006 | g0293 | AMR | PEL | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG01975 | hp1 | a0001 | c0002 | t0002 | g0005 | AMR | PEL | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG01975 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | PEL | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG01978 | hp1 | a0001 | c0001 | t0006 | g0294 | AMR | PEL | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PEL | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG01981 | hp1 | a0001 | c0002 | t0002 | g0010 | AMR | PEL | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PEL | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG01993 | hp1 | a0001 | c0001 | t0004 | g0237 | AMR | PEL | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG01993 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PEL | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | KHV | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG02015 | hp2 | a0001 | c0002 | t0002 | g0060 | EAS | KHV | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG02027 | hp2 | a0001 | c0001 | t0005 | g0219 | EAS | KHV | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG02040 | hp1 | a0001 | c0002 | t0002 | g0023 | EAS | KHV | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG02040 | hp2 | a0001 | c0001 | t0003 | g0187 | EAS | KHV | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG02071 | hp1 | a0001 | c0001 | t0003 | g0183 | EAS | KHV | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG02071 | hp2 | a0001 | c0001 | t0005 | g0315 | EAS | KHV | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG02074 | hp1 | a0001 | c0001 | t0003 | g0013 | EAS | KHV | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG02080 | hp1 | a0001 | c0001 | t0005 | g0299 | EAS | KHV | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | KHV | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG02083 | hp2 | a0001 | c0001 | t0003 | g0190 | EAS | KHV | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG02132 | hp1 | a0004 | c0006 | t0002 | g0005 | EAS | KHV | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG02132 | hp2 | a0001 | c0002 | t0002 | g0127 | EAS | KHV | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG02145 | hp1 | a0001 | c0001 | t0003 | g0201 | AFR | ACB | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0336 | AFR | ACB | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG02148 | hp1 | a0001 | c0002 | t0002 | g0018 | AMR | PEL | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG02148 | hp2 | a0001 | c0001 | t0003 | g0027 | AMR | PEL | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG02155 | hp1 | a0001 | c0001 | t0005 | g0307 | EAS | CDX | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG02155 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | CDX | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG02165 | hp1 | a0001 | c0001 | t0006 | g0290 | EAS | CDX | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | CDX | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG02257 | hp1 | a0001 | c0001 | t0007 | g0282 | AFR | ACB | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG02257 | hp2 | a0001 | c0002 | t0002 | g0011 | AFR | ACB | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG02258 | hp1 | a0001 | c0001 | t0004 | g0272 | AFR | ACB | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | ACB | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG02280 | hp1 | a0001 | c0004 | t0005 | g0177 | AFR | ACB | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG02293 | hp1 | a0001 | c0002 | t0002 | g0004 | AMR | PEL | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG02300 | hp1 | a0001 | c0002 | t0002 | g0018 | AMR | PEL | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG02300 | hp2 | a0001 | c0001 | t0006 | g0288 | AMR | PEL | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG02451 | hp1 | a0001 | c0001 | t0025 | g0247 | AFR | ACB | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG02451 | hp2 | a0001 | c0002 | t0002 | g0052 | AFR | ACB | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG02523 | hp2 | a0001 | c0001 | t0003 | g0192 | EAS | KHV | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG02572 | hp1 | a0001 | c0001 | t0007 | g0285 | AFR | GWD | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG02572 | hp2 | a0001 | c0001 | t0004 | g0275 | AFR | GWD | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG02602 | hp2 | a0001 | c0001 | t0005 | g0328 | SAS | PJL | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG02615 | hp1 | a0001 | c0003 | t0002 | g0117 | AFR | GWD | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG02615 | hp2 | a0001 | c0001 | t0010 | g0162 | AFR | GWD | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG02630 | hp1 | a0001 | c0002 | t0009 | g0043 | AFR | GWD | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0335 | AFR | GWD | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG02647 | hp1 | a0001 | c0002 | t0002 | g0062 | AFR | GWD | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG02647 | hp2 | a0001 | c0001 | t0007 | g0286 | AFR | GWD | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG02683 | hp1 | a0001 | c0002 | t0002 | g0017 | SAS | PJL | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG02683 | hp2 | a0001 | c0001 | t0005 | g0325 | SAS | PJL | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG02698 | hp1 | a0001 | c0001 | t0004 | g0240 | SAS | PJL | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG02698 | hp2 | a0001 | c0001 | t0005 | g0295 | SAS | PJL | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG02717 | hp2 | a0001 | c0003 | t0002 | g0119 | AFR | GWD | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG02735 | hp2 | a0001 | c0001 | t0005 | g0310 | SAS | PJL | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG02738 | hp1 | a0005 | c0008 | t0002 | g0004 | SAS | PJL | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG02738 | hp2 | a0001 | c0002 | t0002 | g0125 | SAS | PJL | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG02809 | hp1 | a0001 | c0001 | t0005 | g0181 | AFR | GWD | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG02809 | hp2 | a0001 | c0001 | t0016 | g0215 | AFR | GWD | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG02818 | hp2 | a0001 | c0002 | t0002 | g0011 | AFR | GWD | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG02886 | hp1 | a0001 | c0003 | t0002 | g0039 | AFR | GWD | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0332 | AFR | GWD | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG02895 | hp2 | a0001 | c0002 | t0009 | g0123 | AFR | GWD | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG02896 | hp1 | a0001 | c0002 | t0009 | g0040 | AFR | GWD | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG02896 | hp2 | a0001 | c0003 | t0002 | g0045 | AFR | GWD | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG02897 | hp2 | a0001 | c0003 | t0002 | g0066 | AFR | GWD | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG02922 | hp1 | a0001 | c0002 | t0002 | g0020 | AFR | ESN | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG02922 | hp2 | a0001 | c0001 | t0011 | g0250 | AFR | ESN | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG02965 | hp1 | a0001 | c0004 | t0005 | g0174 | AFR | ESN | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG02965 | hp2 | a0001 | c0004 | t0005 | g0175 | AFR | ESN | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG02970 | hp1 | a0001 | c0001 | t0005 | g0324 | AFR | ESN | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0333 | AFR | ESN | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG03017 | hp2 | a0001 | c0002 | t0002 | g0017 | SAS | PJL | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG03041 | hp1 | a0001 | c0001 | t0004 | g0265 | AFR | GWD | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG03041 | hp2 | a0001 | c0002 | t0002 | g0173 | AFR | GWD | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG03098 | hp1 | a0001 | c0002 | t0002 | g0050 | AFR | MSL | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | MSL | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG03130 | hp1 | a0001 | c0002 | t0013 | g0136 | AFR | ESN | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG03139 | hp1 | a0001 | c0003 | t0002 | g0034 | AFR | ESN | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG03139 | hp2 | a0001 | c0001 | t0010 | g0148 | AFR | ESN | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG03195 | hp1 | a0001 | c0002 | t0002 | g0011 | AFR | ESN | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG03195 | hp2 | a0001 | c0001 | t0005 | g0329 | AFR | ESN | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG03225 | hp1 | a0001 | c0002 | t0002 | g0020 | AFR | MSL | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG03225 | hp2 | a0001 | c0001 | t0003 | g0216 | AFR | MSL | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG03453 | hp1 | a0001 | c0003 | t0002 | g0118 | AFR | MSL | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG03453 | hp2 | a0001 | c0002 | t0002 | g0061 | AFR | MSL | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG03486 | hp2 | a0001 | c0001 | t0003 | g0191 | AFR | MSL | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG03491 | hp1 | a0001 | c0001 | t0005 | g0319 | SAS | PJL | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG03491 | hp2 | a0001 | c0002 | t0002 | g0041 | SAS | PJL | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG03492 | hp1 | a0001 | c0001 | t0004 | g0243 | SAS | PJL | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG03492 | hp2 | a0001 | c0001 | t0005 | g0320 | SAS | PJL | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG03516 | hp1 | a0001 | c0001 | t0010 | g0163 | AFR | ESN | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG03516 | hp2 | a0001 | c0001 | t0007 | g0284 | AFR | ESN | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG03540 | hp1 | a0001 | c0001 | t0004 | g0260 | AFR | GWD | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG03540 | hp2 | a0001 | c0002 | t0002 | g0128 | AFR | GWD | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | MSL | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG03579 | hp2 | a0001 | c0001 | t0004 | g0269 | AFR | MSL | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG03654 | hp1 | a0001 | c0001 | t0004 | g0256 | SAS | PJL | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG03654 | hp2 | a0001 | c0001 | t0005 | g0305 | SAS | PJL | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG03669 | hp2 | a0001 | c0001 | t0004 | g0267 | SAS | PJL | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG03688 | hp1 | a0001 | c0001 | t0005 | g0296 | SAS | STU | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | STU | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG03704 | hp1 | a0001 | c0001 | t0005 | g0281 | SAS | PJL | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG03704 | hp2 | a0001 | c0001 | t0008 | g0100 | SAS | PJL | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG03710 | hp2 | a0001 | c0001 | t0021 | g0033 | SAS | PJL | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | BEB | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG03831 | hp2 | a0001 | c0001 | t0004 | g0273 | SAS | BEB | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG03834 | hp1 | a0001 | c0002 | t0002 | g0337 | SAS | BEB | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0102 | SAS | BEB | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG03927 | hp1 | a0001 | c0002 | t0002 | g0002 | SAS | BEB | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG03927 | hp2 | a0001 | c0001 | t0014 | g0262 | SAS | BEB | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG03942 | hp1 | a0001 | c0001 | t0004 | g0238 | SAS | BEB | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | BEB | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | BEB | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | BEB | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG04199 | hp1 | a0001 | c0001 | t0004 | g0241 | SAS | STU | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG04199 | hp2 | a0001 | c0001 | t0004 | g0244 | SAS | STU | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG04228 | hp1 | a0001 | c0002 | t0002 | g0051 | SAS | STU | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | STU | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18522 | hp1 | a0001 | c0004 | t0005 | g0179 | AFR | YRI | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18522 | hp2 | a0001 | c0003 | t0002 | g0069 | AFR | YRI | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18612 | hp1 | a0001 | c0001 | t0004 | g0032 | EAS | CHB | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | CHB | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18906 | hp1 | a0001 | c0001 | t0011 | g0248 | AFR | YRI | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | YRI | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18939 | hp1 | a0001 | c0001 | t0003 | g0209 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18939 | hp2 | a0001 | c0001 | t0006 | g0311 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18940 | hp2 | a0001 | c0001 | t0003 | g0213 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18941 | hp1 | a0001 | c0002 | t0002 | g0038 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18941 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18942 | hp1 | a0001 | c0001 | t0006 | g0287 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18943 | hp2 | a0001 | c0001 | t0005 | g0326 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18944 | hp1 | a0001 | c0001 | t0006 | g0291 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18944 | hp2 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18947 | hp1 | a0001 | c0001 | t0005 | g0277 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18949 | hp2 | a0001 | c0001 | t0005 | g0301 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18951 | hp1 | a0001 | c0001 | t0003 | g0208 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18951 | hp2 | a0001 | c0001 | t0004 | g0229 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18952 | hp1 | a0001 | c0001 | t0006 | g0316 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18952 | hp2 | a0001 | c0001 | t0003 | g0205 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18953 | hp1 | a0001 | c0001 | t0003 | g0211 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18954 | hp1 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18956 | hp1 | a0001 | c0001 | t0003 | g0203 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18956 | hp2 | a0001 | c0001 | t0004 | g0242 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18957 | hp1 | a0001 | c0001 | t0004 | g0231 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18957 | hp2 | a0001 | c0001 | t0003 | g0188 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18960 | hp1 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18961 | hp1 | a0001 | c0001 | t0005 | g0317 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18963 | hp2 | a0001 | c0001 | t0004 | g0232 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18965 | hp2 | a0001 | c0001 | t0003 | g0198 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18966 | hp1 | a0001 | c0002 | t0002 | g0057 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18966 | hp2 | a0001 | c0001 | t0004 | g0331 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18967 | hp1 | a0001 | c0002 | t0002 | g0135 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18967 | hp2 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18968 | hp1 | a0001 | c0001 | t0003 | g0199 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18968 | hp2 | a0001 | c0001 | t0005 | g0306 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18970 | hp1 | a0001 | c0002 | t0002 | g0065 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18970 | hp2 | a0001 | c0001 | t0005 | g0313 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18971 | hp1 | a0001 | c0001 | t0005 | g0303 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18971 | hp2 | a0001 | c0002 | t0002 | g0054 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18972 | hp2 | a0001 | c0001 | t0004 | g0032 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18973 | hp1 | a0002 | c0005 | t0005 | g0304 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18973 | hp2 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18974 | hp2 | a0001 | c0001 | t0004 | g0225 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18975 | hp2 | a0001 | c0001 | t0024 | g0234 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18978 | hp1 | a0001 | c0002 | t0002 | g0068 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18982 | hp1 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18982 | hp2 | a0001 | c0001 | t0004 | g0230 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18983 | hp1 | a0001 | c0001 | t0003 | g0217 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18983 | hp2 | a0001 | c0001 | t0004 | g0257 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18984 | hp1 | a0001 | c0001 | t0005 | g0323 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18984 | hp2 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18985 | hp1 | a0001 | c0002 | t0002 | g0019 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18986 | hp1 | a0001 | c0001 | t0015 | g0155 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18988 | hp1 | a0001 | c0001 | t0004 | g0259 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18988 | hp2 | a0001 | c0001 | t0006 | g0318 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18990 | hp1 | a0001 | c0002 | t0002 | g0134 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18990 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18992 | hp2 | a0001 | c0001 | t0005 | g0298 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18993 | hp2 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18994 | hp1 | a0001 | c0002 | t0002 | g0064 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18994 | hp2 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18995 | hp1 | a0001 | c0001 | t0003 | g0212 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18998 | hp2 | a0001 | c0001 | t0005 | g0308 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18999 | hp1 | a0002 | c0005 | t0005 | g0302 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA18999 | hp2 | a0001 | c0001 | t0003 | g0184 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA19000 | hp1 | a0001 | c0001 | t0004 | g0031 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA19000 | hp2 | a0001 | c0001 | t0003 | g0221 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA19001 | hp1 | a0001 | c0001 | t0005 | g0278 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA19001 | hp2 | a0001 | c0001 | t0005 | g0222 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA19002 | hp1 | a0001 | c0002 | t0002 | g0056 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA19002 | hp2 | a0001 | c0001 | t0005 | g0300 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA19003 | hp2 | a0001 | c0001 | t0005 | g0297 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA19004 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA19004 | hp2 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA19005 | hp1 | a0001 | c0001 | t0005 | g0312 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA19005 | hp2 | a0001 | c0001 | t0003 | g0185 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA19006 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA19007 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA19010 | hp1 | a0001 | c0001 | t0003 | g0197 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA19011 | hp1 | a0001 | c0001 | t0005 | g0321 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA19030 | hp1 | a0001 | c0003 | t0023 | g0121 | AFR | LWK | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA19030 | hp2 | a0001 | c0003 | t0012 | g0035 | AFR | LWK | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA19043 | hp1 | a0001 | c0001 | t0007 | g0330 | AFR | LWK | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA19043 | hp2 | a0001 | c0002 | t0002 | g0143 | AFR | LWK | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA19054 | hp2 | a0001 | c0001 | t0019 | g0082 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA19056 | hp1 | a0001 | c0002 | t0002 | g0072 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA19057 | hp2 | a0001 | c0001 | t0003 | g0218 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA19058 | hp1 | a0001 | c0001 | t0004 | g0182 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA19058 | hp2 | a0001 | c0001 | t0005 | g0279 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA19060 | hp1 | a0001 | c0001 | t0005 | g0309 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA19060 | hp2 | a0001 | c0001 | t0004 | g0031 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA19062 | hp1 | a0001 | c0001 | t0003 | g0194 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA19062 | hp2 | a0001 | c0001 | t0004 | g0223 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA19063 | hp1 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA19063 | hp2 | a0001 | c0002 | t0002 | g0044 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA19066 | hp1 | a0001 | c0001 | t0003 | g0195 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA19066 | hp2 | a0001 | c0002 | t0027 | g0042 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA19067 | hp1 | a0001 | c0001 | t0003 | g0189 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA19070 | hp1 | a0001 | c0001 | t0004 | g0227 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA19070 | hp2 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA19072 | hp1 | a0001 | c0001 | t0003 | g0214 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA19072 | hp2 | a0001 | c0001 | t0006 | g0292 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA19076 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA19077 | hp1 | a0001 | c0001 | t0003 | g0193 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA19077 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA19078 | hp2 | a0001 | c0001 | t0004 | g0233 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA19079 | hp2 | a0001 | c0001 | t0005 | g0280 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA19080 | hp1 | a0001 | c0001 | t0004 | g0226 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA19080 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA19081 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA19081 | hp2 | a0001 | c0001 | t0003 | g0210 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA19084 | hp2 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA19085 | hp2 | a0001 | c0002 | t0002 | g0019 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA19086 | hp1 | a0001 | c0002 | t0002 | g0059 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA19086 | hp2 | a0001 | c0001 | t0005 | g0314 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA19087 | hp1 | a0001 | c0001 | t0003 | g0207 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA19087 | hp2 | a0001 | c0001 | t0004 | g0228 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA19090 | hp1 | a0001 | c0001 | t0003 | g0196 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA19091 | hp1 | a0001 | c0001 | t0004 | g0224 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA19091 | hp2 | a0001 | c0001 | t0003 | g0206 | EAS | JPT | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | ASW | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA20129 | hp2 | a0001 | c0003 | t0012 | g0036 | AFR | ASW | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA20905 | hp1 | a0001 | c0001 | t0004 | g0236 | SAS | GIH | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0144 | SAS | GIH | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG01123 | hp1 | a0001 | c0001 | t0004 | g0264 | AMR | CLM | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG01123 | hp2 | a0003 | c0007 | t0002 | g0055 | AMR | CLM | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG02109 | hp1 | a0001 | c0001 | t0007 | g0283 | AFR | ACB | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | ACB | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG02486 | hp2 | a0001 | c0004 | t0005 | g0176 | AFR | ACB | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG02559 | hp1 | a0001 | c0001 | t0011 | g0249 | AFR | ACB | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG02559 | hp2 | a0001 | c0003 | t0022 | g0124 | AFR | ACB | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG03471 | hp1 | a0001 | c0003 | t0002 | g0037 | AFR | MSL | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG03471 | hp2 | a0006 | c0009 | t0004 | g0245 | AFR | MSL | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG06807 | hp1 | a0001 | c0003 | t0026 | g0116 | AFR | USA | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
HG06807 | hp2 | a0001 | c0002 | t0002 | g0115 | AFR | USA | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA20300 | hp1 | a0001 | c0001 | t0004 | g0266 | AFR | USA | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA20300 | hp2 | a0001 | c0004 | t0005 | g0178 | AFR | USA | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA21309 | hp1 | a0001 | c0002 | t0002 | g0172 | AFR | LWK | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
NA21309 | hp2 | a0001 | c0001 | t0004 | g0271 | AFR | LWK | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
homoSapiens | chm13v2 | a0001 | c0001 | t0004 | g0276 | REF | REF | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
homoSapiens | grch38p0 | a0001 | c0002 | t0002 | g0001 | REF | REF | CCNT2_chr2_134913822_134964342 | CCNT2 | chr2 | 134913822 | 134964342 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:134953335 | G | T | 1 | a0006 | 1 | HG03471.hp2 | missense_variant | MODERATE | c.880G>T | p.Gly294Cys | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 9/9 | 913/6920 | 880/2193 | 294/730 | chr2 | 134953335 | |||
chr2:134953374 | T | C | 1 | a0004 | 1 | HG02132.hp1 | missense_variant | MODERATE | c.919T>C | p.Ser307Pro | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 9/9 | 952/6920 | 919/2193 | 307/730 | chr2 | 134953374 | |||
chr2:134953729 | C | T | 1 | a0002 | 2 | NA18973.hp1 NA18999.hp1 |
missense_variant | MODERATE | c.1274C>T | p.Thr425Ile | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 9/9 | 1307/6920 | 1274/2193 | 425/730 | chr2 | 134953729 | |||
chr2:134954181 | T | C | 1 | a0003 | 1 | HG01123.hp2 | missense_variant | MODERATE | c.1726T>C | p.Ser576Pro | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 9/9 | 1759/6920 | 1726/2193 | 576/730 | chr2 | 134954181 | |||
chr2:134954520 | A | C | 1 | a0005 | 1 | HG02738.hp1 | missense_variant | MODERATE | c.2065A>C | p.Lys689Gln | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 9/9 | 2098/6920 | 2065/2193 | 689/730 | chr2 | 134954520 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:134936849 | G | A | 1 | a0001c0004 | 6 | HG02280.hp1 HG02486.hp2 HG02965.hp1 others(3): Show |
synonymous_variant | LOW | c.249G>A | p.Ser83Ser | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 3/9 | 282/6920 | 249/2193 | 83/730 | chr2 | 134936849 | |||
chr2:134953946 | C | T | 5 | a0001c0001 a0001c0003 a0001c0004 others(2): Show |
317 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(314): Show |
synonymous_variant | LOW | c.1491C>T | p.Asp497Asp | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 9/9 | 1524/6920 | 1491/2193 | 497/730 | chr2 | 134953946 | |||
chr2:134954087 | G | A | 4 | a0001c0001 a0001c0004 a0002c0005 others(1): Show |
303 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(300): Show |
synonymous_variant | LOW | c.1632G>A | p.Lys544Lys | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 9/9 | 1665/6920 | 1632/2193 | 544/730 | chr2 | 134954087 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:134954654 | T | C | 1 | a0001c0002t0013 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6T>C | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 9/9 | 6 | chr2 | 134954654 | ||||||
chr2:134954829 | C | T | 1 | a0001c0002t0027 | 1 | NA19066.hp2 | 3_prime_UTR_variant | MODIFIER | c.*181C>T | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 9/9 | 181 | chr2 | 134954829 | ||||||
chr2:134954846 | T | C | 1 | a0001c0001t0014 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*198T>C | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 9/9 | 198 | chr2 | 134954846 | ||||||
chr2:134955511 | A | G | 1 | a0001c0003t0026 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*863A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 9/9 | 863 | chr2 | 134955511 | ||||||
chr2:134955516 | A | G | 1 | a0001c0001t0007 | 6 | HG02109.hp1 HG02257.hp1 HG02572.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*868A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 9/9 | 868 | chr2 | 134955516 | ||||||
chr2:134955815 | TAAAA | T | 5 | a0001c0001t0004 a0001c0001t0011 a0001c0001t0014 others(2): Show |
58 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*1170_*1173delAAAA | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 9/9 | 1170 | INFO_REALIGN_3_PRIME | chr2 | 134955815 | |||||
chr2:134955823 | A | G | 1 | a0001c0001t0024 | 1 | NA18975.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1175A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 9/9 | 1175 | chr2 | 134955823 | ||||||
chr2:134955978 | C | T | 1 | a0001c0001t0010 | 3 | HG02615.hp2 HG03139.hp2 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1330C>T | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 9/9 | 1330 | chr2 | 134955978 | ||||||
chr2:134956132 | C | T | 1 | a0001c0003t0023 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1484C>T | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 9/9 | 1484 | chr2 | 134956132 | ||||||
chr2:134956133 | G | A | 23 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(20): Show |
305 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(302): Show |
3_prime_UTR_variant | MODIFIER | c.*1485G>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 9/9 | 1485 | chr2 | 134956133 | ||||||
chr2:134956473 | G | A | 1 | a0001c0001t0015 | 1 | NA18986.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1825G>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 9/9 | 1825 | chr2 | 134956473 | ||||||
chr2:134956586 | G | A | 2 | a0001c0001t0003 a0001c0001t0016 |
56 | HG00408.hp1 HG00438.hp2 HG00597.hp1 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*1938G>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 9/9 | 1938 | chr2 | 134956586 | ||||||
chr2:134956603 | C | G | 1 | a0001c0001t0021 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1955C>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 9/9 | 1955 | chr2 | 134956603 | ||||||
chr2:134956627 | A | G | 1 | a0001c0001t0020 | 1 | HG01515.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1979A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 9/9 | 1979 | chr2 | 134956627 | ||||||
chr2:134957165 | T | G | 1 | a0001c0002t0009 | 3 | HG02630.hp1 HG02895.hp2 HG02896.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2517T>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 9/9 | 2517 | chr2 | 134957165 | ||||||
chr2:134957308 | A | T | 1 | a0001c0001t0019 | 1 | NA19054.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2660A>T | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 9/9 | 2660 | chr2 | 134957308 | ||||||
chr2:134957361 | A | G | 1 | a0001c0001t0016 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2713A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 9/9 | 2713 | chr2 | 134957361 | ||||||
chr2:134957599 | T | G | 8 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0010 others(5): Show |
124 | HG00544.hp1 HG00558.hp2 HG00597.hp2 others(121): Show |
3_prime_UTR_variant | MODIFIER | c.*2951T>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 9/9 | 2951 | chr2 | 134957599 | ||||||
chr2:134957604 | TC | T | 22 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(19): Show |
303 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(300): Show |
3_prime_UTR_variant | MODIFIER | c.*2957delC | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 9/9 | 2957 | chr2 | 134957604 | ||||||
chr2:134957649 | G | A | 1 | a0001c0001t0008 | 5 | HG01099.hp2 HG01361.hp1 HG01516.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3001G>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 9/9 | 3001 | chr2 | 134957649 | ||||||
chr2:134957895 | ATAAT | A | 22 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(19): Show |
303 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(300): Show |
3_prime_UTR_variant | MODIFIER | c.*3252_*3255delTAAT | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 9/9 | 3252 | INFO_REALIGN_3_PRIME | chr2 | 134957895 | |||||
chr2:134957962 | A | G | 1 | a0001c0001t0007 | 6 | HG02109.hp1 HG02257.hp1 HG02572.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3314A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 9/9 | 3314 | chr2 | 134957962 | ||||||
chr2:134958134 | A | C | 1 | a0001c0001t0006 | 13 | HG00408.hp2 HG00544.hp2 HG00609.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*3486A>C | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 9/9 | 3486 | chr2 | 134958134 | ||||||
chr2:134958387 | A | G | 23 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(20): Show |
305 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(302): Show |
3_prime_UTR_variant | MODIFIER | c.*3739A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 9/9 | 3739 | chr2 | 134958387 | ||||||
chr2:134958400 | C | T | 1 | a0001c0001t0018 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3752C>T | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 9/9 | 3752 | chr2 | 134958400 | ||||||
chr2:134958508 | A | T | 1 | a0001c0001t0017 | 1 | HG01358.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3860A>T | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 9/9 | 3860 | chr2 | 134958508 | ||||||
chr2:134958685 | G | A | 1 | a0001c0003t0012 | 2 | NA19030.hp2 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4037G>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 9/9 | 4037 | chr2 | 134958685 | ||||||
chr2:134958753 | T | C | 2 | a0001c0001t0011 a0001c0001t0025 |
4 | HG02451.hp1 HG02559.hp1 HG02922.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4105T>C | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 9/9 | 4105 | chr2 | 134958753 | ||||||
chr2:134959028 | T | C | 8 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0010 others(5): Show |
124 | HG00544.hp1 HG00558.hp2 HG00597.hp2 others(121): Show |
3_prime_UTR_variant | MODIFIER | c.*4380T>C | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 9/9 | 4380 | chr2 | 134959028 | ||||||
chr2:134959202 | A | C | 1 | a0001c0003t0022 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4554A>C | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 9/9 | 4554 | chr2 | 134959202 | ||||||
chr2:134959291 | T | A | 1 | a0001c0001t0025 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4643T>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 9/9 | 4643 | chr2 | 134959291 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:134919077 | C | T | 11 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0016 others(8): Show |
18 | HG00639.hp1 HG00735.hp2 HG01358.hp2 others(15): Show |
intron_variant | MODIFIER | c.158+65C>T | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 1/8 | chr2 | 134919077 | |||||||
chr2:134919282 | C | T | 178 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0016 others(175): Show |
197 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(194): Show |
intron_variant | MODIFIER | c.158+270C>T | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 1/8 | chr2 | 134919282 | |||||||
chr2:134919348 | C | T | 2 | a0001c0002t0002g0172 a0001c0002t0002g0173 |
2 | HG03041.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.158+336C>T | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 1/8 | chr2 | 134919348 | |||||||
chr2:134919398 | T | C | 1 | a0001c0003t0002g0034 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.158+386T>C | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 1/8 | chr2 | 134919398 | |||||||
chr2:134919419 | G | A | 6 | a0001c0004t0005g0174 a0001c0004t0005g0175 a0001c0004t0005g0176 others(3): Show |
6 | HG02280.hp1 HG02486.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.159-391G>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 1/8 | chr2 | 134919419 | |||||||
chr2:134919465 | T | C | 180 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0016 others(177): Show |
199 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(196): Show |
intron_variant | MODIFIER | c.159-345T>C | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 1/8 | chr2 | 134919465 | |||||||
chr2:134919473 | T | G | 181 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0016 others(178): Show |
200 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(197): Show |
intron_variant | MODIFIER | c.159-337T>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 1/8 | chr2 | 134919473 | |||||||
chr2:134919524 | A | G | 1 | a0001c0001t0004g0331 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.159-286A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 1/8 | chr2 | 134919524 | |||||||
chr2:134919527 | G | C | 2 | a0001c0003t0012g0035 a0001c0003t0012g0036 |
2 | NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.159-283G>C | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 1/8 | chr2 | 134919527 | |||||||
chr2:134919591 | A | G | 32 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(29): Show |
42 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.159-219A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 1/8 | chr2 | 134919591 | |||||||
chr2:134919639 | C | G | 1 | a0001c0001t0007g0330 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.159-171C>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 1/8 | chr2 | 134919639 | |||||||
chr2:134919641 | A | G | 11 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0016 others(8): Show |
18 | HG00639.hp1 HG00735.hp2 HG01358.hp2 others(15): Show |
intron_variant | MODIFIER | c.159-169A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 1/8 | chr2 | 134919641 | |||||||
chr2:134919698 | G | A | 178 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0016 others(175): Show |
197 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(194): Show |
intron_variant | MODIFIER | c.159-112G>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 1/8 | chr2 | 134919698 | |||||||
chr2:134919901 | A | AGTTT | 180 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0016 others(177): Show |
199 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(196): Show |
intron_variant | MODIFIER | c.240+13_240+14insTG others(2): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134919901 | ||||||
chr2:134919982 | G | A | 1 | a0001c0001t0018g0180 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.240+91G>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134919982 | |||||||
chr2:134919987 | C | G | 1 | a0001c0002t0002g0143 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.240+96C>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134919987 | |||||||
chr2:134920111 | G | A | 1 | a0001c0001t0005g0181 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.240+220G>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134920111 | |||||||
chr2:134920247 | A | G | 6 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0139 others(3): Show |
6 | HG00558.hp2 HG00609.hp1 HG03669.hp1 others(3): Show |
intron_variant | MODIFIER | c.240+356A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134920247 | |||||||
chr2:134920377 | G | T | 1 | a0001c0002t0013g0136 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.240+486G>T | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134920377 | |||||||
chr2:134920594 | G | C | 1 | a0001c0001t0001g0144 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.240+703G>C | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134920594 | |||||||
chr2:134920625 | T | C | 1 | a0001c0001t0004g0182 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.240+734T>C | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134920625 | |||||||
chr2:134920690 | C | G | 2 | a0001c0003t0012g0035 a0001c0003t0012g0036 |
2 | NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.240+799C>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134920690 | |||||||
chr2:134920747 | G | T | 1 | a0001c0001t0004g0331 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.240+856G>T | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134920747 | |||||||
chr2:134920871 | A | G | 2 | a0001c0002t0002g0134 a0001c0002t0002g0135 |
2 | NA18967.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.240+980A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134920871 | |||||||
chr2:134921001 | T | G | 1 | a0001c0002t0002g0038 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.240+1110T>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134921001 | |||||||
chr2:134921098 | G | T | 5 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(2): Show |
5 | NA18942.hp2 NA18943.hp1 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.240+1207G>T | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134921098 | |||||||
chr2:134921201 | C | T | 1 | a0001c0001t0005g0329 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.240+1310C>T | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134921201 | |||||||
chr2:134921205 | A | T | 1 | a0001c0002t0002g0128 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.240+1314A>T | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134921205 | |||||||
chr2:134921207 | C | G | 1 | a0001c0002t0002g0038 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.240+1316C>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134921207 | |||||||
chr2:134921231 | C | G | 3 | a0001c0002t0002g0006 a0001c0002t0002g0023 a0001c0002t0002g0127 |
7 | HG00438.hp1 HG00558.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.240+1340C>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134921231 | |||||||
chr2:134921318 | A | G | 119 | a0001c0001t0004g0031 a0001c0001t0004g0032 a0001c0001t0004g0182 others(116): Show |
121 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(118): Show |
intron_variant | MODIFIER | c.240+1427A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134921318 | |||||||
chr2:134921353 | A | AT | 180 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0016 others(177): Show |
199 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(196): Show |
intron_variant | MODIFIER | c.240+1472dupT | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134921353 | ||||||
chr2:134921407 | A | G | 1 | a0001c0001t0001g0126 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.240+1516A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134921407 | |||||||
chr2:134921415 | G | A | 58 | a0001c0001t0004g0031 a0001c0001t0004g0032 a0001c0001t0004g0182 others(55): Show |
60 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.240+1524G>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134921415 | |||||||
chr2:134921478 | T | A | 1 | a0001c0001t0003g0183 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.240+1587T>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134921478 | |||||||
chr2:134921589 | G | C | 4 | a0001c0001t0005g0277 a0001c0001t0005g0278 a0001c0001t0005g0279 others(1): Show |
4 | NA18947.hp1 NA19001.hp1 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.240+1698G>C | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134921589 | |||||||
chr2:134921964 | T | C | 1 | a0001c0004t0005g0174 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.240+2073T>C | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134921964 | |||||||
chr2:134922187 | C | T | 1 | a0001c0002t0002g0125 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.240+2296C>T | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134922187 | |||||||
chr2:134922188 | G | A | 11 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0016 others(8): Show |
18 | HG00639.hp1 HG00735.hp2 HG01358.hp2 others(15): Show |
intron_variant | MODIFIER | c.240+2297G>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134922188 | |||||||
chr2:134922188 | G | T | 2 | a0001c0003t0012g0035 a0001c0003t0012g0036 |
2 | NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.240+2297G>T | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134922188 | |||||||
chr2:134922216 | C | G | 1 | a0001c0001t0004g0182 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.240+2325C>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134922216 | |||||||
chr2:134922416 | T | A | 3 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 |
3 | NA18942.hp2 NA18950.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.240+2525T>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134922416 | |||||||
chr2:134922483 | T | G | 1 | a0001c0003t0002g0039 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.240+2592T>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134922483 | |||||||
chr2:134922535 | C | G | 1 | a0001c0003t0002g0039 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.240+2644C>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134922535 | |||||||
chr2:134922925 | C | G | 2 | a0001c0003t0012g0035 a0001c0003t0012g0036 |
2 | NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.240+3034C>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134922925 | |||||||
chr2:134923061 | C | T | 1 | a0001c0003t0022g0124 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.240+3170C>T | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134923061 | |||||||
chr2:134923094 | A | C | 1 | a0001c0003t0012g0036 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.240+3203A>C | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134923094 | |||||||
chr2:134923151 | C | A | 1 | a0001c0001t0003g0183 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.240+3260C>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134923151 | |||||||
chr2:134923307 | A | G | 2 | a0001c0001t0003g0220 a0001c0001t0003g0221 |
2 | HG00597.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.240+3416A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134923307 | |||||||
chr2:134923765 | C | T | 1 | a0001c0001t0005g0219 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.240+3874C>T | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134923765 | |||||||
chr2:134923823 | A | G | 2 | a0001c0003t0012g0035 a0001c0003t0012g0036 |
2 | NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.240+3932A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134923823 | |||||||
chr2:134923845 | G | C | 1 | a0001c0001t0001g0126 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.240+3954G>C | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134923845 | |||||||
chr2:134923991 | A | G | 2 | a0001c0001t0003g0217 a0001c0001t0003g0218 |
2 | NA18983.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.240+4100A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134923991 | |||||||
chr2:134924006 | A | G | 1 | a0001c0003t0012g0035 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.240+4115A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134924006 | |||||||
chr2:134924027 | T | A | 58 | a0001c0001t0004g0031 a0001c0001t0004g0032 a0001c0001t0004g0182 others(55): Show |
60 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.240+4136T>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134924027 | |||||||
chr2:134924107 | C | T | 1 | a0001c0001t0005g0328 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.240+4216C>T | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134924107 | |||||||
chr2:134924392 | G | A | 1 | a0001c0001t0018g0180 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.240+4501G>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134924392 | |||||||
chr2:134924486 | G | C | 46 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0025 others(43): Show |
56 | HG00408.hp1 HG00438.hp2 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.240+4595G>C | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134924486 | |||||||
chr2:134924524 | G | A | 179 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0016 others(176): Show |
198 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(195): Show |
intron_variant | MODIFIER | c.240+4633G>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134924524 | |||||||
chr2:134924533 | T | A | 2 | a0001c0003t0012g0035 a0001c0003t0012g0036 |
2 | NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.240+4642T>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134924533 | |||||||
chr2:134924638 | C | T | 177 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0016 others(174): Show |
196 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(193): Show |
intron_variant | MODIFIER | c.240+4747C>T | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134924638 | |||||||
chr2:134924719 | G | A | 2 | a0001c0003t0012g0035 a0001c0003t0012g0036 |
2 | NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.240+4828G>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134924719 | |||||||
chr2:134924753 | T | G | 1 | a0001c0001t0005g0219 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.240+4862T>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134924753 | |||||||
chr2:134924758 | T | G | 1 | a0001c0001t0005g0219 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.240+4867T>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134924758 | |||||||
chr2:134924765 | A | G | 1 | a0001c0001t0006g0327 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.240+4874A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134924765 | |||||||
chr2:134924792 | C | T | 6 | a0001c0004t0005g0174 a0001c0004t0005g0175 a0001c0004t0005g0176 others(3): Show |
6 | HG02280.hp1 HG02486.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.240+4901C>T | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134924792 | |||||||
chr2:134924901 | G | A | 1 | a0001c0001t0005g0281 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.240+5010G>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134924901 | |||||||
chr2:134924939 | A | G | 1 | a0001c0001t0005g0326 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.240+5048A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134924939 | |||||||
chr2:134924998 | C | A | 1 | a0001c0001t0018g0180 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.240+5107C>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134924998 | |||||||
chr2:134925124 | G | T | 1 | a0001c0001t0018g0180 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.240+5233G>T | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134925124 | |||||||
chr2:134925178 | C | T | 1 | a0001c0001t0004g0275 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.240+5287C>T | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134925178 | |||||||
chr2:134925222 | T | A | 177 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0016 others(174): Show |
196 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(193): Show |
intron_variant | MODIFIER | c.240+5331T>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134925222 | |||||||
chr2:134925265 | A | G | 2 | a0001c0003t0012g0035 a0001c0003t0012g0036 |
2 | NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.240+5374A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134925265 | |||||||
chr2:134925296 | C | T | 1 | a0001c0004t0005g0179 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.240+5405C>T | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134925296 | |||||||
chr2:134925321 | T | C | 2 | a0001c0002t0002g0143 a0001c0002t0013g0136 |
2 | HG03130.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.240+5430T>C | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134925321 | |||||||
chr2:134925430 | A | G | 11 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0016 others(8): Show |
18 | HG00639.hp1 HG00735.hp2 HG01358.hp2 others(15): Show |
intron_variant | MODIFIER | c.240+5539A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134925430 | |||||||
chr2:134925447 | C | T | 58 | a0001c0001t0004g0031 a0001c0001t0004g0032 a0001c0001t0004g0182 others(55): Show |
60 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.240+5556C>T | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134925447 | |||||||
chr2:134925544 | C | G | 1 | a0001c0002t0009g0123 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.240+5653C>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134925544 | |||||||
chr2:134925610 | T | C | 6 | a0001c0001t0007g0282 a0001c0001t0007g0283 a0001c0001t0007g0284 others(3): Show |
6 | HG02109.hp1 HG02257.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.240+5719T>C | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134925610 | |||||||
chr2:134925793 | G | A | 1 | a0001c0001t0007g0282 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.240+5902G>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134925793 | |||||||
chr2:134925842 | G | C | 3 | a0001c0001t0001g0003 a0001c0001t0001g0145 a0001c0001t0001g0146 |
7 | HG01978.hp2 NA18940.hp1 NA18960.hp2 others(4): Show |
intron_variant | MODIFIER | c.240+5951G>C | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134925842 | |||||||
chr2:134925859 | C | CT | 17 | a0001c0001t0001g0120 a0001c0001t0001g0122 a0001c0001t0001g0142 others(14): Show |
17 | HG00741.hp2 HG02132.hp2 HG02615.hp1 others(14): Show |
intron_variant | MODIFIER | c.240+5992dupT | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134925859 | ||||||
chr2:134925859 | CT | C | 70 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(67): Show |
72 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(69): Show |
intron_variant | MODIFIER | c.240+5992delT | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134925859 | ||||||
chr2:134925859 | CTT | C | 34 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0016 others(31): Show |
43 | HG00609.hp2 HG00639.hp1 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.240+5991_240+5992d others(4): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134925859 | ||||||
chr2:134925859 | CTTT | C | 79 | a0001c0001t0001g0332 a0001c0001t0003g0013 a0001c0001t0003g0014 others(76): Show |
87 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.240+5990_240+5992d others(5): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134925859 | ||||||
chr2:134925952 | A | G | 1 | a0001c0001t0010g0148 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.240+6061A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134925952 | |||||||
chr2:134926030 | A | AT | 101 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(98): Show |
113 | HG00544.hp1 HG00558.hp2 HG00597.hp2 others(110): Show |
intron_variant | MODIFIER | c.240+6146dupT | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134926030 | ||||||
chr2:134926444 | C | A | 1 | a0001c0001t0001g0071 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.240+6553C>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134926444 | |||||||
chr2:134926488 | A | C | 2 | a0001c0001t0005g0181 a0001c0001t0005g0324 |
2 | HG02809.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.240+6597A>C | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134926488 | |||||||
chr2:134926752 | T | C | 2 | a0001c0001t0005g0181 a0001c0001t0005g0324 |
2 | HG02809.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.240+6861T>C | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134926752 | |||||||
chr2:134926839 | T | G | 1 | a0001c0001t0005g0222 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.240+6948T>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134926839 | |||||||
chr2:134927137 | G | T | 1 | a0001c0001t0007g0286 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.240+7246G>T | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134927137 | |||||||
chr2:134927215 | T | C | 1 | a0001c0002t0009g0123 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.240+7324T>C | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134927215 | |||||||
chr2:134927311 | T | G | 2 | a0001c0001t0003g0184 a0001c0001t0003g0185 |
2 | NA18999.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.240+7420T>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134927311 | |||||||
chr2:134927440 | G | A | 1 | a0001c0001t0003g0186 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.240+7549G>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134927440 | |||||||
chr2:134927489 | G | A | 4 | a0001c0001t0001g0003 a0001c0001t0001g0145 a0001c0001t0001g0146 others(1): Show |
8 | HG01978.hp2 NA18940.hp1 NA18960.hp2 others(5): Show |
intron_variant | MODIFIER | c.240+7598G>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134927489 | |||||||
chr2:134927770 | G | A | 46 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0025 others(43): Show |
56 | HG00408.hp1 HG00438.hp2 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.240+7879G>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134927770 | |||||||
chr2:134927850 | A | G | 2 | a0001c0003t0012g0035 a0001c0003t0012g0036 |
2 | NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.240+7959A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134927850 | |||||||
chr2:134927984 | T | C | 2 | a0001c0001t0005g0181 a0001c0001t0005g0324 |
2 | HG02809.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.240+8093T>C | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134927984 | |||||||
chr2:134928129 | C | T | 1 | a0001c0001t0004g0273 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.240+8238C>T | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134928129 | |||||||
chr2:134928274 | C | CT | 119 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(116): Show |
133 | HG00544.hp1 HG00558.hp2 HG00597.hp2 others(130): Show |
intron_variant | MODIFIER | c.240+8402dupT | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134928274 | ||||||
chr2:134928274 | C | CTT | 10 | a0001c0001t0001g0133 a0001c0001t0001g0142 a0001c0001t0001g0146 others(7): Show |
10 | HG01069.hp1 HG01071.hp2 HG01978.hp2 others(7): Show |
intron_variant | MODIFIER | c.240+8401_240+8402d others(4): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134928274 | ||||||
chr2:134928274 | C | CTTTTTT | 9 | a0001c0001t0003g0013 a0001c0001t0003g0188 a0001c0001t0003g0189 others(6): Show |
11 | HG00597.hp1 HG02074.hp1 HG02083.hp2 others(8): Show |
intron_variant | MODIFIER | c.240+8397_240+8402d others(8): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134928274 | ||||||
chr2:134928274 | C | CTTTTTTT | 35 | a0001c0001t0003g0014 a0001c0001t0003g0025 a0001c0001t0003g0026 others(32): Show |
43 | HG00408.hp1 HG00438.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.240+8396_240+8402d others(9): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134928274 | ||||||
chr2:134928274 | C | CTTTTTTT others(1): Show |
21 | a0001c0001t0003g0183 a0001c0001t0003g0207 a0001c0001t0003g0208 others(18): Show |
21 | HG00408.hp2 HG00544.hp2 HG00609.hp2 others(18): Show |
intron_variant | MODIFIER | c.240+8395_240+8402d others(10): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134928274 | ||||||
chr2:134928274 | C | CTTTTTTT others(3): Show |
6 | a0001c0004t0005g0174 a0001c0004t0005g0175 a0001c0004t0005g0176 others(3): Show |
6 | HG02280.hp1 HG02486.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.240+8393_240+8402d others(12): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134928274 | ||||||
chr2:134928274 | C | CTTTTTTT others(5): Show |
1 | a0001c0001t0005g0295 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.240+8391_240+8402d others(14): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134928274 | ||||||
chr2:134928274 | C | CTTTTTTT others(6): Show |
1 | a0001c0001t0005g0296 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.240+8390_240+8402d others(15): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134928274 | ||||||
chr2:134928274 | C | CTTTTTTT others(7): Show |
1 | a0006c0009t0004g0245 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.240+8389_240+8402d others(16): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134928274 | ||||||
chr2:134928274 | C | CTTTTTTT others(12): Show |
5 | a0001c0001t0004g0246 a0001c0001t0005g0297 a0001c0001t0005g0298 others(2): Show |
5 | HG01257.hp1 HG02080.hp1 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.240+8384_240+8402d others(21): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134928274 | ||||||
chr2:134928274 | C | CTTTTTTT others(13): Show |
13 | a0001c0001t0005g0277 a0001c0001t0005g0281 a0001c0001t0005g0300 others(10): Show |
13 | HG02451.hp1 HG02559.hp1 HG03654.hp2 others(10): Show |
intron_variant | MODIFIER | c.240+8402_240+8403i others(22): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134928274 | ||||||
chr2:134928274 | C | CTTTTTTT others(14): Show |
14 | a0001c0001t0005g0278 a0001c0001t0005g0279 a0001c0001t0005g0280 others(11): Show |
14 | HG02155.hp1 HG02602.hp2 HG02735.hp2 others(11): Show |
intron_variant | MODIFIER | c.240+8402_240+8403i others(23): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134928274 | ||||||
chr2:134928274 | C | CTTTTTTT others(15): Show |
6 | a0001c0001t0005g0315 a0001c0001t0005g0317 a0001c0001t0005g0319 others(3): Show |
6 | HG02071.hp2 HG03195.hp2 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.240+8402_240+8403i others(24): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134928274 | ||||||
chr2:134928274 | C | CTTTTTTT others(16): Show |
5 | a0001c0001t0004g0251 a0001c0001t0004g0252 a0001c0001t0004g0253 others(2): Show |
5 | HG00639.hp2 HG01070.hp2 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.240+8402_240+8403i others(25): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134928274 | ||||||
chr2:134928274 | C | CTTTTTTT others(17): Show |
6 | a0001c0001t0004g0254 a0001c0001t0004g0255 a0001c0001t0004g0256 others(3): Show |
6 | HG01192.hp1 HG01255.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.240+8402_240+8403i others(26): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134928274 | ||||||
chr2:134928274 | C | CTTTTTTT others(18): Show |
6 | a0001c0001t0004g0182 a0001c0001t0004g0260 a0001c0001t0004g0261 others(3): Show |
6 | HG00140.hp2 HG00642.hp2 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.240+8402_240+8403i others(27): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134928274 | ||||||
chr2:134928274 | C | CTTTTTTT others(19): Show |
3 | a0001c0001t0004g0265 a0001c0001t0004g0266 a0001c0001t0004g0275 |
3 | HG02572.hp2 HG03041.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.240+8402_240+8403i others(28): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134928274 | ||||||
chr2:134928274 | C | CTTTTTTT others(22): Show |
1 | a0001c0001t0004g0267 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.240+8402_240+8403i others(31): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134928274 | ||||||
chr2:134928274 | C | CTTTTTTT others(24): Show |
1 | a0001c0001t0004g0268 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.240+8402_240+8403i others(33): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134928274 | ||||||
chr2:134928274 | C | CTTTTTTT others(25): Show |
1 | a0001c0001t0004g0269 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.240+8402_240+8403i others(34): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134928274 | ||||||
chr2:134928274 | C | CTTTTTTT others(28): Show |
1 | a0001c0001t0004g0270 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.240+8402_240+8403i others(37): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134928274 | ||||||
chr2:134928274 | C | CTTTTTTT others(30): Show |
1 | a0001c0001t0004g0271 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.240+8402_240+8403i others(39): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134928274 | ||||||
chr2:134928274 | C | CTTTTTTT others(32): Show |
1 | a0001c0001t0004g0272 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.240+8402_240+8403i others(41): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134928274 | ||||||
chr2:134928298 | G | A | 1 | a0001c0002t0002g0050 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.240+8407G>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134928298 | |||||||
chr2:134928332 | G | C | 2 | a0001c0001t0005g0307 a0001c0001t0005g0315 |
2 | HG02071.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.240+8441G>C | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134928332 | |||||||
chr2:134928335 | A | G | 46 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0025 others(43): Show |
56 | HG00408.hp1 HG00438.hp2 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.240+8444A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134928335 | |||||||
chr2:134928405 | A | C | 46 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0025 others(43): Show |
56 | HG00408.hp1 HG00438.hp2 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.241-8436A>C | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134928405 | |||||||
chr2:134928495 | C | G | 2 | a0001c0002t0002g0046 a0001c0002t0002g0067 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.241-8346C>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134928495 | |||||||
chr2:134928579 | A | G | 1 | a0001c0003t0002g0037 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.241-8262A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134928579 | |||||||
chr2:134928599 | C | T | 1 | a0006c0009t0004g0245 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.241-8242C>T | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134928599 | |||||||
chr2:134928614 | T | A | 2 | a0001c0003t0012g0035 a0001c0003t0012g0036 |
2 | NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.241-8227T>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134928614 | |||||||
chr2:134928742 | A | T | 1 | a0001c0003t0022g0124 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.241-8099A>T | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134928742 | |||||||
chr2:134928747 | A | C | 1 | a0001c0003t0002g0039 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.241-8094A>C | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134928747 | |||||||
chr2:134929079 | A | T | 178 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0016 others(175): Show |
197 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(194): Show |
intron_variant | MODIFIER | c.241-7762A>T | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134929079 | |||||||
chr2:134929125 | CAA | C | 178 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0016 others(175): Show |
197 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(194): Show |
intron_variant | MODIFIER | c.241-7712_241-7711d others(4): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134929125 | ||||||
chr2:134929198 | G | A | 6 | a0001c0001t0007g0282 a0001c0001t0007g0283 a0001c0001t0007g0284 others(3): Show |
6 | HG02109.hp1 HG02257.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.241-7643G>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134929198 | |||||||
chr2:134929324 | G | A | 1 | a0001c0002t0002g0051 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.241-7517G>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134929324 | |||||||
chr2:134929388 | A | C | 180 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0016 others(177): Show |
199 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(196): Show |
intron_variant | MODIFIER | c.241-7453A>C | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134929388 | |||||||
chr2:134929449 | T | A | 1 | a0001c0002t0002g0128 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.241-7392T>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134929449 | |||||||
chr2:134929469 | A | G | 1 | a0001c0001t0001g0114 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.241-7372A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134929469 | |||||||
chr2:134929480 | C | T | 1 | a0001c0001t0001g0335 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.241-7361C>T | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134929480 | |||||||
chr2:134929523 | G | A | 1 | a0001c0001t0003g0191 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.241-7318G>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134929523 | |||||||
chr2:134929599 | C | A | 177 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0016 others(174): Show |
196 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(193): Show |
intron_variant | MODIFIER | c.241-7242C>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134929599 | |||||||
chr2:134929607 | C | G | 1 | a0001c0001t0005g0219 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.241-7234C>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134929607 | |||||||
chr2:134929613 | C | CAGAAGAG others(14): Show |
1 | a0001c0001t0001g0075 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.241-7225_241-7224i others(23): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134929613 | ||||||
chr2:134929613 | C | CAGAGAGA others(1): Show |
4 | a0001c0001t0001g0021 a0001c0001t0001g0076 a0001c0002t0002g0143 others(1): Show |
5 | HG02109.hp2 HG02486.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.241-7212_241-7205d others(10): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134929613 | ||||||
chr2:134929613 | C | CAGAGAGA others(3): Show |
1 | a0001c0001t0006g0288 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.241-7214_241-7205d others(12): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134929613 | ||||||
chr2:134929613 | C | CAGAGAGA others(5): Show |
19 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0015 others(16): Show |
30 | HG00639.hp1 HG00735.hp2 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.241-7216_241-7205d others(14): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134929613 | ||||||
chr2:134929613 | C | CAGAGAGA others(7): Show |
53 | a0001c0001t0001g0007 a0001c0001t0001g0024 a0001c0001t0001g0133 others(50): Show |
65 | HG00558.hp2 HG00597.hp1 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.241-7218_241-7205d others(16): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134929613 | ||||||
chr2:134929613 | C | CAGAGAGA others(9): Show |
48 | a0001c0001t0001g0073 a0001c0001t0001g0080 a0001c0001t0001g0081 others(45): Show |
50 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.241-7220_241-7205d others(18): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134929613 | ||||||
chr2:134929613 | C | CAGAGAGA others(11): Show |
40 | a0001c0001t0001g0012 a0001c0001t0001g0022 a0001c0001t0001g0048 others(37): Show |
43 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.241-7222_241-7205d others(20): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134929613 | ||||||
chr2:134929613 | C | CAGAGAGA others(13): Show |
12 | a0001c0001t0001g0047 a0001c0001t0001g0110 a0001c0001t0001g0126 others(9): Show |
13 | HG01243.hp1 HG01358.hp2 HG03017.hp1 others(10): Show |
intron_variant | MODIFIER | c.241-7224_241-7205d others(22): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134929613 | ||||||
chr2:134929613 | C | CAGAGAGA others(15): Show |
8 | a0001c0001t0001g0049 a0001c0001t0001g0070 a0001c0001t0001g0111 others(5): Show |
8 | HG00639.hp2 HG01081.hp2 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.241-7226_241-7205d others(24): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134929613 | ||||||
chr2:134929613 | C | CAGAGAGA others(17): Show |
8 | a0001c0001t0001g0112 a0001c0001t0004g0223 a0001c0001t0004g0227 others(5): Show |
8 | HG00140.hp2 HG02451.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.241-7205_241-7204i others(26): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134929613 | ||||||
chr2:134929613 | C | CAGAGAGA others(19): Show |
12 | a0001c0001t0001g0113 a0001c0001t0004g0032 a0001c0001t0004g0224 others(9): Show |
13 | HG00597.hp2 HG01123.hp1 HG02155.hp1 others(10): Show |
intron_variant | MODIFIER | c.241-7205_241-7204i others(28): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134929613 | ||||||
chr2:134929613 | C | CAGAGAGA others(21): Show |
6 | a0001c0001t0004g0232 a0001c0001t0004g0267 a0001c0001t0004g0274 others(3): Show |
6 | HG01074.hp2 HG02809.hp1 HG03669.hp2 others(3): Show |
intron_variant | MODIFIER | c.241-7205_241-7204i others(30): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134929613 | ||||||
chr2:134929613 | C | CAGAGAGA others(23): Show |
10 | a0001c0001t0004g0233 a0001c0001t0004g0243 a0001c0001t0005g0308 others(7): Show |
10 | HG00544.hp2 HG02922.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.241-7205_241-7204i others(32): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134929613 | ||||||
chr2:134929613 | C | CAGAGAGA others(25): Show |
15 | a0001c0001t0004g0235 a0001c0001t0004g0236 a0001c0001t0005g0309 others(12): Show |
15 | HG01168.hp1 HG01243.hp2 HG02071.hp2 others(12): Show |
intron_variant | MODIFIER | c.241-7205_241-7204i others(34): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134929613 | ||||||
chr2:134929613 | C | CAGAGAGA others(27): Show |
9 | a0001c0001t0004g0237 a0001c0001t0004g0238 a0001c0001t0005g0297 others(6): Show |
9 | HG01993.hp1 HG02257.hp1 HG03516.hp2 others(6): Show |
intron_variant | MODIFIER | c.241-7205_241-7204i others(36): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134929613 | ||||||
chr2:134929613 | C | CAGAGAGA others(29): Show |
4 | a0001c0001t0005g0313 a0001c0001t0005g0319 a0001c0001t0006g0287 others(1): Show |
4 | HG02572.hp1 HG03491.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.241-7205_241-7204i others(38): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134929613 | ||||||
chr2:134929613 | C | CAGAGAGA others(31): Show |
10 | a0001c0001t0004g0239 a0001c0001t0005g0277 a0001c0001t0005g0296 others(7): Show |
10 | HG01358.hp1 HG02165.hp1 HG03492.hp2 others(7): Show |
intron_variant | MODIFIER | c.241-7205_241-7204i others(40): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134929613 | ||||||
chr2:134929613 | C | CAGAGAGA others(33): Show |
7 | a0001c0001t0004g0240 a0001c0001t0005g0279 a0001c0001t0005g0280 others(4): Show |
7 | HG01952.hp2 HG02602.hp2 HG02698.hp1 others(4): Show |
intron_variant | MODIFIER | c.241-7205_241-7204i others(42): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134929613 | ||||||
chr2:134929613 | C | CAGAGAGA others(35): Show |
4 | a0001c0001t0004g0241 a0001c0001t0005g0295 a0001c0001t0005g0299 others(1): Show |
4 | HG02080.hp1 HG02698.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.241-7205_241-7204i others(44): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134929613 | ||||||
chr2:134929613 | C | CAGAGAGA others(37): Show |
3 | a0001c0001t0005g0323 a0001c0001t0006g0294 a0001c0001t0006g0322 |
3 | HG00609.hp2 HG01978.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.241-7205_241-7204i others(46): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134929613 | ||||||
chr2:134929613 | C | CAGAGAGA others(39): Show |
3 | a0001c0001t0005g0314 a0001c0001t0006g0327 a0001c0004t0005g0176 |
3 | HG00408.hp2 HG02486.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.241-7205_241-7204i others(48): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134929613 | ||||||
chr2:134929613 | C | CAGAGAGA others(41): Show |
3 | a0001c0001t0005g0305 a0001c0004t0005g0174 a0001c0004t0005g0177 |
3 | HG02280.hp1 HG02965.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.241-7205_241-7204i others(50): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134929613 | ||||||
chr2:134929613 | C | CAGAGAGA others(45): Show |
2 | a0001c0001t0005g0306 a0001c0004t0005g0178 |
2 | NA18968.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.241-7205_241-7204i others(54): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134929613 | ||||||
chr2:134929613 | C | CAGAGAGA others(55): Show |
1 | a0001c0001t0005g0281 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.241-7205_241-7204i others(64): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134929613 | ||||||
chr2:134929636 | A | AGAGAGAG others(8): Show |
1 | a0001c0001t0001g0165 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.241-7205_241-7204i others(17): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134929636 | |||||||
chr2:134929652 | C | G | 27 | a0001c0001t0004g0031 a0001c0001t0004g0032 a0001c0001t0004g0223 others(24): Show |
29 | HG01074.hp2 HG01168.hp1 HG01358.hp1 others(26): Show |
intron_variant | MODIFIER | c.241-7189C>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134929652 | |||||||
chr2:134929653 | CT | C | 222 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(219): Show |
246 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(243): Show |
intron_variant | MODIFIER | c.241-7174delT | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134929653 | ||||||
chr2:134929660 | T | C | 3 | a0001c0001t0004g0228 a0001c0001t0004g0229 a0001c0001t0004g0331 |
3 | NA18951.hp2 NA18966.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.241-7181T>C | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134929660 | |||||||
chr2:134929810 | C | T | 1 | a0006c0009t0004g0245 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.241-7031C>T | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134929810 | |||||||
chr2:134929838 | G | A | 180 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0016 others(177): Show |
199 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(196): Show |
intron_variant | MODIFIER | c.241-7003G>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134929838 | |||||||
chr2:134929990 | G | A | 1 | a0001c0001t0001g0080 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.241-6851G>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134929990 | |||||||
chr2:134930115 | A | G | 1 | a0001c0003t0022g0124 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.241-6726A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134930115 | |||||||
chr2:134930297 | A | G | 2 | a0001c0003t0012g0035 a0001c0003t0012g0036 |
2 | NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.241-6544A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134930297 | |||||||
chr2:134930432 | G | T | 11 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0016 others(8): Show |
18 | HG00639.hp1 HG00735.hp2 HG01358.hp2 others(15): Show |
intron_variant | MODIFIER | c.241-6409G>T | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134930432 | |||||||
chr2:134930463 | A | G | 2 | a0001c0001t0001g0033 a0001c0001t0021g0033 |
2 | HG01433.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.241-6378A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134930463 | |||||||
chr2:134930533 | T | C | 2 | a0001c0001t0001g0081 a0001c0001t0019g0082 |
2 | NA19054.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.241-6308T>C | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134930533 | |||||||
chr2:134930681 | G | A | 46 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0025 others(43): Show |
56 | HG00408.hp1 HG00438.hp2 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.241-6160G>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134930681 | |||||||
chr2:134930695 | G | A | 6 | a0001c0003t0002g0034 a0001c0003t0002g0117 a0001c0003t0002g0118 others(3): Show |
6 | HG02615.hp1 HG02717.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.241-6146G>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134930695 | |||||||
chr2:134930734 | A | G | 7 | a0001c0002t0002g0006 a0001c0002t0002g0023 a0001c0002t0002g0044 others(4): Show |
11 | HG00438.hp1 HG00558.hp1 HG02040.hp1 others(8): Show |
intron_variant | MODIFIER | c.241-6107A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134930734 | |||||||
chr2:134930750 | A | G | 1 | a0006c0009t0004g0245 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.241-6091A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134930750 | |||||||
chr2:134930810 | T | G | 1 | a0001c0002t0002g0052 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.241-6031T>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134930810 | |||||||
chr2:134930830 | C | T | 1 | a0001c0001t0004g0263 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.241-6011C>T | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134930830 | |||||||
chr2:134930969 | A | AT | 112 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0126 others(109): Show |
124 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.241-5858dupT | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134930969 | ||||||
chr2:134930969 | A | ATT | 9 | a0001c0001t0003g0183 a0001c0001t0003g0198 a0001c0001t0003g0214 others(6): Show |
9 | HG02071.hp1 HG03492.hp1 HG03579.hp2 others(6): Show |
intron_variant | MODIFIER | c.241-5859_241-5858d others(4): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134930969 | ||||||
chr2:134930969 | AT | A | 11 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0016 others(8): Show |
18 | HG00639.hp1 HG00735.hp2 HG01358.hp2 others(15): Show |
intron_variant | MODIFIER | c.241-5858delT | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134930969 | ||||||
chr2:134931024 | G | A | 6 | a0001c0003t0002g0034 a0001c0003t0002g0117 a0001c0003t0002g0118 others(3): Show |
6 | HG02615.hp1 HG02717.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.241-5817G>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134931024 | |||||||
chr2:134931089 | A | G | 1 | a0001c0002t0002g0063 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.241-5752A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134931089 | |||||||
chr2:134931138 | A | G | 103 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(100): Show |
115 | HG00544.hp1 HG00558.hp2 HG00597.hp2 others(112): Show |
intron_variant | MODIFIER | c.241-5703A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134931138 | |||||||
chr2:134931260 | A | ATTTTTTT others(5): Show |
1 | a0001c0001t0003g0214 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.241-5580_241-5579i others(14): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134931260 | ||||||
chr2:134931262 | C | CT | 20 | a0001c0002t0002g0010 a0001c0002t0002g0011 a0001c0002t0002g0019 others(17): Show |
25 | HG01175.hp2 HG01257.hp2 HG01261.hp1 others(22): Show |
intron_variant | MODIFIER | c.241-5554dupT | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134931262 | ||||||
chr2:134931262 | C | CTT | 5 | a0001c0002t0002g0020 a0001c0002t0002g0050 a0001c0002t0002g0062 others(2): Show |
6 | HG02630.hp1 HG02647.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.241-5555_241-5554d others(4): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134931262 | ||||||
chr2:134931262 | C | CTTTTTTT others(5): Show |
1 | a0001c0001t0005g0181 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.241-5565_241-5554d others(14): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134931262 | ||||||
chr2:134931262 | C | CTTTTTTT others(6): Show |
12 | a0001c0001t0003g0027 a0001c0001t0003g0029 a0001c0001t0003g0184 others(9): Show |
14 | HG00408.hp1 HG01346.hp2 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.241-5566_241-5554d others(15): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134931262 | ||||||
chr2:134931262 | C | CTTTTTTT others(7): Show |
12 | a0001c0001t0003g0013 a0001c0001t0003g0030 a0001c0001t0003g0186 others(9): Show |
15 | HG00438.hp2 HG00597.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.241-5567_241-5554d others(16): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134931262 | ||||||
chr2:134931262 | C | CTTTTTTT others(8): Show |
18 | a0001c0001t0003g0014 a0001c0001t0003g0025 a0001c0001t0003g0028 others(15): Show |
22 | HG02071.hp1 HG02083.hp2 NA18939.hp1 others(19): Show |
intron_variant | MODIFIER | c.241-5568_241-5554d others(17): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134931262 | ||||||
chr2:134931262 | C | CTTTTTTT others(9): Show |
34 | a0001c0001t0003g0026 a0001c0001t0003g0197 a0001c0001t0003g0198 others(31): Show |
36 | HG00140.hp2 HG00544.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.241-5569_241-5554d others(18): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134931262 | ||||||
chr2:134931262 | C | CTTTTTTT others(10): Show |
34 | a0001c0001t0001g0147 a0001c0001t0001g0151 a0001c0001t0001g0167 others(31): Show |
34 | HG01069.hp1 HG01071.hp2 HG01168.hp2 others(31): Show |
intron_variant | MODIFIER | c.241-5570_241-5554d others(19): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134931262 | ||||||
chr2:134931262 | C | CTTTTTTT others(11): Show |
23 | a0001c0001t0001g0024 a0001c0001t0001g0144 a0001c0001t0004g0031 others(20): Show |
25 | HG00609.hp2 HG01074.hp1 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.241-5571_241-5554d others(20): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134931262 | ||||||
chr2:134931262 | C | CTTTTTTT others(12): Show |
22 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0145 others(19): Show |
26 | HG00408.hp2 HG00642.hp2 HG01358.hp1 others(23): Show |
intron_variant | MODIFIER | c.241-5572_241-5554d others(21): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134931262 | ||||||
chr2:134931262 | C | CTTTTTTT others(13): Show |
14 | a0001c0001t0001g0007 a0001c0001t0001g0071 a0001c0001t0001g0085 others(11): Show |
17 | HG00609.hp1 HG00621.hp2 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.241-5573_241-5554d others(22): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134931262 | ||||||
chr2:134931262 | C | CTTTTTTT others(14): Show |
22 | a0001c0001t0001g0012 a0001c0001t0001g0070 a0001c0001t0001g0073 others(19): Show |
24 | HG00621.hp1 HG00642.hp1 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.241-5574_241-5554d others(23): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134931262 | ||||||
chr2:134931262 | C | CTTTTTTT others(15): Show |
15 | a0001c0001t0001g0048 a0001c0001t0001g0081 a0001c0001t0001g0091 others(12): Show |
15 | HG00544.hp1 HG01361.hp1 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.241-5575_241-5554d others(24): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134931262 | ||||||
chr2:134931262 | C | CTTTTTTT others(16): Show |
11 | a0001c0001t0001g0022 a0001c0001t0001g0049 a0001c0001t0001g0093 others(8): Show |
12 | HG00597.hp2 HG01123.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.241-5576_241-5554d others(25): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134931262 | ||||||
chr2:134931262 | C | CTTTTTTT others(17): Show |
7 | a0001c0001t0001g0095 a0001c0001t0001g0108 a0001c0001t0001g0129 others(4): Show |
7 | HG01175.hp1 HG03453.hp1 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.241-5577_241-5554d others(26): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134931262 | ||||||
chr2:134931262 | C | CTTTTTTT others(18): Show |
5 | a0001c0001t0001g0110 a0001c0001t0001g0130 a0001c0001t0001g0131 others(2): Show |
5 | HG03139.hp1 NA18950.hp2 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.241-5578_241-5554d others(27): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134931262 | ||||||
chr2:134931262 | C | CTTTTTTT others(19): Show |
2 | a0001c0001t0001g0109 a0001c0001t0005g0329 |
2 | HG02523.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.241-5554_241-5553i others(28): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134931262 | ||||||
chr2:134931262 | C | CTTTTTTT others(20): Show |
2 | a0001c0001t0004g0253 a0001c0001t0005g0281 |
2 | HG00639.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.241-5554_241-5553i others(29): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134931262 | ||||||
chr2:134931262 | C | CTTTTTTT others(21): Show |
3 | a0001c0001t0018g0180 a0002c0005t0005g0302 a0002c0005t0005g0304 |
3 | HG01243.hp2 NA18973.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.241-5554_241-5553i others(30): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134931262 | ||||||
chr2:134931262 | C | CTTTTTTT others(23): Show |
1 | a0001c0001t0001g0080 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.241-5554_241-5553i others(32): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134931262 | ||||||
chr2:134931262 | C | CTTTTTTT others(25): Show |
3 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0140 |
3 | HG00558.hp2 HG03669.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.241-5554_241-5553i others(34): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134931262 | ||||||
chr2:134931262 | C | CTTTTTTT others(26): Show |
1 | a0001c0003t0002g0119 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.241-5554_241-5553i others(35): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134931262 | ||||||
chr2:134931262 | C | CTTTTTTT others(34): Show |
1 | a0001c0001t0001g0096 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.241-5554_241-5553i others(43): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134931262 | ||||||
chr2:134931262 | C | T | 1 | a0001c0001t0003g0214 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.241-5579C>T | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134931262 | |||||||
chr2:134931262 | CT | C | 9 | a0001c0001t0001g0015 a0001c0001t0001g0033 a0001c0001t0001g0101 others(6): Show |
11 | HG00639.hp1 HG01169.hp2 HG01358.hp2 others(8): Show |
intron_variant | MODIFIER | c.241-5554delT | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134931262 | ||||||
chr2:134931262 | CTTTTTTT others(2): Show |
C | 6 | a0001c0001t0007g0282 a0001c0001t0007g0283 a0001c0001t0007g0284 others(3): Show |
6 | HG02109.hp1 HG02257.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.241-5562_241-5554d others(11): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134931262 | ||||||
chr2:134931284 | T | TTTTTTTT others(14): Show |
1 | a0001c0001t0001g0047 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.241-5554_241-5553i others(23): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134931284 | ||||||
chr2:134931351 | T | G | 47 | a0001c0001t0005g0277 a0001c0001t0005g0278 a0001c0001t0005g0279 others(44): Show |
47 | HG00408.hp2 HG00544.hp2 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.241-5490T>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134931351 | |||||||
chr2:134931586 | T | C | 2 | a0001c0003t0002g0045 a0001c0003t0002g0066 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.241-5255T>C | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134931586 | |||||||
chr2:134931618 | G | T | 332 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(329): Show |
383 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(380): Show |
intron_variant | MODIFIER | c.241-5223G>T | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134931618 | |||||||
chr2:134931674 | C | A | 1 | a0001c0001t0004g0241 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.241-5167C>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134931674 | |||||||
chr2:134931802 | G | T | 2 | a0001c0003t0012g0035 a0001c0003t0012g0036 |
2 | NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.241-5039G>T | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134931802 | |||||||
chr2:134931982 | G | T | 10 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0016 others(7): Show |
17 | HG00639.hp1 HG00735.hp2 HG01358.hp2 others(14): Show |
intron_variant | MODIFIER | c.241-4859G>T | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134931982 | |||||||
chr2:134932029 | T | C | 1 | a0001c0001t0003g0205 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.241-4812T>C | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134932029 | |||||||
chr2:134932167 | G | A | 1 | a0001c0001t0005g0219 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.241-4674G>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134932167 | |||||||
chr2:134932186 | ATG | A | 179 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0016 others(176): Show |
198 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(195): Show |
intron_variant | MODIFIER | c.241-4651_241-4650d others(4): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134932186 | ||||||
chr2:134932261 | G | A | 6 | a0001c0004t0005g0174 a0001c0004t0005g0175 a0001c0004t0005g0176 others(3): Show |
6 | HG02280.hp1 HG02486.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.241-4580G>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134932261 | |||||||
chr2:134932263 | A | C | 6 | a0001c0004t0005g0174 a0001c0004t0005g0175 a0001c0004t0005g0176 others(3): Show |
6 | HG02280.hp1 HG02486.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.241-4578A>C | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134932263 | |||||||
chr2:134932288 | A | G | 1 | a0001c0003t0022g0124 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.241-4553A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134932288 | |||||||
chr2:134932296 | C | T | 1 | a0001c0002t0013g0136 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.241-4545C>T | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134932296 | |||||||
chr2:134932475 | A | G | 6 | a0001c0004t0005g0174 a0001c0004t0005g0175 a0001c0004t0005g0176 others(3): Show |
6 | HG02280.hp1 HG02486.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.241-4366A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134932475 | |||||||
chr2:134932491 | C | T | 103 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(100): Show |
115 | HG00544.hp1 HG00558.hp2 HG00597.hp2 others(112): Show |
intron_variant | MODIFIER | c.241-4350C>T | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134932491 | |||||||
chr2:134932788 | T | TA | 47 | a0001c0001t0005g0277 a0001c0001t0005g0278 a0001c0001t0005g0279 others(44): Show |
47 | HG00408.hp2 HG00544.hp2 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.241-4052dupA | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134932788 | ||||||
chr2:134932912 | T | C | 1 | a0001c0001t0005g0219 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.241-3929T>C | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134932912 | |||||||
chr2:134932914 | G | A | 1 | a0001c0001t0005g0306 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.241-3927G>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134932914 | |||||||
chr2:134932925 | A | G | 1 | a0001c0001t0004g0235 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.241-3916A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134932925 | |||||||
chr2:134933497 | A | G | 1 | a0001c0001t0005g0306 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.241-3344A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134933497 | |||||||
chr2:134933621 | G | A | 178 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0016 others(175): Show |
197 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(194): Show |
intron_variant | MODIFIER | c.241-3220G>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134933621 | |||||||
chr2:134933794 | T | G | 1 | a0001c0001t0003g0188 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.241-3047T>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134933794 | |||||||
chr2:134933842 | G | A | 1 | a0001c0001t0004g0273 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.241-2999G>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134933842 | |||||||
chr2:134933903 | A | G | 6 | a0001c0004t0005g0174 a0001c0004t0005g0175 a0001c0004t0005g0176 others(3): Show |
6 | HG02280.hp1 HG02486.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.241-2938A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134933903 | |||||||
chr2:134933925 | G | C | 1 | a0001c0001t0003g0214 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.241-2916G>C | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134933925 | |||||||
chr2:134933926 | C | G | 1 | a0001c0001t0003g0214 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.241-2915C>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134933926 | |||||||
chr2:134933943 | A | G | 1 | a0001c0001t0001g0335 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.241-2898A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134933943 | |||||||
chr2:134934029 | G | A | 19 | a0001c0001t0004g0031 a0001c0001t0004g0032 a0001c0001t0004g0223 others(16): Show |
21 | HG01358.hp1 HG01993.hp1 NA18612.hp1 others(18): Show |
intron_variant | MODIFIER | c.241-2812G>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134934029 | |||||||
chr2:134934089 | A | G | 179 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0016 others(176): Show |
198 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(195): Show |
intron_variant | MODIFIER | c.241-2752A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134934089 | |||||||
chr2:134934155 | A | G | 111 | a0001c0001t0004g0031 a0001c0001t0004g0032 a0001c0001t0004g0182 others(108): Show |
113 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(110): Show |
intron_variant | MODIFIER | c.241-2686A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134934155 | |||||||
chr2:134934470 | A | G | 1 | a0001c0003t0012g0035 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.241-2371A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134934470 | |||||||
chr2:134934750 | C | G | 2 | a0001c0001t0005g0314 a0001c0001t0005g0323 |
2 | NA18984.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.241-2091C>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134934750 | |||||||
chr2:134934785 | C | T | 1 | a0001c0001t0001g0070 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.241-2056C>T | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134934785 | |||||||
chr2:134934794 | GGAAGGAA others(9): Show |
G | 1 | a0001c0001t0010g0163 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.241-2046_241-2031d others(18): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134934794 | |||||||
chr2:134934811 | C | T | 1 | a0001c0001t0010g0163 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.241-2030C>T | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134934811 | |||||||
chr2:134934812 | T | C | 1 | a0001c0001t0010g0163 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.241-2029T>C | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134934812 | |||||||
chr2:134934979 | A | G | 2 | a0001c0001t0004g0266 a0001c0001t0004g0275 |
2 | HG02572.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.241-1862A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134934979 | |||||||
chr2:134935070 | A | G | 27 | a0001c0001t0004g0031 a0001c0001t0004g0032 a0001c0001t0004g0223 others(24): Show |
29 | HG01074.hp2 HG01168.hp1 HG01358.hp1 others(26): Show |
intron_variant | MODIFIER | c.241-1771A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134935070 | |||||||
chr2:134935179 | T | C | 2 | a0001c0003t0002g0045 a0001c0003t0002g0066 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.241-1662T>C | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134935179 | |||||||
chr2:134935257 | T | C | 2 | a0001c0001t0001g0080 a0001c0001t0001g0091 |
2 | HG02080.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.241-1584T>C | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134935257 | |||||||
chr2:134935499 | G | A | 177 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0016 others(174): Show |
196 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(193): Show |
intron_variant | MODIFIER | c.241-1342G>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134935499 | |||||||
chr2:134935667 | T | C | 1 | a0001c0001t0005g0219 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.241-1174T>C | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134935667 | |||||||
chr2:134935807 | TA | T | 7 | a0001c0001t0001g0003 a0001c0001t0001g0145 a0001c0001t0015g0155 others(4): Show |
12 | HG02148.hp1 HG02300.hp1 HG02896.hp2 others(9): Show |
intron_variant | MODIFIER | c.241-1022delA | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134935807 | ||||||
chr2:134935820 | T | A | 45 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0025 others(42): Show |
55 | HG00408.hp1 HG00438.hp2 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.241-1021T>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134935820 | |||||||
chr2:134935886 | C | G | 1 | a0001c0001t0001g0165 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.241-955C>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134935886 | |||||||
chr2:134935967 | C | G | 26 | a0001c0001t0004g0182 a0001c0001t0004g0244 a0001c0001t0004g0246 others(23): Show |
26 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.241-874C>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134935967 | |||||||
chr2:134936011 | A | G | 1 | a0001c0003t0022g0124 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.241-830A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134936011 | |||||||
chr2:134936122 | A | G | 2 | a0001c0003t0012g0035 a0001c0003t0012g0036 |
2 | NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.241-719A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134936122 | |||||||
chr2:134936134 | C | G | 2 | a0001c0003t0012g0035 a0001c0003t0012g0036 |
2 | NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.241-707C>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134936134 | |||||||
chr2:134936151 | C | CT | 6 | a0001c0001t0001g0033 a0001c0001t0005g0181 a0001c0001t0005g0324 others(3): Show |
6 | HG01433.hp2 HG02809.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.241-675dupT | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134936151 | ||||||
chr2:134936151 | CT | C | 108 | a0001c0001t0003g0183 a0001c0001t0004g0031 a0001c0001t0004g0032 others(105): Show |
111 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.241-675delT | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 134936151 | ||||||
chr2:134936211 | C | T | 2 | a0001c0001t0001g0080 a0001c0001t0001g0091 |
2 | HG02080.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.241-630C>T | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134936211 | |||||||
chr2:134936213 | A | G | 6 | a0001c0002t0002g0011 a0001c0002t0002g0020 a0001c0002t0002g0050 others(3): Show |
9 | HG02257.hp2 HG02647.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.241-628A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134936213 | |||||||
chr2:134936419 | A | C | 1 | a0001c0001t0018g0180 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.241-422A>C | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134936419 | |||||||
chr2:134936445 | G | C | 1 | a0001c0001t0003g0194 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.241-396G>C | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134936445 | |||||||
chr2:134936692 | T | A | 1 | a0001c0003t0002g0039 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.241-149T>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134936692 | |||||||
chr2:134936784 | G | C | 177 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0016 others(174): Show |
196 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(193): Show |
intron_variant | MODIFIER | c.241-57G>C | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134936784 | |||||||
chr2:134936809 | C | T | 286 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(283): Show |
317 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(314): Show |
intron_variant | MODIFIER | c.241-32C>T | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134936809 | |||||||
chr2:134936828 | A | C | 1 | a0001c0001t0004g0235 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.241-13A>C | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 2/8 | chr2 | 134936828 | |||||||
chr2:134937026 | G | A | 1 | a0001c0001t0001g0132 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.369+57G>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 3/8 | chr2 | 134937026 | |||||||
chr2:134937038 | A | G | 1 | a0001c0001t0005g0310 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.369+69A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 3/8 | chr2 | 134937038 | |||||||
chr2:134937062 | G | A | 6 | a0001c0001t0007g0282 a0001c0001t0007g0283 a0001c0001t0007g0284 others(3): Show |
6 | HG02109.hp1 HG02257.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.369+93G>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 3/8 | chr2 | 134937062 | |||||||
chr2:134937135 | T | C | 1 | a0001c0004t0005g0175 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.369+166T>C | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 3/8 | chr2 | 134937135 | |||||||
chr2:134937278 | G | A | 288 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(285): Show |
319 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(316): Show |
intron_variant | MODIFIER | c.369+309G>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 3/8 | chr2 | 134937278 | |||||||
chr2:134937279 | C | T | 11 | a0001c0002t0002g0019 a0001c0002t0002g0052 a0001c0002t0002g0059 others(8): Show |
12 | HG02015.hp2 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.369+310C>T | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 3/8 | chr2 | 134937279 | |||||||
chr2:134937497 | G | A | 2 | a0001c0001t0006g0322 a0001c0001t0006g0327 |
2 | HG00408.hp2 HG00609.hp2 |
intron_variant | MODIFIER | c.369+528G>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 3/8 | chr2 | 134937497 | |||||||
chr2:134937582 | AAGAAATA others(3): Show |
A | 1 | a0001c0001t0004g0244 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.369+625_369+634del others(10): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 134937582 | ||||||
chr2:134937694 | T | A | 1 | a0001c0003t0012g0036 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.369+725T>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 3/8 | chr2 | 134937694 | |||||||
chr2:134937728 | C | T | 4 | a0001c0001t0001g0015 a0001c0001t0001g0033 a0001c0001t0001g0335 others(1): Show |
6 | HG00639.hp1 HG01433.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.369+759C>T | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 3/8 | chr2 | 134937728 | |||||||
chr2:134937752 | T | G | 1 | a0001c0001t0005g0298 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.369+783T>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 3/8 | chr2 | 134937752 | |||||||
chr2:134937753 | A | G | 6 | a0001c0001t0007g0282 a0001c0001t0007g0283 a0001c0001t0007g0284 others(3): Show |
6 | HG02109.hp1 HG02257.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.369+784A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 3/8 | chr2 | 134937753 | |||||||
chr2:134938305 | A | G | 2 | a0001c0002t0002g0172 a0001c0002t0002g0173 |
2 | HG03041.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.370-697A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 3/8 | chr2 | 134938305 | |||||||
chr2:134938360 | A | G | 1 | a0001c0001t0001g0098 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.370-642A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 3/8 | chr2 | 134938360 | |||||||
chr2:134938431 | G | T | 1 | a0001c0001t0005g0307 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.370-571G>T | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 3/8 | chr2 | 134938431 | |||||||
chr2:134938481 | G | A | 179 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0016 others(176): Show |
198 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(195): Show |
intron_variant | MODIFIER | c.370-521G>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 3/8 | chr2 | 134938481 | |||||||
chr2:134938697 | C | T | 4 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0332 others(1): Show |
9 | HG00735.hp2 HG02145.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.370-305C>T | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 3/8 | chr2 | 134938697 | |||||||
chr2:134938768 | A | G | 17 | a0001c0002t0002g0011 a0001c0002t0002g0019 a0001c0002t0002g0020 others(14): Show |
21 | HG02015.hp2 HG02257.hp2 HG02451.hp2 others(18): Show |
intron_variant | MODIFIER | c.370-234A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 3/8 | chr2 | 134938768 | |||||||
chr2:134939116 | T | C | 1 | a0001c0001t0018g0180 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.430+54T>C | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 4/8 | chr2 | 134939116 | |||||||
chr2:134939154 | G | C | 2 | a0001c0001t0005g0314 a0001c0001t0005g0323 |
2 | NA18984.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.430+92G>C | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 4/8 | chr2 | 134939154 | |||||||
chr2:134939193 | G | T | 8 | a0001c0001t0005g0181 a0001c0001t0005g0324 a0001c0001t0007g0282 others(5): Show |
8 | HG02109.hp1 HG02257.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.430+131G>T | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 4/8 | chr2 | 134939193 | |||||||
chr2:134939444 | A | G | 181 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0016 others(178): Show |
200 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(197): Show |
intron_variant | MODIFIER | c.430+382A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 4/8 | chr2 | 134939444 | |||||||
chr2:134939454 | T | TTTTA | 6 | a0001c0001t0007g0282 a0001c0001t0007g0283 a0001c0001t0007g0284 others(3): Show |
6 | HG02109.hp1 HG02257.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.430+416_430+419dup others(4): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 134939454 | ||||||
chr2:134939679 | T | A | 103 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(100): Show |
115 | HG00544.hp1 HG00558.hp2 HG00597.hp2 others(112): Show |
intron_variant | MODIFIER | c.430+617T>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 4/8 | chr2 | 134939679 | |||||||
chr2:134939761 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.430+699C>T | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 4/8 | chr2 | 134939761 | |||||||
chr2:134939770 | A | G | 2 | a0001c0003t0012g0035 a0001c0003t0012g0036 |
2 | NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.430+708A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 4/8 | chr2 | 134939770 | |||||||
chr2:134939826 | G | A | 180 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0016 others(177): Show |
199 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(196): Show |
intron_variant | MODIFIER | c.430+764G>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 4/8 | chr2 | 134939826 | |||||||
chr2:134939864 | T | G | 2 | a0001c0001t0001g0021 a0001c0001t0001g0076 |
3 | HG02109.hp2 HG02486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.430+802T>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 4/8 | chr2 | 134939864 | |||||||
chr2:134939973 | C | A | 178 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0016 others(175): Show |
197 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(194): Show |
intron_variant | MODIFIER | c.430+911C>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 4/8 | chr2 | 134939973 | |||||||
chr2:134939987 | A | G | 287 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(284): Show |
318 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(315): Show |
intron_variant | MODIFIER | c.430+925A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 4/8 | chr2 | 134939987 | |||||||
chr2:134940167 | T | C | 180 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0016 others(177): Show |
199 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(196): Show |
intron_variant | MODIFIER | c.430+1105T>C | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 4/8 | chr2 | 134940167 | |||||||
chr2:134940190 | G | C | 103 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(100): Show |
115 | HG00544.hp1 HG00558.hp2 HG00597.hp2 others(112): Show |
intron_variant | MODIFIER | c.430+1128G>C | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 4/8 | chr2 | 134940190 | |||||||
chr2:134940208 | G | A | 1 | a0001c0001t0005g0315 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.430+1146G>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 4/8 | chr2 | 134940208 | |||||||
chr2:134940223 | A | G | 2 | a0001c0001t0003g0200 a0001c0001t0003g0204 |
2 | HG01255.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.430+1161A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 4/8 | chr2 | 134940223 | |||||||
chr2:134940227 | G | T | 177 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0016 others(174): Show |
196 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(193): Show |
intron_variant | MODIFIER | c.430+1165G>T | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 4/8 | chr2 | 134940227 | |||||||
chr2:134940270 | A | AT | 17 | a0001c0001t0004g0031 a0001c0001t0004g0032 a0001c0001t0004g0223 others(14): Show |
19 | NA18612.hp1 NA18951.hp2 NA18956.hp2 others(16): Show |
intron_variant | MODIFIER | c.430+1215dupT | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 134940270 | ||||||
chr2:134940354 | T | TGAAAAAA others(4): Show |
180 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0016 others(177): Show |
199 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(196): Show |
intron_variant | MODIFIER | c.430+1301_430+1302i others(13): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 134940354 | ||||||
chr2:134940386 | CTATATAT others(3): Show |
C | 1 | a0001c0001t0001g0154 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.430+1328_430+1337d others(12): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 134940386 | ||||||
chr2:134940431 | A | G | 178 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0016 others(175): Show |
197 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(194): Show |
intron_variant | MODIFIER | c.430+1369A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 4/8 | chr2 | 134940431 | |||||||
chr2:134940505 | C | T | 178 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0016 others(175): Show |
197 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(194): Show |
intron_variant | MODIFIER | c.430+1443C>T | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 4/8 | chr2 | 134940505 | |||||||
chr2:134940568 | G | A | 11 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0016 others(8): Show |
18 | HG00639.hp1 HG00735.hp2 HG01358.hp2 others(15): Show |
intron_variant | MODIFIER | c.430+1506G>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 4/8 | chr2 | 134940568 | |||||||
chr2:134940637 | G | A | 1 | a0001c0001t0005g0219 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.430+1575G>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 4/8 | chr2 | 134940637 | |||||||
chr2:134940660 | A | T | 1 | a0001c0001t0005g0308 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.430+1598A>T | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 4/8 | chr2 | 134940660 | |||||||
chr2:134940784 | T | C | 2 | a0001c0002t0002g0143 a0001c0002t0013g0136 |
2 | HG03130.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.430+1722T>C | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 4/8 | chr2 | 134940784 | |||||||
chr2:134940793 | C | G | 1 | a0001c0001t0003g0203 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.430+1731C>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 4/8 | chr2 | 134940793 | |||||||
chr2:134940942 | G | T | 46 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0025 others(43): Show |
56 | HG00408.hp1 HG00438.hp2 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.431-1670G>T | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 4/8 | chr2 | 134940942 | |||||||
chr2:134940954 | A | G | 2 | a0001c0001t0003g0028 a0001c0001t0003g0205 |
3 | NA18952.hp2 NA19070.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.431-1658A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 4/8 | chr2 | 134940954 | |||||||
chr2:134940975 | G | A | 1 | a0001c0003t0012g0035 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.431-1637G>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 4/8 | chr2 | 134940975 | |||||||
chr2:134941146 | A | G | 2 | a0001c0001t0001g0088 a0001c0001t0001g0090 |
2 | NA18947.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.431-1466A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 4/8 | chr2 | 134941146 | |||||||
chr2:134941153 | C | T | 1 | a0001c0001t0001g0333 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.431-1459C>T | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 4/8 | chr2 | 134941153 | |||||||
chr2:134941322 | A | G | 1 | a0001c0003t0002g0037 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.431-1290A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 4/8 | chr2 | 134941322 | |||||||
chr2:134941474 | T | C | 2 | a0001c0001t0001g0147 a0001c0001t0001g0151 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.431-1138T>C | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 4/8 | chr2 | 134941474 | |||||||
chr2:134941554 | G | A | 2 | a0001c0003t0012g0035 a0001c0003t0012g0036 |
2 | NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.431-1058G>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 4/8 | chr2 | 134941554 | |||||||
chr2:134941554 | G | C | 178 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0016 others(175): Show |
197 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(194): Show |
intron_variant | MODIFIER | c.431-1058G>C | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 4/8 | chr2 | 134941554 | |||||||
chr2:134941591 | T | C | 1 | a0001c0001t0001g0166 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.431-1021T>C | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 4/8 | chr2 | 134941591 | |||||||
chr2:134941647 | T | C | 2 | a0001c0003t0012g0035 a0001c0003t0012g0036 |
2 | NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.431-965T>C | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 4/8 | chr2 | 134941647 | |||||||
chr2:134941728 | T | C | 3 | a0001c0001t0005g0310 a0001c0001t0005g0319 a0001c0001t0005g0320 |
3 | HG02735.hp2 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.431-884T>C | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 4/8 | chr2 | 134941728 | |||||||
chr2:134942002 | G | C | 1 | a0001c0003t0002g0037 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.431-610G>C | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 4/8 | chr2 | 134942002 | |||||||
chr2:134942003 | C | A | 1 | a0001c0003t0002g0037 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.431-609C>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 4/8 | chr2 | 134942003 | |||||||
chr2:134942049 | T | C | 57 | a0001c0001t0004g0031 a0001c0001t0004g0032 a0001c0001t0004g0182 others(54): Show |
59 | HG00140.hp2 HG00639.hp2 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.431-563T>C | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 4/8 | chr2 | 134942049 | |||||||
chr2:134942276 | A | G | 46 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0025 others(43): Show |
56 | HG00408.hp1 HG00438.hp2 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.431-336A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 4/8 | chr2 | 134942276 | |||||||
chr2:134942361 | A | G | 6 | a0001c0002t0002g0011 a0001c0002t0002g0020 a0001c0002t0002g0050 others(3): Show |
9 | HG02257.hp2 HG02647.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.431-251A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 4/8 | chr2 | 134942361 | |||||||
chr2:134942451 | A | G | 2 | a0001c0003t0002g0045 a0001c0003t0002g0066 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.431-161A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 4/8 | chr2 | 134942451 | |||||||
chr2:134942581 | A | T | 179 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0016 others(176): Show |
198 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(195): Show |
intron_variant | MODIFIER | c.431-31A>T | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 4/8 | chr2 | 134942581 | |||||||
chr2:134942806 | G | A | 2 | a0001c0003t0012g0035 a0001c0003t0012g0036 |
2 | NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.493+132G>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 5/8 | chr2 | 134942806 | |||||||
chr2:134942828 | A | G | 1 | a0001c0001t0004g0264 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.493+154A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 5/8 | chr2 | 134942828 | |||||||
chr2:134942904 | T | G | 4 | a0001c0002t0002g0019 a0001c0002t0002g0059 a0001c0002t0002g0060 others(1): Show |
5 | HG02015.hp2 NA18985.hp1 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.493+230T>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 5/8 | chr2 | 134942904 | |||||||
chr2:134942912 | G | C | 1 | a0001c0001t0004g0237 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.493+238G>C | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 5/8 | chr2 | 134942912 | |||||||
chr2:134942931 | C | T | 1 | a0001c0003t0002g0039 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.493+257C>T | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 5/8 | chr2 | 134942931 | |||||||
chr2:134942933 | A | G | 11 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0016 others(8): Show |
18 | HG00639.hp1 HG00735.hp2 HG01358.hp2 others(15): Show |
intron_variant | MODIFIER | c.493+259A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 5/8 | chr2 | 134942933 | |||||||
chr2:134943070 | T | C | 1 | a0001c0002t0002g0053 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.493+396T>C | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 5/8 | chr2 | 134943070 | |||||||
chr2:134943128 | C | T | 1 | a0001c0001t0005g0279 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.493+454C>T | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 5/8 | chr2 | 134943128 | |||||||
chr2:134943230 | A | G | 2 | a0001c0002t0002g0143 a0001c0002t0013g0136 |
2 | HG03130.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.493+556A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 5/8 | chr2 | 134943230 | |||||||
chr2:134943313 | A | G | 1 | a0001c0003t0012g0036 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.493+639A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 5/8 | chr2 | 134943313 | |||||||
chr2:134943347 | G | T | 3 | a0001c0003t0002g0037 a0001c0003t0002g0045 a0001c0003t0002g0066 |
3 | HG02896.hp2 HG02897.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.493+673G>T | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 5/8 | chr2 | 134943347 | |||||||
chr2:134943387 | G | A | 5 | a0001c0004t0005g0174 a0001c0004t0005g0175 a0001c0004t0005g0176 others(2): Show |
5 | HG02280.hp1 HG02486.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.493+713G>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 5/8 | chr2 | 134943387 | |||||||
chr2:134943411 | A | G | 6 | a0001c0001t0004g0251 a0001c0001t0004g0252 a0001c0001t0004g0254 others(3): Show |
6 | HG00140.hp2 HG00642.hp2 HG01070.hp2 others(3): Show |
intron_variant | MODIFIER | c.493+737A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 5/8 | chr2 | 134943411 | |||||||
chr2:134943454 | C | A | 1 | a0001c0001t0004g0269 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.493+780C>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 5/8 | chr2 | 134943454 | |||||||
chr2:134943701 | A | G | 1 | a0001c0001t0005g0306 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.493+1027A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 5/8 | chr2 | 134943701 | |||||||
chr2:134943870 | T | G | 1 | a0001c0001t0003g0203 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.493+1196T>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 5/8 | chr2 | 134943870 | |||||||
chr2:134943879 | A | G | 1 | a0001c0002t0013g0136 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.493+1205A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 5/8 | chr2 | 134943879 | |||||||
chr2:134943919 | T | C | 175 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0016 others(172): Show |
194 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(191): Show |
intron_variant | MODIFIER | c.493+1245T>C | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 5/8 | chr2 | 134943919 | |||||||
chr2:134944092 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.493+1418G>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 5/8 | chr2 | 134944092 | |||||||
chr2:134944140 | ATGGT | A | 6 | a0001c0003t0002g0034 a0001c0003t0002g0117 a0001c0003t0002g0118 others(3): Show |
6 | HG02615.hp1 HG02717.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.493+1468_493+1471d others(6): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 134944140 | ||||||
chr2:134944230 | A | G | 5 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(2): Show |
5 | NA18942.hp2 NA18943.hp1 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.493+1556A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 5/8 | chr2 | 134944230 | |||||||
chr2:134944259 | G | A | 179 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0016 others(176): Show |
198 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(195): Show |
intron_variant | MODIFIER | c.493+1585G>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 5/8 | chr2 | 134944259 | |||||||
chr2:134944272 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.493+1598G>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 5/8 | chr2 | 134944272 | |||||||
chr2:134944370 | A | T | 1 | a0001c0001t0001g0164 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.493+1696A>T | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 5/8 | chr2 | 134944370 | |||||||
chr2:134944530 | A | G | 2 | a0001c0002t0002g0143 a0001c0002t0013g0136 |
2 | HG03130.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.494-1571A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 5/8 | chr2 | 134944530 | |||||||
chr2:134944566 | C | A | 103 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(100): Show |
115 | HG00544.hp1 HG00558.hp2 HG00597.hp2 others(112): Show |
intron_variant | MODIFIER | c.494-1535C>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 5/8 | chr2 | 134944566 | |||||||
chr2:134944696 | A | G | 1 | a0001c0001t0004g0258 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.494-1405A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 5/8 | chr2 | 134944696 | |||||||
chr2:134944726 | A | G | 1 | a0001c0001t0003g0187 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.494-1375A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 5/8 | chr2 | 134944726 | |||||||
chr2:134944940 | A | C | 1 | a0001c0001t0005g0280 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.494-1161A>C | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 5/8 | chr2 | 134944940 | |||||||
chr2:134944949 | T | C | 1 | a0001c0001t0001g0109 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.494-1152T>C | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 5/8 | chr2 | 134944949 | |||||||
chr2:134944967 | C | G | 4 | a0001c0001t0003g0025 a0001c0001t0003g0028 a0001c0001t0003g0197 others(1): Show |
6 | NA18952.hp2 NA18973.hp2 NA19010.hp1 others(3): Show |
intron_variant | MODIFIER | c.494-1134C>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 5/8 | chr2 | 134944967 | |||||||
chr2:134945387 | G | A | 1 | a0001c0001t0001g0106 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.494-714G>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 5/8 | chr2 | 134945387 | |||||||
chr2:134945388 | A | G | 1 | a0001c0001t0001g0106 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.494-713A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 5/8 | chr2 | 134945388 | |||||||
chr2:134945391 | G | A | 1 | a0001c0001t0001g0106 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.494-710G>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 5/8 | chr2 | 134945391 | |||||||
chr2:134945597 | G | A | 3 | a0001c0003t0002g0037 a0001c0003t0002g0045 a0001c0003t0002g0066 |
3 | HG02896.hp2 HG02897.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.494-504G>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 5/8 | chr2 | 134945597 | |||||||
chr2:134945692 | T | C | 1 | a0001c0002t0002g0054 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.494-409T>C | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 5/8 | chr2 | 134945692 | |||||||
chr2:134945768 | CT | C | 177 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0016 others(174): Show |
196 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(193): Show |
intron_variant | MODIFIER | c.494-323delT | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 134945768 | ||||||
chr2:134946080 | G | GT | 50 | a0001c0001t0004g0259 a0001c0001t0005g0181 a0001c0001t0005g0277 others(47): Show |
50 | HG00408.hp2 HG00544.hp2 HG00609.hp2 others(47): Show |
splice_region_variant&intron_variant | LOW | c.494-8dupT | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 134946080 | ||||||
chr2:134946240 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.539+94G>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 6/8 | chr2 | 134946240 | |||||||
chr2:134946250 | T | A | 1 | a0001c0001t0004g0256 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.539+104T>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 6/8 | chr2 | 134946250 | |||||||
chr2:134946351 | G | T | 1 | a0001c0001t0019g0082 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.539+205G>T | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 6/8 | chr2 | 134946351 | |||||||
chr2:134946492 | C | T | 1 | a0001c0001t0004g0257 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.539+346C>T | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 6/8 | chr2 | 134946492 | |||||||
chr2:134946516 | T | A | 1 | a0001c0001t0001g0106 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.539+370T>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 6/8 | chr2 | 134946516 | |||||||
chr2:134946520 | A | T | 1 | a0001c0001t0001g0106 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.539+374A>T | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 6/8 | chr2 | 134946520 | |||||||
chr2:134946523 | T | C | 1 | a0001c0001t0001g0106 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.539+377T>C | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 6/8 | chr2 | 134946523 | |||||||
chr2:134946681 | C | T | 1 | a0001c0001t0001g0106 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.539+535C>T | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 6/8 | chr2 | 134946681 | |||||||
chr2:134946682 | C | CT | 9 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0139 others(6): Show |
9 | HG00558.hp2 HG00609.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.539+551dupT | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 134946682 | ||||||
chr2:134946682 | C | CTT | 14 | a0001c0002t0002g0011 a0001c0002t0002g0019 a0001c0002t0002g0020 others(11): Show |
18 | HG02015.hp2 HG02257.hp2 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.539+550_539+551dup others(2): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 134946682 | ||||||
chr2:134946682 | CT | C | 116 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0025 others(113): Show |
128 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.539+551delT | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 134946682 | ||||||
chr2:134946682 | CTT | C | 48 | a0001c0001t0004g0182 a0001c0001t0005g0277 a0001c0001t0005g0278 others(45): Show |
48 | HG00408.hp2 HG00544.hp2 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.539+550_539+551del others(2): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 134946682 | ||||||
chr2:134946683 | T | C | 1 | a0001c0001t0001g0106 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.539+537T>C | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 6/8 | chr2 | 134946683 | |||||||
chr2:134946714 | C | T | 1 | a0001c0003t0026g0116 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.539+568C>T | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 6/8 | chr2 | 134946714 | |||||||
chr2:134946744 | A | G | 1 | a0001c0001t0003g0202 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.539+598A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 6/8 | chr2 | 134946744 | |||||||
chr2:134946962 | A | G | 2 | a0001c0001t0001g0144 a0001c0001t0001g0154 |
2 | HG02293.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.540-774A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 6/8 | chr2 | 134946962 | |||||||
chr2:134946967 | G | A | 55 | a0001c0001t0001g0022 a0001c0001t0001g0047 a0001c0001t0001g0048 others(52): Show |
56 | HG00544.hp1 HG00558.hp2 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.540-769G>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 6/8 | chr2 | 134946967 | |||||||
chr2:134947079 | G | A | 5 | a0001c0001t0004g0235 a0001c0001t0004g0238 a0001c0001t0004g0240 others(2): Show |
5 | HG01168.hp1 HG02698.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.540-657G>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 6/8 | chr2 | 134947079 | |||||||
chr2:134947086 | A | G | 13 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0016 others(10): Show |
20 | HG00639.hp1 HG00735.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.540-650A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 6/8 | chr2 | 134947086 | |||||||
chr2:134947238 | T | A | 2 | a0001c0003t0012g0035 a0001c0003t0012g0036 |
2 | NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.540-498T>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 6/8 | chr2 | 134947238 | |||||||
chr2:134947271 | C | T | 1 | a0001c0001t0005g0278 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.540-465C>T | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 6/8 | chr2 | 134947271 | |||||||
chr2:134947461 | A | T | 1 | a0001c0001t0005g0219 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.540-275A>T | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 6/8 | chr2 | 134947461 | |||||||
chr2:134947526 | G | A | 1 | a0001c0001t0018g0180 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.540-210G>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 6/8 | chr2 | 134947526 | |||||||
chr2:134947527 | G | A | 1 | a0001c0001t0005g0219 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.540-209G>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 6/8 | chr2 | 134947527 | |||||||
chr2:134947954 | T | C | 1 | a0001c0001t0018g0180 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.703+55T>C | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 7/8 | chr2 | 134947954 | |||||||
chr2:134947982 | C | T | 6 | a0001c0004t0005g0174 a0001c0004t0005g0175 a0001c0004t0005g0176 others(3): Show |
6 | HG02280.hp1 HG02486.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.703+83C>T | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 7/8 | chr2 | 134947982 | |||||||
chr2:134947988 | G | A | 332 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(329): Show |
383 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(380): Show |
intron_variant | MODIFIER | c.703+89G>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 7/8 | chr2 | 134947988 | |||||||
chr2:134948034 | A | G | 1 | a0001c0001t0003g0202 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.703+135A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 7/8 | chr2 | 134948034 | |||||||
chr2:134948110 | A | C | 1 | a0001c0002t0013g0136 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.703+211A>C | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 7/8 | chr2 | 134948110 | |||||||
chr2:134948111 | G | A | 1 | a0001c0002t0013g0136 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.703+212G>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 7/8 | chr2 | 134948111 | |||||||
chr2:134948129 | G | A | 2 | a0001c0001t0004g0182 a0001c0001t0005g0279 |
2 | NA19058.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.703+230G>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 7/8 | chr2 | 134948129 | |||||||
chr2:134948244 | G | A | 1 | a0001c0001t0001g0075 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.703+345G>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 7/8 | chr2 | 134948244 | |||||||
chr2:134948350 | ATAAG | A | 57 | a0001c0001t0004g0031 a0001c0001t0004g0032 a0001c0001t0004g0223 others(54): Show |
59 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.703+456_703+459del others(4): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr2 | 134948350 | ||||||
chr2:134948634 | A | G | 6 | a0001c0004t0005g0174 a0001c0004t0005g0175 a0001c0004t0005g0176 others(3): Show |
6 | HG02280.hp1 HG02486.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.703+735A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 7/8 | chr2 | 134948634 | |||||||
chr2:134948699 | T | G | 4 | a0001c0002t0002g0044 a0001c0002t0002g0064 a0001c0002t0002g0065 others(1): Show |
4 | NA18970.hp1 NA18978.hp1 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.703+800T>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 7/8 | chr2 | 134948699 | |||||||
chr2:134948714 | A | G | 1 | a0001c0001t0005g0329 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.703+815A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 7/8 | chr2 | 134948714 | |||||||
chr2:134948720 | C | CT | 110 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0016 others(107): Show |
127 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.703+835dupT | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr2 | 134948720 | ||||||
chr2:134948720 | C | CTT | 15 | a0001c0001t0003g0221 a0001c0001t0005g0277 a0001c0001t0005g0278 others(12): Show |
15 | HG02080.hp1 HG03704.hp1 NA18947.hp1 others(12): Show |
intron_variant | MODIFIER | c.703+834_703+835dup others(2): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr2 | 134948720 | ||||||
chr2:134948720 | C | CTTTT | 32 | a0001c0001t0004g0031 a0001c0001t0004g0032 a0001c0001t0004g0223 others(29): Show |
34 | HG01074.hp2 HG01168.hp1 HG01261.hp2 others(31): Show |
intron_variant | MODIFIER | c.703+832_703+835dup others(4): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr2 | 134948720 | ||||||
chr2:134948720 | C | CTTTTT | 25 | a0001c0001t0004g0241 a0001c0001t0004g0244 a0001c0001t0004g0246 others(22): Show |
25 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.703+831_703+835dup others(5): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr2 | 134948720 | ||||||
chr2:134948751 | G | T | 4 | a0001c0001t0001g0024 a0001c0001t0001g0167 a0001c0001t0001g0168 others(1): Show |
5 | HG01069.hp1 HG01071.hp2 HG01074.hp1 others(2): Show |
intron_variant | MODIFIER | c.703+852G>T | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 7/8 | chr2 | 134948751 | |||||||
chr2:134948907 | G | T | 57 | a0001c0001t0004g0031 a0001c0001t0004g0032 a0001c0001t0004g0223 others(54): Show |
59 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.703+1008G>T | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 7/8 | chr2 | 134948907 | |||||||
chr2:134949058 | C | T | 1 | a0001c0001t0015g0155 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.703+1159C>T | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 7/8 | chr2 | 134949058 | |||||||
chr2:134949124 | G | A | 1 | a0001c0003t0012g0035 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.703+1225G>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 7/8 | chr2 | 134949124 | |||||||
chr2:134949175 | C | T | 3 | a0001c0001t0001g0081 a0001c0001t0001g0083 a0001c0001t0001g0120 |
3 | NA19054.hp1 NA19057.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.703+1276C>T | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 7/8 | chr2 | 134949175 | |||||||
chr2:134949179 | C | G | 46 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0025 others(43): Show |
56 | HG00408.hp1 HG00438.hp2 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.703+1280C>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 7/8 | chr2 | 134949179 | |||||||
chr2:134949186 | A | C | 14 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0150 others(11): Show |
19 | HG00621.hp1 HG00621.hp2 HG00673.hp2 others(16): Show |
intron_variant | MODIFIER | c.703+1287A>C | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 7/8 | chr2 | 134949186 | |||||||
chr2:134949188 | G | T | 286 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(283): Show |
317 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(314): Show |
intron_variant | MODIFIER | c.703+1289G>T | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 7/8 | chr2 | 134949188 | |||||||
chr2:134949251 | G | C | 1 | a0001c0003t0022g0124 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.703+1352G>C | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 7/8 | chr2 | 134949251 | |||||||
chr2:134949324 | T | C | 1 | a0006c0009t0004g0245 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.703+1425T>C | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 7/8 | chr2 | 134949324 | |||||||
chr2:134949367 | C | G | 1 | a0001c0003t0023g0121 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.703+1468C>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 7/8 | chr2 | 134949367 | |||||||
chr2:134949559 | A | G | 1 | a0001c0001t0017g0334 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.703+1660A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 7/8 | chr2 | 134949559 | |||||||
chr2:134949581 | C | A | 1 | a0003c0007t0002g0055 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.703+1682C>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 7/8 | chr2 | 134949581 | |||||||
chr2:134949645 | G | A | 1 | a0001c0001t0005g0298 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.703+1746G>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 7/8 | chr2 | 134949645 | |||||||
chr2:134949759 | T | C | 1 | a0001c0002t0002g0056 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.703+1860T>C | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 7/8 | chr2 | 134949759 | |||||||
chr2:134949802 | C | CG | 112 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0015 others(109): Show |
139 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.703+1913dupG | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr2 | 134949802 | ||||||
chr2:134949802 | C | CGG | 29 | a0001c0001t0001g0008 a0001c0001t0001g0085 a0001c0001t0001g0092 others(26): Show |
35 | HG00735.hp2 HG01358.hp2 HG02027.hp2 others(32): Show |
intron_variant | MODIFIER | c.703+1912_703+1913d others(4): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr2 | 134949802 | ||||||
chr2:134949802 | C | CGGG | 61 | a0001c0001t0001g0335 a0001c0001t0003g0013 a0001c0001t0003g0027 others(58): Show |
67 | HG00408.hp1 HG00438.hp2 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.703+1911_703+1913d others(5): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr2 | 134949802 | ||||||
chr2:134949802 | C | CGGGG | 23 | a0001c0001t0003g0025 a0001c0001t0003g0029 a0001c0001t0003g0030 others(20): Show |
26 | HG00140.hp2 HG00597.hp1 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.703+1910_703+1913d others(6): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr2 | 134949802 | ||||||
chr2:134949811 | G | C | 2 | a0001c0001t0001g0033 a0001c0001t0021g0033 |
2 | HG01433.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.703+1912G>C | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 7/8 | chr2 | 134949811 | |||||||
chr2:134949813 | T | G | 1 | a0001c0001t0003g0218 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.703+1914T>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 7/8 | chr2 | 134949813 | |||||||
chr2:134949837 | AGGCTATA others(6): Show |
A | 1 | a0001c0001t0007g0285 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.703+1941_703+1953d others(15): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr2 | 134949837 | ||||||
chr2:134949943 | T | C | 180 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0016 others(177): Show |
199 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(196): Show |
intron_variant | MODIFIER | c.703+2044T>C | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 7/8 | chr2 | 134949943 | |||||||
chr2:134950072 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.703+2173G>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 7/8 | chr2 | 134950072 | |||||||
chr2:134950181 | T | C | 1 | a0001c0001t0004g0243 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.703+2282T>C | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 7/8 | chr2 | 134950181 | |||||||
chr2:134950280 | A | G | 1 | a0001c0002t0002g0053 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.704-2361A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 7/8 | chr2 | 134950280 | |||||||
chr2:134950386 | A | C | 2 | a0001c0003t0012g0035 a0001c0003t0012g0036 |
2 | NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.704-2255A>C | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 7/8 | chr2 | 134950386 | |||||||
chr2:134950411 | C | T | 2 | a0001c0003t0012g0035 a0001c0003t0012g0036 |
2 | NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.704-2230C>T | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 7/8 | chr2 | 134950411 | |||||||
chr2:134950431 | G | A | 1 | a0001c0004t0005g0175 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.704-2210G>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 7/8 | chr2 | 134950431 | |||||||
chr2:134950439 | G | A | 2 | a0001c0001t0001g0088 a0001c0001t0001g0090 |
2 | NA18947.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.704-2202G>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 7/8 | chr2 | 134950439 | |||||||
chr2:134950505 | C | T | 7 | a0001c0001t0003g0026 a0001c0001t0003g0193 a0001c0001t0003g0196 others(4): Show |
8 | NA18951.hp1 NA18967.hp2 NA19004.hp2 others(5): Show |
intron_variant | MODIFIER | c.704-2136C>T | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 7/8 | chr2 | 134950505 | |||||||
chr2:134950514 | A | G | 1 | a0001c0002t0002g0143 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.704-2127A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 7/8 | chr2 | 134950514 | |||||||
chr2:134950545 | G | A | 11 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0016 others(8): Show |
18 | HG00639.hp1 HG00735.hp2 HG01358.hp2 others(15): Show |
intron_variant | MODIFIER | c.704-2096G>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 7/8 | chr2 | 134950545 | |||||||
chr2:134950838 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.704-1803G>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 7/8 | chr2 | 134950838 | |||||||
chr2:134950981 | C | T | 1 | a0001c0001t0018g0180 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.704-1660C>T | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 7/8 | chr2 | 134950981 | |||||||
chr2:134951039 | T | G | 45 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0025 others(42): Show |
55 | HG00408.hp1 HG00438.hp2 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.704-1602T>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 7/8 | chr2 | 134951039 | |||||||
chr2:134951244 | A | C | 46 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0025 others(43): Show |
56 | HG00408.hp1 HG00438.hp2 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.704-1397A>C | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 7/8 | chr2 | 134951244 | |||||||
chr2:134951269 | T | C | 6 | a0001c0004t0005g0174 a0001c0004t0005g0175 a0001c0004t0005g0176 others(3): Show |
6 | HG02280.hp1 HG02486.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.704-1372T>C | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 7/8 | chr2 | 134951269 | |||||||
chr2:134951283 | A | G | 1 | a0001c0001t0018g0180 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.704-1358A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 7/8 | chr2 | 134951283 | |||||||
chr2:134951651 | G | T | 103 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(100): Show |
115 | HG00544.hp1 HG00558.hp2 HG00597.hp2 others(112): Show |
intron_variant | MODIFIER | c.704-990G>T | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 7/8 | chr2 | 134951651 | |||||||
chr2:134951700 | A | C | 1 | a0001c0001t0003g0210 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.704-941A>C | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 7/8 | chr2 | 134951700 | |||||||
chr2:134951789 | C | T | 1 | a0001c0001t0001g0171 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.704-852C>T | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 7/8 | chr2 | 134951789 | |||||||
chr2:134951871 | C | A | 1 | a0001c0001t0001g0152 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.704-770C>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 7/8 | chr2 | 134951871 | |||||||
chr2:134951879 | C | T | 1 | a0001c0003t0002g0039 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.704-762C>T | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 7/8 | chr2 | 134951879 | |||||||
chr2:134951931 | A | G | 29 | a0001c0001t0001g0047 a0001c0001t0001g0073 a0001c0001t0001g0080 others(26): Show |
29 | HG00558.hp2 HG00609.hp1 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.704-710A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 7/8 | chr2 | 134951931 | |||||||
chr2:134952256 | T | C | 6 | a0001c0001t0007g0282 a0001c0001t0007g0283 a0001c0001t0007g0284 others(3): Show |
6 | HG02109.hp1 HG02257.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.704-385T>C | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 7/8 | chr2 | 134952256 | |||||||
chr2:134952358 | AT | A | 11 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0016 others(8): Show |
18 | HG00639.hp1 HG00735.hp2 HG01358.hp2 others(15): Show |
intron_variant | MODIFIER | c.704-273delT | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr2 | 134952358 | ||||||
chr2:134952368 | T | A | 144 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(141): Show |
156 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(153): Show |
intron_variant | MODIFIER | c.704-273T>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 7/8 | chr2 | 134952368 | |||||||
chr2:134952369 | A | T | 144 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(141): Show |
156 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(153): Show |
intron_variant | MODIFIER | c.704-272A>T | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 7/8 | chr2 | 134952369 | |||||||
chr2:134952371 | T | G | 144 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(141): Show |
156 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(153): Show |
intron_variant | MODIFIER | c.704-270T>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 7/8 | chr2 | 134952371 | |||||||
chr2:134952371 | T | TG | 116 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0025 others(113): Show |
128 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.704-263dupG | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr2 | 134952371 | ||||||
chr2:134952374 | G | A | 6 | a0001c0002t0002g0011 a0001c0002t0002g0020 a0001c0002t0002g0050 others(3): Show |
9 | HG02257.hp2 HG02647.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.704-267G>A | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 7/8 | chr2 | 134952374 | |||||||
chr2:134952375 | G | GA | 11 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0016 others(8): Show |
18 | HG00639.hp1 HG00735.hp2 HG01358.hp2 others(15): Show |
intron_variant | MODIFIER | c.704-266_704-265ins others(1): Show |
CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 7/8 | chr2 | 134952375 | |||||||
chr2:134952752 | A | G | 273 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(270): Show |
304 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(301): Show |
intron_variant | MODIFIER | c.774+41A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 8/8 | chr2 | 134952752 | |||||||
chr2:134952929 | A | G | 1 | a0001c0001t0018g0180 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.774+218A>G | CCNT2 | ENSG00000082258.13 | transcript | ENST00000264157.10 | protein_coding | 8/8 | chr2 | 134952929 |