Variant report

Variant	rs73269118
Chromosome Location	chr12:39047064-39047065
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs57000939	1.00[AMR][1000 genomes]
rs73265276	0.84[AFR][1000 genomes]
rs73265279	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73265281	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73265283	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73265284	1.00[AMR][1000 genomes]
rs73269105	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73269109	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73269194	1.00[AFR][1000 genomes]
rs73273192	1.00[AMR][1000 genomes]
rs73273200	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73274725	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73274731	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2422488	chr12:38103874-39070734	ZNF genes & repeats Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
2	nsv469356	chr12:38242029-39187408	Weak transcription Active TSS ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
3	nsv558574	chr12:38242029-39187408	Strong transcription ZNF genes & repeats Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
4	nsv1039538	chr12:38640895-39180750	Weak transcription Flanking Active TSS Strong transcription Active TSS Enhancers ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
5	nsv1039821	chr12:38959645-39121578	Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
6	nsv1053316	chr12:38959645-39122853	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
7	nsv1043831	chr12:38979065-39117868	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
8	nsv541479	chr12:38979065-39117868	ZNF genes & repeats Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
9	nsv1045040	chr12:39038114-39084094	Strong transcription ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region miRNA target site	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:39039400-39053000	Weak transcription	Left Ventricle	heart
2	chr12:39039800-39055800	Weak transcription	Hela-S3	cervix
3	chr12:39041400-39049400	Weak transcription	Primary hematopoietic stem cells	blood
4	chr12:39043200-39049800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr12:39043800-39050600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
6	chr12:39044200-39055400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr12:39045200-39055400	Weak transcription	Sigmoid Colon	Sigmoid Colon
8	chr12:39045400-39068000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr12:39045800-39047400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
10	chr12:39045800-39050200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr12:39046000-39085400	Weak transcription	Aorta	Aorta
12	chr12:39046200-39051400	Weak transcription	Lung	lung
13	chr12:39046200-39055400	Weak transcription	Rectal Mucosa Donor 31	rectum
14	chr12:39046200-39055600	Weak transcription	Adipose Nuclei	Adipose
15	chr12:39046400-39047800	Strong transcription	Liver	Liver
16	chr12:39046400-39047800	Strong transcription	GM12878-XiMat	blood
17	chr12:39046400-39048000	Strong transcription	Monocytes-CD14+_RO01746	blood
18	chr12:39046800-39048000	Strong transcription	Primary monocytes fromperipheralblood	blood
19	chr12:39046800-39080400	Weak transcription	Spleen	Spleen

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dbSNP/dbVar ID: rs12345 /nsv7879
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