Variant report

Variant	rs12741206
Chromosome Location	chr1:210872177-210872178
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs12735867	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes]
rs12754319	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes]
rs17188444	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes]
rs17188465	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes]
rs17260648	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes]
rs34689382	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes]
rs34700735	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes]
rs34965460	0.82[AMR][1000 genomes]
rs35007206	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes]
rs35486198	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes]
rs35504217	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes]
rs35751839	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes]
rs35936572	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes]
rs61827458	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes]
rs61827459	0.95[AMR][1000 genomes]
rs61829465	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv873148	chr1:210665583-210994339	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
2	nsv873150	chr1:210808270-210893233	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region lncRNA miRNA target site	1 gene(s)	inside rSNPs	diseases
3	nsv468083	chr1:210854815-210876192	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
4	nsv549123	chr1:210854815-210876192	Strong transcription Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:210838000-210880400	Weak transcription	Gastric	stomach
2	chr1:210846400-210884600	Weak transcription	Ovary	ovary
3	chr1:210857200-210882600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr1:210858000-210880400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr1:210864400-210889800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr1:210866800-210884800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr1:210869800-210873400	Weak transcription	Fetal Lung	lung
8	chr1:210869800-210882600	Weak transcription	Brain Anterior Caudate	brain
9	chr1:210870400-210879400	Weak transcription	A549	lung
10	chr1:210870800-210873200	Weak transcription	HSMMtube	muscle
11	chr1:210870800-210873600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
12	chr1:210871000-210873400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
13	chr1:210871200-210873400	Weak transcription	Fetal Muscle Leg	muscle
14	chr1:210871200-210932000	Weak transcription	HSMM	muscle
15	chr1:210872000-210872200	Enhancers	Brain Inferior Temporal Lobe	brain
16	chr1:210872000-210872800	Enhancers	Brain Cingulate Gyrus	brain
17	chr1:210872000-210879200	Weak transcription	Brain Hippocampus Middle	brain

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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