Variant report

Variant	rs147978249
Chromosome Location	chr2:213000464-213000465
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 4 )
Associated
traits (count: 0)

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	nsv1011572	chr2:212840066-213152279	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
2	nsv875802	chr2:212867291-213004603	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	nsv875805	chr2:212891401-213164837	Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv875806	chr2:212997024-213211067	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:213000200-213000800	Enhancers	HUVEC	blood vessel
2	chr2:213000400-213000800	Enhancers	Cortex derived primary cultured neurospheres	brain
3	chr2:213000400-213000800	Enhancers	Brain Inferior Temporal Lobe	brain
4	chr2:213000400-213000800	Enhancers	Fetal Brain Female	brain
5	chr2:213000400-213000800	Enhancers	NHLF	lung
6	chr2:213000400-213001000	Enhancers	Brain Hippocampus Middle	brain
7	chr2:213000400-213001200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr2:213000400-213001400	Enhancers	Fetal Heart	heart
9	chr2:213000400-213001400	Enhancers	Fetal Intestine Small	intestine
10	chr2:213000400-213001600	Enhancers	Fetal Intestine Large	intestine

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Input of quick search could be:

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

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