Variant report

Variant	rs542236862
Chromosome Location	chr4:19522282-19522283
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv878732	chr4:19172031-19660947	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv878733	chr4:19335464-19928602	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv878734	chr4:19474680-19598710	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
4	nsv461286	chr4:19488871-19709795	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
5	nsv593786	chr4:19488871-19709795	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
6	esv3464356	chr4:19519454-19523952	Enhancers	n/a	n/a	inside rSNPs	diseases
7	esv3323853	chr4:19520254-19523202	Enhancers	n/a	n/a	inside rSNPs	diseases
8	esv3464358	chr4:19520379-19523427	Enhancers	n/a	n/a	inside rSNPs	diseases
9	esv3398614	chr4:19520704-19523102	Enhancers	n/a	n/a	inside rSNPs	diseases
10	esv3464357	chr4:19521104-19522602	Enhancers	n/a	n/a	inside rSNPs	diseases
11	esv3464359	chr4:19521104-19522602	Enhancers	n/a	n/a	inside rSNPs	diseases
12	nsv593788	chr4:19521736-19535243	Enhancers Weak transcription	lncRNA	n/a	inside rSNPs	diseases
13	nsv593789	chr4:19521736-19541708	Enhancers Weak transcription	lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:19522200-19523000	Enhancers	Brain Hippocampus Middle	brain
2	chr4:19522200-19523000	Enhancers	Brain Inferior Temporal Lobe	brain
3	chr4:19522200-19523000	Enhancers	Fetal Brain Female	brain

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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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