Variant report

Variant	rs200500600
Chromosome Location	chr12:42445541-42445542
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv430505	chr12:42297931-42720773	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
2	nsv832387	chr12:42345541-42465505	Enhancers Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	esv3336680	chr12:42445250-42445648	Weak transcription	n/a	n/a	inside rSNPs	diseases
4	esv3497133	chr12:42445250-42445648	Weak transcription	n/a	n/a	inside rSNPs	diseases
5	esv3497134	chr12:42445250-42445648	Weak transcription	n/a	n/a	inside rSNPs	diseases
6	esv3445049	chr12:42445258-42445672	Weak transcription	n/a	n/a	inside rSNPs	diseases
7	esv3324164	chr12:42445278-42445584	Weak transcription	n/a	n/a	inside rSNPs	diseases
8	esv3358171	chr12:42445333-42445542	Weak transcription	n/a	n/a	inside rSNPs	diseases
9	esv3393980	chr12:42445489-42445545	Weak transcription	n/a	n/a	inside rSNPs	diseases
10	esv1213283	chr12:42445514-42445552	Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:42444800-42447000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland

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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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