Variant report

Variant	rs536425892
Chromosome Location	chr13:95160388-95160389
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 2 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv34004	chr13:94906537-95392644	Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
2	nsv976069	chr13:95160348-95162152	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:95159000-95160400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
2	chr13:95159000-95160400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
3	chr13:95159000-95160400	Enhancers	Primary T helper cells PMA-I stimulated	--
4	chr13:95159000-95160800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
5	chr13:95159000-95161200	Enhancers	Primary T helper cells fromperipheralblood	blood
6	chr13:95159200-95160400	Enhancers	Primary T helper naive cells from peripheral blood	blood
7	chr13:95159200-95160800	Enhancers	Primary T killer memory cells from peripheral blood	blood
8	chr13:95159200-95161200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
9	chr13:95159600-95160800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
10	chr13:95159600-95161800	Enhancers	Dnd41	blood
11	chr13:95159800-95160600	Enhancers	Fetal Thymus	thymus
12	chr13:95159800-95160800	Enhancers	Primary T cells from cord blood	blood

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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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