Variant report

Variant	rs531372685
Chromosome Location	chr5:113335247-113335248
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv471042	chr5:113160490-113440892	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	esv2762537	chr5:113324270-113335389	Active TSS Enhancers	n/a	n/a	inside rSNPs	diseases
3	esv2763922	chr5:113324270-113335389	Active TSS Enhancers	n/a	n/a	inside rSNPs	diseases
4	nsv599418	chr5:113327561-113336598	Enhancers	n/a	n/a	inside rSNPs	diseases
5	nsv599419	chr5:113327561-113339698	Enhancers	n/a	n/a	inside rSNPs	diseases
6	nsv599423	chr5:113330738-113336598	Enhancers	n/a	n/a	inside rSNPs	diseases
7	nsv599427	chr5:113330990-113336598	Enhancers	n/a	n/a	inside rSNPs	diseases
8	nsv599428	chr5:113331136-113336598	Enhancers	n/a	n/a	inside rSNPs	diseases
9	nsv599429	chr5:113331281-113336598	Enhancers	n/a	n/a	inside rSNPs	diseases
10	nsv599430	chr5:113331546-113336598	Enhancers	n/a	n/a	inside rSNPs	diseases
11	nsv599431	chr5:113331616-113336598	Enhancers	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	chr5:113335200-113336200	Enhancers	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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