Variant report

Variant	rs536436719
Chromosome Location	chr18:24791603-24791604
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:19 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv909473	chr18:24655235-24792075	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv909474	chr18:24683823-24832023	Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv530515	chr18:24704459-24883897	Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent/Poised TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv518698	chr18:24779601-24793163	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
5	esv3354552	chr18:24789654-24793852	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
6	esv2443116	chr18:24791159-24792709	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
7	esv2344195	chr18:24791391-24792044	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
8	esv3316595	chr18:24791461-24791981	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
9	esv3516625	chr18:24791484-24791966	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
10	esv3516624	chr18:24791488-24791936	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
11	esv7191	chr18:24791488-24791995	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
12	esv4832	chr18:24791511-24791982	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
13	esv3316597	chr18:24791512-24791954	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
14	esv3316594	chr18:24791513-24791944	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
15	esv3316592	chr18:24791531-24791898	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
16	esv3316593	chr18:24791571-24791878	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
17	esv3516623	chr18:24791583-24791875	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
18	esv3316598	chr18:24791587-24791873	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
19	esv3516626	chr18:24791587-24791873	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:24788000-24793000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
2	chr18:24791400-24793000	Enhancers	Breast Myoepithelial Primary Cells	Breast

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

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