Variant report

Variant	rs200825768
Chromosome Location	chr7:14680890-14680891
allele	-/GCA
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949033	chr7:14086106-14860323	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv1031041	chr7:14624127-14999201	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv538741	chr7:14624127-14999201	Enhancers Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv1015777	chr7:14661754-14730811	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	esv3390952	chr7:14680576-14681306	Weak transcription	n/a	n/a	inside rSNPs	diseases
6	esv2035361	chr7:14680673-14681152	Weak transcription	n/a	n/a	inside rSNPs	diseases
7	esv3380393	chr7:14680756-14681081	Weak transcription	n/a	n/a	inside rSNPs	diseases
8	esv3515725	chr7:14680798-14681038	Weak transcription	n/a	n/a	inside rSNPs	diseases
9	esv3515724	chr7:14680807-14680975	Weak transcription	n/a	n/a	inside rSNPs	diseases
10	esv3477906	chr7:14680840-14680938	Weak transcription	n/a	n/a	inside rSNPs	diseases
11	esv3477907	chr7:14680854-14680934	Weak transcription	n/a	n/a	inside rSNPs	diseases
12	esv3515726	chr7:14680854-14680971	Weak transcription	n/a	n/a	inside rSNPs	diseases
13	esv1008799	chr7:14680865-14680944	Weak transcription	n/a	n/a	inside rSNPs	diseases
14	esv1572679	chr7:14680890-14680970	Weak transcription	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	chr7:14679200-14683200	Weak transcription	Pancreas	Pancrea
2	chr7:14680400-14684800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	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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