Variant report

Variant	rs200625549
Chromosome Location	chr7:108501545-108501546
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	nsv817371	chr7:108199882-108649799	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
2	nsv1031096	chr7:108334543-108596014	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv888945	chr7:108445757-108521842	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
4	esv3391200	chr7:108501216-108502064	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
5	esv3510426	chr7:108501330-108501656	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
6	esv3510422	chr7:108501351-108501632	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
7	esv3510425	chr7:108501358-108501588	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
8	esv3510424	chr7:108501362-108501586	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
9	esv3476577	chr7:108501380-108501576	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
10	esv3510421	chr7:108501386-108501595	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
11	esv3423263	chr7:108501406-108501565	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
12	esv3094	chr7:108501415-108501620	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
13	esv3445836	chr7:108501428-108501547	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
14	esv3476576	chr7:108501431-108501550	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
15	esv3510423	chr7:108501443-108501545	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
16	nsv366315	chr7:108501445-108501545	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
17	esv3476578	chr7:108501445-108501548	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
18	esv3510427	chr7:108501445-108501548	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
19	esv1199838	chr7:108501446-108501547	Weak transcription	Chromatin interactive region	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	chr7:108501400-108501600	Weak transcription	Right Ventricle	heart

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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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