Variant report

Variant	rs190262907
Chromosome Location	chr3:81907962-81907963
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv999992	chr3:81693662-82015969	Active TSS Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
2	nsv536605	chr3:81693662-82015969	Flanking Active TSS Strong transcription Enhancers Weak transcription ZNF genes & repeats Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
3	esv2453055	chr3:81906123-81907991	Weak transcription Enhancers	lncRNA	2 gene(s)	inside rSNPs	n/a
4	esv3434713	chr3:81906712-81908810	Enhancers Weak transcription	n/a	n/a	inside rSNPs	n/a
5	esv6487	chr3:81907260-81908057	Weak transcription Enhancers	n/a	n/a	inside rSNPs	n/a
6	esv2022920	chr3:81907326-81907992	Enhancers Weak transcription	n/a	n/a	inside rSNPs	n/a
7	esv2018755	chr3:81907456-81908016	Weak transcription	n/a	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:81907200-81910000	Weak transcription	Fetal Heart	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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