Variant report

Variant	rs182064868
Chromosome Location	chr2:30608355-30608356
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv533886	chr2:30130019-31068764	ZNF genes & repeats Enhancers Genic enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
2	nsv833648	chr2:30505882-30696275	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
3	nsv873769	chr2:30585638-30625264	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	esv3527832	chr2:30606448-30609846	Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
5	esv3514776	chr2:30606898-30610296	Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
6	esv3514777	chr2:30606898-30610296	Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
7	esv3459510	chr2:30607542-30608719	Enhancers	n/a	n/a	inside rSNPs	diseases
8	esv3527833	chr2:30607576-30608616	Enhancers	n/a	n/a	inside rSNPs	diseases
9	esv3527835	chr2:30607579-30608575	Enhancers	n/a	n/a	inside rSNPs	diseases
10	esv3527834	chr2:30607607-30608600	Enhancers	n/a	n/a	inside rSNPs	diseases
11	esv3459511	chr2:30607672-30608535	Enhancers	n/a	n/a	inside rSNPs	diseases
12	esv3527836	chr2:30607672-30608535	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	chr2:30608000-30608800	Enhancers	Fetal Intestine Large	intestine

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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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