Variant report

Variant	rs376467882
Chromosome Location	chr4:98045135-98045136
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 4 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv879640	chr4:97711707-98697586	Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv1002766	chr4:98006688-98128416	Enhancers ZNF genes & repeats Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv537192	chr4:98006688-98128416	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	esv3370026	chr4:98044823-98067071	Weak transcription Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS	lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:98043800-98048600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
2	chr4:98044800-98045200	Enhancers	H9 Cell Line	embryonic stem cell
3	chr4:98044800-98045200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr4:98044800-98045200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr4:98044800-98045200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr4:98044800-98045400	Enhancers	H1 Cell Line	embryonic stem cell
7	chr4:98045000-98045200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
8	chr4:98045000-98045200	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr4:98045000-98045200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
10	chr4:98045000-98045200	ZNF genes & repeats	Gastric	stomach

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Input of quick search could be:

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

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