Variant report

Variant	rs540025340
Chromosome Location	chr2:211430313-211430314
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 2 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3398091	chr2:211315261-211634200	Active TSS Flanking Active TSS Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	esv3347198	chr2:211430274-211430477	Enhancers Transcr. at gene 5' and 3' Weak transcription Genic enhancers	n/a	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	chr2:211418600-211443200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr2:211423600-211432600	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr2:211423800-211432600	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr2:211426400-211432400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr2:211428400-211432600	Weak transcription	Duodenum Mucosa	Duodenum
6	chr2:211428600-211430400	Weak transcription	Fetal Kidney	kidney
7	chr2:211429000-211431000	Genic enhancers	Fetal Intestine Small	intestine
8	chr2:211429800-211430600	Genic enhancers	Hela-S3	cervix
9	chr2:211430200-211430400	Genic enhancers	Liver	Liver
10	chr2:211430200-211431400	Genic 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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