Variant report

Variant	rs12714226
Chromosome Location	chr2:21255948-21255949
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 3 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:1)

rs_ID	r²[population]
rs12714214	1.00[YRI][hapmap]

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	nsv873728	chr2:21250914-21460786	Enhancers Bivalent Enhancer Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	esv3442957	chr2:21255559-21257877	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:21234800-21262200	Weak transcription	Ovary	ovary
2	chr2:21235000-21261800	Strong transcription	Fetal Intestine Large	intestine
3	chr2:21252000-21256200	Weak transcription	Left Ventricle	heart
4	chr2:21254000-21256200	Strong transcription	Adipose Nuclei	Adipose
5	chr2:21254400-21262000	Strong transcription	Fetal Intestine Small	intestine
6	chr2:21255200-21256400	Strong transcription	Aorta	Aorta
7	chr2:21255200-21258200	Genic enhancers	Liver	Liver
8	chr2:21255200-21260600	Strong transcription	Duodenum Mucosa	Duodenum
9	chr2:21255400-21256600	Genic enhancers	HepG2	liver
10	chr2:21255400-21262800	Weak transcription	Right Atrium	heart

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dbSNP/dbVar ID: rs12345 /nsv7879
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