Variant report

Variant	rs35304218
Chromosome Location	chr14:31741256-31741257
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs10872850	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17097767	0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2378850	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28816478	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs4587868	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57512445	0.89[AMR][1000 genomes]
rs60089901	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs61323238	0.83[EUR][1000 genomes]
rs72672629	0.83[EUR][1000 genomes]
rs956810	0.83[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv901587	chr14:31501505-31752664	Strong transcription Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
2	esv2830427	chr14:31639110-32000034	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
3	nsv1050597	chr14:31711248-31904761	Strong transcription Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:31735400-31743200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr14:31735400-31743400	Weak transcription	Muscle Satellite Cultured Cells	--
3	chr14:31735600-31743400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr14:31738800-31741600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr14:31739200-31742000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr14:31739200-31743200	Weak transcription	Osteobl	bone
7	chr14:31739600-31742600	Weak transcription	NHDF-Ad	bronchial
8	chr14:31739800-31742600	Weak transcription	HUVEC	blood vessel
9	chr14:31740000-31741800	Weak transcription	Liver	Liver
10	chr14:31740000-31741800	Weak transcription	Stomach Mucosa	stomach
11	chr14:31740000-31743200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr14:31740000-31746200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr14:31740000-31746200	Weak transcription	Esophagus	oesophagus
14	chr14:31740800-31743800	Enhancers	HepG2	liver
15	chr14:31741200-31741800	Enhancers	Fetal Intestine Small	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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