Variant report

Variant	rs57887864
Chromosome Location	chr4:22374492-22374493
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs10005140	1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10025938	1.00[EUR][1000 genomes]
rs28380483	0.84[ASN][1000 genomes]
rs28396498	1.00[EUR][1000 genomes]
rs28529338	0.84[ASN][1000 genomes]
rs28759515	0.98[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28885729	1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4697295	0.83[EUR][1000 genomes]
rs58269936	0.88[ASN][1000 genomes]
rs6821621	1.00[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs6855444	1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs73110181	0.82[ASN][1000 genomes]
rs73800904	1.00[EUR][1000 genomes]
rs7676386	1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9993654	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9993802	1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]

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	nsv817467	chr4:21602921-22422816	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv428756	chr4:22239826-22406106	Weak transcription Strong transcription Active TSS Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 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	chr4:22329000-22389400	Weak transcription	Pancreas	Pancrea
2	chr4:22336600-22385400	Weak transcription	Fetal Intestine Large	intestine
3	chr4:22354000-22378200	Weak transcription	Aorta	Aorta
4	chr4:22365600-22386800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr4:22365800-22384600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr4:22366000-22385000	Weak transcription	NHEK	skin
7	chr4:22368800-22418600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr4:22371000-22374600	Weak transcription	Esophagus	oesophagus
9	chr4:22371600-22449800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr4:22371800-22377200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr4:22372000-22400400	Weak transcription	Gastric	stomach
12	chr4:22374000-22376000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr4:22374400-22374800	Enhancers	Fetal Brain Male	brain
14	chr4:22374400-22375000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr4:22374400-22375600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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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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