Variant report

Variant	rs56265309
Chromosome Location	chr4:130284475-130284476
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs12506624	0.84[EUR][1000 genomes]
rs12506696	0.84[EUR][1000 genomes]
rs12510624	0.82[EUR][1000 genomes]
rs1433378	0.82[EUR][1000 genomes]
rs4540061	0.84[EUR][1000 genomes]
rs55792344	0.87[EUR][1000 genomes]
rs56361313	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs56982957	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs61455970	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs61554187	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs62309611	0.84[EUR][1000 genomes]
rs62309616	0.82[EUR][1000 genomes]
rs62317276	0.81[AMR][1000 genomes];0.87[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	nsv534538	chr4:129799138-130431688	Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv830058	chr4:130136025-130315471	Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	esv3466206	chr4:130280102-130284500	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:130280400-130284600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr4:130280400-130284600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr4:130283600-130284600	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr4:130283600-130284800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
5	chr4:130283800-130284600	Enhancers	iPS-20b Cell Line	embryonic stem cell
6	chr4:130283800-130284800	Enhancers	Dnd41	blood
7	chr4:130283800-130285200	Enhancers	HUVEC	blood vessel
8	chr4:130284000-130284600	Enhancers	Fetal Kidney	kidney
9	chr4:130284000-130285000	Enhancers	Colon Smooth Muscle	Colon
10	chr4:130284200-130284600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr4:130284200-130285000	Bivalent Enhancer	Fetal Heart	heart
12	chr4:130284400-130284800	Enhancers	H1 Cell Line	embryonic stem cell
13	chr4:130284400-130284800	Enhancers	Duodenum Smooth Muscle	Duodenum
14	chr4:130284400-130284800	Enhancers	Rectal Smooth Muscle	rectum
15	chr4:130284400-130285200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr4:130284400-130285200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr4:130284400-130285200	Enhancers	Brain Germinal Matrix	brain
18	chr4:130284400-130285200	Enhancers	Fetal Muscle Leg	muscle

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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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