Variant report

Variant	rs73076295
Chromosome Location	chr4:8512302-8512303
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs2222461	0.92[EUR][1000 genomes]
rs3103075	0.85[AFR][1000 genomes]
rs3103076	0.83[EUR][1000 genomes]
rs67332046	0.84[AFR][1000 genomes]
rs67496006	0.84[AFR][1000 genomes]
rs6823826	0.96[EUR][1000 genomes]
rs6830982	0.96[EUR][1000 genomes]
rs6832458	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6857320	0.84[AFR][1000 genomes]
rs73076290	0.82[AFR][1000 genomes]
rs73076294	0.86[AFR][1000 genomes]
rs73076299	0.91[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73076301	0.89[AFR][1000 genomes]
rs7689901	0.91[AMR][1000 genomes];1.00[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	nsv878604	chr4:8315938-8618916	Enhancers Flanking Active TSS Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
2	nsv1002680	chr4:8357163-8721214	Active TSS Flanking Active TSS Strong transcription Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
3	nsv4224	chr4:8503727-8546462	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:8502800-8512800	Enhancers	Placenta	Placenta
2	chr4:8509000-8519200	Weak transcription	Brain Germinal Matrix	brain
3	chr4:8509200-8513200	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr4:8509400-8513200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
5	chr4:8509400-8514000	Weak transcription	HUES6 Cell Line	embryonic stem cell
6	chr4:8509400-8517200	Weak transcription	Skeletal Muscle Female	skeletal muscle
7	chr4:8509600-8514200	Weak transcription	HSMMtube	muscle
8	chr4:8509600-8515200	Weak transcription	Skeletal Muscle Male	skeletal muscle
9	chr4:8509600-8515600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr4:8510000-8515600	Weak transcription	NHDF-Ad	bronchial
11	chr4:8511800-8517800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr4:8512200-8519200	Weak transcription	Spleen	Spleen

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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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