Variant report

Variant	rs176384
Chromosome Location	chr5:107385756-107385757
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs158189	0.89[EUR][1000 genomes]
rs169640	0.87[EUR][1000 genomes]
rs192617	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs286748	0.89[EUR][1000 genomes]
rs286752	0.89[EUR][1000 genomes]
rs286755	0.82[EUR][1000 genomes]
rs286757	0.91[EUR][1000 genomes]
rs286783	0.89[EUR][1000 genomes]
rs286786	0.89[EUR][1000 genomes]
rs286788	0.88[EUR][1000 genomes]
rs286790	0.89[EUR][1000 genomes]
rs288130	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs288140	0.89[EUR][1000 genomes]
rs288148	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs288150	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs288153	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs288155	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs288156	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs288158	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs288162	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs288163	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs288165	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs288166	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs288167	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs288176	0.87[EUR][1000 genomes]
rs288182	0.87[EUR][1000 genomes]
rs289234	0.89[EUR][1000 genomes]
rs2909879	0.89[EUR][1000 genomes]
rs2909880	0.89[EUR][1000 genomes]
rs2909882	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs455394	0.89[EUR][1000 genomes]
rs502790	0.89[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	nsv882682	chr5:107213361-107458336	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv534281	chr5:107357579-107674981	Enhancers Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	nsv1029650	chr5:107370079-107435314	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:107364000-107390000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
2	chr5:107381400-107389600	Weak transcription	Aorta	Aorta
3	chr5:107381800-107390000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
4	chr5:107382000-107386000	Weak transcription	Fetal Muscle Leg	muscle
5	chr5:107383400-107389600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr5:107383400-107390000	Weak transcription	Left Ventricle	heart
7	chr5:107383400-107396400	Weak transcription	Right Ventricle	heart
8	chr5:107383600-107390200	Weak transcription	Gastric	stomach

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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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