Variant report

Variant	rs392723
Chromosome Location	chr5:96404979-96404980
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs10043135	0.81[ASN][1000 genomes]
rs10463198	0.85[ASN][1000 genomes]
rs11748432	0.84[ASN][1000 genomes]
rs11954059	0.81[ASN][1000 genomes]
rs12110061	0.84[ASN][1000 genomes]
rs182625	0.82[ASN][1000 genomes]
rs186413	0.81[ASN][1000 genomes]
rs2544776	0.97[ASN][1000 genomes]
rs316190	0.81[ASN][1000 genomes]
rs316213	0.82[ASN][1000 genomes]
rs316223	0.93[ASN][1000 genomes]
rs316224	0.95[ASN][1000 genomes]
rs316232	0.82[ASN][1000 genomes]
rs316233	0.82[ASN][1000 genomes]
rs316234	0.82[ASN][1000 genomes]
rs389536	0.97[ASN][1000 genomes]
rs6556945	0.83[ASN][1000 genomes]
rs7717829	0.81[ASN][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	nsv432755	chr5:95987984-96657483	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
2	nsv598962	chr5:96057891-96893164	Weak transcription Strong transcription Enhancers Bivalent/Poised TSS Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
3	nsv4924	chr5:96391451-96437233	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:96399600-96407400	Weak transcription	Fetal Kidney	kidney
2	chr5:96399800-96405800	Weak transcription	Fetal Muscle Leg	muscle
3	chr5:96403400-96411200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr5:96404000-96406400	Weak transcription	Colon Smooth Muscle	Colon

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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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