Variant report

Variant	rs1601202
Chromosome Location	chr4:80270953-80270954
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs10000485	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10004440	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10050068	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11733010	0.92[EUR][1000 genomes]
rs1484148	0.91[EUR][1000 genomes]
rs1484149	0.91[EUR][1000 genomes]
rs1601201	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17003721	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs28432328	0.91[EUR][1000 genomes]
rs28516921	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs28619382	0.92[EUR][1000 genomes]
rs28704148	0.92[EUR][1000 genomes]
rs28796992	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2903619	0.92[EUR][1000 genomes]
rs4975046	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4975085	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs6818904	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6823996	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9992718	0.91[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	nsv879505	chr4:79887043-80293046	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv999174	chr4:80212935-80512356	Enhancers Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Bivalent Enhancer Strong transcription Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv980223	chr4:80259303-80276903	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:80265800-80273400	Weak transcription	Colon Smooth Muscle	Colon
2	chr4:80268400-80273600	Weak transcription	Stomach Smooth Muscle	stomach
3	chr4:80268800-80273400	Weak transcription	Adipose Nuclei	Adipose

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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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