Variant report

Variant	rs4422983
Chromosome Location	chr1:166362556-166362557
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs1451605	0.89[EUR][1000 genomes]
rs1551178	0.89[EUR][1000 genomes]
rs16827930	0.83[AMR][1000 genomes]
rs16827931	0.83[AMR][1000 genomes]
rs16827935	0.83[AMR][1000 genomes]
rs16856876	1.00[EUR][1000 genomes]
rs16857044	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1901356	0.89[EUR][1000 genomes]
rs2116525	0.89[EUR][1000 genomes]
rs4256790	0.89[EUR][1000 genomes]
rs4311866	0.89[EUR][1000 genomes]
rs56945226	0.83[AMR][1000 genomes]
rs74119728	0.83[AMR][1000 genomes]
rs74119732	0.83[AMR][1000 genomes]
rs74119733	0.83[AMR][1000 genomes]
rs966152	1.00[EUR][1000 genomes]
rs9970008	0.89[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv916491	chr1:166000783-166948513	Bivalent/Poised TSS Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	38 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	chr1:166356200-166363800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr1:166356200-166364200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr1:166362000-166362600	Enhancers	Psoas Muscle	Psoas
4	chr1:166362400-166362600	Enhancers	Skeletal Muscle Male	skeletal muscle

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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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