Variant report

Variant	rs1969843
Chromosome Location	chr6:33898334-33898335
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs10807129	0.93[EUR][1000 genomes]
rs1324579	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1408503	0.85[EUR][1000 genomes]
rs1535940	0.94[EUR][1000 genomes]
rs1535941	0.94[EUR][1000 genomes]
rs1535943	0.84[EUR][1000 genomes]
rs1535944	0.94[EUR][1000 genomes]
rs1535945	0.94[EUR][1000 genomes]
rs1535946	0.94[EUR][1000 genomes]
rs1535947	0.94[EUR][1000 genomes]
rs2093907	0.91[EUR][1000 genomes]
rs2147423	0.94[EUR][1000 genomes]
rs2147426	0.95[EUR][1000 genomes]
rs2147427	0.96[EUR][1000 genomes]
rs2181916	0.94[EUR][1000 genomes]
rs2477228	0.95[EUR][1000 genomes]
rs2477231	0.95[EUR][1000 genomes]
rs2477232	0.95[EUR][1000 genomes]
rs2477235	0.96[EUR][1000 genomes]
rs2477236	0.96[EUR][1000 genomes]
rs2477237	0.95[EUR][1000 genomes]
rs2499737	0.95[EUR][1000 genomes]
rs4711364	0.89[EUR][1000 genomes]
rs4711365	0.94[EUR][1000 genomes]
rs4713715	0.89[EUR][1000 genomes]
rs4713716	0.89[EUR][1000 genomes]
rs4713717	0.89[EUR][1000 genomes]
rs4713721	0.94[EUR][1000 genomes]
rs6457747	0.89[EUR][1000 genomes]
rs6921366	0.89[EUR][1000 genomes]
rs9296103	0.94[EUR][1000 genomes]
rs9368781	0.91[EUR][1000 genomes]
rs942506	0.89[EUR][1000 genomes]
rs942508	0.94[EUR][1000 genomes]
rs942509	0.94[EUR][1000 genomes]
rs942510	0.94[EUR][1000 genomes]
rs942511	0.82[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	nsv916210	chr6:33804111-34144062	Weak transcription Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	32 gene(s)	inside rSNPs	diseases
2	nsv462899	chr6:33880480-33944014	Weak transcription Bivalent/Poised TSS Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv602841	chr6:33880480-33944014	Enhancers Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers	Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:33894600-33902600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr6:33897400-33898800	Enhancers	HSMMtube	muscle
3	chr6:33897600-33899000	Enhancers	Fetal Muscle Leg	muscle
4	chr6:33898000-33903000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
5	chr6:33898200-33898600	Weak transcription	Fetal Kidney	kidney
6	chr6:33898200-33898600	Weak transcription	Skeletal Muscle Female	skeletal muscle
7	chr6:33898200-33899000	Enhancers	HSMM	muscle

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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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