Variant report

Variant	rs7950791
Chromosome Location	chr11:24379374-24379375
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs1036873	0.82[EUR][1000 genomes]
rs7105553	0.91[EUR][1000 genomes]
rs7928005	0.82[EUR][1000 genomes]
rs7941141	0.82[EUR][1000 genomes]
rs7941806	0.82[EUR][1000 genomes]
rs976427	0.82[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1055026	chr11:24151133-24737122	Enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv1037744	chr11:24174588-24737122	Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:24378400-24379800	Enhancers	Fetal Muscle Leg	muscle
2	chr11:24378600-24379800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
3	chr11:24379000-24379400	Enhancers	Fetal Muscle Trunk	muscle
4	chr11:24379000-24379800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr11:24379000-24379800	Flanking Active TSS	Dnd41	blood
6	chr11:24379200-24379800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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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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