Variant report

Variant	rs2526102
Chromosome Location	chr7:11677347-11677348
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 23 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs1358169	0.85[EUR][1000 genomes]
rs1405327	0.80[AMR][1000 genomes]
rs1526556	0.83[AMR][1000 genomes]
rs1635182	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs1635185	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs1725449	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs1725450	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs2526095	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2526096	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2526100	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2526112	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2681041	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2681042	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2681043	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2681046	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2681047	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs2681048	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs941035	0.84[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1028326	chr7:11221209-11754436	Enhancers Strong transcription Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv538733	chr7:11221209-11754436	Weak transcription Strong transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv1023665	chr7:11457493-11773517	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv887606	chr7:11473561-11771288	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv606199	chr7:11506143-12486659	Active TSS Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:11660800-11681400	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr7:11667000-11678200	Weak transcription	Primary hematopoietic stem cells	blood
3	chr7:11671600-11677600	Weak transcription	Ovary	ovary
4	chr7:11671600-11681600	Weak transcription	A549	lung
5	chr7:11673200-11678000	Weak transcription	Fetal Stomach	stomach
6	chr7:11673400-11678200	Weak transcription	Fetal Lung	lung
7	chr7:11676200-11677800	Weak transcription	Placenta	Placenta
8	chr7:11676400-11681800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland

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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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