Variant report

Variant	rs10275219
Chromosome Location	chr7:150883821-150883822
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs10274484	0.96[EUR][1000 genomes]
rs10275136	0.94[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs28377077	0.87[EUR][1000 genomes]
rs58304055	0.87[EUR][1000 genomes]
rs59806285	0.91[EUR][1000 genomes]
rs61743170	0.94[EUR][1000 genomes]
rs62489631	0.87[EUR][1000 genomes]
rs62489634	0.87[EUR][1000 genomes]
rs62489635	0.87[EUR][1000 genomes]
rs62489646	0.87[EUR][1000 genomes]
rs62489649	0.92[EUR][1000 genomes]
rs73478613	0.81[EUR][1000 genomes]
rs73478622	0.89[EUR][1000 genomes]
rs9987066	0.94[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1821419	chr7:150593315-150974269	Enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	128 gene(s)	inside rSNPs	diseases
2	nsv889476	chr7:150729212-150951819	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	120 gene(s)	inside rSNPs	diseases
3	nsv889478	chr7:150732812-150889527	Strong transcription Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	61 gene(s)	inside rSNPs	diseases
4	nsv831188	chr7:150735204-150912875	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
5	nsv889486	chr7:150775306-150891641	Enhancers Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	48 gene(s)	inside rSNPs	diseases
6	nsv609034	chr7:150830015-150893629	Enhancers Active TSS Weak transcription Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:150882800-150884400	Transcr. at gene 5' and 3'	Skeletal Muscle Male	skeletal muscle
2	chr7:150882800-150885000	Active TSS	Left Ventricle	heart
3	chr7:150883000-150884000	Enhancers	Fetal Muscle Leg	muscle
4	chr7:150883200-150884400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
5	chr7:150883400-150884000	Flanking Active TSS	Right Ventricle	heart
6	chr7:150883400-150885000	Active TSS	Right Atrium	heart
7	chr7:150883400-150885600	Enhancers	Fetal Heart	heart
8	chr7:150883600-150885000	Active TSS	Psoas Muscle	Psoas
9	chr7:150883800-150884000	Active TSS	Skeletal Muscle Female	skeletal muscle
10	chr7:150883800-150884200	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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