Variant report

Variant	rs11979594
Chromosome Location	chr7:12103970-12103971
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs10241146	1.00[EUR][1000 genomes]
rs10251420	1.00[EUR][1000 genomes]
rs10262993	1.00[EUR][1000 genomes]
rs10263331	1.00[EUR][1000 genomes]
rs10266698	1.00[EUR][1000 genomes]
rs10274501	1.00[EUR][1000 genomes]
rs1072262	1.00[EUR][1000 genomes]
rs1595012	1.00[EUR][1000 genomes]
rs16877307	1.00[EUR][1000 genomes]
rs17165535	0.97[AFR][1000 genomes]
rs17165685	1.00[EUR][1000 genomes]
rs2215993	0.91[AFR][1000 genomes]
rs28471043	1.00[EUR][1000 genomes]
rs57308211	1.00[EUR][1000 genomes]
rs57698857	1.00[EUR][1000 genomes]
rs57742006	1.00[EUR][1000 genomes]
rs57812376	1.00[EUR][1000 genomes]
rs58749049	1.00[EUR][1000 genomes]
rs58954316	1.00[EUR][1000 genomes]
rs59080097	1.00[EUR][1000 genomes]
rs60817474	1.00[EUR][1000 genomes]
rs6945705	1.00[AFR][1000 genomes]
rs73289387	1.00[EUR][1000 genomes]
rs73291081	1.00[EUR][1000 genomes]
rs73291082	1.00[EUR][1000 genomes]
rs73292961	1.00[EUR][1000 genomes]
rs73292962	1.00[EUR][1000 genomes]
rs73292964	1.00[EUR][1000 genomes]
rs73292965	1.00[EUR][1000 genomes]
rs73295078	1.00[EUR][1000 genomes]
rs73297023	1.00[EUR][1000 genomes]
rs73297098	1.00[EUR][1000 genomes]
rs73298880	0.97[AFR][1000 genomes]
rs7786770	1.00[EUR][1000 genomes]
rs7786784	1.00[EUR][1000 genomes]
rs7801599	1.00[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	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
2	nsv887614	chr7:11778424-12211198	Bivalent/Poised TSS Active TSS Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
3	esv2758103	chr7:11927239-12109419	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
4	esv2759510	chr7:11927239-12109419	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv830906	chr7:12001764-12177869	Enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv1023608	chr7:12064114-12247520	Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:12103800-12108200	Enhancers	ES-I3 Cell Line	embryonic stem cell

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