Variant report

Variant	rs10230214
Chromosome Location	chr7:11990569-11990570
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 61 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs10224517	1.00[EUR][1000 genomes]
rs10224879	1.00[EUR][1000 genomes]
rs10234847	0.89[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs10237705	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs10241052	1.00[EUR][1000 genomes]
rs10242456	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs10243371	1.00[EUR][1000 genomes]
rs10248300	1.00[EUR][1000 genomes]
rs10254552	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs10254644	1.00[EUR][1000 genomes]
rs10262186	1.00[EUR][1000 genomes]
rs10262661	1.00[EUR][1000 genomes]
rs10269461	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs10270591	0.82[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs10270750	1.00[EUR][1000 genomes]
rs10273844	1.00[EUR][1000 genomes]
rs10274633	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs10275836	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs10277752	0.81[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs13437920	1.00[EUR][1000 genomes]
rs28431052	1.00[EUR][1000 genomes]
rs28452368	1.00[EUR][1000 genomes]
rs28750387	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs28829942	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs6460858	1.00[EUR][1000 genomes]
rs73285074	0.89[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73285075	0.89[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73285077	0.89[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73285079	0.89[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73285081	0.89[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73285087	0.89[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73285088	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73285090	0.87[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73285092	0.87[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73287204	0.87[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73287207	0.87[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73287215	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73287282	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73287290	1.00[EUR][1000 genomes]
rs73287292	1.00[EUR][1000 genomes]
rs73287297	1.00[EUR][1000 genomes]
rs73292721	1.00[EUR][1000 genomes]
rs7779211	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs7783187	1.00[EUR][1000 genomes]
rs7796388	0.86[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs7799871	0.86[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs7800268	0.87[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs7800415	0.89[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs7800416	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 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	nsv887619	chr7:11893588-12043231	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv887620	chr7:11908763-11993510	Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
5	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
6	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
7	nsv606218	chr7:11938060-12000154	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
8	nsv887624	chr7:11941048-12023864	Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
9	nsv464370	chr7:11975557-12010797	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases
10	nsv606219	chr7:11975557-12010797	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS	n/a	n/a	inside rSNPs	diseases
11	nsv887625	chr7:11981995-12046503	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer	n/a	n/a	inside rSNPs	diseases
12	esv3387367	chr7:11982761-12005609	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:11989600-11997200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr7:11989800-11990600	Enhancers	Placenta	Placenta
3	chr7:11989800-11991200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr7:11990400-11990800	Weak transcription	Pancreas	Pancrea
5	chr7:11990400-11991000	Enhancers	Breast Myoepithelial Primary Cells	Breast

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