Variant report

Variant	rs12267169
Chromosome Location	chr10:38079061-38079062
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ZEB1	chr10:38078468-38079081	HepG2	liver:	n/a	n/a
2	GATA3	chr10:38078357-38079069	MCF-7	breast:	n/a	chr10:38078712-38078725 chr10:38078401-38078410 chr10:38078715-38078723
3	ZNF384	chr10:38079041-38079276	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:38072196..38074026-chr10:38077031..38079677,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000260137	TF binding region
ENSG00000226578	Chromatin interaction

Extended variants
information (count: 114 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:109)

rs_ID	r²[population]
rs10827823	0.97[ASN][1000 genomes]
rs10827824	0.97[ASN][1000 genomes]
rs10827825	0.97[ASN][1000 genomes]
rs10827828	0.98[ASN][1000 genomes]
rs10827829	0.95[ASN][1000 genomes]
rs10827831	0.95[ASN][1000 genomes]
rs11011326	0.87[ASN][1000 genomes]
rs11011328	0.87[ASN][1000 genomes]
rs11011330	0.87[ASN][1000 genomes]
rs11011331	0.87[ASN][1000 genomes]
rs11011334	0.90[ASN][1000 genomes]
rs11011346	0.80[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs11011354	0.97[ASN][1000 genomes]
rs11011355	0.97[ASN][1000 genomes]
rs11011363	0.98[ASN][1000 genomes]
rs11011366	0.98[ASN][1000 genomes]
rs11011370	0.98[ASN][1000 genomes]
rs11011372	0.98[ASN][1000 genomes]
rs11011378	0.83[ASN][1000 genomes]
rs11011384	0.81[ASN][1000 genomes]
rs1148287	0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11492508	0.98[ASN][1000 genomes]
rs11511139	0.97[ASN][1000 genomes]
rs11511141	0.97[ASN][1000 genomes]
rs11516808	0.95[ASN][1000 genomes]
rs11523837	0.98[ASN][1000 genomes]
rs11595684	0.98[ASN][1000 genomes]
rs11597286	0.95[ASN][1000 genomes]
rs11599689	0.93[ASN][1000 genomes]
rs1208555	0.85[EUR][1000 genomes]
rs1208556	0.85[EUR][1000 genomes]
rs1208560	0.85[EUR][1000 genomes]
rs1208573	0.85[EUR][1000 genomes]
rs1208587	0.85[EUR][1000 genomes]
rs1208591	0.85[EUR][1000 genomes]
rs1208601	0.81[EUR][1000 genomes]
rs1208633	0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1208645	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1208658	0.85[EUR][1000 genomes]
rs1208683	0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1208695	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1208716	0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1208770	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1208779	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1209425	0.87[ASN][1000 genomes]
rs1212108	0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1212617	0.85[EUR][1000 genomes]
rs12357391	0.93[ASN][1000 genomes]
rs12357418	0.93[ASN][1000 genomes]
rs12358094	0.97[ASN][1000 genomes]
rs12358108	0.97[ASN][1000 genomes]
rs12359608	0.98[ASN][1000 genomes]
rs12360411	0.97[ASN][1000 genomes]
rs12570939	0.97[ASN][1000 genomes]
rs12571820	0.97[ASN][1000 genomes]
rs12763390	0.98[ASN][1000 genomes]
rs12763409	0.98[ASN][1000 genomes]
rs12768391	0.98[ASN][1000 genomes]
rs12776092	0.85[EUR][1000 genomes]
rs12781703	0.97[ASN][1000 genomes]
rs12782327	0.98[ASN][1000 genomes]
rs12783666	0.97[ASN][1000 genomes]
rs12783722	0.97[ASN][1000 genomes]
rs1322319	0.81[ASN][1000 genomes]
rs1619266	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1735621	0.86[EUR][1000 genomes]
rs1735629	0.86[EUR][1000 genomes]
rs1735641	0.86[EUR][1000 genomes]
rs1742235	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1779015	0.97[ASN][1000 genomes]
rs1779068	0.85[EUR][1000 genomes]
rs1779075	0.86[EUR][1000 genomes]
rs1779150	0.97[ASN][1000 genomes]
rs2076809	0.93[ASN][1000 genomes]
rs2144848	0.85[EUR][1000 genomes]
rs2295872	0.81[ASN][1000 genomes]
rs2472149	0.85[EUR][1000 genomes]
rs2738185	0.84[EUR][1000 genomes]
rs2749586	0.83[EUR][1000 genomes]
rs2749588	0.85[EUR][1000 genomes]
rs2749589	0.85[EUR][1000 genomes]
rs2753877	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2753880	0.86[EUR][1000 genomes]
rs2891586	0.95[ASN][1000 genomes]
rs34496143	0.93[ASN][1000 genomes]
rs35872666	0.91[ASN][1000 genomes]
rs35951606	0.98[ASN][1000 genomes]
rs3824584	0.98[ASN][1000 genomes]
rs3824585	0.95[ASN][1000 genomes]
rs61858625	0.93[ASN][1000 genomes]
rs61858626	0.93[ASN][1000 genomes]
rs61859667	0.97[ASN][1000 genomes]
rs61859679	0.93[ASN][1000 genomes]
rs72639533	0.93[ASN][1000 genomes]
rs7476802	0.83[EUR][1000 genomes]
rs9417261	0.95[ASN][1000 genomes]
rs9417262	0.84[ASN][1000 genomes]
rs9417263	0.95[ASN][1000 genomes]
rs9417264	0.92[ASN][1000 genomes]
rs9417265	0.95[ASN][1000 genomes]
rs9417267	0.91[ASN][1000 genomes]
rs9417268	0.95[ASN][1000 genomes]
rs9418288	0.95[ASN][1000 genomes]
rs9418289	0.95[ASN][1000 genomes]
rs9418291	0.83[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9418294	0.95[ASN][1000 genomes]
rs9418297	0.81[ASN][1000 genomes]
rs9418298	0.81[ASN][1000 genomes]
rs9418299	0.81[ASN][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	nsv895030	chr10:37715737-38674609	Weak transcription Active TSS Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
2	nsv1045684	chr10:37765361-38426204	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
3	nsv540564	chr10:37765361-38426204	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
4	nsv1040704	chr10:37940024-38451917	Flanking Active TSS Enhancers ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
5	nsv975812	chr10:37990724-38084639	Weak transcription ZNF genes & repeats Enhancers Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:38072000-38083200	Weak transcription	Skeletal Muscle Male	skeletal muscle
2	chr10:38074600-38081000	Weak transcription	Skeletal Muscle Female	skeletal muscle
3	chr10:38078200-38080600	Weak transcription	Aorta	Aorta
4	chr10:38078400-38079600	Enhancers	HepG2	liver
5	chr10:38079000-38079200	Weak transcription	Left Ventricle	heart

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