Variant report

Variant	rs8068353
Chromosome Location	chr17:33840295-33840296
allele	C/G
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	MAFK	chr17:33840121-33840309	HepG2	liver:	n/a	n/a
2	MAFK	chr17:33840037-33840314	HepG2	liver:	n/a	n/a
3	E2F4	chr17:33840240-33840312	MCF10A-Er-Src	breast:	n/a	n/a

Variant related genes	Relation type
ENSG00000267074	TF binding region

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs16971032	0.94[ASN][1000 genomes]
rs4796093	0.80[CEU][hapmap]
rs55661426	0.95[ASN][1000 genomes]
rs56185101	0.94[ASN][1000 genomes]
rs72828016	0.95[ASN][1000 genomes]
rs8066424	0.80[CEU][hapmap]
rs8070473	1.00[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1055936	chr17:33327166-33884184	Strong transcription Weak transcription Flanking Active TSS Bivalent/Poised TSS Enhancers Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	112 gene(s)	inside rSNPs	diseases
2	nsv543317	chr17:33327166-33884184	Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	112 gene(s)	inside rSNPs	diseases
3	nsv534371	chr17:33456878-34094068	Strong transcription Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	137 gene(s)	inside rSNPs	diseases
4	nsv960581	chr17:33827264-33841554	Strong transcription Weak transcription Genic enhancers Enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:23 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:33835400-33849600	Weak transcription	Spleen	Spleen
2	chr17:33836400-33843800	Strong transcription	Dnd41	blood
3	chr17:33837600-33840400	Weak transcription	Primary T cells from cord blood	blood
4	chr17:33837800-33846800	Weak transcription	Sigmoid Colon	Sigmoid Colon
5	chr17:33838000-33841600	Weak transcription	Duodenum Mucosa	Duodenum
6	chr17:33838400-33840400	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
7	chr17:33838800-33841000	Weak transcription	Fetal Lung	lung
8	chr17:33839000-33841800	Genic enhancers	Primary T helper naive cells from peripheral blood	blood
9	chr17:33839800-33840400	Genic enhancers	Primary T cells fromperipheralblood	blood
10	chr17:33839800-33840600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
11	chr17:33839800-33840800	Genic enhancers	Primary T regulatory cells fromperipheralblood	blood
12	chr17:33839800-33841200	Strong transcription	Primary T helper cells PMA-I stimulated	--
13	chr17:33839800-33841800	Genic enhancers	Primary T helper memory cells from peripheral blood 1	blood
14	chr17:33839800-33842200	Genic enhancers	Primary T killer naive cells fromperipheralblood	blood
15	chr17:33840000-33840600	Genic enhancers	Primary T helper 17 cells PMA-I stimulated	--
16	chr17:33840000-33840800	Genic enhancers	Primary T helper cells fromperipheralblood	blood
17	chr17:33840000-33841200	Genic enhancers	Primary T killer memory cells from peripheral blood	blood
18	chr17:33840000-33841400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
19	chr17:33840000-33842200	Strong transcription	GM12878-XiMat	blood
20	chr17:33840000-33843400	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
21	chr17:33840200-33840400	Bivalent Enhancer	Fetal Brain Male	brain
22	chr17:33840200-33840400	Bivalent Enhancer	Fetal Brain Female	brain
23	chr17:33840200-33841000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood

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