Variant report

Variant	rs68159317
Chromosome Location	chr6:80650730-80650731
allele	-/A
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:80646889..80649492-chr6:80650023..80652919,2	K562	blood:
2	chr6:80646006..80648770-chr6:80649212..80651183,2	MCF-7	breast:
3	chr6:80649918..80652477-chr6:80718505..80720470,2	K562	blood:

Extended variants
information (count: 5 )
Associated
traits (count: 0)

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	nsv1028607	chr6:79853272-80767716	Enhancers Active TSS Genic enhancers Flanking Active TSS Strong transcription Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
2	nsv1032347	chr6:80284809-80694778	Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
3	esv3475140	chr6:80592690-80679283	Active TSS Flanking Bivalent TSS/Enh Enhancers Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
4	esv3475142	chr6:80592789-80679132	Weak transcription Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Active TSS Enhancers Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
5	esv2480577	chr6:80649708-80651056	Weak transcription Genic enhancers Enhancers Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:80618400-80656000	Weak transcription	Aorta	Aorta
2	chr6:80631000-80653000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr6:80632000-80654800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr6:80634800-80651000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr6:80638400-80651000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
6	chr6:80638800-80653000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr6:80640200-80654800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr6:80645800-80651600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr6:80646600-80651000	Weak transcription	HUES6 Cell Line	embryonic stem cell
10	chr6:80646800-80651600	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr6:80647000-80651000	Weak transcription	Thymus	Thymus
12	chr6:80647800-80651600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr6:80648400-80651200	Weak transcription	Fetal Thymus	thymus
14	chr6:80648600-80651000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
15	chr6:80648600-80653000	Weak transcription	H1 Cell Line	embryonic stem cell
16	chr6:80648800-80651000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
17	chr6:80648800-80653000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
18	chr6:80649200-80650800	Weak transcription	HUES64 Cell Line	embryonic stem cell
19	chr6:80649200-80651000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
20	chr6:80649600-80651000	Weak transcription	HUES48 Cell Line	embryonic stem cell
21	chr6:80649600-80651600	Genic enhancers	Dnd41	blood

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