Variant report

Variant	rs569042680
Chromosome Location	chr14:65635494-65635495
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr14:65633532..65639308-chr14:65876570..65881222,11	MCF-7	breast:
2	chr14:65630699..65635625-chr14:65877685..65881184,7	MCF-7	breast:
3	chr14:65629176..65630722-chr14:65633709..65636408,2	K562	blood:

Variant related genes	Relation type
ENSG00000033170	Chromatin interaction

Extended variants
information (count: 2 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832816	chr14:65473244-65644645	Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
2	esv1802727	chr14:65634797-65646536	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:25 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:65624000-65637000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr14:65624000-65637200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr14:65625400-65637200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr14:65626000-65637200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr14:65626400-65637200	Weak transcription	Esophagus	oesophagus
6	chr14:65627200-65637000	Weak transcription	Primary B cells from cord blood	blood
7	chr14:65631600-65635600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
8	chr14:65631800-65637200	Weak transcription	Fetal Intestine Large	intestine
9	chr14:65631800-65637200	Weak transcription	Fetal Intestine Small	intestine
10	chr14:65632000-65636000	Weak transcription	HepG2	liver
11	chr14:65632800-65635600	Enhancers	GM12878-XiMat	blood
12	chr14:65633000-65636000	Enhancers	Brain Hippocampus Middle	brain
13	chr14:65633800-65636000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr14:65633800-65637600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr14:65633800-65637600	Weak transcription	Spleen	Spleen
16	chr14:65634000-65635600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr14:65634200-65637000	Weak transcription	Stomach Mucosa	stomach
18	chr14:65634600-65635600	Weak transcription	Primary B cells from peripheral blood	blood
19	chr14:65635000-65635600	Enhancers	Brain Angular Gyrus	brain
20	chr14:65635000-65635600	Enhancers	Brain Anterior Caudate	brain
21	chr14:65635000-65635600	Enhancers	Brain Cingulate Gyrus	brain
22	chr14:65635000-65635600	Enhancers	Brain Inferior Temporal Lobe	brain
23	chr14:65635000-65636400	Enhancers	Brain Substantia Nigra	brain
24	chr14:65635400-65635600	Enhancers	Muscle Satellite Cultured Cells	--
25	chr14:65635400-65636000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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