Variant report

Variant	rs536536425
Chromosome Location	chr12:50290565-50290566
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:50290402..50293463-chr12:50294998..50297478,3	MCF-7	breast:
2	chr12:50280227..50282176-chr12:50287942..50290577,2	K562	blood:

Variant related genes	Relation type
ENSG00000135472	Chromatin interaction

Extended variants
information (count: 8 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1045327	chr12:49975040-50551375	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS Bivalent/Poised 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	170 gene(s)	inside rSNPs	diseases
2	nsv541490	chr12:49975040-50551375	Weak transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	170 gene(s)	inside rSNPs	diseases
3	nsv522972	chr12:50196394-50410831	Enhancers Flanking Active TSS Strong transcription Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
4	nsv530671	chr12:50233858-50708991	Flanking Active TSS Active TSS Enhancers Weak transcription Genic enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	117 gene(s)	inside rSNPs	diseases
5	nsv832407	chr12:50243268-50412236	Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
6	nsv558835	chr12:50275137-50433234	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS Strong transcription 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	36 gene(s)	inside rSNPs	diseases
7	nsv525920	chr12:50285061-50304949	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
8	nsv558836	chr12:50290023-50316439	Enhancers Bivalent Enhancer Weak transcription Genic enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:26 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:50267000-50297000	Weak transcription	Right Atrium	heart
2	chr12:50275000-50294800	Weak transcription	Fetal Brain Male	brain
3	chr12:50283600-50290600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr12:50287000-50292000	Weak transcription	K562	blood
5	chr12:50287000-50295000	Strong transcription	Brain Germinal Matrix	brain
6	chr12:50287600-50295800	Strong transcription	Fetal Stomach	stomach
7	chr12:50287800-50291800	Enhancers	Esophagus	oesophagus
8	chr12:50288000-50290600	Genic enhancers	Brain Cingulate Gyrus	brain
9	chr12:50288000-50290800	Genic enhancers	Brain Dorsolateral Prefrontal Cortex	brain
10	chr12:50288000-50291200	Genic enhancers	Brain Inferior Temporal Lobe	brain
11	chr12:50288800-50291800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
12	chr12:50288800-50292000	Enhancers	Breast Myoepithelial Primary Cells	Breast
13	chr12:50289000-50290600	Weak transcription	Placenta Amnion	Placenta Amnion
14	chr12:50289200-50291000	Enhancers	Fetal Muscle Leg	muscle
15	chr12:50289200-50292400	Strong transcription	Brain Anterior Caudate	brain
16	chr12:50289600-50290600	Weak transcription	Brain Substantia Nigra	brain
17	chr12:50289600-50291200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr12:50289600-50292400	Strong transcription	Brain Angular Gyrus	brain
19	chr12:50289800-50291000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr12:50289800-50291600	Strong transcription	Fetal Brain Female	brain
21	chr12:50289800-50296200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
22	chr12:50290000-50290600	Weak transcription	Spleen	Spleen
23	chr12:50290000-50290800	Bivalent Enhancer	NHEK	skin
24	chr12:50290000-50293600	Weak transcription	HUES6 Cell Line	embryonic stem cell
25	chr12:50290200-50291400	Weak transcription	Fetal Intestine Small	intestine
26	chr12:50290200-50294800	Strong transcription	Brain Hippocampus Middle	brain

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