Variant report

Variant	rs576011392
Chromosome Location	chr6:35168130-35168131
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:35147825..35149730-chr6:35166517..35168770,2	MCF-7	breast:
2	chr6:35146928..35151829-chr6:35162484..35168348,5	K562	blood:
3	chr6:35167248..35168898-chr6:35172556..35174347,2	MCF-7	breast:

Extended variants
information (count: 3 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3428128	chr6:35150524-35225843	Bivalent Enhancer Enhancers Genic enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	esv2758047	chr6:35168116-35291002	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
3	esv2759419	chr6:35168116-35291002	Weak transcription Flanking Active TSS Active TSS Enhancers Genic enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:28 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:35154000-35169800	Weak transcription	Right Atrium	heart
2	chr6:35154400-35169200	Weak transcription	Fetal Heart	heart
3	chr6:35161600-35169400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr6:35161600-35170000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr6:35163200-35171200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr6:35163600-35171000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr6:35165200-35169400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr6:35165200-35171200	Weak transcription	NH-A	brain
9	chr6:35165600-35169400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr6:35166200-35168800	Enhancers	Breast Myoepithelial Primary Cells	Breast
11	chr6:35167000-35168200	Enhancers	Brain Inferior Temporal Lobe	brain
12	chr6:35167000-35168400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr6:35167000-35168600	Enhancers	Brain Cingulate Gyrus	brain
14	chr6:35167000-35169200	Enhancers	HepG2	liver
15	chr6:35167200-35168200	Enhancers	Brain Hippocampus Middle	brain
16	chr6:35167200-35168400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
17	chr6:35167200-35168400	Enhancers	Brain Substantia Nigra	brain
18	chr6:35167400-35168400	Enhancers	Osteobl	bone
19	chr6:35167400-35168600	Enhancers	Brain Angular Gyrus	brain
20	chr6:35167600-35170200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr6:35167600-35171600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr6:35167800-35168200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr6:35167800-35168200	Enhancers	Brain Anterior Caudate	brain
24	chr6:35167800-35168600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr6:35167800-35168600	Enhancers	HMEC	breast
26	chr6:35167800-35169800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr6:35168000-35169400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr6:35168000-35171200	Weak transcription	Muscle Satellite Cultured Cells	--

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