Variant report

Variant	rs11771895
Chromosome Location	chr7:137093743-137093744
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

rSNPs within LD-proxies of this variant (count:1)

rs_ID	r²[population]
rs4728409	0.87[CEU][hapmap];1.00[CHB][hapmap];0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]

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	nsv1029192	chr7:136433278-137147566	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
2	nsv869820	chr7:136990386-137347718	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
3	nsv1027868	chr7:137004690-137311653	Enhancers Flanking Active TSS Strong transcription Active TSS Weak transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
4	nsv539134	chr7:137004690-137311653	Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:137073800-137095600	Weak transcription	HSMMtube	muscle
2	chr7:137080600-137106000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr7:137085200-137102400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr7:137086000-137102200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr7:137086000-137102400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr7:137088200-137093800	Enhancers	Cortex derived primary cultured neurospheres	brain
7	chr7:137088400-137094600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr7:137091000-137101200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr7:137091400-137124600	Weak transcription	Aorta	Aorta
10	chr7:137091600-137102000	Weak transcription	Muscle Satellite Cultured Cells	--
11	chr7:137092800-137094600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr7:137093200-137094400	Enhancers	Fetal Heart	heart
13	chr7:137093200-137102400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr7:137093400-137093800	Enhancers	Brain Substantia Nigra	brain
15	chr7:137093400-137094200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr7:137093400-137094200	Weak transcription	Brain Angular Gyrus	brain
17	chr7:137093400-137094400	Enhancers	Brain Cingulate Gyrus	brain
18	chr7:137093400-137095600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr7:137093400-137096400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr7:137093400-137103600	Weak transcription	Brain Inferior Temporal Lobe	brain
21	chr7:137093400-137108000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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