Variant report

Variant	rs527569880
Chromosome Location	chr7:137089551-137089552
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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	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
5	nsv518230	chr7:137089537-137090469	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:34 , 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	chr7:137081200-137090000	Weak transcription	Aorta	Aorta
4	chr7:137082200-137089600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr7:137084800-137090200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr7:137085200-137102400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr7:137085400-137090000	Weak transcription	Muscle Satellite Cultured Cells	--
8	chr7:137085400-137091600	Weak transcription	HSMM	muscle
9	chr7:137085600-137089600	Weak transcription	Osteobl	bone
10	chr7:137085800-137089600	Weak transcription	NH-A	brain
11	chr7:137086000-137102200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr7:137086000-137102400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr7:137087600-137089600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr7:137088000-137089600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr7:137088200-137092400	Weak transcription	Brain Germinal Matrix	brain
16	chr7:137088200-137093800	Enhancers	Cortex derived primary cultured neurospheres	brain
17	chr7:137088400-137089600	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr7:137088400-137089800	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr7:137088400-137089800	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr7:137088400-137089800	Enhancers	iPS-20b Cell Line	embryonic stem cell
21	chr7:137088400-137089800	Enhancers	Brain Hippocampus Middle	brain
22	chr7:137088400-137092000	Weak transcription	Brain Inferior Temporal Lobe	brain
23	chr7:137088400-137092400	Weak transcription	Brain Angular Gyrus	brain
24	chr7:137088400-137094600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr7:137088600-137089800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr7:137088800-137091600	Weak transcription	Brain Substantia Nigra	brain
27	chr7:137088800-137092600	Weak transcription	Brain Cingulate Gyrus	brain
28	chr7:137089000-137089600	Weak transcription	HUES48 Cell Line	embryonic stem cell
29	chr7:137089200-137089800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr7:137089200-137090200	Enhancers	NHDF-Ad	bronchial
31	chr7:137089200-137090400	Enhancers	Brain Anterior Caudate	brain
32	chr7:137089200-137091000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr7:137089400-137089600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
34	chr7:137089400-137089800	Enhancers	ES-I3 Cell Line	embryonic stem cell

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