Variant report

Variant	rs576507805
Chromosome Location	chr15:34277034-34277035
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1043046	chr15:33714908-34321330	Enhancers Flanking Active TSS Strong transcription Weak transcription ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
2	nsv456789	chr15:34034421-34426618	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
3	nsv568920	chr15:34034421-34426618	Enhancers Flanking Active TSS Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer 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	29 gene(s)	inside rSNPs	diseases
4	nsv471235	chr15:34035529-34421951	Strong transcription Weak transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
5	nsv1044844	chr15:34065524-34296829	Enhancers Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
6	nsv456790	chr15:34264018-34281733	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	nsv568923	chr15:34264018-34281733	Enhancers Weak transcription Active TSS Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
8	esv2761666	chr15:34275262-34279231	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	inside rSNPs	diseases
9	nsv516347	chr15:34276169-34277907	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	inside rSNPs	diseases
10	nsv456791	chr15:34276169-34277907	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	inside rSNPs	diseases
11	nsv456792	chr15:34276169-34277907	Flanking Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	inside rSNPs	diseases
12	nsv568924	chr15:34276169-34277907	Flanking Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:37 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:34236800-34277200	Weak transcription	Left Ventricle	heart
2	chr15:34238000-34282400	Weak transcription	Ovary	ovary
3	chr15:34261200-34277200	Weak transcription	Brain Anterior Caudate	brain
4	chr15:34263800-34277200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr15:34264800-34281200	Weak transcription	GM12878-XiMat	blood
6	chr15:34265200-34299600	Weak transcription	Sigmoid Colon	Sigmoid Colon
7	chr15:34265400-34294200	Weak transcription	Fetal Stomach	stomach
8	chr15:34265400-34311800	Weak transcription	Liver	Liver
9	chr15:34270200-34277400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
10	chr15:34271600-34277200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
11	chr15:34271600-34277400	Weak transcription	Pancreas	Pancrea
12	chr15:34273000-34277600	Weak transcription	NHEK	skin
13	chr15:34274000-34277200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
14	chr15:34274000-34277400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr15:34274000-34277400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr15:34274200-34277400	Weak transcription	NHLF	lung
17	chr15:34274400-34311000	Weak transcription	Primary B cells from cord blood	blood
18	chr15:34275400-34293200	Weak transcription	Primary T cells from cord blood	blood
19	chr15:34276200-34277200	Weak transcription	Brain Angular Gyrus	brain
20	chr15:34276400-34277200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr15:34276800-34277600	Enhancers	HepG2	liver
22	chr15:34276800-34278200	Enhancers	Brain Cingulate Gyrus	brain
23	chr15:34276800-34278200	Enhancers	Brain Substantia Nigra	brain
24	chr15:34276800-34278400	Enhancers	Brain Hippocampus Middle	brain
25	chr15:34276800-34278400	Enhancers	Placenta	Placenta
26	chr15:34277000-34277200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr15:34277000-34277200	Enhancers	HMEC	breast
28	chr15:34277000-34277400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr15:34277000-34277400	Enhancers	Aorta	Aorta
30	chr15:34277000-34277400	Enhancers	Osteobl	bone
31	chr15:34277000-34277800	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr15:34277000-34278000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr15:34277000-34278000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr15:34277000-34278000	Enhancers	Adipose Nuclei	Adipose
35	chr15:34277000-34278000	Enhancers	Brain Inferior Temporal Lobe	brain
36	chr15:34277000-34278200	Enhancers	Placenta Amnion	Placenta Amnion
37	chr15:34277000-34278200	Enhancers	HSMMtube	muscle

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