Variant report

Variant	rs181978076
Chromosome Location	chr1:76574300-76574301
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 4 )
Associated
traits (count: 0)

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	nsv998499	chr1:76361784-76598712	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv871862	chr1:76525783-76598209	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv518927	chr1:76573614-76586272	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv522056	chr1:76573614-76598209	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:27 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:76548400-76576200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr1:76557400-76605800	Weak transcription	Fetal Intestine Small	intestine
3	chr1:76557600-76588800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr1:76569400-76575400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
5	chr1:76571200-76575000	Weak transcription	Left Ventricle	heart
6	chr1:76571200-76575200	Weak transcription	Sigmoid Colon	Sigmoid Colon
7	chr1:76571200-76575400	Weak transcription	Fetal Lung	lung
8	chr1:76571800-76575000	Weak transcription	Primary B cells from peripheral blood	blood
9	chr1:76572200-76575000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr1:76572200-76575200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
11	chr1:76572200-76577000	Enhancers	Brain Substantia Nigra	brain
12	chr1:76572800-76575000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
13	chr1:76572800-76575600	Weak transcription	Primary B cells from cord blood	blood
14	chr1:76573000-76575000	Weak transcription	Brain Cingulate Gyrus	brain
15	chr1:76573400-76575600	Enhancers	Fetal Kidney	kidney
16	chr1:76573400-76576400	Enhancers	Brain Angular Gyrus	brain
17	chr1:76573600-76575000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr1:76573600-76575000	Enhancers	Brain Hippocampus Middle	brain
19	chr1:76573800-76574400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr1:76573800-76575000	Weak transcription	H1 Cell Line	embryonic stem cell
21	chr1:76574000-76575000	Weak transcription	Brain Inferior Temporal Lobe	brain
22	chr1:76574000-76576800	Enhancers	Brain Anterior Caudate	brain
23	chr1:76574200-76574400	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr1:76574200-76574800	Weak transcription	Adipose Nuclei	Adipose
25	chr1:76574200-76575000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr1:76574200-76575200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
27	chr1:76574200-76575200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin

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