Variant report

Variant	rs565569582
Chromosome Location	chr9:8866968-8866969
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1022796	chr9:8360729-9110046	Enhancers Weak transcription Bivalent Enhancer Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
2	nsv1025800	chr9:8712487-9030627	Enhancers Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	nsv539980	chr9:8712487-9030627	Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	nsv892236	chr9:8745520-8870553	Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	nsv1015898	chr9:8753534-9011443	Active TSS Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
6	esv3326942	chr9:8865090-8872652	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
7	esv3483609	chr9:8865135-8872711	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
8	esv3483610	chr9:8865149-8872716	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
9	nsv522121	chr9:8865925-8870553	Weak transcription Enhancers Flanking Active TSS	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	chr9:8858800-8871400	Enhancers	Fetal Heart	heart
2	chr9:8859400-8870800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr9:8860200-8867400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr9:8860800-8867200	Weak transcription	Brain Germinal Matrix	brain
5	chr9:8861200-8867400	Weak transcription	Fetal Brain Female	brain
6	chr9:8863000-8868200	Enhancers	Brain Cingulate Gyrus	brain
7	chr9:8863400-8868200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr9:8863400-8872000	Weak transcription	Fetal Muscle Leg	muscle
9	chr9:8864600-8868800	Weak transcription	Small Intestine	intestine
10	chr9:8864600-8870800	Weak transcription	H1 Cell Line	embryonic stem cell
11	chr9:8864800-8867000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr9:8864800-8867000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr9:8864800-8867000	Weak transcription	Cortex derived primary cultured neurospheres	brain
14	chr9:8864800-8867200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr9:8864800-8867200	Weak transcription	Brain Inferior Temporal Lobe	brain
16	chr9:8864800-8868600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
17	chr9:8864800-8868600	Weak transcription	HUES48 Cell Line	embryonic stem cell
18	chr9:8864800-8869400	Weak transcription	Aorta	Aorta
19	chr9:8864800-8869400	Weak transcription	Fetal Intestine Small	intestine
20	chr9:8864800-8870800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr9:8864800-8870800	Enhancers	Brain Anterior Caudate	brain
22	chr9:8865000-8867000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr9:8865000-8867200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
24	chr9:8865000-8867200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
25	chr9:8865000-8868800	Weak transcription	HUES6 Cell Line	embryonic stem cell
26	chr9:8865000-8868800	Weak transcription	NH-A	brain
27	chr9:8865600-8867400	Weak transcription	Brain Angular Gyrus	brain
28	chr9:8865800-8870800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
29	chr9:8866200-8870800	Enhancers	Brain Substantia Nigra	brain
30	chr9:8866400-8867200	Enhancers	Brain Hippocampus Middle	brain
31	chr9:8866400-8867800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr9:8866600-8868400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr9:8866800-8867600	Enhancers	HUES64 Cell Line	embryonic stem cell
34	chr9:8866800-8870200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links