Variant report

Variant	rs567780051
Chromosome Location	chr8:69098057-69098058
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:20 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3331644	chr8:68806705-69189171	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv1028889	chr8:69026806-69308725	Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv948687	chr8:69041121-69642540	Flanking Bivalent TSS/Enh Enhancers Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
4	nsv512051	chr8:69096871-69098760	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
5	esv3490151	chr8:69097248-69099346	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
6	esv2472681	chr8:69097485-69099080	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
7	esv1972864	chr8:69097745-69098487	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
8	esv3490153	chr8:69097798-69098441	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
9	esv3479420	chr8:69097798-69098450	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
10	esv3490154	chr8:69097817-69098414	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
11	esv3490155	chr8:69097820-69098382	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
12	esv3479417	chr8:69097830-69098424	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
13	esv3396263	chr8:69097844-69098411	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
14	esv3490156	chr8:69097848-69098383	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
15	esv3479418	chr8:69097852-69098361	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
16	esv1003125	chr8:69097863-69098323	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
17	nsv819415	chr8:69097878-69098368	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
18	nsv471757	chr8:69097901-69098354	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
19	esv3479421	chr8:69097919-69098338	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
20	esv3490157	chr8:69097919-69098338	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:25 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:69043600-69107000	Weak transcription	Brain Substantia Nigra	brain
2	chr8:69052600-69104600	Weak transcription	Brain Hippocampus Middle	brain
3	chr8:69075000-69130800	Weak transcription	Primary hematopoietic stem cells	blood
4	chr8:69075200-69109200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr8:69075200-69113800	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr8:69076400-69104000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr8:69076400-69104200	Weak transcription	Adipose Nuclei	Adipose
8	chr8:69078400-69104400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
9	chr8:69078400-69113600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr8:69086000-69141600	Weak transcription	Fetal Muscle Leg	muscle
11	chr8:69087800-69108800	Weak transcription	Left Ventricle	heart
12	chr8:69090200-69100000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr8:69090400-69126800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr8:69090600-69100000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr8:69090600-69104400	Weak transcription	HUES64 Cell Line	embryonic stem cell
16	chr8:69092800-69115200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr8:69096000-69104400	Weak transcription	HUES48 Cell Line	embryonic stem cell
18	chr8:69096000-69114400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr8:69097000-69104600	Weak transcription	Brain Anterior Caudate	brain
20	chr8:69097400-69104800	Weak transcription	HUES6 Cell Line	embryonic stem cell
21	chr8:69097600-69104400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
22	chr8:69097800-69104600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr8:69097800-69110600	Weak transcription	HUVEC	blood vessel
24	chr8:69097800-69115000	Weak transcription	Fetal Stomach	stomach
25	chr8:69098000-69107600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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