Variant report

Variant	rs535452107
Chromosome Location	chr7:77959855-77959856
allele	-/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:21 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv607654	chr7:77537964-78014329	Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	nsv1022764	chr7:77911072-78316607	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	esv8611	chr7:77959363-77960222	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
4	esv2407744	chr7:77959444-77960168	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
5	esv3476242	chr7:77959517-77960067	Weak transcription	n/a	n/a	inside rSNPs	diseases
6	esv3519551	chr7:77959546-77960054	Weak transcription	n/a	n/a	inside rSNPs	diseases
7	esv3519553	chr7:77959547-77960097	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
8	esv3476240	chr7:77959565-77960037	Weak transcription	n/a	n/a	inside rSNPs	diseases
9	esv3519555	chr7:77959566-77959995	Weak transcription	n/a	n/a	inside rSNPs	diseases
10	esv3476243	chr7:77959574-77960031	Weak transcription	n/a	n/a	inside rSNPs	diseases
11	esv5222	chr7:77959577-77960048	Weak transcription	n/a	n/a	inside rSNPs	diseases
12	esv3519556	chr7:77959584-77960016	Weak transcription	n/a	n/a	inside rSNPs	diseases
13	esv3476239	chr7:77959586-77959986	Weak transcription	n/a	n/a	inside rSNPs	diseases
14	esv3519554	chr7:77959596-77960007	Weak transcription	n/a	n/a	inside rSNPs	diseases
15	esv3418739	chr7:77959604-77959986	Weak transcription	n/a	n/a	inside rSNPs	diseases
16	esv3476244	chr7:77959621-77959968	Weak transcription	n/a	n/a	inside rSNPs	diseases
17	esv3519550	chr7:77959636-77959961	Weak transcription	n/a	n/a	inside rSNPs	diseases
18	esv3476245	chr7:77959637-77959977	Weak transcription	n/a	n/a	inside rSNPs	diseases
19	esv3519557	chr7:77959637-77959977	Weak transcription	n/a	n/a	inside rSNPs	diseases
20	esv996600	chr7:77959642-77959965	Weak transcription	n/a	n/a	inside rSNPs	diseases
21	esv1783865	chr7:77959652-77959976	Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:77946200-77976000	Weak transcription	Aorta	Aorta
2	chr7:77953600-77986600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr7:77955200-77963000	Weak transcription	Esophagus	oesophagus
4	chr7:77956800-77964400	Weak transcription	Ovary	ovary
5	chr7:77957000-77975800	Weak transcription	Brain Angular Gyrus	brain
6	chr7:77957200-77973200	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr7:77957200-77975800	Weak transcription	Brain Substantia Nigra	brain
8	chr7:77957600-77974800	Weak transcription	Brain Hippocampus Middle	brain
9	chr7:77957600-77976000	Weak transcription	Brain Cingulate Gyrus	brain
10	chr7:77957600-77978600	Weak transcription	Brain Anterior Caudate	brain
11	chr7:77958000-77979800	Weak transcription	Fetal Brain Female	brain

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