Variant report

Variant	rs182222798
Chromosome Location	chr8:118223808-118223809
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:118222096..118223964-chr8:118223982..118226303,2	K562	blood:

Extended variants
information (count: 22 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:22 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530386	chr8:117509968-118391406	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
2	nsv1031711	chr8:118134669-118322562	Enhancers Bivalent Enhancer Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv1027039	chr8:118143762-118460954	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv972573	chr8:118221506-118227792	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
5	esv3329468	chr8:118222821-118224819	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
6	esv2439441	chr8:118222936-118224464	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
7	esv3339059	chr8:118223321-118224319	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
8	esv3489832	chr8:118223379-118223952	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
9	esv1999169	chr8:118223385-118224004	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
10	esv3480601	chr8:118223405-118223925	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
11	esv3426819	chr8:118223406-118223944	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
12	esv3489833	chr8:118223436-118223913	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
13	esv3480599	chr8:118223440-118223899	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
14	esv3480600	chr8:118223464-118223882	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
15	esv3398431	chr8:118223472-118223860	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
16	esv4645	chr8:118223475-118223892	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
17	esv3489831	chr8:118223477-118223893	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
18	esv3346638	chr8:118223492-118223830	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
19	esv3480602	chr8:118223530-118223823	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
20	esv3489834	chr8:118223530-118223823	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
21	esv1715127	chr8:118223542-118223822	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
22	nsv397892	chr8:118223543-118223822	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:118217600-118225600	Weak transcription	Pancreatic Islets	Pancreatic Islet

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