Variant report

Variant	rs545694900
Chromosome Location	chr16:80468975-80468976
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr16:80467020..80469434-chr16:80558552..80560756,2	K562	blood:

Extended variants
information (count: 29 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:29 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1061068	chr16:80207546-80537052	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	esv2762333	chr16:80307755-80509983	Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
3	nsv1056026	chr16:80317627-80471469	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
4	nsv542987	chr16:80317627-80471469	Bivalent Enhancer Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
5	nsv833299	chr16:80341745-80549683	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv1061190	chr16:80392009-80471330	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv542988	chr16:80392009-80471330	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Active TSS Strong transcription Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
8	nsv907000	chr16:80405292-80473018	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Active TSS Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
9	nsv907001	chr16:80405292-80620611	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
10	nsv510692	chr16:80432497-80503607	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
11	nsv1055975	chr16:80437861-80513030	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
12	nsv907002	chr16:80441420-80510943	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
13	esv2751614	chr16:80459551-80511649	Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
14	esv3380602	chr16:80467926-80469974	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
15	esv3490725	chr16:80467936-80470103	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
16	esv2457793	chr16:80468193-80469662	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
17	esv6166	chr16:80468372-80469231	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
18	esv2374489	chr16:80468446-80469145	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
19	esv3338020	chr16:80468451-80469449	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
20	esv3490720	chr16:80468496-80469053	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
21	esv3325492	chr16:80468530-80469084	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
22	esv3313057	chr16:80468532-80469046	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
23	esv3313059	chr16:80468544-80469124	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
24	esv3490721	chr16:80468556-80468998	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
25	esv3490719	chr16:80468558-80468982	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
26	esv3313055	chr16:80468565-80469015	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
27	esv3490724	chr16:80468572-80468989	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
28	esv5329	chr16:80468572-80469099	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
29	esv3490723	chr16:80468574-80468995	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	chr16:80468200-80471000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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