Variant report

Variant	rs562686473
Chromosome Location	chr5:97402712-97402713
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 58 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:58 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1016231	chr5:97206242-97420435	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv1021856	chr5:97258323-97414178	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv599062	chr5:97258619-97430527	Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Weak transcription Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	esv2830155	chr5:97278902-97425123	Active TSS Weak transcription Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv882404	chr5:97281641-97638743	Active TSS Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
6	nsv1031989	chr5:97333291-97524353	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
7	nsv1034472	chr5:97357264-97523965	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Active TSS Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
8	nsv1019049	chr5:97373215-97442582	Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS	lncRNA	2 gene(s)	inside rSNPs	diseases
9	esv1821238	chr5:97383980-97402715	Enhancers Weak transcription Active TSS	n/a	n/a	inside rSNPs	diseases
10	esv2758004	chr5:97395508-97550089	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
11	esv2759357	chr5:97395508-97616089	Weak transcription Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
12	esv3468503	chr5:97399596-97404594	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases
13	esv3470569	chr5:97400159-97404048	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases
14	esv3470570	chr5:97400246-97404070	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
15	nsv10721	chr5:97400285-97403045	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
16	esv3348318	chr5:97400396-97403894	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
17	esv3470571	chr5:97400516-97403830	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
18	esv3468500	chr5:97400621-97404069	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases
19	esv1807551	chr5:97400688-97413587	Enhancers Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	inside rSNPs	diseases
20	esv1814114	chr5:97400688-97413587	Enhancers Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases
21	esv3498188	chr5:97400846-97403744	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
22	esv2520936	chr5:97400856-97403272	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
23	esv3468502	chr5:97401085-97403134	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
24	esv2149237	chr5:97401360-97402950	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
25	esv3498187	chr5:97401435-97402859	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
26	esv3468501	chr5:97401436-97402860	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
27	esv3498190	chr5:97401439-97402893	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
28	esv3498183	chr5:97401480-97402793	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
29	esv3468499	chr5:97401487-97402826	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
30	esv3468498	chr5:97401492-97402839	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
31	esv3498184	chr5:97401496-97402816	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
32	esv3468504	chr5:97401500-97402782	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
33	esv3498185	chr5:97401504-97402811	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
34	esv3426640	chr5:97401524-97402781	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
35	esv3062	chr5:97401531-97402850	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
36	nsv821462	chr5:97401540-97402755	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
37	nsv823151	chr5:97401540-97402755	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
38	esv994906	chr5:97401542-97402755	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
39	esv17847	chr5:97401542-97402755	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
40	esv3468505	chr5:97401548-97402765	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
41	esv3498189	chr5:97401558-97402765	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
42	esv3468506	chr5:97401562-97402763	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
43	esv3498191	chr5:97401562-97402763	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
44	nsv819012	chr5:97401568-97402804	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
45	esv1792399	chr5:97401582-97402715	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
46	esv1819057	chr5:97401582-97402715	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
47	esv1823948	chr5:97401582-97402715	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
48	esv1841669	chr5:97401582-97402715	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
49	nsv599067	chr5:97401582-97402715	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
50	esv1842435	chr5:97401582-97402967	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:97400800-97404000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr5:97401400-97402800	Weak transcription	NHDF-Ad	bronchial
3	chr5:97402600-97403000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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