Variant report

Variant	rs192190035
Chromosome Location	chr10:96871396-96871397
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 73 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:73 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv497859	chr10:96058024-97027747	Strong transcription Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
2	nsv529726	chr10:96632494-97106315	Strong transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
3	nsv1043378	chr10:96855366-96876009	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
4	esv21432	chr10:96856006-96996043	Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv1040288	chr10:96857760-96876077	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	inside rSNPs	diseases
6	nsv1040270	chr10:96857760-96882502	Enhancers ZNF genes & repeats Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS	n/a	n/a	inside rSNPs	diseases
7	nsv7498	chr10:96857894-96881940	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	n/a	n/a	inside rSNPs	diseases
8	nsv1054199	chr10:96861570-96875702	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	inside rSNPs	diseases
9	nsv1035517	chr10:96861570-96876009	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
10	nsv551965	chr10:96864805-96872102	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
11	nsv551966	chr10:96864805-96874416	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
12	nsv437691	chr10:96864805-96876696	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	inside rSNPs	diseases
13	esv15617	chr10:96864858-96874954	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
14	nsv1049012	chr10:96865081-96875947	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	inside rSNPs	diseases
15	nsv1051425	chr10:96865081-96875963	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	inside rSNPs	diseases
16	esv1792985	chr10:96865081-96876077	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	inside rSNPs	diseases
17	esv1813761	chr10:96865081-96876077	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
18	esv1828293	chr10:96865081-96876077	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	inside rSNPs	diseases
19	esv1839838	chr10:96865081-96876077	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	inside rSNPs	diseases
20	nsv1051877	chr10:96865081-96876077	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	inside rSNPs	diseases
21	nsv1042421	chr10:96865081-96882502	Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Active TSS	n/a	n/a	inside rSNPs	diseases
22	nsv1046150	chr10:96865081-96885334	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer Flanking Active TSS Active TSS	n/a	n/a	inside rSNPs	diseases
23	esv1837238	chr10:96865093-96876089	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	inside rSNPs	diseases
24	nsv1041130	chr10:96865172-96882502	Bivalent Enhancer ZNF genes & repeats Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
25	nsv1037640	chr10:96865196-96876077	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	inside rSNPs	diseases
26	nsv436103	chr10:96866651-96875162	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
27	esv3316352	chr10:96867106-96875021	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
28	esv3316363	chr10:96867179-96874947	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
29	nsv498738	chr10:96867192-96874943	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
30	esv3316374	chr10:96867193-96874943	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
31	esv3318407	chr10:96869162-96873660	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
32	esv3318419	chr10:96869162-96873660	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
33	nsv551967	chr10:96870565-96871711	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
34	nsv551968	chr10:96870565-96871922	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
35	nsv551969	chr10:96870565-96871974	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
36	nsv551970	chr10:96870565-96872026	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
37	nsv551971	chr10:96870565-96872102	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
38	nsv551972	chr10:96870565-96872142	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
39	nsv551973	chr10:96870565-96872409	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
40	nsv551974	chr10:96870565-96872460	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
41	nsv551975	chr10:96870565-96872731	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
42	nsv551976	chr10:96870565-96872965	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
43	nsv551977	chr10:96870565-96873127	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
44	nsv551978	chr10:96870565-96873303	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
45	nsv551979	chr10:96870565-96873355	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
46	nsv551980	chr10:96870565-96873521	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
47	nsv551981	chr10:96870565-96873763	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
48	nsv551982	chr10:96870565-96873936	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
49	nsv551983	chr10:96870565-96874184	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
50	nsv551984	chr10:96870565-96874416	Weak transcription Enhancers	n/a	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	chr10:96869000-96871600	Enhancers	HepG2	liver

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