Variant report

Variant	rs191635699
Chromosome Location	chr13:65343536-65343537
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 107 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:107 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv455914	chr13:64432922-65368490	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv561965	chr13:64432922-65368490	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	esv3367739	chr13:64805577-65549276	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv1038150	chr13:65224379-65354892	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv1042755	chr13:65300441-65400043	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv561970	chr13:65338673-65352129	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv561971	chr13:65339453-65343969	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
8	nsv561972	chr13:65339575-65343923	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
9	nsv561973	chr13:65339575-65344090	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
10	nsv561974	chr13:65339575-65344159	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
11	nsv511524	chr13:65339575-65350465	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
12	nsv561975	chr13:65339575-65352237	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
13	nsv561976	chr13:65339575-65353103	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
14	nsv561977	chr13:65339575-65353382	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
15	nsv561978	chr13:65339575-65360698	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
16	nsv561979	chr13:65339575-65366000	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
17	esv3518507	chr13:65340751-65346149	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
18	nsv512323	chr13:65341495-65344616	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
19	esv3518551	chr13:65341904-65344715	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
20	esv994619	chr13:65342061-65347087	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
21	esv3518540	chr13:65342291-65344534	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
22	esv989362	chr13:65342334-65344390	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
23	esv3518529	chr13:65342345-65344503	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
24	esv3518518	chr13:65342379-65344524	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
25	esv3518562	chr13:65342428-65344430	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
26	esv11248	chr13:65342512-65344495	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
27	nsv561982	chr13:65342539-65343538	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
28	nsv561983	chr13:65342539-65343762	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
29	nsv561984	chr13:65342539-65343867	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
30	nsv561985	chr13:65342539-65343923	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
31	nsv561986	chr13:65342539-65343969	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
32	nsv561987	chr13:65342539-65344090	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
33	nsv561988	chr13:65342539-65344159	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
34	nsv561989	chr13:65342539-65352129	Enhancers Weak transcription	lncRNA	n/a	inside rSNPs	diseases
35	nsv561990	chr13:65342539-65352237	Enhancers Weak transcription	lncRNA	n/a	inside rSNPs	diseases
36	nsv561991	chr13:65342539-65352759	Enhancers Weak transcription	lncRNA	n/a	inside rSNPs	diseases
37	nsv561992	chr13:65342539-65352940	Weak transcription Enhancers	lncRNA	n/a	inside rSNPs	diseases
38	nsv561993	chr13:65342539-65352958	Enhancers Weak transcription	lncRNA	n/a	inside rSNPs	diseases
39	nsv561994	chr13:65342539-65353103	Weak transcription Enhancers	lncRNA	n/a	inside rSNPs	diseases
40	nsv561995	chr13:65342539-65353382	Weak transcription Enhancers	lncRNA	n/a	inside rSNPs	diseases
41	nsv561996	chr13:65342539-65360698	Weak transcription Enhancers	lncRNA	n/a	inside rSNPs	diseases
42	nsv561997	chr13:65342539-65360737	Enhancers Weak transcription	lncRNA	n/a	inside rSNPs	diseases
43	nsv561998	chr13:65342591-65343710	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
44	nsv561999	chr13:65342591-65343762	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
45	nsv562000	chr13:65342591-65343867	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
46	nsv562001	chr13:65342591-65343923	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
47	nsv562002	chr13:65342591-65343969	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
48	nsv562003	chr13:65342591-65344090	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
49	nsv562004	chr13:65342591-65344159	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
50	nsv562005	chr13:65342591-65352129	Enhancers Weak transcription	lncRNA	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	chr13:65343400-65344200	Enhancers	HUVEC	blood vessel

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