Variant report

Variant	rs531989801
Chromosome Location	chr13:70402844-70402845
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 31 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:31 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1045844	chr13:70038096-70405435	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv900481	chr13:70147851-70560731	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv1054554	chr13:70159715-70502956	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	esv1837120	chr13:70209507-70425056	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
5	nsv482460	chr13:70240630-70419347	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
6	nsv900483	chr13:70254555-70464234	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
7	nsv900486	chr13:70302991-70421896	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
8	nsv832643	chr13:70324440-70486661	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
9	nsv900487	chr13:70327693-70548643	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
10	nsv1041207	chr13:70347748-70473605	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
11	nsv530724	chr13:70393680-71164323	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
12	nsv562208	chr13:70397216-70403590	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
13	nsv562209	chr13:70399003-70406091	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
14	nsv562210	chr13:70399003-70407024	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
15	nsv562211	chr13:70399346-70405460	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
16	nsv562212	chr13:70399346-70407024	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
17	nsv436166	chr13:70401337-70407452	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
18	esv2564277	chr13:70401460-70407643	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
19	esv3518797	chr13:70401821-70406891	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
20	esv3518808	chr13:70401861-70406873	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
21	esv2405237	chr13:70401874-70406985	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
22	esv3518819	chr13:70401913-70406904	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
23	esv3518830	chr13:70401967-70406793	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
24	esv12608	chr13:70401982-70407255	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
25	nsv976131	chr13:70402083-70423358	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
26	esv10859	chr13:70402384-70403675	Enhancers	n/a	n/a	inside rSNPs	diseases
27	nsv562213	chr13:70402522-70405460	Enhancers	n/a	n/a	inside rSNPs	diseases
28	nsv562214	chr13:70402522-70405615	Enhancers	n/a	n/a	inside rSNPs	diseases
29	nsv562215	chr13:70402522-70406769	Enhancers	n/a	n/a	inside rSNPs	diseases
30	nsv562216	chr13:70402522-70407024	Enhancers	n/a	n/a	inside rSNPs	diseases
31	nsv562217	chr13:70402734-70405615	Enhancers	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:70402000-70403600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr13:70402200-70403200	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chr13:70402200-70403400	Enhancers	HUES6 Cell Line	embryonic stem cell
4	chr13:70402600-70403200	Enhancers	Adipose Nuclei	Adipose
5	chr13:70402600-70403200	Enhancers	Placenta Amnion	Placenta Amnion
6	chr13:70402800-70403000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr13:70402800-70403200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell

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