Variant report

Variant	rs532621844
Chromosome Location	chr20:15302585-15302586
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 79 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:79 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1065152	chr20:14781684-15305258	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv1062252	chr20:14964258-15547739	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv544206	chr20:14964258-15547739	Enhancers ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv524481	chr20:15007730-15382919	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
5	nsv916795	chr20:15041479-15345528	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
6	nsv1060275	chr20:15084485-15327541	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
7	nsv1058890	chr20:15234769-15388360	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
8	esv2755557	chr20:15250014-15323282	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
9	nsv912787	chr20:15275538-15309089	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
10	nsv912788	chr20:15275538-15332749	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
11	nsv912789	chr20:15275538-15352001	Flanking Active TSS Weak transcription ZNF genes & repeats Enhancers Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
12	esv2757712	chr20:15282448-15331007	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
13	esv2758786	chr20:15282448-15331007	Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
14	nsv585583	chr20:15289701-15303701	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
15	esv1830261	chr20:15291552-15304048	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
16	nsv585584	chr20:15292533-15303701	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
17	nsv585585	chr20:15299632-15303357	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	inside rSNPs	diseases
18	esv1827682	chr20:15299632-15303701	Active TSS Weak transcription Enhancers Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
19	esv1832488	chr20:15299632-15303701	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	inside rSNPs	diseases
20	nsv585586	chr20:15299632-15303701	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	inside rSNPs	diseases
21	nsv585587	chr20:15299632-15304048	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	inside rSNPs	diseases
22	esv3454128	chr20:15299752-15305150	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
23	esv3454133	chr20:15301227-15304110	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
24	nsv9790	chr20:15301381-15304323	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
25	esv6820	chr20:15301487-15304036	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
26	esv3454134	chr20:15301601-15303862	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
27	esv3454135	chr20:15301645-15303848	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
28	esv3454131	chr20:15301656-15303842	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
29	esv3454132	chr20:15301668-15303796	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
30	nsv828689	chr20:15301684-15303739	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
31	nsv828690	chr20:15301684-15303827	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
32	esv3454129	chr20:15301718-15303773	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
33	nsv179952	chr20:15301732-15303768	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
34	esv3454136	chr20:15301732-15303772	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
35	nsv178993	chr20:15301735-15303771	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
36	esv11488	chr20:15301756-15303851	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
37	nsv585588	chr20:15301783-15303089	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
38	nsv585589	chr20:15301783-15303160	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
39	nsv585590	chr20:15301783-15303357	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
40	nsv585591	chr20:15301783-15303412	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
41	nsv585592	chr20:15301783-15303508	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
42	nsv585593	chr20:15301783-15303644	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
43	esv1832698	chr20:15301783-15303701	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
44	nsv585594	chr20:15301783-15303701	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
45	nsv585595	chr20:15301783-15304048	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
46	nsv828691	chr20:15301803-15303739	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
47	nsv585596	chr20:15301834-15303089	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
48	nsv585597	chr20:15301834-15303266	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
49	nsv585598	chr20:15301834-15303357	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
50	nsv585599	chr20:15301834-15303412	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:15301600-15302600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr20:15302000-15303600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr20:15302200-15303200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr20:15302200-15303800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr20:15302400-15303200	Weak transcription	Fetal Heart	heart
6	chr20:15302400-15303200	Weak transcription	HMEC	breast

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