Variant report

Variant	rs2432027
Chromosome Location	chr5:97402884-97402885
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 28 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:28 , 50 per page) page: 1

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	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
10	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
11	esv3468503	chr5:97399596-97404594	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases
12	esv3470569	chr5:97400159-97404048	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases
13	esv3470570	chr5:97400246-97404070	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
14	nsv10721	chr5:97400285-97403045	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
15	esv3348318	chr5:97400396-97403894	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
16	esv3470571	chr5:97400516-97403830	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
17	esv3468500	chr5:97400621-97404069	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases
18	esv1807551	chr5:97400688-97413587	Enhancers Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	inside rSNPs	diseases
19	esv1814114	chr5:97400688-97413587	Enhancers Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases
20	esv3498188	chr5:97400846-97403744	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
21	esv2520936	chr5:97400856-97403272	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
22	esv3468502	chr5:97401085-97403134	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
23	esv2149237	chr5:97401360-97402950	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
24	esv3498190	chr5:97401439-97402893	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
25	esv1842435	chr5:97401582-97402967	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
26	esv1849438	chr5:97401582-97402967	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
27	esv1810755	chr5:97401738-97402967	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
28	nsv599075	chr5:97402033-97402967	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	chr5:97402600-97403000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr5:97402800-97403200	Enhancers	NHDF-Ad	bronchial

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links