Variant report

Variant	rs72903855
Chromosome Location	chr2:188883897-188883898
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 64 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:54)

rs_ID	r²[population]
rs11673994	1.00[AFR][1000 genomes]
rs11674292	1.00[AFR][1000 genomes]
rs11679720	1.00[AFR][1000 genomes]
rs11685495	1.00[AFR][1000 genomes]
rs11687577	1.00[AFR][1000 genomes]
rs11691788	1.00[AFR][1000 genomes]
rs11692575	1.00[AFR][1000 genomes]
rs11695469	1.00[AFR][1000 genomes]
rs12151778	1.00[AFR][1000 genomes]
rs12185535	1.00[AFR][1000 genomes]
rs12185546	1.00[AFR][1000 genomes]
rs12185596	1.00[AFR][1000 genomes]
rs12185714	1.00[AFR][1000 genomes]
rs72895717	1.00[AFR][1000 genomes]
rs72895720	1.00[AFR][1000 genomes]
rs72895727	1.00[AFR][1000 genomes]
rs72895728	1.00[AFR][1000 genomes]
rs72895740	1.00[AFR][1000 genomes]
rs72895757	1.00[AFR][1000 genomes]
rs72897930	1.00[AFR][1000 genomes]
rs72897939	1.00[AFR][1000 genomes]
rs72899689	1.00[AFR][1000 genomes]
rs72901682	1.00[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs72901686	1.00[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs72903871	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72903876	1.00[AFR][1000 genomes]
rs72903884	1.00[AFR][1000 genomes]
rs72903890	1.00[AFR][1000 genomes]
rs72903892	1.00[AFR][1000 genomes]
rs72903902	1.00[AFR][1000 genomes]
rs72907958	1.00[AFR][1000 genomes]
rs72907969	1.00[AFR][1000 genomes]
rs72907987	1.00[AFR][1000 genomes]
rs72909876	1.00[AFR][1000 genomes]
rs72909889	1.00[AFR][1000 genomes]
rs72909891	1.00[AFR][1000 genomes]
rs72909893	1.00[AFR][1000 genomes]
rs72909895	1.00[AFR][1000 genomes]
rs72911709	1.00[AFR][1000 genomes]
rs72911710	1.00[AFR][1000 genomes]
rs72911713	1.00[AFR][1000 genomes]
rs72911720	1.00[AFR][1000 genomes]
rs72911722	1.00[AFR][1000 genomes]
rs72911729	1.00[AFR][1000 genomes]
rs72911733	1.00[AFR][1000 genomes]
rs72911739	1.00[AFR][1000 genomes]
rs72911740	1.00[AFR][1000 genomes]
rs72911751	1.00[AFR][1000 genomes]
rs72911762	1.00[AFR][1000 genomes]
rs72911775	1.00[AFR][1000 genomes]
rs72911777	1.00[AFR][1000 genomes]
rs72911779	1.00[AFR][1000 genomes]
rs72911782	1.00[AFR][1000 genomes]
rs72911793	1.00[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv533353	chr2:188498301-189024655	Weak transcription Enhancers Bivalent Enhancer Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv875597	chr2:188573244-188916290	Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv1011832	chr2:188631943-188896492	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv536087	chr2:188631943-188896492	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	nsv584041	chr2:188644642-188928433	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv523293	chr2:188774681-188928433	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv470503	chr2:188837548-188896397	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
8	nsv584043	chr2:188837548-188896397	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
9	nsv875600	chr2:188857787-188893936	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
10	nsv875601	chr2:188871436-188934777	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:188875600-188884400	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr2:188882000-188884400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr2:188882800-188884400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links