Variant report

Variant	rs8136113
Chromosome Location	chr22:28935954-28935955
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr22:28934195..28936559-chr22:28940613..28943481,2	K562	blood:

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs11912125	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11912717	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs13053405	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13054496	0.91[EUR][1000 genomes]
rs13054508	0.85[EUR][1000 genomes]
rs13055501	0.91[EUR][1000 genomes]
rs13055576	0.94[EUR][1000 genomes]
rs13055649	0.88[EUR][1000 genomes]
rs13056776	1.00[EUR][1000 genomes]
rs34188840	1.00[EUR][1000 genomes]
rs34277219	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34285557	0.81[EUR][1000 genomes]
rs34780660	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs34843903	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs34928826	0.94[EUR][1000 genomes]
rs34929472	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs34970554	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs34994167	0.83[AFR][1000 genomes];0.91[EUR][1000 genomes]
rs35230579	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs35286648	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs35507981	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs35719457	0.85[EUR][1000 genomes]
rs36100499	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57062250	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs58433661	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs71316850	0.91[EUR][1000 genomes]
rs71325299	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs71325302	0.94[AFR][1000 genomes]
rs71327305	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7286202	0.83[AFR][1000 genomes];0.91[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1067544	chr22:28755418-29055246	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	4 gene(s)	inside rSNPs	diseases
2	nsv544674	chr22:28755418-29055246	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	4 gene(s)	inside rSNPs	diseases
3	nsv588880	chr22:28807277-29001789	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region miRNA	3 gene(s)	inside rSNPs	diseases
4	nsv916473	chr22:28837041-29215603	Weak transcription Bivalent Enhancer Active TSS Enhancers Strong transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	83 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:28916600-28937200	Weak transcription	HepG2	liver
2	chr22:28917600-28943200	Weak transcription	Left Ventricle	heart
3	chr22:28923400-28940400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr22:28932200-28939000	Weak transcription	Fetal Stomach	stomach
5	chr22:28932600-28939000	Weak transcription	Fetal Intestine Small	intestine
6	chr22:28933600-28953800	Weak transcription	HSMMtube	muscle
7	chr22:28934000-28938800	Weak transcription	Cortex derived primary cultured neurospheres	brain
8	chr22:28935000-28936200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
9	chr22:28935400-28940600	Weak transcription	Spleen	Spleen
10	chr22:28935400-28943000	Weak transcription	Fetal Brain Male	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links