Variant report

Variant	rs271927
Chromosome Location	chr5:95741801-95741802
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	chr5:95718819..95721570-chr5:95740186..95742530,2	K562	blood:
2	chr5:95740417..95742590-chr5:95747586..95750354,2	K562	blood:

Variant related genes	Relation type
ENSG00000175426	Chromatin interaction

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs11135450	0.80[CEU][hapmap]
rs11135457	0.81[CEU][hapmap]
rs11741888	0.80[CEU][hapmap]
rs11743265	0.87[CEU][hapmap]
rs11948416	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs155439	0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs155971	0.96[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs155994	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs155995	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs156019	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs156021	0.96[CEU][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs156022	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs271919	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs271921	0.96[CEU][hapmap];0.87[JPT][hapmap];0.91[EUR][1000 genomes]
rs271923	0.95[CEU][hapmap];0.86[JPT][hapmap];0.91[EUR][1000 genomes]
rs271939	0.84[EUR][1000 genomes]
rs3792744	0.81[CEU][hapmap]
rs3811942	0.87[CEU][hapmap]
rs436321	0.95[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs456709	0.96[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs458450	0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4869284	0.83[CEU][hapmap]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1030444	chr5:95353620-95995619	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
2	nsv537810	chr5:95353620-95995619	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:95720800-95745400	Weak transcription	Brain Angular Gyrus	brain
2	chr5:95733000-95745800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr5:95735400-95743200	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr5:95738600-95742200	Weak transcription	HUVEC	blood vessel
5	chr5:95741400-95743400	Enhancers	Hela-S3	cervix

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