Variant report

Variant	rs11211855
Chromosome Location	chr11:106545284-106545285
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GUCY1A2-1	chr11:106544738-106550066	ENSG00000260512.1
2	lnc-GUCY1A2-1	chr11:106544748-106546997	NONHSAT023989

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs10502075	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10890565	0.92[EUR][1000 genomes]
rs11211852	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11211853	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs11211854	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11211856	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11211860	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11211861	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11211863	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11211864	0.86[AFR][1000 genomes];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11211865	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11211866	0.86[AFR][1000 genomes];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11211869	0.86[AFR][1000 genomes];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12360850	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12362289	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12365648	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs17563648	0.86[AFR][1000 genomes];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs17563662	0.86[AFR][1000 genomes];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs17649054	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs61903142	0.87[EUR][1000 genomes]
rs61903143	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs61903144	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs61903145	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs61903146	0.96[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs61903149	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs61903150	0.86[AFR][1000 genomes];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs61903152	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs9645655	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1048381	chr11:105945117-106561574	Weak transcription Enhancers Active TSS Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
2	nsv898359	chr11:106523574-106656863	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
3	nsv556228	chr11:106535709-106576657	Enhancers Weak transcription Strong transcription	Chromatin interactive region lncRNA	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	chr11:106541800-106550400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
2	chr11:106543600-106547600	Weak transcription	Fetal Brain Male	brain
3	chr11:106545000-106550400	Weak transcription	HUES48 Cell Line	embryonic stem cell

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