Variant report

Variant	rs2283261
Chromosome Location	chr11:17462304-17462305
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	FOS	chr11:17462116-17462376	MCF10A-Er-Src	breast:	n/a	n/a
2	FOS	chr11:17462117-17462396	MCF10A-Er-Src	breast:	n/a	n/a
3	NR3C1	chr11:17462019-17462506	A549	lung:	n/a	n/a
4	NR3C1	chr11:17462028-17462556	A549	lung:	n/a	n/a
5	FOS	chr11:17462126-17462406	MCF10A-Er-Src	breast:	n/a	n/a
6	FOS	chr11:17462120-17462353	MCF10A-Er-Src	breast:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:17459219..17462653-chr11:17463041..17467220,4	K562	blood:

Variant related genes	Relation type
SDHCP4	TF binding region
ENSG00000006071	Chromatin interaction

Extended variants
information (count: 53 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs10400389	0.87[EUR][1000 genomes]
rs10766399	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10766400	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10766401	0.88[EUR][1000 genomes]
rs10766402	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10766403	0.80[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs10832788	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10832789	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11024290	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11024295	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11821723	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12417170	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12786125	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12794627	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12803384	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs17775256	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2040653	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2057661	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2073585	0.95[EUR][1000 genomes]
rs2073586	0.92[EUR][1000 genomes]
rs2073587	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2074319	0.84[AMR][1000 genomes]
rs2237973	0.86[EUR][1000 genomes]
rs2237976	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2237977	0.91[EUR][1000 genomes]
rs2237978	0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2237979	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2237980	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2237982	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2237983	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2283259	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2301703	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs3781950	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3815066	0.80[AMR][1000 genomes]
rs3819517	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs3819519	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4148603	0.90[EUR][1000 genomes]
rs4148606	0.86[EUR][1000 genomes]
rs4148609	0.80[AMR][1000 genomes]
rs4148610	0.87[AMR][1000 genomes]
rs4459286	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6486370	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7105391	0.81[AMR][1000 genomes]
rs7117162	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs757109	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7932043	0.85[ASN][1000 genomes]
rs7934185	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7943461	0.87[AMR][1000 genomes]
rs7947326	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7950189	0.85[ASN][1000 genomes]
rs886291	0.81[AMR][1000 genomes]
rs886292	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes];0.97[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv469895	chr11:17368270-17584220	Weak transcription Bivalent Enhancer Genic enhancers Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs2283261	ABCC8	cis	Muscle Skeletal	GTEx

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:17443800-17462600	Weak transcription	Brain Substantia Nigra	brain
2	chr11:17454000-17464000	Weak transcription	Brain Anterior Caudate	brain
3	chr11:17454200-17465800	Weak transcription	Brain Angular Gyrus	brain
4	chr11:17456000-17469200	Weak transcription	Brain Inferior Temporal Lobe	brain
5	chr11:17457000-17467200	Weak transcription	Fetal Brain Male	brain
6	chr11:17457200-17465400	Weak transcription	Cortex derived primary cultured neurospheres	brain
7	chr11:17457400-17464600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr11:17460200-17462400	Strong transcription	Fetal Brain Female	brain
9	chr11:17460800-17474000	Weak transcription	Brain Cingulate Gyrus	brain
10	chr11:17461200-17497400	Weak transcription	Gastric	stomach
11	chr11:17461400-17462400	Weak transcription	Dnd41	blood
12	chr11:17462000-17465200	Strong transcription	Pancreatic Islets	Pancreatic Islet

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