Variant report

Variant	rs2237973
Chromosome Location	chr11:17490571-17490572
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:17484097..17487260-chr11:17487485..17491025,3	MCF-7	breast:
2	chr11:17490196..17492539-chr11:17495004..17496625,2	K562	blood:
3	chr11:17372929..17375866-chr11:17489485..17491410,2	K562	blood:

Variant related genes	Relation type
ENSG00000188211	Chromatin interaction

Extended variants
information (count: 79 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:74)

rs_ID	r²[population]
rs10400389	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10766401	0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10766402	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10766403	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10832788	0.86[EUR][1000 genomes]
rs10832789	0.86[EUR][1000 genomes]
rs10832791	0.88[AMR][1000 genomes];0.80[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11024290	0.86[EUR][1000 genomes]
rs11024295	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11024296	0.89[AMR][1000 genomes];0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11024297	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11024299	0.89[AMR][1000 genomes];0.83[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11826760	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12285976	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12417170	0.86[EUR][1000 genomes]
rs12786125	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12803384	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2057661	0.90[EUR][1000 genomes]
rs2073585	0.90[EUR][1000 genomes]
rs2073586	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2073587	0.85[EUR][1000 genomes]
rs2074319	0.89[ASN][1000 genomes]
rs2237966	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2237967	0.85[ASN][1000 genomes]
rs2237968	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2237969	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2237970	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2237971	0.87[AMR][1000 genomes];0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2237972	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2237974	0.83[AMR][1000 genomes]
rs2237976	0.90[EUR][1000 genomes]
rs2237977	0.80[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2237979	0.83[AMR][1000 genomes]
rs2237980	0.86[EUR][1000 genomes]
rs2237982	0.86[EUR][1000 genomes]
rs2237983	0.86[EUR][1000 genomes]
rs2283254	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2283256	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2283259	0.90[EUR][1000 genomes]
rs2283261	0.86[EUR][1000 genomes]
rs2301703	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs3781950	0.85[EUR][1000 genomes]
rs3815066	0.90[ASN][1000 genomes]
rs3819517	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3819518	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs3819519	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3819520	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs3819521	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs3819522	0.89[ASN][1000 genomes]
rs3819523	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs3819524	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4148601	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4148602	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4148603	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4148604	0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4148605	0.81[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs4148606	0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4148607	0.81[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs4148608	0.81[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs4148609	0.90[ASN][1000 genomes]
rs4148610	0.83[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs4459286	0.86[EUR][1000 genomes]
rs6486370	0.85[EUR][1000 genomes]
rs7105391	0.90[ASN][1000 genomes]
rs7105832	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7106250	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7119716	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7120682	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs71457878	0.81[ASN][1000 genomes]
rs757109	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7934185	0.87[EUR][1000 genomes]
rs7943461	0.83[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs886289	0.81[ASN][1000 genomes]
rs886291	0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 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
2	nsv897019	chr11:17475443-17499547	Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv897020	chr11:17476516-17491386	Strong transcription Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
4	nsv897021	chr11:17478157-17491386	Enhancers Strong transcription Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
5	nsv897022	chr11:17478157-17496516	Enhancers Bivalent Enhancer Strong transcription Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs2237973	ABCC8	cis	Muscle Skeletal	GTEx

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:17461200-17497400	Weak transcription	Gastric	stomach
2	chr11:17465800-17496400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr11:17480200-17494000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr11:17480200-17494200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr11:17480200-17494800	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr11:17481800-17495200	Weak transcription	Brain Hippocampus Middle	brain
7	chr11:17483800-17493400	Weak transcription	Brain Cingulate Gyrus	brain
8	chr11:17485400-17491200	Weak transcription	Brain Angular Gyrus	brain
9	chr11:17486000-17492600	Weak transcription	Spleen	Spleen
10	chr11:17487200-17494200	Weak transcription	Brain Inferior Temporal Lobe	brain
11	chr11:17488600-17492800	Strong transcription	Pancreatic Islets	Pancreatic Islet
12	chr11:17489600-17493200	Strong transcription	Brain Anterior Caudate	brain
13	chr11:17489800-17492000	Strong transcription	Fetal Brain Female	brain
14	chr11:17490200-17496200	Weak transcription	Brain Germinal Matrix	brain
15	chr11:17490400-17490800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain

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