Variant report

Variant	rs11168811
Chromosome Location	chr12:49357514-49357515
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr12:49357444..49360120-chr12:49362245..49365258,3	MCF-7	breast:
2	chr12:49349743..49353633-chr12:49353636..49360057,10	MCF-7	breast:
3	chr12:49356312..49360341-chr12:49373625..49376038,3	MCF-7	breast:
4	chr12:49356930..49359441-chr12:49379101..49381490,2	K562	blood:
5	chr12:49351134..49353553-chr12:49353996..49358640,5	MCF-7	breast:
6	chr12:49356416..49360894-chr12:49369694..49373633,4	MCF-7	breast:
7	chr12:49357111..49358918-chr12:49364300..49365973,2	K562	blood:

Variant related genes	Relation type
ENSG00000134287	Chromatin interaction
ENSG00000272822	Chromatin interaction
ENSG00000125084	Chromatin interaction
ENSG00000169884	Chromatin interaction

Extended variants
information (count: 95 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:92)

rs_ID	r²[population]
rs1051886	0.87[ASN][1000 genomes]
rs1054376	0.85[ASN][1000 genomes]
rs10747557	0.87[ASN][1000 genomes]
rs10747558	0.87[ASN][1000 genomes]
rs10783289	0.81[ASN][1000 genomes]
rs10783290	0.80[ASN][1000 genomes]
rs10783293	0.80[ASN][1000 genomes]
rs10783294	0.80[ASN][1000 genomes]
rs10783295	0.80[ASN][1000 genomes]
rs10783297	0.87[ASN][1000 genomes]
rs10875894	0.80[ASN][1000 genomes]
rs10875895	0.80[ASN][1000 genomes]
rs10875897	0.87[ASN][1000 genomes]
rs10875898	0.87[ASN][1000 genomes]
rs10875899	0.83[ASN][1000 genomes]
rs10875900	0.87[ASN][1000 genomes]
rs10875901	0.88[ASN][1000 genomes]
rs10875902	0.89[ASN][1000 genomes]
rs1111662	0.86[ASN][1000 genomes]
rs11168785	0.80[ASN][1000 genomes]
rs11168790	0.80[ASN][1000 genomes]
rs11168792	0.82[ASN][1000 genomes]
rs11168794	0.82[ASN][1000 genomes]
rs11168795	0.86[ASN][1000 genomes]
rs11168797	0.86[ASN][1000 genomes]
rs11168798	0.82[ASN][1000 genomes]
rs11168800	0.82[ASN][1000 genomes]
rs11168801	0.82[ASN][1000 genomes]
rs11168803	0.87[ASN][1000 genomes]
rs11168812	0.87[ASN][1000 genomes]
rs11610459	0.80[ASN][1000 genomes]
rs11610497	0.80[ASN][1000 genomes]
rs11614474	0.80[ASN][1000 genomes]
rs12229275	0.80[ASN][1000 genomes]
rs12423542	0.82[ASN][1000 genomes]
rs12579249	0.80[ASN][1000 genomes]
rs1690182	0.89[ASN][1000 genomes]
rs1818996	0.87[ASN][1000 genomes]
rs1830192	0.87[ASN][1000 genomes]
rs2030900	0.87[ASN][1000 genomes]
rs2070940	0.87[ASN][1000 genomes]
rs2073480	0.86[ASN][1000 genomes]
rs2131713	0.87[ASN][1000 genomes]
rs2272311	0.86[ASN][1000 genomes]
rs2272312	0.82[ASN][1000 genomes]
rs2293449	0.83[ASN][1000 genomes]
rs2453063	0.87[ASN][1000 genomes]
rs2463175	0.85[ASN][1000 genomes]
rs2641450	0.84[ASN][1000 genomes]
rs2694839	0.86[ASN][1000 genomes]
rs2694840	0.89[ASN][1000 genomes]
rs3741627	0.87[ASN][1000 genomes]
rs3759146	0.82[ASN][1000 genomes]
rs3782353	0.87[ASN][1000 genomes]
rs3825182	0.82[ASN][1000 genomes]
rs4018510	0.87[ASN][1000 genomes]
rs4237854	0.82[ASN][1000 genomes]
rs4526804	0.88[ASN][1000 genomes]
rs4760664	0.88[ASN][1000 genomes]
rs4760666	0.85[ASN][1000 genomes]
rs4760667	0.87[ASN][1000 genomes]
rs4760668	0.87[ASN][1000 genomes]
rs58023472	0.80[ASN][1000 genomes]
rs59087236	0.88[ASN][1000 genomes]
rs61942166	0.84[ASN][1000 genomes]
rs61942167	0.86[ASN][1000 genomes]
rs61942169	0.87[ASN][1000 genomes]
rs61942207	0.88[ASN][1000 genomes]
rs61942209	0.96[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6580696	0.87[ASN][1000 genomes]
rs7297958	0.80[ASN][1000 genomes]
rs7298330	0.80[ASN][1000 genomes]
rs7304942	0.80[ASN][1000 genomes]
rs7313988	0.88[ASN][1000 genomes]
rs7963018	0.87[ASN][1000 genomes]
rs7963160	0.86[ASN][1000 genomes]
rs7976473	0.94[AFR][1000 genomes];0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs833820	0.83[AFR][1000 genomes];0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs833821	0.96[AFR][1000 genomes];0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs833822	0.88[ASN][1000 genomes]
rs833827	0.88[ASN][1000 genomes]
rs833828	0.90[ASN][1000 genomes]
rs833839	0.83[ASN][1000 genomes]
rs833840	0.82[AFR][1000 genomes];0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs833841	0.84[ASN][1000 genomes]
rs833842	0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs833843	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9645813	0.82[ASN][1000 genomes]
rs9783452	0.88[ASN][1000 genomes]
rs9783477	0.88[ASN][1000 genomes]
rs9788029	0.93[AFR][1000 genomes];0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9796008	0.80[ASN][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	nsv832404	chr12:49258560-49458555	Weak transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
2	nsv1051161	chr12:49314550-49828473	Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Active TSS Strong transcription Enhancers Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	322 gene(s)	inside rSNPs	diseases
3	nsv541489	chr12:49314550-49828473	Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers Weak transcription Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	322 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	chr12:49351800-49358600	Weak transcription	Lung	lung
2	chr12:49351800-49365000	Weak transcription	Right Atrium	heart
3	chr12:49352200-49358400	Weak transcription	HUES6 Cell Line	embryonic stem cell
4	chr12:49355400-49358000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr12:49355400-49363000	Weak transcription	Placenta Amnion	Placenta Amnion
6	chr12:49355600-49358000	Weak transcription	HUES64 Cell Line	embryonic stem cell
7	chr12:49355600-49359000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr12:49356000-49360200	Weak transcription	HSMMtube	muscle
9	chr12:49356000-49361800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr12:49356000-49362000	Weak transcription	HSMM	muscle

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