Variant report

Variant	rs11006867
Chromosome Location	chr10:28389289-28389290
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:28387058..28389693-chr6:27776467..27779114,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000203813	Chromatin interaction

Extended variants
information (count: 60 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs10826397	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10826398	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11006818	0.98[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs11006820	0.84[AMR][1000 genomes]
rs11006821	0.84[AMR][1000 genomes]
rs11006822	0.93[AMR][1000 genomes]
rs11006823	0.93[AMR][1000 genomes]
rs11006825	0.98[AMR][1000 genomes];0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11006826	0.84[AMR][1000 genomes]
rs11006827	0.93[AMR][1000 genomes]
rs11006830	0.84[AMR][1000 genomes]
rs11006832	0.97[AMR][1000 genomes];0.80[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11006833	0.97[AMR][1000 genomes];0.80[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11006834	0.97[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs11006836	0.97[AMR][1000 genomes];0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11006839	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11006840	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11006841	0.95[AMR][1000 genomes];0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11006843	0.97[AMR][1000 genomes];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11006855	0.98[AMR][1000 genomes];0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11006863	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11006869	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11006870	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11006873	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11006877	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11006880	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11006881	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs11006883	0.98[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11006884	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12219860	0.92[AMR][1000 genomes]
rs12220659	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1317790	0.98[AMR][1000 genomes];0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs17757844	0.97[AMR][1000 genomes];0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2887213	0.98[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs3885634	0.84[AMR][1000 genomes]
rs3885635	0.89[AMR][1000 genomes];0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs56163384	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56349465	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57764949	0.97[AMR][1000 genomes];0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs59082756	0.97[AMR][1000 genomes];0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs59246203	0.97[AMR][1000 genomes];0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6481499	0.92[AMR][1000 genomes]
rs7071369	0.98[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs72801890	0.98[AMR][1000 genomes];0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7895285	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs927676	0.93[AMR][1000 genomes];0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv917149	chr10:28018919-28688694	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
2	nsv831815	chr10:28235661-28407533	Strong transcription Enhancers Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
3	nsv1042524	chr10:28290149-28506812	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
4	nsv831816	chr10:28304698-28493635	Enhancers Flanking Active TSS Strong transcription Weak transcription ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
5	nsv894988	chr10:28337570-28410989	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS	Chromatin interactive region lncRNA miRNA target site	1 gene(s)	inside rSNPs	diseases
6	nsv525448	chr10:28337570-28563732	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
7	nsv466855	chr10:28341783-28400835	Enhancers Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Active TSS Flanking Active TSS	Chromatin interactive region miRNA target site	1 gene(s)	inside rSNPs	diseases
8	nsv550284	chr10:28341783-28400835	Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region miRNA target site	1 gene(s)	inside rSNPs	diseases
9	nsv831817	chr10:28369836-28539930	Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
10	esv1817535	chr10:28373644-28409054	Weak transcription Strong transcription Active TSS Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
11	esv1848511	chr10:28373644-28464753	Enhancers Genic enhancers Strong transcription Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
12	esv1851923	chr10:28384098-28410989	Strong transcription Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
13	nsv894989	chr10:28384098-28449974	Weak transcription Strong transcription ZNF genes & repeats Enhancers Active TSS Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
14	nsv949151	chr10:28386125-28455221	Weak transcription Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:29 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:28347000-28412200	Weak transcription	Left Ventricle	heart
2	chr10:28347000-28414600	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr10:28364800-28392000	Weak transcription	Gastric	stomach
4	chr10:28364800-28416600	Weak transcription	Pancreas	Pancrea
5	chr10:28367800-28420200	Weak transcription	Rectal Smooth Muscle	rectum
6	chr10:28376000-28438400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
7	chr10:28376600-28416600	Weak transcription	Fetal Intestine Large	intestine
8	chr10:28376800-28392000	Weak transcription	Esophagus	oesophagus
9	chr10:28378000-28418400	Weak transcription	Skeletal Muscle Female	skeletal muscle
10	chr10:28378600-28396200	Weak transcription	Stomach Smooth Muscle	stomach
11	chr10:28378600-28400800	Weak transcription	HSMM	muscle
12	chr10:28378600-28407400	Weak transcription	Duodenum Smooth Muscle	Duodenum
13	chr10:28378600-28412800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
14	chr10:28378600-28425600	Weak transcription	Colon Smooth Muscle	Colon
15	chr10:28378800-28396400	Weak transcription	Primary T cells fromperipheralblood	blood
16	chr10:28378800-28407400	Weak transcription	Primary T helper cells PMA-I stimulated	--
17	chr10:28378800-28408400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr10:28379000-28407000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
19	chr10:28379200-28391800	Weak transcription	Aorta	Aorta
20	chr10:28379200-28394800	Weak transcription	Primary neutrophils fromperipheralblood	blood
21	chr10:28379200-28395600	Weak transcription	Primary monocytes fromperipheralblood	blood
22	chr10:28379200-28406600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
23	chr10:28379200-28416600	Weak transcription	Fetal Intestine Small	intestine
24	chr10:28379800-28407800	Weak transcription	Primary T helper cells fromperipheralblood	blood
25	chr10:28380000-28396000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
26	chr10:28380000-28398400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
27	chr10:28383600-28391600	Weak transcription	Primary T cells from cord blood	blood
28	chr10:28383600-28394800	Weak transcription	Monocytes-CD14+_RO01746	blood
29	chr10:28386200-28394400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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