Variant report

Variant	rs7914592
Chromosome Location	chr10:28377956-28377957
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:28364402..28367665-chr10:28377622..28380231,3	MCF-7	breast:

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs10763638	0.96[ASN][1000 genomes]
rs10763643	0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10826396	0.96[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs10826399	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11006851	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11006852	0.86[EUR][1000 genomes]
rs11006854	0.86[EUR][1000 genomes]
rs12415916	0.87[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs1574418	0.85[EUR][1000 genomes]
rs1781837	0.90[ASN][1000 genomes]
rs1892394	0.86[EUR][1000 genomes]
rs1951935	0.94[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1951936	0.99[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2069202	0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2801848	0.83[ASN][1000 genomes]
rs2997211	0.86[ASN][1000 genomes]
rs4399242	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4749305	0.99[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4749307	0.96[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7085159	0.99[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7086023	0.90[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs7478224	0.86[EUR][1000 genomes]
rs7478236	0.83[EUR][1000 genomes]
rs7478252	0.86[EUR][1000 genomes]
rs7894339	0.83[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7895209	0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7896041	0.99[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7897447	0.83[AFR][1000 genomes]
rs7897848	0.80[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7898446	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7904206	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7919895	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 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

No data

Chromatin state (count:58 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:28347000-28380400	Weak transcription	Rectal Mucosa Donor 31	rectum
2	chr10:28347000-28381000	Weak transcription	Rectal Mucosa Donor 29	rectum
3	chr10:28347000-28412200	Weak transcription	Left Ventricle	heart
4	chr10:28347000-28414600	Weak transcription	Sigmoid Colon	Sigmoid Colon
5	chr10:28348000-28381200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
6	chr10:28357200-28380200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
7	chr10:28364600-28378800	Weak transcription	Fetal Muscle Leg	muscle
8	chr10:28364800-28378400	Weak transcription	HSMMtube	muscle
9	chr10:28364800-28379600	Weak transcription	Adipose Nuclei	Adipose
10	chr10:28364800-28392000	Weak transcription	Gastric	stomach
11	chr10:28364800-28416600	Weak transcription	Pancreas	Pancrea
12	chr10:28365000-28379600	Weak transcription	Pancreatic Islets	Pancreatic Islet
13	chr10:28365200-28379600	Weak transcription	HepG2	liver
14	chr10:28365200-28380200	Weak transcription	Duodenum Mucosa	Duodenum
15	chr10:28367400-28378800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr10:28367800-28420200	Weak transcription	Rectal Smooth Muscle	rectum
17	chr10:28369400-28378800	Strong transcription	Primary T cells from cord blood	blood
18	chr10:28371200-28378800	Strong transcription	Primary T cells fromperipheralblood	blood
19	chr10:28371400-28379800	Strong transcription	Primary T helper cells fromperipheralblood	blood
20	chr10:28373400-28379600	Weak transcription	Lung	lung
21	chr10:28373600-28378600	Strong transcription	Stomach Smooth Muscle	stomach
22	chr10:28373600-28378800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr10:28374000-28378800	Strong transcription	Primary T helper cells PMA-I stimulated	--
24	chr10:28374200-28379000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
25	chr10:28375200-28378600	Strong transcription	Skeletal Muscle Male	skeletal muscle
26	chr10:28375400-28378000	Strong transcription	Skeletal Muscle Female	skeletal muscle
27	chr10:28375400-28378400	Strong transcription	Primary hematopoietic stem cells	blood
28	chr10:28375400-28378600	Strong transcription	Duodenum Smooth Muscle	Duodenum
29	chr10:28375400-28379200	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
30	chr10:28375600-28378200	Strong transcription	Fetal Stomach	stomach
31	chr10:28375600-28378600	Strong transcription	Primary T helper naive cells from peripheral blood	blood
32	chr10:28375600-28379200	Strong transcription	Aorta	Aorta
33	chr10:28375600-28380000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
34	chr10:28375800-28378800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
35	chr10:28376000-28379200	Strong transcription	Fetal Intestine Small	intestine
36	chr10:28376000-28438400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
37	chr10:28376200-28379000	Strong transcription	Primary B cells from cord blood	blood
38	chr10:28376600-28378400	Enhancers	Hela-S3	cervix
39	chr10:28376600-28378600	Strong transcription	Colon Smooth Muscle	Colon
40	chr10:28376600-28378600	Enhancers	HMEC	breast
41	chr10:28376600-28379200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr10:28376600-28379200	Enhancers	Muscle Satellite Cultured Cells	--
43	chr10:28376600-28382200	Enhancers	HUVEC	blood vessel
44	chr10:28376600-28416600	Weak transcription	Fetal Intestine Large	intestine
45	chr10:28376800-28378200	Enhancers	NH-A	brain
46	chr10:28376800-28378600	Strong transcription	HSMM	muscle
47	chr10:28376800-28378800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr10:28376800-28392000	Weak transcription	Esophagus	oesophagus
49	chr10:28377000-28378800	Strong transcription	Primary T killer memory cells from peripheral blood	blood
50	chr10:28377200-28378200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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