Variant report

Variant	rs11007003
Chromosome Location	chr10:28597308-28597309
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:28590374..28593337-chr10:28595037..28598622,5	MCF-7	breast:

Variant related genes	Relation type
ENSG00000150054	Chromatin interaction

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs10826445	0.85[AMR][1000 genomes]
rs10826446	0.85[AMR][1000 genomes]
rs11006913	0.84[MEX][hapmap]
rs11006928	0.82[CHB][hapmap];1.00[MEX][hapmap]
rs11006937	0.91[MEX][hapmap]
rs11006958	0.82[CHB][hapmap];0.82[GIH][hapmap];1.00[MEX][hapmap]
rs11006989	0.83[AMR][1000 genomes]
rs11006990	0.81[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs11006992	0.87[CHB][hapmap];1.00[MEX][hapmap]
rs11006993	0.86[CHB][hapmap];0.86[JPT][hapmap]
rs11006994	0.81[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs11006995	0.87[CHB][hapmap];1.00[MEX][hapmap];0.83[AMR][1000 genomes]
rs11006997	0.81[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs11006998	0.83[AMR][1000 genomes]
rs11006999	0.81[AMR][1000 genomes]
rs11007000	0.85[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs11007004	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11007005	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11007006	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11007010	0.91[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs11007012	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs11007013	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs12218186	0.91[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12218294	0.81[AMR][1000 genomes]
rs12570440	0.82[ASN][1000 genomes]
rs1762186	0.84[ASN][1000 genomes]
rs17831816	0.82[CHB][hapmap]
rs1984853	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2368306	0.81[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs35016093	0.81[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs3842931	0.87[CHB][hapmap];0.83[AMR][1000 genomes]
rs3843586	0.91[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs4317882	0.84[MEX][hapmap]
rs4506531	0.84[MEX][hapmap]
rs4598572	0.81[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs4604776	0.83[AMR][1000 genomes]
rs57441879	0.83[AMR][1000 genomes]
rs7901835	0.85[AMR][1000 genomes]
rs7902785	0.83[AMR][1000 genomes]
rs7903242	0.86[CHB][hapmap];0.86[JPT][hapmap];0.83[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs7916067	0.83[AMR][1000 genomes]
rs7916711	0.85[AMR][1000 genomes]
rs7916740	0.85[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 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	nsv1041555	chr10:28419399-29304934	Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers Strong transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
3	nsv1037863	chr10:28419399-29378871	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
4	nsv540521	chr10:28419399-29378871	Flanking Active TSS Enhancers Weak transcription Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	46 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:22 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:28592800-28606600	Weak transcription	Colon Smooth Muscle	Colon
2	chr10:28593000-28607600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
3	chr10:28593200-28597400	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr10:28593200-28600200	Weak transcription	Psoas Muscle	Psoas
5	chr10:28593200-28603000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
6	chr10:28593200-28605800	Weak transcription	Primary T cells fromperipheralblood	blood
7	chr10:28593200-28615400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
8	chr10:28593400-28597400	Enhancers	Primary neutrophils fromperipheralblood	blood
9	chr10:28593400-28613400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
10	chr10:28593400-28615200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
11	chr10:28594000-28606600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
12	chr10:28595800-28597400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
13	chr10:28595800-28597400	Enhancers	Left Ventricle	heart
14	chr10:28596000-28597400	Enhancers	Primary T cells from cord blood	blood
15	chr10:28596200-28597400	Enhancers	Primary T helper cells fromperipheralblood	blood
16	chr10:28596400-28597600	Enhancers	Primary T helper naive cells from peripheral blood	blood
17	chr10:28596800-28618800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
18	chr10:28597000-28597400	Enhancers	Lung	lung
19	chr10:28597200-28597400	Enhancers	Primary T helper cells PMA-I stimulated	--
20	chr10:28597200-28597400	Enhancers	HSMMtube	muscle
21	chr10:28597200-28605400	Weak transcription	Monocytes-CD14+_RO01746	blood
22	chr10:28597200-28611000	Weak transcription	Pancreas	Pancrea

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