Variant report

Variant	rs7107526
Chromosome Location	chr11:17743949-17743950
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:17735220..17735764-chr11:17743713..17744525,2	MCF-7	breast:
2	chr11:17619891..17621109-chr11:17743288..17744431,5	MCF-7	breast:
3	chr11:17620217..17621179-chr11:17742829..17744247,6	MCF-7	breast:

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

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs10766416	0.81[EUR][1000 genomes]
rs10766420	0.84[EUR][1000 genomes]
rs10766425	0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10832842	0.81[EUR][1000 genomes]
rs10832845	0.85[EUR][1000 genomes]
rs10832851	0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10832852	0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11024384	0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11603216	0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11603221	0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2336849	0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs28609365	0.80[EUR][1000 genomes]
rs2878806	0.80[CEU][hapmap]
rs3858493	0.80[EUR][1000 genomes]
rs3858494	0.80[EUR][1000 genomes]
rs3858495	0.80[EUR][1000 genomes]
rs3858496	0.80[EUR][1000 genomes]
rs3858498	0.80[EUR][1000 genomes]
rs3858506	0.85[CEU][hapmap];1.00[CHB][hapmap]
rs3858508	0.86[EUR][1000 genomes]
rs3890009	0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3901226	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[GIH][hapmap];0.82[JPT][hapmap];1.00[MEX][hapmap];0.91[TSI][hapmap];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3911833	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[GIH][hapmap];0.82[JPT][hapmap];1.00[MEX][hapmap];0.94[TSI][hapmap];0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3928366	0.80[EUR][1000 genomes]
rs4081578	1.00[CHB][hapmap]
rs4083362	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4756912	0.84[CEU][hapmap];1.00[CHB][hapmap]
rs4757570	0.85[CEU][hapmap];1.00[CHB][hapmap];0.86[MEX][hapmap]
rs4757574	0.85[CEU][hapmap];1.00[CHB][hapmap];0.83[GIH][hapmap];0.93[MEX][hapmap]
rs6416178	0.82[EUR][1000 genomes]
rs6486390	0.82[EUR][1000 genomes]
rs7101870	0.80[EUR][1000 genomes]
rs7106809	0.85[EUR][1000 genomes]
rs7109072	0.85[CEU][hapmap];1.00[CHB][hapmap];0.82[JPT][hapmap];0.93[MEX][hapmap];0.83[TSI][hapmap]
rs7128599	0.80[EUR][1000 genomes]
rs7930233	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7937727	0.81[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1040065	chr11:17556031-17753467	Enhancers Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv467717	chr11:17713507-17791822	Bivalent Enhancer Bivalent/Poised TSS Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv553588	chr11:17713507-17791822	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv825772	chr11:17723530-17783128	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Enhancers Active TSS Weak transcription Genic enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	nsv1037585	chr11:17730586-17768346	Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Active TSS Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
6	esv3351059	chr11:17739776-17744374	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:17740600-17744400	Active TSS	HSMMtube	muscle
2	chr11:17741800-17750200	Weak transcription	Right Atrium	heart
3	chr11:17742000-17744000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
4	chr11:17742000-17744200	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
5	chr11:17742000-17744200	Transcr. at gene 5' and 3'	Skeletal Muscle Male	skeletal muscle
6	chr11:17743000-17744000	Bivalent Enhancer	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr11:17743400-17744000	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
8	chr11:17743400-17744200	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
9	chr11:17743400-17744600	Transcr. at gene 5' and 3'	HSMM	muscle
10	chr11:17743600-17744200	Active TSS	Psoas Muscle	Psoas
11	chr11:17743800-17744000	Bivalent Enhancer	Brain Substantia Nigra	brain
12	chr11:17743800-17744000	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
13	chr11:17743800-17744400	Transcr. at gene 5' and 3'	Muscle Satellite Cultured Cells	--

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