Variant report

Variant	rs1178166
Chromosome Location	chr7:18790781-18790782
allele	A/C/G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs11764116	0.91[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1178130	0.85[EUR][1000 genomes]
rs1178131	0.82[EUR][1000 genomes]
rs1178132	0.80[EUR][1000 genomes]
rs1178142	0.89[EUR][1000 genomes]
rs1178143	0.88[EUR][1000 genomes]
rs1178146	0.80[EUR][1000 genomes]
rs1178147	0.82[EUR][1000 genomes]
rs1178148	0.82[EUR][1000 genomes]
rs1178149	0.84[EUR][1000 genomes]
rs1178150	0.92[EUR][1000 genomes]
rs1178151	0.84[EUR][1000 genomes]
rs1178152	0.92[EUR][1000 genomes]
rs1178153	0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1178154	0.85[EUR][1000 genomes]
rs1178155	0.85[EUR][1000 genomes]
rs1178156	0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1178158	0.98[ASN][1000 genomes]
rs1178159	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1178160	0.91[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1178162	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1178164	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1178165	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1178171	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1178172	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1178174	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1178176	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1178179	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs212672	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs212674	0.91[EUR][1000 genomes]
rs3852249	0.84[ASN][1000 genomes]
rs727851	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs894978	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2755157	chr7:18337660-18805860	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv830917	chr7:18612436-18817712	Enhancers Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv531368	chr7:18677922-18836920	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv498112	chr7:18677922-18991946	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv887813	chr7:18720135-18995552	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv887814	chr7:18751998-18886177	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	esv2757218	chr7:18767714-18801340	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Active TSS Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
8	esv2759516	chr7:18767714-18801340	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:18765200-18810600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr7:18787400-18801800	Weak transcription	Psoas Muscle	Psoas
3	chr7:18787800-18792400	Weak transcription	Primary B cells from peripheral blood	blood
4	chr7:18787800-18810800	Weak transcription	Skeletal Muscle Female	skeletal muscle
5	chr7:18788200-18790800	Weak transcription	Monocytes-CD14+_RO01746	blood
6	chr7:18788800-18801800	Weak transcription	Primary monocytes fromperipheralblood	blood
7	chr7:18789000-18794000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr7:18789000-18807800	Weak transcription	Aorta	Aorta
9	chr7:18789000-18808600	Weak transcription	Left Ventricle	heart
10	chr7:18789600-18792400	Weak transcription	HSMMtube	muscle
11	chr7:18790600-18792800	Weak transcription	HSMM	muscle
12	chr7:18790600-18835000	Weak transcription	Primary B cells from cord blood	blood

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