Variant report

Variant	rs1178111
Chromosome Location	chr7:18745723-18745724
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs1178102	0.81[CHD][hapmap];0.82[TSI][hapmap]
rs1178103	0.82[CEU][hapmap];0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1178105	0.88[CEU][hapmap];0.80[ASN][1000 genomes]
rs1178107	0.94[CEU][hapmap];0.80[JPT][hapmap];0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1178108	0.88[CEU][hapmap];0.94[CHD][hapmap];0.80[JPT][hapmap];0.82[TSI][hapmap];0.82[ASN][1000 genomes]
rs1178109	0.82[CEU][hapmap];0.93[CHD][hapmap];0.84[JPT][hapmap];0.82[MEX][hapmap];0.85[TSI][hapmap];0.92[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1178110	0.94[CEU][hapmap];0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1178112	0.94[CEU][hapmap];0.80[JPT][hapmap];0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1178113	0.92[CEU][hapmap];0.83[JPT][hapmap];0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1178116	0.88[CEU][hapmap];0.81[EUR][1000 genomes]
rs1178118	0.88[CEU][hapmap];0.94[CHD][hapmap];0.92[GIH][hapmap];0.85[TSI][hapmap];0.86[ASN][1000 genomes]
rs1178119	0.82[CEU][hapmap];0.89[EUR][1000 genomes]
rs1178120	0.82[CEU][hapmap];0.97[CHD][hapmap]
rs12669789	0.90[CHD][hapmap]
rs17139675	0.80[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:5 , 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

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:18688800-18746400	Weak transcription	Primary hematopoietic stem cells	blood
2	chr7:18699600-18776000	Weak transcription	Aorta	Aorta
3	chr7:18726200-18790200	Weak transcription	Primary B cells from cord blood	blood
4	chr7:18743600-18746000	Weak transcription	Fetal Heart	heart
5	chr7:18743800-18746400	Weak transcription	Left Ventricle	heart
6	chr7:18743800-18747800	Weak transcription	Psoas Muscle	Psoas

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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