Variant report

Variant	rs7142351
Chromosome Location	chr14:84495421-84495422
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:84489726..84491906-chr14:84495009..84496588,2	MCF-7	breast:
2	chr14:84493242..84495734-chr14:84508485..84511044,2	K562	blood:

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

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs10131505	0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10132537	0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10133221	0.92[ASN][1000 genomes]
rs10137482	0.94[ASN][1000 genomes]
rs10139559	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10148456	0.94[ASN][1000 genomes]
rs10151367	0.94[ASN][1000 genomes]
rs11851518	0.96[ASN][1000 genomes]
rs12432538	0.82[ASN][1000 genomes]
rs12434360	0.96[ASN][1000 genomes]
rs12435170	0.88[ASN][1000 genomes]
rs12436496	0.93[ASN][1000 genomes]
rs12587047	0.93[ASN][1000 genomes]
rs12587356	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12589135	0.85[ASN][1000 genomes]
rs12590331	0.94[ASN][1000 genomes]
rs12590725	0.88[ASN][1000 genomes]
rs12887780	0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12887904	0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs17119380	0.88[ASN][1000 genomes]
rs17119453	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1999279	0.85[ASN][1000 genomes]
rs2183523	0.88[ASN][1000 genomes]
rs2210184	0.83[ASN][1000 genomes]
rs2210185	0.85[ASN][1000 genomes]
rs28793601	0.94[ASN][1000 genomes]
rs34326388	0.88[ASN][1000 genomes]
rs4904151	0.88[ASN][1000 genomes]
rs4904152	0.88[ASN][1000 genomes]
rs4904153	0.94[ASN][1000 genomes]
rs59954455	0.93[ASN][1000 genomes]
rs6574764	0.85[ASN][1000 genomes]
rs71412380	0.85[ASN][1000 genomes]
rs7148040	0.94[ASN][1000 genomes]
rs7153137	0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7155319	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs72701039	0.94[ASN][1000 genomes]
rs7493561	0.94[ASN][1000 genomes]
rs8007316	0.88[ASN][1000 genomes]
rs8022815	0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs8022878	0.88[ASN][1000 genomes]
rs952821	0.93[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1382	chr14:84487547-84532237	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:84494800-84496000	Weak transcription	Adipose Nuclei	Adipose
2	chr14:84494800-84496200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
3	chr14:84495400-84495600	Enhancers	Fetal Lung	lung

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