Variant report

Variant	rs8013875
Chromosome Location	chr14:80930299-80930300
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	chr14:80924960..80926463-chr14:80928354..80930711,2	MCF-7	breast:

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs10131256	0.89[ASN][1000 genomes]
rs10483951	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs10498538	0.89[ASN][1000 genomes]
rs11159465	0.93[ASN][1000 genomes]
rs12436273	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12587661	0.93[ASN][1000 genomes]
rs12588053	0.88[ASN][1000 genomes]
rs12892902	0.84[AMR][1000 genomes]
rs12894810	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12895468	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12897856	0.93[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1551070	0.89[ASN][1000 genomes]
rs17528984	0.91[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs17600960	0.87[ASN][1000 genomes]
rs2122431	0.88[ASN][1000 genomes]
rs2197986	0.89[ASN][1000 genomes]
rs34806974	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs35334352	0.87[AMR][1000 genomes]
rs4415953	0.89[AMR][1000 genomes]
rs4899768	0.83[AMR][1000 genomes]
rs4899769	0.87[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs4903915	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61991590	0.93[ASN][1000 genomes]
rs6574574	0.82[AMR][1000 genomes]
rs6574575	0.84[AMR][1000 genomes]
rs6574579	0.89[ASN][1000 genomes]
rs6574580	0.89[ASN][1000 genomes]
rs6574581	0.89[ASN][1000 genomes]
rs67982332	0.89[ASN][1000 genomes]
rs7143237	0.89[ASN][1000 genomes]
rs7143355	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7145557	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7145603	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7149914	0.89[ASN][1000 genomes]
rs7156166	0.89[ASN][1000 genomes]
rs8005349	0.87[AMR][1000 genomes]
rs8011476	0.91[ASN][1000 genomes]
rs935728	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv15289	chr14:80900600-80939903	Active TSS Enhancers Weak transcription Bivalent Enhancer Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
2	nsv869348	chr14:80921098-81535754	Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:80923400-80941200	Weak transcription	HSMM	muscle
2	chr14:80925200-80941400	Weak transcription	Psoas Muscle	Psoas
3	chr14:80926000-80937000	Weak transcription	Skeletal Muscle Female	skeletal muscle
4	chr14:80926200-80936200	Weak transcription	Skeletal Muscle Male	skeletal muscle
5	chr14:80929600-80939200	Weak transcription	Thymus	Thymus
6	chr14:80930200-80930400	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
7	chr14:80930200-80930400	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell

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