Variant report

Variant	rs56111431
Chromosome Location	chr14:79967857-79967858
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:79962362..79964375-chr14:79965844..79968447,2	K562	blood:

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10083466	0.83[ASN][1000 genomes]
rs10130663	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs10133502	0.81[ASN][1000 genomes]
rs10144362	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10150805	0.81[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs10483923	0.84[ASN][1000 genomes]
rs1080129	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11845632	0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11848580	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11848640	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11849345	0.95[EUR][1000 genomes]
rs11850075	0.87[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11850956	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs17109313	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs17763953	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2043585	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2196447	0.84[ASN][1000 genomes]
rs2217889	0.85[EUR][1000 genomes]
rs35879888	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs61504574	0.81[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs61995170	0.96[EUR][1000 genomes]
rs61995179	0.90[EUR][1000 genomes]
rs61995180	0.90[EUR][1000 genomes]
rs7150181	0.81[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7151972	0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8020593	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9323673	0.81[AMR][1000 genomes];0.97[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	nsv902110	chr14:79624492-79998294	Bivalent/Poised TSS Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv1045241	chr14:79885361-80734201	Weak transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
3	nsv1039622	chr14:79908702-80266601	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv902112	chr14:79939393-80050771	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv521160	chr14:79963569-79971835	Enhancers Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
6	esv1811223	chr14:79967761-79981954	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:79966000-79976400	Weak transcription	Stomach Smooth Muscle	stomach
2	chr14:79967600-79968800	Weak transcription	Brain Germinal Matrix	brain
3	chr14:79967800-79968000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
4	chr14:79967800-79969400	Enhancers	Placenta Amnion	Placenta Amnion

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