Variant report

Variant	rs61002775
Chromosome Location	chr14:80020557-80020558
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	chr14:80018191..80021124-chr14:80031002..80033246,2	K562	blood:

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

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs11847465	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11848738	1.00[AMR][1000 genomes]
rs11852085	1.00[AMR][1000 genomes]
rs55708063	1.00[AMR][1000 genomes]
rs57252489	1.00[AMR][1000 genomes]
rs57281369	1.00[AMR][1000 genomes]
rs57656995	1.00[AMR][1000 genomes]
rs58351352	1.00[AMR][1000 genomes]
rs58357059	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59078244	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59472910	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59693725	1.00[AFR][1000 genomes]
rs59809006	1.00[AMR][1000 genomes]
rs60319911	1.00[AMR][1000 genomes]
rs60502118	1.00[AMR][1000 genomes]
rs60734338	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61029849	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61309702	1.00[AMR][1000 genomes]
rs72696784	1.00[AMR][1000 genomes]
rs74068005	1.00[AMR][1000 genomes]
rs74068052	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74068054	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74068066	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74068069	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74068072	1.00[AMR][1000 genomes]
rs74068091	1.00[AMR][1000 genomes]
rs74068696	1.00[AMR][1000 genomes]
rs74070211	1.00[AMR][1000 genomes]
rs74070212	1.00[AMR][1000 genomes]
rs74070239	1.00[AMR][1000 genomes]
rs74070242	1.00[AMR][1000 genomes]
rs74070257	1.00[AMR][1000 genomes]
rs74070258	1.00[AMR][1000 genomes]
rs74070263	1.00[AMR][1000 genomes]
rs74070265	1.00[AMR][1000 genomes]
rs74070266	1.00[AMR][1000 genomes]
rs74070271	1.00[AMR][1000 genomes]
rs74070273	1.00[AMR][1000 genomes]
rs74070276	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	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
3	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
4	nsv869542	chr14:80009619-80118315	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 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	chr14:80011800-80069200	Weak transcription	Stomach Smooth Muscle	stomach
2	chr14:80014400-80037800	Weak transcription	Aorta	Aorta
3	chr14:80015800-80021000	Enhancers	Placenta Amnion	Placenta Amnion
4	chr14:80018000-80020600	Enhancers	Hela-S3	cervix
5	chr14:80019000-80020800	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chr14:80020000-80021400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr14:80020000-80027200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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