Variant report

Variant	rs17107516
Chromosome Location	chr14:78874013-78874014
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	chr14:78861659..78863872-chr14:78874003..78876017,2	K562	blood:

Extended variants
information (count: 62 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:61)

rs_ID	r²[population]
rs10132376	1.00[CHB][hapmap]
rs10138731	1.00[CHB][hapmap]
rs10140699	1.00[CHB][hapmap]
rs10141923	1.00[CHB][hapmap]
rs10483898	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10873318	1.00[CHB][hapmap]
rs12323467	1.00[CHB][hapmap]
rs12431997	1.00[CHB][hapmap]
rs12432145	1.00[CHB][hapmap]
rs12432323	1.00[CHB][hapmap]
rs12435491	1.00[CHB][hapmap]
rs12435510	1.00[CHB][hapmap]
rs12436134	1.00[CHB][hapmap]
rs12437077	1.00[CHB][hapmap]
rs17107424	1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs17107444	1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs17107504	0.82[JPT][hapmap]
rs17107519	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs17107523	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs17107530	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs17107594	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs17107601	1.00[JPT][hapmap]
rs17107611	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs17107847	1.00[CHB][hapmap]
rs56923572	1.00[AMR][1000 genomes]
rs58330928	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs59762056	1.00[AMR][1000 genomes]
rs59819728	1.00[AMR][1000 genomes]
rs61052532	1.00[AMR][1000 genomes]
rs61199699	0.81[ASN][1000 genomes]
rs7147592	1.00[CHB][hapmap]
rs732176	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs73308947	0.81[ASN][1000 genomes]
rs73308971	0.81[ASN][1000 genomes]
rs73308985	0.81[ASN][1000 genomes]
rs73309000	0.81[ASN][1000 genomes]
rs73310817	0.81[ASN][1000 genomes]
rs73310826	0.81[ASN][1000 genomes]
rs73316006	0.94[ASN][1000 genomes]
rs73316040	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73316042	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73316045	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73316421	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73316436	1.00[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs73316456	1.00[AMR][1000 genomes]
rs73316459	1.00[AMR][1000 genomes]
rs73316471	1.00[AMR][1000 genomes]
rs73316478	1.00[AMR][1000 genomes]
rs73319533	0.81[ASN][1000 genomes]
rs73319535	0.81[ASN][1000 genomes]
rs73319540	0.81[ASN][1000 genomes]
rs73320490	1.00[AMR][1000 genomes]
rs73320491	1.00[AMR][1000 genomes]
rs73324490	1.00[AMR][1000 genomes]
rs73327195	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73327200	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73329110	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs73329120	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs73329172	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs8015539	1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[ASN][1000 genomes]
rs9323666	1.00[CHB][hapmap]

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	nsv832837	chr14:78766805-78946526	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:78869400-78875000	Active TSS	GM12878-XiMat	blood
2	chr14:78871200-78874400	Enhancers	Brain Substantia Nigra	brain
3	chr14:78872600-78874200	Enhancers	Brain Cingulate Gyrus	brain
4	chr14:78873200-78874200	Enhancers	Brain Hippocampus Middle	brain
5	chr14:78873400-78880600	Weak transcription	Brain Inferior Temporal Lobe	brain
6	chr14:78873400-78881400	Weak transcription	Brain Anterior Caudate	brain
7	chr14:78873600-78876600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
8	chr14:78873600-78880600	Weak transcription	Brain Angular Gyrus	brain

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