Variant report

Variant	rs17106020
Chromosome Location	chr14:37500250-37500251
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	chr14:37499430..37501111-chr14:37506004..37508252,2	K562	blood:

Extended variants
information (count: 58 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:54)

rs_ID	r²[population]
rs11846664	1.00[EUR][1000 genomes]
rs17105663	1.00[CEU][hapmap]
rs17105856	1.00[EUR][1000 genomes]
rs17105876	1.00[EUR][1000 genomes]
rs17105909	1.00[EUR][1000 genomes]
rs17105921	1.00[EUR][1000 genomes]
rs17105928	1.00[EUR][1000 genomes]
rs17105938	1.00[EUR][1000 genomes]
rs17105941	1.00[EUR][1000 genomes]
rs17105957	0.83[AFR][1000 genomes]
rs17105972	0.81[ASW][hapmap];0.86[LWK][hapmap];1.00[YRI][hapmap]
rs17105973	1.00[YRI][hapmap]
rs17105991	0.81[ASW][hapmap];0.84[LWK][hapmap];1.00[YRI][hapmap];0.83[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17105999	0.88[YRI][hapmap];0.89[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17106194	1.00[EUR][1000 genomes]
rs17106252	1.00[EUR][1000 genomes]
rs17106300	1.00[EUR][1000 genomes]
rs17106370	1.00[EUR][1000 genomes]
rs17106427	1.00[EUR][1000 genomes]
rs17106428	1.00[EUR][1000 genomes]
rs17106431	1.00[EUR][1000 genomes]
rs2093087	1.00[EUR][1000 genomes]
rs2144319	1.00[EUR][1000 genomes]
rs55764696	1.00[EUR][1000 genomes]
rs55987900	1.00[EUR][1000 genomes]
rs56167909	1.00[EUR][1000 genomes]
rs56395950	1.00[EUR][1000 genomes]
rs57432181	1.00[EUR][1000 genomes]
rs57545427	1.00[EUR][1000 genomes]
rs60179583	1.00[EUR][1000 genomes]
rs60717098	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60846053	1.00[EUR][1000 genomes]
rs60910364	1.00[EUR][1000 genomes]
rs61192357	0.87[AFR][1000 genomes]
rs61200961	1.00[EUR][1000 genomes]
rs7147703	1.00[EUR][1000 genomes]
rs73256266	1.00[EUR][1000 genomes]
rs73256270	1.00[EUR][1000 genomes]
rs73256271	1.00[EUR][1000 genomes]
rs73256284	1.00[EUR][1000 genomes]
rs73256290	1.00[EUR][1000 genomes]
rs73256292	0.87[AFR][1000 genomes]
rs73256295	1.00[EUR][1000 genomes]
rs73258212	1.00[EUR][1000 genomes]
rs73260317	1.00[EUR][1000 genomes]
rs73260392	1.00[EUR][1000 genomes]
rs73264172	1.00[EUR][1000 genomes]
rs73266178	1.00[EUR][1000 genomes]
rs74045252	1.00[EUR][1000 genomes]
rs74045477	1.00[EUR][1000 genomes]
rs8009539	1.00[EUR][1000 genomes]
rs8009729	1.00[EUR][1000 genomes]
rs9671258	1.00[EUR][1000 genomes]
rs9672077	1.00[EUR][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	nsv534288	chr14:37254539-37697745	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	17 gene(s)	inside rSNPs	diseases
2	nsv1036201	chr14:37498841-37542041	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv1037719	chr14:37498841-37546359	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv526786	chr14:37499904-37537352	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats 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	chr14:37494800-37503400	Weak transcription	Muscle Satellite Cultured Cells	--
2	chr14:37499800-37500400	Enhancers	iPS-18 Cell Line	embryonic stem cell
3	chr14:37500000-37500400	Enhancers	HUES64 Cell Line	embryonic stem cell
4	chr14:37500200-37500400	Enhancers	iPS-15b Cell Line	embryonic stem cell

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