Variant report

Variant	rs35429023
Chromosome Location	chr13:39503836-39503837
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr13:39497714..39500454-chr13:39501817..39503959,2	K562	blood:

Extended variants
information (count: 105 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:104)

rs_ID	r²[population]
rs11618742	1.00[ASN][1000 genomes]
rs12864816	1.00[ASN][1000 genomes]
rs12869426	1.00[ASN][1000 genomes]
rs12869876	1.00[ASN][1000 genomes]
rs12869917	1.00[ASN][1000 genomes]
rs12875224	1.00[ASN][1000 genomes]
rs1333506	1.00[ASN][1000 genomes]
rs1333508	1.00[ASN][1000 genomes]
rs1945496	1.00[ASN][1000 genomes]
rs34127262	0.86[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs34943621	1.00[ASN][1000 genomes]
rs35252750	1.00[ASN][1000 genomes]
rs35459396	1.00[ASN][1000 genomes]
rs35657252	1.00[ASN][1000 genomes]
rs35944548	1.00[ASN][1000 genomes]
rs35986835	0.86[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs36088006	1.00[ASN][1000 genomes]
rs4287442	1.00[ASN][1000 genomes]
rs4334155	1.00[ASN][1000 genomes]
rs4369521	1.00[ASN][1000 genomes]
rs4397983	1.00[ASN][1000 genomes]
rs4426230	1.00[ASN][1000 genomes]
rs4426231	1.00[ASN][1000 genomes]
rs4533148	1.00[ASN][1000 genomes]
rs4643179	1.00[ASN][1000 genomes]
rs4943606	1.00[ASN][1000 genomes]
rs4943607	1.00[ASN][1000 genomes]
rs4943608	1.00[ASN][1000 genomes]
rs4943609	1.00[ASN][1000 genomes]
rs4943610	1.00[ASN][1000 genomes]
rs4943611	1.00[ASN][1000 genomes]
rs4943612	1.00[ASN][1000 genomes]
rs4943615	0.86[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs61945515	1.00[ASN][1000 genomes]
rs61945516	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61945763	1.00[ASN][1000 genomes]
rs61947983	1.00[ASN][1000 genomes]
rs61948017	1.00[ASN][1000 genomes]
rs61948018	1.00[ASN][1000 genomes]
rs66889481	1.00[ASN][1000 genomes]
rs71198492	1.00[ASN][1000 genomes]
rs71423186	1.00[ASN][1000 genomes]
rs71423187	1.00[ASN][1000 genomes]
rs71439788	1.00[ASN][1000 genomes]
rs71439789	1.00[ASN][1000 genomes]
rs73169477	1.00[ASN][1000 genomes]
rs7328953	0.86[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs7331927	0.86[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs7982313	1.00[ASN][1000 genomes]
rs9532285	1.00[ASN][1000 genomes]
rs9532287	1.00[ASN][1000 genomes]
rs9532288	1.00[ASN][1000 genomes]
rs9532294	1.00[ASN][1000 genomes]
rs9532297	1.00[ASN][1000 genomes]
rs9532298	1.00[ASN][1000 genomes]
rs9532310	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9548466	1.00[ASN][1000 genomes]
rs9548467	1.00[ASN][1000 genomes]
rs9548468	1.00[ASN][1000 genomes]
rs9548471	1.00[ASN][1000 genomes]
rs9548473	1.00[ASN][1000 genomes]
rs9548474	1.00[ASN][1000 genomes]
rs9548475	1.00[ASN][1000 genomes]
rs9548476	1.00[ASN][1000 genomes]
rs9548478	1.00[ASN][1000 genomes]
rs9548479	1.00[ASN][1000 genomes]
rs9548480	1.00[ASN][1000 genomes]
rs9548488	1.00[ASN][1000 genomes]
rs9548489	1.00[ASN][1000 genomes]
rs9548490	1.00[ASN][1000 genomes]
rs9548492	1.00[ASN][1000 genomes]
rs9548493	1.00[ASN][1000 genomes]
rs9548494	1.00[ASN][1000 genomes]
rs9548495	1.00[ASN][1000 genomes]
rs9548496	1.00[ASN][1000 genomes]
rs9548497	1.00[ASN][1000 genomes]
rs9548498	1.00[ASN][1000 genomes]
rs9548499	1.00[ASN][1000 genomes]
rs9548500	1.00[ASN][1000 genomes]
rs9548501	1.00[ASN][1000 genomes]
rs9548502	1.00[ASN][1000 genomes]
rs9548503	1.00[ASN][1000 genomes]
rs9548504	1.00[ASN][1000 genomes]
rs9548505	1.00[ASN][1000 genomes]
rs9548507	1.00[ASN][1000 genomes]
rs9548515	0.86[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs9548521	0.86[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs9548523	1.00[ASN][1000 genomes]
rs9548524	1.00[ASN][1000 genomes]
rs9548525	1.00[ASN][1000 genomes]
rs9548531	1.00[ASN][1000 genomes]
rs9548532	1.00[ASN][1000 genomes]
rs9548535	1.00[ASN][1000 genomes]
rs9548552	1.00[ASN][1000 genomes]
rs9548554	1.00[ASN][1000 genomes]
rs9548555	1.00[ASN][1000 genomes]
rs9548556	1.00[ASN][1000 genomes]
rs9548557	1.00[ASN][1000 genomes]
rs9548560	1.00[ASN][1000 genomes]
rs9548562	1.00[ASN][1000 genomes]
rs9548563	1.00[ASN][1000 genomes]
rs9548569	1.00[ASN][1000 genomes]
rs9548573	1.00[ASN][1000 genomes]
rs9548576	1.00[ASN][1000 genomes]

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	esv2754118	chr13:39347702-40222644	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:39503200-39504600	Enhancers	HUES64 Cell Line	embryonic stem cell
2	chr13:39503400-39504200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
3	chr13:39503600-39504400	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr13:39503600-39504400	Enhancers	iPS-18 Cell Line	embryonic stem cell
5	chr13:39503600-39504400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr13:39503600-39504600	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr13:39503600-39504600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr13:39503600-39504600	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr13:39503800-39504200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr13:39503800-39504400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
11	chr13:39503800-39505000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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