Variant report

Variant	rs35242629
Chromosome Location	chr3:115789866-115789867
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	chr3:115782312..115784390-chr3:115787119..115790072,2	K562	blood:
2	chr3:115784918..115786597-chr3:115787841..115790560,2	K562	blood:

Extended variants
information (count: 54 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs11425708	1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11918080	1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs13100914	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1344131	0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs17697994	0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1920379	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2091669	0.99[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2222827	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2864066	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2864067	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs28735793	0.81[ASN][1000 genomes]
rs33956431	0.87[ASN][1000 genomes]
rs34844901	0.87[ASN][1000 genomes]
rs34930794	0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs35619123	0.93[AFR][1000 genomes];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35780065	0.87[ASN][1000 genomes]
rs35914238	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4263291	0.88[ASN][1000 genomes]
rs4831227	0.87[ASN][1000 genomes]
rs4831228	1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4831229	0.80[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4831230	0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs5004406	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs56121547	0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs62269168	0.88[ASN][1000 genomes]
rs62269170	0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs66490447	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6765355	0.99[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6772113	1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs73139202	0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7632265	0.80[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7637650	1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9289042	0.95[ASN][1000 genomes]
rs9816425	0.99[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9821865	1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9822568	0.99[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9836963	0.87[ASN][1000 genomes]
rs9837276	0.87[ASN][1000 genomes]
rs9839078	1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9854345	0.87[ASN][1000 genomes]
rs9854711	1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9855097	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9857520	0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9866484	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9873576	0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9877662	0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9985471	0.81[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv931948	chr3:114884574-115802562	Bivalent Enhancer Enhancers Flanking Active TSS Strong transcription Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
2	esv2760762	chr3:115476222-115807650	Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
3	nsv829685	chr3:115643521-115812913	Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
4	nsv1012260	chr3:115680931-115935968	Enhancers Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	esv2756413	chr3:115721898-115908480	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
6	nsv1001538	chr3:115746561-115791116	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
7	esv2751975	chr3:115766285-115902901	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:115766200-115794200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr3:115780400-115830000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr3:115780600-115803800	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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