Variant report

Variant	rs9978235
Chromosome Location	chr21:15613779-15613780
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	chr21:15612009..15614501-chr21:15615453..15618275,2	K562	blood:

Extended variants
information (count: 68 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:64)

rs_ID	r²[population]
rs13048936	0.82[ASN][1000 genomes]
rs2041609	0.90[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs2080098	0.84[ASN][1000 genomes]
rs2080099	0.84[ASN][1000 genomes]
rs2080100	0.84[ASN][1000 genomes]
rs2098260	0.84[ASN][1000 genomes]
rs2192165	0.84[ASN][1000 genomes]
rs2245549	0.90[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs2245629	0.90[AFR][1000 genomes];0.84[ASN][1000 genomes]
rs2245630	0.90[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs2245631	0.88[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs2403761	0.84[ASN][1000 genomes]
rs2822444	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2822446	0.84[ASN][1000 genomes]
rs2822447	0.84[ASN][1000 genomes]
rs2822452	0.84[ASN][1000 genomes]
rs2822454	0.84[ASN][1000 genomes]
rs2822457	0.84[ASN][1000 genomes]
rs2822478	0.84[ASN][1000 genomes]
rs2822479	0.82[ASN][1000 genomes]
rs2822480	0.84[ASN][1000 genomes]
rs2822481	0.84[ASN][1000 genomes]
rs2822482	0.83[AFR][1000 genomes];0.84[ASN][1000 genomes]
rs2822483	0.83[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs2822485	0.86[ASN][1000 genomes]
rs2822486	0.83[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs2822487	0.83[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs2822488	0.83[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs2822489	0.89[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs2822491	0.88[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs2822493	0.90[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs2822494	0.86[ASN][1000 genomes]
rs2822495	0.89[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs2822496	0.90[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs2822497	0.89[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs2822498	0.90[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs2822499	0.86[ASN][1000 genomes]
rs2822500	0.90[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs2822501	0.90[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs2822502	0.99[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28450820	0.90[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs3937457	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4350835	0.90[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs4384867	0.84[ASN][1000 genomes]
rs7282747	0.84[ASN][1000 genomes]
rs8128641	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs8128704	0.84[ASN][1000 genomes]
rs9305261	0.84[ASN][1000 genomes]
rs9974101	0.88[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs9974145	0.89[AFR][1000 genomes];0.85[ASN][1000 genomes]
rs9974227	0.84[ASN][1000 genomes]
rs9974337	0.84[ASN][1000 genomes]
rs9974434	0.84[ASN][1000 genomes]
rs9974778	0.88[AFR][1000 genomes];0.85[ASN][1000 genomes]
rs9975653	0.84[ASN][1000 genomes]
rs9976642	0.84[ASN][1000 genomes]
rs9977630	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9978140	0.86[ASN][1000 genomes]
rs9978229	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9978241	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9979382	0.90[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs9982191	0.84[ASN][1000 genomes]
rs9982795	0.84[ASN][1000 genomes]
rs9982809	0.90[AFR][1000 genomes];0.86[ASN][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	nsv1058202	chr21:14706767-15628668	Weak transcription Active TSS ZNF genes & repeats Enhancers Genic enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	38 gene(s)	inside rSNPs	diseases
2	nsv869466	chr21:15482572-15683385	Active TSS Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv1056588	chr21:15583231-15615520	Enhancers Bivalent/Poised TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv1066738	chr21:15587815-15642948	Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 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	chr21:15613000-15614600	Enhancers	Primary T helper cells PMA-I stimulated	--
2	chr21:15613200-15614400	Enhancers	Primary T helper naive cells from peripheral blood	blood
3	chr21:15613200-15614600	Enhancers	Primary T helper cells fromperipheralblood	blood
4	chr21:15613200-15614800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
5	chr21:15613400-15614000	Enhancers	Primary hematopoietic stem cells short term culture	blood
6	chr21:15613400-15614600	Enhancers	Dnd41	blood
7	chr21:15613600-15614000	Enhancers	K562	blood
8	chr21:15613600-15614200	Enhancers	Primary T killer memory cells from peripheral blood	blood

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