Variant report

Variant	rs4683461
Chromosome Location	chr3:142903366-142903367
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr3:142883459..142885076-chr3:142902502..142904668,2	K562	blood:
2	chr3:142837194..142839590-chr3:142902275..142903779,2	K562	blood:
3	chr3:142901683..142905677-chr3:142909688..142913196,5	K562	blood:
4	chr3:142875650..142878540-chr3:142902217..142903747,2	K562	blood:

Variant related genes	Relation type
ENSG00000211483	Chromatin interaction
ENSG00000175040	Chromatin interaction

Extended variants
information (count: 61 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10935485	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11715203	0.81[ASN][1000 genomes]
rs169808	0.81[ASN][1000 genomes]
rs186077	0.81[ASN][1000 genomes]
rs2165520	0.81[ASN][1000 genomes]
rs294465	0.81[ASN][1000 genomes]
rs294469	0.81[ASN][1000 genomes]
rs294470	0.88[ASN][1000 genomes]
rs294471	0.81[ASN][1000 genomes]
rs294472	0.81[ASN][1000 genomes]
rs294473	0.81[ASN][1000 genomes]
rs4371486	0.83[CHB][hapmap];0.90[CHD][hapmap];0.83[JPT][hapmap];0.81[ASN][1000 genomes]
rs4839588	0.81[ASN][1000 genomes]
rs4839591	0.81[ASN][1000 genomes]
rs4839616	0.81[ASN][1000 genomes]
rs4839617	0.81[ASN][1000 genomes]
rs4839618	0.81[ASN][1000 genomes]
rs4839619	0.81[ASN][1000 genomes]
rs4839621	0.81[ASN][1000 genomes]
rs4839625	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4839629	0.81[ASN][1000 genomes]
rs4839656	0.81[ASN][1000 genomes]
rs54520	0.83[CHB][hapmap];0.83[JPT][hapmap];0.81[ASN][1000 genomes]
rs6414352	0.81[ASN][1000 genomes]
rs6440149	0.81[ASN][1000 genomes]
rs6440150	0.81[ASN][1000 genomes]
rs6440151	0.81[ASN][1000 genomes]
rs6440152	0.81[ASN][1000 genomes]
rs6440153	0.81[ASN][1000 genomes]
rs6765181	0.81[ASN][1000 genomes]
rs6767762	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6776634	0.81[ASN][1000 genomes]
rs6777882	0.81[ASN][1000 genomes]
rs6778330	0.81[ASN][1000 genomes]
rs6781821	0.81[ASN][1000 genomes]
rs6781909	0.81[ASN][1000 genomes]
rs6785002	0.81[ASN][1000 genomes]
rs6786129	0.81[ASN][1000 genomes]
rs6788806	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6795908	0.81[ASN][1000 genomes]
rs6796353	0.81[ASN][1000 genomes]
rs6803862	0.81[ASN][1000 genomes]
rs7611317	0.81[ASN][1000 genomes]
rs7632649	0.81[ASN][1000 genomes]
rs834906	0.81[ASN][1000 genomes]
rs834907	0.81[ASN][1000 genomes]
rs834908	0.81[ASN][1000 genomes]
rs834909	0.81[ASN][1000 genomes]
rs834910	0.81[ASN][1000 genomes]
rs9289656	0.81[ASN][1000 genomes]
rs9809153	0.81[ASN][1000 genomes]
rs9821086	0.83[CHB][hapmap];0.83[JPT][hapmap]
rs990738	0.81[ASN][1000 genomes]
rs991419	0.81[ASN][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	esv2757893	chr3:142720230-142962932	Enhancers Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
2	esv2759183	chr3:142720230-142964373	Strong transcription Weak transcription Enhancers Bivalent Enhancer Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
3	nsv949288	chr3:142793323-143585882	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
4	nsv508250	chr3:142842454-142943722	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	esv34280	chr3:142887460-142962075	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv818171	chr3:142894411-142960273	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	nsv1009573	chr3:142896048-142959777	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region lncRNA	2 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	chr3:142893200-142909200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
2	chr3:142900200-142903400	Enhancers	Primary hematopoietic stem cells	blood
3	chr3:142902400-142908600	Weak transcription	Primary T cells from cord blood	blood
4	chr3:142902600-142904800	Weak transcription	Dnd41	blood
5	chr3:142902600-142909200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
6	chr3:142902600-142909200	Weak transcription	Primary T helper cells PMA-I stimulated	--
7	chr3:142902800-142903400	Enhancers	Primary B cells from cord blood	blood
8	chr3:142903000-142903600	Enhancers	Fetal Muscle Leg	muscle
9	chr3:142903000-142906800	Enhancers	K562	blood
10	chr3:142903200-142903400	Enhancers	Primary T helper cells fromperipheralblood	blood
11	chr3:142903200-142908000	Weak transcription	Fetal Thymus	thymus

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