Variant report

Variant	rs4473651
Chromosome Location	chr4:15770911-15770912
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs1004124	0.81[JPT][hapmap]
rs1112243	0.81[JPT][hapmap]
rs1112244	0.81[JPT][hapmap]
rs11574928	0.81[JPT][hapmap]
rs11945730	0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12502292	0.82[ASN][1000 genomes]
rs12647844	0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs16892438	0.81[JPT][hapmap]
rs16892441	0.81[JPT][hapmap]
rs1800051	0.81[JPT][hapmap]
rs2286553	0.80[JPT][hapmap]
rs28464016	0.95[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs28520979	0.95[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs28660365	0.95[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs3756243	0.87[JPT][hapmap]
rs3796865	0.81[JPT][hapmap]
rs3796866	0.81[JPT][hapmap]
rs3796871	0.81[JPT][hapmap]
rs3822257	0.87[JPT][hapmap]
rs4508877	0.81[JPT][hapmap]
rs6449194	0.82[EUR][1000 genomes]
rs6449195	0.91[CEU][hapmap];0.87[JPT][hapmap]
rs6449197	1.00[CEU][hapmap];0.87[JPT][hapmap];0.89[TSI][hapmap];0.82[EUR][1000 genomes]
rs6449198	0.81[EUR][1000 genomes]
rs6836374	0.81[JPT][hapmap]
rs6855636	0.86[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7690685	0.81[JPT][hapmap]
rs953870	0.81[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3448986	chr4:14928802-15805558	Active TSS Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Enhancers ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
2	nsv1012988	chr4:15597510-16091527	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
3	nsv10460	chr4:15757611-15818206	ZNF genes & repeats Enhancers Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	esv2760884	chr4:15759680-15776181	Enhancers Bivalent Enhancer Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv1013204	chr4:15762970-15836237	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Weak transcription Bivalent/Poised TSS Strong transcription Bivalent Enhancer Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:31 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:15764800-15775800	Weak transcription	Primary neutrophils fromperipheralblood	blood
2	chr4:15766800-15771000	Enhancers	Primary T helper cells fromperipheralblood	blood
3	chr4:15766800-15771200	Enhancers	Primary T killer memory cells from peripheral blood	blood
4	chr4:15767000-15771200	Enhancers	Primary T cells fromperipheralblood	blood
5	chr4:15767200-15771000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
6	chr4:15767200-15771200	Enhancers	Primary T helper naive cells from peripheral blood	blood
7	chr4:15767200-15771200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
8	chr4:15767200-15771200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
9	chr4:15767200-15779400	Weak transcription	Spleen	Spleen
10	chr4:15768000-15771000	Weak transcription	Right Ventricle	heart
11	chr4:15768200-15772400	Weak transcription	Monocytes-CD14+_RO01746	blood
12	chr4:15768200-15775200	Enhancers	Primary T helper cells PMA-I stimulated	--
13	chr4:15768200-15777200	Enhancers	Fetal Thymus	thymus
14	chr4:15768400-15772800	Weak transcription	Primary monocytes fromperipheralblood	blood
15	chr4:15768800-15771000	Weak transcription	GM12878-XiMat	blood
16	chr4:15768800-15773400	Weak transcription	Sigmoid Colon	Sigmoid Colon
17	chr4:15768800-15774800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
18	chr4:15769000-15771200	Enhancers	Primary T cells from cord blood	blood
19	chr4:15769000-15772400	Weak transcription	Primary hematopoietic stem cells	blood
20	chr4:15769000-15772400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr4:15769000-15772800	Weak transcription	Primary B cells from cord blood	blood
22	chr4:15769000-15772800	Weak transcription	Duodenum Mucosa	Duodenum
23	chr4:15769000-15773400	Weak transcription	Rectal Mucosa Donor 29	rectum
24	chr4:15769200-15778600	Weak transcription	Skeletal Muscle Female	skeletal muscle
25	chr4:15769800-15772400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
26	chr4:15769800-15772400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr4:15769800-15773400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
28	chr4:15770000-15773000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
29	chr4:15770600-15772800	Genic enhancers	Dnd41	blood
30	chr4:15770800-15771000	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
31	chr4:15770800-15771200	Enhancers	Thymus	Thymus

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