Variant report

Variant	rs4698418
Chromosome Location	chr4:15818916-15818917
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs11574923	0.94[AMR][1000 genomes];0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11574927	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs13104011	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs13124795	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13136498	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13143035	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs13147551	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs16892403	0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs17408310	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs17408338	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs34252100	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs34324179	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs34747980	0.80[ASN][1000 genomes]
rs34762270	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs36125685	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs3756242	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3796864	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3796868	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4698121	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4698122	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4698123	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4698419	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4698421	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4698422	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.89[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs57904440	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs60090018	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs62290649	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6815245	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6816486	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs71601499	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7655635	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7678866	0.81[EUR][1000 genomes]
rs9637595	0.96[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[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	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
2	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
3	nsv1010597	chr4:15776181-15836237	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
4	nsv916742	chr4:15797994-16064232	Strong transcription Enhancers Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:26 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:15808400-15819400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr4:15810800-15821600	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr4:15811400-15819400	Weak transcription	Primary T cells fromperipheralblood	blood
4	chr4:15811400-15819800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
5	chr4:15811400-15820000	Weak transcription	Primary T helper cells PMA-I stimulated	--
6	chr4:15811400-15827000	Weak transcription	Skeletal Muscle Female	skeletal muscle
7	chr4:15811400-15851200	Weak transcription	Rectal Mucosa Donor 29	rectum
8	chr4:15811400-15852200	Weak transcription	Spleen	Spleen
9	chr4:15811600-15821600	Weak transcription	Primary neutrophils fromperipheralblood	blood
10	chr4:15811800-15819000	Weak transcription	Primary T helper cells fromperipheralblood	blood
11	chr4:15811800-15842200	Weak transcription	Skeletal Muscle Male	skeletal muscle
12	chr4:15812200-15840000	Strong transcription	Dnd41	blood
13	chr4:15813800-15834600	Weak transcription	Psoas Muscle	Psoas
14	chr4:15814000-15819000	Weak transcription	Monocytes-CD14+_RO01746	blood
15	chr4:15814000-15819200	Weak transcription	Primary monocytes fromperipheralblood	blood
16	chr4:15817800-15819600	Strong transcription	Fetal Thymus	thymus
17	chr4:15818000-15821000	Strong transcription	Primary T cells from cord blood	blood
18	chr4:15818000-15821600	Strong transcription	Primary B cells from cord blood	blood
19	chr4:15818200-15819400	Strong transcription	Thymus	Thymus
20	chr4:15818200-15821000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr4:15818200-15821200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
22	chr4:15818400-15821000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr4:15818600-15819200	Strong transcription	Duodenum Mucosa	Duodenum
24	chr4:15818600-15820200	Strong transcription	Primary hematopoietic stem cells	blood
25	chr4:15818600-15821200	Strong transcription	Primary B cells from peripheral blood	blood
26	chr4:15818800-15821200	Strong transcription	Primary T helper naive cells fromperipheralblood	blood

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