Variant report

Variant	rs10021442
Chromosome Location	chr4:47589896-47589897
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	chr4:47582229..47585198-chr4:47587871..47590442,2	K562	blood:

Variant related genes	Relation type
ENSG00000145246	Chromatin interaction

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs10004038	1.00[CHB][hapmap]
rs11930255	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11932436	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11941639	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs11947712	1.00[CHB][hapmap]
rs1316782	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1316783	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13435606	0.87[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.98[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16860404	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17462783	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs17572227	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17572234	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17572617	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap]
rs4599383	1.00[CHB][hapmap]
rs4694851	1.00[CHB][hapmap]
rs4695239	1.00[CHB][hapmap]
rs4695243	1.00[CHB][hapmap]
rs6447564	1.00[CHB][hapmap]
rs67707778	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6835978	1.00[CHB][hapmap]
rs6842769	1.00[CHB][hapmap]
rs6855797	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73238611	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73238616	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7674353	1.00[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv829923	chr4:47436139-47678443	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	nsv1008515	chr4:47488431-47906835	Weak transcription Strong transcription Flanking Bivalent TSS/Enh Enhancers Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
3	nsv948568	chr4:47488431-47907524	Enhancers Strong transcription Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
4	nsv1004939	chr4:47488573-47901460	Bivalent Enhancer Enhancers Strong transcription Weak transcription Active TSS Genic enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
5	nsv537080	chr4:47488573-47901460	Weak transcription Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
6	nsv997471	chr4:47489412-47895223	Weak transcription Strong transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
7	nsv998892	chr4:47493552-47863354	Weak transcription Strong transcription Flanking Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
8	nsv537081	chr4:47493552-47863354	Strong transcription Weak transcription Enhancers Bivalent/Poised TSS Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
9	nsv1000337	chr4:47493907-47902019	Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
10	nsv594118	chr4:47560386-47917730	Weak transcription Strong transcription Bivalent/Poised TSS ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:93 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:47534600-47592000	Strong transcription	Monocytes-CD14+_RO01746	blood
2	chr4:47555800-47594800	Weak transcription	Stomach Mucosa	stomach
3	chr4:47567600-47598400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr4:47567800-47590800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
5	chr4:47568000-47592000	Strong transcription	Primary B cells from peripheral blood	blood
6	chr4:47568200-47592200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr4:47568200-47595800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
8	chr4:47570000-47592200	Strong transcription	Stomach Smooth Muscle	stomach
9	chr4:47570200-47592200	Strong transcription	Primary B cells from cord blood	blood
10	chr4:47570400-47591800	Strong transcription	Dnd41	blood
11	chr4:47570400-47595400	Strong transcription	Primary monocytes fromperipheralblood	blood
12	chr4:47570600-47592000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr4:47570800-47595800	Strong transcription	Osteobl	bone
14	chr4:47570800-47596000	Strong transcription	Placenta	Placenta
15	chr4:47571000-47591800	Strong transcription	Duodenum Smooth Muscle	Duodenum
16	chr4:47573400-47593600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr4:47573800-47591000	Weak transcription	Brain Germinal Matrix	brain
18	chr4:47574400-47595000	Weak transcription	Fetal Brain Female	brain
19	chr4:47575000-47610200	Weak transcription	Fetal Brain Male	brain
20	chr4:47575200-47592400	Weak transcription	Rectal Smooth Muscle	rectum
21	chr4:47577600-47592200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr4:47577600-47592200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr4:47577600-47592400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr4:47577600-47592400	Weak transcription	Fetal Intestine Small	intestine
25	chr4:47578200-47590400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
26	chr4:47578200-47592600	Strong transcription	HMEC	breast
27	chr4:47578600-47590400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
28	chr4:47579800-47592000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr4:47580800-47591400	Weak transcription	Primary T cells fromperipheralblood	blood
30	chr4:47580800-47592200	Strong transcription	HSMM	muscle
31	chr4:47581200-47595600	Weak transcription	HUVEC	blood vessel
32	chr4:47583600-47592000	Strong transcription	Liver	Liver
33	chr4:47583600-47592200	Strong transcription	Muscle Satellite Cultured Cells	--
34	chr4:47583800-47590200	Strong transcription	Fetal Kidney	kidney
35	chr4:47583800-47591400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr4:47583800-47591600	Strong transcription	Ovary	ovary
37	chr4:47585200-47592200	Weak transcription	Brain Inferior Temporal Lobe	brain
38	chr4:47585200-47592200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
39	chr4:47586200-47605400	Weak transcription	Fetal Stomach	stomach
40	chr4:47587600-47590800	Strong transcription	Fetal Intestine Large	intestine
41	chr4:47587600-47591800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr4:47587600-47591800	Strong transcription	Brain Hippocampus Middle	brain
43	chr4:47587600-47592400	Strong transcription	Duodenum Mucosa	Duodenum
44	chr4:47587600-47592400	Strong transcription	Fetal Lung	lung
45	chr4:47587800-47590000	Strong transcription	Rectal Mucosa Donor 31	rectum
46	chr4:47587800-47590200	Strong transcription	Cortex derived primary cultured neurospheres	brain
47	chr4:47587800-47590200	Strong transcription	Brain Substantia Nigra	brain
48	chr4:47587800-47591200	Strong transcription	Brain Anterior Caudate	brain
49	chr4:47587800-47592200	Strong transcription	Adipose Nuclei	Adipose
50	chr4:47587800-47592400	Strong transcription	HSMMtube	muscle

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