Variant report

Variant	rs7692406
Chromosome Location	chr4:87867958-87867959
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:13)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:87866421..87869517-chr4:87926538..87929020,3	MCF-7	breast:
2	chr4:87866229..87868544-chr4:87942788..87945492,2	K562	blood:
3	chr4:87864190..87869754-chr4:87925812..87929793,8	K562	blood:
4	chr4:87866938..87869563-chr4:87883119..87884691,2	K562	blood:
5	chr4:87867281..87868896-chr4:87929541..87932174,2	MCF-7	breast:
6	chr4:87866844..87868969-chr4:88158554..88161014,2	K562	blood:
7	chr4:87859835..87862279-chr4:87865985..87868737,2	MCF-7	breast:
8	chr4:87854383..87857849-chr4:87866968..87869833,6	K562	blood:
9	chr4:87853595..87871697-chr4:87924007..87941983,77	K562	blood:
10	chr4:87857968..87859669-chr4:87867267..87869680,2	MCF-7	breast:
11	chr4:87867208..87869675-chr4:87927269..87929156,3	MCF-7	breast:
12	chr4:87867715..87870000-chr4:87883212..87884800,2	K562	blood:
13	chr4:87866229..87868745-chr4:87943992..87946336,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000163633	Chromatin interaction
ENSG00000172493	Chromatin interaction

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs13109353	1.00[AMR][1000 genomes]
rs2594275	1.00[AMR][1000 genomes]
rs6811156	1.00[AMR][1000 genomes]
rs6815870	1.00[AMR][1000 genomes]
rs6840031	1.00[AMR][1000 genomes]
rs6846015	1.00[AMR][1000 genomes]
rs6857047	1.00[AMR][1000 genomes]
rs7671962	1.00[AMR][1000 genomes]
rs7699431	0.82[YRI][hapmap];1.00[AMR][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	nsv594787	chr4:87221827-87888667	Enhancers Weak transcription Strong transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
2	nsv1013308	chr4:87769694-87870168	Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
3	nsv508297	chr4:87778783-87868508	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
4	nsv1009937	chr4:87795314-88008345	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	42 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:105 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:87857600-87882000	Weak transcription	Spleen	Spleen
2	chr4:87857800-87880200	Weak transcription	HSMM	muscle
3	chr4:87858200-87869400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr4:87858600-87881000	Weak transcription	Stomach Smooth Muscle	stomach
5	chr4:87861000-87878000	Weak transcription	HMEC	breast
6	chr4:87861400-87868000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
7	chr4:87861400-87877200	Weak transcription	Placenta Amnion	Placenta Amnion
8	chr4:87861400-87880800	Weak transcription	Aorta	Aorta
9	chr4:87861600-87868000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr4:87861600-87868000	Weak transcription	Fetal Lung	lung
11	chr4:87861600-87868000	Weak transcription	Skeletal Muscle Male	skeletal muscle
12	chr4:87861600-87868400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr4:87861600-87868400	Weak transcription	Brain Cingulate Gyrus	brain
14	chr4:87861600-87869200	Weak transcription	Brain Hippocampus Middle	brain
15	chr4:87861600-87870400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
16	chr4:87861800-87868000	Weak transcription	Colonic Mucosa	Colon
17	chr4:87861800-87868200	Weak transcription	Adipose Nuclei	Adipose
18	chr4:87861800-87871600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr4:87861800-87871600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr4:87861800-87878000	Weak transcription	Osteobl	bone
21	chr4:87861800-87880000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr4:87861800-87880600	Weak transcription	Fetal Kidney	kidney
23	chr4:87862400-87871200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
24	chr4:87863200-87868200	Enhancers	HUES6 Cell Line	embryonic stem cell
25	chr4:87863400-87869200	Enhancers	Dnd41	blood
26	chr4:87863400-87871600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr4:87863600-87871800	Weak transcription	NHDF-Ad	bronchial
28	chr4:87863800-87868200	Weak transcription	Primary T cells from cord blood	blood
29	chr4:87864000-87868000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
30	chr4:87864000-87868200	Weak transcription	Brain Anterior Caudate	brain
31	chr4:87864000-87868400	Weak transcription	Pancreatic Islets	Pancreatic Islet
32	chr4:87864000-87868400	Enhancers	Placenta	Placenta
33	chr4:87864000-87870000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr4:87864000-87871800	Weak transcription	NHEK	skin
35	chr4:87864000-87878000	Weak transcription	Muscle Satellite Cultured Cells	--
36	chr4:87864200-87868000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
37	chr4:87864200-87868000	Weak transcription	Rectal Mucosa Donor 31	rectum
38	chr4:87864400-87868000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
39	chr4:87864400-87868000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
40	chr4:87864400-87868200	Enhancers	GM12878-XiMat	blood
41	chr4:87864400-87868200	Weak transcription	HUVEC	blood vessel
42	chr4:87864400-87868400	Weak transcription	Fetal Intestine Small	intestine
43	chr4:87864400-87871800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr4:87864400-87871800	Weak transcription	Fetal Intestine Large	intestine
45	chr4:87864400-87874400	Weak transcription	Liver	Liver
46	chr4:87864400-87880600	Weak transcription	Gastric	stomach
47	chr4:87864400-87880800	Weak transcription	Rectal Mucosa Donor 29	rectum
48	chr4:87864600-87874400	Weak transcription	Hela-S3	cervix
49	chr4:87865000-87868600	Enhancers	HUES48 Cell Line	embryonic stem cell
50	chr4:87865400-87868400	Enhancers	HUES64 Cell Line	embryonic stem cell

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