Variant report

Variant	rs7085189
Chromosome Location	chr10:5936111-5936112
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1)
CpG islands
(count:0)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr10:5935995-5936156	GM12878	blood:	n/a	n/a

No data

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:5935195..5937102-chr10:6243588..6245241,2	MCF-7	breast:
2	chr10:5726920..5728949-chr10:5933520..5936437,2	K562	blood:
3	chr10:5852595..5861125-chr10:5921136..5936216,31	MCF-7	breast:
4	chr10:5934107..5937505-chr10:5944279..5947723,3	K562	blood:
5	chr10:5852308..5856409-chr10:5935538..5939554,4	K562	blood:
6	chr10:5853439..5857708-chr10:5926443..5936823,24	K562	blood:

No data

Variant related genes	Relation type
FBXO18	TF binding region
ANKRD16	TF binding region
ENSG00000057608	Chromatin interaction
ENSG00000272764	Chromatin interaction
ENSG00000134452	Chromatin interaction
ENSG00000213994	Chromatin interaction
ENSG00000108021	Chromatin interaction
ENSG00000170525	Chromatin interaction

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:1)

rs_ID	r²[population]
rs8177728	1.00[MEX][hapmap]

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	esv34147	chr10:5726821-6105717	Strong transcription Weak transcription Genic enhancers Enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
2	esv34061	chr10:5726821-6225187	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Genic enhancers 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 miRNA target site	50 gene(s)	inside rSNPs	diseases
3	nsv1042286	chr10:5795129-6578445	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	76 gene(s)	inside rSNPs	diseases
4	nsv831775	chr10:5804335-6000849	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
5	nsv825229	chr10:5886905-5967697	Enhancers Genic enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
6	nsv466724	chr10:5920836-5938544	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	15 gene(s)	inside rSNPs	diseases
7	nsv549906	chr10:5920836-5938544	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	15 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:5933200-5936400	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr10:5933200-5948200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr10:5933200-5949800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
4	chr10:5933200-5977000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
5	chr10:5933400-5936400	Weak transcription	Colonic Mucosa	Colon
6	chr10:5933400-5936400	Weak transcription	Fetal Kidney	kidney
7	chr10:5933400-5936600	Weak transcription	HSMMtube	muscle
8	chr10:5933400-5938800	Enhancers	Primary T helper cells PMA-I stimulated	--
9	chr10:5933400-5948200	Weak transcription	Ovary	ovary
10	chr10:5933400-5948400	Weak transcription	Placenta Amnion	Placenta Amnion
11	chr10:5933400-5949800	Weak transcription	Fetal Brain Male	brain
12	chr10:5933600-5936200	Weak transcription	A549	lung
13	chr10:5933600-5937000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr10:5933600-5948200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
15	chr10:5933600-5951600	Weak transcription	Stomach Mucosa	stomach
16	chr10:5933800-5936400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr10:5933800-5936400	Enhancers	Right Ventricle	heart
18	chr10:5933800-5939200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
19	chr10:5933800-5941200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr10:5934000-5936400	Weak transcription	Brain Angular Gyrus	brain
21	chr10:5934000-5936400	Weak transcription	Rectal Smooth Muscle	rectum
22	chr10:5934000-5939800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr10:5934200-5936400	Weak transcription	Brain Substantia Nigra	brain
24	chr10:5934200-5937800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
25	chr10:5934200-5938600	Strong transcription	Fetal Intestine Large	intestine
26	chr10:5934200-5939400	Strong transcription	Fetal Muscle Leg	muscle
27	chr10:5934400-5936200	Weak transcription	Brain Anterior Caudate	brain
28	chr10:5934400-5936400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
29	chr10:5934400-5936400	Weak transcription	Fetal Brain Female	brain
30	chr10:5934400-5936400	Enhancers	HUVEC	blood vessel
31	chr10:5934400-5937600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
32	chr10:5934400-5938000	Strong transcription	HUES48 Cell Line	embryonic stem cell
33	chr10:5934600-5936200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr10:5934600-5937400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
35	chr10:5934600-5941000	Strong transcription	NHEK	skin
36	chr10:5934800-5936400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr10:5934800-5940200	Weak transcription	Colon Smooth Muscle	Colon
38	chr10:5934800-5948000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr10:5935000-5936400	Enhancers	Thymus	Thymus
40	chr10:5935000-5937200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
41	chr10:5935000-5938000	Strong transcription	Dnd41	blood
42	chr10:5935200-5937600	Strong transcription	HUES64 Cell Line	embryonic stem cell
43	chr10:5935200-5941800	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr10:5935200-5947400	Weak transcription	Small Intestine	intestine
45	chr10:5935400-5936400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr10:5935400-5936400	Strong transcription	Primary B cells from peripheral blood	blood
47	chr10:5935400-5936800	Strong transcription	Primary B cells from cord blood	blood
48	chr10:5935400-5937000	Strong transcription	Primary T cells fromperipheralblood	blood
49	chr10:5935400-5937200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr10:5935400-5937800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell

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