Variant report

Variant	rs10947450
Chromosome Location	chr6:33795964-33795965
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:33794613..33797241-chr6:33797718..33800343,2	K562	blood:
2	chr6:33794679..33797387-chr6:33799948..33801747,2	MCF-7	breast:
3	chr6:33785785..33787790-chr6:33794712..33797065,2	K562	blood:
4	chr6:33755377..33757050-chr6:33795236..33797558,2	MCF-7	breast:
5	chr6:33795530..33798300-chr6:33803409..33806426,4	MCF-7	breast:
6	chr6:33788574..33790183-chr6:33793587..33795973,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000161904	Chromatin interaction

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs6899677	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9461911	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9461915	0.87[ASN][1000 genomes]
rs9461916	0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9461917	0.84[EUR][1000 genomes]
rs9469603	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]

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	nsv885773	chr6:33778964-33813043	Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
2	nsv885774	chr6:33778964-33840121	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats	Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv885775	chr6:33788055-33828178	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv1032074	chr6:33795671-33835988	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Active TSS	Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv1022403	chr6:33795671-33847345	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:43 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:33790800-33796000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr6:33790800-33796000	Weak transcription	Right Ventricle	heart
3	chr6:33791000-33796000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr6:33791000-33796200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr6:33791000-33796400	Weak transcription	HUES64 Cell Line	embryonic stem cell
6	chr6:33791600-33796400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr6:33792800-33797000	Weak transcription	Ovary	ovary
8	chr6:33793000-33796000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
9	chr6:33793000-33798800	Weak transcription	Spleen	Spleen
10	chr6:33794400-33796000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr6:33794600-33796600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr6:33794600-33796600	Enhancers	Rectal Mucosa Donor 31	rectum
13	chr6:33794600-33799400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
14	chr6:33794800-33796400	Enhancers	Stomach Smooth Muscle	stomach
15	chr6:33795000-33796000	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr6:33795000-33796000	Enhancers	Osteobl	bone
17	chr6:33795000-33796200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr6:33795000-33796200	Enhancers	Duodenum Mucosa	Duodenum
19	chr6:33795000-33796200	Enhancers	Fetal Intestine Large	intestine
20	chr6:33795000-33796200	Enhancers	HSMMtube	muscle
21	chr6:33795000-33796600	Enhancers	Fetal Intestine Small	intestine
22	chr6:33795000-33799600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr6:33795200-33796000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr6:33795200-33796000	Enhancers	Brain Cingulate Gyrus	brain
25	chr6:33795200-33796000	Enhancers	Rectal Mucosa Donor 29	rectum
26	chr6:33795200-33796200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr6:33795200-33796400	Bivalent Enhancer	HepG2	liver
28	chr6:33795400-33796000	Enhancers	Colonic Mucosa	Colon
29	chr6:33795400-33797200	Enhancers	H1 Cell Line	embryonic stem cell
30	chr6:33795600-33796000	Bivalent Enhancer	NH-A	brain
31	chr6:33795600-33797000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr6:33795600-33797200	Enhancers	Colon Smooth Muscle	Colon
33	chr6:33795800-33796200	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr6:33795800-33796400	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
35	chr6:33795800-33796400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr6:33795800-33796400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
37	chr6:33795800-33796600	Enhancers	Rectal Smooth Muscle	rectum
38	chr6:33795800-33796600	Enhancers	A549	lung
39	chr6:33795800-33797000	Enhancers	Fetal Kidney	kidney
40	chr6:33795800-33797200	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
41	chr6:33795800-33797200	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
42	chr6:33795800-33798000	Enhancers	HUES48 Cell Line	embryonic stem cell
43	chr6:33795800-33798600	Enhancers	HUES6 Cell Line	embryonic stem cell

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