Variant report

Variant	rs57665994
Chromosome Location	chr2:33718679-33718680
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:33718664..33721605-chr2:33823247..33825969,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000119812	Chromatin interaction

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs10495789	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13009528	0.93[ASN][1000 genomes]
rs13009794	0.81[ASN][1000 genomes]
rs17013126	0.81[ASN][1000 genomes]
rs17013137	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17013166	0.82[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs34160168	0.96[ASN][1000 genomes]
rs35799810	0.81[ASN][1000 genomes]
rs35807143	0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs55844722	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs56354744	0.96[ASN][1000 genomes]
rs57476168	0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs57647413	0.81[ASN][1000 genomes]
rs6705101	0.93[ASN][1000 genomes]
rs6757351	0.83[ASN][1000 genomes]
rs6758071	0.81[ASN][1000 genomes]
rs719546	0.96[ASN][1000 genomes]
rs72804238	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1005435	chr2:33136117-33747159	Weak transcription Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	22 gene(s)	inside rSNPs	diseases
2	nsv535624	chr2:33136117-33747159	Weak transcription Enhancers Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	22 gene(s)	inside rSNPs	diseases
3	esv1829750	chr2:33704194-33740571	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	esv1798854	chr2:33708860-33720009	Enhancers Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	esv3457478	chr2:33716912-33727989	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
6	esv3457477	chr2:33717011-33728006	Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
7	esv3457479	chr2:33717011-33728006	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent Enhancer Strong transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
8	nsv828775	chr2:33717066-33727682	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Active TSS Genic enhancers	Chromatin interactive region	2 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	chr2:33710400-33775400	Weak transcription	Pancreas	Pancrea
2	chr2:33712200-33747600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr2:33712800-33718800	Enhancers	Psoas Muscle	Psoas
4	chr2:33714400-33718800	Enhancers	Left Ventricle	heart
5	chr2:33714400-33726000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr2:33715600-33719000	Genic enhancers	Primary B cells from peripheral blood	blood
7	chr2:33715600-33719200	Weak transcription	NHDF-Ad	bronchial
8	chr2:33716000-33721400	Weak transcription	Primary T helper cells PMA-I stimulated	--
9	chr2:33716800-33719400	Weak transcription	Brain Anterior Caudate	brain
10	chr2:33717000-33720200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr2:33717000-33722200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr2:33717000-33723600	Weak transcription	Lung	lung
13	chr2:33717200-33721600	Weak transcription	Primary T helper cells fromperipheralblood	blood
14	chr2:33717400-33719600	Genic enhancers	Primary B cells from cord blood	blood
15	chr2:33717600-33719400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
16	chr2:33717800-33720000	Weak transcription	Fetal Heart	heart
17	chr2:33718000-33719200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr2:33718000-33719200	Weak transcription	Brain Hippocampus Middle	brain
19	chr2:33718000-33719400	Weak transcription	Primary hematopoietic stem cells	blood
20	chr2:33718200-33719000	Flanking Active TSS	GM12878-XiMat	blood
21	chr2:33718400-33721000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr2:33718400-33722400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr2:33718400-33724200	Weak transcription	Right Atrium	heart
24	chr2:33718600-33719200	Weak transcription	Right Ventricle	heart
25	chr2:33718600-33719600	Weak transcription	Skeletal Muscle Female	skeletal muscle
26	chr2:33718600-33720800	Weak transcription	Skeletal Muscle Male	skeletal muscle

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links