Variant report

Variant	rs7557280
Chromosome Location	chr2:127873161-127873162
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr2:127868348..127869960-chr2:127871605..127873219,2	MCF-7	breast:
2	chr2:127865657..127869658-chr2:127871080..127873352,3	K562	blood:
3	chr2:127853337..127855770-chr2:127871735..127873345,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC114783.1.1-4	chr2:127871993-127874626	NONHSAT074143

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs12989701	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12994284	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12994718	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13004848	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs13009551	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs13029812	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28434131	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34608578	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34745987	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34854727	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs35832505	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs35860453	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs36085158	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4663096	0.94[EUR][1000 genomes]
rs4663097	0.94[EUR][1000 genomes]
rs6710467	0.90[EUR][1000 genomes]
rs6720234	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs71414738	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7583814	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs873270	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv999422	chr2:127464647-127956543	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
2	nsv1004930	chr2:127477369-127938234	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
3	nsv875012	chr2:127800981-127895573	Enhancers ZNF genes & repeats Weak transcription Genic enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv1006112	chr2:127830117-128032546	Transcr. at gene 5' and 3' Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
5	esv2757832	chr2:127830943-128006514	Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
6	esv2759090	chr2:127830943-128006514	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
7	nsv1005149	chr2:127841930-127880106	Bivalent Enhancer ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Genic enhancers Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	nsv1011378	chr2:127841930-128020546	Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Weak transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
9	nsv999809	chr2:127841930-128032546	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
10	nsv1010669	chr2:127848860-128032546	Active TSS Enhancers Weak transcription Genic enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
11	nsv1003599	chr2:127871183-128059407	Strong transcription Active TSS Enhancers Weak transcription Genic enhancers Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
12	nsv535920	chr2:127871183-128059407	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:127866200-127873200	Weak transcription	Gastric	stomach
2	chr2:127867400-127874800	Weak transcription	Brain Anterior Caudate	brain
3	chr2:127870600-127898400	Weak transcription	Right Atrium	heart
4	chr2:127871800-127873200	Weak transcription	Brain Substantia Nigra	brain
5	chr2:127872200-127876200	Enhancers	Brain Hippocampus Middle	brain
6	chr2:127872400-127873200	Enhancers	Fetal Muscle Leg	muscle
7	chr2:127872400-127874000	Enhancers	Fetal Intestine Large	intestine
8	chr2:127872400-127874200	Enhancers	Liver	Liver
9	chr2:127872400-127874200	Enhancers	Fetal Intestine Small	intestine
10	chr2:127872400-127874200	Enhancers	Stomach Mucosa	stomach
11	chr2:127872600-127873200	Enhancers	Fetal Muscle Trunk	muscle
12	chr2:127872800-127873200	Weak transcription	Spleen	Spleen
13	chr2:127872800-127873400	Enhancers	Duodenum Mucosa	Duodenum
14	chr2:127873000-127873200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
15	chr2:127873000-127873400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr2:127873000-127873400	Enhancers	Brain Cingulate Gyrus	brain
17	chr2:127873000-127873600	Enhancers	Brain Angular Gyrus	brain
18	chr2:127873000-127873600	Enhancers	A549	lung
19	chr2:127873000-127874000	Enhancers	Brain Inferior Temporal Lobe	brain
20	chr2:127873000-127874000	Enhancers	Rectal Mucosa Donor 31	rectum
21	chr2:127873000-127874200	Bivalent Enhancer	HepG2	liver

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