Variant report

Variant	rs10204965
Chromosome Location	chr2:127873505-127873506
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs10198772	0.96[ASN][1000 genomes]
rs11674215	0.96[ASN][1000 genomes]
rs11688714	0.96[ASN][1000 genomes]
rs11688763	0.96[ASN][1000 genomes]
rs11692858	0.89[ASN][1000 genomes]
rs11695202	0.96[ASN][1000 genomes]
rs13416395	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs13417002	1.00[ASN][1000 genomes]
rs13417187	1.00[ASN][1000 genomes]
rs13419729	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs13427080	1.00[ASN][1000 genomes]
rs3845673	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs56772251	1.00[ASN][1000 genomes]
rs56827597	1.00[ASN][1000 genomes]
rs56853185	1.00[ASN][1000 genomes]
rs6751498	1.00[ASN][1000 genomes]
rs72959054	1.00[ASN][1000 genomes]
rs72959055	1.00[ASN][1000 genomes]
rs72959057	0.96[ASN][1000 genomes]
rs72959066	0.96[ASN][1000 genomes]
rs72959067	0.96[ASN][1000 genomes]
rs7575579	0.96[ASN][1000 genomes]
rs7583814	0.87[ASN][1000 genomes]
rs7584040	0.87[ASN][1000 genomes]
rs7600660	1.00[ASN][1000 genomes]
rs9653201	0.89[ASN][1000 genomes]
rs9653202	0.96[ASN][1000 genomes]
rs9653203	0.96[ASN][1000 genomes]
rs9653206	0.96[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:22 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:127867400-127874800	Weak transcription	Brain Anterior Caudate	brain
2	chr2:127870600-127898400	Weak transcription	Right Atrium	heart
3	chr2:127872200-127876200	Enhancers	Brain Hippocampus Middle	brain
4	chr2:127872400-127874000	Enhancers	Fetal Intestine Large	intestine
5	chr2:127872400-127874200	Enhancers	Liver	Liver
6	chr2:127872400-127874200	Enhancers	Fetal Intestine Small	intestine
7	chr2:127872400-127874200	Enhancers	Stomach Mucosa	stomach
8	chr2:127873000-127873600	Enhancers	Brain Angular Gyrus	brain
9	chr2:127873000-127873600	Enhancers	A549	lung
10	chr2:127873000-127874000	Enhancers	Brain Inferior Temporal Lobe	brain
11	chr2:127873000-127874000	Enhancers	Rectal Mucosa Donor 31	rectum
12	chr2:127873000-127874200	Bivalent Enhancer	HepG2	liver
13	chr2:127873200-127873800	Enhancers	Brain Substantia Nigra	brain
14	chr2:127873200-127874000	Enhancers	Gastric	stomach
15	chr2:127873200-127875200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr2:127873200-127878000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr2:127873200-127878200	Weak transcription	Fetal Muscle Trunk	muscle
18	chr2:127873200-127878200	Weak transcription	Fetal Muscle Leg	muscle
19	chr2:127873400-127874000	Weak transcription	Duodenum Mucosa	Duodenum
20	chr2:127873400-127874800	Weak transcription	Brain Cingulate Gyrus	brain
21	chr2:127873400-127879400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr2:127873400-127886000	Weak transcription	Spleen	Spleen

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