Variant report

Variant	rs11681838
Chromosome Location	chr2:11741193-11741194
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:11739453..11742441-chr2:11747484..11750945,3	MCF-7	breast:
2	chr2:11740125..11742102-chr2:11743265..11746041,3	K562	blood:

Variant related genes	Relation type
ENSG00000265583	Chromatin interaction

Extended variants
information (count: 23 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11688915	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11689869	0.95[ASN][1000 genomes]
rs13431704	1.00[CHD][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs13432243	1.00[CHD][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs1435547	0.84[ASW][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1865575	1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2252958	1.00[CHB][hapmap];1.00[CHD][hapmap]
rs2304399	1.00[CHB][hapmap];1.00[CHD][hapmap]
rs36030386	0.90[ASN][1000 genomes]
rs4669756	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62118318	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6735957	1.00[CHB][hapmap];1.00[CHD][hapmap];0.88[GIH][hapmap];1.00[MEX][hapmap]
rs6736604	0.90[ASN][1000 genomes]
rs6744817	1.00[CHD][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs7557063	1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7559835	1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs7576944	1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs7596162	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs880858	0.90[ASN][1000 genomes]
rs9287733	1.00[JPT][hapmap];0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1010506	chr2:11430965-12057286	Enhancers Strong transcription Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
2	nsv535585	chr2:11430965-12057286	Enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
3	nsv873663	chr2:11664349-11783775	Genic enhancers Weak transcription ZNF genes & repeats Strong transcription Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	41 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:51 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:11678400-11757000	Weak transcription	Right Ventricle	heart
2	chr2:11694800-11755200	Weak transcription	Gastric	stomach
3	chr2:11700000-11767000	Weak transcription	Right Atrium	heart
4	chr2:11714400-11765000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr2:11717600-11767000	Weak transcription	Fetal Intestine Small	intestine
6	chr2:11719400-11750800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr2:11724400-11788600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
8	chr2:11724600-11766800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr2:11724600-11766800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr2:11724800-11749600	Weak transcription	Brain Cingulate Gyrus	brain
11	chr2:11725000-11743800	Weak transcription	Fetal Kidney	kidney
12	chr2:11725400-11742400	Strong transcription	Ovary	ovary
13	chr2:11725600-11766800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
14	chr2:11733400-11750800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr2:11733600-11750600	Weak transcription	Pancreas	Pancrea
16	chr2:11733600-11784000	Strong transcription	HepG2	liver
17	chr2:11735200-11744600	Strong transcription	H9 Cell Line	embryonic stem cell
18	chr2:11735200-11746400	Strong transcription	HUES6 Cell Line	embryonic stem cell
19	chr2:11735600-11745000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr2:11735600-11746600	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr2:11736000-11743000	Weak transcription	Stomach Smooth Muscle	stomach
22	chr2:11736200-11765000	Weak transcription	Fetal Lung	lung
23	chr2:11736400-11755400	Weak transcription	Brain Substantia Nigra	brain
24	chr2:11736600-11750600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
25	chr2:11736800-11762800	Weak transcription	Fetal Heart	heart
26	chr2:11737000-11744600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr2:11737400-11741600	Strong transcription	Brain Hippocampus Middle	brain
28	chr2:11737600-11742000	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
29	chr2:11737600-11744400	Strong transcription	Fetal Stomach	stomach
30	chr2:11737800-11745000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
31	chr2:11737800-11746400	Strong transcription	HUES64 Cell Line	embryonic stem cell
32	chr2:11738000-11744600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
33	chr2:11738400-11744000	Strong transcription	HUES48 Cell Line	embryonic stem cell
34	chr2:11738600-11741400	Strong transcription	H1 Cell Line	embryonic stem cell
35	chr2:11738600-11743400	Strong transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr2:11738600-11744800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr2:11739200-11743000	Weak transcription	Left Ventricle	heart
38	chr2:11739200-11751400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr2:11739200-11752000	Weak transcription	Skeletal Muscle Male	skeletal muscle
40	chr2:11739600-11744800	Strong transcription	Fetal Muscle Leg	muscle
41	chr2:11739600-11750800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr2:11740000-11742200	Strong transcription	ES-I3 Cell Line	embryonic stem cell
43	chr2:11740000-11745200	Strong transcription	Cortex derived primary cultured neurospheres	brain
44	chr2:11740200-11745200	Strong transcription	Fetal Muscle Trunk	muscle
45	chr2:11740400-11741400	Strong transcription	Liver	Liver
46	chr2:11740400-11743800	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
47	chr2:11740800-11742000	Strong transcription	Pancreatic Islets	Pancreatic Islet
48	chr2:11741000-11741200	Strong transcription	Brain Anterior Caudate	brain
49	chr2:11741000-11741400	Strong transcription	Brain Angular Gyrus	brain
50	chr2:11741000-11741600	Strong transcription	Brain Inferior Temporal Lobe	brain

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