Variant report

Variant	rs11603531
Chromosome Location	chr11:56971717-56971718
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs10792077	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11603194	0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11604352	0.81[ASN][1000 genomes]
rs11820215	0.94[AFR][1000 genomes];0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1893937	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2077190	0.91[AFR][1000 genomes];0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3017577	0.85[AFR][1000 genomes];0.80[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4442567	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4939113	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs514354	0.91[AFR][1000 genomes];0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs567766	0.95[AFR][1000 genomes];0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs609763	0.95[AFR][1000 genomes];0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs622932	0.91[AFR][1000 genomes];0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs948851	0.95[AFR][1000 genomes];0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv915640	chr11:56814841-57139786	Weak transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
2	nsv482317	chr11:56857026-57028631	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:30 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:56967200-56973000	Enhancers	Fetal Lung	lung
2	chr11:56967400-56973600	Enhancers	Fetal Stomach	stomach
3	chr11:56967800-56973600	Enhancers	Fetal Muscle Leg	muscle
4	chr11:56968200-56973000	Enhancers	Left Ventricle	heart
5	chr11:56968200-56974400	Enhancers	Fetal Muscle Trunk	muscle
6	chr11:56968200-56975200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
7	chr11:56968600-56972800	Enhancers	Spleen	Spleen
8	chr11:56968800-56972400	Enhancers	Right Ventricle	heart
9	chr11:56969000-56972200	Weak transcription	Brain Anterior Caudate	brain
10	chr11:56969800-56973000	Enhancers	Placenta	Placenta
11	chr11:56970000-56972400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr11:56970000-56972600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr11:56970200-56972600	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
14	chr11:56970600-56972400	Weak transcription	Fetal Heart	heart
15	chr11:56970800-56972000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
16	chr11:56970800-56972800	Enhancers	Lung	lung
17	chr11:56970800-56974000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr11:56971000-56972200	Weak transcription	HUES64 Cell Line	embryonic stem cell
19	chr11:56971000-56972200	Weak transcription	Brain Substantia Nigra	brain
20	chr11:56971200-56972200	Weak transcription	H9 Cell Line	embryonic stem cell
21	chr11:56971200-56972200	Weak transcription	HUES6 Cell Line	embryonic stem cell
22	chr11:56971200-56972200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
23	chr11:56971200-56974000	Enhancers	H1 Cell Line	embryonic stem cell
24	chr11:56971200-56978000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr11:56971400-56972400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr11:56971600-56971800	Enhancers	Duodenum Mucosa	Duodenum
27	chr11:56971600-56972200	Weak transcription	Duodenum Smooth Muscle	Duodenum
28	chr11:56971600-56973600	Enhancers	Adipose Nuclei	Adipose
29	chr11:56971600-56974800	Weak transcription	Right Atrium	heart
30	chr11:56971600-56974800	Weak transcription	Stomach Smooth Muscle	stomach

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links