Variant report

Variant	rs16927218
Chromosome Location	chr11:35286999-35287000
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs10488814	1.00[EUR][1000 genomes]
rs16927196	1.00[YRI][hapmap]
rs16927209	1.00[EUR][1000 genomes]
rs16927212	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16927214	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16927220	0.82[YRI][hapmap];1.00[EUR][1000 genomes]
rs16927255	1.00[EUR][1000 genomes]
rs16927281	1.00[EUR][1000 genomes]
rs16927304	0.83[AFR][1000 genomes]
rs6484773	1.00[EUR][1000 genomes]
rs6484777	1.00[EUR][1000 genomes]
rs7102949	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7106060	1.00[EUR][1000 genomes]
rs7109108	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7125980	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7130500	1.00[EUR][1000 genomes]
rs73439144	1.00[EUR][1000 genomes]
rs7941569	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7947035	1.00[AMR][1000 genomes];1.00[EUR][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	nsv1045837	chr11:34893992-35395190	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
2	nsv541004	chr11:35122694-35297414	Strong transcription Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
3	nsv832120	chr11:35277410-35490304	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:29 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:35265800-35305800	Weak transcription	HepG2	liver
2	chr11:35270200-35292600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
3	chr11:35270400-35296400	Weak transcription	Brain Cingulate Gyrus	brain
4	chr11:35270400-35307000	Weak transcription	Fetal Brain Male	brain
5	chr11:35274600-35287400	Weak transcription	HSMMtube	muscle
6	chr11:35282200-35297000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr11:35282200-35297000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr11:35282400-35289200	Strong transcription	Cortex derived primary cultured neurospheres	brain
9	chr11:35282400-35296600	Weak transcription	Aorta	Aorta
10	chr11:35282600-35288600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr11:35282600-35296800	Weak transcription	Skeletal Muscle Female	skeletal muscle
12	chr11:35282800-35287400	Weak transcription	HSMM	muscle
13	chr11:35283000-35289400	Weak transcription	NHDF-Ad	bronchial
14	chr11:35283000-35302000	Weak transcription	Brain Inferior Temporal Lobe	brain
15	chr11:35283800-35288400	Weak transcription	NHLF	lung
16	chr11:35284600-35296600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
17	chr11:35284600-35300800	Weak transcription	Brain Angular Gyrus	brain
18	chr11:35284800-35296600	Weak transcription	Brain Hippocampus Middle	brain
19	chr11:35285200-35287600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr11:35285400-35287600	Strong transcription	Brain Germinal Matrix	brain
21	chr11:35285400-35287800	Strong transcription	Fetal Brain Female	brain
22	chr11:35285400-35288000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr11:35285800-35289800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr11:35285800-35308800	Weak transcription	Gastric	stomach
25	chr11:35286000-35287000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr11:35286000-35289600	Enhancers	Primary hematopoietic stem cells	blood
27	chr11:35286400-35287400	Enhancers	Pancreas	Pancrea
28	chr11:35286400-35293800	Weak transcription	Brain Anterior Caudate	brain
29	chr11:35286800-35287600	Strong transcription	Liver	Liver

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links