Variant report

Variant	rs34263105
Chromosome Location	chr1:227459063-227459064
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:227457997..227462821-chr1:227486670..227490328,4	K562	blood:

Extended variants
information (count: 94 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:89)

rs_ID	r²[population]
rs1015815	0.96[EUR][1000 genomes]
rs1015816	0.94[EUR][1000 genomes]
rs10495258	0.86[AMR][1000 genomes]
rs10916109	0.95[EUR][1000 genomes]
rs10916114	0.98[EUR][1000 genomes]
rs11801994	0.94[EUR][1000 genomes]
rs11803590	0.94[EUR][1000 genomes]
rs11803761	0.90[EUR][1000 genomes]
rs11805298	0.90[EUR][1000 genomes]
rs11806511	0.94[EUR][1000 genomes]
rs11806937	0.90[EUR][1000 genomes]
rs11808928	0.94[EUR][1000 genomes]
rs11810328	0.98[EUR][1000 genomes]
rs11811358	0.96[EUR][1000 genomes]
rs12401556	0.83[AMR][1000 genomes]
rs12402456	0.94[EUR][1000 genomes]
rs12403650	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12403833	0.86[AMR][1000 genomes]
rs12403986	0.94[EUR][1000 genomes]
rs12404627	0.86[AMR][1000 genomes]
rs12405363	0.95[EUR][1000 genomes]
rs12407061	0.86[AMR][1000 genomes]
rs12408913	0.80[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12410327	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12741049	0.89[EUR][1000 genomes]
rs1464076	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1464077	0.98[EUR][1000 genomes]
rs1513602	0.94[EUR][1000 genomes]
rs1513603	0.90[EUR][1000 genomes]
rs1546557	0.98[EUR][1000 genomes]
rs1606549	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs16847492	0.95[EUR][1000 genomes]
rs16847634	0.95[EUR][1000 genomes]
rs17605533	0.86[AMR][1000 genomes]
rs17613166	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs34400564	0.90[EUR][1000 genomes]
rs41270149	0.94[EUR][1000 genomes]
rs4255349	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs4282782	0.98[EUR][1000 genomes]
rs4300186	0.95[EUR][1000 genomes]
rs4354510	0.95[EUR][1000 genomes]
rs4434814	0.98[EUR][1000 genomes]
rs4437846	0.96[EUR][1000 genomes]
rs4518864	0.98[EUR][1000 genomes]
rs4543764	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4551563	0.86[AMR][1000 genomes]
rs55805110	0.98[EUR][1000 genomes]
rs55882852	0.94[EUR][1000 genomes]
rs55946024	0.96[EUR][1000 genomes]
rs57276421	0.94[EUR][1000 genomes]
rs57758974	0.98[EUR][1000 genomes]
rs58489467	0.95[EUR][1000 genomes]
rs59116340	0.90[EUR][1000 genomes]
rs59121440	0.98[EUR][1000 genomes]
rs59859849	0.94[EUR][1000 genomes]
rs60068245	0.98[EUR][1000 genomes]
rs60235610	0.94[EUR][1000 genomes]
rs60742095	0.96[EUR][1000 genomes]
rs60958272	0.95[EUR][1000 genomes]
rs61081394	0.98[EUR][1000 genomes]
rs61522132	0.90[EUR][1000 genomes]
rs6659506	0.98[EUR][1000 genomes]
rs6668367	0.80[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs73088658	0.90[EUR][1000 genomes]
rs73090612	0.90[EUR][1000 genomes]
rs73094351	0.92[EUR][1000 genomes]
rs73094393	0.94[EUR][1000 genomes]
rs73094400	0.95[EUR][1000 genomes]
rs73096317	0.95[EUR][1000 genomes]
rs73096350	0.95[EUR][1000 genomes]
rs73096353	0.95[EUR][1000 genomes]
rs73096358	0.93[EUR][1000 genomes]
rs73096374	0.99[EUR][1000 genomes]
rs73098390	0.95[EUR][1000 genomes]
rs73098398	0.95[EUR][1000 genomes]
rs73102307	0.95[EUR][1000 genomes]
rs7413768	0.86[AMR][1000 genomes]
rs74140153	0.98[EUR][1000 genomes]
rs7515739	0.98[EUR][1000 genomes]
rs7519099	0.93[EUR][1000 genomes]
rs7526283	0.82[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs7534286	0.92[EUR][1000 genomes]
rs7535010	0.92[EUR][1000 genomes]
rs7539037	0.90[EUR][1000 genomes]
rs7539750	0.90[EUR][1000 genomes]
rs7542505	0.82[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs7544923	0.93[EUR][1000 genomes]
rs7545775	0.95[EUR][1000 genomes]
rs7551556	0.98[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1003656	chr1:227034700-227559665	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
2	nsv535318	chr1:227034700-227559665	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
3	nsv534002	chr1:227315186-228047108	Bivalent/Poised TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	54 gene(s)	inside rSNPs	diseases
4	nsv873242	chr1:227371906-227579344	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
5	nsv549271	chr1:227411003-227581017	Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	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	chr1:227414000-227459200	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr1:227431600-227486200	Weak transcription	NHDF-Ad	bronchial
3	chr1:227432000-227459200	Weak transcription	Fetal Lung	lung
4	chr1:227433000-227469000	Weak transcription	Aorta	Aorta
5	chr1:227434600-227468800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr1:227443400-227474000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr1:227447200-227473600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr1:227449600-227473600	Weak transcription	NH-A	brain
9	chr1:227449800-227465200	Weak transcription	K562	blood
10	chr1:227452800-227463800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr1:227453000-227468600	Weak transcription	Lung	lung
12	chr1:227454200-227470400	Weak transcription	Ovary	ovary
13	chr1:227456600-227459600	Enhancers	A549	lung
14	chr1:227456600-227468800	Weak transcription	Left Ventricle	heart
15	chr1:227457200-227459400	Weak transcription	Brain Anterior Caudate	brain
16	chr1:227457800-227459200	Weak transcription	Skeletal Muscle Male	skeletal muscle
17	chr1:227458400-227459200	Enhancers	Brain Cingulate Gyrus	brain
18	chr1:227458400-227459400	Enhancers	NHEK	skin
19	chr1:227458400-227459600	Enhancers	Brain Substantia Nigra	brain
20	chr1:227458600-227469400	Weak transcription	Duodenum Smooth Muscle	Duodenum
21	chr1:227458800-227472200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr1:227459000-227459400	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet

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