Variant report

Variant	rs12266386
Chromosome Location	chr10:96897796-96897797
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 105 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:101)

rs_ID	r²[population]
rs10128123	0.82[ASN][1000 genomes]
rs10218877	0.87[AFR][1000 genomes];0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10509682	0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10509683	0.82[ASN][1000 genomes]
rs10786186	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10786187	0.83[ASN][1000 genomes]
rs10786188	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10786189	0.83[ASN][1000 genomes]
rs10786190	0.83[ASN][1000 genomes]
rs10882542	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10882543	0.83[ASN][1000 genomes]
rs10882546	0.83[ASN][1000 genomes]
rs10882551	0.86[AFR][1000 genomes];0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10882562	0.90[AFR][1000 genomes];0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10882564	0.84[AFR][1000 genomes];0.91[AMR][1000 genomes];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10882565	0.84[AFR][1000 genomes];0.91[AMR][1000 genomes];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10882566	0.86[AFR][1000 genomes];0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10882568	0.82[ASN][1000 genomes]
rs11188189	0.83[ASN][1000 genomes]
rs11188190	0.83[ASN][1000 genomes]
rs11188192	0.83[ASN][1000 genomes]
rs11188196	0.83[ASN][1000 genomes]
rs11188197	0.83[ASN][1000 genomes]
rs11188200	0.83[ASN][1000 genomes]
rs11188214	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11188219	0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11188223	0.94[AMR][1000 genomes];0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11188225	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11188227	0.83[ASN][1000 genomes]
rs11188228	0.82[ASN][1000 genomes]
rs11188229	0.82[ASN][1000 genomes]
rs11599884	0.82[ASN][1000 genomes]
rs12245722	0.82[ASN][1000 genomes]
rs12261370	0.83[ASN][1000 genomes]
rs12262878	0.82[ASN][1000 genomes]
rs12354433	0.84[AFR][1000 genomes];0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12769820	0.82[ASN][1000 genomes]
rs12782731	0.83[ASN][1000 genomes]
rs1575930	0.83[ASN][1000 genomes]
rs16872	0.82[ASN][1000 genomes]
rs17451604	0.84[AFR][1000 genomes];0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs17524438	0.82[ASN][1000 genomes]
rs2449809	0.83[ASN][1000 genomes]
rs2449810	0.83[ASN][1000 genomes]
rs2478477	0.80[ASN][1000 genomes]
rs2478478	0.83[ASN][1000 genomes]
rs2478479	0.83[ASN][1000 genomes]
rs2901829	0.83[ASN][1000 genomes]
rs34999658	0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs35306243	0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs35999600	0.82[ASN][1000 genomes]
rs4532969	0.83[ASN][1000 genomes]
rs585381	0.83[ASN][1000 genomes]
rs591157	0.83[ASN][1000 genomes]
rs594402	0.83[ASN][1000 genomes]
rs604022	0.83[ASN][1000 genomes]
rs604373	0.83[ASN][1000 genomes]
rs610046	0.83[ASN][1000 genomes]
rs611416	0.83[ASN][1000 genomes]
rs613340	0.83[ASN][1000 genomes]
rs614682	0.83[ASN][1000 genomes]
rs620196	0.83[ASN][1000 genomes]
rs626415	0.83[ASN][1000 genomes]
rs632113	0.83[ASN][1000 genomes]
rs634269	0.83[ASN][1000 genomes]
rs637724	0.83[ASN][1000 genomes]
rs638895	0.83[ASN][1000 genomes]
rs641198	0.83[ASN][1000 genomes]
rs644437	0.83[ASN][1000 genomes]
rs646845	0.83[ASN][1000 genomes]
rs648638	0.83[ASN][1000 genomes]
rs6583980	0.83[ASN][1000 genomes]
rs663473	0.83[ASN][1000 genomes]
rs666679	0.83[ASN][1000 genomes]
rs666786	0.83[ASN][1000 genomes]
rs672428	0.83[ASN][1000 genomes]
rs672860	0.83[ASN][1000 genomes]
rs675332	0.83[ASN][1000 genomes]
rs678165	0.83[ASN][1000 genomes]
rs679025	0.83[ASN][1000 genomes]
rs680918	0.83[ASN][1000 genomes]
rs682477	0.83[ASN][1000 genomes]
rs7079861	0.83[ASN][1000 genomes]
rs7082502	0.83[ASN][1000 genomes]
rs7087492	0.83[ASN][1000 genomes]
rs7087618	0.83[ASN][1000 genomes]
rs7089303	0.80[ASN][1000 genomes]
rs7094658	0.83[ASN][1000 genomes]
rs752415	0.83[ASN][1000 genomes]
rs752416	0.83[ASN][1000 genomes]
rs752417	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7907627	0.83[ASN][1000 genomes]
rs7907827	0.83[ASN][1000 genomes]
rs7921561	0.83[ASN][1000 genomes]
rs815265	0.83[ASN][1000 genomes]
rs815266	0.83[ASN][1000 genomes]
rs815268	0.83[ASN][1000 genomes]
rs815269	0.83[ASN][1000 genomes]
rs815270	0.83[ASN][1000 genomes]
rs943313	0.83[ASN][1000 genomes]
rs943315	0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv497859	chr10:96058024-97027747	Strong transcription Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
2	nsv529726	chr10:96632494-97106315	Strong transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
3	esv21432	chr10:96856006-96996043	Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS Active TSS Bivalent Enhancer 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	nsv551985	chr10:96870565-96920198	ZNF genes & repeats Enhancers Weak transcription Strong transcription Active TSS Bivalent Enhancer Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:96890000-96897800	Weak transcription	Brain Angular Gyrus	brain
2	chr10:96890600-96904400	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr10:96891200-96902400	Weak transcription	Aorta	Aorta
4	chr10:96893000-96903800	Weak transcription	Pancreas	Pancrea
5	chr10:96893400-96900600	Weak transcription	Primary hematopoietic stem cells	blood
6	chr10:96893400-96901000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
7	chr10:96893600-96898400	Weak transcription	Liver	Liver
8	chr10:96894000-96906600	Weak transcription	Primary B cells from cord blood	blood
9	chr10:96895800-96902600	Weak transcription	Left Ventricle	heart
10	chr10:96896600-96899400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr10:96896600-96904400	Weak transcription	Fetal Intestine Large	intestine
12	chr10:96896800-96902400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
13	chr10:96896800-96902400	Weak transcription	Fetal Intestine Small	intestine
14	chr10:96897000-96899200	Enhancers	HepG2	liver

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