Variant report

Variant	rs17826952
Chromosome Location	chr14:66218871-66218872
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 75 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:69)

rs_ID	r²[population]
rs10130526	0.85[ASN][1000 genomes]
rs10143920	0.85[ASN][1000 genomes]
rs11847101	0.98[ASN][1000 genomes]
rs11849249	0.98[ASN][1000 genomes]
rs11849792	0.94[ASN][1000 genomes]
rs12431694	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs12431772	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12432032	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs12432326	1.00[AFR][1000 genomes]
rs12432422	0.98[ASN][1000 genomes]
rs12433273	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs12433830	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs12433947	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs12433950	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs12434375	1.00[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs12434465	1.00[EUR][1000 genomes]
rs12434626	0.85[ASN][1000 genomes]
rs12435769	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12435809	0.89[ASN][1000 genomes]
rs12435971	0.98[ASN][1000 genomes]
rs12436148	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs12436349	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs12436402	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs12436434	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs12436482	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs12436677	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs12436771	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12436975	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs12437088	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs17102839	0.89[ASN][1000 genomes]
rs17102854	0.96[ASN][1000 genomes]
rs17102894	0.98[ASN][1000 genomes]
rs17102898	0.98[ASN][1000 genomes]
rs17102910	0.83[ASN][1000 genomes]
rs17246385	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs17246441	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17246504	1.00[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs17246532	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17826892	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17826946	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1952605	1.00[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs2073295	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2268965	0.96[ASN][1000 genomes]
rs2295360	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2300863	0.94[ASN][1000 genomes]
rs2300866	0.94[ASN][1000 genomes]
rs2300870	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs28496380	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2898701	0.98[ASN][1000 genomes]
rs58087042	0.85[ASN][1000 genomes]
rs59036531	0.98[ASN][1000 genomes]
rs61417186	0.85[ASN][1000 genomes]
rs61987778	0.98[ASN][1000 genomes]
rs61987810	0.85[ASN][1000 genomes]
rs6573636	1.00[AFR][1000 genomes]
rs74056820	0.85[ASN][1000 genomes]
rs74056844	0.83[ASN][1000 genomes]
rs74056845	0.83[ASN][1000 genomes]
rs74056851	0.81[ASN][1000 genomes]
rs74056863	1.00[EUR][1000 genomes]
rs74058505	0.81[ASN][1000 genomes]
rs74058525	0.85[ASN][1000 genomes]
rs74058541	0.85[ASN][1000 genomes]
rs74058560	0.96[ASN][1000 genomes]
rs74058562	0.96[ASN][1000 genomes]
rs8004564	0.94[ASN][1000 genomes]
rs8008391	1.00[AFR][1000 genomes]
rs956582	0.96[ASN][1000 genomes]
rs997794	0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1043943	chr14:65782466-66698411	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	55 gene(s)	inside rSNPs	diseases
2	nsv542120	chr14:65782466-66698411	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	55 gene(s)	inside rSNPs	diseases
3	nsv1039168	chr14:65811750-66308343	Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	35 gene(s)	inside rSNPs	diseases
4	esv3366524	chr14:65924360-66423862	Weak transcription Enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	27 gene(s)	inside rSNPs	diseases
5	nsv1045000	chr14:66010886-66372518	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	nsv1042671	chr14:66010886-66399888	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:66201800-66219200	Weak transcription	Brain Anterior Caudate	brain
2	chr14:66209400-66219200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr14:66209600-66219000	Weak transcription	Thymus	Thymus
4	chr14:66209600-66219200	Weak transcription	Stomach Mucosa	stomach
5	chr14:66215600-66239800	Weak transcription	Primary T cells from cord blood	blood
6	chr14:66217400-66220200	Enhancers	Rectal Mucosa Donor 31	rectum
7	chr14:66217400-66221000	Enhancers	Fetal Intestine Small	intestine
8	chr14:66217800-66219600	Enhancers	HepG2	liver
9	chr14:66217800-66220400	Enhancers	Rectal Mucosa Donor 29	rectum
10	chr14:66218000-66219200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr14:66218000-66221000	Enhancers	Fetal Intestine Large	intestine
12	chr14:66218400-66219200	Weak transcription	Duodenum Mucosa	Duodenum
13	chr14:66218400-66219200	Weak transcription	Small Intestine	intestine
14	chr14:66218400-66220200	Weak transcription	Sigmoid Colon	Sigmoid Colon
15	chr14:66218600-66219000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr14:66218800-66219600	Enhancers	Colonic Mucosa	Colon

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