Variant report

Variant	rs332791
Chromosome Location	chr1:174678922-174678923
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 67 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:63)

rs_ID	r²[population]
rs1016466	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10753086	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10912797	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10912804	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10912807	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10912813	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11804541	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11804941	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12060177	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12074753	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12088073	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12094143	0.80[ASN][1000 genomes]
rs1653626	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1653627	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1653632	0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1754349	0.83[EUR][1000 genomes]
rs1754351	0.81[AFR][1000 genomes];0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1754355	0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1793297	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1793300	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1793308	0.92[ASN][1000 genomes]
rs1793309	0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2072760	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2142633	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2187562	0.85[EUR][1000 genomes]
rs2981894	0.85[EUR][1000 genomes]
rs2987869	0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2987874	0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs3018410	0.83[EUR][1000 genomes]
rs3118980	0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs3133270	0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs332765	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs332770	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs332771	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs332773	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs332789	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs332795	0.81[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs332805	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs34819375	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4233195	0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs444678	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs461910	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs56199565	0.81[AMR][1000 genomes]
rs56347239	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6425282	0.81[AMR][1000 genomes]
rs6425283	0.81[AMR][1000 genomes]
rs6425287	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6664864	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6668053	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6671824	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6672148	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6683602	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6689170	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6696197	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs67967476	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs727279	0.81[AMR][1000 genomes]
rs7542389	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7545910	0.81[EUR][1000 genomes]
rs7555533	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9425784	0.89[ASN][1000 genomes]
rs9628627	0.90[ASN][1000 genomes]
rs9700904	0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs989423	0.85[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	nsv1014637	chr1:174265631-174826765	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv535208	chr1:174265631-174826765	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
3	nsv1014753	chr1:174271770-174694838	Weak transcription Strong transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	esv2755184	chr1:174388343-174970343	Flanking Active TSS Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	54 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:23 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:174646800-174680400	Weak transcription	Ovary	ovary
2	chr1:174665800-174680000	Weak transcription	Fetal Intestine Large	intestine
3	chr1:174665800-174682600	Weak transcription	Left Ventricle	heart
4	chr1:174668400-174682600	Weak transcription	Gastric	stomach
5	chr1:174669600-174684000	Weak transcription	Primary T helper cells PMA-I stimulated	--
6	chr1:174672600-174682600	Weak transcription	Right Ventricle	heart
7	chr1:174673000-174679400	Weak transcription	GM12878-XiMat	blood
8	chr1:174674800-174679000	Weak transcription	Thymus	Thymus
9	chr1:174677400-174679000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr1:174677600-174679000	ZNF genes & repeats	Primary hematopoietic stem cells	blood
11	chr1:174677800-174679200	Strong transcription	Primary B cells from cord blood	blood
12	chr1:174677800-174680000	Weak transcription	Duodenum Mucosa	Duodenum
13	chr1:174678200-174689000	Weak transcription	Primary T helper cells fromperipheralblood	blood
14	chr1:174678200-174689200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
15	chr1:174678200-174708600	Weak transcription	Primary T cells from cord blood	blood
16	chr1:174678600-174680000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr1:174678600-174680200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr1:174678600-174682600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
19	chr1:174678600-174684400	Weak transcription	Rectal Smooth Muscle	rectum
20	chr1:174678600-174706400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
21	chr1:174678800-174680000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr1:174678800-174680000	Weak transcription	Fetal Intestine Small	intestine
23	chr1:174678800-174681400	Weak transcription	Primary B cells from peripheral blood	blood

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