Variant report

Variant	rs10919250
Chromosome Location	chr1:169784563-169784564
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs10489172	0.89[YRI][hapmap];0.94[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1062976	0.89[YRI][hapmap];0.94[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10800468	1.00[ASN][1000 genomes]
rs10919246	0.81[EUR][1000 genomes]
rs10919252	0.89[YRI][hapmap];0.96[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs10919255	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10919256	0.96[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs10919258	0.90[AFR][1000 genomes]
rs10919259	0.90[AFR][1000 genomes]
rs10919267	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1131498	1.00[ASN][1000 genomes]
rs11576078	0.89[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11589247	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12064636	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12084893	1.00[ASN][1000 genomes]
rs12089057	0.81[AFR][1000 genomes];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12405525	0.96[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs12410352	0.94[AFR][1000 genomes];0.82[AMR][1000 genomes]
rs12742961	0.94[AFR][1000 genomes];0.82[AMR][1000 genomes]
rs12760399	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16862745	0.89[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17525350	1.00[ASN][1000 genomes]
rs17529513	0.98[AFR][1000 genomes];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17603022	0.88[YRI][hapmap];0.94[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2205846	0.88[AFR][1000 genomes];0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs2272918	0.96[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs35296671	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs4987280	1.00[ASN][1000 genomes]
rs6678351	0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6694855	0.86[AFR][1000 genomes];0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67274208	0.94[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs73026213	0.86[AFR][1000 genomes];0.90[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73026223	0.80[AMR][1000 genomes]
rs73026243	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73026245	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3451367	chr1:169630075-169976964	Strong transcription Flanking Active TSS Genic enhancers Enhancers Weak transcription Active TSS ZNF genes & repeats 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 target site	37 gene(s)	inside rSNPs	diseases
2	esv1814601	chr1:169782006-169885186	Weak transcription Active TSS Flanking Active TSS Enhancers Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
3	esv1821503	chr1:169782006-169885186	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
4	esv1847722	chr1:169782006-169885186	Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
5	esv2757760	chr1:169782006-169885186	Strong transcription Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
6	esv2758976	chr1:169782006-169885186	Strong transcription Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Enhancers Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
7	nsv428268	chr1:169782006-169885186	Strong transcription ZNF genes & repeats Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
8	esv1845220	chr1:169782006-169933886	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:110 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:169764800-169793200	Weak transcription	Aorta	Aorta
2	chr1:169764800-169793200	Weak transcription	Brain Hippocampus Middle	brain
3	chr1:169764800-169793400	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr1:169764800-169795200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
5	chr1:169764800-169796200	Weak transcription	Spleen	Spleen
6	chr1:169764800-169818200	Weak transcription	Esophagus	oesophagus
7	chr1:169764800-169818200	Weak transcription	Lung	lung
8	chr1:169764800-169823600	Weak transcription	Gastric	stomach
9	chr1:169765000-169786000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
10	chr1:169765000-169793200	Weak transcription	Fetal Brain Male	brain
11	chr1:169765000-169808000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr1:169765000-169821800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
13	chr1:169765200-169793200	Weak transcription	H9 Cell Line	embryonic stem cell
14	chr1:169765200-169793200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr1:169765200-169793400	Weak transcription	Fetal Kidney	kidney
16	chr1:169765200-169797400	Weak transcription	HSMMtube	muscle
17	chr1:169765200-169802000	Weak transcription	Skeletal Muscle Male	skeletal muscle
18	chr1:169765200-169807800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr1:169765200-169808000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr1:169765200-169809000	Weak transcription	Primary T helper cells fromperipheralblood	blood
21	chr1:169765200-169814800	Weak transcription	Brain Anterior Caudate	brain
22	chr1:169765200-169815200	Weak transcription	Rectal Smooth Muscle	rectum
23	chr1:169765200-169818800	Weak transcription	Brain Angular Gyrus	brain
24	chr1:169765200-169820600	Weak transcription	Psoas Muscle	Psoas
25	chr1:169765200-169823400	Weak transcription	Right Ventricle	heart
26	chr1:169765400-169788200	Weak transcription	Placenta Amnion	Placenta Amnion
27	chr1:169765400-169796800	Weak transcription	Colon Smooth Muscle	Colon
28	chr1:169765400-169798400	Weak transcription	Brain Germinal Matrix	brain
29	chr1:169765400-169798400	Weak transcription	Rectal Mucosa Donor 31	rectum
30	chr1:169765400-169808000	Weak transcription	Fetal Heart	heart
31	chr1:169765400-169822600	Weak transcription	Colonic Mucosa	Colon
32	chr1:169765600-169808000	Weak transcription	Small Intestine	intestine
33	chr1:169765600-169818200	Weak transcription	NHLF	lung
34	chr1:169765800-169793200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
35	chr1:169765800-169808000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr1:169765800-169815200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
37	chr1:169765800-169818400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
38	chr1:169766000-169796800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr1:169766000-169797000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr1:169766000-169797400	Weak transcription	Muscle Satellite Cultured Cells	--
41	chr1:169769400-169785800	Strong transcription	HUES64 Cell Line	embryonic stem cell
42	chr1:169770400-169785000	Strong transcription	Dnd41	blood
43	chr1:169771200-169785800	Strong transcription	Fetal Thymus	thymus
44	chr1:169771800-169784600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr1:169772400-169784600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
46	chr1:169773400-169796200	Weak transcription	HMEC	breast
47	chr1:169773400-169798400	Weak transcription	Primary B cells from peripheral blood	blood
48	chr1:169773400-169808000	Weak transcription	Primary T helper cells PMA-I stimulated	--
49	chr1:169773800-169796200	Weak transcription	NH-A	brain
50	chr1:169773800-169796200	Weak transcription	Osteobl	bone

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