Variant report

Variant	rs645081
Chromosome Location	chr1:227306048-227306049
allele	C/T
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:32)

rs_ID	r²[population]
rs10458379	0.92[AFR][1000 genomes];0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10916098	0.94[AFR][1000 genomes];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12033050	0.83[AMR][1000 genomes]
rs12035190	0.83[AMR][1000 genomes]
rs12035998	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12080452	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12095674	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12097121	0.97[AFR][1000 genomes];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1929859	0.97[AFR][1000 genomes];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2104863	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2458523	0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2482453	1.00[ASN][1000 genomes]
rs4065211	0.83[AMR][1000 genomes]
rs4551562	0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4653477	0.82[ASN][1000 genomes]
rs4653788	0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4653790	0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs477373	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs482032	0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs533134	0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs567467	0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58442036	0.97[AFR][1000 genomes];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs595155	0.88[AFR][1000 genomes];0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs61700597	0.82[AMR][1000 genomes]
rs61834563	0.80[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs61834564	0.82[AFR][1000 genomes];0.87[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs61836477	0.97[AFR][1000 genomes];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6664803	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs688718	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72757311	0.83[AMR][1000 genomes]
rs7536444	0.97[AFR][1000 genomes];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs871210	0.97[AFR][1000 genomes];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 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	nsv1011654	chr1:227196502-227308416	Weak transcription Strong transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv832792	chr1:227211378-227364992	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv873239	chr1:227222125-227361072	Strong transcription Enhancers Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv468227	chr1:227223736-227340790	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv549269	chr1:227223736-227340790	Strong transcription Enhancers Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	nsv873240	chr1:227228946-227361072	Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
9	nsv873241	chr1:227242247-227361072	Strong transcription Weak transcription ZNF genes & repeats Enhancers Genic enhancers Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
10	nsv549270	chr1:227290139-227361072	Genic enhancers Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
11	esv2830098	chr1:227295716-227422234	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:83 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:227214800-227329200	Weak transcription	Right Ventricle	heart
2	chr1:227257800-227312200	Weak transcription	HUES6 Cell Line	embryonic stem cell
3	chr1:227259400-227349000	Weak transcription	Colonic Mucosa	Colon
4	chr1:227272800-227331000	Weak transcription	Lung	lung
5	chr1:227273000-227312400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr1:227282600-227318000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr1:227285600-227308600	Weak transcription	Pancreas	Pancrea
8	chr1:227285600-227313800	Weak transcription	Gastric	stomach
9	chr1:227286400-227328200	Weak transcription	Brain Germinal Matrix	brain
10	chr1:227287400-227360800	Weak transcription	Psoas Muscle	Psoas
11	chr1:227288000-227326400	Weak transcription	A549	lung
12	chr1:227288200-227332400	Weak transcription	Sigmoid Colon	Sigmoid Colon
13	chr1:227288400-227343000	Weak transcription	Rectal Smooth Muscle	rectum
14	chr1:227288400-227398000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
15	chr1:227288600-227310800	Weak transcription	Brain Inferior Temporal Lobe	brain
16	chr1:227288600-227312200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
17	chr1:227288600-227313000	Weak transcription	H1 Cell Line	embryonic stem cell
18	chr1:227288600-227316000	Weak transcription	Fetal Muscle Trunk	muscle
19	chr1:227288600-227328200	Weak transcription	Fetal Stomach	stomach
20	chr1:227288600-227332400	Weak transcription	NHLF	lung
21	chr1:227288600-227333600	Weak transcription	Esophagus	oesophagus
22	chr1:227288800-227317200	Weak transcription	NHEK	skin
23	chr1:227288800-227330000	Weak transcription	NHDF-Ad	bronchial
24	chr1:227289000-227312000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
25	chr1:227290200-227309800	Weak transcription	Fetal Intestine Small	intestine
26	chr1:227295200-227316000	Weak transcription	Fetal Kidney	kidney
27	chr1:227295200-227346400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr1:227295400-227310800	Weak transcription	Brain Angular Gyrus	brain
29	chr1:227295400-227313800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr1:227296000-227310600	Weak transcription	Small Intestine	intestine
31	chr1:227296400-227326200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr1:227296600-227316400	Weak transcription	HSMMtube	muscle
33	chr1:227296600-227326200	Weak transcription	Fetal Lung	lung
34	chr1:227298600-227351800	Weak transcription	Hela-S3	cervix
35	chr1:227299200-227318800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr1:227299800-227306600	Weak transcription	HUVEC	blood vessel
37	chr1:227299800-227313800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
38	chr1:227299800-227319600	Weak transcription	Fetal Intestine Large	intestine
39	chr1:227299800-227332600	Weak transcription	Skeletal Muscle Male	skeletal muscle
40	chr1:227300000-227310800	Weak transcription	Brain Cingulate Gyrus	brain
41	chr1:227300000-227310800	Weak transcription	Brain Hippocampus Middle	brain
42	chr1:227300000-227311800	Weak transcription	HUES64 Cell Line	embryonic stem cell
43	chr1:227300000-227312000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
44	chr1:227300000-227312600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr1:227300000-227315800	Weak transcription	Duodenum Smooth Muscle	Duodenum
46	chr1:227300000-227316200	Weak transcription	Rectal Mucosa Donor 31	rectum
47	chr1:227300000-227316400	Weak transcription	Osteobl	bone
48	chr1:227300000-227321800	Weak transcription	Colon Smooth Muscle	Colon
49	chr1:227300000-227325800	Weak transcription	Rectal Mucosa Donor 29	rectum
50	chr1:227300000-227326400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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