Variant report

Variant	rs56711752
Chromosome Location	chr3:139393365-139393366
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:139392662..139394391-chr3:139394909..139396842,2	K562	blood:

Variant related genes	Relation type
ENSG00000163864	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs10935341	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12186041	0.99[ASN][1000 genomes]
rs12632145	0.90[ASN][1000 genomes]
rs12634170	0.99[ASN][1000 genomes]
rs13074121	0.83[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16849303	0.91[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16849305	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16849307	0.88[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16849309	0.90[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs35449667	0.99[ASN][1000 genomes]
rs35657101	0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3922940	0.81[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4474999	0.83[ASN][1000 genomes]
rs4518082	0.99[ASN][1000 genomes]
rs4535184	0.99[ASN][1000 genomes]
rs4549242	0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4615039	0.99[ASN][1000 genomes]
rs57304307	0.99[ASN][1000 genomes]
rs59476496	0.93[ASN][1000 genomes]
rs62270189	0.90[ASN][1000 genomes]
rs62270193	0.90[ASN][1000 genomes]
rs62273120	0.96[ASN][1000 genomes]
rs62273121	0.96[ASN][1000 genomes]
rs62273122	0.93[ASN][1000 genomes]
rs6808215	0.89[AFR][1000 genomes];0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs71627866	0.86[ASN][1000 genomes]
rs7617537	0.89[AFR][1000 genomes];0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7636269	0.86[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs7651551	0.89[AFR][1000 genomes];0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9289581	0.99[ASN][1000 genomes]
rs9810042	0.90[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9810049	0.90[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9815708	0.90[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9833539	0.90[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9836944	0.86[ASN][1000 genomes]
rs9848375	0.90[AFR][1000 genomes];0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9865942	0.99[ASN][1000 genomes]
rs9871543	0.90[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9878498	0.99[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	nsv1003154	chr3:139060841-139788752	ZNF genes & repeats Flanking Active TSS Strong transcription Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
2	nsv536729	chr3:139060841-139788752	Active TSS Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
3	nsv916193	chr3:139187767-139821526	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
4	nsv530058	chr3:139243971-139814419	Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:36 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:139369800-139395200	Weak transcription	Primary hematopoietic stem cells	blood
2	chr3:139374200-139394000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr3:139374200-139395600	Weak transcription	Gastric	stomach
4	chr3:139374400-139394600	Weak transcription	Pancreas	Pancrea
5	chr3:139374400-139394800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr3:139375200-139393800	Weak transcription	Ovary	ovary
7	chr3:139375400-139394400	Weak transcription	Brain Anterior Caudate	brain
8	chr3:139375400-139395600	Weak transcription	Pancreatic Islets	Pancreatic Islet
9	chr3:139375600-139395800	Weak transcription	Adipose Nuclei	Adipose
10	chr3:139380400-139394800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr3:139383200-139395600	Weak transcription	Rectal Mucosa Donor 29	rectum
12	chr3:139384000-139394400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
13	chr3:139384400-139396000	Weak transcription	Left Ventricle	heart
14	chr3:139388800-139396000	Weak transcription	Lung	lung
15	chr3:139389000-139395800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
16	chr3:139389800-139394600	Weak transcription	Skeletal Muscle Male	skeletal muscle
17	chr3:139390200-139395000	Weak transcription	Duodenum Mucosa	Duodenum
18	chr3:139390400-139395400	Enhancers	Brain Germinal Matrix	brain
19	chr3:139391800-139393400	Strong transcription	Fetal Intestine Small	intestine
20	chr3:139391800-139394000	Weak transcription	Brain Angular Gyrus	brain
21	chr3:139392000-139395400	Weak transcription	Skeletal Muscle Female	skeletal muscle
22	chr3:139392000-139395800	Weak transcription	Brain Hippocampus Middle	brain
23	chr3:139392000-139395800	Weak transcription	Brain Substantia Nigra	brain
24	chr3:139392200-139394000	Weak transcription	H9 Cell Line	embryonic stem cell
25	chr3:139392200-139394800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr3:139392400-139395200	Weak transcription	Stomach Smooth Muscle	stomach
27	chr3:139392600-139395800	Weak transcription	Brain Cingulate Gyrus	brain
28	chr3:139392800-139393600	Weak transcription	Fetal Brain Female	brain
29	chr3:139392800-139393800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr3:139393000-139393400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr3:139393000-139394200	Weak transcription	Fetal Muscle Leg	muscle
32	chr3:139393000-139394800	Enhancers	ES-I3 Cell Line	embryonic stem cell
33	chr3:139393000-139395600	Weak transcription	Primary T cells from cord blood	blood
34	chr3:139393000-139395800	Weak transcription	Psoas Muscle	Psoas
35	chr3:139393200-139394000	Weak transcription	Brain Inferior Temporal Lobe	brain
36	chr3:139393200-139394600	Enhancers	Fetal Brain Male	brain

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