Variant report

Variant	rs3774548
Chromosome Location	chr3:53751064-53751065
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:53740542..53743254-chr3:53751040..53753856,2	MCF-7	breast:
2	chr3:53749411..53751208-chr3:54008710..54010882,2	K562	blood:

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs1020822	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11130380	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2248381	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2306866	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2633723	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2633726	0.84[EUR][1000 genomes]
rs898423	0.83[AMR][1000 genomes];0.91[EUR][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	nsv1003621	chr3:53448934-54425322	Active TSS Strong transcription Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
2	nsv1001128	chr3:53659570-53927842	Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
3	nsv1013783	chr3:53694418-53934781	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
4	nsv1007655	chr3:53742148-53767689	Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
5	nsv1002452	chr3:53742148-53802811	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
6	nsv1000280	chr3:53742736-53770588	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:34 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:53740200-53764400	Weak transcription	Brain Cingulate Gyrus	brain
2	chr3:53741200-53751400	Weak transcription	Fetal Brain Female	brain
3	chr3:53742600-53778000	Weak transcription	Pancreas	Pancrea
4	chr3:53744200-53753800	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr3:53744200-53764600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr3:53744400-53756600	Weak transcription	Lung	lung
7	chr3:53744400-53758600	Weak transcription	Stomach Smooth Muscle	stomach
8	chr3:53744400-53763800	Weak transcription	Rectal Mucosa Donor 29	rectum
9	chr3:53744600-53755000	Weak transcription	Brain Anterior Caudate	brain
10	chr3:53744600-53755000	Weak transcription	Brain Inferior Temporal Lobe	brain
11	chr3:53744600-53756400	Weak transcription	Liver	Liver
12	chr3:53744600-53761200	Weak transcription	Duodenum Mucosa	Duodenum
13	chr3:53745000-53753800	Strong transcription	Fetal Intestine Small	intestine
14	chr3:53745200-53762800	Strong transcription	Fetal Intestine Large	intestine
15	chr3:53748400-53752800	Weak transcription	Spleen	Spleen
16	chr3:53748600-53756200	Weak transcription	Fetal Brain Male	brain
17	chr3:53749200-53751200	Enhancers	NH-A	brain
18	chr3:53749200-53752400	Strong transcription	Fetal Lung	lung
19	chr3:53750000-53755200	Weak transcription	Left Ventricle	heart
20	chr3:53750400-53752400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
21	chr3:53750400-53755000	Weak transcription	NHDF-Ad	bronchial
22	chr3:53750400-53755200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr3:53750400-53755200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr3:53750600-53753400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr3:53750600-53755000	Weak transcription	Osteobl	bone
26	chr3:53750800-53751400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr3:53750800-53751600	Enhancers	Primary monocytes fromperipheralblood	blood
28	chr3:53750800-53751600	Enhancers	Primary neutrophils fromperipheralblood	blood
29	chr3:53750800-53751600	Enhancers	Primary hematopoietic stem cells short term culture	blood
30	chr3:53750800-53751600	Enhancers	Monocytes-CD14+_RO01746	blood
31	chr3:53750800-53752400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
32	chr3:53751000-53751400	Enhancers	Primary B cells from peripheral blood	blood
33	chr3:53751000-53751400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
34	chr3:53751000-53752000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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