Variant report

Variant	rs474281
Chromosome Location	chr10:44749120-44749121
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr10:44730852..44733719-chr10:44748011..44750876,2	MCF-7	breast:
2	chr10:44744429..44746085-chr10:44747966..44749573,2	K562	blood:
3	chr10:44731064..44733763-chr10:44747711..44749635,2	MCF-7	breast:

Extended variants
information (count: 64 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:62)

rs_ID	r²[population]
rs1632484	0.89[EUR][1000 genomes]
rs1657345	0.83[EUR][1000 genomes]
rs1746047	0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1746048	0.94[EUR][1000 genomes]
rs1746049	0.89[EUR][1000 genomes]
rs1746050	0.89[EUR][1000 genomes]
rs1746052	0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2576354	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2576355	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2760670	0.81[AFR][1000 genomes];0.81[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs2781543	0.88[ASN][1000 genomes]
rs473501	0.81[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs479596	0.89[EUR][1000 genomes]
rs487465	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs492152	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs494207	0.81[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs498810	0.81[AFR][1000 genomes];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs501120	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs504799	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs510785	0.81[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs513391	0.81[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs518594	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs522293	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs534079	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs535176	0.81[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs535949	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs541483	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs546659	0.81[AFR][1000 genomes];0.81[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs554565	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs559469	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs559580	0.81[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs573141	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs579058	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs583489	0.81[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs587375	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs604674	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs605414	0.98[ASN][1000 genomes]
rs605445	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs607363	0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs607592	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs607609	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs607760	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs617035	0.99[ASN][1000 genomes]
rs617542	0.81[AFR][1000 genomes];0.81[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs620356	0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs620828	0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs622472	0.81[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs622956	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs634963	0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs635612	0.81[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs646890	0.81[AFR][1000 genomes];0.81[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs649192	0.81[AFR][1000 genomes];0.81[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs665855	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs670056	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs671765	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs683297	0.81[AFR][1000 genomes];0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs684196	0.82[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs684521	0.93[AFR][1000 genomes];0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs684666	0.81[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs687175	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs694425	0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs915083	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1038511	chr10:44596885-44870030	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	nsv508579	chr10:44709770-44799256	Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:31 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:44745600-44749200	Weak transcription	Left Ventricle	heart
2	chr10:44748800-44750000	Enhancers	Fetal Heart	heart
3	chr10:44749000-44749400	Enhancers	Fetal Intestine Small	intestine
4	chr10:44749000-44749400	Enhancers	Placenta	Placenta
5	chr10:44749000-44749400	Enhancers	Lung	lung
6	chr10:44749000-44749400	Enhancers	Pancreas	Pancrea
7	chr10:44749000-44749400	Enhancers	Right Ventricle	heart
8	chr10:44749000-44749400	Enhancers	NHLF	lung
9	chr10:44749000-44749600	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr10:44749000-44749600	Enhancers	Fetal Intestine Large	intestine
11	chr10:44749000-44749600	Enhancers	Fetal Muscle Leg	muscle
12	chr10:44749000-44749600	Enhancers	Gastric	stomach
13	chr10:44749000-44749600	Enhancers	Stomach Smooth Muscle	stomach
14	chr10:44749000-44749800	Enhancers	Adipose Nuclei	Adipose
15	chr10:44749000-44749800	Enhancers	Ovary	ovary
16	chr10:44749000-44749800	Enhancers	Rectal Smooth Muscle	rectum
17	chr10:44749000-44749800	Enhancers	Skeletal Muscle Male	skeletal muscle
18	chr10:44749000-44749800	Enhancers	Skeletal Muscle Female	skeletal muscle
19	chr10:44749000-44750000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr10:44749000-44750000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr10:44749000-44750000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr10:44749000-44750000	Enhancers	Liver	Liver
23	chr10:44749000-44750000	Enhancers	Colon Smooth Muscle	Colon
24	chr10:44749000-44750000	Enhancers	Fetal Stomach	stomach
25	chr10:44749000-44750000	Enhancers	HSMM	muscle
26	chr10:44749000-44750000	Enhancers	HSMMtube	muscle
27	chr10:44749000-44750000	Enhancers	Osteobl	bone
28	chr10:44749000-44750200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr10:44749000-44750200	Enhancers	Fetal Lung	lung
30	chr10:44749000-44750200	Enhancers	NHDF-Ad	bronchial
31	chr10:44749000-44757600	Enhancers	HepG2	liver

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