Variant report

Variant	rs604674
Chromosome Location	chr10:44756894-44756895
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 70 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:68)

rs_ID	r²[population]
rs1159931	0.81[JPT][hapmap]
rs1632484	0.92[EUR][1000 genomes]
rs1657345	0.86[EUR][1000 genomes]
rs1746047	0.85[AFR][1000 genomes];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1746048	0.84[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1746049	0.81[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs1746050	0.81[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs1746052	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2209065	0.81[JPT][hapmap]
rs2576354	0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2576355	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2760670	0.95[ASN][1000 genomes]
rs2781543	0.83[ASN][1000 genomes]
rs473501	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs474281	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs475926	0.84[YRI][hapmap];0.85[AFR][1000 genomes]
rs479596	1.00[CEU][hapmap];0.86[YRI][hapmap];0.87[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs487465	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs492152	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs494207	0.95[ASN][1000 genomes]
rs498810	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs501120	0.84[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs504799	0.82[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs510785	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs513391	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs518594	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs522293	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs534079	0.83[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs535176	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs535949	0.83[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs541483	0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs546659	0.95[ASN][1000 genomes]
rs554565	0.84[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs559469	0.83[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs559580	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs573141	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs579058	0.84[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs583489	0.95[ASN][1000 genomes]
rs587375	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs605414	0.93[ASN][1000 genomes]
rs605445	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs605956	0.92[AFR][1000 genomes]
rs607363	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap];0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs607592	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs607609	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs607760	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs617035	0.94[ASN][1000 genomes]
rs617542	0.95[ASN][1000 genomes]
rs620356	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.87[YRI][hapmap];0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs620828	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.87[YRI][hapmap];0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs622472	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs622956	0.84[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs634963	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap];0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs635612	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs646890	0.95[ASN][1000 genomes]
rs649192	0.95[ASN][1000 genomes]
rs665855	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs670056	0.81[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs671765	0.83[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs683297	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs684196	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs684521	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs684666	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs687175	0.83[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs694425	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7082209	0.95[JPT][hapmap]
rs800330	0.95[JPT][hapmap]
rs915083	0.82[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[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:36 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:44749000-44757600	Enhancers	HepG2	liver
2	chr10:44753000-44757800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr10:44754600-44758400	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr10:44755200-44757000	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr10:44755200-44757800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr10:44755400-44757000	Weak transcription	Fetal Intestine Small	intestine
7	chr10:44755400-44757000	Weak transcription	Pancreas	Pancrea
8	chr10:44755400-44758200	Enhancers	Fetal Heart	heart
9	chr10:44755800-44757800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
10	chr10:44755800-44758400	Enhancers	Right Ventricle	heart
11	chr10:44756000-44757400	Bivalent Enhancer	Fetal Stomach	stomach
12	chr10:44756000-44758400	Enhancers	Spleen	Spleen
13	chr10:44756000-44759200	Enhancers	NHDF-Ad	bronchial
14	chr10:44756000-44761000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr10:44756200-44757800	Enhancers	Placenta	Placenta
16	chr10:44756200-44757800	Enhancers	Left Ventricle	heart
17	chr10:44756200-44760800	Enhancers	Rectal Smooth Muscle	rectum
18	chr10:44756400-44757000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
19	chr10:44756400-44757000	Enhancers	Stomach Smooth Muscle	stomach
20	chr10:44756400-44757200	Weak transcription	Lung	lung
21	chr10:44756400-44757800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
22	chr10:44756400-44758000	Enhancers	Fetal Muscle Leg	muscle
23	chr10:44756400-44760200	Enhancers	Colon Smooth Muscle	Colon
24	chr10:44756600-44757200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr10:44756600-44757600	Enhancers	Esophagus	oesophagus
26	chr10:44756600-44757800	Enhancers	Colonic Mucosa	Colon
27	chr10:44756600-44758000	Enhancers	Right Atrium	heart
28	chr10:44756600-44758200	Enhancers	Ovary	ovary
29	chr10:44756600-44759200	Enhancers	Skeletal Muscle Male	skeletal muscle
30	chr10:44756600-44760200	Enhancers	Adipose Nuclei	Adipose
31	chr10:44756800-44757000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr10:44756800-44757000	Enhancers	GM12878-XiMat	blood
33	chr10:44756800-44757400	Enhancers	Osteobl	bone
34	chr10:44756800-44757600	Enhancers	Duodenum Smooth Muscle	Duodenum
35	chr10:44756800-44757800	Enhancers	Skeletal Muscle Female	skeletal muscle
36	chr10:44756800-44759800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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