Variant report

Variant	rs73152013
Chromosome Location	chr3:99440781-99440782
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs10935921	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12107242	0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12486703	0.82[EUR][1000 genomes]
rs12494720	0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13080329	0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs13088056	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs13088851	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13099452	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1971381	0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs28820982	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs34218799	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs34303842	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs34906671	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35495890	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35577846	0.99[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4408901	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4928144	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4928219	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55648906	0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6440807	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7613580	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7614366	0.84[EUR][1000 genomes]
rs7632327	0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv877217	chr3:99418950-99496351	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:26 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:99428200-99442800	Weak transcription	Aorta	Aorta
2	chr3:99433600-99449200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr3:99438200-99442200	Enhancers	HUVEC	blood vessel
4	chr3:99438600-99442600	Enhancers	Muscle Satellite Cultured Cells	--
5	chr3:99439600-99440800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr3:99439800-99440800	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr3:99439800-99440800	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr3:99439800-99440800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr3:99439800-99441200	Enhancers	Fetal Lung	lung
10	chr3:99439800-99441400	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr3:99440000-99441000	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr3:99440200-99458000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr3:99440400-99440800	Enhancers	iPS-20b Cell Line	embryonic stem cell
14	chr3:99440400-99442800	Weak transcription	Adipose Nuclei	Adipose
15	chr3:99440400-99444600	Weak transcription	NHLF	lung
16	chr3:99440400-99448600	Weak transcription	HSMM	muscle
17	chr3:99440400-99450200	Weak transcription	HSMMtube	muscle
18	chr3:99440400-99458000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr3:99440400-99458200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr3:99440400-99471000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr3:99440600-99440800	Flanking Active TSS	NH-A	brain
22	chr3:99440600-99441000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr3:99440600-99441000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr3:99440600-99441200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr3:99440600-99441400	Weak transcription	Osteobl	bone
26	chr3:99440600-99449200	Weak transcription	NHDF-Ad	bronchial

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