Variant report

Variant	rs7632272
Chromosome Location	chr3:143354316-143354317
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs11712583	0.91[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs13089318	0.95[AFR][1000 genomes];0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1534161	0.98[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1978913	0.91[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2030817	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4425252	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6779887	0.90[AFR][1000 genomes];0.88[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6779888	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs9809563	0.94[AFR][1000 genomes]
rs9811274	0.92[AFR][1000 genomes]
rs9811842	0.95[AFR][1000 genomes];0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.81[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	nsv949288	chr3:142793323-143585882	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
2	nsv829745	chr3:143278512-143405626	Weak transcription Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:143328200-143376200	Weak transcription	Ovary	ovary
2	chr3:143339200-143355200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
3	chr3:143346400-143363200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr3:143346600-143355600	Weak transcription	Primary T cells from cord blood	blood
5	chr3:143348200-143355400	Weak transcription	Monocytes-CD14+_RO01746	blood
6	chr3:143351600-143369800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
7	chr3:143352000-143355600	Weak transcription	Primary T helper cells fromperipheralblood	blood
8	chr3:143352800-143354400	Enhancers	Duodenum Mucosa	Duodenum
9	chr3:143353200-143354400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr3:143353600-143354600	Enhancers	Rectal Mucosa Donor 29	rectum
11	chr3:143354000-143354600	Enhancers	Breast Myoepithelial Primary Cells	Breast
12	chr3:143354000-143354800	Weak transcription	Dnd41	blood
13	chr3:143354200-143354600	Enhancers	Duodenum Smooth Muscle	Duodenum
14	chr3:143354200-143373600	Weak transcription	Sigmoid Colon	Sigmoid Colon
15	chr3:143354200-143374000	Weak transcription	Esophagus	oesophagus

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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