Variant report

Variant	rs1599383
Chromosome Location	chr3:160829820-160829821
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	chr3:160827858..160830677-chr3:160937623..160940393,2	K562	blood:

Variant related genes	Relation type
ENSG00000169251	Chromatin interaction

Extended variants
information (count: 59 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:55)

rs_ID	r²[population]
rs1026572	0.85[EUR][1000 genomes]
rs1037888	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs10936223	0.85[EUR][1000 genomes]
rs12493960	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12631850	0.85[EUR][1000 genomes]
rs13066683	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1599374	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1599376	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1599378	0.94[AFR][1000 genomes];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1599379	0.88[EUR][1000 genomes]
rs1599381	0.91[EUR][1000 genomes]
rs1599386	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1599389	0.91[EUR][1000 genomes]
rs1599390	0.91[EUR][1000 genomes]
rs1609688	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1610158	0.91[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2306061	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4342141	0.81[EUR][1000 genomes]
rs4414866	0.81[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs4557202	0.91[EUR][1000 genomes]
rs4616689	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs4618258	0.80[EUR][1000 genomes]
rs5004752	0.83[AMR][1000 genomes]
rs6441354	0.91[EUR][1000 genomes]
rs6765270	0.90[AFR][1000 genomes];0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6769642	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs6772578	0.83[AMR][1000 genomes]
rs6774635	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs6778254	0.82[EUR][1000 genomes]
rs6783085	0.91[EUR][1000 genomes]
rs6789244	0.91[EUR][1000 genomes]
rs6799130	0.90[EUR][1000 genomes]
rs7614375	0.81[AFR][1000 genomes];0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7617204	0.91[EUR][1000 genomes]
rs7619011	0.90[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7622047	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7625363	0.89[EUR][1000 genomes]
rs7630674	0.88[AFR][1000 genomes];0.98[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7630768	0.91[EUR][1000 genomes]
rs7633857	0.91[EUR][1000 genomes]
rs7637086	0.91[EUR][1000 genomes]
rs7647285	0.90[EUR][1000 genomes]
rs7650703	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs7651087	0.91[EUR][1000 genomes]
rs898680	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs898681	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs9290065	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs9290069	0.82[EUR][1000 genomes]
rs980975	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs980976	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs9820825	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9847866	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs9848239	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs9860360	0.83[AMR][1000 genomes]
rs9867582	0.88[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv931072	chr3:160669567-161159779	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	98 gene(s)	inside rSNPs	diseases
2	nsv877704	chr3:160806859-160836006	Active TSS Strong transcription Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv877705	chr3:160818188-160836006	Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv877707	chr3:160820175-160836006	Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:160823200-160832800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr3:160823800-160830400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr3:160824200-160830800	Weak transcription	Ovary	ovary
4	chr3:160826800-160834400	Weak transcription	Left Ventricle	heart

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