Variant report

Variant	rs57013196
Chromosome Location	chr6:45361874-45361875
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:45343263..45347310-chr6:45361550..45366697,4	K562	blood:
2	chr6:45344122..45347310-chr6:45361550..45366697,4	K562	blood:

Variant related genes	Relation type
ENSG00000196284	Chromatin interaction

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs1004130	0.80[ASN][1000 genomes]
rs10498760	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11498195	0.80[ASN][1000 genomes]
rs11963804	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11966462	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11966902	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11968177	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17209846	0.83[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17209853	0.83[ASN][1000 genomes]
rs17209874	0.80[ASN][1000 genomes]
rs17209881	0.80[ASN][1000 genomes]
rs17288355	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17288376	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17288397	0.80[ASN][1000 genomes]
rs1977152	0.83[ASN][1000 genomes]
rs3749864	0.80[ASN][1000 genomes]
rs3792952	0.80[ASN][1000 genomes]
rs3805811	0.80[ASN][1000 genomes]
rs3805818	0.80[ASN][1000 genomes]
rs3828722	0.80[ASN][1000 genomes]
rs3828723	0.80[ASN][1000 genomes]
rs4370348	0.80[ASN][1000 genomes]
rs4413613	0.80[ASN][1000 genomes]
rs4413614	0.80[ASN][1000 genomes]
rs56789892	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58571027	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59397804	0.80[ASN][1000 genomes]
rs61467394	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6921145	0.80[ASN][1000 genomes]
rs7768466	0.80[ASN][1000 genomes]
rs7768666	0.80[ASN][1000 genomes]
rs7771980	0.80[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	nsv1028393	chr6:44875558-45822335	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
2	nsv538211	chr6:44875558-45822335	ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	38 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:45356800-45382800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr6:45358400-45383000	Weak transcription	Osteobl	bone
3	chr6:45360600-45362600	Weak transcription	Right Atrium	heart
4	chr6:45361000-45363000	Enhancers	Placenta	Placenta
5	chr6:45361800-45363600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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