Variant report

Variant	rs73825165
Chromosome Location	chr3:28489204-28489205
allele	C/G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:28388988..28390557-chr3:28488307..28491237,2	K562	blood:

Variant related genes	Relation type
ENSG00000163512	Chromatin interaction

Extended variants
information (count: 56 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs10510608	1.00[EUR][1000 genomes]
rs11914283	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11914462	1.00[EUR][1000 genomes]
rs11914828	1.00[EUR][1000 genomes]
rs11917441	1.00[EUR][1000 genomes]
rs11918676	1.00[EUR][1000 genomes]
rs11921493	1.00[EUR][1000 genomes]
rs11924235	1.00[EUR][1000 genomes]
rs17021276	1.00[EUR][1000 genomes]
rs17021326	1.00[EUR][1000 genomes]
rs1955313	1.00[EUR][1000 genomes]
rs34490679	1.00[EUR][1000 genomes]
rs4605504	1.00[EUR][1000 genomes]
rs55859737	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56316071	1.00[EUR][1000 genomes]
rs56854865	0.80[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57260178	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58228744	1.00[AMR][1000 genomes]
rs59014991	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59574091	1.00[EUR][1000 genomes]
rs60199196	1.00[EUR][1000 genomes]
rs60457049	1.00[EUR][1000 genomes]
rs60812941	1.00[EUR][1000 genomes]
rs61107194	1.00[EUR][1000 genomes]
rs73822329	1.00[EUR][1000 genomes]
rs73822336	1.00[EUR][1000 genomes]
rs73822577	1.00[EUR][1000 genomes]
rs73822578	1.00[EUR][1000 genomes]
rs73822640	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73822641	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73822642	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73822643	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73825127	1.00[EUR][1000 genomes]
rs73825128	1.00[EUR][1000 genomes]
rs73825130	1.00[EUR][1000 genomes]
rs73825142	1.00[EUR][1000 genomes]
rs73825144	1.00[EUR][1000 genomes]
rs73825146	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73825147	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73825148	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73825149	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73825152	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73825156	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73825163	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73825167	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7638742	0.83[AMR][1000 genomes]
rs7642252	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7642709	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9682725	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3328565	chr3:27991169-28915035	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
2	nsv876649	chr3:28126595-28718454	Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
3	nsv876650	chr3:28427029-28613602	Enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv1015015	chr3:28461972-28728494	Bivalent/Poised TSS Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	nsv916364	chr3:28468275-29146280	Enhancers Bivalent Enhancer Weak transcription ZNF genes & repeats Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
6	nsv590010	chr3:28469830-28727214	Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
7	nsv979813	chr3:28478897-28489553	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	2 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	chr3:28473200-28492400	Weak transcription	Gastric	stomach
2	chr3:28479800-28509000	Weak transcription	Left Ventricle	heart
3	chr3:28483600-28497000	Weak transcription	Brain Substantia Nigra	brain
4	chr3:28483800-28497600	Weak transcription	Ovary	ovary

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