Variant report

Variant	rs35577995
Chromosome Location	chr8:130656284-130656285
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs10099422	0.92[ASN][1000 genomes]
rs10101101	0.82[EUR][1000 genomes]
rs12707937	0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs13256760	0.84[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs13263733	0.84[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs13264700	0.84[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs13265576	0.84[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs13267039	0.82[ASN][1000 genomes]
rs13267746	0.84[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs13280368	0.81[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs34092021	0.94[ASN][1000 genomes]
rs34319381	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34390591	0.82[ASN][1000 genomes]
rs34716000	0.88[ASN][1000 genomes]
rs34865413	0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs35125576	0.82[ASN][1000 genomes]
rs35226520	0.88[ASN][1000 genomes]
rs35509786	0.92[ASN][1000 genomes]
rs35778967	0.91[ASN][1000 genomes]
rs4382437	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs56049814	0.82[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs59672682	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs60812642	0.89[ASN][1000 genomes]
rs62523768	0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs66910128	0.84[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs67986379	0.94[ASN][1000 genomes]
rs68077667	0.91[ASN][1000 genomes]
rs6998742	0.92[ASN][1000 genomes]
rs7004790	0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs72716385	0.91[ASN][1000 genomes]
rs7841674	0.83[ASN][1000 genomes]
rs9297796	0.91[ASN][1000 genomes]
rs9918807	0.92[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	nsv612230	chr8:130624121-130661901	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Genic enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
2	nsv891446	chr8:130656205-130710638	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:130654400-130656400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr8:130654800-130656400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr8:130655200-130656800	Enhancers	Fetal Muscle Leg	muscle
4	chr8:130656000-130657800	Enhancers	Fetal Lung	lung
5	chr8:130656200-130656800	Enhancers	Primary hematopoietic stem cells	blood
6	chr8:130656200-130657200	Enhancers	Osteobl	bone

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