Variant report

Variant	rs7002378
Chromosome Location	chr8:10528550-10528551
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	chr8:10528112..10530692-chr8:10696880..10699073,2	K562	blood:
2	chr8:10527187..10529394-chr8:10534040..10536905,2	K562	blood:

Variant related genes	Relation type
ENSG00000258724	Chromatin interaction
ENSG00000253695	Chromatin interaction
ENSG00000254093	Chromatin interaction

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs10094968	0.93[ASN][1000 genomes]
rs10097577	0.93[ASN][1000 genomes]
rs10098956	0.86[ASN][1000 genomes]
rs10107820	0.93[ASN][1000 genomes]
rs10216539	0.93[ASN][1000 genomes]
rs11990311	0.93[ASN][1000 genomes]
rs12680711	0.80[ASN][1000 genomes]
rs13258730	1.00[EUR][1000 genomes]
rs28463918	0.93[ASN][1000 genomes]
rs28488675	0.87[ASN][1000 genomes]
rs28665435	0.93[ASN][1000 genomes]
rs34043696	0.93[ASN][1000 genomes]
rs35639780	0.86[ASN][1000 genomes]
rs59276210	0.86[ASN][1000 genomes]
rs59329830	0.86[ASN][1000 genomes]
rs60270701	0.80[ASN][1000 genomes]
rs60410697	0.80[ASN][1000 genomes]
rs60672851	0.86[ASN][1000 genomes]
rs6601505	0.86[ASN][1000 genomes]
rs6601507	0.86[ASN][1000 genomes]
rs6601508	0.86[ASN][1000 genomes]
rs6991320	0.93[ASN][1000 genomes]
rs7003456	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7006325	0.93[ASN][1000 genomes]
rs73530796	0.93[ASN][1000 genomes]
rs73532605	0.93[ASN][1000 genomes]
rs73532619	0.86[ASN][1000 genomes]
rs73532620	0.86[ASN][1000 genomes]
rs73532622	0.86[ASN][1000 genomes]
rs73536579	0.80[ASN][1000 genomes]
rs73541440	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73541442	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73541445	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73541496	0.87[ASN][1000 genomes]
rs7815184	0.93[ASN][1000 genomes]
rs7820334	0.80[ASN][1000 genomes]
rs7822666	0.80[ASN][1000 genomes]
rs7828426	0.93[ASN][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	nsv1030934	chr8:10065169-10561161	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
2	nsv1022994	chr8:10190618-10660122	Strong transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
3	nsv539466	chr8:10190618-10660122	Enhancers Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
4	nsv1025557	chr8:10216726-10555187	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
5	nsv917085	chr8:10237508-10828204	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
6	nsv1015932	chr8:10357101-10597856	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Bivalent/Poised TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
7	nsv1021048	chr8:10504395-10591896	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	18 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	chr8:10520800-10529000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr8:10524800-10529600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr8:10526400-10529000	Weak transcription	HUVEC	blood vessel
4	chr8:10526800-10537600	Weak transcription	Gastric	stomach
5	chr8:10528200-10530000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland

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