Variant report

Variant	rs10821280
Chromosome Location	chr9:96764777-96764778
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:96727798..96728815-chr9:96764497..96765503,14	MCF-7	breast:
2	chr9:96581793..96583854-chr9:96762877..96764983,2	MCF-7	breast:
3	chr9:96444144..96445247-chr9:96764543..96765553,7	MCF-7	breast:
4	chr9:96759109..96762774-chr9:96763478..96766072,3	MCF-7	breast:
5	chr9:96763518..96767786-chr9:96791932..96794541,3	MCF-7	breast:
6	chr9:96761819..96764816-chr9:96950228..96952225,2	K562	blood:
7	chr9:96444182..96444858-chr9:96764335..96765029,3	K562	blood:
8	chr9:96762892..96765043-chr9:96770336..96774570,3	MCF-7	breast:
9	chr9:96727876..96728832-chr9:96764494..96765342,5	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000158079	Chromatin interaction

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs10114421	0.80[EUR][1000 genomes]
rs10114811	0.82[EUR][1000 genomes]
rs10116489	0.82[EUR][1000 genomes]
rs10116746	0.80[EUR][1000 genomes]
rs10122071	0.82[EUR][1000 genomes]
rs10761311	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10761312	0.88[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs10761314	0.82[EUR][1000 genomes]
rs10821277	0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10821278	0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10821281	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10821283	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10821289	0.80[EUR][1000 genomes]
rs10993009	0.84[EUR][1000 genomes]
rs10993028	0.83[EUR][1000 genomes]
rs10993032	0.82[EUR][1000 genomes]
rs10993035	0.80[EUR][1000 genomes]
rs10993039	0.80[EUR][1000 genomes]
rs10993044	0.82[EUR][1000 genomes]
rs11795301	0.84[EUR][1000 genomes]
rs12338762	0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12340234	0.82[EUR][1000 genomes]
rs1316934	0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1592152	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1854836	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1963282	0.82[EUR][1000 genomes]
rs2094929	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2153061	0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2211361	0.82[EUR][1000 genomes]
rs2225937	0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4743942	0.80[EUR][1000 genomes]
rs4744306	0.91[AFR][1000 genomes]
rs57094654	0.84[EUR][1000 genomes]
rs7020044	0.82[EUR][1000 genomes]
rs7045483	0.80[EUR][1000 genomes]
rs7866395	0.84[EUR][1000 genomes]
rs7868385	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv893589	chr9:96624645-96884544	Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:96759000-96767800	Weak transcription	Pancreas	Pancrea
2	chr9:96760200-96766000	Weak transcription	Stomach Mucosa	stomach
3	chr9:96762600-96768000	Weak transcription	Fetal Intestine Large	intestine
4	chr9:96763400-96767200	Weak transcription	Gastric	stomach
5	chr9:96764200-96765000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr9:96764200-96765000	Enhancers	Stomach Smooth Muscle	stomach
7	chr9:96764200-96765000	Enhancers	Osteobl	bone
8	chr9:96764400-96774200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr9:96764600-96765000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr9:96764600-96765000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr9:96764600-96765000	Enhancers	Fetal Stomach	stomach

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