Variant report

Variant	rs73075888
Chromosome Location	chr3:56433449-56433450
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:56431485..56433512-chr3:56441532..56444158,2	MCF-7	breast:

Extended variants
information (count: 64 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:63)

rs_ID	r²[population]
rs1317750	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55968316	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56138618	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56216904	1.00[ASN][1000 genomes]
rs56227347	1.00[ASN][1000 genomes]
rs56286622	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56354761	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56383777	1.00[ASN][1000 genomes]
rs56988974	1.00[ASN][1000 genomes]
rs57708875	1.00[ASN][1000 genomes]
rs58067804	1.00[ASN][1000 genomes]
rs58449031	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58720638	1.00[ASN][1000 genomes]
rs59412382	1.00[ASN][1000 genomes]
rs59923603	1.00[ASN][1000 genomes]
rs60120946	1.00[ASN][1000 genomes]
rs60419369	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61092323	1.00[ASN][1000 genomes]
rs61163420	1.00[ASN][1000 genomes]
rs61248828	1.00[ASN][1000 genomes]
rs61524165	1.00[ASN][1000 genomes]
rs6802166	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73073904	0.90[AFR][1000 genomes];0.87[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73073905	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73073910	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73073974	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73073978	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73073985	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73073992	0.93[AFR][1000 genomes];0.87[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73075823	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73075825	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73075831	0.88[AFR][1000 genomes];0.87[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73075832	0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73075858	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73075865	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73075881	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73075891	1.00[ASN][1000 genomes]
rs73075902	1.00[ASN][1000 genomes]
rs73077703	1.00[ASN][1000 genomes]
rs73077704	1.00[ASN][1000 genomes]
rs73077719	1.00[ASN][1000 genomes]
rs73079872	1.00[ASN][1000 genomes]
rs73082476	1.00[ASN][1000 genomes]
rs73086422	1.00[ASN][1000 genomes]
rs73086435	1.00[ASN][1000 genomes]
rs73086436	1.00[ASN][1000 genomes]
rs73086437	1.00[ASN][1000 genomes]
rs73086439	1.00[ASN][1000 genomes]
rs73086440	1.00[ASN][1000 genomes]
rs73086441	1.00[ASN][1000 genomes]
rs73086449	1.00[ASN][1000 genomes]
rs73088517	1.00[ASN][1000 genomes]
rs73088520	1.00[ASN][1000 genomes]
rs73088522	1.00[ASN][1000 genomes]
rs73088532	1.00[ASN][1000 genomes]
rs73088534	1.00[ASN][1000 genomes]
rs73090547	0.81[AFR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73090555	0.88[AFR][1000 genomes];0.87[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73090565	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73090570	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73090572	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7615413	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs969242	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	nsv876816	chr3:56422771-56457705	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:56424000-56447400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr3:56433000-56433600	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr3:56433200-56433600	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr3:56433200-56433600	Enhancers	HUES6 Cell Line	embryonic stem cell
5	chr3:56433200-56434000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr3:56433200-56434000	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr3:56433200-56434200	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr3:56433200-56435000	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr3:56433400-56436400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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