Variant report

Variant	rs972957
Chromosome Location	chr2:172986576-172986577
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	chr2:172561285..172564164-chr2:172986386..172988674,2	K562	blood:
2	chr2:172737244..172739400-chr2:172984997..172987788,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000077380	Chromatin interaction

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs10930516	0.88[EUR][1000 genomes]
rs11675271	0.90[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs11675320	0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11675761	0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11681688	0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11890561	0.88[EUR][1000 genomes]
rs1319695	0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1386354	0.88[EUR][1000 genomes]
rs16860015	0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2357316	0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2357317	0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4972429	0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6433332	0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6708019	0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6724614	0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6735574	0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6748154	0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6748291	0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs73020553	0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs73022510	0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs73022564	0.88[EUR][1000 genomes]
rs7566889	0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7569224	1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7583008	0.80[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7590382	0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7590626	0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7590815	0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7593498	0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs991484	0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:172983400-172986600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr2:172983400-172986800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr2:172983400-172987600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr2:172984000-172987400	Enhancers	HMEC	breast
5	chr2:172985800-172986600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr2:172985800-172986600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr2:172986000-172986800	Enhancers	NHDF-Ad	bronchial
8	chr2:172986200-172986600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr2:172986200-172986600	Enhancers	Osteobl	bone
10	chr2:172986200-172986800	Enhancers	Muscle Satellite Cultured Cells	--
11	chr2:172986200-172986800	Flanking Active TSS	NHEK	skin
12	chr2:172986400-172986600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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