Variant report

Variant	rs60086789
Chromosome Location	chr2:205729816-205729817
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:205728566..205731008-chr2:205734010..205736358,2	MCF-7	breast:

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs55941034	1.00[AMR][1000 genomes]
rs57531270	1.00[AMR][1000 genomes]
rs58416129	1.00[AMR][1000 genomes]
rs59381758	1.00[AMR][1000 genomes]
rs60446736	1.00[AMR][1000 genomes]
rs61001089	1.00[AMR][1000 genomes]
rs61286794	1.00[AMR][1000 genomes]
rs6713878	1.00[AMR][1000 genomes]
rs6753755	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73982523	1.00[AMR][1000 genomes]
rs73982525	1.00[AMR][1000 genomes]
rs73982529	1.00[AMR][1000 genomes]
rs73982531	1.00[AMR][1000 genomes]
rs73982532	1.00[AMR][1000 genomes]
rs73982556	1.00[AMR][1000 genomes]
rs73982587	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73982600	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73984428	1.00[AMR][1000 genomes]
rs73984429	1.00[AMR][1000 genomes]
rs73984430	1.00[AMR][1000 genomes]
rs73984488	1.00[AMR][1000 genomes]
rs73984489	1.00[AMR][1000 genomes]
rs73984490	1.00[AMR][1000 genomes]
rs7579299	1.00[AMR][1000 genomes]
rs7597714	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv998485	chr2:205407813-206184006	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv536122	chr2:205407813-206184006	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	nsv1010210	chr2:205489653-206076013	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	esv2757846	chr2:205539832-205841174	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	esv2759111	chr2:205539832-205841174	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv875725	chr2:205572718-205760800	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:205725200-205730000	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr2:205725200-205734600	Weak transcription	Pancreas	Pancrea
3	chr2:205725400-205733600	Weak transcription	Fetal Lung	lung
4	chr2:205725400-205734400	Weak transcription	Adipose Nuclei	Adipose
5	chr2:205725800-205733400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr2:205728400-205733600	Weak transcription	Rectal Smooth Muscle	rectum
7	chr2:205729000-205732400	Weak transcription	Colon Smooth Muscle	Colon
8	chr2:205729000-205732600	Weak transcription	Ovary	ovary
9	chr2:205729000-205733400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr2:205729600-205734400	Weak transcription	HUES48 Cell Line	embryonic stem cell

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