Variant report

Variant	rs28408980
Chromosome Location	chr12:124026942-124026943
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr12:124018963..124020649-chr12:124025084..124027162,2	MCF-7	breast:
2	chr12:123942696..123944552-chr12:124025092..124028061,2	K562	blood:
3	chr12:124014613..124020427-chr12:124021757..124030921,10	MCF-7	breast:

Variant related genes	Relation type
ENSG00000184209	Chromatin interaction
ENSG00000188026	Chromatin interaction

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs1057879	0.85[ASN][1000 genomes]
rs10846526	0.87[ASN][1000 genomes]
rs10846528	0.93[ASN][1000 genomes]
rs11057297	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2048615	0.85[ASN][1000 genomes]
rs2333831	0.85[ASN][1000 genomes]
rs28371124	0.85[ASN][1000 genomes]
rs28430750	0.85[ASN][1000 genomes]
rs28454032	0.82[ASN][1000 genomes]
rs28465339	0.87[ASN][1000 genomes]
rs28478446	0.85[ASN][1000 genomes]
rs28497190	0.85[ASN][1000 genomes]
rs28539789	0.87[ASN][1000 genomes]
rs28654896	0.87[ASN][1000 genomes]
rs28701527	0.85[ASN][1000 genomes]
rs28707421	0.85[ASN][1000 genomes]
rs28712858	0.85[ASN][1000 genomes]
rs28741988	0.85[ASN][1000 genomes]
rs28758342	0.87[ASN][1000 genomes]
rs28834793	0.94[ASN][1000 genomes]
rs5027860	0.82[ASN][1000 genomes]
rs61953552	0.87[ASN][1000 genomes]
rs61953557	0.87[ASN][1000 genomes]
rs71458805	0.85[ASN][1000 genomes]
rs7307227	0.82[ASN][1000 genomes]
rs7313751	0.81[EUR][1000 genomes]
rs7315326	0.96[ASN][1000 genomes]
rs7398935	0.81[EUR][1000 genomes]
rs786454	0.91[ASN][1000 genomes]
rs7956299	0.81[EUR][1000 genomes]
rs7959727	0.91[ASN][1000 genomes]
rs7962151	0.82[EUR][1000 genomes]
rs7965334	0.82[ASN][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	nsv1038841	chr12:123757305-124087671	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
2	nsv541622	chr12:123757305-124087671	Enhancers Strong transcription Genic enhancers Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
3	nsv1050598	chr12:123991646-124214332	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
4	nsv541623	chr12:123991646-124214332	Active TSS Weak transcription Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
5	nsv498024	chr12:123994372-124459856	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
6	esv2422416	chr12:124009676-124085689	Strong transcription Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	28 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:124019400-124028200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr12:124026000-124027000	Active TSS	HepG2	liver

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