Variant report

Variant	rs2003524
Chromosome Location	chr7:139971473-139971474
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:139967905..139969636-chr7:139970125..139972118,2	MCF-7	breast:
2	chr7:139970498..139972137-chr7:139976828..139978399,2	K562	blood:
3	chr7:139969481..139972137-chr7:139976037..139978399,3	K562	blood:

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs2003523	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2003525	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2429202	0.80[ASN][1000 genomes]
rs2429204	0.80[ASN][1000 genomes]
rs2429225	0.80[ASN][1000 genomes]
rs2429226	0.80[ASN][1000 genomes]
rs2429228	0.80[ASN][1000 genomes]
rs2471282	0.80[ASN][1000 genomes]
rs2471283	0.80[ASN][1000 genomes]
rs2471285	0.80[ASN][1000 genomes]
rs2471286	0.80[ASN][1000 genomes]
rs2471287	0.80[ASN][1000 genomes]
rs2471288	0.80[ASN][1000 genomes]
rs2471289	0.80[ASN][1000 genomes]
rs2471290	0.80[ASN][1000 genomes]
rs2471291	0.80[ASN][1000 genomes]
rs2471292	0.80[ASN][1000 genomes]
rs2471293	0.80[ASN][1000 genomes]
rs2471294	0.80[ASN][1000 genomes]
rs2471295	0.80[ASN][1000 genomes]
rs2471296	0.80[ASN][1000 genomes]
rs2471297	0.80[ASN][1000 genomes]
rs2471298	0.80[ASN][1000 genomes]
rs2471303	0.80[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	nsv889247	chr7:139855216-140033631	Weak transcription Flanking Active TSS Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	nsv1015840	chr7:139912355-139987681	Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv1026255	chr7:139944473-140043299	Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Strong transcription Genic enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
4	esv2761371	chr7:139964350-139979655	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
5	nsv520097	chr7:139969051-139979843	Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
6	nsv519667	chr7:139969051-139992387	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:139960400-139975200	Weak transcription	Right Atrium	heart
2	chr7:139965400-139973400	Weak transcription	HepG2	liver
3	chr7:139969400-139974800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr7:139970800-139971800	Active TSS	Placenta	Placenta
5	chr7:139971400-139973200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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