Variant report

Variant	rs34782082
Chromosome Location	chr1:223467235-223467236
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	chr1:223466163..223468186-chr1:223469482..223472172,2	MCF-7	breast:
2	chr1:223466621..223469312-chr1:223470297..223473880,3	K562	blood:

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs1095170	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1341291	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1356481	0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1356482	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs17161993	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17161994	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17163762	0.87[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs17163773	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs17163774	1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs17518279	0.91[EUR][1000 genomes]
rs2203763	0.97[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2678367	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2795063	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs34013846	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs34283624	0.95[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs34788475	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs34827745	0.92[AFR][1000 genomes]
rs35133329	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs35345711	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4661252	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs6662301	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1012537	chr1:222755091-223512243	Weak transcription Strong transcription Enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
2	nsv1000039	chr1:223429733-223527845	Enhancers Weak transcription Strong transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:223443800-223472600	Weak transcription	Gastric	stomach
2	chr1:223459000-223474200	Weak transcription	Primary T helper cells PMA-I stimulated	--
3	chr1:223460800-223473400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
4	chr1:223461200-223469600	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr1:223464400-223472800	Weak transcription	Brain Cingulate Gyrus	brain
6	chr1:223465800-223469600	Weak transcription	Esophagus	oesophagus
7	chr1:223466400-223471800	Weak transcription	Ovary	ovary
8	chr1:223466400-223480400	Weak transcription	Pancreas	Pancrea
9	chr1:223467200-223469200	Weak transcription	Primary T cells from cord blood	blood

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