Variant report

Variant	rs211674
Chromosome Location	chr1:76073747-76073748
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr1:76064706..76067511-chr1:76072450..76074334,2	K562	blood:
2	chr1:76073216..76076150-chr1:76081319..76083961,2	MCF-7	breast:
3	chr1:76071710..76074403-chr1:76079679..76081378,2	K562	blood:
4	chr1:76070009..76076148-chr1:76078248..76081967,7	K562	blood:

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

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

rs_ID	r²[population]
rs1265895	0.80[EUR][1000 genomes]
rs169830	0.88[EUR][1000 genomes]
rs169831	0.80[EUR][1000 genomes]
rs1739901	0.80[EUR][1000 genomes]
rs190026	0.83[EUR][1000 genomes]
rs211677	0.88[EUR][1000 genomes]
rs211680	0.88[EUR][1000 genomes]
rs211697	0.88[EUR][1000 genomes]
rs211698	0.83[EUR][1000 genomes]
rs211701	0.88[EUR][1000 genomes]
rs211704	0.88[EUR][1000 genomes]
rs211741	0.83[EUR][1000 genomes]
rs211742	0.88[EUR][1000 genomes]
rs211743	0.88[EUR][1000 genomes]
rs211760	0.88[EUR][1000 genomes]
rs211761	0.88[EUR][1000 genomes]
rs211763	0.83[EUR][1000 genomes]
rs211765	0.83[EUR][1000 genomes]
rs211766	0.88[EUR][1000 genomes]
rs211767	0.83[EUR][1000 genomes]
rs378926	0.88[EUR][1000 genomes]
rs388870	0.88[EUR][1000 genomes]
rs408340	0.88[EUR][1000 genomes]
rs431959	0.88[EUR][1000 genomes]
rs6593582	0.88[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv519329	chr1:75830438-76358591	Enhancers Strong transcription Flanking Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
2	esv3445096	chr1:75933216-76126980	Active TSS Weak transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	esv2757737	chr1:75986904-76187748	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
4	esv2758943	chr1:75986904-76187748	Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
5	nsv427675	chr1:76070382-76187748	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:76070000-76078400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr1:76072600-76075200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr1:76072600-76077600	Weak transcription	Fetal Brain Male	brain

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