Variant report

Variant	rs7593033
Chromosome Location	chr2:149140982-149140983
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs10164630	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs10181225	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs10188234	0.80[EUR][1000 genomes]
rs10191789	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs10198939	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs10204642	0.84[AFR][1000 genomes];0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10928395	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs12613727	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12615490	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs12616001	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs12691792	0.81[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs12992721	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs13427268	0.81[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs1404185	0.80[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs1916960	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2140606	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs34228226	0.83[AFR][1000 genomes];0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs35630407	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs35715730	0.84[AFR][1000 genomes];0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4635473	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6706914	0.84[EUR][1000 genomes]
rs6708633	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs6723914	0.81[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs6745934	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs6748825	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs6758931	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7355758	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs7425880	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs7567204	0.81[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs7606618	0.80[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs7607930	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2753542	chr2:149004714-149268503	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv1012275	chr2:149031668-149316793	Enhancers Strong transcription Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv1012123	chr2:149078500-149151358	Enhancers Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
4	nsv583289	chr2:149091754-149170115	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
5	nsv875277	chr2:149094415-149178974	Enhancers Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
6	nsv875278	chr2:149094415-149201775	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
7	nsv875279	chr2:149111470-149201775	Enhancers ZNF genes & repeats Weak transcription Strong transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
8	nsv875280	chr2:149115432-149198275	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
9	nsv875281	chr2:149115432-149206943	ZNF genes & repeats Enhancers Bivalent Enhancer Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
10	nsv583290	chr2:149117734-149170115	ZNF genes & repeats Weak transcription Enhancers Bivalent Enhancer Strong transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:149137200-149152600	Weak transcription	Primary T cells from cord blood	blood

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