Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:105128438..105130994-chr1:105132786..105134781,2	K562	blood:

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs10120233	0.97[ASN][1000 genomes]
rs10120239	0.97[ASN][1000 genomes]
rs10122635	0.97[ASN][1000 genomes]
rs10810090	0.97[ASN][1000 genomes]
rs10961395	0.80[EUR][1000 genomes]
rs10961403	0.92[ASN][1000 genomes]
rs10961408	0.92[ASN][1000 genomes]
rs10961409	0.92[ASN][1000 genomes]
rs10961410	0.92[ASN][1000 genomes]
rs10961423	0.92[ASN][1000 genomes]
rs10961432	0.86[ASN][1000 genomes]
rs10961438	0.92[ASN][1000 genomes]
rs1105394	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs11788463	0.92[ASN][1000 genomes]
rs11789395	1.00[ASN][1000 genomes]
rs11794684	1.00[ASN][1000 genomes]
rs72688899	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72688902	0.95[ASN][1000 genomes]
rs7856186	0.97[ASN][1000 genomes]
rs7856193	0.92[ASN][1000 genomes]
rs7856205	0.97[ASN][1000 genomes]
rs7856329	0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1010903	chr1:104483363-105468941	Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	esv2762170	chr1:104817700-105411596	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv872081	chr1:105009637-105455991	Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv1004836	chr1:105104358-105173095	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv999490	chr1:105105338-105173095	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv1013052	chr1:105105338-105175991	Enhancers ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv547218	chr1:105111443-105134662	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:105127800-105134800	Weak transcription	Primary B cells from peripheral blood	blood

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