Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:127489751..127491692-chr4:127495242..127497629,2	K562	blood:
2	chr4:127351878..127354231-chr4:127491279..127492861,2	K562	blood:

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

rs_ID	r²[population]
rs11727424	1.00[ASN][1000 genomes]
rs1355111	1.00[ASN][1000 genomes]
rs167506	1.00[ASN][1000 genomes]
rs313103	1.00[ASN][1000 genomes]
rs313130	1.00[ASN][1000 genomes]
rs313131	1.00[ASN][1000 genomes]
rs313134	1.00[ASN][1000 genomes]
rs313137	1.00[ASN][1000 genomes]
rs313138	1.00[ASN][1000 genomes]
rs432446	1.00[ASN][1000 genomes]
rs4444841	1.00[ASN][1000 genomes]
rs4834125	1.00[ASN][1000 genomes]
rs60133914	1.00[ASN][1000 genomes]
rs62321712	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62321713	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62321715	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62321722	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62321723	1.00[ASN][1000 genomes]
rs62322676	1.00[ASN][1000 genomes]
rs62322678	1.00[ASN][1000 genomes]
rs62322679	1.00[ASN][1000 genomes]
rs62322680	1.00[ASN][1000 genomes]
rs62322683	1.00[ASN][1000 genomes]
rs62322684	1.00[ASN][1000 genomes]
rs62324762	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1012833	chr4:127468474-127760933	Enhancers Weak transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv537242	chr4:127468474-127760933	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv524850	chr4:127470903-127768849	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:127474800-127493400	Weak transcription	K562	blood
2	chr4:127490600-127491600	Enhancers	Brain Substantia Nigra	brain

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