Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:58243274..58245439-chr2:58246837..58248682,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FANCL-1	chr2:58243792-58245216	ENSG00000250445
2	lnc-FANCL-1	chr2:58243792-58245214	NONHSAT070845

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10164499	1.00[MEX][hapmap];0.90[MKK][hapmap]
rs10168038	1.00[YRI][hapmap]
rs10187411	0.85[LWK][hapmap];1.00[MEX][hapmap];0.97[MKK][hapmap];0.87[AMR][1000 genomes]
rs10191766	1.00[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10201793	0.96[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10518852	1.00[ASW][hapmap];0.97[LWK][hapmap];1.00[MEX][hapmap];0.97[MKK][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11883874	0.96[MKK][hapmap]
rs11890639	1.00[YRI][hapmap]
rs13382369	0.97[MKK][hapmap]
rs13400997	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs13431271	0.97[MKK][hapmap]
rs2165100	0.97[MKK][hapmap]
rs4459722	0.87[AMR][1000 genomes]
rs57597086	0.87[AMR][1000 genomes]
rs72949131	0.87[AMR][1000 genomes]
rs72949137	0.87[AMR][1000 genomes]
rs72949158	0.87[AMR][1000 genomes]
rs7590976	0.82[MKK][hapmap]
rs7600213	1.00[MEX][hapmap];0.96[MKK][hapmap];0.87[AMR][1000 genomes]
rs9973928	0.93[MKK][hapmap]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv834159	chr2:58101262-58283655	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
2	nsv525988	chr2:58161520-58427786	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
3	nsv874200	chr2:58163178-58262016	Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv999591	chr2:58214871-58316147	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:58244200-58244800	ZNF genes & repeats	Primary B cells from cord blood	blood

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