Variant report

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FER-5	chr5:108555955-108558658	ucscGeneNc_uc003kor_1

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs10051034	0.85[CHB][hapmap]
rs10055161	0.85[CHB][hapmap]
rs10069467	1.00[CHB][hapmap]
rs10074150	0.93[CHB][hapmap]
rs1036214	0.93[CHB][hapmap]
rs10477438	0.84[CHB][hapmap]
rs10477439	0.93[CHB][hapmap]
rs11746231	0.85[CHB][hapmap]
rs11749629	0.93[CHB][hapmap]
rs11750370	0.85[CHB][hapmap]
rs11952637	0.85[CHB][hapmap]
rs15402	0.90[ASN][1000 genomes]
rs17161612	0.85[CHB][hapmap]
rs17407717	1.00[CHB][hapmap]
rs4130644	0.85[CHB][hapmap]
rs4957569	0.85[CHB][hapmap]
rs4957801	0.95[AFR][1000 genomes]
rs4957807	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62376812	0.81[AFR][1000 genomes]
rs62376813	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6870061	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6870080	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6870224	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6870394	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6873546	0.85[CHB][hapmap]
rs6882531	0.93[CHB][hapmap]
rs6891839	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6894369	0.95[AFR][1000 genomes]
rs72793026	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9326764	0.84[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1027163	chr5:108445447-108839913	Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
2	nsv599338	chr5:108528729-108675737	Weak transcription Strong transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:108555200-108559600	Weak transcription	Ovary	ovary
2	chr5:108555400-108559400	Weak transcription	Fetal Muscle Leg	muscle
3	chr5:108555400-108559400	Weak transcription	Pancreas	Pancrea
4	chr5:108555800-108558200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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