Variant report

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SUCLA2-4	chr13:48464985-48466403	XLOC_010601

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

rs_ID	r²[population]
rs12869557	0.95[ASN][1000 genomes]
rs12873785	0.94[AFR][1000 genomes];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1555722	0.93[ASN][1000 genomes]
rs1974039	0.90[AFR][1000 genomes];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2104373	0.92[ASN][1000 genomes]
rs2104374	0.91[ASN][1000 genomes]
rs4553498	0.91[ASN][1000 genomes]
rs4942710	0.92[ASN][1000 genomes]
rs7317860	0.94[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7323277	0.93[ASN][1000 genomes]
rs7334095	0.95[ASN][1000 genomes]
rs7334463	0.94[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7336952	0.94[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7337766	0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7981260	0.90[ASN][1000 genomes]
rs7986369	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7993360	0.90[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs7993810	0.96[ASN][1000 genomes]
rs7994427	0.93[ASN][1000 genomes]
rs7998886	0.94[AFR][1000 genomes];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9562779	0.93[ASN][1000 genomes]
rs9567940	0.91[ASN][1000 genomes]
rs9567943	0.95[ASN][1000 genomes]
rs9567948	0.87[ASN][1000 genomes]
rs9595813	0.91[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	esv3510679	chr13:48236624-48498185	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	esv3510680	chr13:48236624-48498185	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv933980	chr13:48431000-48557419	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:48451000-48480200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr13:48453800-48471600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr13:48457200-48478000	Weak transcription	Adipose Nuclei	Adipose
4	chr13:48461000-48472200	Weak transcription	Spleen	Spleen
5	chr13:48461000-48472400	Weak transcription	Lung	lung
6	chr13:48461000-48478200	Weak transcription	Left Ventricle	heart
7	chr13:48463600-48474600	Weak transcription	Brain Cingulate Gyrus	brain
8	chr13:48464600-48467400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr13:48464800-48469800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr13:48465000-48467400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
11	chr13:48465000-48467400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr13:48465000-48484000	Weak transcription	Primary T cells from cord blood	blood
13	chr13:48465200-48478200	Weak transcription	Skeletal Muscle Female	skeletal muscle
14	chr13:48465800-48466600	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chr13:48465800-48468000	Weak transcription	HSMMtube	muscle
16	chr13:48466000-48466600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
17	chr13:48466200-48466400	Enhancers	H9 Cell Line	embryonic stem cell
18	chr13:48466200-48466400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
19	chr13:48466200-48466800	Enhancers	HUES6 Cell Line	embryonic stem cell

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