Variant report

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs10266314	0.83[EUR][1000 genomes]
rs10267307	0.82[EUR][1000 genomes]
rs10499979	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11521007	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1357685	0.94[EUR][1000 genomes]
rs1464744	0.80[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1524271	0.80[AFR][1000 genomes];0.92[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1524273	0.95[EUR][1000 genomes]
rs1616510	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1721445	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1721447	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1721448	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1721898	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1721899	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1721908	0.82[EUR][1000 genomes]
rs17463939	0.93[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs17464044	0.80[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1880236	0.82[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1880237	0.94[AFR][1000 genomes];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2140585	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2140587	0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs2396133	0.83[EUR][1000 genomes]
rs56165817	0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs62473267	0.97[AMR][1000 genomes];0.99[EUR][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	nsv1023379	chr7:109003574-109355234	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv608079	chr7:109098364-109862289	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv1020761	chr7:109208187-109275700	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:109211800-109234000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr7:109221200-109234400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr7:109225800-109230000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
4	chr7:109226400-109229600	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
5	chr7:109227200-109229200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
6	chr7:109227400-109229400	Weak transcription	H1 Cell Line	embryonic stem cell
7	chr7:109228000-109228400	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
8	chr7:109228200-109228400	Flanking Active TSS	H9 Cell Line	embryonic stem cell
9	chr7:109228200-109228800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
10	chr7:109228200-109228800	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell

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