Variant report

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs10236816	0.81[AFR][1000 genomes]
rs10241279	0.80[EUR][1000 genomes]
rs10267558	0.90[YRI][hapmap];1.00[EUR][1000 genomes]
rs10268108	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10272342	1.00[CEU][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10278132	1.00[EUR][1000 genomes]
rs12540623	0.94[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs28483889	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs28676380	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs57449818	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs73363781	0.80[EUR][1000 genomes]
rs73365659	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73365677	1.00[EUR][1000 genomes]
rs73365680	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73365685	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs73365688	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs73367513	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[EUR][1000 genomes]

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	nsv519090	chr7:70085934-71071896	Weak transcription Enhancers Bivalent/Poised TSS Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
2	nsv1015261	chr7:70404302-71255933	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:70908400-70935200	Weak transcription	Fetal Lung	lung
2	chr7:70923800-70935200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr7:70927200-70937800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr7:70928200-70932400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr7:70928800-70930800	Enhancers	Right Ventricle	heart
6	chr7:70929200-70932400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr7:70929200-70932800	Enhancers	H1 Cell Line	embryonic stem cell
8	chr7:70929200-70933000	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr7:70929400-70930800	Enhancers	H9 Cell Line	embryonic stem cell
10	chr7:70929400-70931200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
11	chr7:70929400-70933000	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr7:70929400-70936000	Weak transcription	Ovary	ovary
13	chr7:70929600-70931000	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr7:70929600-70931200	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr7:70929600-70932800	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr7:70929800-70933000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr7:70930000-70931200	Enhancers	Fetal Heart	heart
18	chr7:70930400-70930600	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
19	chr7:70930400-70930600	Genic enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr7:70930400-70930800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell

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