Variant report

Variant	rs73358129
Chromosome Location	chr7:70798255-70798256
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs11971278	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11971711	1.00[AMR][1000 genomes]
rs11973091	1.00[AMR][1000 genomes]
rs11974045	1.00[AMR][1000 genomes]
rs11976034	1.00[AMR][1000 genomes]
rs11982964	1.00[AMR][1000 genomes]
rs58768169	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59592502	1.00[AMR][1000 genomes]
rs60204871	1.00[AMR][1000 genomes]
rs73354290	1.00[AMR][1000 genomes]
rs73356047	1.00[AMR][1000 genomes]
rs73356056	1.00[AMR][1000 genomes]
rs73356066	1.00[AMR][1000 genomes]
rs73358126	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73358132	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73358163	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73358191	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73360114	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73360128	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73360129	1.00[AMR][1000 genomes]
rs73360132	1.00[AMR][1000 genomes]
rs73360136	1.00[AMR][1000 genomes]
rs73360139	1.00[AMR][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	chr7:70784000-70808200	Weak transcription	Aorta	Aorta
2	chr7:70790800-70799200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr7:70790800-70804800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr7:70793600-70802200	Weak transcription	Left Ventricle	heart
5	chr7:70794000-70800600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr7:70794400-70799000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr7:70794400-70801400	Weak transcription	H1 Cell Line	embryonic stem cell
8	chr7:70794400-70801400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr7:70794600-70799400	Weak transcription	Fetal Lung	lung
10	chr7:70794600-70800600	Weak transcription	HUES64 Cell Line	embryonic stem cell
11	chr7:70794600-70800800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
12	chr7:70794600-70801400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
13	chr7:70794600-70801400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr7:70794600-70801400	Weak transcription	HUES48 Cell Line	embryonic stem cell
15	chr7:70794600-70806600	Weak transcription	HUES6 Cell Line	embryonic stem cell
16	chr7:70794800-70801200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr7:70794800-70804800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
18	chr7:70796000-70798600	Weak transcription	Fetal Muscle Leg	muscle
19	chr7:70796000-70798800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr7:70796000-70804200	Weak transcription	Ovary	ovary

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