Variant report

Variant	rs797823
Chromosome Location	chr7:83586714-83586715
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:83566155..83568449-chr7:83585105..83587262,2	K562	blood:
2	chr7:83580423..83584240-chr7:83586287..83589174,3	K562	blood:
3	chr7:83566534..83568449-chr7:83584344..83587262,2	K562	blood:

Extended variants
information (count: 29 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11975852	0.87[ASN][1000 genomes]
rs13236626	0.87[ASN][1000 genomes]
rs1623312	1.00[CHB][hapmap];0.94[CHD][hapmap];0.81[GIH][hapmap];0.82[JPT][hapmap];0.83[ASN][1000 genomes]
rs1626663	0.83[ASN][1000 genomes]
rs1627397	0.83[ASN][1000 genomes]
rs1639559	1.00[CHB][hapmap];0.82[JPT][hapmap];0.85[ASN][1000 genomes]
rs1639582	0.87[ASN][1000 genomes]
rs1639583	0.82[ASN][1000 genomes]
rs2535786	0.89[CHB][hapmap];0.94[CHD][hapmap];0.82[JPT][hapmap];0.87[ASN][1000 genomes]
rs2691695	0.87[ASN][1000 genomes]
rs3801594	0.87[ASN][1000 genomes]
rs4385417	0.85[ASN][1000 genomes]
rs701311	0.87[AFR][1000 genomes];0.86[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs701314	0.89[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs701320	1.00[CHB][hapmap];0.94[CHD][hapmap];0.82[JPT][hapmap];0.81[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs797802	0.81[AFR][1000 genomes];0.86[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs797804	1.00[CHB][hapmap];0.87[ASN][1000 genomes]
rs797805	0.81[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs797818	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs797820	1.00[ASW][hapmap];0.88[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];0.92[GIH][hapmap];0.82[JPT][hapmap];1.00[MEX][hapmap];0.95[TSI][hapmap];1.00[YRI][hapmap];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs797822	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs797826	0.87[AFR][1000 genomes];0.86[AMR][1000 genomes];0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs797828	0.87[AFR][1000 genomes];0.86[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs797831	0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs797833	0.81[AFR][1000 genomes];0.86[AMR][1000 genomes];0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv607707	chr7:83381032-83646816	Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv888620	chr7:83459908-83593805	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv888622	chr7:83526743-83631376	Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv1020784	chr7:83577402-83687108	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:83579200-83590400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr7:83581800-83588000	Weak transcription	Colon Smooth Muscle	Colon
3	chr7:83584600-83593000	Weak transcription	NHLF	lung
4	chr7:83584800-83588600	Weak transcription	NHDF-Ad	bronchial
5	chr7:83585000-83590200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr7:83585600-83587400	Weak transcription	Fetal Brain Male	brain
7	chr7:83585600-83597800	Weak transcription	Gastric	stomach
8	chr7:83586000-83588000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr7:83586000-83590600	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr7:83586400-83586800	Enhancers	Fetal Lung	lung
11	chr7:83586400-83590200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
12	chr7:83586600-83586800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
13	chr7:83586600-83587600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr7:83586600-83590000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr7:83586600-83590200	Weak transcription	HUES6 Cell Line	embryonic stem cell

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