Variant report

Variant	rs797822
Chromosome Location	chr7:83589551-83589552
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs11975852	0.87[ASN][1000 genomes]
rs13236626	0.87[ASN][1000 genomes]
rs1623312	0.83[ASN][1000 genomes]
rs1626663	0.83[ASN][1000 genomes]
rs1627397	0.83[ASN][1000 genomes]
rs1639559	0.85[ASN][1000 genomes]
rs1639582	0.87[ASN][1000 genomes]
rs1639583	0.82[ASN][1000 genomes]
rs2535786	0.87[ASN][1000 genomes]
rs2691695	0.87[ASN][1000 genomes]
rs3801594	0.87[ASN][1000 genomes]
rs4385417	0.85[ASN][1000 genomes]
rs701311	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs701312	0.80[EUR][1000 genomes]
rs701314	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs701320	0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs797802	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs797804	0.81[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs797805	0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs797818	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs797820	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs797823	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs797826	0.88[AMR][1000 genomes];0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs797828	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs797831	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs797833	0.84[AMR][1000 genomes];0.81[EUR][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:34 , 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	chr7:83584600-83593000	Weak transcription	NHLF	lung
3	chr7:83585000-83590200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr7:83585600-83597800	Weak transcription	Gastric	stomach
5	chr7:83586000-83590600	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr7:83586400-83590200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
7	chr7:83586600-83590000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr7:83586600-83590200	Weak transcription	HUES6 Cell Line	embryonic stem cell
9	chr7:83586800-83590600	Weak transcription	Fetal Lung	lung
10	chr7:83586800-83592800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr7:83587600-83589800	Weak transcription	HUES64 Cell Line	embryonic stem cell
12	chr7:83587600-83593000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr7:83587800-83590600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr7:83588000-83592600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr7:83588000-83593800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr7:83588200-83590000	Weak transcription	HUES48 Cell Line	embryonic stem cell
17	chr7:83588200-83605200	Weak transcription	Colon Smooth Muscle	Colon
18	chr7:83588600-83592800	Strong transcription	NHDF-Ad	bronchial
19	chr7:83588800-83590400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
20	chr7:83588800-83590400	Weak transcription	Fetal Kidney	kidney
21	chr7:83588800-83590400	Weak transcription	Stomach Smooth Muscle	stomach
22	chr7:83588800-83599400	Weak transcription	Fetal Brain Male	brain
23	chr7:83588800-83624600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr7:83589000-83590400	Weak transcription	Fetal Brain Female	brain
25	chr7:83589000-83590600	Weak transcription	H1 Cell Line	embryonic stem cell
26	chr7:83589000-83590600	Weak transcription	Fetal Muscle Trunk	muscle
27	chr7:83589000-83590600	Weak transcription	Fetal Muscle Leg	muscle
28	chr7:83589000-83605000	Weak transcription	Hela-S3	cervix
29	chr7:83589000-83654600	Weak transcription	Fetal Stomach	stomach
30	chr7:83589200-83591200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr7:83589200-83616600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr7:83589400-83592000	Weak transcription	Duodenum Smooth Muscle	Duodenum
33	chr7:83589400-83592400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr7:83589400-83605200	Weak transcription	Fetal Intestine Small	intestine

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