Variant report

Variant	rs73299920
Chromosome Location	chr8:91988510-91988511
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10490979	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1060583	0.98[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11994240	0.84[EUR][1000 genomes]
rs16905862	0.84[ASN][1000 genomes]
rs16906071	0.87[ASN][1000 genomes]
rs16907242	0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs34503257	0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4645524	0.99[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55999403	0.84[EUR][1000 genomes]
rs56871170	0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs58183914	0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs58624537	0.99[AFR][1000 genomes];0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58807337	0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs59695689	0.81[EUR][1000 genomes]
rs60121972	0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6471263	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6651175	0.81[AFR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7006863	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73298014	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs73299912	0.86[EUR][1000 genomes]
rs73299915	0.84[EUR][1000 genomes]
rs73299946	0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs73299965	0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs73299977	0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs73299979	0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs73299981	0.81[AFR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7818979	0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1028628	chr8:91680968-92418954	Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
2	nsv539672	chr8:91680968-92418954	Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
3	nsv891185	chr8:91923776-92056288	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
4	nsv1028201	chr8:91968527-92009964	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region miRNA target site	11 gene(s)	inside rSNPs	diseases
5	esv2758623	chr8:91974499-92273724	Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
6	esv2759629	chr8:91974499-92273724	Weak transcription Flanking Active TSS Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	26 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:43 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:91958200-91996000	Weak transcription	Fetal Stomach	stomach
2	chr8:91964600-91989800	Weak transcription	Left Ventricle	heart
3	chr8:91964800-91996600	Weak transcription	Ovary	ovary
4	chr8:91971800-91996600	Weak transcription	Thymus	Thymus
5	chr8:91975400-91991000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr8:91977800-91996200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr8:91978000-91996200	Weak transcription	Right Ventricle	heart
8	chr8:91978000-91996400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
9	chr8:91979200-91996600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr8:91979400-91996400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr8:91979600-91996200	Weak transcription	Primary hematopoietic stem cells	blood
12	chr8:91979800-91996800	Weak transcription	Adipose Nuclei	Adipose
13	chr8:91980800-91996400	Weak transcription	Fetal Kidney	kidney
14	chr8:91981000-91996400	Weak transcription	Osteobl	bone
15	chr8:91981600-91996200	Weak transcription	NHLF	lung
16	chr8:91981600-91996400	Weak transcription	Muscle Satellite Cultured Cells	--
17	chr8:91981600-91996400	Weak transcription	Fetal Muscle Leg	muscle
18	chr8:91982400-91996600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr8:91983000-91989800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr8:91983000-91990600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr8:91983000-91991200	Weak transcription	Fetal Lung	lung
22	chr8:91983000-91992400	Weak transcription	Gastric	stomach
23	chr8:91983000-91994600	Weak transcription	Cortex derived primary cultured neurospheres	brain
24	chr8:91983000-91996600	Weak transcription	Aorta	Aorta
25	chr8:91983000-91996800	Weak transcription	HSMM	muscle
26	chr8:91985400-91989600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr8:91985400-91996400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr8:91986800-91989000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr8:91986800-91990400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr8:91986800-91991400	Weak transcription	Colon Smooth Muscle	Colon
31	chr8:91986800-91994000	Weak transcription	Stomach Smooth Muscle	stomach
32	chr8:91986800-91995800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
33	chr8:91986800-91996400	Weak transcription	H1 Cell Line	embryonic stem cell
34	chr8:91986800-91996400	Weak transcription	HUES6 Cell Line	embryonic stem cell
35	chr8:91986800-91996800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
36	chr8:91987000-91991000	Weak transcription	K562	blood
37	chr8:91987000-91995800	Weak transcription	NHDF-Ad	bronchial
38	chr8:91987200-91994800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
39	chr8:91987400-91990400	Weak transcription	HUES64 Cell Line	embryonic stem cell
40	chr8:91987400-91991000	Weak transcription	HUES48 Cell Line	embryonic stem cell
41	chr8:91987600-91995600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
42	chr8:91987800-91991800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
43	chr8:91988400-91989600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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