Variant report

Variant	rs16888491
Chromosome Location	chr8:39849530-39849531
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs1362847	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2032723	0.83[ASN][1000 genomes]
rs4736794	0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4736929	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4736961	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4736962	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs56767874	0.93[ASN][1000 genomes]
rs57804443	0.81[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs62511373	0.84[ASN][1000 genomes]
rs62511374	0.80[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs62511375	0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs62511376	0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs62513785	0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7001170	0.89[YRI][hapmap];0.81[AFR][1000 genomes]
rs73621309	0.81[AFR][1000 genomes]
rs73621318	0.84[AFR][1000 genomes]
rs7820968	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7837357	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.80[EUR][1000 genomes];0.81[ASN][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	nsv539555	chr8:39683857-40673606	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
2	nsv1033371	chr8:39749437-39899540	Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:30 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:39835200-39853600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr8:39843000-39853000	Weak transcription	Lung	lung
3	chr8:39847000-39849800	Enhancers	Fetal Muscle Leg	muscle
4	chr8:39847200-39851200	Enhancers	Rectal Smooth Muscle	rectum
5	chr8:39847400-39849800	Weak transcription	Right Ventricle	heart
6	chr8:39847600-39849600	Enhancers	Sigmoid Colon	Sigmoid Colon
7	chr8:39847600-39849800	Enhancers	Stomach Smooth Muscle	stomach
8	chr8:39847600-39850000	Enhancers	Liver	Liver
9	chr8:39847600-39851200	Enhancers	Fetal Heart	heart
10	chr8:39847600-39851400	Enhancers	Colon Smooth Muscle	Colon
11	chr8:39847600-39853600	Weak transcription	Fetal Muscle Trunk	muscle
12	chr8:39847800-39849600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr8:39847800-39851200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr8:39847800-39854800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr8:39848200-39850200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr8:39848400-39849600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr8:39848400-39849600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr8:39848400-39850200	Enhancers	A549	lung
19	chr8:39848600-39849600	Weak transcription	Duodenum Mucosa	Duodenum
20	chr8:39848800-39849800	Weak transcription	Cortex derived primary cultured neurospheres	brain
21	chr8:39848800-39850200	Weak transcription	Fetal Stomach	stomach
22	chr8:39849000-39849800	Weak transcription	H1 Cell Line	embryonic stem cell
23	chr8:39849000-39849800	Weak transcription	Ovary	ovary
24	chr8:39849000-39850200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr8:39849000-39850200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr8:39849000-39850200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr8:39849000-39853400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
28	chr8:39849200-39850200	Weak transcription	Duodenum Smooth Muscle	Duodenum
29	chr8:39849400-39850000	Enhancers	Pancreas	Pancrea
30	chr8:39849400-39850600	Enhancers	Right Atrium	heart

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