Variant report

Variant	rs10095190
Chromosome Location	chr8:10239612-10239613
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs11249994	0.84[CEU][hapmap]
rs11779480	0.83[CEU][hapmap]
rs12674649	0.82[JPT][hapmap]
rs12682070	0.96[JPT][hapmap];0.88[ASN][1000 genomes]
rs13249940	0.82[CHB][hapmap];0.91[JPT][hapmap];0.82[ASN][1000 genomes]
rs3750314	0.82[JPT][hapmap]
rs6601449	0.81[CEU][hapmap]
rs7015768	0.91[JPT][hapmap];0.83[ASN][1000 genomes]
rs9329221	0.83[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1030934	chr8:10065169-10561161	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
2	nsv890347	chr8:10153082-10331636	Flanking Active TSS ZNF genes & repeats Weak transcription Enhancers Flanking Bivalent TSS/Enh Strong transcription Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
3	nsv1022994	chr8:10190618-10660122	Strong transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
4	nsv539466	chr8:10190618-10660122	Enhancers Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
5	nsv527326	chr8:10199548-10320019	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
6	nsv1025557	chr8:10216726-10555187	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
7	nsv917085	chr8:10237508-10828204	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	37 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs10095190	BLK	Cis_chr	lymphoblastoid	RTeQTL

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:10192600-10282400	Weak transcription	Gastric	stomach
2	chr8:10224000-10255800	Weak transcription	Stomach Smooth Muscle	stomach
3	chr8:10228600-10247800	Weak transcription	Liver	Liver
4	chr8:10233800-10240000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr8:10233800-10241400	Weak transcription	Primary neutrophils fromperipheralblood	blood
6	chr8:10233800-10252400	Weak transcription	Fetal Brain Male	brain
7	chr8:10234000-10241200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr8:10235200-10252400	Weak transcription	Brain Hippocampus Middle	brain
9	chr8:10235400-10239800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr8:10235400-10256800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr8:10235600-10239800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr8:10235600-10240600	Weak transcription	Fetal Brain Female	brain
13	chr8:10235600-10241600	Weak transcription	Placenta Amnion	Placenta Amnion
14	chr8:10235600-10244000	Weak transcription	Cortex derived primary cultured neurospheres	brain
15	chr8:10235600-10244400	Weak transcription	Duodenum Mucosa	Duodenum
16	chr8:10235800-10241600	Weak transcription	Right Atrium	heart
17	chr8:10236000-10239800	Weak transcription	Left Ventricle	heart
18	chr8:10236200-10240000	Weak transcription	Spleen	Spleen
19	chr8:10236200-10247400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
20	chr8:10236200-10252600	Weak transcription	Brain Inferior Temporal Lobe	brain
21	chr8:10236200-10255800	Weak transcription	Pancreas	Pancrea
22	chr8:10236200-10255800	Weak transcription	Right Ventricle	heart
23	chr8:10236400-10241400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr8:10236800-10241800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr8:10237200-10247400	Weak transcription	Lung	lung
26	chr8:10239000-10241600	Enhancers	Psoas Muscle	Psoas
27	chr8:10239200-10241800	Enhancers	Primary T cells from cord blood	blood
28	chr8:10239200-10241800	Enhancers	Skeletal Muscle Female	skeletal muscle
29	chr8:10239600-10239800	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
30	chr8:10239600-10242000	Enhancers	Fetal Muscle Leg	muscle

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