Variant report

Variant	rs7824675
Chromosome Location	chr8:10243418-10243419
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:10230455..10233257-chr8:10241195..10243671,2	K562	blood:

Extended variants
information (count: 52 )
Associated
traits (count: 7 )

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs10096337	0.91[ASN][1000 genomes]
rs10105867	0.91[ASN][1000 genomes]
rs10283145	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.93[GIH][hapmap];1.00[JPT][hapmap];0.89[MEX][hapmap];0.82[MKK][hapmap];0.86[TSI][hapmap];0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11774221	1.00[CHD][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs11777976	0.89[GIH][hapmap];0.82[JPT][hapmap];0.89[MEX][hapmap];0.87[TSI][hapmap];0.85[EUR][1000 genomes]
rs11990519	0.82[JPT][hapmap]
rs13252982	0.82[JPT][hapmap];0.85[EUR][1000 genomes]
rs13254263	0.82[JPT][hapmap];0.85[EUR][1000 genomes]
rs17151843	1.00[CHD][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs17151854	1.00[CHD][hapmap];0.85[JPT][hapmap]
rs17151859	0.85[JPT][hapmap]
rs17708276	1.00[CHD][hapmap]
rs17709397	1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs17765901	1.00[CHB][hapmap];1.00[CHD][hapmap];0.93[GIH][hapmap];1.00[JPT][hapmap];0.94[MEX][hapmap];0.87[TSI][hapmap];0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs17767019	0.82[JPT][hapmap]
rs2001364	1.00[JPT][hapmap]
rs28507213	0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs28712068	0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2952184	1.00[CHB][hapmap]
rs2952185	1.00[CHD][hapmap]
rs2975675	1.00[CHB][hapmap]
rs3750310	0.82[JPT][hapmap]
rs3812495	0.82[ASN][1000 genomes]
rs4074083	0.82[JPT][hapmap]
rs4260895	1.00[CHB][hapmap]
rs4342552	0.82[JPT][hapmap]
rs4433149	1.00[CHB][hapmap];1.00[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.94[MEX][hapmap];0.87[TSI][hapmap];0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4526367	0.82[JPT][hapmap]
rs4610752	1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4840480	1.00[CHD][hapmap];0.85[JPT][hapmap]
rs4841329	0.84[EUR][1000 genomes]
rs4841352	0.82[JPT][hapmap]
rs6601443	1.00[CHB][hapmap];1.00[CHD][hapmap]
rs6601450	0.81[CEU][hapmap]
rs6601451	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs68071218	0.82[ASN][1000 genomes]
rs6984111	1.00[CHD][hapmap];0.85[JPT][hapmap]
rs6989657	0.82[JPT][hapmap]
rs7818437	1.00[CHB][hapmap]
rs7831557	0.82[JPT][hapmap]
rs7833781	0.82[JPT][hapmap]
rs7838901	1.00[CHB][hapmap]
rs7841921	1.00[CHD][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 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
8	nsv465460	chr8:10241411-10290566	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
9	nsv610265	chr8:10241411-10290566	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases

mRNA abundance (count:7)

SNP	Gene	Cis/trans	Tissue	Source
rs7824675	C8orf5	Cis_1M	lymphoblastoid	RTeQTL
rs7824675	CTSB	cis	cerebellum	SCAN
rs7824675	C8orf13	Cis_chr	lymphoblastoid	RTeQTL
rs7824675	CLDN23	cis	multi-tissue	Pritchard
rs7824675	BLK	Cis_chr	lymphoblastoid	RTeQTL
rs7824675	MFHAS1	cis	cerebellum	SCAN
rs7824675	FLJ10661	cis	cerebellum	SCAN

Chromatin state (count:27 , 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	chr8:10233800-10252400	Weak transcription	Fetal Brain Male	brain
5	chr8:10235200-10252400	Weak transcription	Brain Hippocampus Middle	brain
6	chr8:10235400-10256800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr8:10235600-10244000	Weak transcription	Cortex derived primary cultured neurospheres	brain
8	chr8:10235600-10244400	Weak transcription	Duodenum Mucosa	Duodenum
9	chr8:10236200-10247400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
10	chr8:10236200-10252600	Weak transcription	Brain Inferior Temporal Lobe	brain
11	chr8:10236200-10255800	Weak transcription	Pancreas	Pancrea
12	chr8:10236200-10255800	Weak transcription	Right Ventricle	heart
13	chr8:10237200-10247400	Weak transcription	Lung	lung
14	chr8:10240400-10256000	Weak transcription	Adipose Nuclei	Adipose
15	chr8:10240400-10256800	Weak transcription	Left Ventricle	heart
16	chr8:10241200-10247400	Weak transcription	Spleen	Spleen
17	chr8:10241400-10245000	Strong transcription	Primary neutrophils fromperipheralblood	blood
18	chr8:10241800-10246800	Weak transcription	Primary T cells from cord blood	blood
19	chr8:10241800-10249600	Weak transcription	Skeletal Muscle Female	skeletal muscle
20	chr8:10242000-10243600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr8:10242000-10246200	Weak transcription	Fetal Muscle Leg	muscle
22	chr8:10242000-10255800	Weak transcription	Brain Germinal Matrix	brain
23	chr8:10242200-10248200	Weak transcription	Fetal Brain Female	brain
24	chr8:10242400-10244000	Weak transcription	Placenta Amnion	Placenta Amnion
25	chr8:10242800-10244600	Weak transcription	H1 Cell Line	embryonic stem cell
26	chr8:10243000-10246200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr8:10243400-10244400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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