Variant report

Variant	rs1484648
Chromosome Location	chr8:10053882-10053883
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 51 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs10085917	0.81[CEU][hapmap];0.86[CHB][hapmap];0.81[JPT][hapmap];0.86[AMR][1000 genomes];0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10093457	0.81[ASN][1000 genomes]
rs10097315	0.89[CEU][hapmap];0.91[CHD][hapmap];0.95[GIH][hapmap];0.92[MEX][hapmap];0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs10104463	0.81[CEU][hapmap]
rs10283047	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11249972	0.81[AMR][1000 genomes]
rs11249973	0.91[CHB][hapmap];0.88[CHD][hapmap];0.93[GIH][hapmap];0.89[JPT][hapmap];0.84[MEX][hapmap];0.87[ASN][1000 genomes]
rs11777161	0.81[ASN][1000 genomes]
rs11783143	0.81[CHB][hapmap];0.86[CHD][hapmap];0.86[JPT][hapmap];0.83[ASN][1000 genomes]
rs11786117	0.86[CHB][hapmap];0.81[JPT][hapmap];0.84[ASN][1000 genomes]
rs11786120	0.85[CHB][hapmap];0.84[ASN][1000 genomes]
rs13257383	0.82[CHD][hapmap]
rs17748267	0.86[CHB][hapmap];0.81[JPT][hapmap];0.82[MEX][hapmap];0.80[TSI][hapmap];0.81[ASN][1000 genomes]
rs17748464	0.92[CEU][hapmap]
rs1905630	0.89[CEU][hapmap]
rs1905631	0.89[CEU][hapmap];0.85[JPT][hapmap]
rs1905633	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1905634	1.00[CEU][hapmap];0.81[CHD][hapmap];0.95[GIH][hapmap];0.86[JPT][hapmap];0.92[MEX][hapmap];0.87[TSI][hapmap];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2409623	0.91[AFR][1000 genomes];0.87[AMR][1000 genomes];0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs28380058	0.80[ASN][1000 genomes]
rs28660563	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs28701812	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs2898240	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4255142	0.82[CHB][hapmap];0.84[CHD][hapmap];0.81[JPT][hapmap]
rs4448276	0.85[CEU][hapmap];0.85[CHD][hapmap];0.84[MEX][hapmap]
rs57515357	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs60032918	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs60999585	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6601420	0.85[CEU][hapmap];0.80[AMR][1000 genomes]
rs6982806	0.96[CEU][hapmap];0.83[CHB][hapmap];0.91[CHD][hapmap];0.91[GIH][hapmap];0.84[MEX][hapmap];0.96[YRI][hapmap];0.85[AFR][1000 genomes];0.85[AMR][1000 genomes];0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6994636	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6996281	0.93[AMR][1000 genomes];0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs6997464	0.85[CEU][hapmap];0.89[GIH][hapmap];0.92[MEX][hapmap];0.84[TSI][hapmap];0.91[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7004224	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7006628	0.85[CEU][hapmap];0.82[CHD][hapmap];0.89[GIH][hapmap];0.84[MEX][hapmap];0.81[AMR][1000 genomes]
rs7009475	0.88[ASN][1000 genomes]
rs7011004	0.80[CEU][hapmap];0.86[CHB][hapmap];0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7011281	0.89[CEU][hapmap];0.81[CHB][hapmap];0.82[CHD][hapmap];0.93[GIH][hapmap];0.81[JPT][hapmap];0.92[MEX][hapmap];0.89[TSI][hapmap];0.84[AMR][1000 genomes];0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7011821	0.89[CEU][hapmap];0.82[CHD][hapmap];0.93[GIH][hapmap];0.81[JPT][hapmap];0.88[MEX][hapmap];0.89[TSI][hapmap];0.80[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7812517	0.89[CEU][hapmap];0.86[CHD][hapmap];0.93[GIH][hapmap];0.81[JPT][hapmap];0.83[MEX][hapmap];0.82[AMR][1000 genomes]
rs7820236	0.81[CEU][hapmap];0.81[CHB][hapmap];0.81[JPT][hapmap];0.85[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs7822181	0.81[AFR][1000 genomes];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7829478	0.89[CEU][hapmap];0.88[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7845503	0.89[CEU][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	nsv610263	chr8:9941021-10090149	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
2	nsv831230	chr8:9953343-10139350	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
3	nsv1027280	chr8:9958259-10058984	Enhancers Active TSS Genic enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv1021921	chr8:9958259-10212555	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv890344	chr8:9995515-10060638	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
6	nsv831231	chr8:10001214-10189094	Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	nsv1026335	chr8:10037279-10139782	Weak transcription Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs1484648	MORN3	trans	parietal	SCAN

Chromatin state (count:24 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:10050000-10057800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr8:10050000-10068000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr8:10050400-10054600	Weak transcription	HMEC	breast
4	chr8:10050400-10054600	Weak transcription	NHEK	skin
5	chr8:10050400-10055000	Weak transcription	HSMMtube	muscle
6	chr8:10050400-10058000	Weak transcription	Aorta	Aorta
7	chr8:10050600-10054800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr8:10050600-10055000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr8:10051600-10058400	Enhancers	Fetal Brain Male	brain
10	chr8:10052200-10054000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr8:10052200-10056200	Weak transcription	Brain Inferior Temporal Lobe	brain
12	chr8:10052400-10058000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr8:10053200-10054000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr8:10053400-10054200	Enhancers	Fetal Muscle Trunk	muscle
15	chr8:10053600-10054000	Enhancers	Primary neutrophils fromperipheralblood	blood
16	chr8:10053600-10054000	Enhancers	Brain Angular Gyrus	brain
17	chr8:10053600-10054600	Weak transcription	Fetal Brain Female	brain
18	chr8:10053600-10062400	Weak transcription	Pancreas	Pancrea
19	chr8:10053600-10065000	Weak transcription	Brain Germinal Matrix	brain
20	chr8:10053800-10054000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr8:10053800-10054800	Weak transcription	Brain Substantia Nigra	brain
22	chr8:10053800-10055000	Weak transcription	Left Ventricle	heart
23	chr8:10053800-10062400	Weak transcription	Liver	Liver
24	chr8:10053800-10087000	Weak transcription	Spleen	Spleen

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