Variant report

Variant	rs953372
Chromosome Location	chr9:72615869-72615870
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 55 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs1027283	0.94[ASN][1000 genomes]
rs1027284	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10735572	0.88[ASN][1000 genomes]
rs10780718	0.88[ASN][1000 genomes]
rs10780724	0.88[ASN][1000 genomes]
rs10868291	0.88[ASN][1000 genomes]
rs10868299	0.89[ASN][1000 genomes]
rs10868327	0.87[AFR][1000 genomes];0.89[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10868358	0.86[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10868378	0.94[ASN][1000 genomes]
rs1121607	0.88[ASN][1000 genomes]
rs1121608	0.88[ASN][1000 genomes]
rs1389125	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1473520	0.96[ASN][1000 genomes]
rs1493046	0.85[ASN][1000 genomes]
rs1493047	0.88[ASN][1000 genomes]
rs1542769	0.94[ASN][1000 genomes]
rs1586914	0.88[ASN][1000 genomes]
rs1873825	0.90[ASN][1000 genomes]
rs1907956	0.88[ASN][1000 genomes]
rs1907959	0.88[ASN][1000 genomes]
rs2035922	0.90[ASN][1000 genomes]
rs2975859	0.94[ASN][1000 genomes]
rs2975860	0.94[ASN][1000 genomes]
rs2975926	0.93[ASN][1000 genomes]
rs3015226	0.94[ASN][1000 genomes]
rs4403478	0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4413835	0.94[ASN][1000 genomes]
rs4418399	0.88[AFR][1000 genomes];0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4445287	0.95[JPT][hapmap];0.94[ASN][1000 genomes]
rs4487845	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4490905	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4574911	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4636269	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4744583	0.88[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4744584	0.94[ASN][1000 genomes]
rs7019025	0.90[ASN][1000 genomes]
rs7023406	0.93[ASN][1000 genomes]
rs7025044	0.88[ASN][1000 genomes]
rs7029606	0.88[ASN][1000 genomes]
rs7035415	0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7037671	0.88[ASN][1000 genomes]
rs7847934	0.88[ASN][1000 genomes]
rs7863165	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7863229	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs870011	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs902964	0.92[ASN][1000 genomes]
rs931500	0.96[ASN][1000 genomes]
rs996375	0.88[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	nsv893438	chr9:72363992-72720438	Weak transcription Enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
2	nsv831612	chr9:72473778-72634253	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv1049457	chr9:72539144-72765913	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv1035668	chr9:72555053-72632796	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	nsv1051004	chr9:72557761-72632015	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
6	nsv831613	chr9:72586058-72740061	Weak transcription Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs953372	MAMDC2	cis	parietal	SCAN
rs953372	PGM5	cis	cerebellum	SCAN

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:72612400-72619200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr9:72612400-72622600	Weak transcription	NHEK	skin
3	chr9:72612800-72620800	Weak transcription	Colon Smooth Muscle	Colon
4	chr9:72613400-72618600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr9:72614600-72618600	Weak transcription	HSMMtube	muscle
6	chr9:72614800-72618800	Weak transcription	Fetal Lung	lung
7	chr9:72615400-72616200	Enhancers	Cortex derived primary cultured neurospheres	brain

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