Variant report

Variant	rs7302200
Chromosome Location	chr12:56449435-56449436
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 23 )
Associated
traits (count: 6 )

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs10876866	0.96[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1689510	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1701704	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1702877	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2017445	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2292239	0.82[EUR][1000 genomes]
rs2456973	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2640562	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2640564	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs34415530	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs3741499	0.85[EUR][1000 genomes]
rs4759229	0.85[EUR][1000 genomes]
rs61938962	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs61938963	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs705696	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs705704	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs705705	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs772921	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs877636	0.82[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1051961	chr12:56262220-56629427	Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	284 gene(s)	inside rSNPs	diseases
2	nsv832424	chr12:56275226-56466917	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	121 gene(s)	inside rSNPs	diseases
3	nsv1043988	chr12:56348185-56534900	Weak transcription Flanking Active TSS Enhancers Genic enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	189 gene(s)	inside rSNPs	diseases
4	nsv832427	chr12:56392545-56512774	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	152 gene(s)	inside rSNPs	diseases

mRNA abundance (count:6)

SNP	Gene	Cis/trans	Tissue	Source
rs7302200	AC034102.1	cis	Muscle Skeletal	GTEx
rs7302200	RPS26	cis	multi-tissue	Pritchard
rs7302200	LOC644166///LOC644191///LOC728937///RPS26	Cis_1M	lymphoblastoid	RTeQTL
rs7302200	RAB5B	cis	Muscle Skeletal	GTEx
rs7302200	DEFB124	trans	lymphoblastoid	RTeQTL
rs7302200	SUOX	cis	Thyroid	GTEx

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:56437000-56472800	Weak transcription	Right Atrium	heart
2	chr12:56437800-56450000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr12:56439600-56449600	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr12:56440800-56454000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr12:56440800-56455600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr12:56445400-56449600	Enhancers	Placenta	Placenta
7	chr12:56449000-56450200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr12:56449000-56453800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr12:56449000-56454000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr12:56449000-56454000	Weak transcription	HMEC	breast
11	chr12:56449000-56454000	Weak transcription	NHEK	skin
12	chr12:56449200-56449600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
13	chr12:56449200-56456400	Weak transcription	Muscle Satellite Cultured Cells	--
14	chr12:56449400-56454000	Weak transcription	Osteobl	bone

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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