Variant report

Variant	rs9370284
Chromosome Location	chr6:54177403-54177404
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 30 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs1058768	0.90[ASN][1000 genomes]
rs1316576	0.96[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1353708	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs1508638	0.99[AMR][1000 genomes];0.92[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1605675	0.96[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1605676	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1813105	0.87[ASN][1000 genomes]
rs1848439	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1848440	0.83[ASN][1000 genomes]
rs1934791	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1995768	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs2202802	0.97[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2221666	0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs3777652	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs3798278	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs6458994	1.00[YRI][hapmap];0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs682088	0.99[AMR][1000 genomes];0.92[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7740868	0.94[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7740970	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7754752	0.97[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7760842	0.97[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7766669	0.85[AMR][1000 genomes]
rs9367561	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9367562	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs9370290	0.83[ASN][1000 genomes]
rs9382323	0.83[ASN][1000 genomes]
rs9474801	0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1067663	chr6:53796341-54449718	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv529158	chr6:53796341-54449718	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
3	nsv885888	chr6:54132353-54266032	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs9370284	TINAG	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:54173000-54178000	Active TSS	Fetal Intestine Large	intestine
2	chr6:54173000-54178200	Active TSS	Fetal Intestine Small	intestine
3	chr6:54176200-54177600	Weak transcription	Fetal Kidney	kidney
4	chr6:54176600-54191800	Weak transcription	Rectal Mucosa Donor 29	rectum
5	chr6:54176600-54191800	Weak transcription	Rectal Mucosa Donor 31	rectum

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