Variant report

Variant	rs60730410
Chromosome Location	chr7:122193089-122193090
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs11768210	0.84[ASN][1000 genomes]
rs12668581	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2058264	0.84[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2191276	0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2430023	0.83[EUR][1000 genomes]
rs3808171	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs55728082	0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs56326140	0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs61594727	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs61692498	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs73218224	0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs73218225	0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs73218228	0.90[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs73218230	0.84[AFR][1000 genomes];0.92[AMR][1000 genomes];0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs73218231	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs73218232	0.84[AFR][1000 genomes];0.92[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs73218233	0.84[AFR][1000 genomes];0.92[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs73218235	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs73218236	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs740812	0.94[ASN][1000 genomes]
rs740813	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7786557	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1017029	chr7:121958574-122338623	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	esv3326794	chr7:122186590-122196256	Enhancers Weak transcription Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:122184400-122226000	Weak transcription	Left Ventricle	heart
2	chr7:122184600-122197400	Weak transcription	Lung	lung
3	chr7:122184800-122197200	Weak transcription	Pancreas	Pancrea
4	chr7:122187800-122196200	Weak transcription	Duodenum Mucosa	Duodenum
5	chr7:122188200-122194000	Weak transcription	Liver	Liver
6	chr7:122189000-122196600	Weak transcription	Colon Smooth Muscle	Colon
7	chr7:122192400-122193200	Enhancers	Fetal Heart	heart
8	chr7:122192400-122194400	Strong transcription	Fetal Lung	lung
9	chr7:122192600-122196800	Weak transcription	Stomach Smooth Muscle	stomach
10	chr7:122192800-122196600	Weak transcription	Duodenum Smooth Muscle	Duodenum
11	chr7:122193000-122193200	Enhancers	Placenta Amnion	Placenta Amnion

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