Variant report

Variant	rs62296870
Chromosome Location	chr4:19631392-19631393
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs10024291	0.82[ASN][1000 genomes]
rs10025939	0.82[ASN][1000 genomes]
rs10026163	0.82[ASN][1000 genomes]
rs10027111	0.89[ASN][1000 genomes]
rs10031839	0.89[ASN][1000 genomes]
rs11942433	0.85[AFR][1000 genomes];0.89[AMR][1000 genomes];0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17570085	0.89[ASN][1000 genomes]
rs17570168	0.81[AMR][1000 genomes];0.80[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2200748	0.89[ASN][1000 genomes]
rs28674625	0.89[ASN][1000 genomes]
rs4371613	0.82[ASN][1000 genomes]
rs4425370	0.89[ASN][1000 genomes]
rs4593130	0.89[ASN][1000 genomes]
rs62296887	0.81[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs62296905	0.85[AFR][1000 genomes];0.84[AMR][1000 genomes];0.80[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6846330	0.89[ASN][1000 genomes]
rs6846645	0.89[ASN][1000 genomes]
rs6848523	0.81[AMR][1000 genomes];0.80[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6853029	0.88[AFR][1000 genomes];0.89[AMR][1000 genomes];0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73099628	0.82[ASN][1000 genomes]
rs73249357	0.89[ASN][1000 genomes]
rs73249365	0.89[ASN][1000 genomes]
rs73249369	0.89[ASN][1000 genomes]
rs73249379	0.89[ASN][1000 genomes]
rs73249381	0.89[ASN][1000 genomes]
rs7665257	0.83[AFR][1000 genomes];0.82[AMR][1000 genomes]
rs7666136	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7667493	0.82[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs7681473	0.93[AFR][1000 genomes];0.80[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7682477	0.82[ASN][1000 genomes]
rs7682588	0.89[ASN][1000 genomes]
rs7686699	0.89[ASN][1000 genomes]
rs7691992	0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv878732	chr4:19172031-19660947	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv878733	chr4:19335464-19928602	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv461286	chr4:19488871-19709795	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
4	nsv593786	chr4:19488871-19709795	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
5	nsv829873	chr4:19582263-19742515	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv1001485	chr4:19585423-19655316	Enhancers Weak transcription Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv1013517	chr4:19611067-19655316	Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
8	esv3337676	chr4:19630260-19631884	Enhancers	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:19630800-19631600	Enhancers	Fetal Lung	lung
2	chr4:19630800-19632000	Enhancers	Fetal Kidney	kidney
3	chr4:19631200-19631800	Enhancers	Colon Smooth Muscle	Colon

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