Variant report

Variant	rs62307199
Chromosome Location	chr4:96559218-96559219
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs10018665	1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10021321	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11097476	1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1436571	0.93[AMR][1000 genomes];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17581436	0.84[AMR][1000 genomes]
rs62306733	0.90[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs62307193	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62307200	1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[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	nsv830012	chr4:96547783-96746163	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	esv1844506	chr4:96554889-96704333	Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv1007133	chr4:96556072-96614235	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:96550400-96560000	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr4:96558200-96561600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr4:96558400-96561800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr4:96558600-96559600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr4:96558600-96559800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr4:96558600-96559800	Weak transcription	Brain Cingulate Gyrus	brain
7	chr4:96558600-96560000	Weak transcription	Brain Substantia Nigra	brain
8	chr4:96558600-96560200	Weak transcription	Brain Anterior Caudate	brain
9	chr4:96558600-96560200	Weak transcription	Brain Inferior Temporal Lobe	brain
10	chr4:96558600-96560400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr4:96558600-96561600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr4:96558600-96561800	Weak transcription	HUES48 Cell Line	embryonic stem cell
13	chr4:96558600-96561800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
14	chr4:96558600-96561800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
15	chr4:96558800-96560000	Weak transcription	HMEC	breast
16	chr4:96559200-96559800	Enhancers	Dnd41	blood

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

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