Variant report

Variant	rs10779630
Chromosome Location	chr1:215094706-215094707
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs10399921	0.94[ASN][1000 genomes]
rs10864141	0.86[ASN][1000 genomes]
rs11120444	0.95[ASN][1000 genomes]
rs11120450	0.85[ASN][1000 genomes]
rs12022738	0.80[ASN][1000 genomes]
rs12025511	0.94[ASN][1000 genomes]
rs12045695	0.84[ASN][1000 genomes]
rs1377178	0.95[ASN][1000 genomes]
rs17042163	0.85[ASN][1000 genomes]
rs472961	0.82[AMR][1000 genomes]
rs476910	0.82[AMR][1000 genomes]
rs478664	0.82[AMR][1000 genomes]
rs494808	0.82[AMR][1000 genomes]
rs506436	0.82[AMR][1000 genomes]
rs520394	0.81[AMR][1000 genomes]
rs554343	0.83[AMR][1000 genomes]
rs6540871	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72743806	0.85[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv873167	chr1:214950361-215116947	Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:215085800-215097800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr1:215092800-215096400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr1:215093600-215095200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr1:215094400-215094800	Enhancers	NHEK	skin
5	chr1:215094400-215095600	Enhancers	HMEC	breast
6	chr1:215094600-215095200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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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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