Variant report

Variant	rs1003757
Chromosome Location	chr2:234829869-234829870
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs1003756	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.90[TSI][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10170647	0.86[CEU][hapmap]
rs10180847	0.83[GIH][hapmap]
rs10203291	1.00[CEU][hapmap];0.85[EUR][1000 genomes]
rs10490013	0.86[CEU][hapmap]
rs10519356	1.00[CEU][hapmap];0.89[GIH][hapmap];0.85[EUR][1000 genomes]
rs10803664	0.86[CEU][hapmap]
rs11562975	0.86[CEU][hapmap]
rs11563212	0.86[CEU][hapmap]
rs12466401	0.86[CEU][hapmap]
rs12476852	0.86[CEU][hapmap]
rs17863851	0.86[CEU][hapmap]
rs17864744	0.86[CEU][hapmap]
rs2017655	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2108806	1.00[CEU][hapmap];0.89[GIH][hapmap];0.87[TSI][hapmap];0.81[EUR][1000 genomes]
rs2108807	1.00[CEU][hapmap];0.89[GIH][hapmap];0.81[EUR][1000 genomes]
rs4497869	0.86[CEU][hapmap]
rs4663344	0.86[CEU][hapmap]
rs4663345	0.86[CEU][hapmap]
rs4663984	0.97[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4663985	0.86[CEU][hapmap]
rs4663987	0.83[GIH][hapmap]
rs4663991	0.86[CEU][hapmap]
rs6712540	0.86[CEU][hapmap]
rs735551	0.86[CEU][hapmap]
rs735552	1.00[CEU][hapmap];0.83[GIH][hapmap]
rs737635	0.86[CEU][hapmap]
rs7569987	0.86[CEU][hapmap]
rs7577157	0.86[CEU][hapmap];0.91[CHB][hapmap];0.82[CHD][hapmap];0.90[GIH][hapmap];0.95[JPT][hapmap];0.89[MEX][hapmap]
rs7582832	1.00[CEU][hapmap];0.85[EUR][1000 genomes]
rs7595960	0.86[CEU][hapmap];0.91[CHB][hapmap];0.82[CHD][hapmap];0.87[GIH][hapmap];0.95[JPT][hapmap];0.83[MEX][hapmap]

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	nsv1013712	chr2:234558457-235495825	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
2	nsv532476	chr2:234595695-235134381	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:234826200-234830000	Weak transcription	Brain Germinal Matrix	brain
2	chr2:234827600-234834000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr2:234827800-234833600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr2:234829800-234830000	Enhancers	Cortex derived primary cultured neurospheres	brain

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