Variant report

Variant	rs11012573
Chromosome Location	chr10:18370496-18370497
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs10764297	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs11012314	0.85[CEU][hapmap]
rs11012333	0.85[CEU][hapmap]
rs11012350	0.85[CEU][hapmap]
rs11012579	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12256910	0.84[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs12355062	0.85[CEU][hapmap]
rs12358478	0.85[CEU][hapmap]
rs12358488	0.85[CEU][hapmap]
rs16916785	0.85[CEU][hapmap]
rs16916787	0.85[CEU][hapmap]
rs16916794	0.85[CEU][hapmap]
rs7893893	0.85[CEU][hapmap]
rs7921720	0.85[CEU][hapmap]

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	nsv550039	chr10:18363924-18425519	Enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv550040	chr10:18365380-18399519	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv1045547	chr10:18366749-18397247	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:18369000-18371600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr10:18369000-18374400	Weak transcription	Fetal Lung	lung
3	chr10:18369000-18374600	Weak transcription	Fetal Stomach	stomach
4	chr10:18369800-18372200	Weak transcription	Brain Cingulate Gyrus	brain
5	chr10:18370000-18371200	Weak transcription	Fetal Heart	heart
6	chr10:18370200-18372400	Weak transcription	Brain Anterior Caudate	brain

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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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