Variant report

Variant	rs7903292
Chromosome Location	chr10:23130424-23130425
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs10734042	0.94[ASN][1000 genomes]
rs10741009	0.93[ASN][1000 genomes]
rs10741010	0.93[AFR][1000 genomes];0.82[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs10764346	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10764347	0.91[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs10764355	0.81[EUR][1000 genomes]
rs10764356	0.82[EUR][1000 genomes]
rs10764357	0.81[EUR][1000 genomes]
rs10764358	0.82[EUR][1000 genomes]
rs10828345	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10828346	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10828348	0.80[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11013151	0.84[ASN][1000 genomes]
rs11814688	0.81[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs35687987	0.81[AMR][1000 genomes]
rs67531879	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs7098978	0.94[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7899129	0.98[ASN][1000 genomes]
rs9988672	0.94[ASN][1000 genomes]

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	esv2764013	chr10:23087298-23239345	Enhancers Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
2	nsv894966	chr10:23090535-23202522	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:23122600-23131400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr10:23124000-23135000	Weak transcription	Brain Angular Gyrus	brain
3	chr10:23125400-23135000	Weak transcription	Brain Hippocampus Middle	brain
4	chr10:23126600-23137600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr10:23129000-23131000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
6	chr10:23129000-23133800	Weak transcription	Aorta	Aorta
7	chr10:23129200-23131000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
8	chr10:23129200-23131200	Weak transcription	HUES48 Cell Line	embryonic stem cell

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Input of quick search could be:

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

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