Variant report

Variant	rs4747345
Chromosome Location	chr10:18712352-18712353
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs11593522	1.00[CHB][hapmap];0.86[CHD][hapmap];0.82[GIH][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs1325990	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[YRI][hapmap];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1575835	0.92[CEU][hapmap]
rs4748463	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6482385	0.89[CEU][hapmap];0.85[EUR][1000 genomes]
rs7074010	0.93[ASW][hapmap];0.96[CEU][hapmap];0.83[CHD][hapmap];0.87[MEX][hapmap];0.95[TSI][hapmap];0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7908861	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[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	nsv550042	chr10:18683267-18994583	ZNF genes & repeats Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
2	nsv1053675	chr10:18703895-18722912	Enhancers Weak transcription Flanking Active TSS Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:18690200-18713000	Weak transcription	Ovary	ovary
2	chr10:18692000-18712600	Weak transcription	Cortex derived primary cultured neurospheres	brain
3	chr10:18703600-18732000	Weak transcription	Pancreas	Pancrea
4	chr10:18707800-18713000	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr10:18707800-18713000	Weak transcription	Left Ventricle	heart
6	chr10:18708000-18713000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr10:18708000-18713200	Weak transcription	HUES64 Cell Line	embryonic stem cell
8	chr10:18710800-18715200	Enhancers	Fetal Heart	heart
9	chr10:18711200-18713000	Weak transcription	Pancreatic Islets	Pancreatic Islet
10	chr10:18711400-18713400	Enhancers	Placenta	Placenta
11	chr10:18712200-18712600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
12	chr10:18712200-18713200	Enhancers	Stomach Smooth Muscle	stomach
13	chr10:18712200-18713400	Enhancers	Right Ventricle	heart
14	chr10:18712200-18713600	Enhancers	Brain Anterior Caudate	brain

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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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