Variant report

Variant	rs7326700
Chromosome Location	chr13:30044351-30044352
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 5 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs3013639	0.87[JPT][hapmap]
rs4390442	0.87[JPT][hapmap]
rs9508464	0.87[JPT][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	nsv427927	chr13:29729315-30062054	Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv983696	chr13:30034016-30090454	Enhancers Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:30015200-30054800	Weak transcription	Dnd41	blood
2	chr13:30040000-30054200	Weak transcription	Aorta	Aorta
3	chr13:30040400-30052800	Weak transcription	Left Ventricle	heart
4	chr13:30040600-30045600	Weak transcription	K562	blood
5	chr13:30040600-30053400	Weak transcription	Right Ventricle	heart
6	chr13:30041400-30054000	Weak transcription	Fetal Muscle Leg	muscle
7	chr13:30041600-30045800	Weak transcription	Fetal Muscle Trunk	muscle
8	chr13:30042000-30045800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr13:30042200-30045600	Weak transcription	Primary monocytes fromperipheralblood	blood
10	chr13:30042200-30046000	Weak transcription	Primary hematopoietic stem cells	blood
11	chr13:30042400-30045600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
12	chr13:30043400-30046000	Weak transcription	Monocytes-CD14+_RO01746	blood
13	chr13:30044200-30044400	Genic enhancers	Fetal Heart	heart

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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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