Variant report

Variant	rs146212719
Chromosome Location	chr11:71910975-71910976
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 3 )
Associated
traits (count: 0)

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	nsv530623	chr11:71088949-72020418	Enhancers Transcr. at gene 5' and 3' Active TSS Strong transcription Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	134 gene(s)	inside rSNPs	diseases
2	esv3322828	chr11:71910304-71914502	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
3	esv1118262	chr11:71910975-71910977	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:71906200-71912200	Enhancers	Placenta	Placenta
2	chr11:71907400-71911200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr11:71909800-71911000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
4	chr11:71910000-71911000	Enhancers	Primary monocytes fromperipheralblood	blood
5	chr11:71910600-71914000	Weak transcription	Hela-S3	cervix
6	chr11:71910600-71915200	Weak transcription	Monocytes-CD14+_RO01746	blood

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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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