Variant report

Variant	rs185892236
Chromosome Location	chr7:128704939-128704940
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 2 )
Associated
traits (count: 0)

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	esv1829719	chr7:128602992-128810971	Enhancers Flanking Active TSS Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
2	nsv5947	chr7:128704900-128749885	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:128695800-128706200	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr7:128696200-128706400	Weak transcription	Right Atrium	heart
3	chr7:128696600-128706200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr7:128703200-128706800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
5	chr7:128703800-128705800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr7:128704600-128705200	Enhancers	Monocytes-CD14+_RO01746	blood
7	chr7:128704600-128705800	Enhancers	Fetal Intestine Large	intestine
8	chr7:128704800-128705600	Enhancers	GM12878-XiMat	blood
9	chr7:128704800-128706000	Enhancers	K562	blood

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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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