Variant report

Variant	rs10018047
Chromosome Location	chr4:173971614-173971615
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

rSNPs within LD-proxies of this variant (count:1)

rs_ID	r²[population]
rs10017507	1.00[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949126	chr4:173466221-174051451	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:173961800-173972800	Weak transcription	Aorta	Aorta
2	chr4:173962000-173972200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
3	chr4:173968400-173972400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr4:173968400-173972800	Weak transcription	HSMMtube	muscle
5	chr4:173968400-173977200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr4:173968600-173972200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr4:173968800-173972400	Weak transcription	Fetal Muscle Leg	muscle
8	chr4:173970600-173972200	Weak transcription	HUES64 Cell Line	embryonic stem cell
9	chr4:173971200-173972000	Weak transcription	HUES48 Cell Line	embryonic stem cell
10	chr4:173971200-173975400	Weak transcription	Stomach Mucosa	stomach

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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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