Variant report

Variant	rs17156638
Chromosome Location	chr10:45068656-45068657
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 4 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs12416165	0.98[ASN][1000 genomes]
rs17156655	0.98[ASN][1000 genomes]
rs7918194	0.97[ASN][1000 genomes]

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	esv2422287	chr10:45044161-45257684	Active TSS Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 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	chr10:45044600-45070200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr10:45065800-45070400	Weak transcription	Fetal Muscle Trunk	muscle
3	chr10:45065800-45072400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr10:45066200-45072000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr10:45066800-45071600	Weak transcription	Fetal Muscle Leg	muscle
6	chr10:45067200-45072000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr10:45067600-45071800	Weak transcription	Muscle Satellite Cultured Cells	--
8	chr10:45067600-45071800	Weak transcription	NHDF-Ad	bronchial
9	chr10:45068000-45071600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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