Variant report

Variant	rs7914010
Chromosome Location	chr10:89860428-89860429
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 6 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs10160194	0.88[ASN][1000 genomes]
rs10788582	0.96[CEU][hapmap];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs10887784	0.90[CHB][hapmap];0.86[JPT][hapmap]
rs1360952	0.84[ASN][1000 genomes]
rs6586120	0.82[CEU][hapmap];0.95[AMR][1000 genomes];0.93[EUR][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	nsv831940	chr10:89811247-89989199	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:89853800-89860800	Weak transcription	GM12878-XiMat	blood
2	chr10:89856000-89864800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr10:89857000-89860800	Weak transcription	Muscle Satellite Cultured Cells	--
4	chr10:89858400-89861000	Weak transcription	Primary B cells from cord blood	blood
5	chr10:89858600-89863200	Weak transcription	Primary monocytes fromperipheralblood	blood
6	chr10:89859200-89861400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
7	chr10:89860000-89861600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr10:89860200-89860600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr10:89860200-89861000	Enhancers	NHDF-Ad	bronchial
10	chr10:89860400-89861000	Weak transcription	NHLF	lung
11	chr10:89860400-89861400	Enhancers	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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