Variant report

Variant	rs1749323
Chromosome Location	chr10:95914097-95914098
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs1228531	1.00[AMR][1000 genomes]
rs1346045	1.00[AMR][1000 genomes]
rs1749324	1.00[AMR][1000 genomes]
rs2689696	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2689701	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2764342	1.00[AMR][1000 genomes]
rs2949003	1.00[AMR][1000 genomes]
rs57730765	1.00[AMR][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	nsv1036676	chr10:95851376-96103876	Strong transcription Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:95906000-95924800	Weak transcription	A549	lung
2	chr10:95906400-95914600	Weak transcription	Fetal Intestine Small	intestine
3	chr10:95906400-95930800	Weak transcription	Fetal Stomach	stomach
4	chr10:95906800-95930800	Weak transcription	Cortex derived primary cultured neurospheres	brain
5	chr10:95906800-95931200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr10:95908200-95915800	Weak transcription	Right Atrium	heart
7	chr10:95911000-95915200	Weak transcription	Left Ventricle	heart
8	chr10:95911000-95915800	Weak transcription	HSMMtube	muscle

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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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