Variant report

Variant	rs11120469
Chromosome Location	chr1:215205469-215205470
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs11120470	0.80[AFR][1000 genomes]
rs11120471	0.80[AFR][1000 genomes]
rs11120472	0.97[AFR][1000 genomes]
rs11120474	0.94[AFR][1000 genomes]
rs12061587	0.91[AFR][1000 genomes]
rs12062465	0.94[AFR][1000 genomes]
rs12066174	0.94[AFR][1000 genomes]
rs12069528	0.91[AFR][1000 genomes]
rs12069674	0.94[AFR][1000 genomes]
rs12078139	0.94[AFR][1000 genomes]
rs12082755	1.00[AFR][1000 genomes]
rs12084973	0.90[AFR][1000 genomes]
rs12087979	0.80[AFR][1000 genomes]
rs12088528	1.00[AFR][1000 genomes]
rs12089490	1.00[AFR][1000 genomes]
rs12092077	1.00[AFR][1000 genomes]
rs12096956	0.80[AFR][1000 genomes]
rs12097853	0.94[AFR][1000 genomes]

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	nsv468105	chr1:215167236-215248417	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv549182	chr1:215167236-215248417	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:215177200-215211200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr1:215198000-215206200	Weak transcription	Osteobl	bone
3	chr1:215199400-215206000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr1:215204800-215206600	Weak transcription	NHDF-Ad	bronchial

Quick Search:

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

what's new

Quick links