Variant report

Variant	rs11983151
Chromosome Location	chr7:116879802-116879803
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs10265828	1.00[EUR][1000 genomes]
rs11980583	1.00[EUR][1000 genomes]
rs11981502	1.00[EUR][1000 genomes]
rs17139469	1.00[EUR][1000 genomes]
rs2106627	1.00[EUR][1000 genomes]
rs4430033	1.00[EUR][1000 genomes]
rs4730767	1.00[EUR][1000 genomes]
rs60356864	1.00[EUR][1000 genomes]
rs60412272	1.00[EUR][1000 genomes]
rs6967851	1.00[EUR][1000 genomes]
rs73470843	1.00[EUR][1000 genomes]
rs73714631	1.00[EUR][1000 genomes]
rs73714633	1.00[EUR][1000 genomes]
rs73714637	1.00[EUR][1000 genomes]
rs7804397	1.00[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	nsv831108	chr7:116749534-116952011	Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:116879800-116880200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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