Variant report

Variant	rs11032479
Chromosome Location	chr11:34013535-34013536
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11032478	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11603098	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12280158	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12281999	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12282130	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12283374	0.95[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12417112	0.80[AFR][1000 genomes]
rs7102479	0.95[AMR][1000 genomes];0.86[EUR][1000 genomes]

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:34006400-34018200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr11:34012800-34013600	Enhancers	Primary T helper cells fromperipheralblood	blood
3	chr11:34012800-34013600	Enhancers	Fetal Thymus	thymus
4	chr11:34013400-34013600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr11:34013400-34018400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
6	chr11:34013400-34018800	Weak transcription	Dnd41	blood

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