Variant report

Variant	rs7110141
Chromosome Location	chr11:86132413-86132414
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 4 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs11234634	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6592290	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7928674	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7935933	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:86106600-86134600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr11:86108600-86138600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr11:86117800-86142200	Weak transcription	Fetal Stomach	stomach
4	chr11:86118200-86151000	Weak transcription	Skeletal Muscle Female	skeletal muscle
5	chr11:86118400-86142800	Weak transcription	Left Ventricle	heart
6	chr11:86119400-86135000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr11:86119600-86142200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr11:86122600-86133400	Weak transcription	Ovary	ovary
9	chr11:86123600-86136800	Weak transcription	Brain Hippocampus Middle	brain
10	chr11:86124600-86142200	Weak transcription	Aorta	Aorta
11	chr11:86124800-86136600	Weak transcription	Brain Anterior Caudate	brain
12	chr11:86127800-86133200	Weak transcription	K562	blood
13	chr11:86128200-86133200	Weak transcription	Fetal Intestine Large	intestine
14	chr11:86130400-86134600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr11:86131200-86133000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr11:86131400-86142400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr11:86131600-86133400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr11:86131600-86136000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr11:86132200-86142200	Weak transcription	Spleen	Spleen

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