Variant report

Variant	rs10832612
Chromosome Location	chr11:16491212-16491213
allele	C/T
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:2)

rs_ID	r²[population]
rs11023956	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4582933	0.84[AMR][1000 genomes];0.98[ASN][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	nsv553566	chr11:16329009-16799044	Strong transcription Weak transcription Enhancers Bivalent/Poised TSS ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
2	nsv897016	chr11:16455794-16691743	Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:16461600-16510000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr11:16480800-16497000	Weak transcription	Left Ventricle	heart
3	chr11:16480800-16497800	Weak transcription	Skeletal Muscle Male	skeletal muscle
4	chr11:16489800-16492000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr11:16490000-16492400	Enhancers	Adipose Nuclei	Adipose
6	chr11:16490400-16491800	Enhancers	Skeletal Muscle Female	skeletal muscle
7	chr11:16490600-16491600	Weak transcription	Fetal Lung	lung
8	chr11:16490600-16492400	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr11:16490800-16492200	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr11:16490800-16492400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr11:16490800-16492400	Enhancers	HUES64 Cell Line	embryonic stem cell
12	chr11:16491000-16492000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr11:16491000-16492000	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chr11:16491000-16492200	Enhancers	iPS-20b Cell Line	embryonic stem cell
15	chr11:16491000-16492400	Enhancers	Cortex derived primary cultured neurospheres	brain
16	chr11:16491200-16491800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr11:16491200-16492600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr11:16491200-16494000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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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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