Variant report

Variant	rs73515153
Chromosome Location	chr11:83535790-83535791
allele	A/C/G/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:3)

rs_ID	r²[population]
rs61177004	0.82[AFR][1000 genomes]
rs61546028	0.94[AFR][1000 genomes]
rs73515149	0.86[AFR][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	esv14634	chr11:83532806-83538775	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:83527800-83539200	Weak transcription	Brain Angular Gyrus	brain
2	chr11:83529800-83537800	Weak transcription	Muscle Satellite Cultured Cells	--
3	chr11:83531000-83536800	Weak transcription	Brain Substantia Nigra	brain
4	chr11:83535000-83537800	Weak transcription	NH-A	brain
5	chr11:83535000-83538800	Weak transcription	Brain Inferior Temporal Lobe	brain
6	chr11:83535000-83546600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr11:83535200-83536600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr11:83535200-83536600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr11:83535200-83537200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr11:83535400-83539000	Weak transcription	Brain Cingulate Gyrus	brain
11	chr11:83535600-83538800	Weak transcription	Brain Hippocampus Middle	brain

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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