Variant report

Variant	rs7933648
Chromosome Location	chr11:106825968-106825969
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs17574845	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17650405	1.00[AFR][1000 genomes]
rs17653598	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17654146	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7101706	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7104886	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7117556	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7119611	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7122744	1.00[AMR][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	nsv531938	chr11:106760733-107156814	Enhancers Bivalent/Poised TSS Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
2	esv1818906	chr11:106786428-106831384	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Active TSS	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:106807400-106826600	Weak transcription	Fetal Lung	lung
2	chr11:106808000-106827800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
3	chr11:106809000-106830400	Weak transcription	Fetal Muscle Leg	muscle
4	chr11:106821200-106827600	Weak transcription	Fetal Muscle Trunk	muscle
5	chr11:106821400-106827600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr11:106822000-106829600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr11:106822200-106827800	Weak transcription	Fetal Heart	heart
8	chr11:106825400-106836200	Weak transcription	Fetal Brain Male	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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