Variant report

Variant	rs2103030
Chromosome Location	chr7:99404234-99404235
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs1036374	0.91[EUR][1000 genomes]
rs17161937	0.91[EUR][1000 genomes]
rs1851426	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2023548	0.91[EUR][1000 genomes]
rs2461610	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2687105	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2687116	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2738262	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2740566	0.81[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2740574	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28988583	0.86[EUR][1000 genomes]
rs4281055	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs667660	0.85[AFR][1000 genomes]
rs73393660	0.91[EUR][1000 genomes]
rs892753	0.91[EUR][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	esv1827709	chr7:99353500-99440051	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:99403600-99404400	Enhancers	Dnd41	blood
2	chr7:99404200-99405800	Flanking Active TSS	K562	blood

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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