Variant report

Variant	rs934902
Chromosome Location	chr10:92769529-92769530
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 2 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:1)

rs_ID	r²[population]
rs7897249	0.84[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	nsv831945	chr10:92590576-92793582	Active TSS Enhancers Flanking Active TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:92761800-92782800	Weak transcription	Aorta	Aorta
2	chr10:92765200-92770000	Enhancers	Fetal Thymus	thymus
3	chr10:92766800-92769600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr10:92767200-92770600	Weak transcription	Osteobl	bone
5	chr10:92767400-92781400	Weak transcription	HSMM	muscle
6	chr10:92768000-92770000	Enhancers	Dnd41	blood
7	chr10:92768200-92769600	Weak transcription	Brain Substantia Nigra	brain
8	chr10:92768600-92769800	Enhancers	Fetal Muscle Leg	muscle
9	chr10:92768600-92770000	Enhancers	Breast Myoepithelial Primary Cells	Breast
10	chr10:92768800-92769600	Enhancers	Brain Anterior Caudate	brain
11	chr10:92768800-92769800	Enhancers	Primary B cells from peripheral blood	blood
12	chr10:92769200-92769600	Flanking Active TSS	GM12878-XiMat	blood

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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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