Variant report

Variant	rs6929731
Chromosome Location	chr6:145624624-145624625
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs1396645	1.00[EUR][1000 genomes]
rs4566900	1.00[EUR][1000 genomes]
rs59400283	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59536308	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59839423	1.00[EUR][1000 genomes]
rs6899864	1.00[EUR][1000 genomes]
rs73559143	1.00[EUR][1000 genomes]
rs73559156	1.00[EUR][1000 genomes]
rs73560914	1.00[EUR][1000 genomes]
rs73562162	1.00[EUR][1000 genomes]
rs73575448	1.00[EUR][1000 genomes]
rs7742823	1.00[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	nsv1022965	chr6:145374851-145635385	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:145623800-145625600	Enhancers	Stomach Mucosa	stomach
2	chr6:145624200-145625600	Enhancers	Pancreatic Islets	Pancreatic Islet
3	chr6:145624400-145625600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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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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