Variant report

Variant	rs6699778
Chromosome Location	chr1:215253661-215253662
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs10779637	0.88[ASN][1000 genomes]
rs11120483	0.80[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs11120486	0.94[ASN][1000 genomes]
rs12088480	0.92[ASN][1000 genomes]
rs12092312	0.94[ASN][1000 genomes]
rs12092515	0.92[ASN][1000 genomes]
rs12136349	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1377184	0.91[EUR][1000 genomes]
rs28545309	0.94[ASN][1000 genomes]
rs66943143	0.94[ASN][1000 genomes]
rs67098096	0.92[ASN][1000 genomes]
rs7522445	0.94[ASN][1000 genomes]
rs7528306	0.92[ASN][1000 genomes]
rs7528988	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][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	esv2754411	chr1:215235605-215281605	Bivalent/Poised TSS Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	1 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	chr1:215252600-215254200	Enhancers	NHDF-Ad	bronchial
2	chr1:215253400-215254400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr1:215253400-215255000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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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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