Variant report

Variant	rs7127750
Chromosome Location	chr11:60068076-60068077
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 6 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs10750930	0.82[ASN][1000 genomes]
rs1365246	0.81[ASN][1000 genomes]
rs2194962	0.82[ASN][1000 genomes]
rs4644658	0.82[ASN][1000 genomes]
rs7104122	0.81[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	nsv832174	chr11:59909267-60073908	Enhancers ZNF genes & repeats Weak transcription Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:60056800-60069000	Weak transcription	Placenta	Placenta
2	chr11:60058000-60074800	Weak transcription	Primary hematopoietic stem cells	blood
3	chr11:60059200-60078400	Weak transcription	Primary B cells from cord blood	blood
4	chr11:60066600-60068600	Weak transcription	Primary monocytes fromperipheralblood	blood
5	chr11:60066800-60068200	Weak transcription	Monocytes-CD14+_RO01746	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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