Variant report

Variant	rs11945137
Chromosome Location	chr4:141987607-141987608
allele	C/T
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]
rs11931760	0.90[AFR][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	nsv880167	chr4:141616979-142092124	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:141962400-141995400	Weak transcription	Ovary	ovary
2	chr4:141980600-141988600	Weak transcription	Colon Smooth Muscle	Colon
3	chr4:141984200-141994200	Weak transcription	Left Ventricle	heart
4	chr4:141984200-141994200	Weak transcription	Right Ventricle	heart
5	chr4:141985000-141994400	Weak transcription	Fetal Heart	heart
6	chr4:141987000-141988600	Enhancers	Pancreatic Islets	Pancreatic Islet
7	chr4:141987400-141994400	Weak transcription	Psoas Muscle	Psoas

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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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