Variant report

Variant	rs11931644
Chromosome Location	chr4:78335732-78335733
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 5 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs10021560	0.89[ASN][1000 genomes]
rs12643983	0.81[ASN][1000 genomes]
rs4859836	0.89[ASN][1000 genomes]
rs7690027	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	nsv829974	chr4:78240718-78415642	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:78333400-78336000	Enhancers	Fetal Muscle Leg	muscle
2	chr4:78334200-78336200	Enhancers	Fetal Stomach	stomach
3	chr4:78334400-78335800	Weak transcription	Fetal Muscle Trunk	muscle
4	chr4:78334800-78335800	Enhancers	Fetal Lung	lung
5	chr4:78335000-78336000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
6	chr4:78335600-78336000	Enhancers	Fetal Intestine Small	intestine

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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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