Variant report

Variant	rs6745941
Chromosome Location	chr2:39780559-39780560
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs12712645	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12994521	0.81[EUR][1000 genomes]
rs13015976	0.93[EUR][1000 genomes]
rs1405085	0.93[EUR][1000 genomes]
rs1526027	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2241162	0.84[AMR][1000 genomes]
rs34677610	0.89[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs4670944	0.94[EUR][1000 genomes]
rs6740771	0.91[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs71439259	0.94[EUR][1000 genomes]
rs714855	0.83[AMR][1000 genomes]
rs7586289	0.89[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs7608399	0.83[AMR][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	nsv833858	chr2:39684483-39856498	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 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	chr2:39762200-39785000	Weak transcription	HSMMtube	muscle
2	chr2:39770800-39789600	Weak transcription	Left Ventricle	heart
3	chr2:39778000-39788000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr2:39778400-39791800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr2:39778800-39797400	Weak transcription	Fetal Heart	heart
6	chr2:39780400-39783200	Weak transcription	HepG2	liver

Quick Search:

Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

what's new

Quick links