Variant report

Variant	rs61570927
Chromosome Location	chr4:96272827-96272828
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs11937484	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1351772	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1542616	0.88[EUR][1000 genomes]
rs1843018	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2621439	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2621462	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2621463	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2626050	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2626051	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2626057	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2626062	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2626063	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2626069	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4699419	0.84[EUR][1000 genomes]
rs56184934	0.93[EUR][1000 genomes]
rs56219612	0.88[EUR][1000 genomes]
rs56663807	0.93[EUR][1000 genomes]
rs56916207	0.93[EUR][1000 genomes]
rs58809210	0.93[EUR][1000 genomes]
rs59179643	0.93[EUR][1000 genomes]
rs61076479	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs62307079	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6532550	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6846883	0.88[EUR][1000 genomes]
rs6856212	0.93[EUR][1000 genomes]
rs72659904	0.93[EUR][1000 genomes]
rs7436599	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7440986	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7441683	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869528	chr4:95537649-96368018	Weak transcription Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
2	nsv1001955	chr4:96216118-96445841	Enhancers Weak transcription Bivalent Enhancer Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:96239600-96284400	Weak transcription	Aorta	Aorta
2	chr4:96264200-96273000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr4:96264400-96283600	Weak transcription	Fetal Stomach	stomach
4	chr4:96272200-96273600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr4:96272200-96273600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
6	chr4:96272200-96274000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr4:96272400-96282400	Weak transcription	Brain Inferior Temporal Lobe	brain

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