Variant report

Variant	rs36084087
Chromosome Location	chr4:27122283-27122284
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs11727911	0.84[EUR][1000 genomes]
rs12503097	0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs13108236	0.83[EUR][1000 genomes]
rs13113425	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs35241736	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs35281978	0.84[EUR][1000 genomes]
rs4234985	0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4501207	0.81[ASN][1000 genomes]
rs4692163	0.86[EUR][1000 genomes]
rs55833139	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6844289	0.88[EUR][1000 genomes]
rs741130	0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs741137	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs757632	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs759113	0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7696691	0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1002082	chr4:27078850-27377252	Flanking Bivalent TSS/Enh Weak transcription Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv997608	chr4:27085524-27371848	Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv999134	chr4:27115301-27270500	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:27117400-27122800	Weak transcription	HUES48 Cell Line	embryonic stem cell
2	chr4:27117400-27123600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr4:27117600-27122600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr4:27117600-27122800	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr4:27117600-27122800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr4:27117600-27122800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr4:27117800-27122800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr4:27118600-27122600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr4:27121200-27122600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr4:27121800-27122600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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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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