Variant report

Variant	rs11735278
Chromosome Location	chr4:62424399-62424400
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs10031433	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10866124	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11131329	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11131334	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12715704	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs13123888	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1391321	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1472425	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1497901	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1497906	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1497916	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1603660	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs17239080	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1846160	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2343250	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4860417	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4860418	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs6551634	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs67669396	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6813075	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6817476	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6835374	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs72636199	0.84[ASN][1000 genomes]
rs9685140	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv868844	chr4:62241702-62497248	Weak transcription Enhancers Bivalent/Poised TSS Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	esv2753138	chr4:62271444-62442507	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Active TSS Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	nsv461377	chr4:62368762-62883431	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv594328	chr4:62368762-62883431	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv1004815	chr4:62398737-62553769	ZNF genes & repeats Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	nsv537110	chr4:62398737-62553769	ZNF genes & repeats Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	nsv1004432	chr4:62408333-62444506	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
8	nsv537111	chr4:62408333-62444506	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
9	nsv594329	chr4:62416593-62478230	Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
10	nsv879077	chr4:62419426-62545435	Enhancers ZNF genes & repeats Weak transcription Active TSS Strong transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:62419200-62424600	Enhancers	Fetal Intestine Large	intestine
2	chr4:62419600-62425600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chr4:62420800-62424400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
4	chr4:62422000-62425200	Weak transcription	HUES64 Cell Line	embryonic stem cell
5	chr4:62422000-62425400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr4:62422200-62425200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr4:62422400-62425200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr4:62422400-62433200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr4:62422600-62428800	Weak transcription	Fetal Muscle Leg	muscle
10	chr4:62423600-62429000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr4:62424200-62424400	Enhancers	Fetal Brain Female	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links