Variant report

Variant	rs4370469
Chromosome Location	chr7:78345659-78345660
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs10237271	0.88[ASN][1000 genomes]
rs10252981	0.86[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs10255125	0.83[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs10256096	0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs10267607	0.92[AFR][1000 genomes];0.86[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs10269389	0.84[ASN][1000 genomes]
rs10274288	0.90[AFR][1000 genomes];0.87[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs1075221	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10953675	0.84[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs11768116	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12531323	0.80[ASN][1000 genomes]
rs13234228	0.84[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs13240156	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13242288	1.00[AFR][1000 genomes];0.88[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs13246026	0.88[ASN][1000 genomes]
rs1390824	0.85[AFR][1000 genomes];0.87[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs1496779	0.90[AFR][1000 genomes];0.87[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs1496780	0.90[AFR][1000 genomes];0.87[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs17384271	0.85[AFR][1000 genomes];0.87[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs4727750	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6948326	0.89[AFR][1000 genomes];0.85[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs9640732	0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1022199	chr7:78054639-78469370	Enhancers Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv538986	chr7:78054639-78469370	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv1019355	chr7:78319575-78399845	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv607657	chr7:78329795-78483211	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:78341200-78346800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr7:78342200-78346000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr7:78343600-78346600	Weak transcription	Pancreas	Pancrea
4	chr7:78343600-78347600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr7:78344000-78346000	Weak transcription	HUES6 Cell Line	embryonic stem cell
6	chr7:78344200-78346200	Weak transcription	HUES48 Cell Line	embryonic stem cell
7	chr7:78344400-78346200	Weak transcription	HUES64 Cell Line	embryonic stem cell
8	chr7:78344600-78346000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
9	chr7:78344600-78347400	Weak transcription	Brain Inferior Temporal Lobe	brain
10	chr7:78344600-78348200	Weak transcription	Brain Cingulate Gyrus	brain
11	chr7:78344600-78348200	Weak transcription	Brain Hippocampus Middle	brain
12	chr7:78345200-78350200	Weak transcription	Pancreatic Islets	Pancreatic Islet
13	chr7:78345600-78346800	Enhancers	iPS-20b Cell Line	embryonic stem cell
14	chr7:78345600-78348200	Enhancers	Fetal Heart	heart

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links