Variant report

Variant	rs61223906
Chromosome Location	chr7:39447726-39447727
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs10259786	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs10282168	0.92[EUR][1000 genomes]
rs2073546	0.93[ASN][1000 genomes]
rs2074934	0.90[AFR][1000 genomes]
rs2190890	0.92[ASN][1000 genomes]
rs2190892	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2190893	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2215138	0.92[ASN][1000 genomes]
rs2237395	0.92[ASN][1000 genomes]
rs2237402	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2237403	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2237404	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2299133	0.91[ASN][1000 genomes]
rs3778934	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs56408610	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7459210	0.93[ASN][1000 genomes]
rs933370	0.86[AMR][1000 genomes];0.90[EUR][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	nsv1021180	chr7:39424988-39642261	Flanking Active TSS ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv1026951	chr7:39429036-39642261	Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	nsv981456	chr7:39431071-39454006	Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Bivalent Enhancer Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:39446000-39447800	Enhancers	H1 Cell Line	embryonic stem cell
2	chr7:39446200-39447800	Enhancers	iPS-18 Cell Line	embryonic stem cell
3	chr7:39446200-39447800	Enhancers	Fetal Intestine Small	intestine
4	chr7:39446200-39448200	Enhancers	Fetal Intestine Large	intestine
5	chr7:39446400-39447800	Enhancers	Fetal Muscle Leg	muscle
6	chr7:39446400-39453400	Weak transcription	Pancreas	Pancrea
7	chr7:39446800-39448600	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr7:39447000-39448000	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr7:39447200-39448000	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr7:39447200-39453400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr7:39447600-39448000	Weak transcription	Pancreatic Islets	Pancreatic Islet
12	chr7:39447600-39453200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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