Variant report

Variant	rs72659569
Chromosome Location	chr4:94752067-94752068
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs11731687	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11734082	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11737153	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4605616	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs72659563	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs72659564	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7438447	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[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	nsv1008055	chr4:94169131-95030074	Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv931979	chr4:94289958-95121723	Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
3	nsv821636	chr4:94439636-95116590	Bivalent Enhancer Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
4	esv1792557	chr4:94738158-95027272	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Enhancers Flanking Active TSS Weak transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 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	chr4:94751200-94753200	Weak transcription	Pancreas	Pancrea
2	chr4:94751200-94753200	Bivalent/Poised TSS	Rectal Mucosa Donor 31	rectum
3	chr4:94751400-94752400	Bivalent/Poised TSS	Duodenum Mucosa	Duodenum
4	chr4:94751400-94752400	Bivalent/Poised TSS	Fetal Intestine Large	intestine
5	chr4:94751400-94752600	Bivalent/Poised TSS	Fetal Intestine Small	intestine
6	chr4:94751400-94753600	Bivalent/Poised TSS	Rectal Mucosa Donor 29	rectum
7	chr4:94751400-94755200	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
8	chr4:94751600-94753400	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
9	chr4:94751600-94753400	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
10	chr4:94751800-94752200	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
11	chr4:94751800-94752600	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
12	chr4:94751800-94753400	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
13	chr4:94751800-94753400	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
14	chr4:94752000-94753200	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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