Variant report

Variant	rs72656806
Chromosome Location	chr4:149248509-149248510
allele	A/C
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:12)

rs_ID	r²[population]
rs10519962	1.00[AMR][1000 genomes]
rs17024607	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17024702	1.00[AMR][1000 genomes]
rs1858415	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs3910060	1.00[AMR][1000 genomes]
rs72645698	1.00[AMR][1000 genomes]
rs72655224	1.00[AMR][1000 genomes]
rs72656849	1.00[AMR][1000 genomes]
rs72656898	1.00[AMR][1000 genomes]
rs72658613	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs878232	1.00[AMR][1000 genomes]
rs907619	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1027263	chr4:149127120-149320135	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv537296	chr4:149127120-149320135	Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv1031815	chr4:149172485-149282928	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv1028105	chr4:149199913-149284620	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv537297	chr4:149199913-149284620	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	nsv1016966	chr4:149209467-149341037	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	nsv1019350	chr4:149232430-149282117	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:149235000-149266800	Weak transcription	Rectal Mucosa Donor 31	rectum
2	chr4:149237000-149249600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
3	chr4:149244400-149257600	Weak transcription	Rectal Mucosa Donor 29	rectum
4	chr4:149245000-149251200	Weak transcription	HUES48 Cell Line	embryonic stem cell
5	chr4:149245200-149251400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr4:149245400-149248600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr4:149245400-149251200	Weak transcription	HUES64 Cell Line	embryonic stem cell
8	chr4:149245400-149251400	Weak transcription	HUES6 Cell Line	embryonic stem cell
9	chr4:149245400-149257200	Weak transcription	Primary T helper cells PMA-I stimulated	--
10	chr4:149245600-149248600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
11	chr4:149247400-149252000	Weak transcription	Aorta	Aorta
12	chr4:149247800-149250000	Enhancers	Breast Myoepithelial Primary Cells	Breast
13	chr4:149248400-149248800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr4:149248400-149252800	Enhancers	Fetal Heart	heart

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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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