Variant report

Variant	rs4557236
Chromosome Location	chr4:173955750-173955751
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs10019310	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10020676	0.85[CEU][hapmap];0.86[CHB][hapmap];0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11132976	0.86[CHB][hapmap]
rs11721460	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs11722826	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11939508	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13125629	0.86[CHB][hapmap];0.82[EUR][1000 genomes]
rs13145272	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs17059107	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs28451718	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28569824	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3905287	0.85[CEU][hapmap];0.86[CHB][hapmap];0.89[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4331761	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4695821	0.84[EUR][1000 genomes]
rs62341925	0.97[ASN][1000 genomes]
rs6832095	0.84[EUR][1000 genomes]
rs6833557	0.84[EUR][1000 genomes]
rs7669563	0.86[CHB][hapmap]
rs7680255	0.96[CEU][hapmap];0.86[CHB][hapmap];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv948856	chr4:173388217-173967546	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv949126	chr4:173466221-174051451	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:173950400-173959400	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr4:173950800-173958000	Weak transcription	HUES6 Cell Line	embryonic stem cell
3	chr4:173951200-173960400	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr4:173951600-173959200	Weak transcription	HUES48 Cell Line	embryonic stem cell
5	chr4:173953200-173957800	Weak transcription	Stomach Mucosa	stomach
6	chr4:173955600-173955800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr4:173955600-173955800	Enhancers	Rectal Mucosa Donor 31	rectum
8	chr4:173955600-173956000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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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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