Variant report

Variant	rs2818224
Chromosome Location	chr13:54835024-54835025
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:17)

rs_ID	r²[population]
rs12429973	0.82[AMR][1000 genomes]
rs12430260	0.86[ASN][1000 genomes]
rs17604306	0.86[ASN][1000 genomes]
rs17667588	0.86[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs17667614	0.86[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs2782502	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2784567	1.00[CHB][hapmap]
rs2818222	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2818223	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4883886	0.86[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs4883887	0.86[AMR][1000 genomes]
rs4884928	0.86[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs57804893	0.86[ASN][1000 genomes]
rs682930	0.88[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs684299	0.90[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs795647	0.90[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs795649	0.86[AMR][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	esv3375545	chr13:54517432-54908108	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
2	nsv1051063	chr13:54777487-54997866	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA miRNA	2 gene(s)	inside rSNPs	diseases
3	nsv541778	chr13:54777487-54997866	Weak transcription Enhancers Strong transcription Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA miRNA	2 gene(s)	inside rSNPs	diseases
4	nsv471132	chr13:54788842-54885744	ZNF genes & repeats Genic enhancers Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:54822800-54835600	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr13:54831800-54835600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr13:54832200-54839000	Enhancers	HUES64 Cell Line	embryonic stem cell
4	chr13:54832400-54835800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr13:54832600-54836200	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr13:54833400-54840000	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr13:54834000-54836000	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr13:54834200-54838200	Weak transcription	H1 Cell Line	embryonic stem cell

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