Variant report

Variant	rs16849561
Chromosome Location	chr4:74377433-74377434
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs1247684	1.00[AMR][1000 genomes]
rs16849294	1.00[AMR][1000 genomes]
rs16849506	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16849521	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16849524	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs41386245	1.00[AMR][1000 genomes]
rs41494947	1.00[AMR][1000 genomes]
rs56043949	1.00[AMR][1000 genomes]
rs59078835	1.00[AMR][1000 genomes]
rs72865471	1.00[AMR][1000 genomes]
rs72865474	1.00[AMR][1000 genomes]
rs72865476	1.00[AMR][1000 genomes]
rs72865480	1.00[AMR][1000 genomes]
rs72865485	1.00[AMR][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	esv3430875	chr4:74243646-74420354	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv1001725	chr4:74354050-74860924	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
3	nsv530126	chr4:74376622-74843892	Bivalent Enhancer Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Active TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:74374600-74383800	Weak transcription	Fetal Intestine Small	intestine
2	chr4:74374600-74399000	Weak transcription	Fetal Intestine Large	intestine
3	chr4:74377400-74378600	Genic enhancers	Liver	Liver

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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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