Variant report

Variant	rs57825313
Chromosome Location	chr4:152786114-152786115
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs56169032	1.00[EUR][1000 genomes]
rs60722156	1.00[EUR][1000 genomes]
rs73862271	1.00[EUR][1000 genomes]
rs73862585	1.00[EUR][1000 genomes]
rs73865529	1.00[EUR][1000 genomes]
rs7692744	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv432644	chr4:152635395-153023402	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
2	esv2753949	chr4:152764038-152794700	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
3	esv2757086	chr4:152776271-152809738	Weak transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	esv2759289	chr4:152776271-152809738	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Bivalent/Poised TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	esv16590	chr4:152778545-152790136	Enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv1030973	chr4:152779838-152792879	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:152779000-152788600	Weak transcription	Pancreas	Pancrea
2	chr4:152780800-152789000	Enhancers	Fetal Brain Male	brain
3	chr4:152781200-152794800	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr4:152785200-152789400	Enhancers	Primary monocytes fromperipheralblood	blood
5	chr4:152785400-152786400	Weak transcription	Fetal Brain Female	brain
6	chr4:152785800-152786400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
7	chr4:152785800-152788600	Enhancers	Fetal Thymus	thymus
8	chr4:152786000-152786200	Enhancers	Brain Cingulate Gyrus	brain
9	chr4:152786000-152786400	Enhancers	Right Ventricle	heart
10	chr4:152786000-152786600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
11	chr4:152786000-152786800	Enhancers	Stomach Smooth Muscle	stomach
12	chr4:152786000-152786800	Enhancers	GM12878-XiMat	blood
13	chr4:152786000-152787000	Enhancers	Skeletal Muscle Male	skeletal muscle
14	chr4:152786000-152787000	Enhancers	Dnd41	blood
15	chr4:152786000-152787200	Enhancers	Adipose Nuclei	Adipose
16	chr4:152786000-152788000	Enhancers	Fetal Heart	heart
17	chr4:152786000-152789000	Enhancers	Primary neutrophils fromperipheralblood	blood
18	chr4:152786000-152789000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood

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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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