Variant report

Variant	rs374749096
Chromosome Location	chr3:141571416-141571417
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 3 )
Associated
traits (count: 0)

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	nsv949709	chr3:141295050-142178144	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
2	nsv1013352	chr3:141541105-141870293	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
3	nsv591894	chr3:141570294-141572848	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:141550800-141571800	Weak transcription	Esophagus	oesophagus
2	chr3:141560600-141572600	Weak transcription	Spleen	Spleen
3	chr3:141565000-141572000	Weak transcription	Adipose Nuclei	Adipose
4	chr3:141565000-141578000	Weak transcription	Fetal Intestine Small	intestine
5	chr3:141567600-141574600	Enhancers	Primary monocytes fromperipheralblood	blood
6	chr3:141568600-141572400	Weak transcription	Primary neutrophils fromperipheralblood	blood
7	chr3:141568600-141572400	Weak transcription	Sigmoid Colon	Sigmoid Colon
8	chr3:141568600-141579600	Weak transcription	Fetal Thymus	thymus
9	chr3:141569000-141572000	Weak transcription	K562	blood
10	chr3:141569800-141572600	Enhancers	HUVEC	blood vessel
11	chr3:141570600-141571800	Weak transcription	Lung	lung
12	chr3:141570800-141571800	Weak transcription	Primary hematopoietic stem cells	blood
13	chr3:141570800-141572400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
14	chr3:141570800-141578600	Weak transcription	Left Ventricle	heart
15	chr3:141571000-141572000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr3:141571400-141571800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr3:141571400-141571800	Enhancers	Monocytes-CD14+_RO01746	blood

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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

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