Variant report

Variant	rs73084227
Chromosome Location	chr4:7401247-7401248
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv916610	chr4:7238883-7731946	Bivalent Enhancer Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases
2	nsv593569	chr4:7291363-7626136	Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases
3	nsv1011547	chr4:7318232-7637410	Active TSS ZNF genes & repeats Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
4	nsv537017	chr4:7318232-7637410	Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
5	nsv1003679	chr4:7319111-7449262	Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv469758	chr4:7370083-7546250	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Active TSS Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
7	esv3437934	chr4:7400351-7405049	Enhancers Bivalent Enhancer Weak transcription	n/a	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	chr4:7391800-7402000	Enhancers	Brain Germinal Matrix	brain
2	chr4:7396800-7401400	Enhancers	Brain Cingulate Gyrus	brain
3	chr4:7397400-7401800	Enhancers	Breast Myoepithelial Primary Cells	Breast
4	chr4:7397600-7401600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr4:7398800-7401400	Enhancers	Brain Inferior Temporal Lobe	brain
6	chr4:7399000-7401400	Enhancers	Brain Angular Gyrus	brain
7	chr4:7399400-7401400	Enhancers	Brain Anterior Caudate	brain
8	chr4:7399400-7401400	Enhancers	Brain Hippocampus Middle	brain
9	chr4:7399400-7401600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr4:7399600-7401800	Enhancers	Fetal Brain Female	brain
11	chr4:7399800-7404200	Weak transcription	Rectal Smooth Muscle	rectum
12	chr4:7400000-7404800	Weak transcription	Left Ventricle	heart
13	chr4:7400200-7404800	Weak transcription	Pancreas	Pancrea
14	chr4:7400800-7404200	Weak transcription	Colon Smooth Muscle	Colon
15	chr4:7400800-7404200	Weak transcription	Stomach Smooth Muscle	stomach
16	chr4:7401000-7401600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr4:7401200-7401400	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
18	chr4:7401200-7402000	Enhancers	Primary Natural Killer cells fromperipheralblood	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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