Variant report

Variant	rs186694714
Chromosome Location	chr4:82417119-82417120
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 4 )
Associated
traits (count: 0)

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	nsv999729	chr4:81802554-82627820	Genic enhancers Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	nsv537156	chr4:81802554-82627820	Flanking Active TSS Strong transcription Enhancers Weak transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
3	nsv829986	chr4:82345163-82509860	Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv1005254	chr4:82416237-82521768	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:82413800-82425200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr4:82414200-82419200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
3	chr4:82415400-82417200	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr4:82415400-82421000	Weak transcription	Brain Anterior Caudate	brain
5	chr4:82415800-82417200	Enhancers	Primary B cells from cord blood	blood
6	chr4:82415800-82417200	Enhancers	Primary T cells from cord blood	blood
7	chr4:82415800-82417400	Enhancers	Monocytes-CD14+_RO01746	blood
8	chr4:82415800-82420400	Weak transcription	Fetal Lung	lung
9	chr4:82415800-82421000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
10	chr4:82415800-82423800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr4:82415800-82425800	Weak transcription	Right Atrium	heart
12	chr4:82415800-82426000	Weak transcription	Rectal Mucosa Donor 31	rectum
13	chr4:82416000-82421000	Weak transcription	Fetal Thymus	thymus
14	chr4:82416400-82421600	Weak transcription	Adipose Nuclei	Adipose
15	chr4:82416600-82427600	Weak transcription	Fetal Intestine Small	intestine
16	chr4:82416800-82420400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr4:82417000-82419600	Weak transcription	Primary T helper cells PMA-I stimulated	--
18	chr4:82417000-82420000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
19	chr4:82417000-82420400	Weak transcription	Primary hematopoietic stem cells	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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