Variant report

Variant	rs144053138
Chromosome Location	chr4:100495593-100495594
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	nsv879656	chr4:99976646-100533722	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
2	nsv933074	chr4:100460951-100630600	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	esv1833664	chr4:100495571-100504985	Strong transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 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	chr4:100493800-100495800	Enhancers	Cortex derived primary cultured neurospheres	brain
2	chr4:100494200-100495800	Weak transcription	Skeletal Muscle Female	skeletal muscle
3	chr4:100494400-100495800	Weak transcription	Aorta	Aorta
4	chr4:100494600-100495600	Enhancers	Fetal Intestine Large	intestine
5	chr4:100494600-100495800	Enhancers	Fetal Intestine Small	intestine
6	chr4:100495000-100495600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr4:100495000-100495800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr4:100495000-100495800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr4:100495000-100496400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
10	chr4:100495200-100495800	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr4:100495200-100495800	Weak transcription	Ovary	ovary
12	chr4:100495200-100495800	Weak transcription	Rectal Smooth Muscle	rectum
13	chr4:100495200-100496000	Weak transcription	Duodenum Smooth Muscle	Duodenum
14	chr4:100495200-100496000	Flanking Active TSS	HepG2	liver
15	chr4:100495400-100495600	Active TSS	Duodenum Mucosa	Duodenum
16	chr4:100495400-100496200	Flanking Active TSS	Liver	Liver
17	chr4:100495400-100497000	Enhancers	HUES64 Cell Line	embryonic stem cell

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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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