Variant report

Variant	rs533665049
Chromosome Location	chr4:152989329-152989330
allele	A/G
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	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	nsv880341	chr4:152861685-153110256	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
3	nsv931416	chr4:152877808-153440553	Genic enhancers Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
4	nsv461679	chr4:152935555-152992741	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv595734	chr4:152935555-152992741	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	n/a	inside rSNPs	diseases
6	esv3466425	chr4:152988702-152994200	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
7	nsv968029	chr4:152988941-152994456	Weak transcription Enhancers	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	chr4:152983800-153000800	Enhancers	Fetal Thymus	thymus
2	chr4:152985200-152990000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
3	chr4:152985200-152993400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr4:152985200-152996200	Weak transcription	HUES6 Cell Line	embryonic stem cell
5	chr4:152985200-153000000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
6	chr4:152986200-152990000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
7	chr4:152986400-152989800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
8	chr4:152986600-152989600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
9	chr4:152986600-152993200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr4:152986800-152998000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
11	chr4:152987200-152989400	Weak transcription	Primary T helper cells fromperipheralblood	blood
12	chr4:152987600-152989600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
13	chr4:152987600-152989600	Weak transcription	Primary T helper cells PMA-I stimulated	--
14	chr4:152987600-152990000	Weak transcription	Primary T cells fromperipheralblood	blood
15	chr4:152988000-152989600	Weak transcription	Dnd41	blood
16	chr4:152988200-152989400	Weak transcription	Thymus	Thymus
17	chr4:152988800-152993600	Weak transcription	Right Atrium	heart
18	chr4:152989200-152992200	Enhancers	Primary T cells from cord blood	blood

Quick Search:

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

what's new

Quick links