Variant report

Variant	rs533820746
Chromosome Location	chr13:49310049-49310050
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:18 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1049117	chr13:49089476-49928945	Enhancers Strong transcription Weak transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
2	nsv832605	chr13:49171305-49344970	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
3	esv2758327	chr13:49283983-49472517	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	esv2759936	chr13:49283983-49472517	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	esv3492096	chr13:49309870-49310232	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
6	esv3387282	chr13:49309874-49310250	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
7	esv3492094	chr13:49309893-49310110	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
8	esv3492095	chr13:49309907-49310178	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
9	esv3347197	chr13:49309913-49310080	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
10	esv3510385	chr13:49309925-49310157	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
11	esv3510397	chr13:49309925-49310157	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
12	esv3396927	chr13:49309936-49310103	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
13	esv3289	chr13:49309942-49310254	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
14	esv1001486	chr13:49309951-49310059	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
15	nsv64104	chr13:49309952-49310060	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
16	esv3492099	chr13:49309952-49310152	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
17	esv3492098	chr13:49309954-49310192	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
18	esv1487703	chr13:49310042-49310151	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:49303000-49312200	Weak transcription	Fetal Lung	lung
2	chr13:49306400-49311800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr13:49306600-49312200	Weak transcription	Left Ventricle	heart
4	chr13:49306800-49312000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr13:49307600-49311800	Weak transcription	Dnd41	blood
6	chr13:49308400-49312200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr13:49308600-49312600	Weak transcription	Right Ventricle	heart
8	chr13:49309200-49310200	Weak transcription	Fetal Brain Female	brain
9	chr13:49309200-49310400	Enhancers	HUES6 Cell Line	embryonic stem cell
10	chr13:49309400-49310200	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr13:49310000-49312200	Weak transcription	iPS-18 Cell Line	embryonic stem cell

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