Variant report

Variant	rs183880895
Chromosome Location	chr13:53774950-53774951
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1050969	chr13:53665927-54064861	Bivalent Enhancer Enhancers Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	esv3427175	chr13:53773776-53776324	Bivalent Enhancer Bivalent/Poised TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
3	esv3386985	chr13:53774176-53776724	Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	Chromatin interactive region	n/a	inside rSNPs	n/a
4	esv16748	chr13:53774609-53776399	Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3'	Chromatin interactive region	n/a	inside rSNPs	n/a
5	esv1819513	chr13:53774627-53776265	Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	n/a	inside rSNPs	n/a
6	esv1835841	chr13:53774627-53776265	Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Flanking Active TSS Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a
7	esv1834091	chr13:53774627-53784083	Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	n/a	inside rSNPs	n/a
8	esv1838050	chr13:53774627-53784083	Bivalent Enhancer Active TSS Enhancers Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	n/a	inside rSNPs	n/a
9	esv1835986	chr13:53774627-53786026	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	n/a	inside rSNPs	n/a
10	esv1840677	chr13:53774627-53791895	Bivalent/Poised TSS Bivalent Enhancer Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:35 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:53773400-53775400	Weak transcription	Brain Anterior Caudate	brain
2	chr13:53774200-53776200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr13:53774200-53776200	ZNF genes & repeats	Spleen	Spleen
4	chr13:53774200-53776600	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr13:53774400-53775200	Transcr. at gene 5' and 3'	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr13:53774400-53776600	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr13:53774400-53776600	Enhancers	Pancreas	Pancrea
8	chr13:53774600-53775200	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
9	chr13:53774600-53775400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr13:53774600-53776000	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
11	chr13:53774600-53776000	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
12	chr13:53774800-53775000	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
13	chr13:53774800-53775000	Bivalent Enhancer	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr13:53774800-53775000	Flanking Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr13:53774800-53775000	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr13:53774800-53775000	Bivalent Enhancer	Esophagus	oesophagus
17	chr13:53774800-53775200	Active TSS	H9 Cell Line	embryonic stem cell
18	chr13:53774800-53775200	Bivalent Enhancer	Primary hematopoietic stem cells	blood
19	chr13:53774800-53775200	Flanking Bivalent TSS/Enh	Brain Germinal Matrix	brain
20	chr13:53774800-53775200	Bivalent Enhancer	Fetal Brain Male	brain
21	chr13:53774800-53775200	Flanking Bivalent TSS/Enh	Fetal Brain Female	brain
22	chr13:53774800-53775400	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
23	chr13:53774800-53775400	Bivalent/Poised TSS	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr13:53774800-53775400	Bivalent Enhancer	Fetal Stomach	stomach
25	chr13:53774800-53775600	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
26	chr13:53774800-53775600	Bivalent Enhancer	Sigmoid Colon	Sigmoid Colon
27	chr13:53774800-53775800	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
28	chr13:53774800-53775800	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
29	chr13:53774800-53775800	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr13:53774800-53775800	Bivalent Enhancer	Fetal Muscle Leg	muscle
31	chr13:53774800-53775800	Enhancers	Gastric	stomach
32	chr13:53774800-53776000	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
33	chr13:53774800-53776400	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
34	chr13:53774800-53776400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
35	chr13:53774800-53776400	Bivalent Enhancer	Lung	lung

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