Variant report

Variant	rs566343754
Chromosome Location	chr10:18503262-18503263
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:21 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3469840	chr10:18501971-18504819	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
2	esv3346215	chr10:18502321-18504569	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
3	esv3468729	chr10:18502796-18504044	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
4	esv3470951	chr10:18502955-18503680	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
5	esv3495772	chr10:18502969-18503700	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
6	esv3438118	chr10:18502976-18503683	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
7	esv3495771	chr10:18502988-18503631	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
8	esv3495770	chr10:18502996-18503626	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
9	esv3472062	chr10:18503001-18503657	Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
10	esv3474285	chr10:18503003-18503654	Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
11	esv3467618	chr10:18503016-18503606	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
12	esv3495775	chr10:18503017-18503639	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
13	esv3495776	chr10:18503035-18503640	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
14	esv3348675	chr10:18503037-18503609	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
15	esv4994	chr10:18503046-18503751	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
16	esv3473173	chr10:18503062-18503594	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
17	esv3495773	chr10:18503072-18503593	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
18	nsv24155	chr10:18503076-18503589	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
19	esv3475396	chr10:18503076-18503591	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
20	esv3495777	chr10:18503076-18503591	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
21	nsv24229	chr10:18503077-18503590	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:22 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:18485000-18503800	Weak transcription	Duodenum Smooth Muscle	Duodenum
2	chr10:18493800-18503800	Weak transcription	Fetal Brain Male	brain
3	chr10:18494400-18503600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr10:18499200-18511000	Weak transcription	Aorta	Aorta
5	chr10:18500000-18504800	Enhancers	Rectal Smooth Muscle	rectum
6	chr10:18500200-18506000	Weak transcription	Right Atrium	heart
7	chr10:18500400-18503600	Enhancers	Colon Smooth Muscle	Colon
8	chr10:18501200-18503400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr10:18502000-18504400	Enhancers	Cortex derived primary cultured neurospheres	brain
10	chr10:18502200-18503600	Weak transcription	Brain Angular Gyrus	brain
11	chr10:18502200-18503600	Weak transcription	Left Ventricle	heart
12	chr10:18502200-18503600	Weak transcription	Ovary	ovary
13	chr10:18502400-18503600	Weak transcription	Fetal Stomach	stomach
14	chr10:18502400-18503600	Weak transcription	Pancreas	Pancrea
15	chr10:18502400-18503800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr10:18502400-18513600	Weak transcription	Right Ventricle	heart
17	chr10:18502600-18503600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr10:18502800-18503600	Weak transcription	Skeletal Muscle Female	skeletal muscle
19	chr10:18502800-18505400	Weak transcription	Pancreatic Islets	Pancreatic Islet
20	chr10:18503000-18503400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
21	chr10:18503000-18503400	Weak transcription	Fetal Heart	heart
22	chr10:18503000-18503400	Weak transcription	Stomach Smooth Muscle	stomach

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