Variant report

Variant	rs563262827
Chromosome Location	chr10:49917072-49917073
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv895371	chr10:49492075-50232180	Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	35 gene(s)	inside rSNPs	diseases
2	nsv895372	chr10:49576878-49933488	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
3	nsv1049259	chr10:49901984-49924310	Strong transcription Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv895373	chr10:49911737-49933488	Strong transcription Weak transcription Bivalent Enhancer Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	nsv512162	chr10:49915860-49919375	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	esv3361529	chr10:49916471-49918494	Enhancers Strong transcription Weak transcription Bivalent Enhancer Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	inside rSNPs	diseases
7	esv2472494	chr10:49916628-49918127	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer	TF binding region	1 gene(s)	inside rSNPs	diseases
8	esv9654	chr10:49916903-49917755	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	inside rSNPs	diseases
9	esv3371552	chr10:49916946-49917994	Weak transcription Strong transcription Bivalent Enhancer Enhancers Genic enhancers	TF binding region	1 gene(s)	inside rSNPs	diseases
10	esv1991692	chr10:49916969-49917692	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region	1 gene(s)	inside rSNPs	diseases
11	esv3498285	chr10:49917050-49917557	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region	1 gene(s)	inside rSNPs	diseases
12	nsv523003	chr10:49917061-49920608	Weak transcription Flanking Active TSS Strong transcription Enhancers Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
13	esv3519489	chr10:49917064-49917564	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	1 gene(s)	inside rSNPs	diseases
14	esv3519495	chr10:49917068-49917587	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:24 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:49897000-49918200	Genic enhancers	Primary B cells from peripheral blood	blood
2	chr10:49907400-49917800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
3	chr10:49908200-49922800	Weak transcription	Spleen	Spleen
4	chr10:49910800-49917800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr10:49911000-49917800	Weak transcription	Primary hematopoietic stem cells	blood
6	chr10:49911000-49917800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr10:49913000-49930600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr10:49914200-49922600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
9	chr10:49915200-49917200	Enhancers	Primary monocytes fromperipheralblood	blood
10	chr10:49915400-49918800	Enhancers	Fetal Muscle Leg	muscle
11	chr10:49915400-49921600	Strong transcription	GM12878-XiMat	blood
12	chr10:49916400-49918800	Weak transcription	Fetal Muscle Trunk	muscle
13	chr10:49916600-49917400	Weak transcription	Fetal Lung	lung
14	chr10:49916600-49917800	Weak transcription	Primary B cells from cord blood	blood
15	chr10:49916600-49917800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
16	chr10:49916800-49917600	Weak transcription	Monocytes-CD14+_RO01746	blood
17	chr10:49916800-49917800	Weak transcription	Left Ventricle	heart
18	chr10:49916800-49918800	Weak transcription	Fetal Stomach	stomach
19	chr10:49916800-49918800	Weak transcription	Right Ventricle	heart
20	chr10:49916800-49919200	Enhancers	Fetal Heart	heart
21	chr10:49916800-49920400	Weak transcription	Sigmoid Colon	Sigmoid Colon
22	chr10:49916800-49921600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr10:49916800-49921600	Weak transcription	Right Atrium	heart
24	chr10:49917000-49917600	Weak transcription	Primary neutrophils fromperipheralblood	blood

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