Variant report

Variant	rs146544814
Chromosome Location	chr10:49918473-49918474
allele	A/C
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	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	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

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:49908200-49922800	Weak transcription	Spleen	Spleen
2	chr10:49913000-49930600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr10:49914200-49922600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
4	chr10:49915400-49918800	Enhancers	Fetal Muscle Leg	muscle
5	chr10:49915400-49921600	Strong transcription	GM12878-XiMat	blood
6	chr10:49916400-49918800	Weak transcription	Fetal Muscle Trunk	muscle
7	chr10:49916800-49918800	Weak transcription	Fetal Stomach	stomach
8	chr10:49916800-49918800	Weak transcription	Right Ventricle	heart
9	chr10:49916800-49919200	Enhancers	Fetal Heart	heart
10	chr10:49916800-49920400	Weak transcription	Sigmoid Colon	Sigmoid Colon
11	chr10:49916800-49921600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr10:49916800-49921600	Weak transcription	Right Atrium	heart
13	chr10:49917600-49920200	Strong transcription	Primary neutrophils fromperipheralblood	blood
14	chr10:49917600-49921200	Strong transcription	Monocytes-CD14+_RO01746	blood
15	chr10:49917800-49919800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
16	chr10:49917800-49920800	Strong transcription	Primary monocytes fromperipheralblood	blood
17	chr10:49917800-49921400	Strong transcription	Primary B cells from cord blood	blood
18	chr10:49917800-49921400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
19	chr10:49917800-49921600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr10:49917800-49921800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr10:49917800-49922400	Strong transcription	Primary hematopoietic stem cells	blood
22	chr10:49918200-49922800	Strong transcription	Primary B cells from peripheral blood	blood
23	chr10:49918400-49919800	Enhancers	Fetal Brain Male	brain
24	chr10:49918400-49922400	Enhancers	Left Ventricle	heart

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