Variant report

Variant	rs372365971
Chromosome Location	chr11:93920038-93920039
allele	C/T
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	nsv898184	chr11:93741612-93969726	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
2	nsv1046092	chr11:93833446-93964452	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
3	nsv898185	chr11:93851048-93927529	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
4	nsv469980	chr11:93864321-93962121	Weak transcription Flanking Active TSS Strong transcription Enhancers Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
5	nsv468795	chr11:93864321-93964917	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
6	nsv555966	chr11:93864321-93964917	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
7	nsv1038294	chr11:93918837-93982605	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:70 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:93901400-93921200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr11:93912200-93921000	Weak transcription	Brain Anterior Caudate	brain
3	chr11:93913600-93929400	Weak transcription	Gastric	stomach
4	chr11:93913800-93921400	Weak transcription	Fetal Brain Male	brain
5	chr11:93914400-93920400	Weak transcription	Primary B cells from cord blood	blood
6	chr11:93914800-93920400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr11:93914800-93920600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
8	chr11:93914800-93921000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
9	chr11:93914800-93921600	Weak transcription	Thymus	Thymus
10	chr11:93914800-93926200	Weak transcription	Esophagus	oesophagus
11	chr11:93914800-93926200	Weak transcription	Spleen	Spleen
12	chr11:93915000-93921000	Weak transcription	Right Ventricle	heart
13	chr11:93915600-93920400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
14	chr11:93915600-93929400	Weak transcription	Placenta Amnion	Placenta Amnion
15	chr11:93916200-93920800	Weak transcription	Primary hematopoietic stem cells	blood
16	chr11:93916200-93921200	Weak transcription	Primary T cells from cord blood	blood
17	chr11:93916400-93922000	Weak transcription	Brain Germinal Matrix	brain
18	chr11:93916800-93920200	Weak transcription	Fetal Muscle Trunk	muscle
19	chr11:93916800-93920200	Enhancers	NHLF	lung
20	chr11:93916800-93920600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr11:93916800-93926200	Weak transcription	HMEC	breast
22	chr11:93917000-93920800	Weak transcription	Primary monocytes fromperipheralblood	blood
23	chr11:93917200-93920200	Weak transcription	Dnd41	blood
24	chr11:93917200-93926200	Weak transcription	NHEK	skin
25	chr11:93917400-93921000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr11:93917400-93921200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr11:93917400-93922000	Weak transcription	Lung	lung
28	chr11:93917600-93923000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
29	chr11:93917600-93925600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
30	chr11:93917600-93934200	Weak transcription	Fetal Intestine Small	intestine
31	chr11:93917800-93920400	Weak transcription	Colon Smooth Muscle	Colon
32	chr11:93917800-93926400	Weak transcription	Cortex derived primary cultured neurospheres	brain
33	chr11:93918000-93920400	Enhancers	NHDF-Ad	bronchial
34	chr11:93918000-93925600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
35	chr11:93918600-93921200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr11:93918800-93920200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
37	chr11:93919000-93920400	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr11:93919000-93920600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr11:93919000-93920600	Strong transcription	Stomach Smooth Muscle	stomach
40	chr11:93919200-93920400	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr11:93919200-93920800	Weak transcription	Monocytes-CD14+_RO01746	blood
42	chr11:93919200-93921000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr11:93919200-93921600	Weak transcription	Fetal Stomach	stomach
44	chr11:93919200-93922200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr11:93919200-93925800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
46	chr11:93919400-93920400	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr11:93919400-93920600	Strong transcription	Aorta	Aorta
48	chr11:93919400-93921000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr11:93919400-93921200	Weak transcription	Left Ventricle	heart
50	chr11:93919400-93925400	Weak transcription	HUES48 Cell Line	embryonic stem cell

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