Variant report

Variant	rs370095982
Chromosome Location	chrX:138914365-138914366
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 3 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532936	chrX:138687855-139384681	Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	148 gene(s)	inside rSNPs	diseases
2	nsv491760	chrX:138780768-139283477	Active TSS Weak transcription Enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	147 gene(s)	inside rSNPs	diseases
3	nsv917353	chrX:138912620-139283492	Active TSS Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	146 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:71 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:138855000-138915400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
2	chrX:138869000-138915600	Weak transcription	Fetal Stomach	stomach
3	chrX:138900200-138915200	Weak transcription	Brain Germinal Matrix	brain
4	chrX:138907000-138916800	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chrX:138907200-138916000	Enhancers	Liver	Liver
6	chrX:138908200-138917000	Weak transcription	K562	blood
7	chrX:138909800-138923200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chrX:138910200-138915200	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chrX:138910600-138915600	Weak transcription	Fetal Intestine Small	intestine
10	chrX:138910600-138916400	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chrX:138910800-138915600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chrX:138911200-138915000	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chrX:138911400-138914400	Weak transcription	H1 Cell Line	embryonic stem cell
14	chrX:138911800-138914800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chrX:138912200-138915800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chrX:138912400-138914800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chrX:138912400-138914800	Enhancers	Cortex derived primary cultured neurospheres	brain
18	chrX:138912400-138915400	Enhancers	iPS-20b Cell Line	embryonic stem cell
19	chrX:138912600-138914600	Enhancers	Primary hematopoietic stem cells	blood
20	chrX:138912600-138914600	Enhancers	Adipose Nuclei	Adipose
21	chrX:138912600-138914800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chrX:138912600-138915000	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chrX:138912600-138915200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chrX:138912600-138915600	Enhancers	Osteobl	bone
25	chrX:138912800-138914600	Enhancers	Primary monocytes fromperipheralblood	blood
26	chrX:138912800-138914600	Enhancers	Primary neutrophils fromperipheralblood	blood
27	chrX:138912800-138915600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
28	chrX:138913000-138914400	Enhancers	Primary T cells from cord blood	blood
29	chrX:138913000-138914400	Enhancers	Fetal Heart	heart
30	chrX:138913000-138915200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chrX:138913200-138914600	Enhancers	H9 Cell Line	embryonic stem cell
32	chrX:138913200-138914600	Enhancers	Primary hematopoietic stem cells short term culture	blood
33	chrX:138913200-138914600	Enhancers	Muscle Satellite Cultured Cells	--
34	chrX:138913200-138914600	Enhancers	Stomach Mucosa	stomach
35	chrX:138913200-138914800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chrX:138913200-138915600	Enhancers	NHLF	lung
37	chrX:138913200-138915800	Enhancers	HUVEC	blood vessel
38	chrX:138913400-138914400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
39	chrX:138913400-138914600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
40	chrX:138913400-138914600	Weak transcription	Duodenum Smooth Muscle	Duodenum
41	chrX:138913400-138915000	Enhancers	NHDF-Ad	bronchial
42	chrX:138913600-138914400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
43	chrX:138913600-138914400	Enhancers	Left Ventricle	heart
44	chrX:138913600-138914600	Enhancers	Primary B cells from peripheral blood	blood
45	chrX:138913600-138914600	Enhancers	Primary T helper cells fromperipheralblood	blood
46	chrX:138913600-138914600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
47	chrX:138913600-138914600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chrX:138913600-138914600	Enhancers	Fetal Muscle Leg	muscle
49	chrX:138913600-138914600	Enhancers	Dnd41	blood
50	chrX:138913600-138914800	Enhancers	Primary B cells from cord blood	blood

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