Variant report

Variant	rs180706335
Chromosome Location	chrX:138913695-138913696
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chrX:138907383..138910299-chrX:138911001..138913816,2	K562	blood:

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:76 , 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:138868600-138914000	Weak transcription	Stomach Smooth Muscle	stomach
3	chrX:138869000-138915600	Weak transcription	Fetal Stomach	stomach
4	chrX:138881400-138913800	Weak transcription	Sigmoid Colon	Sigmoid Colon
5	chrX:138899800-138914200	Weak transcription	Primary T cells fromperipheralblood	blood
6	chrX:138900200-138915200	Weak transcription	Brain Germinal Matrix	brain
7	chrX:138907000-138916800	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chrX:138907200-138916000	Enhancers	Liver	Liver
9	chrX:138907600-138914200	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chrX:138908200-138917000	Weak transcription	K562	blood
11	chrX:138909000-138913800	Weak transcription	Duodenum Mucosa	Duodenum
12	chrX:138909200-138914000	Weak transcription	HSMM	muscle
13	chrX:138909800-138923200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chrX:138910200-138915200	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chrX:138910600-138914200	Weak transcription	A549	lung
16	chrX:138910600-138915600	Weak transcription	Fetal Intestine Small	intestine
17	chrX:138910600-138916400	Enhancers	HUES64 Cell Line	embryonic stem cell
18	chrX:138910800-138915600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chrX:138911200-138915000	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chrX:138911400-138914400	Weak transcription	H1 Cell Line	embryonic stem cell
21	chrX:138911800-138914200	Weak transcription	HMEC	breast
22	chrX:138911800-138914800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
23	chrX:138912200-138915800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chrX:138912400-138914800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chrX:138912400-138914800	Enhancers	Cortex derived primary cultured neurospheres	brain
26	chrX:138912400-138915400	Enhancers	iPS-20b Cell Line	embryonic stem cell
27	chrX:138912600-138914600	Enhancers	Primary hematopoietic stem cells	blood
28	chrX:138912600-138914600	Enhancers	Adipose Nuclei	Adipose
29	chrX:138912600-138914800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chrX:138912600-138915000	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chrX:138912600-138915200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chrX:138912600-138915600	Enhancers	Osteobl	bone
33	chrX:138912800-138914600	Enhancers	Primary monocytes fromperipheralblood	blood
34	chrX:138912800-138914600	Enhancers	Primary neutrophils fromperipheralblood	blood
35	chrX:138912800-138915600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
36	chrX:138913000-138913800	Enhancers	GM12878-XiMat	blood
37	chrX:138913000-138914000	Weak transcription	Fetal Brain Male	brain
38	chrX:138913000-138914200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
39	chrX:138913000-138914200	Enhancers	Brain Hippocampus Middle	brain
40	chrX:138913000-138914200	Enhancers	Small Intestine	intestine
41	chrX:138913000-138914400	Enhancers	Primary T cells from cord blood	blood
42	chrX:138913000-138914400	Enhancers	Fetal Heart	heart
43	chrX:138913000-138915200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chrX:138913200-138914600	Enhancers	H9 Cell Line	embryonic stem cell
45	chrX:138913200-138914600	Enhancers	Primary hematopoietic stem cells short term culture	blood
46	chrX:138913200-138914600	Enhancers	Muscle Satellite Cultured Cells	--
47	chrX:138913200-138914600	Enhancers	Stomach Mucosa	stomach
48	chrX:138913200-138914800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chrX:138913200-138915600	Enhancers	NHLF	lung
50	chrX:138913200-138915800	Enhancers	HUVEC	blood vessel

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