Variant report

Variant	rs530882121
Chromosome Location	chrX:138915690-138915691
allele	-/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chrX:138910196..138912152-chrX:138915456..138917020,2	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:28 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:138907000-138916800	Enhancers	iPS-15b Cell Line	embryonic stem cell
2	chrX:138907200-138916000	Enhancers	Liver	Liver
3	chrX:138908200-138917000	Weak transcription	K562	blood
4	chrX:138909800-138923200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chrX:138910600-138916400	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chrX:138912200-138915800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chrX:138913200-138915800	Enhancers	HUVEC	blood vessel
8	chrX:138913800-138915800	Weak transcription	Pancreas	Pancrea
9	chrX:138914400-138917200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chrX:138914400-138931800	Weak transcription	Primary T cells from cord blood	blood
11	chrX:138914600-138916800	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chrX:138914600-138916800	Weak transcription	Primary T helper cells fromperipheralblood	blood
13	chrX:138914600-138918800	Weak transcription	HMEC	breast
14	chrX:138914600-138926400	Weak transcription	Primary B cells from peripheral blood	blood
15	chrX:138914600-138934400	Weak transcription	Primary hematopoietic stem cells	blood
16	chrX:138915000-138915800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
17	chrX:138915000-138916200	Weak transcription	GM12878-XiMat	blood
18	chrX:138915000-138916400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
19	chrX:138915200-138916000	Enhancers	Cortex derived primary cultured neurospheres	brain
20	chrX:138915400-138916600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
21	chrX:138915600-138915800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
22	chrX:138915600-138915800	Enhancers	Fetal Intestine Small	intestine
23	chrX:138915600-138915800	Enhancers	Fetal Stomach	stomach
24	chrX:138915600-138915800	Enhancers	Rectal Mucosa Donor 31	rectum
25	chrX:138915600-138916400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
26	chrX:138915600-138916400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chrX:138915600-138916600	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chrX:138915600-138916800	Weak transcription	Osteobl	bone

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