Variant report

Variant	rs5972325
Chromosome Location	chrX:31189180-31189181
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs12391957	0.90[CEU][hapmap]
rs12557265	0.90[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap]
rs12557283	0.90[CEU][hapmap]
rs12687954	0.90[CEU][hapmap]
rs1484854	0.90[CEU][hapmap];0.90[CHB][hapmap];0.86[JPT][hapmap]
rs1921383	1.00[CHB][hapmap]
rs1921385	0.89[CEU][hapmap]
rs1921386	0.90[CEU][hapmap]
rs1921394	0.87[CEU][hapmap]
rs1921395	0.90[CEU][hapmap]
rs2178538	0.90[CEU][hapmap];1.00[CHB][hapmap]
rs2404495	0.90[CEU][hapmap]
rs2404496	0.90[CEU][hapmap]
rs2404497	0.90[CEU][hapmap];1.00[CHB][hapmap];0.85[JPT][hapmap]
rs2896876	0.90[CEU][hapmap]
rs3747385	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs3788887	0.82[CEU][hapmap]
rs426228	0.89[CEU][hapmap]
rs4397574	0.88[CEU][hapmap]
rs4829210	0.90[CEU][hapmap];1.00[CHB][hapmap]
rs5926986	0.90[CHB][hapmap]
rs5927689	0.89[CHB][hapmap]
rs5972328	0.90[CEU][hapmap];1.00[CHB][hapmap];0.85[JPT][hapmap]
rs6527061	0.90[CEU][hapmap];1.00[CHB][hapmap]
rs6527062	0.89[CEU][hapmap];1.00[CHB][hapmap]
rs6653848	0.90[CEU][hapmap];0.90[CHB][hapmap]
rs7057738	0.90[CEU][hapmap];0.90[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530449	chrX:30962926-31375215	Strong transcription Flanking Bivalent TSS/Enh Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	esv3416705	chrX:31099481-31213379	Strong transcription Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA miRNA target site	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:26 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:31140200-31227600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chrX:31140600-31206000	Weak transcription	Skeletal Muscle Female	skeletal muscle
3	chrX:31142000-31236600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chrX:31156800-31224800	Weak transcription	Skeletal Muscle Male	skeletal muscle
5	chrX:31161800-31199800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
6	chrX:31163000-31209000	Weak transcription	Ovary	ovary
7	chrX:31164600-31196000	Weak transcription	Left Ventricle	heart
8	chrX:31164800-31189600	Weak transcription	Duodenum Smooth Muscle	Duodenum
9	chrX:31165000-31203400	Weak transcription	HUES64 Cell Line	embryonic stem cell
10	chrX:31166000-31196000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chrX:31173600-31193600	Strong transcription	Hela-S3	cervix
12	chrX:31177800-31202800	Weak transcription	Brain Angular Gyrus	brain
13	chrX:31182000-31227000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chrX:31183000-31199800	Weak transcription	HUES6 Cell Line	embryonic stem cell
15	chrX:31184400-31197200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chrX:31184800-31190400	Weak transcription	HepG2	liver
17	chrX:31185000-31190200	Strong transcription	Liver	Liver
18	chrX:31185000-31200600	Weak transcription	Pancreas	Pancrea
19	chrX:31185800-31189200	Weak transcription	Brain Cingulate Gyrus	brain
20	chrX:31186000-31189200	Enhancers	Primary B cells from peripheral blood	blood
21	chrX:31186400-31196400	Weak transcription	HSMMtube	muscle
22	chrX:31186800-31201800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
23	chrX:31186800-31203200	Weak transcription	Fetal Muscle Leg	muscle
24	chrX:31186800-31217600	Weak transcription	Fetal Intestine Small	intestine
25	chrX:31187000-31196000	Weak transcription	Adipose Nuclei	Adipose
26	chrX:31187800-31195400	Weak transcription	GM12878-XiMat	blood

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