Variant report

Variant	rs5916269
Chromosome Location	chrX:5810299-5810300
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs11094874	0.85[CEU][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap]
rs3810687	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap]
rs6529896	0.92[CEU][hapmap];1.00[CHD][hapmap];0.89[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap]
rs7049300	1.00[CEU][hapmap];1.00[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869027	chrX:5052974-6043003	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
2	esv2830398	chrX:5618240-5882060	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
3	nsv949393	chrX:5637763-5883977	Strong transcription Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
4	nsv817415	chrX:5803207-5833017	Enhancers Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island lncRNA miRNA target site	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:5792600-5821800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chrX:5799600-5828600	Weak transcription	Ovary	ovary
3	chrX:5805400-5820200	Weak transcription	Fetal Brain Female	brain
4	chrX:5805600-5820600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chrX:5806000-5820400	Weak transcription	Cortex derived primary cultured neurospheres	brain
6	chrX:5806600-5810400	Weak transcription	HUES64 Cell Line	embryonic stem cell
7	chrX:5806800-5833200	Strong transcription	Dnd41	blood
8	chrX:5808400-5820200	Weak transcription	Fetal Stomach	stomach
9	chrX:5808800-5810400	Weak transcription	HUES6 Cell Line	embryonic stem cell
10	chrX:5809000-5811600	Strong transcription	iPS-18 Cell Line	embryonic stem cell
11	chrX:5809400-5811800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
12	chrX:5809600-5811200	Strong transcription	H1 Cell Line	embryonic stem cell
13	chrX:5809600-5811200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chrX:5809600-5811200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chrX:5809600-5811800	Strong transcription	H9 Cell Line	embryonic stem cell
16	chrX:5809600-5811800	Strong transcription	HUES48 Cell Line	embryonic stem cell
17	chrX:5809800-5810600	Genic enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
18	chrX:5809800-5811000	Strong transcription	Fetal Thymus	thymus
19	chrX:5810000-5811000	Strong transcription	Brain Germinal Matrix	brain
20	chrX:5810000-5823000	Weak transcription	iPS-15b Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links