Variant report

Variant	rs5918974
Chromosome Location	chrX:65274335-65274336
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chrX:65273217..65275089-chrX:65276067..65278791,2	K562	blood:

Variant related genes	Relation type
ENSG00000215168	Chromatin interaction

Extended variants
information (count: 57 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:54)

rs_ID	r²[population]
rs1011526	0.86[MEX][hapmap]
rs1028348	0.89[CEU][hapmap];0.81[LWK][hapmap];0.93[MEX][hapmap];0.89[YRI][hapmap]
rs1068537	0.86[MEX][hapmap]
rs1068538	0.85[MEX][hapmap]
rs1091486	0.86[MEX][hapmap]
rs1264212	0.86[MEX][hapmap]
rs1264216	0.86[MEX][hapmap]
rs1325561	1.00[CEU][hapmap];1.00[MEX][hapmap]
rs2206203	0.86[MEX][hapmap]
rs3848897	0.86[MEX][hapmap]
rs3848900	0.93[MEX][hapmap];0.92[TSI][hapmap]
rs3848901	0.93[MEX][hapmap];0.83[TSI][hapmap]
rs3903921	0.89[CEU][hapmap];0.93[MEX][hapmap]
rs4145625	1.00[CEU][hapmap]
rs4827449	1.00[CEU][hapmap];0.90[GIH][hapmap];1.00[MEX][hapmap];0.92[TSI][hapmap]
rs582787	0.88[CEU][hapmap];1.00[GIH][hapmap];0.93[MEX][hapmap];0.92[TSI][hapmap]
rs585069	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];0.92[TSI][hapmap]
rs586789	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];0.92[TSI][hapmap]
rs587657	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];0.92[TSI][hapmap]
rs5918579	1.00[CEU][hapmap];0.89[YRI][hapmap]
rs5918587	1.00[CEU][hapmap];1.00[GIH][hapmap];0.85[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.89[YRI][hapmap]
rs5918594	0.86[MEX][hapmap]
rs5918975	1.00[CEU][hapmap];0.84[YRI][hapmap]
rs5918977	1.00[CEU][hapmap]
rs5964480	0.86[MEX][hapmap]
rs5964482	0.86[MEX][hapmap]
rs5964483	0.86[MEX][hapmap]
rs5964486	0.93[MEX][hapmap];0.92[TSI][hapmap]
rs5964487	0.93[MEX][hapmap];0.83[TSI][hapmap]
rs5964488	0.93[MEX][hapmap];0.84[TSI][hapmap]
rs5964500	0.86[MEX][hapmap]
rs5965077	0.86[MEX][hapmap]
rs5965083	0.89[CEU][hapmap];0.93[MEX][hapmap]
rs5965105	0.86[MEX][hapmap]
rs5965106	0.86[MEX][hapmap]
rs606886	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];0.83[TSI][hapmap]
rs614506	1.00[CEU][hapmap];0.83[YRI][hapmap]
rs6624844	1.00[ASW][hapmap];1.00[CEU][hapmap];0.90[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.84[YRI][hapmap]
rs6624875	0.86[MEX][hapmap]
rs670546	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];0.92[TSI][hapmap]
rs699863	0.86[MEX][hapmap]
rs7054364	0.86[MEX][hapmap]
rs7062799	0.86[MEX][hapmap]
rs707302	0.86[MEX][hapmap]
rs708966	0.86[MEX][hapmap]
rs708968	0.86[MEX][hapmap]
rs708969	0.85[MEX][hapmap]
rs760867	1.00[CEU][hapmap];0.90[GIH][hapmap];1.00[MEX][hapmap];0.92[TSI][hapmap]
rs7891437	0.86[MEX][hapmap]
rs806607	0.86[MEX][hapmap]
rs806608	0.86[MEX][hapmap]
rs809363	0.86[MEX][hapmap]
rs942844	1.00[CEU][hapmap]
rs9633155	0.93[MEX][hapmap];0.83[TSI][hapmap]

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	esv3429625	chrX:64787230-65458721	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
2	nsv995042	chrX:65121634-65953299	Weak transcription Enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	40 gene(s)	inside rSNPs	diseases
3	nsv916393	chrX:65269672-65521616	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:65265200-65274800	Enhancers	Primary monocytes fromperipheralblood	blood
2	chrX:65269400-65275800	Enhancers	Primary neutrophils fromperipheralblood	blood
3	chrX:65273600-65274600	Enhancers	Primary T cells fromperipheralblood	blood
4	chrX:65273800-65275000	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
5	chrX:65274000-65274400	Enhancers	Primary B cells from cord blood	blood
6	chrX:65274000-65274600	Enhancers	Primary hematopoietic stem cells short term culture	blood
7	chrX:65274000-65274800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chrX:65274000-65274800	Bivalent Enhancer	Adipose Nuclei	Adipose
9	chrX:65274200-65274600	Enhancers	Primary hematopoietic stem cells	blood
10	chrX:65274200-65278600	Weak transcription	Primary T cells from cord blood	blood

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