Variant report

Variant	rs10753795
Chromosome Location	chr1:169752102-169752103
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr1:169751349..169757764-chr1:169760418..169766538,11	K562	blood:
2	chr1:169453908..169455963-chr1:169751227..169752986,2	K562	blood:
3	chr1:169751559..169753241-chr1:169780241..169782649,2	MCF-7	breast:
4	chr1:169751112..169752655-chr1:169758575..169760981,2	MCF-7	breast:
5	chr1:169750643..169754945-chr1:169761592..169765030,6	MCF-7	breast:
6	chr1:169751762..169754671-chr1:169756355..169758348,3	K562	blood:

Variant related genes	Relation type
ENSG00000171806	Chromatin interaction
ENSG00000213062	Chromatin interaction
ENSG00000117479	Chromatin interaction
ENSG00000000460	Chromatin interaction

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10157246	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs10157266	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[YRI][hapmap];0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10753794	1.00[CEU][hapmap];0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs10753796	0.93[CEU][hapmap];0.87[EUR][1000 genomes]
rs10919236	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs10919237	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs10919238	1.00[CEU][hapmap];0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs10919240	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs10919242	1.00[CEU][hapmap];0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs10919243	0.89[CEU][hapmap];0.85[EUR][1000 genomes]
rs11588275	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12035144	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12129417	1.00[CEU][hapmap];0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12404614	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2420507	0.92[EUR][1000 genomes]
rs3753311	0.82[CEU][hapmap]
rs6427216	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6427219	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6676623	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6676718	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6683782	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6686522	1.00[CEU][hapmap];0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6696884	0.89[CEU][hapmap];0.84[EUR][1000 genomes]
rs6701718	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs722511	1.00[CEU][hapmap];0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs9728301	0.82[AMR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3451367	chr1:169630075-169976964	Strong transcription Flanking Active TSS Genic enhancers Enhancers Weak transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:169748200-169753600	Enhancers	HUVEC	blood vessel
2	chr1:169749400-169761400	Weak transcription	Liver	Liver
3	chr1:169750000-169752400	Enhancers	Placenta	Placenta
4	chr1:169750200-169753000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr1:169750400-169754400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr1:169750800-169762800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr1:169751400-169752600	Enhancers	Placenta Amnion	Placenta Amnion
8	chr1:169751600-169753000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr1:169751600-169760200	Weak transcription	HUES48 Cell Line	embryonic stem cell
10	chr1:169751600-169762600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr1:169752000-169752400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr1:169752000-169753200	Weak transcription	HMEC	breast

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links