Variant report

Variant	rs35575236
Chromosome Location	chr15:76056912-76056913
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:76048264..76050108-chr15:76055339..76058185,2	K562	blood:
2	chr15:76050226..76052609-chr15:76056345..76058198,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000260288	Chromatin interaction

Extended variants
information (count: 66 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:62)

rs_ID	r²[population]
rs10519109	0.91[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs11852712	0.85[AMR][1000 genomes]
rs11854305	0.84[AMR][1000 genomes]
rs11858818	0.85[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs12898509	0.85[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs12899163	0.85[AMR][1000 genomes]
rs12899303	0.91[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs12900007	0.84[AMR][1000 genomes]
rs12900167	0.84[AMR][1000 genomes]
rs12903661	0.91[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs12905062	0.91[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs12905730	0.88[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs1964473	0.82[ASN][1000 genomes]
rs1964474	0.81[ASN][1000 genomes]
rs1996302	0.88[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs1996303	0.88[AMR][1000 genomes]
rs2004630	0.81[ASN][1000 genomes]
rs2004920	0.88[AMR][1000 genomes]
rs2009508	0.86[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs2010392	0.81[ASN][1000 genomes]
rs2017312	0.84[AMR][1000 genomes]
rs2290484	0.91[AMR][1000 genomes]
rs2405718	0.91[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs2405882	0.86[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs28404806	0.84[AMR][1000 genomes]
rs28541422	0.86[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs28651447	0.86[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs28657001	0.86[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs28688252	0.86[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs28695212	0.86[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs28695716	0.83[AMR][1000 genomes]
rs28744558	0.86[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs28833005	0.86[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs28837134	0.86[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs34243492	0.82[ASN][1000 genomes]
rs34469290	0.88[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs34571038	0.88[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs34605750	0.88[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs34611707	0.82[AMR][1000 genomes]
rs34941412	0.83[AMR][1000 genomes]
rs35019194	0.89[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs35135316	0.84[AMR][1000 genomes]
rs35136767	0.90[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs35147271	0.90[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs35745834	0.90[AMR][1000 genomes]
rs35842909	0.90[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs36057011	0.90[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs3861184	0.83[ASN][1000 genomes]
rs4503758	0.82[AMR][1000 genomes]
rs55744943	0.91[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs57905971	0.88[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs66838310	0.82[ASN][1000 genomes]
rs67908345	0.86[AMR][1000 genomes]
rs71403504	0.86[AMR][1000 genomes]
rs71403505	0.81[AMR][1000 genomes]
rs7165531	0.88[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs7181595	0.86[AMR][1000 genomes]
rs74026532	0.90[AMR][1000 genomes]
rs8026234	0.91[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs8027311	0.82[AMR][1000 genomes]
rs8028002	0.83[AMR][1000 genomes]
rs8037672	0.84[AMR][1000 genomes];0.83[ASN][1000 genomes]

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	nsv531903	chr15:75889302-76342128	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	97 gene(s)	inside rSNPs	diseases
2	nsv527186	chr15:75924443-76107730	Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	69 gene(s)	inside rSNPs	diseases
3	nsv904396	chr15:75961518-76071105	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	26 gene(s)	inside rSNPs	diseases
4	nsv974599	chr15:76033068-76101142	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:76051400-76057000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr15:76051400-76059000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr15:76051400-76063200	Weak transcription	Right Atrium	heart
4	chr15:76053200-76058200	Enhancers	HepG2	liver
5	chr15:76056400-76057800	Weak transcription	Pancreas	Pancrea
6	chr15:76056600-76062000	Weak transcription	Liver	Liver

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links