Variant report

Variant	rs28551086
Chromosome Location	chr11:68400739-68400740
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:68399359..68401842-chr11:68855467..68857380,2	MCF-7	breast:
2	chr11:68400378..68400956-chr11:68855833..68856663,2	K562	blood:
3	chr11:68400175..68400936-chr11:68495016..68495727,2	MCF-7	breast:
4	chr11:68400417..68400956-chr11:68811436..68811940,2	MCF-7	breast:
5	chr11:68400009..68400995-chr11:68657393..68658012,3	MCF-7	breast:

Extended variants
information (count: 61 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:51)

rs_ID	r²[population]
rs10791987	0.81[ASN][1000 genomes]
rs10791988	0.81[ASN][1000 genomes]
rs11228313	0.81[ASN][1000 genomes]
rs11601281	0.82[ASN][1000 genomes]
rs11605472	0.83[ASN][1000 genomes]
rs12286536	0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12293615	0.93[AFR][1000 genomes];0.87[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs17149179	0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2186937	0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2510380	0.82[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs2510382	0.82[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs2510397	0.81[ASN][1000 genomes]
rs2513280	0.81[ASN][1000 genomes]
rs2513281	0.81[ASN][1000 genomes]
rs2513282	0.81[ASN][1000 genomes]
rs2513286	0.87[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2513289	0.81[ASN][1000 genomes]
rs2513299	0.83[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs3018716	0.84[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs35989399	0.91[ASN][1000 genomes]
rs4544002	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4930236	0.81[ASN][1000 genomes]
rs4930237	0.83[ASN][1000 genomes]
rs4930581	0.81[ASN][1000 genomes]
rs4930582	0.81[ASN][1000 genomes]
rs4930583	0.81[ASN][1000 genomes]
rs4930584	0.81[ASN][1000 genomes]
rs4930585	0.81[ASN][1000 genomes]
rs4930587	0.81[ASN][1000 genomes]
rs4930588	0.81[ASN][1000 genomes]
rs4930589	0.81[ASN][1000 genomes]
rs55761963	0.83[AFR][1000 genomes];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs55975204	0.91[ASN][1000 genomes]
rs57813595	0.82[AFR][1000 genomes];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs59919614	0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs60538784	0.92[AFR][1000 genomes];0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs61705449	0.83[AFR][1000 genomes];0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs61889616	0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7102308	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7102438	0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7107613	0.81[ASN][1000 genomes]
rs7116288	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7116363	0.81[ASN][1000 genomes]
rs7128942	0.91[ASN][1000 genomes]
rs7129320	0.81[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs72936524	0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs72936570	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs72936599	0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7932726	0.81[ASN][1000 genomes]
rs948861	0.81[ASN][1000 genomes]
rs948863	0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3431317	chr11:68282676-68411867	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	esv3478641	chr11:68282679-68411856	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
3	esv3478652	chr11:68282679-68411856	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
4	esv3425206	chr11:68282708-68411817	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
5	esv3511614	chr11:68282726-68411806	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
6	esv3511615	chr11:68282726-68411806	Weak transcription Genic enhancers Strong transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
7	esv3348204	chr11:68282891-68411839	Strong transcription Enhancers Weak transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
8	nsv832195	chr11:68286383-68474611	Strong transcription Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
9	nsv430403	chr11:68297201-68448324	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
10	nsv897864	chr11:68367007-68453429	Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Enhancers Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs28551086	CPT1A	Cis_1M	lymphoblastoid	RTeQTL

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:68398000-68400800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr11:68400000-68401200	Enhancers	HUES6 Cell Line	embryonic stem cell
3	chr11:68400200-68400800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr11:68400200-68400800	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr11:68400200-68400800	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr11:68400200-68401000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr11:68400200-68401000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
8	chr11:68400200-68401200	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr11:68400200-68401200	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr11:68400600-68400800	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell

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