Variant report

Variant	rs2511391
Chromosome Location	chr11:93703244-93703245
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:93698163..93699732-chr11:93702050..93703572,2	K562	blood:
2	chr11:93700752..93703504-chr11:93704529..93706599,2	K562	blood:
3	chr11:93700458..93703504-chr11:93704523..93708049,5	K562	blood:

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs11020618	0.83[EUR][1000 genomes]
rs11605140	0.88[EUR][1000 genomes]
rs12222414	0.84[EUR][1000 genomes]
rs1401180	0.86[ASN][1000 genomes]
rs1506658	0.83[EUR][1000 genomes]
rs1518567	0.92[ASN][1000 genomes]
rs1518568	0.92[ASN][1000 genomes]
rs1518569	0.83[ASN][1000 genomes]
rs1518574	0.85[ASN][1000 genomes]
rs1914724	0.85[ASN][1000 genomes]
rs1960895	0.85[ASN][1000 genomes]
rs2135526	0.81[ASN][1000 genomes]
rs2139091	0.85[ASN][1000 genomes]
rs2139092	0.84[ASN][1000 genomes]
rs2174638	0.92[ASN][1000 genomes]
rs2174640	0.85[ASN][1000 genomes]
rs2203794	0.84[ASN][1000 genomes]
rs2213109	0.84[ASN][1000 genomes]
rs2256323	0.95[ASN][1000 genomes]
rs2256426	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2456557	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2460038	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2460039	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2460051	0.82[ASN][1000 genomes]
rs2462741	0.85[ASN][1000 genomes]
rs2462742	0.85[ASN][1000 genomes]
rs2511382	0.84[ASN][1000 genomes]
rs2511388	0.92[ASN][1000 genomes]
rs2511392	0.96[ASN][1000 genomes]
rs2511404	0.84[ASN][1000 genomes]
rs2939619	0.85[EUR][1000 genomes]
rs3018380	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs3020007	0.93[EUR][1000 genomes]
rs59527139	0.83[EUR][1000 genomes]
rs60833228	0.83[EUR][1000 genomes]
rs67268439	0.88[EUR][1000 genomes]
rs7113975	0.83[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv508650	chr11:93609010-93713576	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
2	nsv1049467	chr11:93651025-93778717	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Active TSS Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv442	chr11:93665117-93717973	Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	esv2757466	chr11:93676224-93714950	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	esv2759854	chr11:93676224-93714950	Enhancers Bivalent Enhancer Weak transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	esv3495079	chr11:93694004-93703302	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
7	esv1821420	chr11:93695235-93703637	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:93702000-93703400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland

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