Variant report

Variant	rs72964611
Chromosome Location	chr11:93702511-93702512
allele	C/T
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: 45 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs11020619	0.87[EUR][1000 genomes]
rs11823303	0.81[EUR][1000 genomes]
rs11823785	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11823836	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11828737	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12278077	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1518573	0.84[EUR][1000 genomes]
rs16919810	0.81[EUR][1000 genomes]
rs16919815	0.81[EUR][1000 genomes]
rs2460058	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2462743	0.84[EUR][1000 genomes]
rs2511390	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4415716	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56355412	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7107851	0.81[EUR][1000 genomes]
rs72964608	0.91[AFR][1000 genomes];0.83[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs72964616	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72964618	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72964621	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72964623	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72964624	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72964625	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72964634	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72964664	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72964672	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72964674	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72964683	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72964690	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72964693	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72966603	1.00[ASN][1000 genomes]
rs72966608	0.81[EUR][1000 genomes]
rs72966637	0.81[EUR][1000 genomes]
rs925005	0.84[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 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	esv3495078	chr11:93694454-93703152	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
8	esv2511618	chr11:93694604-93702872	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
9	nsv8864	chr11:93694672-93702559	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
10	esv1819337	chr11:93694753-93702531	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
11	esv1821420	chr11:93695235-93703637	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
12	nsv983209	chr11:93695606-93702578	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs72964611	HEPHL1	cis	Artery Tibial	GTEx

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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