Variant report

Variant	rs1866171
Chromosome Location	chr15:93246839-93246840
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr15:93229485..93231177-chr15:93245143..93247617,2	K562	blood:
2	chr15:93245067..93247571-chr15:93251644..93254423,2	K562	blood:
3	chr15:93245067..93247571-chr15:93251644..93254423,3	K562	blood:
4	chr15:92928446..92930218-chr15:93246533..93249274,2	MCF-7	breast:
5	chr15:93224785..93226821-chr15:93245528..93247882,2	MCF-7	breast:

Extended variants
information (count: 25 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs17648050	0.83[CEU][hapmap]
rs34161004	0.83[CEU][hapmap]
rs34188575	0.81[ASN][1000 genomes]
rs34327113	0.80[ASN][1000 genomes]
rs34913881	0.81[ASN][1000 genomes]
rs35277112	0.81[ASN][1000 genomes]
rs35351684	0.87[ASN][1000 genomes]
rs35839849	0.82[ASN][1000 genomes]
rs35984805	0.88[ASN][1000 genomes]
rs4777729	0.80[ASN][1000 genomes]
rs4777730	0.80[ASN][1000 genomes]
rs67759391	0.82[ASN][1000 genomes]
rs71412559	0.81[ASN][1000 genomes]
rs71412560	0.81[ASN][1000 genomes]
rs71412561	0.81[ASN][1000 genomes]
rs71412562	0.81[ASN][1000 genomes]
rs71412563	0.83[ASN][1000 genomes]
rs71412564	0.81[ASN][1000 genomes]
rs71412566	0.81[ASN][1000 genomes]
rs71412567	0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1037972	chr15:92804908-93270761	Flanking Bivalent TSS/Enh Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
2	nsv904499	chr15:92914795-93472582	Bivalent Enhancer Flanking Active TSS Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	163 gene(s)	inside rSNPs	diseases
3	nsv948738	chr15:93070742-93728147	Strong transcription Weak transcription Flanking Active TSS Enhancers Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	169 gene(s)	inside rSNPs	diseases
4	nsv1049490	chr15:93134405-93591660	Enhancers Genic enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	151 gene(s)	inside rSNPs	diseases
5	nsv1040501	chr15:93177153-93286393	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs1866171	LOC400451	cis	multi-tissue	Pritchard
rs1866171	ANPEP	cis	parietal	SCAN
rs1866171	FAM174B	cis	cerebellum	SCAN

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:93245600-93257400	Weak transcription	Skeletal Muscle Male	skeletal muscle
2	chr15:93246200-93257400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain

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