Variant report

Variant	rs881801
Chromosome Location	chr7:118099658-118099659
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:118093376..118094985-chr7:118098864..118100577,2	K562	blood:
2	chr7:118093376..118097334-chr7:118098069..118100577,4	K562	blood:
3	chr7:118098838..118101158-chr7:118104567..118106399,2	K562	blood:

Extended variants
information (count: 30 )
Associated
traits (count: 4 )

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs1548812	0.81[EUR][1000 genomes]
rs2192234	0.84[EUR][1000 genomes]
rs2402357	0.83[EUR][1000 genomes]
rs41912	0.80[EUR][1000 genomes]
rs41921	0.82[EUR][1000 genomes]
rs41923	0.82[EUR][1000 genomes]
rs41924	0.82[EUR][1000 genomes]
rs41930	0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs41931	0.85[EUR][1000 genomes]
rs41936	0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs41962	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs41989	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4260839	0.82[AFR][1000 genomes];0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4730862	0.81[EUR][1000 genomes]
rs4730866	0.83[EUR][1000 genomes]
rs4730868	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6466657	0.84[EUR][1000 genomes]
rs6651117	0.84[EUR][1000 genomes]
rs6963274	0.84[CEU][hapmap]
rs6964858	0.83[EUR][1000 genomes]
rs71314617	0.84[EUR][1000 genomes]
rs7801976	0.82[EUR][1000 genomes]
rs7811687	0.94[AFR][1000 genomes];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][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	nsv869971	chr7:117420583-118274149	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
2	esv1804964	chr7:117960973-118188573	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv889093	chr7:117977091-118709754	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv889094	chr7:117981820-118186543	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	esv2829882	chr7:118009306-118222312	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	esv1806893	chr7:118093537-118160303	Enhancers Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	esv1813338	chr7:118093537-118160303	Flanking Active TSS Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

mRNA abundance (count:4)

SNP	Gene	Cis/trans	Tissue	Source
rs881801	ANKRD7	cis	parietal	SCAN
rs881801	LSM8	cis	multi-tissue	Pritchard
rs881801	KCND2	cis	parietal	SCAN
rs881801	NAA38	cis	lymphoblastoid	seeQTL

Chromatin state (count:0 , 50 per page) page:

No data

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