Variant report

Variant	rs7557365
Chromosome Location	chr2:7346878-7346879
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:7337101..7339316-chr2:7346517..7348557,2	K562	blood:

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs17627382	0.86[ASN][1000 genomes]
rs17627644	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17628027	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17628092	0.90[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs17678724	0.95[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs17679036	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2056634	0.90[ASN][1000 genomes]
rs2056637	0.90[ASN][1000 genomes]
rs35238941	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55680060	0.90[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55935532	0.90[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56007885	0.94[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56344406	0.94[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62104661	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62104666	0.90[AMR][1000 genomes];0.80[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs62104669	0.90[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62104707	0.82[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs62104708	0.90[ASN][1000 genomes]
rs62104709	0.80[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs62104710	0.90[ASN][1000 genomes]
rs62106503	0.86[ASN][1000 genomes]
rs62106508	0.86[ASN][1000 genomes]
rs72770008	0.90[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72770026	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72770038	0.90[ASN][1000 genomes]
rs72770045	0.90[ASN][1000 genomes]
rs72770048	0.90[ASN][1000 genomes]
rs72770050	0.90[ASN][1000 genomes]
rs72770051	0.81[ASN][1000 genomes]
rs72770052	0.85[ASN][1000 genomes]
rs72770055	0.85[ASN][1000 genomes]
rs72770056	0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv915888	chr2:7197783-7461967	Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv1000136	chr2:7337270-7379211	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
3	nsv833337	chr2:7337273-7521146	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:7342400-7349600	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr2:7343200-7348800	Weak transcription	HUES64 Cell Line	embryonic stem cell
3	chr2:7343200-7349200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
4	chr2:7343600-7348200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
5	chr2:7344400-7347400	Weak transcription	Fetal Brain Male	brain
6	chr2:7345200-7349800	Weak transcription	Lung	lung
7	chr2:7345600-7347000	Enhancers	Primary monocytes fromperipheralblood	blood
8	chr2:7345600-7347200	Enhancers	Primary neutrophils fromperipheralblood	blood
9	chr2:7345600-7347200	Enhancers	Monocytes-CD14+_RO01746	blood
10	chr2:7346200-7349200	Weak transcription	H9 Cell Line	embryonic stem cell

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