Variant report

Variant	rs11768578
Chromosome Location	chr7:14623723-14623724
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 41 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10227646	0.99[ASN][1000 genomes]
rs10236011	0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1357864	0.98[ASN][1000 genomes]
rs1357865	0.98[ASN][1000 genomes]
rs1357866	0.87[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1357867	0.98[ASN][1000 genomes]
rs1357868	0.98[ASN][1000 genomes]
rs1357869	0.98[ASN][1000 genomes]
rs1474385	0.98[ASN][1000 genomes]
rs1525083	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1525089	0.90[ASN][1000 genomes]
rs1560478	0.98[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs17150062	0.86[ASN][1000 genomes]
rs17168296	0.85[ASN][1000 genomes]
rs17168298	0.85[ASN][1000 genomes]
rs17168299	0.83[ASN][1000 genomes]
rs17595206	0.93[AFR][1000 genomes];0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17595234	0.84[AFR][1000 genomes];0.83[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs3795245	0.87[AFR][1000 genomes];0.92[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3951243	0.99[ASN][1000 genomes]
rs4537212	0.96[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs55681155	0.83[ASN][1000 genomes]
rs62443555	0.84[AFR][1000 genomes];0.83[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs62443556	0.84[AFR][1000 genomes];0.83[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs62443557	0.84[AFR][1000 genomes];0.83[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs66473448	0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6944740	0.98[ASN][1000 genomes]
rs73059484	0.83[ASN][1000 genomes]
rs73059497	0.81[ASN][1000 genomes]
rs7777504	0.98[ASN][1000 genomes]
rs7796807	0.86[ASN][1000 genomes]
rs7809502	0.98[ASN][1000 genomes]
rs879693	0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs940690	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs940691	0.97[ASN][1000 genomes]
rs953604	0.83[ASN][1000 genomes]
rs953605	0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949033	chr7:14086106-14860323	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv915603	chr7:14443884-14624268	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv887710	chr7:14587948-14653702	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv887711	chr7:14619026-14671325	ZNF genes & repeats Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:14603800-14624200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr7:14604200-14624000	Weak transcription	Cortex derived primary cultured neurospheres	brain
3	chr7:14620000-14624000	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr7:14622200-14623800	Enhancers	Liver	Liver
5	chr7:14622400-14625000	Weak transcription	Rectal Mucosa Donor 31	rectum
6	chr7:14623400-14624400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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