Variant report

Variant	rs11620108
Chromosome Location	chr13:38523618-38523619
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr13:38523391..38525686-chr13:38530354..38532093,2	K562	blood:
2	chr13:38514672..38518463-chr13:38523225..38527429,4	K562	blood:

Extended variants
information (count: 58 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:55)

rs_ID	r²[population]
rs10161861	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10219814	0.91[ASN][1000 genomes]
rs10467366	0.91[ASN][1000 genomes]
rs10467459	0.91[ASN][1000 genomes]
rs11147677	0.87[ASN][1000 genomes]
rs11617568	0.91[ASN][1000 genomes]
rs11618727	0.91[ASN][1000 genomes]
rs11619292	1.00[AFR][1000 genomes];0.85[ASN][1000 genomes]
rs11619577	0.91[ASN][1000 genomes]
rs12430942	0.91[ASN][1000 genomes]
rs12864438	0.91[ASN][1000 genomes]
rs1337647	0.91[ASN][1000 genomes]
rs1572503	0.91[ASN][1000 genomes]
rs1886201	0.91[ASN][1000 genomes]
rs1886202	0.91[ASN][1000 genomes]
rs1886203	0.91[ASN][1000 genomes]
rs1890125	0.91[ASN][1000 genomes]
rs2225872	0.91[ASN][1000 genomes]
rs2245073	0.91[ASN][1000 genomes]
rs2245074	0.91[ASN][1000 genomes]
rs2255148	0.83[ASN][1000 genomes]
rs2256009	0.91[ASN][1000 genomes]
rs2256119	0.91[ASN][1000 genomes]
rs2265458	0.91[ASN][1000 genomes]
rs2485491	0.91[ASN][1000 genomes]
rs2485492	0.87[ASN][1000 genomes]
rs2785959	0.91[ASN][1000 genomes]
rs4943546	0.81[ASN][1000 genomes]
rs4943550	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4943552	0.91[ASN][1000 genomes]
rs61955036	0.91[ASN][1000 genomes]
rs67142536	0.91[ASN][1000 genomes]
rs71439740	0.91[ASN][1000 genomes]
rs9315522	0.91[ASN][1000 genomes]
rs9315523	0.91[ASN][1000 genomes]
rs9315524	0.91[ASN][1000 genomes]
rs9315525	0.87[ASN][1000 genomes]
rs9315550	1.00[AFR][1000 genomes]
rs9532136	0.91[ASN][1000 genomes]
rs9532137	0.91[ASN][1000 genomes]
rs9532142	1.00[JPT][hapmap]
rs9548098	0.91[ASN][1000 genomes]
rs9548099	0.91[ASN][1000 genomes]
rs9548100	0.91[ASN][1000 genomes]
rs9548101	0.91[ASN][1000 genomes]
rs9548102	0.91[ASN][1000 genomes]
rs9548103	0.91[ASN][1000 genomes]
rs9548110	0.91[ASN][1000 genomes]
rs9548111	0.91[ASN][1000 genomes]
rs9548114	0.91[ASN][1000 genomes]
rs9548129	0.91[ASN][1000 genomes]
rs9548136	0.91[ASN][1000 genomes]
rs9594241	0.91[ASN][1000 genomes]
rs9594242	0.91[ASN][1000 genomes]
rs9603278	0.86[EUR][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	nsv915901	chr13:38199035-39032633	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
2	nsv899996	chr13:38459224-38577056	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv899998	chr13:38480878-38582178	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:38520800-38524000	Weak transcription	Fetal Intestine Small	intestine
2	chr13:38523200-38524800	Enhancers	Fetal Intestine Large	intestine

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