Variant report

Variant	rs11250011
Chromosome Location	chr8:10292078-10292079
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MSRA-1	chr8:10291182-10295822	ENSG00000261451.1

Extended variants
information (count: 40 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs10903327	0.97[ASN][1000 genomes]
rs11250010	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11250012	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11250013	0.86[AFR][1000 genomes];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11774291	0.86[EUR][1000 genomes]
rs11774920	0.86[EUR][1000 genomes]
rs11781243	0.86[EUR][1000 genomes]
rs11782465	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11783249	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12546721	0.86[EUR][1000 genomes]
rs13257718	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13266986	0.85[AFR][1000 genomes];0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1986358	0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs34675714	0.85[AFR][1000 genomes];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs34975042	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs35073964	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs35335292	0.85[AFR][1000 genomes];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs35479789	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4410951	0.97[ASN][1000 genomes]
rs4471098	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4840484	0.82[EUR][1000 genomes]
rs4841342	0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs57759396	0.83[EUR][1000 genomes]
rs61510468	0.86[EUR][1000 genomes]
rs6601462	0.83[ASN][1000 genomes]
rs6601466	0.88[EUR][1000 genomes]
rs67173113	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6980700	0.86[EUR][1000 genomes]
rs6989757	0.94[ASN][1000 genomes]
rs6995374	0.86[EUR][1000 genomes]
rs7837520	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1030934	chr8:10065169-10561161	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
2	nsv890347	chr8:10153082-10331636	Flanking Active TSS ZNF genes & repeats Weak transcription Enhancers Flanking Bivalent TSS/Enh Strong transcription Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
3	nsv1022994	chr8:10190618-10660122	Strong transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
4	nsv539466	chr8:10190618-10660122	Enhancers Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
5	nsv527326	chr8:10199548-10320019	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
6	nsv1025557	chr8:10216726-10555187	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
7	nsv917085	chr8:10237508-10828204	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
8	nsv610266	chr8:10250758-10294330	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
9	nsv610267	chr8:10268736-10526742	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	17 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs11250011	BLK	Cis_chr	lymphoblastoid	RTeQTL

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:10276000-10293600	Weak transcription	Brain Substantia Nigra	brain
2	chr8:10282600-10295200	Strong transcription	Primary neutrophils fromperipheralblood	blood
3	chr8:10282800-10293800	Weak transcription	Primary T cells from cord blood	blood
4	chr8:10283200-10293600	Weak transcription	Left Ventricle	heart
5	chr8:10283200-10294000	Weak transcription	Gastric	stomach
6	chr8:10283200-10295200	Weak transcription	Primary T cells fromperipheralblood	blood
7	chr8:10285400-10293000	Weak transcription	Brain Angular Gyrus	brain
8	chr8:10285400-10293800	Weak transcription	Stomach Smooth Muscle	stomach
9	chr8:10285800-10292800	Weak transcription	Fetal Intestine Small	intestine
10	chr8:10285800-10305200	Weak transcription	Lung	lung
11	chr8:10288400-10293800	Weak transcription	Fetal Brain Female	brain
12	chr8:10288800-10292200	Weak transcription	Spleen	Spleen
13	chr8:10289800-10293600	Weak transcription	Adipose Nuclei	Adipose
14	chr8:10290000-10294200	Strong transcription	Liver	Liver
15	chr8:10290600-10292200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr8:10290600-10292200	Enhancers	Fetal Brain Male	brain
17	chr8:10291000-10293000	Weak transcription	Fetal Intestine Large	intestine
18	chr8:10291200-10292400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr8:10291200-10292400	Strong transcription	Brain Germinal Matrix	brain
20	chr8:10291400-10301200	Weak transcription	Pancreas	Pancrea
21	chr8:10291800-10294000	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain

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