Variant report

Variant	rs10106574
Chromosome Location	chr8:10817928-10817929
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:10813776..10816525-chr8:10817526..10819399,2	K562	blood:

Extended variants
information (count: 51 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs10086778	1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs10086872	1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs10087376	0.80[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs10094007	1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10094337	0.89[EUR][1000 genomes]
rs10094684	1.00[JPT][hapmap];0.80[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs10095039	1.00[JPT][hapmap];0.80[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs10095261	1.00[JPT][hapmap];0.80[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs10095390	1.00[ASN][1000 genomes]
rs10096624	1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs10096634	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10096872	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs10097626	1.00[JPT][hapmap];0.80[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs10098549	1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10101503	1.00[ASN][1000 genomes]
rs10102369	0.85[EUR][1000 genomes]
rs10107544	1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10107591	0.82[ASN][1000 genomes]
rs10107658	1.00[JPT][hapmap];0.80[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs10111178	1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10112255	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10903334	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11250096	0.82[ASN][1000 genomes]
rs11250100	1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11783935	0.80[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs11985330	1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11990141	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs11995188	1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11996961	0.82[ASN][1000 genomes]
rs28542689	0.82[ASN][1000 genomes]
rs28546463	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs28712086	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4265148	1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs4314618	1.00[JPT][hapmap]
rs4434585	1.00[JPT][hapmap];0.80[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs4623374	1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs4626559	1.00[JPT][hapmap]
rs4645525	1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs4840527	0.82[ASN][1000 genomes]
rs55958006	0.82[ASN][1000 genomes]
rs56048959	0.82[ASN][1000 genomes]
rs57698321	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6601540	1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs6982751	0.82[ASN][1000 genomes]
rs6982927	1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs7006612	0.82[ASN][1000 genomes]
rs7008460	1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs73537380	0.89[EUR][1000 genomes]
rs7816172	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	nsv521721	chr8:10802102-10836472	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:10807400-10818200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr8:10810400-10818200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr8:10815000-10820800	Enhancers	Fetal Muscle Leg	muscle
4	chr8:10815200-10818200	Weak transcription	Brain Inferior Temporal Lobe	brain
5	chr8:10815400-10818600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr8:10816000-10818400	Weak transcription	Brain Hippocampus Middle	brain
7	chr8:10817600-10819400	Enhancers	Fetal Brain Male	brain
8	chr8:10817600-10820000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr8:10817800-10818800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr8:10817800-10819400	Enhancers	Fetal Brain Female	brain
11	chr8:10817800-10819800	Enhancers	Fetal Muscle Trunk	muscle
12	chr8:10817800-10820000	Enhancers	Primary T helper cells fromperipheralblood	blood
13	chr8:10817800-10820000	Enhancers	Primary T killer naive cells fromperipheralblood	blood

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