Variant report

Variant	rs961027
Chromosome Location	chr10:25589710-25589711
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 66 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:65)

rs_ID	r²[population]
rs10741085	0.95[JPT][hapmap]
rs10764548	0.95[JPT][hapmap]
rs10828776	0.85[CEU][hapmap];0.88[CHB][hapmap];0.94[JPT][hapmap]
rs10828800	0.95[JPT][hapmap]
rs11014552	0.95[JPT][hapmap]
rs1329258	0.85[CEU][hapmap];0.84[CHB][hapmap];0.95[JPT][hapmap]
rs1329267	0.95[JPT][hapmap]
rs1329268	0.84[CHB][hapmap];0.94[JPT][hapmap]
rs1334057	0.85[CEU][hapmap];0.84[CHB][hapmap];0.95[JPT][hapmap]
rs1341961	0.95[JPT][hapmap]
rs1341962	1.00[JPT][hapmap]
rs1341967	0.84[CHB][hapmap];0.95[JPT][hapmap]
rs1361633	0.95[JPT][hapmap]
rs1410928	0.95[JPT][hapmap]
rs1410935	0.84[CHB][hapmap];0.95[JPT][hapmap]
rs1413396	0.85[CEU][hapmap]
rs1413398	0.94[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs1418126	0.95[JPT][hapmap]
rs1418129	0.95[JPT][hapmap]
rs1576319	0.85[CEU][hapmap];0.95[JPT][hapmap]
rs1612726	0.95[JPT][hapmap]
rs1754246	0.95[JPT][hapmap]
rs1754248	0.95[JPT][hapmap]
rs1754270	0.95[JPT][hapmap]
rs1754277	0.95[JPT][hapmap]
rs1754281	0.95[JPT][hapmap]
rs1760750	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1760757	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs1773615	0.85[CEU][hapmap];0.84[CHB][hapmap];0.95[JPT][hapmap]
rs1773624	0.85[CEU][hapmap];0.83[CHB][hapmap];0.94[JPT][hapmap]
rs1773631	0.85[CEU][hapmap];0.84[CHB][hapmap];0.95[JPT][hapmap]
rs1773652	0.80[ASN][1000 genomes]
rs1773654	0.95[JPT][hapmap]
rs1773656	0.95[JPT][hapmap]
rs1773658	0.95[JPT][hapmap]
rs1773663	0.95[JPT][hapmap]
rs1773678	0.95[JPT][hapmap]
rs1773681	0.84[CHB][hapmap];0.95[JPT][hapmap];0.83[MEX][hapmap]
rs1773682	0.95[JPT][hapmap]
rs1812401	1.00[CEU][hapmap];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1854471	0.85[CEU][hapmap];0.84[CHB][hapmap];0.94[JPT][hapmap]
rs1855462	0.93[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.80[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2262990	0.84[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs2480351	0.89[JPT][hapmap]
rs3949311	0.95[JPT][hapmap]
rs4271295	0.95[JPT][hapmap]
rs4405201	0.85[CEU][hapmap];0.84[CHB][hapmap];0.94[JPT][hapmap]
rs4749022	0.95[JPT][hapmap]
rs539357	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap]
rs545616	0.92[CEU][hapmap];0.83[CHB][hapmap];1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs545905	0.85[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];0.88[GIH][hapmap];1.00[JPT][hapmap];0.84[MEX][hapmap];0.89[MKK][hapmap];0.85[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs564371	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.92[MEX][hapmap];0.89[MKK][hapmap];0.90[TSI][hapmap];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs577382	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.83[MEX][hapmap];0.82[MKK][hapmap];0.84[TSI][hapmap];0.86[AMR][1000 genomes];0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7392687	0.95[JPT][hapmap]
rs768540	0.85[CEU][hapmap];0.84[CHB][hapmap];0.95[JPT][hapmap]
rs7924230	0.84[CHB][hapmap];0.95[JPT][hapmap]
rs824153	0.86[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs824591	0.84[CHB][hapmap];0.95[JPT][hapmap]
rs824594	0.95[JPT][hapmap]
rs824601	0.84[CHB][hapmap];0.95[JPT][hapmap]
rs824602	0.84[CHB][hapmap];0.95[JPT][hapmap]
rs844042	0.84[CHB][hapmap];0.94[JPT][hapmap]
rs956085	0.95[JPT][hapmap]
rs956086	0.95[JPT][hapmap]
rs956088	0.84[CHB][hapmap];0.95[JPT][hapmap]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2761583	chr10:25525657-25722444	Weak transcription Enhancers ZNF genes & repeats Active TSS Strong transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:25582000-25592000	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr10:25588800-25589800	Enhancers	HUES6 Cell Line	embryonic stem cell
3	chr10:25589000-25589800	Enhancers	HUES64 Cell Line	embryonic stem cell
4	chr10:25589200-25589800	Enhancers	iPS-18 Cell Line	embryonic stem cell

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