Variant report

Variant	rs577382
Chromosome Location	chr10:25619275-25619276
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 67 )
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	0.92[CEU][hapmap];0.88[CHB][hapmap];0.94[JPT][hapmap]
rs10828800	0.95[JPT][hapmap]
rs11014552	0.95[JPT][hapmap]
rs1329258	0.92[CEU][hapmap];0.83[CHB][hapmap];0.95[JPT][hapmap]
rs1329267	0.95[JPT][hapmap]
rs1329268	0.85[CEU][hapmap];0.83[CHB][hapmap];0.94[JPT][hapmap]
rs1334057	0.92[CEU][hapmap];0.83[CHB][hapmap];0.95[JPT][hapmap]
rs1341961	0.95[JPT][hapmap]
rs1341962	1.00[JPT][hapmap]
rs1341967	0.85[CEU][hapmap];0.83[CHB][hapmap];0.95[JPT][hapmap]
rs1361633	0.95[JPT][hapmap]
rs1410928	0.95[JPT][hapmap]
rs1410935	0.83[CHB][hapmap];0.95[JPT][hapmap]
rs1413396	0.92[CEU][hapmap]
rs1413398	0.85[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs1418126	0.95[JPT][hapmap]
rs1418129	0.95[JPT][hapmap]
rs1576319	0.92[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	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs1760757	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[YRI][hapmap];0.83[AFR][1000 genomes];0.88[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs1773615	0.92[CEU][hapmap];0.83[CHB][hapmap];0.95[JPT][hapmap]
rs1773624	0.92[CEU][hapmap];0.83[CHB][hapmap];0.94[JPT][hapmap]
rs1773631	0.92[CEU][hapmap];0.83[CHB][hapmap];0.95[JPT][hapmap]
rs1773652	0.84[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	0.85[CEU][hapmap];0.83[CHB][hapmap];0.95[JPT][hapmap]
rs1773682	0.95[JPT][hapmap]
rs1812401	0.92[CEU][hapmap];0.89[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs1854471	0.92[CEU][hapmap];0.83[CHB][hapmap];0.94[JPT][hapmap]
rs1855462	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.82[YRI][hapmap];0.87[AMR][1000 genomes];0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2262990	0.81[AFR][1000 genomes];0.91[AMR][1000 genomes];0.83[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2480351	0.89[JPT][hapmap]
rs3949311	0.95[JPT][hapmap]
rs4271295	0.95[JPT][hapmap]
rs4405201	0.92[CEU][hapmap];0.83[CHB][hapmap];0.94[JPT][hapmap]
rs4749022	0.95[JPT][hapmap]
rs539357	1.00[ASW][hapmap];0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.82[TSI][hapmap];1.00[YRI][hapmap]
rs545616	0.84[CEU][hapmap];0.83[CHB][hapmap];0.84[AMR][1000 genomes];0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs545905	1.00[ASW][hapmap];0.92[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];0.91[GIH][hapmap];1.00[JPT][hapmap];0.84[MEX][hapmap];0.92[MKK][hapmap];0.82[TSI][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes];0.92[AMR][1000 genomes];0.82[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs564371	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.92[MEX][hapmap];0.92[MKK][hapmap];0.93[TSI][hapmap];0.91[YRI][hapmap];0.80[AFR][1000 genomes];0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7392687	0.95[JPT][hapmap]
rs768540	0.92[CEU][hapmap];0.83[CHB][hapmap];0.95[JPT][hapmap]
rs7924230	0.83[CHB][hapmap];0.95[JPT][hapmap]
rs824153	0.85[AFR][1000 genomes];0.88[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs824591	0.83[CHB][hapmap];0.95[JPT][hapmap]
rs824594	0.95[JPT][hapmap]
rs824601	0.85[CEU][hapmap];0.83[CHB][hapmap];0.95[JPT][hapmap]
rs824602	0.85[CEU][hapmap];0.83[CHB][hapmap];0.95[JPT][hapmap]
rs844042	0.85[CEU][hapmap];0.83[CHB][hapmap];0.94[JPT][hapmap]
rs956085	0.95[JPT][hapmap]
rs956086	0.95[JPT][hapmap]
rs956088	0.85[CEU][hapmap];0.83[CHB][hapmap];0.95[JPT][hapmap]
rs961027	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]

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	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
2	esv3349863	chr10:25614571-25946379	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:25616600-25619400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr10:25618400-25619600	Weak transcription	Placenta	Placenta
3	chr10:25619200-25622000	Enhancers	HUES64 Cell Line	embryonic stem cell

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