Variant report

Variant	rs1773624
Chromosome Location	chr10:25668699-25668700
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	chr10:25667594..25669629-chr10:25671940..25673892,2	MCF-7	breast:

Extended variants
information (count: 84 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:79)

rs_ID	r²[population]
rs10741085	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs10764548	0.88[CHB][hapmap];1.00[JPT][hapmap]
rs10828776	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs10828800	0.82[CHB][hapmap];1.00[JPT][hapmap]
rs11014552	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs1329258	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap]
rs1329267	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs1329268	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1334057	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap];0.81[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1341961	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs1341962	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs1341967	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs1361633	0.89[CHB][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs1410928	0.88[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs1410935	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs1413395	0.84[ASN][1000 genomes]
rs1413396	1.00[CEU][hapmap];0.88[CHB][hapmap];0.92[EUR][1000 genomes]
rs1413398	0.93[CEU][hapmap];0.89[CHB][hapmap];0.95[JPT][hapmap];0.86[YRI][hapmap];0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1418126	0.89[CHB][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs1418129	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs1576319	1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1612726	0.88[CHB][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs1754246	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs1754248	0.88[CHB][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs1754252	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1754259	0.81[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1754263	0.85[AFR][1000 genomes];0.91[AMR][1000 genomes];0.83[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1754266	0.93[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs1754270	0.89[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs1754276	0.82[ASN][1000 genomes]
rs1754277	0.89[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs1754281	0.88[CHB][hapmap];1.00[JPT][hapmap]
rs1760750	0.93[CEU][hapmap];0.84[CHB][hapmap];0.95[JPT][hapmap]
rs1760757	0.85[CEU][hapmap];0.83[CHB][hapmap];0.94[JPT][hapmap]
rs1773604	0.88[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs1773611	0.89[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs1773615	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1773631	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs1773652	0.81[ASN][1000 genomes]
rs1773654	1.00[JPT][hapmap];0.87[AMR][1000 genomes]
rs1773655	0.84[ASN][1000 genomes]
rs1773656	0.89[CHB][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs1773657	0.85[ASN][1000 genomes]
rs1773658	0.88[CHB][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs1773659	0.94[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs1773663	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs1773678	0.88[CHB][hapmap];1.00[JPT][hapmap]
rs1773681	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1773682	0.88[CHB][hapmap];1.00[JPT][hapmap]
rs1773688	0.87[ASN][1000 genomes]
rs1812401	0.85[CEU][hapmap]
rs1854471	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs1855462	0.93[CEU][hapmap];0.84[CHB][hapmap];0.90[JPT][hapmap]
rs2480351	0.83[CHB][hapmap];0.95[JPT][hapmap]
rs3949311	0.88[CHB][hapmap];1.00[JPT][hapmap]
rs4271295	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs4405201	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs4749022	0.88[CHB][hapmap];1.00[JPT][hapmap]
rs539357	0.82[CHB][hapmap];0.94[JPT][hapmap]
rs545905	0.84[CEU][hapmap];0.83[CHB][hapmap];0.94[JPT][hapmap]
rs564371	0.92[CEU][hapmap];0.83[CHB][hapmap];0.94[JPT][hapmap]
rs577382	0.92[CEU][hapmap];0.83[CHB][hapmap];0.94[JPT][hapmap]
rs7072189	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7081326	0.85[ASN][1000 genomes]
rs7097708	0.85[ASN][1000 genomes]
rs7392687	0.88[CHB][hapmap];1.00[JPT][hapmap]
rs768540	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs7924230	1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs824591	0.83[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs824594	0.89[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs824596	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs824601	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs824602	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs824604	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs844042	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs956085	0.88[CHB][hapmap];1.00[JPT][hapmap]
rs956086	0.88[CHB][hapmap];1.00[JPT][hapmap]
rs956088	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs961027	0.85[CEU][hapmap];0.83[CHB][hapmap];0.94[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:5 , 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
3	esv3342880	chr10:25644995-25682820	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv550225	chr10:25653017-25671382	Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv550226	chr10:25653017-25693426	ZNF genes & repeats Enhancers Strong transcription Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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