Variant report

Variant	rs10860995
Chromosome Location	chr12:103800981-103800982
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:103799013..103801250-chr12:103801844..103804662,2	MCF-7	breast:

Extended variants
information (count: 57 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:53)

rs_ID	r²[population]
rs10161218	0.88[CEU][hapmap];0.81[CHB][hapmap];0.80[CHD][hapmap];0.92[GIH][hapmap];0.81[TSI][hapmap];0.88[EUR][1000 genomes]
rs10466955	1.00[CEU][hapmap];0.85[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs10467022	0.87[CEU][hapmap];0.85[GIH][hapmap]
rs10467023	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs10745966	1.00[CEU][hapmap];0.94[GIH][hapmap];1.00[TSI][hapmap];0.85[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10745969	0.94[CEU][hapmap];0.90[EUR][1000 genomes]
rs10778245	1.00[CEU][hapmap];0.81[CHD][hapmap];0.94[GIH][hapmap];1.00[TSI][hapmap];0.85[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10861006	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs10861012	0.93[EUR][1000 genomes]
rs10861023	0.86[EUR][1000 genomes]
rs10861024	0.93[CEU][hapmap];0.86[EUR][1000 genomes]
rs10861027	0.85[EUR][1000 genomes]
rs11111565	0.81[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1112754	0.86[EUR][1000 genomes]
rs1316751	0.94[CEU][hapmap];0.94[GIH][hapmap];0.96[TSI][hapmap];0.88[EUR][1000 genomes]
rs1319091	0.93[CEU][hapmap];0.86[EUR][1000 genomes]
rs1320348	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2374049	0.86[GIH][hapmap];0.81[TSI][hapmap]
rs2374063	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2374067	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2374075	0.93[EUR][1000 genomes]
rs2374076	0.94[CEU][hapmap];0.89[EUR][1000 genomes]
rs2374077	0.94[CEU][hapmap];0.80[CHD][hapmap];0.85[GIH][hapmap];1.00[TSI][hapmap];0.93[EUR][1000 genomes]
rs2888730	1.00[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2888731	0.88[CEU][hapmap];0.89[TSI][hapmap];0.84[EUR][1000 genomes]
rs3953541	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4015523	0.88[CEU][hapmap];0.91[EUR][1000 genomes]
rs4015525	0.88[CEU][hapmap];0.89[TSI][hapmap];0.83[EUR][1000 genomes]
rs4015527	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4015536	0.94[CEU][hapmap];0.88[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs4433658	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4488299	0.94[EUR][1000 genomes]
rs4506750	0.88[CEU][hapmap];0.86[EUR][1000 genomes]
rs4764960	0.94[EUR][1000 genomes]
rs6539076	0.93[CEU][hapmap];0.93[EUR][1000 genomes]
rs7295666	0.87[CEU][hapmap];0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7295986	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7296215	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.92[TSI][hapmap];0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7299547	1.00[CEU][hapmap];0.85[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7301105	0.88[CEU][hapmap];1.00[CHB][hapmap];0.96[CHD][hapmap];0.92[GIH][hapmap];1.00[JPT][hapmap];0.89[MEX][hapmap];0.86[MKK][hapmap];0.89[TSI][hapmap];0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7302598	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7307779	0.82[EUR][1000 genomes]
rs7308343	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.92[TSI][hapmap];0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7312427	0.88[CEU][hapmap];0.94[GIH][hapmap];0.96[TSI][hapmap];0.91[EUR][1000 genomes]
rs7316757	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7958520	0.94[CEU][hapmap];0.89[MEX][hapmap];1.00[TSI][hapmap];0.92[EUR][1000 genomes]
rs7959115	1.00[CEU][hapmap];1.00[CHB][hapmap];0.96[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.92[TSI][hapmap];0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7960043	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7964462	0.86[EUR][1000 genomes]
rs7965797	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7969700	1.00[CEU][hapmap];0.85[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7977907	0.85[EUR][1000 genomes]
rs9669745	0.88[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv455703	chr12:103692799-103818049	Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
2	nsv560037	chr12:103692799-103818049	Enhancers Bivalent Enhancer Strong transcription Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
3	nsv899477	chr12:103747515-103817326	Enhancers Strong transcription Weak transcription ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
4	nsv899478	chr12:103747515-103834275	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:103795200-103801600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr12:103795200-103814000	Weak transcription	Primary B cells from peripheral blood	blood
3	chr12:103799000-103802800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr12:103799600-103801600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr12:103799600-103801800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr12:103799600-103803000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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