Variant report

Variant	rs11012486
Chromosome Location	chr10:21301981-21301982
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:21301785..21302400-chr7:30698509..30699321,2	MCF-7	breast:

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs10764300	0.97[ASN][1000 genomes]
rs10764301	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs10828173	1.00[CHB][hapmap];0.95[JPT][hapmap];0.95[ASN][1000 genomes]
rs10828174	0.98[ASN][1000 genomes]
rs10828175	0.95[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs10828176	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs11012479	1.00[CHB][hapmap];0.96[JPT][hapmap];0.96[ASN][1000 genomes]
rs11012483	0.96[CHB][hapmap];0.91[JPT][hapmap];0.97[ASN][1000 genomes]
rs11012485	1.00[CHB][hapmap];0.95[JPT][hapmap];0.98[ASN][1000 genomes]
rs11012489	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs11012491	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs11012492	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs11816130	1.00[CHB][hapmap];0.95[JPT][hapmap];0.98[ASN][1000 genomes]
rs11817951	1.00[CHB][hapmap];0.96[JPT][hapmap];0.98[ASN][1000 genomes]
rs12220884	0.99[ASN][1000 genomes]
rs16921415	1.00[CHB][hapmap];0.95[JPT][hapmap];0.98[ASN][1000 genomes]
rs3858200	0.91[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs55647529	0.98[ASN][1000 genomes]
rs55687305	0.98[ASN][1000 genomes]
rs56070435	0.98[ASN][1000 genomes]
rs58448284	0.97[ASN][1000 genomes]
rs6482158	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs661924	0.86[CHB][hapmap];0.95[JPT][hapmap]
rs7073838	1.00[ASN][1000 genomes]
rs7079324	0.96[ASN][1000 genomes]
rs7079790	1.00[CHB][hapmap];0.95[JPT][hapmap];0.97[ASN][1000 genomes]
rs7896773	0.97[ASN][1000 genomes]
rs7904906	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs7920067	1.00[CHB][hapmap];0.96[JPT][hapmap];0.98[ASN][1000 genomes]

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	nsv530148	chr10:21065080-21724565	Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:21290200-21309200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr10:21290400-21319800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr10:21290600-21311200	Weak transcription	Brain Substantia Nigra	brain
4	chr10:21290800-21305000	Weak transcription	Brain Anterior Caudate	brain
5	chr10:21291000-21303800	Weak transcription	Brain Inferior Temporal Lobe	brain
6	chr10:21291000-21305000	Weak transcription	Brain Angular Gyrus	brain
7	chr10:21292400-21309200	Weak transcription	Brain Cingulate Gyrus	brain
8	chr10:21292600-21308000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr10:21299000-21311000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr10:21300800-21310600	Weak transcription	Right Atrium	heart

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