Variant report

Variant	rs17190051
Chromosome Location	chr2:56403523-56403524
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr16:75033537..75035200-chr2:56403126..56405221,2	MCF-7	breast:
2	chr2:56395307..56398284-chr2:56402876..56406233,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000103091	Chromatin interaction
ENSG00000186187	Chromatin interaction

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs10490395	1.00[CEU][hapmap];1.00[AFR][1000 genomes];0.96[EUR][1000 genomes]
rs10490396	1.00[CEU][hapmap];1.00[AFR][1000 genomes];0.96[EUR][1000 genomes]
rs10490398	1.00[CEU][hapmap];1.00[AFR][1000 genomes];0.96[EUR][1000 genomes]
rs10490399	1.00[CEU][hapmap];1.00[AFR][1000 genomes];0.96[EUR][1000 genomes]
rs17190058	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap];1.00[AFR][1000 genomes];0.96[EUR][1000 genomes]
rs17190100	1.00[CEU][hapmap];0.92[GIH][hapmap];1.00[TSI][hapmap];1.00[AFR][1000 genomes];0.96[EUR][1000 genomes]
rs17190121	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs17190149	1.00[CEU][hapmap];1.00[AFR][1000 genomes];0.96[EUR][1000 genomes]
rs17190156	1.00[CEU][hapmap];1.00[AFR][1000 genomes];0.96[EUR][1000 genomes]
rs17190163	1.00[CEU][hapmap];1.00[AFR][1000 genomes];0.96[EUR][1000 genomes]
rs17190170	1.00[CEU][hapmap];1.00[AFR][1000 genomes];0.96[EUR][1000 genomes]
rs17268619	1.00[AFR][1000 genomes]
rs17268653	1.00[CEU][hapmap];1.00[AFR][1000 genomes];0.96[EUR][1000 genomes]
rs17268688	1.00[CEU][hapmap];0.92[GIH][hapmap];1.00[TSI][hapmap];1.00[AFR][1000 genomes];0.91[EUR][1000 genomes]
rs17268695	1.00[CEU][hapmap];1.00[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs55644642	1.00[AFR][1000 genomes];0.96[EUR][1000 genomes]
rs56007407	1.00[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs56017486	1.00[AFR][1000 genomes];0.96[EUR][1000 genomes]
rs56207598	0.96[EUR][1000 genomes]
rs72801150	1.00[AFR][1000 genomes]
rs72801161	0.96[EUR][1000 genomes]
rs72801165	1.00[AFR][1000 genomes];0.96[EUR][1000 genomes]
rs72801168	1.00[AFR][1000 genomes];0.96[EUR][1000 genomes]
rs72801171	1.00[AFR][1000 genomes];0.96[EUR][1000 genomes]
rs72801179	0.96[EUR][1000 genomes]
rs72801180	0.96[EUR][1000 genomes]
rs72801181	1.00[AFR][1000 genomes];0.96[EUR][1000 genomes]
rs72801182	1.00[AFR][1000 genomes];0.91[EUR][1000 genomes]
rs72801189	1.00[AFR][1000 genomes]
rs72801196	0.96[EUR][1000 genomes]
rs72801198	1.00[AFR][1000 genomes];0.96[EUR][1000 genomes]
rs72801199	1.00[AFR][1000 genomes];0.96[EUR][1000 genomes]
rs72801200	1.00[AFR][1000 genomes];0.96[EUR][1000 genomes]
rs72803004	1.00[AFR][1000 genomes];0.96[EUR][1000 genomes]
rs72803010	0.96[EUR][1000 genomes]
rs72803016	1.00[AFR][1000 genomes];0.96[EUR][1000 genomes]

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	esv2757799	chr2:56178439-56472394	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	34 gene(s)	inside rSNPs	diseases
2	esv2759051	chr2:56178439-56472394	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	34 gene(s)	inside rSNPs	diseases
3	nsv874162	chr2:56255832-56480571	Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
4	nsv874169	chr2:56383762-56473480	Flanking Bivalent TSS/Enh Active TSS Enhancers Weak transcription Strong transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
5	esv2762648	chr2:56386656-56422448	Bivalent Enhancer Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:56398800-56406000	Weak transcription	Adipose Nuclei	Adipose
2	chr2:56398800-56409200	Weak transcription	Placenta	Placenta
3	chr2:56399600-56404400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr2:56400400-56410200	Weak transcription	HUVEC	blood vessel
5	chr2:56401000-56410600	Weak transcription	Left Ventricle	heart

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