Variant report

Variant	rs7179903
Chromosome Location	chr15:45873752-45873753
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:45871737..45874925-chr15:45877626..45879711,4	MCF-7	breast:
2	chr15:45871932..45875099-chr15:45877644..45881217,5	K562	blood:

Variant related genes	Relation type
ENSG00000104164	Chromatin interaction
ENSG00000260170	Chromatin interaction

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs16945097	1.00[ASN][1000 genomes]
rs17627219	1.00[ASN][1000 genomes]
rs1966763	0.98[ASN][1000 genomes]
rs55806911	0.98[ASN][1000 genomes]
rs55913172	0.82[ASN][1000 genomes]
rs55997350	0.84[ASN][1000 genomes]
rs56179992	0.84[ASN][1000 genomes]
rs56304405	0.98[ASN][1000 genomes]
rs57291883	1.00[ASN][1000 genomes]
rs59593563	0.98[ASN][1000 genomes]
rs60351453	0.95[ASN][1000 genomes]
rs60378269	1.00[ASN][1000 genomes]
rs60992352	0.84[ASN][1000 genomes]
rs61209164	0.83[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs68044128	0.98[ASN][1000 genomes]
rs7164956	0.95[ASN][1000 genomes]
rs7165827	0.95[ASN][1000 genomes]
rs7178395	0.93[ASN][1000 genomes]
rs7178879	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7179265	1.00[ASN][1000 genomes]
rs7181436	0.98[ASN][1000 genomes]
rs72711301	0.84[ASN][1000 genomes]
rs72713103	0.84[ASN][1000 genomes]
rs72713104	0.84[ASN][1000 genomes]
rs72713105	0.84[ASN][1000 genomes]
rs72713106	1.00[ASN][1000 genomes]
rs72713107	1.00[ASN][1000 genomes]
rs72713168	0.85[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs72713169	0.81[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs72713171	0.81[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs72713172	0.81[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs72713175	1.00[ASN][1000 genomes]
rs72713177	0.98[ASN][1000 genomes]
rs72713178	0.93[ASN][1000 genomes]
rs72713182	0.95[ASN][1000 genomes]
rs72713185	0.95[ASN][1000 genomes]
rs72713191	0.91[ASN][1000 genomes]
rs72713197	0.82[ASN][1000 genomes]
rs72713199	0.82[ASN][1000 genomes]
rs72713201	0.82[ASN][1000 genomes]
rs72715003	0.82[ASN][1000 genomes]
rs72715005	0.81[ASN][1000 genomes]
rs8025407	0.84[ASN][1000 genomes]
rs8041902	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1045556	chr15:45777396-45884854	Strong transcription Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
2	nsv904188	chr15:45801035-45941689	Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	57 gene(s)	inside rSNPs	diseases
3	nsv904189	chr15:45821158-46298458	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:45866200-45876400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr15:45871600-45875600	Weak transcription	K562	blood
3	chr15:45872400-45875400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
4	chr15:45873400-45878000	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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