Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:74136294..74138011-chr15:74140455..74142778,2	MCF-7	breast:

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs10519015	0.83[ASN][1000 genomes]
rs10519016	0.83[ASN][1000 genomes]
rs11632590	0.87[EUR][1000 genomes]
rs11635478	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11636381	0.83[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs11636619	0.98[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs12591658	0.91[EUR][1000 genomes]
rs12592471	0.82[ASN][1000 genomes]
rs1452388	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1452390	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1452391	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs16958333	0.82[ASN][1000 genomes]
rs16958334	0.82[ASN][1000 genomes]
rs16958379	0.82[ASN][1000 genomes]
rs2127016	0.88[EUR][1000 genomes]
rs2127017	0.88[EUR][1000 genomes]
rs2415232	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2415233	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs28493876	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs35127778	0.82[ASN][1000 genomes]
rs35192808	0.82[EUR][1000 genomes]
rs4996372	0.82[ASN][1000 genomes]
rs55841941	0.84[EUR][1000 genomes]
rs56047016	0.84[EUR][1000 genomes]
rs58492359	0.82[ASN][1000 genomes]
rs61319694	0.82[ASN][1000 genomes]
rs74023570	0.82[ASN][1000 genomes]
rs746655	0.82[ASN][1000 genomes]
rs8023384	0.82[ASN][1000 genomes]
rs8030364	0.83[ASN][1000 genomes]
rs8031663	0.82[ASN][1000 genomes]
rs896591	0.90[EUR][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	nsv1043335	chr15:74078689-74241186	Weak transcription Flanking Active TSS Strong transcription Enhancers Bivalent Enhancer Genic enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:74132400-74146600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr15:74134400-74140800	Weak transcription	Fetal Brain Male	brain
3	chr15:74134600-74137000	Weak transcription	Right Atrium	heart
4	chr15:74135000-74137000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr15:74135000-74137000	Weak transcription	H1 Cell Line	embryonic stem cell
6	chr15:74136800-74137400	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr15:74136800-74137400	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr15:74136800-74137400	Enhancers	iPS-18 Cell Line	embryonic stem cell

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