Variant report

(count:1 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ZNF384	chr7:128076371-128076582	GM12878	blood:	n/a	n/a

No data

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

No.	Distal block	Cell Line	Cell type
1	chr7:128075023..128077569-chr7:128095918..128098804,2	K562	blood:
2	chr7:128048480..128050287-chr7:128075489..128078227,2	MCF-7	breast:
3	chr7:128066083..128070069-chr7:128074107..128077404,7	MCF-7	breast:
4	chr7:128066135..128077193-chr7:128094256..128102719,54	MCF-7	breast:
5	chr7:128071934..128079559-chr7:128081793..128086197,10	MCF-7	breast:

No data

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs10228542	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs10239919	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10247945	0.82[EUR][1000 genomes]
rs11562031	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12111997	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs12113427	0.82[EUR][1000 genomes]
rs1560215	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs17152065	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28429588	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4731449	0.82[EUR][1000 genomes]
rs57075087	0.86[EUR][1000 genomes]
rs6978246	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72624928	0.86[EUR][1000 genomes]
rs7779455	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7779818	0.86[AFR][1000 genomes];0.87[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7779945	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7781310	0.81[EUR][1000 genomes]
rs7783540	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7784120	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7784564	0.91[AFR][1000 genomes];0.87[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7806193	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv831124	chr7:127970345-128147910	Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
2	esv1801356	chr7:128073366-128084133	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:128051400-128086200	Weak transcription	Right Atrium	heart
2	chr7:128071800-128078600	Weak transcription	Adipose Nuclei	Adipose
3	chr7:128073800-128083800	Weak transcription	Esophagus	oesophagus
4	chr7:128075000-128076600	Enhancers	Fetal Lung	lung
5	chr7:128075600-128083600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr7:128075600-128093800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr7:128075600-128093800	Weak transcription	Pancreas	Pancrea
8	chr7:128076000-128084000	Weak transcription	HUES64 Cell Line	embryonic stem cell
9	chr7:128076200-128080600	Weak transcription	HUES6 Cell Line	embryonic stem cell
10	chr7:128076200-128081800	Weak transcription	HepG2	liver
11	chr7:128076400-128076800	Enhancers	A549	lung
12	chr7:128076400-128079600	Enhancers	Primary B cells from peripheral blood	blood
13	chr7:128076400-128083400	Weak transcription	Placenta	Placenta
14	chr7:128076400-128083600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr7:128076400-128084000	Weak transcription	iPS-15b Cell Line	embryonic stem cell

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