Variant report

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ZNF384	chr14:65573881-65574489	K562	blood:	n/a	n/a
2	CEBPD	chr14:65573790-65574434	K562	blood:	n/a	n/a
3	GATA1	chr14:65573738-65574911	K562	blood:	n/a	n/a
4	CEBPD	chr14:65573819-65574433	K562	blood:	n/a	n/a
5	TAL1	chr14:65573908-65574427	K562	blood:	n/a	chr14:65574039-65574047
6	STAT5A	chr14:65573837-65574398	K562	blood:	n/a	n/a
7	MYC	chr14:65574000-65574743	K562	blood:	n/a	n/a
8	GATA1	chr14:65573501-65574399	PBDE	blood:	n/a	chr14:65573675-65573684 chr14:65573678-65573687
9	EP300	chr14:65573765-65574593	K562	blood:	n/a	n/a
10	ARID3A	chr14:65573750-65574459	K562	blood:	n/a	n/a
11	JUND	chr14:65573821-65574765	K562	blood:	n/a	n/a
12	TEAD4	chr14:65573827-65574402	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:65568317..65571529-chr14:65572429..65574819,6	K562	blood:
2	chr14:65568317..65571554-chr14:65571608..65574819,5	K562	blood:

Variant related genes	Relation type
MAX	TF binding region
ENSG00000125952	Chromatin interaction

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs11626796	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs12101257	1.00[CEU][hapmap];0.94[CHB][hapmap];0.89[JPT][hapmap];0.80[YRI][hapmap];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1256415	0.91[ASN][1000 genomes]
rs12588412	0.82[ASN][1000 genomes]
rs12590701	0.83[ASN][1000 genomes]
rs1262269	0.94[ASN][1000 genomes]
rs12895232	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs1953230	0.93[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs1953231	0.93[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs1953233	1.00[CEU][hapmap];0.89[CHB][hapmap];0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1957947	0.89[ASN][1000 genomes]
rs2225676	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2277500	0.93[CHB][hapmap];0.80[ASN][1000 genomes]
rs2781371	0.94[CHB][hapmap];1.00[JPT][hapmap];0.82[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs6573590	0.90[ASN][1000 genomes]
rs7151350	0.88[ASN][1000 genomes]
rs7152879	0.81[CHB][hapmap];0.84[JPT][hapmap]
rs7153893	0.89[CHB][hapmap];0.82[ASN][1000 genomes]
rs8011293	1.00[CEU][hapmap];0.83[CHB][hapmap];0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs945013	0.89[CHB][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.82[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	nsv832816	chr14:65473244-65644645	Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	19 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:65572400-65575000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr14:65572800-65574800	Enhancers	Primary hematopoietic stem cells	blood
3	chr14:65573200-65574800	Enhancers	Primary hematopoietic stem cells short term culture	blood
4	chr14:65573400-65574600	Enhancers	GM12878-XiMat	blood
5	chr14:65573800-65574400	Enhancers	Fetal Heart	heart
6	chr14:65574000-65574400	Enhancers	Dnd41	blood
7	chr14:65574000-65574600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr14:65574000-65574600	Flanking Active TSS	K562	blood
9	chr14:65574200-65574800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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