Variant report

(count:20 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	NFIC	chr4:74271609-74277969	HepG2	liver:	n/a	n/a
2	CEBPB	chr4:74272976-74273344	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:74272842-74273336	HepG2	liver:	n/a	n/a
4	NFIC	chr4:74272820-74273524	HepG2	liver:	n/a	n/a
5	POLR2A	chr4:74272841-74273371	HepG2	liver:	n/a	n/a
6	HEY1	chr4:74269686-74276424	HepG2	liver:	n/a	n/a
7	POLR2A	chr4:74270579-74276367	HepG2	liver:	n/a	n/a
8	POLR2A	chr4:74272888-74273621	HepG2	liver:	n/a	n/a
9	POLR2A	chr4:74269720-74276302	HepG2	liver:	n/a	n/a
10	NR2F2	chr4:74272808-74273577	HepG2	liver:	n/a	n/a
11	MBD4	chr4:74271454-74276372	HepG2	liver:	n/a	n/a
12	MBD4	chr4:74269575-74278337	HepG2	liver:	n/a	n/a
13	HEY1	chr4:74271395-74274631	HepG2	liver:	n/a	n/a
14	MYBL2	chr4:74272796-74273364	HepG2	liver:	n/a	n/a
15	TEAD4	chr4:74271474-74275073	HepG2	liver:	n/a	n/a
16	POLR2A	chr4:74271823-74273636	HepG2	liver:	n/a	n/a
17	POLR2A	chr4:74272785-74273658	HepG2	liver:	n/a	n/a
18	MYBL2	chr4:74269121-74276395	HepG2	liver:	n/a	n/a
19	POLR2A	chr4:74271650-74274575	HepG2	liver:	n/a	n/a
20	POLR2A	chr4:74269783-74288816	HepG2	liver:	n/a	n/a

No data

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:74271142..74273142-chr4:74275880..74278467,2	K562	blood:

No data

Variant related genes	Relation type
ALB	TF binding region
ENSG00000163631	Chromatin interaction

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs11933644	0.82[JPT][hapmap]
rs12651581	1.00[CEU][hapmap];0.88[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs56247162	0.88[EUR][1000 genomes]
rs6446927	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs66600903	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs67784283	0.88[EUR][1000 genomes]
rs7678298	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7679277	0.82[JPT][hapmap]

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	esv3430875	chr4:74243646-74420354	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv879490	chr4:74258832-74285223	Enhancers Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 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	chr4:74271600-74283200	Transcr. at gene 5' and 3'	HepG2	liver
2	chr4:74272000-74283400	Transcr. at gene 5' and 3'	Liver	Liver
3	chr4:74272000-74298200	Weak transcription	Pancreas	Pancrea
4	chr4:74272200-74273600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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