Variant report

Variant	rs147104631
Chromosome Location	chr11:74023446-74023447
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	FOXA2	chr11:74023426-74023763	A549	lung:	n/a	n/a
2	FOXA1	chr11:74023384-74023784	HepG2	liver:	n/a	chr11:74023534-74023549
3	FOS	chr11:74023390-74023660	MCF10A-Er-Src	breast:	n/a	n/a
4	CEBPB	chr11:74023398-74023778	HepG2	liver:	n/a	chr11:74023581-74023592
5	CEBPB	chr11:74023396-74023801	A549	lung:	n/a	chr11:74023581-74023592
6	CEBPB	chr11:74023423-74023752	K562	blood:	n/a	chr11:74023581-74023592
7	POLR2A	chr11:74023390-74023567	MCF10A-Er-Src	breast:	n/a	n/a
8	FOXA1	chr11:74023312-74023660	HepG2	liver:	n/a	chr11:74023534-74023549
9	FOXA1	chr11:74023309-74023699	HepG2	liver:	n/a	chr11:74023534-74023549
10	CEBPB	chr11:74023386-74023824	A549	lung:	n/a	chr11:74023581-74023592
11	FOS	chr11:74023421-74023615	MCF10A-Er-Src	breast:	n/a	n/a
12	CEBPB	chr11:74023438-74023800	MCF-7	breast:	n/a	chr11:74023581-74023592
13	CEBPB	chr11:74023394-74023814	Hela-S3	cervix:	n/a	chr11:74023581-74023592
14	CEBPB	chr11:74023406-74023802	IMR90	lung:	n/a	chr11:74023581-74023592
15	FOS	chr11:74023426-74023662	MCF10A-Er-Src	breast:	n/a	n/a
16	FOXA2	chr11:74023401-74023662	HepG2	liver:	n/a	n/a
17	MYC	chr11:74023402-74023697	MCF10A-Er-Src	breast:	n/a	n/a
18	FOXA1	chr11:74023296-74023641	HepG2	liver:	n/a	chr11:74023534-74023549
19	CEBPB	chr11:74023395-74023856	A549	lung:	n/a	chr11:74023816-74023829 chr11:74023581-74023592
20	FOXA2	chr11:74023306-74023762	A549	lung:	n/a	n/a
21	CEBPB	chr11:74023429-74023756	HepG2	liver:	n/a	chr11:74023581-74023592
22	STAT3	chr11:74023320-74023583	MCF10A-Er-Src	breast:	n/a	n/a

Variant related genes	Relation type
P4HA3	TF binding region

Extended variants
information (count: 7 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2757451	chr11:73842609-74545888	Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Enhancers Genic enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
2	esv2759837	chr11:73842609-74557597	Flanking Active TSS Enhancers Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
3	esv34979	chr11:73878688-74533452	Enhancers Weak transcription Active TSS ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	85 gene(s)	inside rSNPs	diseases
4	esv2758277	chr11:73887567-74557597	Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	85 gene(s)	inside rSNPs	diseases
5	nsv825994	chr11:73936667-74534455	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	83 gene(s)	inside rSNPs	diseases
6	esv3442682	chr11:74019804-74024402	Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	esv3462630	chr11:74022904-74029002	Bivalent Enhancer Flanking Active TSS Enhancers Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:74022600-74023600	Enhancers	Primary neutrophils fromperipheralblood	blood
2	chr11:74023000-74023600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr11:74023000-74023800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr11:74023000-74028600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr11:74023200-74023600	Enhancers	Primary monocytes fromperipheralblood	blood
6	chr11:74023200-74023800	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
7	chr11:74023200-74023800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr11:74023200-74023800	Enhancers	Muscle Satellite Cultured Cells	--
9	chr11:74023200-74023800	Enhancers	Monocytes-CD14+_RO01746	blood
10	chr11:74023200-74027600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr11:74023200-74036800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr11:74023400-74028600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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