Variant report

Variant	rs184144303
Chromosome Location	chr4:152403065-152403066
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	HNF4A	chr4:152403012-152403275	HepG2	liver:	n/a	chr4:152403166-152403180 chr4:152403166-152403179 chr4:152403165-152403180 chr4:152403165-152403180 chr4:152403165-152403180 chr4:152403165-152403180
2	HNF4G	chr4:152403052-152403272	HepG2	liver:	n/a	chr4:152403166-152403180 chr4:152403166-152403179 chr4:152403165-152403180 chr4:152403165-152403180 chr4:152403165-152403180

Variant related genes	Relation type
FAM160A1	TF binding region

Extended variants
information (count: 8 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv880262	chr4:151712054-152519899	Enhancers Weak transcription Strong transcription Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats 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 target site	53 gene(s)	inside rSNPs	diseases
2	nsv881526	chr4:151968295-152489087	Flanking Active TSS Enhancers Active TSS Strong transcription Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
3	nsv1025192	chr4:152202627-152498890	Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
4	nsv537307	chr4:152202627-152498890	Enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
5	nsv880624	chr4:152280646-152549112	Flanking Bivalent TSS/Enh Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
6	nsv432643	chr4:152335395-152417635	Weak transcription Enhancers Bivalent/Poised TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv881342	chr4:152363772-152560449	Enhancers Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
8	nsv830114	chr4:152401288-152548606	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:25 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:152391800-152405400	Weak transcription	NHEK	skin
2	chr4:152395000-152413200	Weak transcription	Duodenum Mucosa	Duodenum
3	chr4:152396800-152404600	Weak transcription	HSMM	muscle
4	chr4:152396800-152405400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr4:152396800-152405600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr4:152397200-152406600	Weak transcription	Psoas Muscle	Psoas
7	chr4:152400200-152405200	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr4:152400600-152405400	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr4:152400600-152405400	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr4:152401600-152412200	Weak transcription	Ovary	ovary
11	chr4:152402000-152404600	Weak transcription	H1 Cell Line	embryonic stem cell
12	chr4:152402000-152405400	Weak transcription	H9 Cell Line	embryonic stem cell
13	chr4:152402600-152404600	Enhancers	Liver	Liver
14	chr4:152402600-152405800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
15	chr4:152402800-152403200	Enhancers	Fetal Intestine Large	intestine
16	chr4:152402800-152403400	Enhancers	HepG2	liver
17	chr4:152402800-152405400	Enhancers	HUES64 Cell Line	embryonic stem cell
18	chr4:152403000-152403200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
19	chr4:152403000-152403200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr4:152403000-152403200	Enhancers	Fetal Intestine Small	intestine
21	chr4:152403000-152403400	Enhancers	HSMMtube	muscle
22	chr4:152403000-152403800	Weak transcription	Skeletal Muscle Female	skeletal muscle
23	chr4:152403000-152405200	Enhancers	iPS-20b Cell Line	embryonic stem cell
24	chr4:152403000-152405400	Enhancers	HUES6 Cell Line	embryonic stem cell
25	chr4:152403000-152405400	Enhancers	iPS-15b Cell Line	embryonic stem cell

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