Variant report

Variant	rs73873370
Chromosome Location	chr4:186686221-186686222
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	FOS	chr4:186686099-186686352	MCF10A-Er-Src	breast:	n/a	chr4:186686261-186686272
2	GATA2	chr4:186685850-186686585	HUVEC	blood vessel:	n/a	chr4:186686425-186686435
3	FOS	chr4:186686040-186686445	MCF10A-Er-Src	breast:	n/a	chr4:186686425-186686434 chr4:186686261-186686272
4	FOS	chr4:186686061-186686400	MCF10A-Er-Src	breast:	n/a	chr4:186686261-186686272
5	STAT3	chr4:186686068-186686349	MCF10A-Er-Src	breast:	n/a	n/a
6	FOS	chr4:186686066-186686413	MCF10A-Er-Src	breast:	n/a	chr4:186686261-186686272
7	FOS	chr4:186685954-186686438	HUVEC	blood vessel:	n/a	chr4:186686425-186686434 chr4:186686261-186686272

Variant related genes	Relation type
SORBS2	TF binding region

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs11937003	1.00[AMR][1000 genomes]
rs58973669	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73873362	1.00[AMR][1000 genomes]
rs73873365	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73873366	1.00[AMR][1000 genomes]
rs73873367	1.00[AMR][1000 genomes]
rs73873373	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv432684	chr4:186412851-186742851	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	nsv1028146	chr4:186503899-187338335	Strong transcription Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
3	nsv1020731	chr4:186512433-186724031	Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv1023917	chr4:186533075-186997806	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	nsv537420	chr4:186533075-186997806	Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
6	nsv830171	chr4:186610113-186789271	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv1023412	chr4:186613289-186707428	Enhancers Weak transcription Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	nsv537421	chr4:186613289-186707428	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
9	nsv427702	chr4:186618031-186782377	Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
10	nsv530178	chr4:186659940-187478310	Bivalent Enhancer Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
11	nsv1015931	chr4:186683165-186734480	Enhancers Genic enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:30 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:186655200-186701400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr4:186661400-186694600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr4:186662200-186688800	Weak transcription	Aorta	Aorta
4	chr4:186664800-186693400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr4:186667600-186691400	Weak transcription	H1 Cell Line	embryonic stem cell
6	chr4:186673000-186714000	Weak transcription	Ovary	ovary
7	chr4:186676600-186694000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr4:186676800-186690800	Weak transcription	Fetal Intestine Small	intestine
9	chr4:186677000-186687200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr4:186677200-186690400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr4:186680600-186702600	Weak transcription	Gastric	stomach
12	chr4:186681000-186688800	Weak transcription	HepG2	liver
13	chr4:186683400-186687200	Enhancers	HUVEC	blood vessel
14	chr4:186683400-186687400	Weak transcription	Liver	Liver
15	chr4:186683400-186690400	Enhancers	Fetal Heart	heart
16	chr4:186683400-186692400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
17	chr4:186683400-186694000	Weak transcription	H9 Cell Line	embryonic stem cell
18	chr4:186683400-186694600	Weak transcription	Rectal Smooth Muscle	rectum
19	chr4:186683400-186695400	Weak transcription	Colon Smooth Muscle	Colon
20	chr4:186683400-186695600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr4:186683600-186687200	Weak transcription	Left Ventricle	heart
22	chr4:186683600-186687200	Weak transcription	Pancreas	Pancrea
23	chr4:186683600-186694200	Weak transcription	HSMM	muscle
24	chr4:186683800-186691400	Weak transcription	HSMMtube	muscle
25	chr4:186683800-186692600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr4:186684600-186687200	Weak transcription	Right Ventricle	heart
27	chr4:186685600-186686600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr4:186685800-186686600	Enhancers	Muscle Satellite Cultured Cells	--
29	chr4:186685800-186686600	Enhancers	Osteobl	bone
30	chr4:186686200-186687200	Weak transcription	NH-A	brain

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