Variant report

Variant	rs7231089
Chromosome Location	chr18:7750979-7750980
allele	A/C
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	CEBPB	chr18:7750692-7751262	HepG2	liver:	n/a	chr18:7750816-7750833
2	EP300	chr18:7750930-7751346	HepG2	liver:	n/a	n/a
3	TEAD4	chr18:7750909-7751385	HepG2	liver:	n/a	n/a
4	FOXA2	chr18:7750961-7751378	HepG2	liver:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr18:7749744..7751445-chr18:7751627..7754409,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000266767	TF binding region
PTPRM	TF binding region

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs10163760	0.88[ASN][1000 genomes]
rs12165086	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12326071	0.88[ASN][1000 genomes]
rs13380901	0.92[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13381592	1.00[ASN][1000 genomes]
rs1530516	1.00[ASN][1000 genomes]
rs1664980	0.89[ASN][1000 genomes]
rs4121619	0.82[ASN][1000 genomes]
rs613706	0.89[ASN][1000 genomes]
rs629562	0.89[ASN][1000 genomes]
rs6506526	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs679873	0.89[ASN][1000 genomes]
rs7230332	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7231079	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7239716	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73389595	0.88[ASN][1000 genomes]
rs73389600	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73391565	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73939351	0.87[ASN][1000 genomes]
rs8085995	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8089054	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9954459	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:22 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1064597	chr18:7169490-7762738	Active TSS Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv543636	chr18:7169490-7762738	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv534374	chr18:7438812-8412546	Enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
4	nsv458016	chr18:7488133-7934001	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv576399	chr18:7488133-7934001	Weak transcription ZNF genes & repeats Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	esv2762810	chr18:7492090-7924728	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Active TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
7	nsv1062911	chr18:7561991-8088274	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
8	nsv543637	chr18:7561991-8088274	Weak transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
9	nsv1064345	chr18:7562051-8088274	Enhancers Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
10	nsv543638	chr18:7562051-8088274	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
11	nsv1064869	chr18:7730116-7760969	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
12	nsv1061538	chr18:7730116-7762149	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Active TSS Strong transcription	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
13	nsv1067394	chr18:7730116-7768536	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Strong transcription	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
14	esv2656311	chr18:7732141-7761056	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Strong transcription Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
15	nsv1057760	chr18:7732188-7760969	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
16	nsv431970	chr18:7732188-7770950	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Strong transcription	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
17	nsv525328	chr18:7732917-7760498	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
18	nsv576421	chr18:7732917-7761056	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
19	nsv576422	chr18:7732917-7763363	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
20	nsv576423	chr18:7732917-7788329	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
21	nsv576424	chr18:7740473-7761056	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
22	nsv576425	chr18:7747873-7859757	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:57 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:7742000-7751400	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr18:7746800-7751400	Enhancers	Right Ventricle	heart
3	chr18:7746800-7752000	Enhancers	Skeletal Muscle Male	skeletal muscle
4	chr18:7746800-7753600	Enhancers	HepG2	liver
5	chr18:7747000-7752000	Enhancers	Fetal Heart	heart
6	chr18:7748000-7751000	Enhancers	HUVEC	blood vessel
7	chr18:7748200-7751400	Enhancers	Fetal Kidney	kidney
8	chr18:7748400-7751800	Enhancers	A549	lung
9	chr18:7748600-7751400	Enhancers	Skeletal Muscle Female	skeletal muscle
10	chr18:7748600-7752200	Enhancers	Adipose Nuclei	Adipose
11	chr18:7748600-7784000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr18:7749000-7751000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr18:7749200-7751200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr18:7749200-7754400	Weak transcription	Gastric	stomach
15	chr18:7749200-7757000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr18:7749800-7751000	Weak transcription	Ovary	ovary
17	chr18:7749800-7754400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr18:7749800-7754400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr18:7749800-7754400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr18:7749800-7754400	Weak transcription	Small Intestine	intestine
21	chr18:7749800-7754600	Weak transcription	Stomach Smooth Muscle	stomach
22	chr18:7749800-7755000	Weak transcription	Sigmoid Colon	Sigmoid Colon
23	chr18:7750000-7751000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr18:7750000-7752000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr18:7750000-7753600	Weak transcription	Fetal Intestine Small	intestine
26	chr18:7750000-7753800	Weak transcription	Fetal Intestine Large	intestine
27	chr18:7750000-7754200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr18:7750000-7754200	Weak transcription	Osteobl	bone
29	chr18:7750000-7754600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr18:7750000-7760800	Weak transcription	Fetal Stomach	stomach
31	chr18:7750200-7751800	Enhancers	Fetal Lung	lung
32	chr18:7750200-7753800	Weak transcription	Colon Smooth Muscle	Colon
33	chr18:7750200-7754400	Weak transcription	Duodenum Smooth Muscle	Duodenum
34	chr18:7750200-7755000	Weak transcription	HUES64 Cell Line	embryonic stem cell
35	chr18:7750400-7751000	Weak transcription	HUES6 Cell Line	embryonic stem cell
36	chr18:7750400-7751200	Flanking Active TSS	Fetal Thymus	thymus
37	chr18:7750400-7751400	Enhancers	Placenta	Placenta
38	chr18:7750400-7751400	Enhancers	Right Atrium	heart
39	chr18:7750400-7751800	Enhancers	Psoas Muscle	Psoas
40	chr18:7750400-7752000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr18:7750400-7752000	Enhancers	Left Ventricle	heart
42	chr18:7750400-7754400	Weak transcription	NH-A	brain
43	chr18:7750400-7754600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
44	chr18:7750400-7755000	Weak transcription	Rectal Smooth Muscle	rectum
45	chr18:7750600-7751200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr18:7750600-7751400	Enhancers	Pancreas	Pancrea
47	chr18:7750600-7754000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr18:7750600-7754400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
49	chr18:7750600-7756200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr18:7750800-7751000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain

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