Variant report

Variant	rs9960156
Chromosome Location	chr18:7632909-7632910
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs10502358	0.94[YRI][hapmap];0.86[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs16952213	0.83[AMR][1000 genomes]
rs2105669	0.94[LWK][hapmap];0.86[YRI][hapmap];0.91[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs28402175	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28728381	0.83[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs6506522	1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7226532	0.83[AMR][1000 genomes]
rs7230088	0.83[AMR][1000 genomes]
rs7236112	0.94[YRI][hapmap];0.90[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs8091470	0.83[YRI][hapmap]
rs9945442	0.94[YRI][hapmap];0.85[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs9957180	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2656232	chr18:7111033-7658679	Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	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
3	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
4	nsv1063350	chr18:7215275-7659999	Enhancers Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	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
6	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
7	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
8	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
9	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
10	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
11	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
12	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

No data

Chromatin state (count:32 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:7620400-7633400	Weak transcription	Aorta	Aorta
2	chr18:7627200-7636000	Weak transcription	Gastric	stomach
3	chr18:7627200-7637800	Weak transcription	Rectal Smooth Muscle	rectum
4	chr18:7627400-7633000	Weak transcription	HSMM	muscle
5	chr18:7627600-7636600	Weak transcription	Fetal Muscle Leg	muscle
6	chr18:7627800-7633000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr18:7627800-7637200	Weak transcription	NHLF	lung
8	chr18:7627800-7637400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr18:7628200-7633000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr18:7628200-7633000	Weak transcription	A549	lung
11	chr18:7628200-7636000	Weak transcription	Lung	lung
12	chr18:7628400-7635800	Weak transcription	HepG2	liver
13	chr18:7628800-7633000	Enhancers	Skeletal Muscle Male	skeletal muscle
14	chr18:7629000-7646200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr18:7629600-7634200	Enhancers	Left Ventricle	heart
16	chr18:7629600-7634600	Enhancers	Right Ventricle	heart
17	chr18:7630600-7641800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr18:7631000-7636600	Weak transcription	Fetal Lung	lung
19	chr18:7631000-7637400	Weak transcription	Ovary	ovary
20	chr18:7631000-7662800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr18:7632000-7633200	Enhancers	Skeletal Muscle Female	skeletal muscle
22	chr18:7632000-7634400	Enhancers	Psoas Muscle	Psoas
23	chr18:7632200-7633000	Enhancers	Monocytes-CD14+_RO01746	blood
24	chr18:7632200-7633400	Enhancers	Primary monocytes fromperipheralblood	blood
25	chr18:7632200-7636800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr18:7632400-7633000	Enhancers	Fetal Brain Female	brain
27	chr18:7632400-7633200	Enhancers	Primary neutrophils fromperipheralblood	blood
28	chr18:7632600-7633000	Enhancers	Stomach Smooth Muscle	stomach
29	chr18:7632600-7633200	Weak transcription	Right Atrium	heart
30	chr18:7632600-7633600	Enhancers	NHDF-Ad	bronchial
31	chr18:7632800-7633600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr18:7632800-7633800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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