Variant report

Variant	rs12606212
Chromosome Location	chr18:7922616-7922617
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr18:7921540..7923960-chr18:7924672..7926506,2	K562	blood:

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs10502365	0.90[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.91[YRI][hapmap];0.98[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11873831	0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12606381	1.00[CEU][hapmap];0.91[CHB][hapmap];0.95[JPT][hapmap];0.83[YRI][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12607648	1.00[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1372061	0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2120320	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2165412	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28854345	0.82[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs55742047	0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs55869040	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs56082106	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7227767	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7237870	1.00[CEU][hapmap];0.94[YRI][hapmap];0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7244035	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs73379961	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs8082717	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs8087211	1.00[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9676009	0.81[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.88[YRI][hapmap];0.94[AMR][1000 genomes];0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]

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	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
2	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
3	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
4	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
5	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
6	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
7	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
8	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:47 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:7905800-7923000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr18:7907800-7926600	Weak transcription	Aorta	Aorta
3	chr18:7916000-7924800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr18:7920600-7925000	Enhancers	HMEC	breast
5	chr18:7921000-7923400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr18:7921600-7923600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr18:7921800-7923000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr18:7921800-7923200	Enhancers	Stomach Mucosa	stomach
9	chr18:7921800-7923400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr18:7921800-7923400	Enhancers	NHDF-Ad	bronchial
11	chr18:7921800-7923400	Enhancers	NHLF	lung
12	chr18:7921800-7923600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr18:7921800-7924400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr18:7922000-7922800	Flanking Active TSS	HUVEC	blood vessel
15	chr18:7922000-7923400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr18:7922000-7923400	Enhancers	Psoas Muscle	Psoas
17	chr18:7922000-7923600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr18:7922000-7924000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr18:7922000-7924800	Enhancers	Placenta	Placenta
20	chr18:7922200-7922800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
21	chr18:7922200-7922800	Flanking Active TSS	NH-A	brain
22	chr18:7922200-7923400	Weak transcription	Pancreatic Islets	Pancreatic Islet
23	chr18:7922200-7923400	Enhancers	Lung	lung
24	chr18:7922200-7923400	Enhancers	Pancreas	Pancrea
25	chr18:7922200-7923400	Enhancers	Right Ventricle	heart
26	chr18:7922200-7923400	Enhancers	Stomach Smooth Muscle	stomach
27	chr18:7922200-7923400	Enhancers	HSMM	muscle
28	chr18:7922200-7924200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr18:7922200-7924400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr18:7922200-7925000	Weak transcription	Rectal Smooth Muscle	rectum
31	chr18:7922200-7925600	Enhancers	Left Ventricle	heart
32	chr18:7922200-7926600	Weak transcription	Skeletal Muscle Male	skeletal muscle
33	chr18:7922400-7922800	Weak transcription	Right Atrium	heart
34	chr18:7922400-7923000	Active TSS	A549	lung
35	chr18:7922400-7923200	Weak transcription	Colon Smooth Muscle	Colon
36	chr18:7922400-7923600	Enhancers	Adipose Nuclei	Adipose
37	chr18:7922400-7923800	Enhancers	Muscle Satellite Cultured Cells	--
38	chr18:7922400-7924200	Enhancers	NHEK	skin
39	chr18:7922400-7925200	Enhancers	HepG2	liver
40	chr18:7922400-7925600	Enhancers	Hela-S3	cervix
41	chr18:7922400-7926000	Weak transcription	Duodenum Smooth Muscle	Duodenum
42	chr18:7922400-7927200	Weak transcription	Skeletal Muscle Female	skeletal muscle
43	chr18:7922400-7940600	Weak transcription	Gastric	stomach
44	chr18:7922600-7922800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr18:7922600-7923200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr18:7922600-7923600	Enhancers	Osteobl	bone
47	chr18:7922600-7925200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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