Variant report

Variant	rs12942993
Chromosome Location	chr17:67080984-67080985
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr17:67074676..67077837-chr17:67079761..67081398,3	K562	blood:
2	chr17:67042180..67045074-chr17:67080026..67082668,2	K562	blood:

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs11077942	0.98[ASN][1000 genomes]
rs11654867	0.99[ASN][1000 genomes]
rs11657954	0.99[ASN][1000 genomes]
rs12453921	0.98[ASN][1000 genomes]
rs12942011	0.99[ASN][1000 genomes]
rs2098034	0.98[ASN][1000 genomes]
rs2302132	0.98[ASN][1000 genomes]
rs2302133	0.98[ASN][1000 genomes]
rs2302290	0.98[ASN][1000 genomes]
rs2364315	0.95[ASN][1000 genomes]
rs4968833	0.99[ASN][1000 genomes]
rs4968995	0.99[ASN][1000 genomes]
rs740517	0.98[ASN][1000 genomes]
rs763920	0.98[ASN][1000 genomes]
rs9914684	0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1067334	chr17:66695039-67221585	Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Enhancers Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
2	nsv543411	chr17:66695039-67221585	Flanking Active TSS Strong transcription Enhancers Weak transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
3	nsv833526	chr17:66980758-67137034	Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
4	nsv1066998	chr17:67060038-67090475	Weak transcription Enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv908705	chr17:67061898-67112456	Weak transcription Enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region lncRNA miRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:41 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:67065600-67088600	Weak transcription	Pancreas	Pancrea
2	chr17:67067200-67099600	Weak transcription	Gastric	stomach
3	chr17:67067200-67111600	Weak transcription	Rectal Mucosa Donor 31	rectum
4	chr17:67071800-67091400	Weak transcription	Brain Anterior Caudate	brain
5	chr17:67074600-67083800	Strong transcription	Skeletal Muscle Female	skeletal muscle
6	chr17:67075200-67081200	Strong transcription	Skeletal Muscle Male	skeletal muscle
7	chr17:67075600-67085600	Strong transcription	Fetal Lung	lung
8	chr17:67076800-67109800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
9	chr17:67077600-67082600	Weak transcription	Brain Angular Gyrus	brain
10	chr17:67077800-67137800	Weak transcription	Brain Inferior Temporal Lobe	brain
11	chr17:67078000-67081200	Strong transcription	Fetal Muscle Leg	muscle
12	chr17:67078400-67081200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
13	chr17:67078600-67081200	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr17:67078600-67081400	Strong transcription	Stomach Smooth Muscle	stomach
15	chr17:67078800-67081000	Weak transcription	Spleen	Spleen
16	chr17:67079000-67082600	Weak transcription	Colonic Mucosa	Colon
17	chr17:67079400-67081000	Weak transcription	Right Ventricle	heart
18	chr17:67079400-67081400	Strong transcription	Ovary	ovary
19	chr17:67079400-67081800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr17:67079400-67084200	Strong transcription	Adipose Nuclei	Adipose
21	chr17:67079400-67087400	Weak transcription	Colon Smooth Muscle	Colon
22	chr17:67079400-67090600	Weak transcription	Fetal Muscle Trunk	muscle
23	chr17:67079400-67093600	Weak transcription	Fetal Stomach	stomach
24	chr17:67079400-67095600	Weak transcription	Psoas Muscle	Psoas
25	chr17:67079400-67112200	Strong transcription	Liver	Liver
26	chr17:67079400-67112600	Weak transcription	Sigmoid Colon	Sigmoid Colon
27	chr17:67079400-67117600	Weak transcription	Esophagus	oesophagus
28	chr17:67079600-67081200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr17:67079600-67081600	Weak transcription	Brain Cingulate Gyrus	brain
30	chr17:67079600-67091600	Weak transcription	Pancreatic Islets	Pancreatic Islet
31	chr17:67079600-67101200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr17:67079600-67114200	Weak transcription	NHDF-Ad	bronchial
33	chr17:67080000-67085000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr17:67080400-67081400	ZNF genes & repeats	Left Ventricle	heart
35	chr17:67080600-67083600	Weak transcription	Lung	lung
36	chr17:67080600-67086600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr17:67080800-67081800	Weak transcription	Duodenum Smooth Muscle	Duodenum
38	chr17:67080800-67088000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr17:67080800-67088600	Weak transcription	GM12878-XiMat	blood
40	chr17:67080800-67090800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
41	chr17:67080800-67112000	Weak transcription	Brain Substantia Nigra	brain

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