Variant report

Variant	rs36150169
Chromosome Location	chr5:52981720-52981721
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs13079095	1.00[ASN][1000 genomes]
rs13090559	1.00[ASN][1000 genomes]
rs1841733	1.00[ASN][1000 genomes]
rs34584516	1.00[ASN][1000 genomes]
rs34925538	1.00[ASN][1000 genomes]
rs4682026	1.00[ASN][1000 genomes]
rs4682032	1.00[ASN][1000 genomes]
rs62273765	1.00[ASN][1000 genomes]
rs73229188	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2752745	chr5:52422063-53343529	Transcr. at gene 5' and 3' ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
2	nsv1032632	chr5:52667145-53655624	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
3	nsv880868	chr5:52799618-53002783	Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
4	nsv880689	chr5:52847995-53002783	ZNF genes & repeats Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	nsv881604	chr5:52885100-53035301	Weak transcription Genic enhancers Enhancers Active TSS ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	nsv1032504	chr5:52908394-53398435	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
7	nsv537763	chr5:52908394-53398435	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
8	nsv880673	chr5:52965574-53002783	Strong transcription Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
9	nsv881152	chr5:52965574-53028303	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
10	nsv881028	chr5:52965574-53035301	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
11	nsv880806	chr5:52967967-53002783	ZNF genes & repeats Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
12	nsv880377	chr5:52967967-53028303	Strong transcription Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
13	nsv881185	chr5:52967967-53060893	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
14	nsv830298	chr5:52973912-53193398	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:45 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:52929000-52981800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
2	chr5:52940000-52982000	Weak transcription	Skeletal Muscle Male	skeletal muscle
3	chr5:52941400-52985200	Weak transcription	Rectal Smooth Muscle	rectum
4	chr5:52945400-52985000	Weak transcription	Brain Hippocampus Middle	brain
5	chr5:52945600-52983000	Weak transcription	Fetal Muscle Trunk	muscle
6	chr5:52945600-52983600	Weak transcription	Fetal Thymus	thymus
7	chr5:52955800-52982200	Weak transcription	Dnd41	blood
8	chr5:52956000-52982600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr5:52961600-52984200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr5:52961800-52989200	Weak transcription	Ovary	ovary
11	chr5:52963600-52984400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr5:52968000-52983400	Weak transcription	Duodenum Mucosa	Duodenum
13	chr5:52970200-52984800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr5:52973000-52983600	Weak transcription	Brain Anterior Caudate	brain
15	chr5:52974400-52983200	Weak transcription	Spleen	Spleen
16	chr5:52975600-52982400	Weak transcription	Osteobl	bone
17	chr5:52976000-52982400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr5:52976400-52983000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
19	chr5:52977600-52981800	Weak transcription	Brain Substantia Nigra	brain
20	chr5:52978400-52985400	Weak transcription	Primary B cells from cord blood	blood
21	chr5:52979200-52984800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
22	chr5:52979400-52982600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
23	chr5:52979400-52982600	Weak transcription	Duodenum Smooth Muscle	Duodenum
24	chr5:52979600-52982000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
25	chr5:52980000-52983800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr5:52980200-52982000	Weak transcription	Fetal Muscle Leg	muscle
27	chr5:52980200-52982600	Weak transcription	Primary monocytes fromperipheralblood	blood
28	chr5:52980200-52983200	Weak transcription	Monocytes-CD14+_RO01746	blood
29	chr5:52980200-52983800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
30	chr5:52980400-52981800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr5:52980400-52982200	Weak transcription	Left Ventricle	heart
32	chr5:52980400-52982600	Weak transcription	Pancreas	Pancrea
33	chr5:52980400-52983400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr5:52980600-52982200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr5:52980600-52983000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
36	chr5:52980600-52985200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr5:52980600-52985400	Weak transcription	Aorta	Aorta
38	chr5:52980800-52982000	Weak transcription	Primary B cells from peripheral blood	blood
39	chr5:52980800-52982000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr5:52980800-52982600	Weak transcription	HSMM	muscle
41	chr5:52980800-52983200	Weak transcription	Stomach Smooth Muscle	stomach
42	chr5:52980800-52985000	Weak transcription	Primary hematopoietic stem cells	blood
43	chr5:52980800-52985600	Weak transcription	Liver	Liver
44	chr5:52981200-52982000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr5:52981200-52982200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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