Variant report

Variant	rs79037110
Chromosome Location	chr5:37620720-37620721
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1026554	chr5:37112133-37734859	Strong transcription Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases
2	nsv537726	chr5:37112133-37734859	Weak transcription Strong transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases
3	nsv949716	chr5:37179341-37967352	Weak transcription Strong transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	58 gene(s)	inside rSNPs	diseases
4	nsv1015983	chr5:37240827-37666601	Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
5	nsv1021284	chr5:37264275-37630188	ZNF genes & repeats Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
6	nsv1023871	chr5:37330018-37804744	Enhancers Strong transcription Weak transcription Active TSS ZNF genes & repeats Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
7	nsv537729	chr5:37330018-37804744	Weak transcription Flanking Active TSS Strong transcription Genic enhancers Enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
8	nsv432744	chr5:37374124-37743077	ZNF genes & repeats Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
9	nsv1034094	chr5:37406859-37666704	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
10	nsv537731	chr5:37406859-37666704	ZNF genes & repeats Strong transcription Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
11	nsv597846	chr5:37430215-37813591	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
12	nsv880890	chr5:37443079-37681646	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
13	nsv1030250	chr5:37478163-37734859	ZNF genes & repeats Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
14	nsv881383	chr5:37485316-37773877	Strong transcription Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
15	esv3338424	chr5:37620365-37621362	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:56 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:37540000-37621000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr5:37588800-37628000	Weak transcription	Ovary	ovary
3	chr5:37600800-37627200	Weak transcription	Fetal Intestine Small	intestine
4	chr5:37601600-37620800	Weak transcription	Primary hematopoietic stem cells	blood
5	chr5:37601600-37628600	Weak transcription	Brain Hippocampus Middle	brain
6	chr5:37602000-37630800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
7	chr5:37602200-37626200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
8	chr5:37602800-37628000	Weak transcription	Sigmoid Colon	Sigmoid Colon
9	chr5:37603000-37621800	Weak transcription	Primary monocytes fromperipheralblood	blood
10	chr5:37603600-37627600	Weak transcription	Liver	Liver
11	chr5:37603600-37628000	Weak transcription	Thymus	Thymus
12	chr5:37604000-37627200	Weak transcription	Lung	lung
13	chr5:37604800-37625400	Weak transcription	Rectal Mucosa Donor 29	rectum
14	chr5:37604800-37630400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
15	chr5:37605000-37628800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
16	chr5:37605400-37622600	Weak transcription	Fetal Muscle Leg	muscle
17	chr5:37605400-37628800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
18	chr5:37606200-37629000	Weak transcription	Fetal Thymus	thymus
19	chr5:37606400-37637800	Weak transcription	Esophagus	oesophagus
20	chr5:37607200-37628000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr5:37607800-37620800	Weak transcription	GM12878-XiMat	blood
22	chr5:37608200-37627200	Weak transcription	Left Ventricle	heart
23	chr5:37608400-37621000	Weak transcription	Primary B cells from peripheral blood	blood
24	chr5:37608600-37620800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr5:37608600-37626600	Weak transcription	Primary T helper cells PMA-I stimulated	--
26	chr5:37609400-37627400	Weak transcription	Monocytes-CD14+_RO01746	blood
27	chr5:37610000-37627800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
28	chr5:37610200-37624600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
29	chr5:37613800-37637600	Weak transcription	Skeletal Muscle Male	skeletal muscle
30	chr5:37615800-37626200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr5:37615800-37628800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr5:37616200-37621000	Weak transcription	HSMM	muscle
33	chr5:37616200-37622400	Weak transcription	NHDF-Ad	bronchial
34	chr5:37616200-37622800	Weak transcription	Adipose Nuclei	Adipose
35	chr5:37616200-37630200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr5:37616200-37639400	Weak transcription	Fetal Heart	heart
37	chr5:37618600-37629200	Weak transcription	Fetal Intestine Large	intestine
38	chr5:37619200-37620800	Enhancers	Rectal Smooth Muscle	rectum
39	chr5:37619400-37621200	Enhancers	Colon Smooth Muscle	Colon
40	chr5:37619400-37622000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
41	chr5:37619400-37626600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
42	chr5:37619400-37632000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr5:37619600-37627200	Weak transcription	Fetal Stomach	stomach
44	chr5:37619600-37629000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
45	chr5:37619800-37627200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr5:37619800-37629200	Weak transcription	Osteobl	bone
47	chr5:37619800-37630800	Weak transcription	Gastric	stomach
48	chr5:37620200-37621000	Weak transcription	Primary T cells fromperipheralblood	blood
49	chr5:37620200-37629200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr5:37620400-37621200	Strong transcription	Primary B cells from cord blood	blood

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