Variant report

Variant	rs575292479
Chromosome Location	chr16:12192397-12192398
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

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	nsv905347	chr16:12010444-12243329	Genic enhancers Strong transcription Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
2	nsv1043096	chr16:12013915-12840769	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
3	nsv1043959	chr16:12039346-12285269	Weak transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
4	nsv977111	chr16:12161129-12220593	Weak transcription Strong transcription Bivalent Enhancer Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	nsv1039492	chr16:12176517-12210702	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv571460	chr16:12181702-12238602	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	nsv1052973	chr16:12188092-12307880	ZNF genes & repeats Enhancers Strong transcription Weak transcription Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
8	esv3337175	chr16:12191551-12195249	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:83 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:12178600-12199600	Weak transcription	Aorta	Aorta
2	chr16:12184200-12193000	Enhancers	Fetal Thymus	thymus
3	chr16:12184400-12231200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
4	chr16:12186800-12213400	Weak transcription	Sigmoid Colon	Sigmoid Colon
5	chr16:12188000-12194400	Strong transcription	GM12878-XiMat	blood
6	chr16:12188400-12193600	Enhancers	Placenta	Placenta
7	chr16:12188800-12192400	Enhancers	Fetal Stomach	stomach
8	chr16:12188800-12192400	Enhancers	Rectal Mucosa Donor 31	rectum
9	chr16:12189200-12192400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr16:12189200-12192600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr16:12189200-12192600	Enhancers	Spleen	Spleen
12	chr16:12189600-12192400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr16:12189600-12192400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr16:12189600-12192400	Enhancers	Duodenum Mucosa	Duodenum
15	chr16:12189600-12192800	Enhancers	Brain Inferior Temporal Lobe	brain
16	chr16:12189600-12192800	Enhancers	Fetal Lung	lung
17	chr16:12189600-12193600	Weak transcription	H1 Cell Line	embryonic stem cell
18	chr16:12189600-12194000	Enhancers	Fetal Muscle Leg	muscle
19	chr16:12189600-12194000	Enhancers	Ovary	ovary
20	chr16:12189600-12204000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
21	chr16:12189600-12204800	Weak transcription	Primary hematopoietic stem cells	blood
22	chr16:12189600-12204800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr16:12189800-12192400	Enhancers	Brain Hippocampus Middle	brain
24	chr16:12189800-12192800	Weak transcription	Primary T cells from cord blood	blood
25	chr16:12189800-12192800	Enhancers	Brain Cingulate Gyrus	brain
26	chr16:12189800-12205000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr16:12189800-12209600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
28	chr16:12189800-12220400	Weak transcription	Primary T helper cells fromperipheralblood	blood
29	chr16:12190000-12199600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
30	chr16:12190000-12220200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
31	chr16:12190000-12220400	Weak transcription	Primary T cells fromperipheralblood	blood
32	chr16:12190200-12194400	Strong transcription	Primary B cells from cord blood	blood
33	chr16:12190200-12210600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr16:12190400-12192400	Enhancers	Fetal Kidney	kidney
35	chr16:12190400-12193800	Enhancers	Esophagus	oesophagus
36	chr16:12190600-12192400	Enhancers	Liver	Liver
37	chr16:12190600-12194600	Strong transcription	Monocytes-CD14+_RO01746	blood
38	chr16:12190600-12195800	Strong transcription	Primary B cells from peripheral blood	blood
39	chr16:12190800-12192400	Genic enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr16:12190800-12192400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
41	chr16:12190800-12195000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
42	chr16:12190800-12210600	Weak transcription	Pancreas	Pancrea
43	chr16:12191000-12192800	Enhancers	K562	blood
44	chr16:12191000-12197400	Weak transcription	Pancreatic Islets	Pancreatic Islet
45	chr16:12191200-12192400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
46	chr16:12191200-12192600	Enhancers	iPS-15b Cell Line	embryonic stem cell
47	chr16:12191200-12193600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr16:12191200-12194200	Enhancers	Fetal Muscle Trunk	muscle
49	chr16:12191200-12223200	Weak transcription	Rectal Mucosa Donor 29	rectum
50	chr16:12191400-12193600	Weak transcription	Skeletal Muscle Male	skeletal muscle

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