Variant report

Variant	rs372463149
Chromosome Location	chr1:186846493-186846494
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 4 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2762854	chr1:186547101-186847574	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
2	nsv872590	chr1:186557453-187500338	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
3	nsv947343	chr1:186846236-186851365	Enhancers Weak transcription Strong transcription	n/a	n/a	inside rSNPs	diseases
4	esv3370350	chr1:186846479-186848527	Enhancers Weak transcription Strong transcription	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:26 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:186839200-186884800	Weak transcription	Duodenum Mucosa	Duodenum
2	chr1:186840400-186849200	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr1:186841000-186853600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
4	chr1:186841000-186853800	Weak transcription	Primary hematopoietic stem cells	blood
5	chr1:186841600-186850200	Weak transcription	Primary monocytes fromperipheralblood	blood
6	chr1:186841800-186846600	Enhancers	Rectal Smooth Muscle	rectum
7	chr1:186841800-186850000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr1:186841800-186862400	Weak transcription	Hela-S3	cervix
9	chr1:186843000-186847600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr1:186843400-186849200	Weak transcription	Cortex derived primary cultured neurospheres	brain
11	chr1:186843400-186853800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr1:186844200-186851600	Weak transcription	HUES64 Cell Line	embryonic stem cell
13	chr1:186844400-186850200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr1:186844800-186846600	Enhancers	Adipose Nuclei	Adipose
15	chr1:186844800-186847000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr1:186844800-186848000	Enhancers	NHEK	skin
17	chr1:186845000-186846600	Enhancers	NHDF-Ad	bronchial
18	chr1:186845200-186851400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
19	chr1:186845200-186856800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr1:186845400-186846800	Enhancers	Colon Smooth Muscle	Colon
21	chr1:186846000-186846600	Strong transcription	Monocytes-CD14+_RO01746	blood
22	chr1:186846000-186847600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr1:186846000-186848400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr1:186846200-186850000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr1:186846400-186847800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr1:186846400-186849200	Weak transcription	Stomach Smooth Muscle	stomach

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