Variant report

Variant	rs561869632
Chromosome Location	chr4:55102895-55102896
allele	A/G
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	nsv1008793	chr4:55060925-55535807	Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
2	nsv537098	chr4:55060925-55535807	Enhancers Active TSS Genic enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
3	nsv1002905	chr4:55093677-55115698	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	esv2763361	chr4:55102425-55107618	Strong transcription Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:55100600-55104400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr4:55101000-55103800	Weak transcription	Colonic Mucosa	Colon
3	chr4:55101000-55104200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr4:55101000-55104400	Weak transcription	HMEC	breast
5	chr4:55101000-55105200	Weak transcription	Aorta	Aorta
6	chr4:55101200-55105800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr4:55101200-55106400	Weak transcription	Right Atrium	heart
8	chr4:55101400-55103000	Weak transcription	Cortex derived primary cultured neurospheres	brain
9	chr4:55101400-55103200	Weak transcription	Fetal Stomach	stomach
10	chr4:55101400-55104000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr4:55101400-55104600	Weak transcription	Colon Smooth Muscle	Colon
12	chr4:55101400-55110200	Weak transcription	Fetal Kidney	kidney
13	chr4:55101600-55103400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr4:55102200-55103000	Weak transcription	Fetal Lung	lung
15	chr4:55102200-55105200	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr4:55102400-55103400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr4:55102400-55103800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr4:55102600-55103400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr4:55102600-55103400	Weak transcription	NHLF	lung
20	chr4:55102600-55103600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr4:55102600-55103600	Weak transcription	Osteobl	bone
22	chr4:55102600-55103800	Weak transcription	NHDF-Ad	bronchial
23	chr4:55102600-55106200	Enhancers	Ovary	ovary
24	chr4:55102800-55103000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr4:55102800-55106200	Enhancers	Placenta	Placenta
26	chr4:55102800-55109000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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